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Plants, Volume 13, Issue 18 (September-2 2024) – 133 articles

Cover Story (view full-size image): The yield stability of durum wheat (DW), a major Mediterranean crop, is seriously threatened by increased day/night (d/n) temperatures. The introgression of chromosome segments from wild wheat relatives is a promising strategy for coping with heat stress (HS). We explored DW–Thinopyrum spp. introgression lines (ILs) for their physiological response and production ability after intense HS (37/27 °C d/n) applied at anthesis. The work highlights the value of wild germplasm in improving DW’s tolerance to even extreme stress conditions, as ILs carrying Th. ponticum or Th. ponticum/Th. elongatum segments on a DW 7AL arm showed higher relative water content, osmolyte accumulation, and photosynthetic efficiency in flag leaves, as well as better yield performance compared to control lines with no introgression. View this paper
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21 pages, 16292 KiB  
Article
Unveiling the Neem (Azadirachta indica) Effects on Biofilm Formation of Food-Borne Bacteria and the Potential Mechanism Using a Molecular Docking Approach
by Ghada Abd-Elmonsef Mahmoud, Nahed M. Rashed, Sherif M. El-Ganainy and Shimaa H. Salem
Plants 2024, 13(18), 2669; https://doi.org/10.3390/plants13182669 - 23 Sep 2024
Viewed by 1746
Abstract
Biofilms currently represent the most prevalent bacterial lifestyle, enabling them to resist environmental stress and antibacterial drugs. Natural antibacterial agents could be a safe solution for controlling bacterial biofilms in food industries without affecting human health and environmental safety. A methanolic extract of [...] Read more.
Biofilms currently represent the most prevalent bacterial lifestyle, enabling them to resist environmental stress and antibacterial drugs. Natural antibacterial agents could be a safe solution for controlling bacterial biofilms in food industries without affecting human health and environmental safety. A methanolic extract of Azadirachta indica (neem) leaves was prepared and analyzed using gas chromatography–mass spectrometry for the identification of its phytochemical constituents. Four food-borne bacterial pathogens (Bacillus cereus, Novosphingobium aromaticivorans, Klebsiella pneumoniae, and Serratia marcescens) were tested for biofilm formation qualitatively and quantitatively. The antibacterial and antibiofilm properties of the extract were estimated using liquid cultures and a microtiter plate assay. The biofilm inhibition mechanisms were investigated using a light microscope and molecular docking technique. The methanolic extract contained 45 identified compounds, including fatty acids, ester, phenols, flavonoids, terpenes, steroids, and antioxidants with antimicrobial, anticancer, and anti-inflammatory properties. Substantial antibacterial activity in relation to the extract was recorded, especially at 100 μg/mL against K. pneumoniae and S. marcescens. The extract inhibited biofilm formation at 100 μg/mL by 83.83% (S. marcescens), 73.12% (K. pneumoniae), and 54.4% (N. aromaticivorans). The results indicate efficient biofilm formation by the Gram-negative bacteria S. marcescens, K. pneumoniae, and N. aromaticivorans, giving 0.74, 0.292, and 0.219 OD at 595 nm, respectively, while B. cereus was found to have a low biofilm formation potential, i.e., 0.14 OD at 595 nm. The light microscope technique shows the antibiofilm activities with the biofilm almost disappearing at 75 μg/mL and 100 μg/mL concentrations. This antibiofilm property was attributed to DNA gyrase inhibition as illustrated by the molecular docking approach. Full article
(This article belongs to the Special Issue Phytochemical and Biological Activity of Plant Extracts)
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<p>Gas chromatography–mass spectrometry (GC-MS) chromatogram of the methanolic extract of neem (<span class="html-italic">A. indica</span>); numbers above the peaks represented the retention times.</p>
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<p>Qualitative assessment of bacterial biofilm using Congo Red agar medium showing the black color as positive biofilm formation and no color changes as negative biofilm formation.</p>
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<p>Biofilm biomass assessment of <span class="html-italic">B. cereus</span>, <span class="html-italic">N. aromaticivorans</span>, <span class="html-italic">K. pneumoniae</span>, and <span class="html-italic">S. marcescens</span> (OD at 595 nm) using microtiter plate assay.</p>
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<p>Antimicrobial activities of neem (<span class="html-italic">A. indica</span>) extract (10, 25, 50, 75, and 100 μg/mL) against (<b>a</b>): <span class="html-italic">K. pneumoniae</span>, (<b>b</b>): <span class="html-italic">S. marcescens</span>, and (<b>c</b>): <span class="html-italic">N. aromaticivorans</span> bacterial growth comparing with chloramphenicol (CHL) as positive control.</p>
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<p>Antibiofilm efficacy of different concentrations of neem (<span class="html-italic">A. indica</span>) extract on <span class="html-italic">S. marcescens</span>, <span class="html-italic">K. pneumoniae</span>, and <span class="html-italic">N. aromaticivorans</span> as assessed by crystal violet quantification of biofilm. Gentamicin was used as the positive control (PC).</p>
Full article ">Figure 5 Cont.
<p>Antibiofilm efficacy of different concentrations of neem (<span class="html-italic">A. indica</span>) extract on <span class="html-italic">S. marcescens</span>, <span class="html-italic">K. pneumoniae</span>, and <span class="html-italic">N. aromaticivorans</span> as assessed by crystal violet quantification of biofilm. Gentamicin was used as the positive control (PC).</p>
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<p>Light microscopic analysis of <span class="html-italic">Serratia marcescens</span> (Sm-26) biofilm treated with 10, 25, 50, 75, and 100 μg/mL of <span class="html-italic">A. indica</span> methanolic extract compared with the control sample.</p>
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<p>Light microscopic analysis of <span class="html-italic">Klebsiella pneumonia</span> (Kp-38) treated with 10, 25, 50, 75, and 100 μg/mL of <span class="html-italic">A. indica</span> methanolic extract compared with the control sample.</p>
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<p>Light microscopic analysis of <span class="html-italic">Novosphingobium aromaticivorans</span> (ASU 35) treated with 10, 25, 50, 75, and 100 μg/mL of <span class="html-italic">A. indica</span> methanolic extract compared with the control sample.</p>
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<p>Docking models of pseudosolasodine diacetate and 9-oximino-2,7-diethoxyfluorene with DNA gyrase. (<b>A</b>,<b>B</b>) Stick model and surface map of pseudosolasodine diacetate docked model with DNA gyrase; it forms a hydrogen bond with ARG76. (<b>C</b>,<b>D</b>) Stick model and surface map of 9-oximino-2,7-diethoxyfluorene docked model with DNA gyrase; it forms hydrogen bonds with ARG136, THR165, and ASP73.</p>
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<p>Docking models of sarreroside and ergosta-5,22-dien-3-ol, acetate, (3a,22E)- with DNA gyrase. (<b>A</b>,<b>B</b>) Stick model and surface map of sarreroside docked model with DNA gyrase; it forms a hydrogen bond with ASN46. (<b>C</b>,<b>D</b>) Stick model and surface map of Ergosta-5,22-dien-3-ol, acetate, (3a,22E)-docked model with DNA gyrase; it exhibits hydrophobic interactions with VAL43, VAL71, VAL120, ILE78, and ILE90.</p>
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<p>Docking models of cholestan-3-ol, 2-methylene-, (3a,5a)- and estra-1,3,5(10)-trien-17a-ol with DNA gyrase. (<b>A</b>,<b>B</b>) Stick model and surface map of cholestan-3-ol, 2-methylene-, (3a,5a)- docked model with DNA gyrase; it exhibits hydrophobic interactions with VAL71, THR165, and ILE78. (<b>C</b>,<b>D</b>) Stick model and surface map of estra-1,3,5(10)-trien-17a-ol docked model with DNA gyrase; it exhibits hydrophobic interaction with VAL120, VAL167, ILE78, and THR165.</p>
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<p>Surface representation of the superimposed redocked protein–ligand complex on the co-crystalized complex. Redocked ligand is blue, co-crystalized ligand is green.</p>
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41 pages, 5070 KiB  
Review
Insights into Chemical Diversity and Potential Health-Promoting Effects of Ferns
by Ashaimaa Y. Moussa, Jinhai Luo and Baojun Xu
Plants 2024, 13(18), 2668; https://doi.org/10.3390/plants13182668 - 23 Sep 2024
Viewed by 1185
Abstract
The scientific community is focusing on how to enhance human health and immunity through functional foods, and dietary supplements are proven to have a positive as well as a protective effect against infectious and chronic diseases. Ferns act as a taxonomical linkage between [...] Read more.
The scientific community is focusing on how to enhance human health and immunity through functional foods, and dietary supplements are proven to have a positive as well as a protective effect against infectious and chronic diseases. Ferns act as a taxonomical linkage between higher and lower plants and are endowed with a wide chemical diversity not subjected to sufficient scrutinization before. Even though a wealth of traditional medicinal fern uses were recorded in Chinese medicine, robust phytochemical and biological investigations of these plants are lacking. Herein, an extensive search was conducted using the keywords ferns and compounds, ferns and NMR, ferns and toxicity, and the terms ferns and chemistry, lignans, Polypodiaceae, NMR, isolation, bioactive compounds, terpenes, phenolics, phloroglucinols, monoterpenes, alkaloids, phenolics, and fatty acids were utilized with the Boolean operators AND, OR, and NOT. Databases such as PubMed, Web of Science, Science Direct, Scopus, Google Scholar, and Reaxys were utilized to reveal a wealth of information regarding fern chemistry and their health-promoting effects. Terpenes followed by phenolics represented the largest number of isolated active compounds. Regarding the neuroprotective effects, Psilotium, Polypodium, and Dryopteris species possessed as their major phenolics component unique chemical moieties including catechins, procyanidins, and bioflavonoids. In this updated chemical review, the pharmacological and chemical aspects of ferns are compiled manifesting their chemical diversity in the last seven years (2017–2024) together with a special focus on their nutritive and potential health-promoting effects. Full article
(This article belongs to the Section Phytochemistry)
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<p>Polyketide-terpene compounds <b>1-67</b> isolated from ferns (2017–2023). The two chiral centers have the same configuration, denoted as R*. The two chiral centers have opposite configurations, denoted as S*.</p>
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<p>Polyketide compounds <b>68-116</b> isolated from ferns (2017–2023).</p>
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<p>Polyketide compounds <b>117-159</b> isolated from ferns (2017–2023).</p>
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<p>Polyketide compounds <b>160-207</b> isolated from ferns (2017–2023).</p>
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<p>Polyketide compounds <b>208-234</b> isolated from ferns (2017–2023).</p>
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<p>Fatty acid and steroidal compounds <b>236-244</b> isolated from ferns (2017–2023).</p>
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<p>Terpene compounds <b>245-279</b> isolated from ferns (2017–2023).</p>
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<p>Terpene compounds <b>280-320</b> isolated from ferns (2017–2023).</p>
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<p>Terpene compounds isolated from ferns (2017–2023).</p>
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<p>Illustration of ferns’ chemical diversity and biological effects.</p>
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17 pages, 4093 KiB  
Article
Genetic Diversity of Tulipa alberti and T. greigii Populations from Kazakhstan Based on Application of Expressed Sequence Tag Simple Sequence Repeat Markers
by Moldir Yermagambetova, Shyryn Almerekova, Anna Ivashchenko, Yerlan Turuspekov and Saule Abugalieva
Plants 2024, 13(18), 2667; https://doi.org/10.3390/plants13182667 - 23 Sep 2024
Cited by 1 | Viewed by 843
Abstract
The genus Tulipa L., renowned for its ornamental and ecological significance, encompasses a diversity of species primarily concentrated in the Tian Shan and Pamir-Alay Mountain ranges. With its varied landscapes, Kazakhstan harbors 42 Tulipa species, including the endangered Tulipa alberti Regel and Tulipa [...] Read more.
The genus Tulipa L., renowned for its ornamental and ecological significance, encompasses a diversity of species primarily concentrated in the Tian Shan and Pamir-Alay Mountain ranges. With its varied landscapes, Kazakhstan harbors 42 Tulipa species, including the endangered Tulipa alberti Regel and Tulipa greigii Regel, which are critical for biodiversity yet face significant threats from human activities. This study aimed to assess these two species’ genetic diversity and population structure using 15 expressed sequence tag simple sequence repeat (EST-SSR) markers. Leaf samples from 423 individuals across 23 natural populations, including 11 populations of T. alberti and 12 populations of T. greigii, were collected and genetically characterized using EST-SSR markers. The results revealed relatively high levels of genetic variation in T. greigii compared to T. alberti. The average number of alleles per locus was 1.9 for T. alberti and 2.8 for T. greigii. AMOVA indicated substantial genetic variation within populations (75% for T. alberti and 77% for T. greigii). The Bayesian analysis of the population structure of the two species indicated an optimal value of K = 3 for both species, splitting all sampled populations into three distinct genetic clusters. Populations with the highest level of genetic diversity were identified in both species. The results underscore the importance of conserving the genetic diversity of Tulipa populations, which can help develop strategies for their preservation in stressed ecological conditions. Full article
(This article belongs to the Section Plant Genetics, Genomics and Biotechnology)
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<p>Principal coordinate analysis (PCoA) plots for <span class="html-italic">Tulipa alberti</span> populations (<b>A</b>); <span class="html-italic">Tulipa greigii</span> populations (<b>B</b>); and for <span class="html-italic">Tulia alberti</span> and <span class="html-italic">Tulipa greigii</span> populations (<b>C</b>). T.A.—<span class="html-italic">Tulipa alberti</span>; T.Gr.—<span class="html-italic">Tulipa greigii</span>.</p>
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<p>Unweighted pair group method with arithmetic mean (UPGMA) tree constructed from polymorphic EST-SSR loci of <span class="html-italic">Tulipa alberti and Tulipa greigii</span> populations. T.A.—<span class="html-italic">Tulipa alberti</span>; T.Gr.—<span class="html-italic">Tulipa greigii</span>.</p>
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<p>Genetic structure of <span class="html-italic">Tulipa alberti</span> (T.A.) populations. Distribution of <span class="html-italic">Tulipa alberti</span> populations (<b>A</b>); UPGMA tree of <span class="html-italic">Tulipa alberti</span> populations (<b>B</b>); STRUCTURE analysis graphic with the Evanno method showing optimal K = 3 (<b>C</b>); and Bayesian inference clustering of 207 individuals from 11 <span class="html-italic">Tulipa alberti</span> populations (<b>D</b>).</p>
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<p>Genetic structure of <span class="html-italic">Tulipa greigii</span> (T.Gr.) populations. Distribution of <span class="html-italic">T. greigii</span> populations (<b>A</b>); UPGMA tree of <span class="html-italic">T. greigii</span> populations (<b>B</b>); STRUCTURE analysis graphic with the Evanno method showing optimal K = 3 (<b>C</b>); and Bayesian inference clustering of 216 individuals from 12 <span class="html-italic">T. greigii</span> populations (<b>D</b>).</p>
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<p><span class="html-italic">Tulipa alberti</span> (<b>A</b>) and <span class="html-italic">Tulipa greigii</span> (<b>B</b>) species in nature. Photos were taken by Oleg Belyalov.</p>
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<p>Location of sampled <span class="html-italic">Tulipa alberti</span> (<b>A</b>) and <span class="html-italic">Tulipa greigii</span> (<b>B</b>) populations in Kazakhstan. Pop—population; numeration according to <a href="#plants-13-02667-t001" class="html-table">Table 1</a>. T.A.—<span class="html-italic">Tulipa alberti</span>; T.Gr.—<span class="html-italic">Tulipa greigii</span>.</p>
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19 pages, 3319 KiB  
Review
Prion–like Proteins in Plants: Key Regulators of Development and Environmental Adaptation via Phase Separation
by Peisong Wu and Yihao Li
Plants 2024, 13(18), 2666; https://doi.org/10.3390/plants13182666 - 23 Sep 2024
Cited by 1 | Viewed by 1423
Abstract
Prion–like domains (PrLDs), a unique type of low–complexity domain (LCD) or intrinsically disordered region (IDR), have been shown to mediate protein liquid–liquid phase separation (LLPS). Recent research has increasingly focused on how prion–like proteins (PrLPs) regulate plant growth, development, and stress responses. This [...] Read more.
Prion–like domains (PrLDs), a unique type of low–complexity domain (LCD) or intrinsically disordered region (IDR), have been shown to mediate protein liquid–liquid phase separation (LLPS). Recent research has increasingly focused on how prion–like proteins (PrLPs) regulate plant growth, development, and stress responses. This review provides a comprehensive overview of plant PrLPs. We analyze the structural features of PrLPs and the mechanisms by which PrLPs undergo LLPS. Through gene ontology (GO) analysis, we highlight the diverse molecular functions of PrLPs and explore how PrLPs influence plant development and stress responses via phase separation. Finally, we address unresolved questions about PrLP regulatory mechanisms, offering prospects for future research. Full article
(This article belongs to the Special Issue Responses of Plant Molecular Physiology to Environments)
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<p>Gene Ontology (GO) analysis of prion–like protein (PrLP) genes across 10 plant species (Brachypodium distachyon, Hordeum vulgare, Oryza sativa, Sorghum bicolor, Triticum aestivum, Arabidopsis thaliana, Glycine max, Helianthus annuus, Prunus persica, and Solanum lycopersicum). Bubble size represents the number of genes, while color variation represents different <span class="html-italic">p</span>–values.</p>
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<p>Prion−like proteins (PrLPs) regulate plant meristem maintenance and light signaling. (<b>A</b>) STM, BELLs, and MED8 form condensates to maintain the SAM. (<b>B</b>) PLTs form NBs with WOX5 and RNA to control the destiny of the CSC and sustain the RAM. (<b>C</b>) PYCO1 forms pyrenoids to bind rubisco, enhancing the efficiency of CO<sub>2</sub> fixation in photosynthesis. (<b>D</b>) The SWAP/SFPS/RRC1 complex interacts with photobodies to regulate alternative splicing of pre–mRNAs. Diamonds indicate PrLPs; ellipses represent other proteins; dashed circles indicate droplet–like condensates; solid–line circles represent gel–like condensates. BELL: BEL1−like; CSC: columella stem cell; NB: nuclear body; Pfr: physiological active far−red form; phyB: phytochrome B; PLT: PLETHORA; Pr: physiological inactive red form; PYCO1: pyrenoid component 1; RAM: root apical meristem; RRC1: REDUCED RED−LIGHT RESPONSES IN CRY1CRY2 BACKGROUND1; SAM: shoot apical meristem; SFPS: SPLICING FACTOR FOR PHYTOCHROME SIGNALING; snRNP: small nuclear ribonucleoproteins; STM: SHOOT MERISTEMLESS; SWAP1: SUPPRESSOR OF WHITE APRICOT/SURP RNA−BINDING DOMAIN CONTAINING PROTEIN1; WOX5: WUSCHEL−RELATED HOMEOBOX 5.</p>
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<p>Prion–like proteins (PrLPs) regulate plant reproductive growth. (<b>A</b>) PrLPs regulate flowering and fruit development. (<b>B</b>) SPRI2/SRS7 condensates facilitate the development of interspecific reproductive barriers. (<b>C</b>) YTH07 and EHD6 bind to m<sup>6</sup>A–modified mRNA and form condensates to initiate flowering in rice. (<b>D</b>) TMF and TFAM1/2/3/11 form condensates to modulate the development of inflorescences in tomatoes. Diamonds indicate PrLPs; ellipses represent other proteins; dashed circles indicate droplet–like condensates; solid–line circles represent gel–like condensates. AN: ANANTHA; DCP5: DECAPPING 5; EHD6: EARLY HEADING DATE 6; FCA: FLOWERING CONTROL LOCUS A; FLC: FLOWERING LOCUS C; FLD: FLOWERING LOCUS D; FLM: FLOWERING LOCUS M; FRI: FRIGIDA; FRL: FRIGIDA like; FT: FLOWERING LOCUS T; H3K4me1: monomethylated H3K4; H3K27me3: trimethylated H3K27; H3K36me3: trimethylated H3K36; HRLP: hnRNP R–LIKE PROTEIN; LD: LUMINIDEPENDENS; m<sup>6</sup>A: N<sup>6</sup>–methyladenosine; OsCOL4: CONSTANS–like 4; RNA Pol II: RNA polymerase II; SDG26: SET DOMAIN GROUP 26; SPRI2: STIGMATIC PRIVACY 2; SR45: SERINE/ARGININE–RICH 45; SSF: SISTER OF FCA; TFAM: TMF family member; TMF: TERMINATING FLOWER.</p>
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<p>PrLPs regulate plant adaptation to stresses. (<b>A</b>) PrLPs coordinate the plant’s response to abiotic stress. (<b>a</b>,<b>b</b>). PrLPs modulate plant responses to hyperosmotic stress. (<b>b</b>–<b>d</b>). PrLPs modulate plant responses to salt stress. (<b>e</b>,<b>f</b>). PrLPs govern plant responses to heat stress. (<b>B</b>) PrLPs exhibit responses to biotic stressors. (<b>a</b>,<b>b</b>). SGs or PB for immune responses. (<b>c</b>). D–bodies involved in pri–miRNA processing. (<b>d</b>). SGs assemble in response to allelopathic effects. Diamonds indicate PrLPs; ellipses represent other proteins; dashed circles indicate droplet–like condensates. AGO1: ARGONAUTE1; BELL: BEL1–like; CARP9: CONSTITUTIVE ALTERATIONS IN THE SMALL RNA PATHWAYS9; D–body: dicing body; DCL1: Dicer–like1; DCP: DECAPPING; ECT: EVOLUTIONARILY CONSERVED C–TERMINAL REGION; ELF3: EARLY FLOWERING 3; ELF4: EARLY FLOWERING 4; HYL1: Hyponastic Leaves1; m6A: N6–methyladenosine; PA: phenolic acid; PB: processing body; pri–miRNA: primary microRNA; RBP: RNA–binding protein; RBP47B: RNA–binding protein 47B; RH: RNA helicase; RNAi: RNA interference; RNP: ribonucleoprotein; RP: ribosome protein; SA: salicylic acid; SE: SERRATE; SEU: SEUSS; SG: stress granule; SGS3: SUPPRESSOR OF GENE SILENCING 3; STM: SHOOT MERISTEMLESS; TuMV: Turnip mosaic virus; UBP1b: OLIGOURIDYLATE BINDING PROTEIN 1b; VCS: VARICOSE; XRN: 5′–to–3′ exonuclease exoribonuclease.</p>
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16 pages, 4638 KiB  
Essay
Effects of Fertilization and Planting Modes on Soil Organic Carbon and Microbial Community Formation of Tree Seedlings
by Sutong Fan, Yao Tang, Hongzhi Yang, Yuda Hu, Yelin Zeng, Yonghong Wang, Yunlin Zhao, Xiaoyong Chen, Yaohui Wu and Guangjun Wang
Plants 2024, 13(18), 2665; https://doi.org/10.3390/plants13182665 - 23 Sep 2024
Cited by 1 | Viewed by 1537
Abstract
Biochar and organic fertilizer can significantly increase soil organic carbon (SOC) and promote agricultural production, but it is still unclear how they affect forest SOC after. Here, low-quality plantation soil was subjected to four distinct fertilization treatments: (CK, without fertilization; BC, tea seed [...] Read more.
Biochar and organic fertilizer can significantly increase soil organic carbon (SOC) and promote agricultural production, but it is still unclear how they affect forest SOC after. Here, low-quality plantation soil was subjected to four distinct fertilization treatments: (CK, without fertilization; BC, tea seed shell biochar alone; OF, tea meal organic fertilizer alone; BCF, tea seed shell biochar plus tea meal organic fertilizer). Cunninghamia lanceolata (Lamb.) Hook and Cyclobalanopsis glauca (Thunb.) Oersted seedlings were then planted in pots at the ratios of 2:0, 1:1, and 0:2 (SS, SQ, QQ) and grown for one year. The results showed that the BCF treatment had the best effect on promoting seedling growth and increasing SOC content. BCF changed soil pH and available nutrient content, resulting in the downregulation of certain oligotrophic groups (Acidobacteria and Basidiomycetes) and the upregulation of eutrophic groups (Ascomycota and Proteobacteria). Key bacterial groups, which were identified by Line Discriminant Analysis Effect Size analysis, were closely associated with microbial biomass carbon (MBC) and SOC. Pearson correlation analysis showed that bacterial community composition exhibited a positive correlation with SOC, MBC, available phosphorus, seedling biomass, and plant height, whereas fungal community composition was predominantly positively correlated with seedling underground biomass. It suggested that environmental differences arising from fertilization and planting patterns selectively promote microbial communities that contribute to organic carbon formation. In summary, the combination of biochar and organic fertilizers would enhance the improvement and adaptation of soil microbial communities, playing a crucial role in increasing forest soil organic carbon and promoting tree growth. Full article
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<p>The above and below-ground biomass (<b>A</b>) and plant height (<b>B</b>) in potted plants by three plant modes (SS, QQ, SQ) treated with four fertilizations (CK, BC, OF, BCF). Data present means (<span class="html-italic">n</span> = 3) and standard errors. Each bar represents the average of the growth characteristics of two plants planted in the soil with the corresponding fertilization type, for example, the first blue bar represents the average shoot biomass of two <span class="html-italic">Cunninghamia lanceolata</span> seedlings planted in unfertilized soil (CK). Different uppercase and lowercase letters indicate significant differences between different planting patterns and fertilization treatments at <span class="html-italic">p</span> &lt; 0.05 level. (SS, QQ, and SQ represent the planting treatment groups: <span class="html-italic">Cunninghamia lanceolata</span> + <span class="html-italic">Cunninghamia lanceolata</span>, <span class="html-italic">Cyclobalanopsis gilva</span> + <span class="html-italic">Cyclobalanopsis gilva</span>, <span class="html-italic">Cyclobalanopsis gilva</span> + <span class="html-italic">Cunninghamia lanceolata</span>, respectively. CK, BC, OF, and BCF represent the fertilization treatment groups: no fertilizer, biochar alone, organic fertilizer alone, and biochar + organic fertilizer, respectively).</p>
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<p>Alpha diversity of microbial community (mean ± SEM). Fungal (<b>a</b>) and bacterial α diversity (<b>b</b>) in the soil of seedling pots under each treatment (SS, QQ, and SQ represent the planting treatment groups: <span class="html-italic">Cunninghamia lanceolata</span> + <span class="html-italic">Cunninghamia lanceolata</span>, <span class="html-italic">Cyclobalanopsis gilva</span> + <span class="html-italic">Cyclobalanopsis gilva</span>, <span class="html-italic">Cyclobalanopsis gilva</span> + <span class="html-italic">Cunninghamia lanceolata</span>, respectively. CK, BC, OF, and BCF represent the fertilization treatment groups: no fertilizer, biochar alone, organic fertilizer alone, and biochar + organic fertilizer, respectively). The red asterisk and blue asterisk indicate significant diversity among different planting patterns and fertilization treatments, respectively. Note: asterisks denote the significance level. * 0.01 &lt; <span class="html-italic">p</span> &lt; 0.05, ** 0.001 &lt; <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>PCoA analysis of fungal (<b>a</b>) and bacterial (<b>b</b>) community structures in three plantations (SS, QQ, and SQ represent the planting treatment groups: <span class="html-italic">Cunninghamia lanceolata</span> + <span class="html-italic">Cunninghamia lanceolata</span>, <span class="html-italic">Cyclobalanopsis gilva</span> + <span class="html-italic">Cyclobalanopsis gilva</span>, <span class="html-italic">Cyclobalanopsis gilva</span> + <span class="html-italic">Cunninghamia lanceolata</span>, respectively) based on Bray–Curtis distance. PCoA analysis of fungal (<b>c</b>) and bacterial (<b>d</b>) in four ways of fertilization (CK, BC, OF, and BCF represent the fertilization treatment groups: no fertilizer, biochar alone, organic fertilizer alone, and biochar + organic fertilizer, respectively). The ellipse was drawn assuming a multivariate normal distribution (confidence level: 0.95).</p>
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<p>Relative abundance of dominant fungi (<b>a</b>) and bacteria (<b>b</b>). The figure shows the top 10 phyla in relative abundance, with the rest classified as others (SS, QQ, and SQ represent the planting treatment groups: <span class="html-italic">Cunninghamia lanceolata</span> + <span class="html-italic">Cunninghamia lanceolata</span>, <span class="html-italic">Cyclobalanopsis gilva</span> + <span class="html-italic">Cyclobalanopsis gilva</span>, <span class="html-italic">Cyclobalanopsis gilva</span> + <span class="html-italic">Cunninghamia lanceolata</span>, respectively. CK, BC, OF, and BCF represent the fertilization treatment groups: no fertilizer, biochar alone, organic fertilizer alone, and biochar + organic fertilizer, respectively).</p>
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<p>Fungal (<b>a</b>,<b>b</b>) and bacterial (<b>c</b>,<b>d</b>) taxa with different changes in plant pots between fertilization, irrespective of plant species (<b>b</b>,<b>d</b>) and between plant species, irrespective of fertilizer treatment (<b>c</b>,<b>d</b>) as detected by LEfSe analysis. Taxa with absolute LDA scores over 3 and <span class="html-italic">p</span>-values less than 0.05 are shown. The circles radiating from inside to outside represent taxonomic levels from phylum to genus; each small circle at a different taxonomic level represents a taxon at that level, and the diameter of the small circle is proportional to the relative abundance.</p>
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<p>Correlation network analysis showed that soil fungal genera (<b>a</b>) and bacterial genera (<b>b</b>) that have significant correlations with soil biochemical properties. The red and blue lines indicate positive and negative correlations, respectively.</p>
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<p>Pairwise comparisons of soil variables shown with a color gradient representing Pearson’s correlation coefficients. “*” and “**” denote the significance level at 0.01 &lt; <span class="html-italic">p</span> &lt; 0.05, and <span class="html-italic">p</span> &lt; 0.01, respectively. Mantel tests depict the association between taxonomic composition (16 S OTUs, ITS OTUs) and soil variables, as well as seedling growth characteristics. The width of each edge matches Mantel’s r statistic for the equivalent distance correlations. Solid lines indicate significant correlation, and dashed lines indicate insignificant correlation.</p>
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24 pages, 5391 KiB  
Article
Viromes of Monocotyledonous Weeds Growing in Crop Fields Reveal Infection by Several Viruses Suggesting Their Virus Reservoir Role
by Zsuzsanna N. Galbács, Evans Duah Agyemang, György Pásztor, András Péter Takács and Éva Várallyay
Plants 2024, 13(18), 2664; https://doi.org/10.3390/plants13182664 - 23 Sep 2024
Viewed by 1182
Abstract
In 2019, random samples of Panicum miliaceum growing as a weed were surveyed to uncover their virus infections at two locations in Hungary. This pilot study revealed infection with three viruses, two appearing for the first time in the country. As follow-up research, [...] Read more.
In 2019, random samples of Panicum miliaceum growing as a weed were surveyed to uncover their virus infections at two locations in Hungary. This pilot study revealed infection with three viruses, two appearing for the first time in the country. As follow-up research, in the summer of 2021, we collected symptomatic leaves of several monocotyledonous plants in the same locations and determined their viromes using small RNA high-throughput sequencing (HTS). As a result, we have identified the presence of wheat streak mosaic virus (WSMV), barley yellow striate mosaic virus (BYSMV), barley virus G (BVG), and two additional viruses, namely Aphis glycines virus 1 (ApGlV1) and Ljubljana dicistrovirus 1 (LDV1), which are described for the first time in Hungary. New hosts of the viruses were identified: Cynodon dactylon is a new host of BYSMV and LDV1, Echinocloa crus-galli is a new host of BVG, ApGlV1 and LDV1, Sorghum halepense is a new host of ApGlV1, and Panicum miliaceum is a new host of LDV1. At the same time, Zea mays is a new host of ApGlV1 and LDV1. Small RNA HTS diagnosed acute infections but failed to detect persistent ones, which could be revealed using RT-PCR. The infection rates at the different locations and plant species were different. The phylogenetic analyses of the sequenced virus variants suggest that the tested monocotyledonous weeds can host different viruses and play a virus reservoir role. Viral spread from the reservoir species relies on the activity of insect vectors, which is why their management requires an active role in plant protection strategies, which need careful planning in the changing environment. Full article
(This article belongs to the Section Plant Protection and Biotic Interactions)
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Graphical abstract

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<p>Investigation of the mapped viral reads in the case of WSMV. (<b>a</b>) shows the genome organization, while (<b>b</b>) shows the coverage of the viral genome by sRNAs and the size distribution of the viral reads in the indicated libraries. Plots are presented for libraries where the presence of the virus has been detected by RT-PCR. Green marks libraries where sRNA HTS detected the presence of the virus. On (<b>a</b>) CP encodes the coat protein of the virus. On (<b>b</b>) blue marks the small RNAs with sense and red with antisense orientation.</p>
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<p>Investigation of the mapped viral reads in the case of BYSMV (<b>a</b>) shows the genome organization, while (<b>b</b>) shows the coverage of the viral genome by sRNAs and the size distribution of the viral reads in the indicated libraries. Plots are presented for libraries where the presence of the virus has been detected by RT-PCR. Green marks libraries where sRNA HTS detected the presence of the virus. On (<b>a</b>) P and L encode the P and L protein and N-CP is the coat protein of the virus. On (<b>b</b>) blue marks the small RNAs with sense and red with antisense orientation.</p>
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<p>Investigation of the mapped viral reads in the case of BVG (<b>a</b>) shows the genome organization, while (<b>b</b>) shows the coverage of the viral genome by sRNAs and the size distribution of the viral reads in the viral reads in the indicated libraries. Plots are presented for libraries where the presence of the virus has been detected by RT-PCR. Green marks libraries where sRNA HTS detected the presence of the virus. On (<b>a</b>) P0 and P1 encodes the P0 and P1 protein, RdRP is the RNA-dependent RNA polymerase, MP is the movement protein, and CP is the coat protein of the virus. On (<b>b</b>) blue marks the small RNAs with sense and red with antisense orientation.</p>
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<p>The investigation of the mapped viral reads in the case of ApGlV1 (<b>a</b>) shows the genome organization, while (<b>b</b>) shows the coverage of the viral genome by sRNAs and the size distribution of the viral reads in the indicated libraries. Plots are presented for libraries where the presence of the virus has been detected by RT-PCR. Green marks the libraries where sRNA HTS detected the presence of the virus. On (<b>a</b>) VP4 and VP3 encodes the P4 and P3 protein, and RdRP is the RNA-dependent RNA polymerase of the virus. On (<b>b</b>) blue marks the small RNAs with sense and red with antisense orientation.</p>
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<p>The investigation of the mapped viral reads in the case of LDV1 (<b>a</b>) shows the genome organization, while (<b>b</b>) shows the coverage of the viral genome by sRNAs and the size distribution of the viral reads in the indicated libraries. Plots are presented for libraries where the presence of the virus has been detected by RT-PCR. Green marks libraries where sRNA HTS detected the presence of the virus. On (<b>a</b>) RdRP encodes the RNA-dependent RNA polymerase, and CP is the coat protein of the virus. On (<b>b</b>) blue marks the small RNAs with sense and red with antisense orientation.</p>
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<p>Virus diagnostics using RT-PCR and virus-specific primers. Circles indicate positive results, green when Sanger sequencing confirmed the presence of the virus, and red when Sanger sequencing did not confirm the RT-PCR result. Each library is represented only by one circle. Filled circles show cases with the same sRNA HTS result. M—stands for a GenRuler 100 bpPlus, used as a molecular marker. ÚS—Újmajor susnyás; U—Újmajor; BA—Büdös árok; M—<span class="html-italic">P. miliaceum</span>; ECG—<span class="html-italic">E. crus-galli</span>; SV—<span class="html-italic">S. viridis</span>; CD—<span class="html-italic">C. dactylon</span>; Ma—<span class="html-italic">Z. mays</span>. K− is the negative control, while K+ is the positive control.</p>
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<p>Virus diagnostics using RT-PCR to test the presence of WSMV in the sampled individuals amplifying a 755 bp long part of the WSMV genome using WSMV_8499F and WSMV_9253R primers (Sequences are available in <a href="#app1-plants-13-02664" class="html-app">Table S4</a>). M—stands for a GenRuler 100 bpPlus, used as a molecular marker. K− is the negative, while K+ is the positive control. Red indicates positive individuals. The codes of the sRNA HTS libraries and the numbered individuals are marked based on <a href="#plants-13-02664-t0A1" class="html-table">Table A1</a>. The infection rate of the plant species is also indicated.</p>
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<p>The phylogenetical analysis of the WSMV strains originating from BA and US. The phylogenetic tree was constructed based on the 755 nt long amplified and Sanger-sequenced, polyprotein-encoding (containing CP coding) part of the viral genome using the Neighbour-Joining analysis and the Jukes–Cantor model, with 1000x bootstrap replications. Bars represent 4% nucleotide diversity. Sequences originating from our previous study are marked with circles, while sequences from this study are marked with stars. Green represents US, while blue represents BA. Sequences of the different strains are marked with their GenBank accession numbers, host species, and countries of origin. HU—Hungary, CZ—Czechia; PL—Poland; RU—Russia; FR—France; TR—Turkey; NA—North America; IR—Iran. Green—US, blue—BA. ONMV—Oat necrotic mottle virus, used as an outgroup to root the tree.</p>
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<p>Virus diagnostics using RT-PCR to test the presence of BYSMV in the sampled individuals, amplifying a 1287 bp long part of the BYSMV genome using BYSMV_158F and BYSMV_1444R primers (sequences are available in <a href="#app1-plants-13-02664" class="html-app">Table S4</a>). M stands for a GenRuler 100 bpPlus, used as a molecular marker. K− is the negative control, while K+ is the positive control. Red indicates positive individuals The codes of the sRNA HTS libraries and the numbered individuals are marked based on <a href="#plants-13-02664-t0A1" class="html-table">Table A1</a>. The infection rate of the plant species is also indicated.</p>
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<p>Phylogenetic analysis of the BYSMV strains originating from BA and US. The phylogenetic tree was constructed based on the 1287 nt long amplified and Sanger-sequenced, CP-coding part of the viral genome using Neighbour-Joining analysis and the Jukes–Cantor model, with 1000x bootstrap replications. Bars represent 4% nucleotide diversity. Sequences originating from our previous study are marked with circles, while sequences from this study are marked with stars. Green represents US, while blue represents BA. Sequences of the different strains are marked with their GenBank accession numbers, host species, and countries of origin. HU—Hungary. MSSV—maize sterile stunt virus (MSSV), used as an outgroup to root the tree.</p>
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<p>Virus diagnostics using RT-PCR to test the presence of BVG in the sampled individuals. amplifying a 523 bp long part of the BVG genome using BVG_700F and BVG_1223R in cases of 1_M_US and 5_M_BA and a 607 bp long part of the BVG genome using BVG_3508F and BVG_4115R primers in case of 6_ECGSV_BA (sequences are available in <a href="#app1-plants-13-02664" class="html-app">Table S4</a>). M stands for a GenRuler 100 bpPlus, used as a molecular marker. K− is the negative control, while K+ is the positive control. Red indicates positive individuals. The codes of the sRNA HTS libraries and the numbered individuals are marked based on <a href="#plants-13-02664-t0A1" class="html-table">Table A1</a>. The infection rate of the plant species is also indicated.</p>
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<p>Phylogenetic analysis of the BVG strains originating from BA and US. The phylogenetic tree was constructed based on (<b>a</b>) nearly full (5362 nt long) BVG genomes and (<b>b</b>) on the 608 bp long amplified and Sanger-sequenced, CP-coding part of the viral genome using the Neighbour-Joining analysis and the Jukes–Cantor model, with 1000x bootstrap replications. Bars represent (<b>a</b>) 7% and (<b>b</b>) 0.3% nucleotide diversity. Sequences originating from our previous study are marked with circles, while sequences from this study are marked with stars. Green represents US, while blue represents BA. Sequences of the different strains are marked with their GenBank accession numbers, host species, and countries of origin. GR—Great Britain; SLo—Slovenia; FR—France; HU—Hungary; N—the Netherlands; SKo—South Korea; AUS—Australia; D—Germany. MYDWV—Maize yellow dwarf virus, used as an outgroup to root the tree.</p>
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<p>Virus diagnostics using RT-PCR to test the presence of ApGlV1 in the sampled individuals amplifying a 906 bp long part of the ApGlV1 genome using ApGlV1_439F and ApGlV1_1323R primers (sequences are available in <a href="#app1-plants-13-02664" class="html-app">Table S4</a>). M stands for a GenRuler 100 bpPlus, used as a molecular marker. K− is the negative control, while K+ is the positive control. Red indicates positive individuals. The codes of the sRNA HTS libraries and the numbered individuals are marked based on <a href="#plants-13-02664-t0A1" class="html-table">Table A1</a>. The infection rate of the plant species is also indicated.</p>
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<p>Phylogenetic analysis of the ApGlV1 strains originating from U and BA. The phylogenetic tree was constructed based on the 906 nt long amplified and Sanger-sequenced, VP4/VP3-coding part of the viral genome using the Neighbour-Joining analysis and the Jukes–Cantor model, with 1000x bootstrap replications. Bars represent 1% nucleotide diversity. Sequences originating from this study are indicated with stars. Green represents US, while blue represents BA. Sequences of the different strains are marked with GenBank accession numbers, host species, and countries of origin. SLo—Slovenia; POR—Portugal; HU—Hungary. PP791011—Tetranychus truncatus picorna-like virus 2 (TTPV2), used as an outgroup to root the tree.</p>
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<p>Virus diagnostics using RT-PCR to test the presence of LDV1 in the sampled individuals amplifying an 838 bp long part of the LDV1 genome using LDV1_5664F and LDV1_6480R primers (sequences are available in <a href="#app1-plants-13-02664" class="html-app">Table S4</a>). M stands for a GenRuler 100 bpPlus, used as a molecular marker. K− is the negative control, while K+ is the positive control. Red indicates positive individuals. The codes of the sRNA HTS libraries and the numbered individuals are marked based on <a href="#plants-13-02664-t0A1" class="html-table">Table A1</a>. The infection rate of the plant species is also indicated.</p>
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<p>Phylogenetic analysis of the LDV1 strains originating from US and BA. The phylogenetic tree was constructed based on the 838 nt long amplified and the Sanger-sequenced part of the viral genome, encoding the end of the viral RdRP and the beginning of the CP, using the Neighbour-Joining analysis and the Jukes–Cantor model, with 1000x bootstrap replications. Bars represent 4% nucleotide diversity. Sequences originating from this study are indicated with stars. Green represents US, while blue represents BA. Sequences of the different strains are marked with their GenBank accession numbers, host species, and countries of origin. SLo—Slovenia; HU—Hungary. MN231041—Bemisia-associated dicistrovirus 2 (BaDCV2), used as an outgroup to root the tree.</p>
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16 pages, 5278 KiB  
Article
A Flowering Morphological Investigation, Fruit Fatty Acids, and Mineral Elements Dynamic Changes of Idesia polycarpa Maxim
by Yanpeng Wang, Cuiyu Liu, Jiasong Hu, Kaiyun Wu, Bangchu Gong and Yang Xu
Plants 2024, 13(18), 2663; https://doi.org/10.3390/plants13182663 - 23 Sep 2024
Cited by 1 | Viewed by 817
Abstract
Idesia polycarpa Maxim is a high-value species of fruit oil with edible, abundant linoleic acid and polyphenols. Idesia polycarpa is described as a dioecious species, and the flowers are male; female and bisexual flowers are produced on separate plants. In order to explore [...] Read more.
Idesia polycarpa Maxim is a high-value species of fruit oil with edible, abundant linoleic acid and polyphenols. Idesia polycarpa is described as a dioecious species, and the flowers are male; female and bisexual flowers are produced on separate plants. In order to explore the flower types of Idesia polycarpa, the morphology of its flowers and inflorescence were investigated in this study. The flower and inflorescence types, the diameter, and the flowering sequencing in male and female inflorescence were determined. We also detected the length, width, and fresh weight of leaves, shoots, and female inflorescence, as well as the length and fresh weight of the petiole during the development. Additionally, we compared the length, width, the length/width ratio, and the flowering density between 5- and 7-year-old female trees. The phenological period observation of Idesia polycarpa showed that the development process can be roughly divided into 12 stages, including bud burst, leaf expansion, inflorescence growth, initial flowering, full flowering, flower decline, initial fruiting, fruit enlargement, fruit color change, fruit ripening, post-ripening of fruit, and leaf fall periods. Furthermore, four elites’ fruit determined the oil content and the composition of fatty acid content during the development. The dynamic of fatty acids contents, the palrnitic acid, palmitoleic acid, stearic acid, oleic acid, and linolenic acid contents were detected during the fruit development of four elites. Moreover, the mineral elements content of fruit of four elites during development were determined. The patterns of vegetative and reproductive growth in young dioecious trees of Idesia polycarpa provided the theoretical basis for artificial pruning and training. Full article
(This article belongs to the Section Plant Development and Morphogenesis)
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<p>Diameter of the flower aspects of different flower types of <span class="html-italic">Idesia polycarpa</span>. (<b>A</b>): male flower; (<b>B</b>–<b>F</b>): bisexual flowers. Red arrow: stamen, blue arrow: pistil. (<b>G</b>): female flower; (<b>H</b>): determination of the flower diameter of different flower types during flowering. FT1: female flower; FT2: male flower; FT3–5: different types of bisexual flowers; (<b>I</b>): the morphological observation of male and female flowers during different development. Horizontal first row: male flower, horizontal second row: female flower. (<b>J</b>): diameter of different types of flowers during flowering.</p>
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<p>The determination of leaf, petiole, and shoot during development. (<b>A</b>): the length, width and fresh weight of leaves during the growing periods, (<b>B</b>): the length and fresh weight of the petiole during the growing periods, (<b>C</b>): the length, diameter and fresh weight of shoots during the growing periods.</p>
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<p>Different types of inflorescences of <span class="html-italic">Idesia polycarpa</span>. (<b>A</b>): the inflorescence of female flowers; (<b>B</b>): the inflorescence is mainly female flowers, with a small amount of bisexual flowers; (<b>C</b>): the inflorescence of mainly female flowers, with a small amount of male flowers and less bisexual flowers; (<b>D</b>): the inflorescence is mainly bisexual flowers, with a small amount of female and male flowers; (<b>E</b>): the inflorescence of bisexual flowers; (<b>F</b>): the inflorescence is mainly bisexual flowers, with less male flowers; (<b>G</b>): the inflorescence is half bisexual flowers and half male flowers; (<b>H</b>): the inflorescence is mainly male flowers, with less bisexual flowers; (<b>I</b>): the inflorescence of male flowers. (<b>J</b>): male inflorescence; (<b>K</b>): female inflorescence; (<b>L</b>): the length, width and fresh weight of inflorescence during development; (<b>M</b>): the transverse diameter and longitudinal diameter of fruit in different time during development.</p>
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<p>The fruit fatty acid content in fruit of four elites of <span class="html-italic">Idesia polycarpa</span> during development. Different letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) within the different lines.</p>
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<p>Dynamic changes in fatty acid composition contents in different <span class="html-italic">Idesia polycarpa</span> elites during fruit development. (<b>A</b>): Palrnitic acid (C16:0), (<b>B</b>): palmitoleic acid (C16:1), (<b>C</b>): stearic acid (C18:0), (<b>D</b>): oleic acid (C18:1), (<b>E</b>): linoleic acid (C18:2), (<b>F</b>): linolenic acid (C18:3). Different letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) within the different lines.</p>
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<p>The dynamic of mineral elements in four elites’ fruit during the development. (<b>A</b>): N content, (<b>B</b>): P content, (<b>C</b>): K content, (<b>D</b>): Ca content, (<b>E</b>): Mg content, (<b>F</b>): Fe content, (<b>G</b>): Mn content, (<b>H</b>): Cu content, (<b>I</b>): Zn content. Different letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) within the different lines.</p>
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20 pages, 1768 KiB  
Review
Sesame, an Underutilized Oil Seed Crop: Breeding Achievements and Future Challenges
by Saeed Rauf, Taiyyibah Basharat, Adane Gebeyehu, Mohammed Elsafy, Mahbubjon Rahmatov, Rodomiro Ortiz and Yalcin Kaya
Plants 2024, 13(18), 2662; https://doi.org/10.3390/plants13182662 - 23 Sep 2024
Viewed by 3360
Abstract
Sesame seeds and their edible oil are highly nutritious and rich in mono- and polyunsaturated fatty acids. Bioactive compounds such as sterols, tocopherols, and sesamol provide significant medicinal benefits. The high oil content (50%) and favorable mono- and polyunsaturated fatty acid balance, as [...] Read more.
Sesame seeds and their edible oil are highly nutritious and rich in mono- and polyunsaturated fatty acids. Bioactive compounds such as sterols, tocopherols, and sesamol provide significant medicinal benefits. The high oil content (50%) and favorable mono- and polyunsaturated fatty acid balance, as well as resilience to water stress, make sesame a promising candidate crop for global agricultural expansion. However, sesame production faces challenges such as low yields, poor response to agricultural inputs, and losses due to capsule dehiscence. To enhance yield, traits like determinate growth, dwarfism, a high harvest index, non-shattering capsules, disease resistance, and photoperiod sensitivity are needed. These traits can be achieved through variation or induced mutation breeding. Crossbreeding methods often result in unwanted genetic changes. The gene editing CRISPR/Cas9 technology has the potential to suppress detrimental alleles and improve the fatty acid profile by inhibiting polyunsaturated fatty acid biosynthesis. Even though sesame is an orphan crop, it has entered the genomic era, with available sequences assisting molecular breeding efforts. This progress aids in associating single-nucleotide polymorphisms (SNPs) and simple sequence repeats (SSR) with key economic traits, as well as identifying genes related to adaptability, oil production, fatty acid synthesis, and photosynthesis. Additionally, transcriptomic research can reveal genes involved in abiotic stress responses and adaptation to diverse climates. The mapping of quantitative trait loci (QTL) can identify loci linked to key traits such as capsule size, seed count per capsule, and capsule number per plant. This article reviews recent advances in sesame breeding, discusses ongoing challenges, and explores potential strategies for future improvement. Hence, integrating advanced genomic tools and breeding strategies provides promising ways to enhance sesame production to meet global demands. Full article
(This article belongs to the Section Plant Genetic Resources)
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<p>Flow chart of activities related to sesame breeding and germplasm conservation.</p>
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<p>Cluster and phylogenetic analysis among various accessions of <span class="html-italic">Glycine max</span>, <span class="html-italic">Sesamum indicum</span>, and <span class="html-italic">Helianthus annuus</span> based on the <span class="html-italic">FAD2</span> gene. Phylogenetic analysis was based on the sequence homology of FAD2 transcripts downloaded from gene bank <a href="https://www.ncbi.nlm.nih.gov/genbank/" target="_blank">https://www.ncbi.nlm.nih.gov/genbank/</a>, accessed on 9 May 2024 and analyzed through MEGA X software.</p>
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<p>Sesame wilting syndrome after delayed irrigation (<b>A</b>), under high temperature (<b>B</b>), high-temperature effects on sesame causing stunted growth, flower shedding, and mal capsule formation (<b>C</b>), and sesame pod rotting in humid conditions (<b>D</b>). Phyllody disease causing the conversion of the capsule into a flower-like structure (<b>E</b>) and the sesame crop affected by the weed infestation (<span class="html-italic">Cucumis callosus</span>) causing the suppression of pod formation during the reproductive phase (<b>F</b>).</p>
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<p>Sesame wilting syndrome after delayed irrigation (<b>A</b>), under high temperature (<b>B</b>), high-temperature effects on sesame causing stunted growth, flower shedding, and mal capsule formation (<b>C</b>), and sesame pod rotting in humid conditions (<b>D</b>). Phyllody disease causing the conversion of the capsule into a flower-like structure (<b>E</b>) and the sesame crop affected by the weed infestation (<span class="html-italic">Cucumis callosus</span>) causing the suppression of pod formation during the reproductive phase (<b>F</b>).</p>
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22 pages, 12133 KiB  
Article
Abiotic Stress Effect on Agastache mexicana subsp. mexicana Yield: Cultivated in Two Contrasting Environments with Organic Nutrition and Artificial Shading
by Judith Morales-Barrera, Juan Reséndiz-Muñoz, Blas Cruz-Lagunas, José Luis Fernández-Muñoz, Flaviano Godínez-Jaimes, Tania de Jesús Adame-Zambrano, Mirna Vázquez-Villamar, Teollincacihuatl Romero-Rosales, María Teresa Zagaceta-Álvarez, Karen Alicia Aguilar-Cruz, Jorge Estrada-Martínez and Miguel Angel Gruintal-Santos
Plants 2024, 13(18), 2661; https://doi.org/10.3390/plants13182661 - 23 Sep 2024
Cited by 1 | Viewed by 797
Abstract
Research on medicinal plants is essential for their conservation, propagation, resistance to environmental stress, and domestication. The use of organic nutrition has been demonstrated to improve soil fertility and plant quality. It is also important to study the effects of the Basic Cation [...] Read more.
Research on medicinal plants is essential for their conservation, propagation, resistance to environmental stress, and domestication. The use of organic nutrition has been demonstrated to improve soil fertility and plant quality. It is also important to study the effects of the Basic Cation Saturation Ratio (BCSR) approach, which is a topic where there is currently controversy and limited scientific information. Evaluating the growth and yields of Agastache mexicana subsp. mexicana (Amm) in different environments is crucial for developing effective propagation and domestication strategies. This includes examining warm and subhumid environments with rain in summer in comparison to mild environments with summer rain. Significant differences were observed in the effects of cold, waterlogging, and heat stresses on the plant’s biomass yield and the morphometric-quantitative modeling by means of isolines. The biomass yield was 56% higher in environment one compared to environment two, 19% higher in environment one with organic nutrition, and 48% higher in environment two with organic nutrition compared to using only BCSR nutrition. In the second harvesting cycle, the plants in environment one did not survive, while the plants in environment two managed to survive without needing additional nutrition. Statistical and mathematical analyses provided information about the population or sample. Additionally, further analysis using isolines as a new approach revealed new insights into understanding phenology and growth issues. Full article
(This article belongs to the Special Issue Abiotic Stress Responses in Plants)
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<p>Shows the temperature and relative humidity profiles (maximum and minimum), for both environments: (<b>a</b>) Temperature in E1, (<b>b</b>) Temperature in E2, (<b>c</b>) RH in E1, (<b>d</b>) RH in E2.</p>
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<p>Isolines of L<sub>N</sub>, obtained through relationship RH and Temperature; (<b>a</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>b</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>c</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>3</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>d</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>4</mn> </mrow> </msub> </mrow> </semantics></math>.</p>
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<p>Isolines for relationship among H<sub>Pl</sub>, temperature and L<sub>N</sub>, (<b>a</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>b</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>c</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>3</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>d</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>4</mn> </mrow> </msub> </mrow> </semantics></math>.</p>
Full article ">Figure 3 Cont.
<p>Isolines for relationship among H<sub>Pl</sub>, temperature and L<sub>N</sub>, (<b>a</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>b</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>c</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>3</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>d</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>4</mn> </mrow> </msub> </mrow> </semantics></math>.</p>
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<p>Isolines for relationship among H<sub>Pl</sub>, RH, and L<sub>N</sub>: (<b>a</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>b</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>c</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>3</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>d</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>4</mn> </mrow> </msub> </mrow> </semantics></math>.</p>
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<p>Isolines for relationship among H<sub>Pl</sub>, Crops time, and L<sub>N</sub>: (<b>a</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>b</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>c</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>3</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>d</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>4</mn> </mrow> </msub> </mrow> </semantics></math>.</p>
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<p>Isolines for relationship among H<sub>Pl</sub>, B<sub>N</sub>, and L<sub>N</sub>: (<b>a</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>b</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>c</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>3</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>d</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>4</mn> </mrow> </msub> </mrow> </semantics></math>.</p>
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<p>Isolines for relationship among H<sub>Pl</sub>, SS<sub>N</sub>, and L<sub>N</sub>: (<b>a</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>b</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>c</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>3</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>d</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>4</mn> </mrow> </msub> </mrow> </semantics></math>.</p>
Full article ">Figure 7 Cont.
<p>Isolines for relationship among H<sub>Pl</sub>, SS<sub>N</sub>, and L<sub>N</sub>: (<b>a</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>b</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>c</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>3</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>d</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>4</mn> </mrow> </msub> </mrow> </semantics></math>.</p>
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<p>Isolines for relationship among H<sub>Pl</sub>, I<sub>N</sub>, and L<sub>N</sub>: (<b>a</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>b</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>c</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>3</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>d</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>4</mn> </mrow> </msub> </mrow> </semantics></math>.</p>
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<p>Isolines for relationship among H<sub>Pl</sub>, D<sub>T</sub>, and L<sub>N</sub>: (<b>a</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>b</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>c</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>3</mn> </mrow> </msub> </mrow> </semantics></math>, (<b>d</b>) <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>τ</mi> </mrow> <mrow> <mn>4</mn> </mrow> </msub> </mrow> </semantics></math>.</p>
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17 pages, 4491 KiB  
Article
Comparative Analysis of Water Stress Regimes in Avocado Plants during the Early Development Stage
by Tatiana Rondon, Manuel Guzmán-Hernández, Maria C. Torres-Madronero, Maria Casamitjana, Lucas Cano, July Galeano and Manuel Goez
Plants 2024, 13(18), 2660; https://doi.org/10.3390/plants13182660 - 23 Sep 2024
Viewed by 1084
Abstract
The avocado cv. Hass requires a suitable rootstock for optimal development under water stress. This study evaluated the performance of two avocado rootstocks (ANRR88 and ANGI52) grafted onto cv. Hass under four water stress conditions, 50% and 25% deficit, and 50% and 25% [...] Read more.
The avocado cv. Hass requires a suitable rootstock for optimal development under water stress. This study evaluated the performance of two avocado rootstocks (ANRR88 and ANGI52) grafted onto cv. Hass under four water stress conditions, 50% and 25% deficit, and 50% and 25% excess during the nursery stage. Plant height, leaf area (LA), dry matter (DM), and Carbon (OC) content in the roots, stems, and leaves were measured. Root traits were evaluated using digital imaging, and three vegetation indices (NDVI, CIRE, and MTCI) were used to quantify stress. The results showed that genotype significantly influenced the response to water stress. ANRR88 exhibited adaptation to moderate to high water deficits. ANGI52 adapted better to both water deficit and excess, and showed greater root exploration. LA and DM reductions of up to 60% were observed in ANRR88, suggesting a higher sensitivity to extreme changes in water availability. More than 90% of the total OC accumulation was observed in the stem and roots. The NDVI and the MTCI quantified the presence and levels of stress applied, and the 720 nm band provided high precision and speed for detecting stress. These insights are crucial for selecting rootstocks that ensure optimal performance under varying water availability, enhancing productivity and sustainability. Full article
(This article belongs to the Special Issue Responses of Crops to Abiotic Stress)
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<p>Average plant height (cm) for the different treatments evaluated: water restriction of (T1) 50% and (T2) 25%, water excess of (T3) 25% and (T4) 50%, and (T5) control. Values represent the mean of the two rootstocks evaluated. Both rootstocks were combined with a common cv. Hass scion. Different letters indicate statistical differences at a significance of <span class="html-italic">p</span> ≤ 0.05 according to the Tukey test.</p>
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<p>Leaf area (cm<sup>2</sup>) of the avocado plants using rootstock (<b>A</b>) ANRR88 and (<b>B</b>) ANGI52 for the different treatments evaluated: water restriction of (T1) 50% and (T2) 25%, water excess of (T3) 25% and (T4) 50%, and (T5) control. Both rootstocks were combined with a common cv. Hass scion. Different letters indicate statistical differences at a significance of <span class="html-italic">p</span> ≤ 0.05 according to the Tukey test.</p>
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<p>Dry matter (g m<sup>–2</sup>) partitioning per plant organ: leaves (light blue), stem (medium blue), and roots (dark blue) for ANRR88 (<b>A</b>) and ANGI52 (<b>B</b>). Treatments: water restriction of (T1) 50% and (T2) 25%, water excess of (T3) 25% and (T4) 50%, and (T5) control. Both rootstocks were combined with a common cv. Hass scion. Different letters indicate statistical differences at a significance of <span class="html-italic">p</span> ≤ 0.05 according to the Tukey test.</p>
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<p>Organic Carbon (mg OC g<sup>–1</sup> DT) partitioning per plant organ: leaves (light blue), stem (medium blue), and roots (dark blue) for ANRR88 (<b>A</b>) and ANGI52 (<b>B</b>). Treatments: water restriction of (T1) 50% and (T2) 25%, water excess of (T3) 25% and (T4) 50%, and (T5) control. Both rootstocks were combined with a common cv. Hass scion. Different letters indicate statistical differences at a significance at the <span class="html-italic">p</span> ≤ 0.05 according to the Tukey test.</p>
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<p>Mean values per treatment for (<b>A</b>) NDVI, (<b>B</b>) MTCI, and (<b>C</b>) CI<sub>RE</sub>. Treatments: water restriction of (T1) 50% and (T2) 25%, water excess of (T3) 25% and (T4) 50%, and (T5) control. Both rootstocks were combined with a common cv. Hass scion. Different letters indicate statistical differences at a significance of 0.05 level, according to the Tukey test.</p>
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<p>Process of avocado root conditioning for imaging: (<b>A</b>) washing, (<b>B</b>) sample before imaging, (<b>C</b>) angle opening data calculated by the software, and (<b>D</b>) density area occupied estimated by the software.</p>
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17 pages, 2969 KiB  
Article
Characterization of Plant-Growth-Promoting Rhizobacteria for Tea Plant (Camellia sinensis) Development and Soil Nutrient Enrichment
by Mengjiao Wang, Haiyan Sun, Huiping Dai and Zhimin Xu
Plants 2024, 13(18), 2659; https://doi.org/10.3390/plants13182659 - 23 Sep 2024
Cited by 2 | Viewed by 1034
Abstract
Plant-growth-promoting rhizobacteria (PGPR) play an important role in plant growth and rhizosphere soil. In order to evaluate the effects of PGPR strains on tea plant growth and the rhizosphere soil microenvironment, 38 PGPR strains belonging to the phyla Proteobacteria with different growth-promoting properties [...] Read more.
Plant-growth-promoting rhizobacteria (PGPR) play an important role in plant growth and rhizosphere soil. In order to evaluate the effects of PGPR strains on tea plant growth and the rhizosphere soil microenvironment, 38 PGPR strains belonging to the phyla Proteobacteria with different growth-promoting properties were isolated from the rhizosphere soil of tea plants. Among them, two PGPR strains with the best growth-promoting properties were then selected for the root irrigation. The PGPR treatment groups had a higher Chlorophyll (Chl) concentration in the eighth leaf of tea plants and significantly promoted the plant height and major soil elements. There were significant differences in microbial diversity and metabolite profiles in the rhizosphere between different experimental groups. PGPR improved the diversity of beneficial rhizosphere microorganisms and enhanced the root metabolites through the interaction between PGPR and tea plants. The results of this research are helpful for understanding the relationship between PGPR strains, tea plant growing, and rhizosphere soil microenvironment improvement. Moreover, they could be used as guidance to develop environmentally friendly biofertilizers with the selected PGPR instead of chemical fertilizers for tea plants. Full article
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<p>Growth-promoting characteristics of PGPR strains: (<b>a</b>) phosphorus-solubilizing capacity, (<b>b</b>) auxin production, (<b>c</b>) colony diameters of PGPR strains in silicate media, and (<b>d</b>) colony diameters of PGPR strains in A Sugai’s medium.</p>
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<p>Nutritional element contents in rhizosphere soils of control and treatment groups. The OCC (<b>a</b>), TNC (<b>b</b>), HNC (<b>b</b>), TPOC (<b>c</b>), APOC (<b>c</b>), TPHC (<b>d</b>), and APHC (<b>d</b>) contents in rhizosphere soils. A significant difference between the data (<span class="html-italic">p</span> &lt; 0.05) was indicated by bars with different letters.</p>
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<p>The distribution of microorganism with relative abundance greater than or equal to 1% in tea plant rhizosphere soil samples. Bacterial phyla (CK-B, C15-B, and C20-B) and fungal phyla (CK-P, C15-P, and C20-P) in soil.</p>
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<p>Differences in microorganism community structures in tea plant rhizospheres. Panels (<b>a</b>,<b>b</b>) show the differences in bacterial and fungal community structures, respectively.</p>
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<p>LEfSe analysis of microorganism for (<b>a</b>) differential enrichments of the bacterial features; and (<b>b</b>) fungi in tea plant rhizospheres.</p>
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<p>Data analysis and classification of identified metabolites in tea plant roots via HPLC-MS. (<b>a</b>) Classification of significantly different metabolites. (<b>b</b>) Top 20 pathways of upregulated and downregulated metabolites and DAMs on KEGG (rich factor on the X-axis and pathway on the Y-axis). The size of bubble indicates the number of involved DAMs. The color of bubble represents the degree of pathway enrichment. (<b>c</b>) DAMs’ up- and downregulation in various treatment groups.</p>
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<p>The relationship between the PGPR strains, rhizosphere microenvironmental factors, and tea plant growing. Notes: The red arrows indicate the correlations. The thicker the arrow line, the stronger the correlation.</p>
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12 pages, 1456 KiB  
Article
Advancements in Cold-Region Rice Breeding: The 4S Phenotypic-Design Breeding System and Its Applications in Heilongjiang
by Baohai Liu, Shoujun Nie, Shiwei Gao, Qing Liu, Yuqiang Liu, Fengchen Mu, Bo Zhang, Beiping Zhao, Hongru Gao, Licheng Wu, Minggang Xiao and Kun Li
Plants 2024, 13(18), 2658; https://doi.org/10.3390/plants13182658 - 23 Sep 2024
Cited by 1 | Viewed by 914
Abstract
Heilongjiang, located in the cold region, is China’s largest rice-producing and commercializing province. The variety selection of rice in cold regions (RCR) is indispensable in promoting the rice industry’s development, and technological innovation in breeding theory plays a significant role in breeding breakthrough. Based [...] Read more.
Heilongjiang, located in the cold region, is China’s largest rice-producing and commercializing province. The variety selection of rice in cold regions (RCR) is indispensable in promoting the rice industry’s development, and technological innovation in breeding theory plays a significant role in breeding breakthrough. Based primarily on long-term research, contemplation, and breeding practices, the 4S (selected topic, selected breeding, selected progenies, and selected promotion) phenotypic-design breeding technical system for RCR, which has revolutionized the theoretical basis and deepened the conceptual model, has been developed through systematic analyses and generalization. The system covers several key aspects such as scientific question formulation, breeding objective optimization, parental taxa hybridization, progeny population selection, and innovation dissemination, aiming to improve the foresight, precision, and efficiency of breeding. Furthermore, the system has demonstrated successful cases of rice variety breeding over the past 20 years, such as for Suijing 3, Suijing 4, Suijing 18, and a series of other rice varieties, providing theoretical and technical supports for cold-region rice breeding. Full article
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<p>The 4S conceptual model for phenotypic-design breeding in RCR.</p>
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<p>Conceptual model of the methodology for formulating scientific questions in RCR breeding.</p>
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<p>Pressure–state–response (PSR) conceptual model for hybrid progeny selection in Heilongjiang Japonica rice.</p>
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<p>Conceptual model of a multidisciplinary, three-stage transformation of scientific and technological achievements.</p>
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15 pages, 18012 KiB  
Article
Impact of Quorum Sensing on the Virulence and Survival Traits of Burkholderia plantarii
by Minhee Kang, Duyoung Lee, Mohamed Mannaa, Gil Han, Haeun Choi, Seungchul Lee, Gah-Hyun Lim, Sang-Woo Kim, Tae-Jin Kim and Young-Su Seo
Plants 2024, 13(18), 2657; https://doi.org/10.3390/plants13182657 - 23 Sep 2024
Cited by 1 | Viewed by 1080
Abstract
Quorum sensing (QS) is a mechanism by which bacteria detect and respond to cell density, regulating collective behaviors. Burkholderia plantarii, the causal agent of rice seedling blight, employs the LuxIR-type QS system, common among Gram-negative bacteria, where LuxI-type synthase produces QS signals [...] Read more.
Quorum sensing (QS) is a mechanism by which bacteria detect and respond to cell density, regulating collective behaviors. Burkholderia plantarii, the causal agent of rice seedling blight, employs the LuxIR-type QS system, common among Gram-negative bacteria, where LuxI-type synthase produces QS signals recognized by LuxR-type regulators to control gene expression. This study aimed to elucidate the QS mechanism in B. plantarii KACC18965. Through whole-genome analysis and autoinducer assays, the plaI gene, responsible for QS signal production, was identified. Motility assays confirmed that C8-homoserine lactone (C8-HSL) serves as the QS signal. Physiological experiments revealed that the QS-defective mutant exhibited reduced virulence, impaired swarming motility, and delayed biofilm formation compared to the wild type. Additionally, the QS mutant demonstrated weakened antibacterial activity against Escherichia coli and decreased phosphate solubilization. These findings indicate that QS in B. plantarii significantly influences various pathogenicity and survival traits, including motility, biofilm formation, antibacterial activity, and nutrient acquisition, highlighting the critical role of QS in pathogen virulence and adaptability. Full article
(This article belongs to the Section Plant Protection and Biotic Interactions)
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<p>Autoinducers (AIs) production of <span class="html-italic">B. plantarii</span> KACC18965 strains. Detection of C8-HSL and C6-HSL was performed using the biosensor strain <span class="html-italic">Chromobacterium violaceum</span> on thin-layer chromatography (TLC). (<b>A</b>) AI production was undetectable in the <span class="html-italic">plaI</span> deletion mutant (Bp65 ∆<span class="html-italic">plaI</span>) compared to the wild type (Bp65 WT) and other <span class="html-italic">plaI</span> deletion mutants (Bp65 ∆<span class="html-italic">plaI2</span> and Bp65 ∆<span class="html-italic">plaI3</span>). (<b>B</b>) AI production was absent in the <span class="html-italic">plaI</span> deletion mutant (Bp65 ∆<span class="html-italic">plaI</span>) but was restored in the complemented strain (Bp65 C<span class="html-italic">plaI</span>).</p>
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<p>Virulence of <span class="html-italic">B. plantarii</span> KACC18965 strains. (<b>A</b>) Photographs representing the seedlings infected with <span class="html-italic">B. plantarii</span> strains, including the wild type (Bp65 WT), <span class="html-italic">plaI</span> deletion mutant (Bp65 ∆<span class="html-italic">plaI</span>), and <span class="html-italic">plaI</span> complemented strain (Bp65 C<span class="html-italic">plaI</span>), compared to a negative control. (<b>B</b>) Quantitative analysis of shoot and root lengths of seedlings. Seedlings infected with the <span class="html-italic">plaI</span> deletion mutant (Bp65 ∆<span class="html-italic">plaI</span>) exhibited longer root lengths compared to those infected with the wild type or <span class="html-italic">plaI</span> complemented strain. Significant differences according to LSD test in root lengths are indicated by an asterisk (*, <span class="html-italic">p</span> &lt; 0.05). (<b>C</b>) Photographs representing the disease symptoms on rice panicles caused by the different <span class="html-italic">B. plantari</span>i strains and the negative control. (<b>D</b>) Disease severity index of rice panicles infected with the <span class="html-italic">B. plantarii</span> strains. The <span class="html-italic">plaI</span> deletion mutant (Bp65 ∆<span class="html-italic">plaI</span>) showed a lower disease severity index compared to the wild type and <span class="html-italic">plaI</span> complemented strain. Different letters on the error bar indicate statistically significant differences between groups according to LSD test at (<span class="html-italic">p</span> &lt; 0.05). (<b>E</b>) Distribution of disease severity indices among different treatment groups, illustrating the proportion of panicles within each severity category.</p>
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<p>Motility of <span class="html-italic">B. plantarii</span> KACC18965 strains. Swarming and swimming motilities of <span class="html-italic">B. plantarii</span> strains, including wild type (Bp65 WT), <span class="html-italic">plaI</span> deletion mutant (Bp65 ∆<span class="html-italic">plaI</span>), <span class="html-italic">plaI</span> complemented strain (Bp65 C<span class="html-italic">plaI</span>), and <span class="html-italic">plaI</span> deletion mutant supplemented with 1 µM C8-HSL. Swarming motility (top row) was significantly reduced in the <span class="html-italic">plaI</span> deletion mutant (Bp65 ∆<span class="html-italic">plaI</span>) compared to the wild type (Bp65 WT) and the <span class="html-italic">plaI</span> complemented strain (Bp65 C<span class="html-italic">plaI</span>). The addition of 1 µM C8-HSL to the <span class="html-italic">plaI</span> deletion mutant restored swarming motility to the wild-type level. Swimming motility (bottom row) showed no significant difference among the wild type, <span class="html-italic">plaI</span> deletion mutant, and <span class="html-italic">plaI</span> complemented strain.</p>
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<p>Biofilm formation of <span class="html-italic">B. plantarii</span> KACC18965 strains. (<b>A</b>) Biofilm formation in static cultures of <span class="html-italic">B. plantarii</span> strains over time. Representative images show biofilm formation at the air–liquid interface at 24, 48, 72, and 96 h for the wild type (Bp65 WT), <span class="html-italic">plaI</span> deletion mutant (Bp65 ∆<span class="html-italic">plaI</span>), and <span class="html-italic">plaI</span> complemented strain (Bp65 C<span class="html-italic">plaI</span>). The <span class="html-italic">plaI</span> deletion mutant exhibited delayed biofilm formation compared to the wild type and complemented strain. (<b>B</b>) Quantification of air-dried biofilm mass produced by the tested strains. Bars represent the mean ± standard error of the mean from three independent replicates (<span class="html-italic">n</span> = 3). Different letters above the error bars indicate statistically significant differences as determined by the Duncan’s multiple range test (<span class="html-italic">p</span> &lt; 0.05). (<b>C</b>) Microscopic images of biofilms formed by <span class="html-italic">B. plantarii</span> strains 48 h after incubation, stained with safranin. Left: Wild-type (Bp65 WT) biofilm shows a dense, continuous structure. Middle: <span class="html-italic">plaI</span> deletion mutant (Bp65 ∆<span class="html-italic">plaI</span>) biofilm is fragmented with significantly reduced biofilm mass. Right: <span class="html-italic">plaI</span> complemented strain (Bp65 C<span class="html-italic">plaI</span>) shows restored biofilm formation similar to the wild type. Scale bar = 10 μm.</p>
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<p>Antibacterial activity of <span class="html-italic">B. plantarii</span> KACC18965 strains. (<b>A</b>) Co-culture assay showing the survival of <span class="html-italic">E. coli</span> when co-cultured with <span class="html-italic">B. plantarii</span> strains. Serial dilutions (10<sup>0</sup> to 10<sup>−5</sup>) of <span class="html-italic">E. coli</span> were plated after co-culture with wild type (Bp65 WT), <span class="html-italic">plaI</span> deletion mutant (Bp65 ∆<span class="html-italic">plaI</span>), and <span class="html-italic">plaI</span> complemented strain (Bp65 C<span class="html-italic">plaI</span>). <span class="html-italic">E. coli</span> co-cultured with the wild type or complemented strain did not survive, while <span class="html-italic">E. coli</span> co-cultured with the <span class="html-italic">plaI</span> deletion mutant showed significant survival. (<b>B</b>) Quantitative analysis of <span class="html-italic">E. coli</span> survival in co-culture assays. The log (cfu/mL) values of <span class="html-italic">E. coli</span> are shown. <span class="html-italic">E. coli</span> only (control) had the highest survival rate, while <span class="html-italic">E. coli</span> co-cultured with the wild type or complemented strain had significantly lower survival rates. Different letters on the error bar indicate statistically significant differences between according to LSD test at (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Phosphate solubilizing activity of <span class="html-italic">B. plantarii</span> KACC18965 strains. (<b>A</b>) Photographs showing the phosphate solubilizing activity of <span class="html-italic">B. plantarii</span> strains on Pikovskaya’s agar media. The diameter of the halo around the colonies indicates the extent of phosphate solubilization. The <span class="html-italic">plaI</span> deletion mutant (Bp65 ∆<span class="html-italic">plaI</span>) formed a smaller halo compared to the wild type (Bp65 WT) and the <span class="html-italic">plaI</span> complemented strain (Bp65 C<span class="html-italic">plaI</span>). (<b>B</b>) Quantitative analysis of the diameter of phosphate solubilization halos. The diameter of the halos was measured, showing that the <span class="html-italic">plaI</span> deletion mutant (Bp65 ∆<span class="html-italic">plaI</span>) had significantly reduced phosphate solubilizing activity compared to the wild type and complemented strain. Different letters on the error bar indicate statistically significant differences according to LSD test between groups at (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Gene clusters and relative expression levels of T3SS and T6SS genes in <span class="html-italic">B. plantarii</span> KACC18965 strains. (<b>A</b>) Schematic representation of the <span class="html-italic">B. plantarii</span> T3SS gene cluster, highlighting the selected genes analyzed in this study (in red), including <span class="html-italic">T3SP</span>, <span class="html-italic">hrpB1</span>, <span class="html-italic">hrpB2</span>, <span class="html-italic">PTTL</span>, <span class="html-italic">HP1</span>, and <span class="html-italic">hrpK1</span>. (<b>B</b>) Quantitative PCR (qPCR) analysis showing relative expression levels of the selected T3SS genes in the wild-type strain (Bp65 WT) and the <span class="html-italic">plaI</span> deletion mutant (Bp65 ∆<span class="html-italic">plaI</span>). Expression levels of these genes are significantly lower in the <span class="html-italic">plaI</span> deletion mutant compared to the wild type. Significant differences in gene expression between the wild type and the mutant are indicated by an asterisk (*, <span class="html-italic">p</span> &lt; 0.05). (<b>C</b>) Schematic representation of the <span class="html-italic">B. plantarii</span> T6SS gene cluster, highlighting the selected genes analyzed (in red), including <span class="html-italic">tssL</span>, <span class="html-italic">HP2</span>, <span class="html-italic">tssB</span>, <span class="html-italic">tssC</span>, <span class="html-italic">tssD</span>, and <span class="html-italic">tssE</span>. (<b>D</b>) qPCR analysis demonstrating the relative expression levels of these T6SS genes in the wild type (Bp65 WT) versus the Bp65 ∆<span class="html-italic">plaI</span>. Significant differences in gene expression between the wild type and the mutant are indicated by an asterisk (*, <span class="html-italic">p</span> &lt; 0.05).</p>
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30 pages, 4060 KiB  
Article
Growth, Biochemical Traits, Antioxidant Enzymes, and Essential Oils of Four Aromatic and Medicinal Plants Cultivated in Phosphate-Mine Residues
by Khadija Ait Elallem, Widad Ben Bakrim, Abdelaziz Yasri and Ali Boularbah
Plants 2024, 13(18), 2656; https://doi.org/10.3390/plants13182656 - 22 Sep 2024
Cited by 1 | Viewed by 1502
Abstract
Revegetation emerges as a promising approach to alleviate the adverse impacts of mining residues. However, it is essential to evaluate the characteristics of these materials and select suitable plant species to ensure successful ecosystem restoration. This study aimed to investigate the effects of [...] Read more.
Revegetation emerges as a promising approach to alleviate the adverse impacts of mining residues. However, it is essential to evaluate the characteristics of these materials and select suitable plant species to ensure successful ecosystem restoration. This study aimed to investigate the effects of phosphate-mine residues (MR) on the growth, biochemical properties, and essential oil concentration of Rosmarinus officinalis L., Salvia Officinalis L., Lavandula dentata L., and Origanum majorana L. The results showed that R. officinalis L. appeared to be particularly well-suited to thriving in MR soil. Our finding also revealed that L. dentata L., O. majorana L., and S. officinalis L. grown in MR exhibited significantly lower growth performance (lower shoot length, smaller leaves, and altered root structure) and higher antioxidant activities, with an alterations of photosynthetic pigment composition. They showed a decrease in total chlorophylls when grown on MR (0.295, 0.453, and 0.562 mg g−1 FW, respectively) compared to the control (0.465, 0.807, and 0.808 mg g−1 FW, respectively); however, they produced higher essential oil content (1.8%, 3.06%, and 2.88%, respectively). The outcomes of this study could offer valuable insights for the advancement of revegetation technologies and the utilization of plant products derived from phosphate-mine residues. Full article
(This article belongs to the Section Plant Ecology)
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<p>Change in the survival and the growth of the aerial parts of <span class="html-italic">R. officinalis</span> L., <span class="html-italic">S. officinalis</span> L., <span class="html-italic">L. dentata</span> L., and <span class="html-italic">O. majorana</span> L. cultivated in phosphate-mine residue and control soil.</p>
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<p>WinRHIZO image of <span class="html-italic">O. majorana</span> L. (<b>a</b>) C and (<b>b</b>) MR <span class="html-italic">S. officinalis</span> L; (<b>c</b>) C and (<b>d</b>) MR; <span class="html-italic">L. dentata</span> L. (<b>e</b>) C and (<b>f</b>) MR; <span class="html-italic">R. officinalis</span> L. (<b>g</b>) C and (<b>h</b>) MR) roots. C: Agriculture soil; MR: mine residue.</p>
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<p>Change in (<b>a</b>) proline, (<b>b</b>) MDA, (<b>c</b>) polyphenols, (<b>d</b>) flavonoids, (<b>e</b>) soluble sugars, and (<b>f</b>) proteins content of <span class="html-italic">R. officinalis</span> L., <span class="html-italic">S. officinalis</span> L., <span class="html-italic">L. dentata</span> L., and <span class="html-italic">O. majorana</span> L. cultivated in phosphate-mine residues and control soil. C: Agriculture soil; MR: mine residue. Bars with superscript asterisks are statistically different (ns: not significant; ≤0.001: ***) using Student’s <span class="html-italic">t</span>-test.</p>
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<p>Change in enzymatic activities of (<b>a</b>) APX and (<b>b</b>) GuPX of <span class="html-italic">R. officinalis</span> L., <span class="html-italic">S. officinalis</span> L., <span class="html-italic">L. dentata</span> L., and <span class="html-italic">O. majorana</span> L. cultivated in phosphate-mine residue and control soil. C: Agriculture soil; MR: mine residue; APX: ascorbate peroxidase; GuPX: guaiacol peroxidase. Bars with superscript asterisks are statistically (ns: not significant; ≤0.01: **; ≤0.001: ***) using Student’s <span class="html-italic">t</span>-test.</p>
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18 pages, 11034 KiB  
Article
Dual-Stream Architecture Enhanced by Soft-Attention Mechanism for Plant Species Classification
by Imran Ullah Khan, Haseeb Ali Khan and Jong Weon Lee
Plants 2024, 13(18), 2655; https://doi.org/10.3390/plants13182655 - 22 Sep 2024
Viewed by 922
Abstract
Plants play a vital role in numerous domains, including medicine, agriculture, and environmental balance. Furthermore, they contribute to the production of oxygen and the retention of carbon dioxide, both of which are necessary for living beings. Numerous researchers have conducted thorough research in [...] Read more.
Plants play a vital role in numerous domains, including medicine, agriculture, and environmental balance. Furthermore, they contribute to the production of oxygen and the retention of carbon dioxide, both of which are necessary for living beings. Numerous researchers have conducted thorough research in the classification of plant species where certain studies have focused on limited numbers of classes, while others have employed conventional machine-learning and deep-learning models to classify them. To address these limitations, this paper introduces a novel dual-stream neural architecture embedded with a soft-attention mechanism specifically developed for accurately classifying plant species. The proposed model utilizes residual and inception blocks enhanced with dilated convolutional layers for acquiring both local and global information. Following the extraction of features, both streams are combined, and a soft-attention technique is used to improve the distinct characteristics. The efficacy of the model is shown via extensive experimentation on varied datasets, including several plant species. Moreover, we have contributed a novel dataset that comprises 48 classes of different plant species. The results demonstrate a higher level of performance when compared to current models, emphasizing the capability of the dual-stream design in improving accuracy and model generalization. The integration of a dual-stream architecture, dilated convolutions, and soft attention provides a strong and reliable foundation for the botanical community, supporting advancement in the field of plant species classification. Full article
(This article belongs to the Section Plant Modeling)
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<p>A high-level generic diagram of the proposed study, comprising three distinct phases: Phase (1) contains different augmentation techniques to mitigate the data-scarcity problem. Phase (2) showcases a dual-stream network, employing two different networks, such as residual block and inception block, followed by a soft-attention module for effective feature learning. Finally, Phase (3) signifies the testing phase, where the proposed network is evaluated on testing data.</p>
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<p>The soft-attention function of converting feature map to attention maps and postprocessing procedure.</p>
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<p>Shows the different types of plant species samples from our proposed dataset.</p>
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<p>Demonstrates the classification performance of our proposed model on testing samples, where (<b>a</b>–<b>c</b>) shows samples from our custom dataset, while (<b>d</b>–<b>f</b>) shows samples from the Flower299 dataset.</p>
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16 pages, 1741 KiB  
Article
Water-Light Interaction and Its Effect on the Morphophysiology of Cedrela fissilis Vell. Seedlings
by Juliana Milene Silverio, Silvana de Paula Quintão Scalon, Cleberton Correia Santos, Jéssica Aline Linné, Anderson dos Santos Dias, Rodrigo da Silva Bernardes and Thaise Dantas
Plants 2024, 13(18), 2654; https://doi.org/10.3390/plants13182654 - 22 Sep 2024
Viewed by 744
Abstract
Plant responses to different light and water availability are variable among species and their respective phenotypic plasticity, and the combination between these two abiotic factors can alleviate or intensify stressful effects. This study aimed to evaluate the impacts of exposure time of Cedrela [...] Read more.
Plant responses to different light and water availability are variable among species and their respective phenotypic plasticity, and the combination between these two abiotic factors can alleviate or intensify stressful effects. This study aimed to evaluate the impacts of exposure time of Cedrela fissilis Vell. seedlings to different water and light availability considering natural radiation variations and the interaction of these factors. Seedlings were submitted to combinations of three shading levels—SH (0, 30 and 70%) and three water regimes based on the water holding capacity (WHC) in the substrate, constituting nine cultivation conditions: T1—0% SH + 40% WHC; T2—0% SH + 70% WHC; T3—0% SH + 100% WHC; T4—30% SH + 40% WHC; T5—30% SH + 70% WHC; T6—30% SH + 100% WHC; T7—70% SH + 40% WHC; T8—70% SH + 70% WHC; T9—70% SH + 100% WHC. C. fissilis seedlings are sensitive to water deficit, here represented by 40% WHC, regardless of exposure time, and when cultivated in full sun even though there are variations in radiation, the stressful effects were enhanced, acting in a synergistic manner. The condition that provided better gas exchange performance and greater total dry mass accumulation for C. fissilis seedlings was 30% shading combined with 100% WHC. C. fissilis seedlings have physiological plasticity and resilience to survive under different water and light conditions. Full article
(This article belongs to the Special Issue Physiology and Seedling Production of Plants)
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<p>Visual aspects of <span class="html-italic">Cedrela fissilis</span> Vell. seedlings of cultivation under different water and light availability. WHC—water holding capacity.</p>
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<p>Net photosynthetic rate—<span class="html-italic">A</span> (<b>A</b>), stomatal conductance—<span class="html-italic">g</span><sub>s</sub> (<b>B</b>), Rubisco carboxylation efficiencies—<span class="html-italic">A/C</span><sub>i</sub> (<b>C</b>), and transpiration rate—<span class="html-italic">E</span> (<b>D</b>) of <span class="html-italic">Cedrela fissilis</span> Vell. seedlings evaluated at 15, 30, 45, and 60 treatment days under different water and light availability. T1—0% SH + 40% WHC; T2—0% SH + 70% WHC; T3—0% SH + 100% WHC; T4—30% SH + 40% WHC; T5—30% SH + 70% WHC; T6—30% SH + 100% WHC; T7—70% SH + 40% WHC; T8—70% SH + 70% WHC; T9—70% SH + 100% WHC. SH—shading and WHC—water holding capacity. Equal lowercase letters between markers of different colors in each evaluation period do not differ statistically by the Scott-Knott test (<span class="html-italic">p</span> ≤ 0.05) ± standard error for cultivation conditions.</p>
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<p>Water use efficiency—<span class="html-italic">WUE</span> (<b>A</b>,<b>B</b>) and chlorophyll index—SPAD (<b>C</b>) of <span class="html-italic">Cedrela fissilis</span> Vell. under different availability of water and light evaluated at 15, 30, 45 and 60 treatment days. T1—0% SH + 40% WHC; T2—0% SH + 70% WHC; T3—0% SH + 100% WHC; T4—30% SH + 40% WHC; T5—30% SH + 70% WHC; T6—30% SH + 100% WHC; T7—70% SH + 40% WHC; T8—70% SH +70% WHC; T9—70% SH + 100% WHC. SH—shading and WHC—water holding capacity. Equal lowercase letters between columns or markers of different colors in each evaluation period do not differ statistically according to the Scott-Knott test (<span class="html-italic">p</span> ≤ 0.05) ± standard error for cultivation conditions.</p>
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<p>Effective quantum yield of photochemical energy conversion in PSII—F<sub>v</sub>/F<sub>0</sub> (<b>A</b>,<b>B</b>) and potential quantum efficiency of PSII—F<sub>v</sub>/F<sub>m</sub> (<b>C</b>,<b>D</b>) of <span class="html-italic">Cedrela fissilis</span> Vell. under different availability of water and light evaluated at 15, 30, 45, and 60 treatment days. T1—0% SH + 40% WHC; T2—0% SH + 70% WHC; T3—0% SH + 100% WHC; T4—30% SH + 40% WHC; T5—30% SH + 70% WHC; T6—30% SH + 100% WHC; T7—70% SH + 40% WHC; T8—70% SH +70% WHC; T9—70% SH + 100% WHC. SH—shading and WHC—water holding capacity. Equal lowercase letters between columns in each evaluation period do not differ statistically according to the Scott-Knott test (<span class="html-italic">p</span> ≤ 0.05) ± standard error for cultivation conditions.</p>
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<p>Relative water content of leaves—RWC (<b>A</b>), leaf area—LA (<b>B</b>), root length—RL (<b>C</b>), and total dry mass—TDM (<b>D</b>) of <span class="html-italic">Cedrela fissilis</span> Vell. under different availability of water and light evaluated at 15 and 60 treatment days. T1—0% SH + 40% WHC; T2—0% SH + 70% WHC; T3—0% SH + 100% WHC; T4—30% SH + 40% WHC; T5—30% SH + 70% WHC; T6—30% SH + 100% WHC; T7—70% SH + 40% WHC; T8—70% SH + 70% WHC; T9—70% SH + 100% WHC. SH—shading and WHC—water holding capacity. Lowercase letters compare the effect of cultivation conditions at each evaluation time using the Scott-Knott test (<span class="html-italic">p</span> ≤ 0.05), and uppercase letters compare the effect of days of cultivation within each cultivation condition using the F test (<span class="html-italic">p</span> ≤ 0.05) ± standard error.</p>
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<p>Experimental design exemplifying the origin of the 9 treatments is the interaction between the three levels of shading with the three water retention capacities and the four periods in which the seedlings of all treatments were evaluated.</p>
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<p>Maintenance of the WHC, with the aid of scales on <span class="html-italic">Cedrella fissilis</span> Vell. seedlings (<b>A</b>). Pots with plastic protection used to reduce soil water evapotranspiration (<b>B</b>).</p>
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14 pages, 5392 KiB  
Article
Phenotypic Analysis and Gene Cloning of Rice Floury Endosperm Mutant wcr (White-Core Rice)
by Yihao Yang, Xiaoyi Yang, Lingjun Wu, Zixing Sun, Yi Zhang, Ziyan Shen, Juan Zhou, Min Guo and Changjie Yan
Plants 2024, 13(18), 2653; https://doi.org/10.3390/plants13182653 - 22 Sep 2024
Viewed by 939
Abstract
The composition and distribution of storage substances in rice endosperm directly affect grain quality. A floury endosperm mutant, wcr (white-core rice), was identified, exhibiting a loose arrangement of starch granules with a floury opaque appearance in the inner layer of mature grains, resulting [...] Read more.
The composition and distribution of storage substances in rice endosperm directly affect grain quality. A floury endosperm mutant, wcr (white-core rice), was identified, exhibiting a loose arrangement of starch granules with a floury opaque appearance in the inner layer of mature grains, resulting in reduced grain weight. The total starch and amylose content remained unchanged, but the levels of the four component proteins in the mutant brown rice significantly decreased. Additionally, the milled rice (inner endosperm) showed a significant decrease in total starch and amylose content, accompanied by a nearly threefold increase in albumin content. The swelling capacity of mutant starch was reduced, and its chain length distribution was altered. The target gene was mapped on chromosome 5 within a 65 kb region. A frameshift mutation occurred due to an insertion of an extra C base in the second exon of the cyOsPPDKB gene, which encodes pyruvate phosphate dikinase. Expression analysis revealed that wcr not only affected genes involved in starch metabolism but also downregulated expression levels of genes associated with storage protein synthesis. Overall, wcr plays a crucial role as a regulator factor influencing protein synthesis and starch metabolism in rice grains. Full article
(This article belongs to the Special Issue Crop Functional Genomics and Biological Breeding)
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<p>Phenotypic and crop traits analysis of the <span class="html-italic">wcr</span> mutant and wild type. (<b>A</b>) The whole plants of the Sa-Sasanishiki wild-type and <span class="html-italic">wcr</span>, scale bar = 10 cm. (<b>B</b>) The brown rice of the Sa and <span class="html-italic">wcr</span>, scale bar = 10 mm. (<b>C</b>) The cross-section of the Sa and <span class="html-italic">wcr</span> grains, scale bar = 1 mm. (<b>D</b>) Electron microscopic scanning of the endosperm of Sa and <span class="html-italic">wcr</span>, black scale bar = 10 μm, white scale bar = 200 μm. Different colored boxes represent local enlargements of starch structures. (<b>E</b>–<b>J</b>) The crop traits of Sa and <span class="html-italic">wcr</span>. Different upper case letters denote significant statistical differences between Sa (orange) and <span class="html-italic">wcr</span> (blue) plants, with the <span class="html-italic">p</span>-value &lt; 0.01.</p>
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<p>Physicochemical properties of mature grains of Sa and <span class="html-italic">wcr</span> mutant. (<b>A</b>–<b>F</b>) The contents of total starch, amylose, albumin, globulin, prolamin, and glutelin in brown rice flour and milled rice flour of Sa and <span class="html-italic">wcr</span> mutant. Different small case letters denote statistical differences between Sa (orange) and <span class="html-italic">wcr</span> (blue) plants in the same rice type (brown or milled); different upper case letters denote statistical differences between brown or milled rice types in the same wild type or <span class="html-italic">wcr</span> plants. (<b>G</b>) The SDS-PAGE analysis of storage proteins of Sa and <span class="html-italic">wcr</span> mutant rice flour. (<b>H</b>) Changes in the contents of storage substances in the inner and outer endosperm of <span class="html-italic">wcr</span> compared to wild type (the yellow part indicates the outer endosperm; the white part indicates the inner endosperm; Red arrows represent up-regulated levels, light green and dark green arrows represent down-regulated levels, and purple horizontal lines indicate unchanged levels; TSC, total starch content; AC, amylose content; Alb, albumin; Glo, globulin; Prol, prolamin; Glut, glutelin).</p>
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<p>Gelatinization characteristics and amylopectin structure analysis of <span class="html-italic">wcr</span> mutant. (<b>A</b>,<b>B</b>) Comparison of the swelling volume of brown rice flour between Sa and <span class="html-italic">wcr</span> mutant under different urea concentrations. The <span class="html-italic">p</span>-values &lt; 0.05 * and &lt;0.01 ** calculated using an independent-samples <span class="html-italic">t</span>-test. (<b>C</b>) Determination of amylopectin chain length distribution in Sa and <span class="html-italic">wcr</span> mutant brown rice flour.</p>
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<p>Fine mapping of the <span class="html-italic">wcr</span> gene. (<b>A</b>) The MutMap analysis of the <span class="html-italic">wcr</span> gene. (<b>B</b>) Fine mapping of the <span class="html-italic">wcr</span> gene using linkage analysis. (<b>C</b>) The gene structure of the <span class="html-italic">LOC_Os05g33570</span>. (<b>D</b>) The Sanger chromatogram of the WT and <span class="html-italic">wcr</span>.</p>
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<p>Gene expression analysis of storage substance-related genes of Sa and the <span class="html-italic">wcr</span> mutant. (<b>A</b>) Gene expression analysis of grain protein biosynthesis genes. (<b>B</b>) Gene expression analysis of grain starch metabolism genes.</p>
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<p>The structure of <span class="html-italic">cyOsPPDKB</span>. The <span class="html-italic">wcr</span> mutant is highlighted in red boxes. Previously reported allelic mutants of <span class="html-italic">cyOsPPDKB</span> are indicated in blue boxes.</p>
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15 pages, 6972 KiB  
Article
Metabolomics Revealed the Tolerance and Growth Dynamics of Arbuscular Mycorrhizal Fungi (AMF) to Soil Salinity in Licorice
by Li Fan, Chen Zhang, Jiafeng Li, Zhongtao Zhao and Yan Liu
Plants 2024, 13(18), 2652; https://doi.org/10.3390/plants13182652 - 22 Sep 2024
Viewed by 773
Abstract
Several studies have been devoted to seeking some beneficial plant-related microorganisms for a long time, and on this basis, it has been found that arbuscular mycorrhizal fungi (AMF) have a considerable positive impact on plant health as a biological fungal agent. In this [...] Read more.
Several studies have been devoted to seeking some beneficial plant-related microorganisms for a long time, and on this basis, it has been found that arbuscular mycorrhizal fungi (AMF) have a considerable positive impact on plant health as a biological fungal agent. In this study, we focused on the effects of different AMF on the growth dynamics and root configuration of licorice under saline and alkali conditions. The metabolites of licorice under different AMF were assessed using liquid chromatography–tandem mass spectrometry (LC-MS/MS). Funneliformis mosseae (Fm) and Rhizophagus intraradices (Ri) were added as different AMF treatments, while the sterilized saline–alkali soil was treated as a control. Samples were taken in the R1 period (15 d after AMF treatment) and the R2 period (45 d after AMF treatment). The results showed that the application of AMF significantly increased the root growth of licorice and significantly increased the biomass of both shoot and root. A total of 978 metabolites were detected and divided into 12 groups including lipids, which accounted for 15.44%; organic acids and their derivatives, at 5.83%; benzene compounds and organic heterocyclic compounds, at 5.42%; organic oxides, at 3.78%; and ketones, accounting for 3.17%. Compared with the control, there were significant changes in the differential metabolites with treatment inoculated with AMF; the metabolic pathways and biosynthesis of secondary metabolites were the main differential metabolite enrichment pathways in the R1 period, and those in the R2 period were microbial metabolism in diverse environments and the degradation of aromatic compounds. In conclusion, the use of AMF as biofertilizer can effectively improve the growth of licorice, especially in terms of the root development and metabolites, in saline–alkali soil conditions. Full article
(This article belongs to the Special Issue Role of Microbes in Alleviating Abiotic Stress in Plants)
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Figure 1
<p>Changes in plant growth performance for R1 period (<b>a</b>) and R2 period (<b>b</b>); shoot (<b>c</b>) and root (<b>d</b>) biomass production; and root mycorrhizal colonization rate (<b>e</b>). Data followed by different letters above the bars indicate significant (<span class="html-italic">p</span> &lt; 0.05) differences. Abbreviations: R1 and R2, the different periods; CK, treatment with no inoculation; Fm, treatment with <span class="html-italic">Funneliformis mosseae</span> inoculation; Ri, treatment with <span class="html-italic">Rhizophagus intraradices</span> inoculation.</p>
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<p>Changes in root system architecture in R1 period (<b>a</b>) and R2 period (<b>b</b>). Abbreviations: R1 and R2, the different periods; CK, treatment with no inoculation; Fm, treatment with <span class="html-italic">Funneliformis mosseae</span> inoculation; Ri, treatment with <span class="html-italic">Rhizophagus intraradices</span> inoculation.</p>
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<p>Classification statistics of compounds in the root of licorice.</p>
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<p>Number of differential metabolites in roots of licorice in R1 period for CK_vs._Fm (<b>a</b>) and CK_vs._Ri (<b>b</b>) treatments, and in R2 period for CK_vs._Fm (<b>c</b>) and CK_vs._Ri (<b>d</b>) treatments. Abbreviations: R1 and R2, the different periods; CK, treatment with no inoculation; Fm, treatment with <span class="html-italic">Funneliformis mosseae</span> inoculation; Ri, treatment with <span class="html-italic">Rhizophagus intraradices</span> inoculation.</p>
Full article ">Figure 4 Cont.
<p>Number of differential metabolites in roots of licorice in R1 period for CK_vs._Fm (<b>a</b>) and CK_vs._Ri (<b>b</b>) treatments, and in R2 period for CK_vs._Fm (<b>c</b>) and CK_vs._Ri (<b>d</b>) treatments. Abbreviations: R1 and R2, the different periods; CK, treatment with no inoculation; Fm, treatment with <span class="html-italic">Funneliformis mosseae</span> inoculation; Ri, treatment with <span class="html-italic">Rhizophagus intraradices</span> inoculation.</p>
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<p>Heatmap of metabolites in licorice root in R1 period for CK_vs._Fm_vs._Ri (<b>a</b>) treatment, and in R2 period for CK_vs._Fm_vs._Ri (<b>b</b>) treatment. Abbreviations: R1 and R2, the different periods; CK, treatment with no inoculation; Fm, treatment with <span class="html-italic">Funneliformis mosseae</span> inoculation; Ri, treatment with <span class="html-italic">Rhizophagus intraradices</span> inoculation.</p>
Full article ">Figure 5 Cont.
<p>Heatmap of metabolites in licorice root in R1 period for CK_vs._Fm_vs._Ri (<b>a</b>) treatment, and in R2 period for CK_vs._Fm_vs._Ri (<b>b</b>) treatment. Abbreviations: R1 and R2, the different periods; CK, treatment with no inoculation; Fm, treatment with <span class="html-italic">Funneliformis mosseae</span> inoculation; Ri, treatment with <span class="html-italic">Rhizophagus intraradices</span> inoculation.</p>
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<p>Top 20 differential metabolites in roots of licorice in R1 period for CK_vs._Fm (<b>a</b>) and CK_vs._Ri (<b>b</b>) treatments, and in R2 period for CK_vs._Fm (<b>c</b>) and CK_vs._Ri (<b>d</b>) treatments. Abbreviations: R1 and R2, the different periods; CK, treatment with no inoculation; Fm, treatment with <span class="html-italic">Funneliformis mosseae</span> inoculation; Ri, treatment with <span class="html-italic">Rhizophagus intraradices</span> inoculation.</p>
Full article ">Figure 6 Cont.
<p>Top 20 differential metabolites in roots of licorice in R1 period for CK_vs._Fm (<b>a</b>) and CK_vs._Ri (<b>b</b>) treatments, and in R2 period for CK_vs._Fm (<b>c</b>) and CK_vs._Ri (<b>d</b>) treatments. Abbreviations: R1 and R2, the different periods; CK, treatment with no inoculation; Fm, treatment with <span class="html-italic">Funneliformis mosseae</span> inoculation; Ri, treatment with <span class="html-italic">Rhizophagus intraradices</span> inoculation.</p>
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<p>Top 20 metabolic pathways of differential metabolites annotated by KEEG in roots of licorice between R1 period for CK_vs._Fm (<b>a</b>) and CK_vs._Ri (<b>b</b>) treatments and R2 period for CK_vs._Fm (<b>c</b>) and CK_vs._Ri (<b>d</b>) treatments. Abbreviations: R1 and R2, the different periods; CK, treatment with no inoculation; Fm, treatment with <span class="html-italic">Funneliformis mosseae</span> inoculation; Ri, treatment with <span class="html-italic">Rhizophagus intraradices</span> inoculation.</p>
Full article ">Figure 7 Cont.
<p>Top 20 metabolic pathways of differential metabolites annotated by KEEG in roots of licorice between R1 period for CK_vs._Fm (<b>a</b>) and CK_vs._Ri (<b>b</b>) treatments and R2 period for CK_vs._Fm (<b>c</b>) and CK_vs._Ri (<b>d</b>) treatments. Abbreviations: R1 and R2, the different periods; CK, treatment with no inoculation; Fm, treatment with <span class="html-italic">Funneliformis mosseae</span> inoculation; Ri, treatment with <span class="html-italic">Rhizophagus intraradices</span> inoculation.</p>
Full article ">Figure 7 Cont.
<p>Top 20 metabolic pathways of differential metabolites annotated by KEEG in roots of licorice between R1 period for CK_vs._Fm (<b>a</b>) and CK_vs._Ri (<b>b</b>) treatments and R2 period for CK_vs._Fm (<b>c</b>) and CK_vs._Ri (<b>d</b>) treatments. Abbreviations: R1 and R2, the different periods; CK, treatment with no inoculation; Fm, treatment with <span class="html-italic">Funneliformis mosseae</span> inoculation; Ri, treatment with <span class="html-italic">Rhizophagus intraradices</span> inoculation.</p>
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21 pages, 3338 KiB  
Article
Biochemical and Epigenetic Regulation of Glutamate Metabolism in Maize (Zea mays L.) Leaves under Salt Stress
by Alexander T. Eprintsev, Galina B. Anokhina, Polina S. Selivanova, Polina P. Moskvina and Abir U. Igamberdiev
Plants 2024, 13(18), 2651; https://doi.org/10.3390/plants13182651 - 21 Sep 2024
Cited by 3 | Viewed by 1076
Abstract
The effect of salt stress (150 mM NaCl) on the expression of genes, methylation of their promoters, and enzymatic activity of glutamate dehydrogenase (GDH), glutamate decarboxylase (GAD), and the 2-oxoglutarate (2-OG)–dehydrogenase (2-OGDH) complex was studied in maize (Zea mays L.). GDH activity [...] Read more.
The effect of salt stress (150 mM NaCl) on the expression of genes, methylation of their promoters, and enzymatic activity of glutamate dehydrogenase (GDH), glutamate decarboxylase (GAD), and the 2-oxoglutarate (2-OG)–dehydrogenase (2-OGDH) complex was studied in maize (Zea mays L.). GDH activity increased continuously under salt stress, being 3-fold higher after 24 h. This was accompanied by the appearance of a second isoform with lower electrophoretic mobility. The expression of the Gdh1 gene strongly increased after 6–12 h of incubation, which corresponded to the demethylation of its promoter, while Gdh2 gene expression slightly increased after 2–6 h and then decreased. GAD activity gradually increased in the first 12 h, and then returned to the control level. This corresponded to the increase of Gad expression and its demethylation. Salt stress led to a 2-fold increase in the activity of 2-OGDH during the first 6 h of NaCl treatment, then the activity returned to the control level. Expression of the genes Ogdh1 and Ogdh3 peaked after 1–2 h of incubation. After 6–8 h with NaCl, the expression of these genes declined below the control levels, which correlated with the higher methylation of their promoters. We conclude that salt stress causes a redirection of the 2-OG flux to the γ-aminobutyric acid shunt via its amination to glutamate, by altering the expression of the Gdh1 and Gdh2 genes, which likely promotes the assembly of the native GDH molecule having a different subunit composition and greater affinity for 2-OG. Full article
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<p>Effect of salt stress on the operation of the 2-oxoglutarate dehydrogenase (2-OGDH) complex. Changes in the activity of the 2-OGDH complex (<b>A</b>), in the relative levels of transcripts and the fraction of methylation of promoters (black triangles) of the genes <span class="html-italic">Ogdh1</span> (<b>B</b>) and <span class="html-italic">Ogdh3</span> (<b>C</b>) in maize leaves in the course of incubation of maize plants in 150 mM NaCl (red circles) as compared to the control plants (green squares). The data represent the means of three biological repeats ± SD. Statistically significant differences in activity and expression as compared to the control (<span class="html-italic">p</span> ≤ 0.05) are shown by stars.</p>
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<p>Results of analysis of the promoters of the genes <span class="html-italic">Ogdh1</span> (<b>A</b>) and <span class="html-italic">Ogdh3</span> (<b>B</b>) of <span class="html-italic">Zea mays</span> for the presence of CpG islands. Vertical lines indicate the positions of CpG dinucleotides. The outlined arrows indicate the position of the start codon. Thin blue arrows show the change of scale to outline the region used for designing three groups (I, II, III) of primers to the different CpG dinucleotides.</p>
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<p>Effect of salt stress on glutamate dehydrogenase activity and expression in maize leaves. Changes in the activity of glutamate dehydrogenase (GDH) (<b>A</b>), in the relative levels of transcripts and the fraction of methylation of promoters (black triangles) of the genes <span class="html-italic">Gdh1</span> (<b>B</b>) and <span class="html-italic">Gdh2</span> (<b>C</b>) in maize leaves in the course of incubation of maize plants in 150 mM NaCl (red circles) as compared to the control plants (green squares). The data represent the means of three biological repeats ± SD. Statistically significant differences in activity and expression as compared to the control (<span class="html-italic">p</span> ≤ 0.05) are shown by stars.</p>
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<p>Effect of salt stress on the isoenzyme composition of GDH in maize leaves. PAGE electropherogram of GDH from maize leaves under salt stress: 0, 1, 6, 12, 24—incubation time in the NaCl solution (hours); P1, P2—protein bands representing native GDH protein molecules (isoenzymes) stained by the tetrazolium method; and F—dye front.</p>
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<p>Results of analysis of the promoters of the genes <span class="html-italic">Gdh1</span> (<b>A</b>) and <span class="html-italic">Gdh2</span> (<b>B</b>) of <span class="html-italic">Zea mays</span> for the presence of CpG islands. Vertical lines indicate the positions of CpG dinucleotides. The outlined arrows indicate the position of the start codon. Thin blue arrows show the change of scale to outline the region used for designing three groups (I, II, III) of primers to the different CpG dinucleotides.</p>
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<p>Effect of salt stress on glutamate decarboxylase (GAD) activity and expression in maize leaves. Changes in the total enzymatic activity of GAD (<b>A</b>), and in the relative levels of transcripts and the fraction of methylation of the promoters (black triangles) of the gene <span class="html-italic">Gad</span> (<b>B</b>) in maize leaves in the course of incubation of maize plants in 150 mM NaCl (red circles) as compared to the control plants (green squares). The data represent the means of three biological repeats ± SD. Statistically significant differences in activity and expression as compared to the control (<span class="html-italic">p</span> ≤ 0.05) are shown by stars.</p>
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<p>Analysis of <span class="html-italic">Gad</span> gene promoters of <span class="html-italic">Zea mays</span> for the presence of CpG islands. Vertical lines indicate the positions of CpG dinucleotides. The outlined arrow indicates the position of the start codon. Thin blue arrows show the change of scale to outline the region used for designing three groups (I, II, III) of primers to the different CpG dinucleotides.</p>
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<p>Regulation of glutamate metabolism in plant cells under salt stress. Abbreviations: TCA cycle, tricarboxylic acid cycle; 2-OG, 2-oxoglutarate; OGDH, 2-oxoglutarate dehydrogenase complex; GDH1 and GDH2, polypeptides encoded by the <span class="html-italic">Gdh1</span> and <span class="html-italic">Gdh2</span> genes, respectively; Glu, glutamate; GABA, γ-aminobutyric acid; SSA, succinic acid semialdehyde; Suc, succinate. Salt stress affects plant cell metabolism in two stages: 1. During the first 6 h of salt stress, 2-OGDH activity increases, while GDH, due to the induction of <span class="html-italic">Gdh2</span> gene expression, acts as a supplier of 2-OG, the source of which is glutamate (red arrow). 2. After 6 h, 2-OGDH is inhibited, GDH redirects the flow of 2-OG to glutamate due to the induction of the <span class="html-italic">Gdh1</span> gene, 2-OG is converted into glutamate, which is used for the synthesis of GABA (blue arrow). −CH<sub>3</sub> indicates the methylation of gene promoter.</p>
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17 pages, 10109 KiB  
Article
Virus-Induced galactinol-sucrose galactosyltransferase 2 Silencing Delays Tomato Fruit Ripening
by Pengcheng Zhang, Jingjing Wang, Yajie Yang, Jingjing Pan, Xuelian Bai, Ting Zhou and Tongfei Lai
Plants 2024, 13(18), 2650; https://doi.org/10.3390/plants13182650 - 21 Sep 2024
Viewed by 1041
Abstract
Tomato fruit ripening is an elaborate genetic trait correlating with significant changes at physiological and biochemical levels. Sugar metabolism plays an important role in this highly orchestrated process and ultimately determines the quality and nutritional value of fruit. However, the mode of molecular [...] Read more.
Tomato fruit ripening is an elaborate genetic trait correlating with significant changes at physiological and biochemical levels. Sugar metabolism plays an important role in this highly orchestrated process and ultimately determines the quality and nutritional value of fruit. However, the mode of molecular regulation is not well understood. Galactinoal-sucrose galactosyltransferase (GSGT), a key enzyme in the biosynthesis of raffinose family oligosaccharides (RFOs), can transfer the galactose unit from 1-α-D-galactosyl-myo-inositol to sucrose and yield raffinose, or catalyze the reverse reaction. In the present study, the expression of SlGSGT2 was decreased by Potato Virus X (PVX)-mediated gene silencing, which led to an unripe phenotype in tomato fruit. The physiological and biochemical changes induced by SlGSGT2 silencing suggested that the process of fruit ripening was delayed as well. SlGSGT2 silencing also led to significant changes in gene expression levels associated with ethylene production, pigment accumulation, and ripening-associated transcription factors (TFs). In addition, the interaction between SlGSGT2 and SlSPL-CNR indicated a possible regulatory mechanism via ripening-related TFs. These findings would contribute to illustrating the biological functions of GSGT2 in tomato fruit ripening and quality forming. Full article
(This article belongs to the Section Plant Development and Morphogenesis)
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<p>Developmental expression of <span class="html-italic">SlGSGT2</span> in different parts of plants (<b>A</b>) or different ripening stages of tomato cultivar Ailsa Craig fruit (<b>B</b>). The values represent the means of three biological replicates, and the bars represent the standard deviation of the means. Lowercase letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05. DPA: days post anthesis; B+5: 5 days after breaker; B+10: 10 days after breaker.</p>
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<p>Characterization of the nuclear localization signal for GSGT2-sGFP in <span class="html-italic">N. benthamiana</span> leaf cells. Leaves infiltrated with Agrobacterium (strain GV3101, Tiangen, Beijing, China) serve as controls. Leaves are taken on the seventh day post-inoculation and examined under a confocal microscope.</p>
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<p>In vitro transcription of PVX/<span class="html-italic">pSlGSGT2</span>. (<b>A</b>) The schematic representation of the PVX/<span class="html-italic">pSlGSGT2</span> vector. (<b>B</b>) The linearization of PVX and PVX<span class="html-italic">/pSlGSGT2</span> vectors by a restriction endonuclease <span class="html-italic">Spe</span> I. (<b>C</b>) The in vitro transcription RNA products of PVX and PVX/<span class="html-italic">pSlGSGT2</span>. (<b>D</b>) RT-PCR detection of PVX and PVX/<span class="html-italic">pSlGSGT2</span> in infected leaves of <span class="html-italic">N. benthamiana</span>. (<b>E</b>) The phenotypes of <span class="html-italic">N. benthamiana</span> with PVX and PVX/<span class="html-italic">pSlGSGT2</span> through mechanical inoculation after 10 days of culturing. The plant is mock inoculated with H<sub>2</sub>O as the negative control.</p>
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<p>PVX-induced <span class="html-italic">SlGSGT2</span> silencing delays tomato fruit ripening. (<b>A</b>) Ripening phenotypes of wild-type AC fruit and fruit injected with PVX or PVX/<span class="html-italic">pGSGT2</span> at 5 days after breaker. (<b>B</b>) RT-PCR detection of PVX and PVX/<span class="html-italic">pGSGT2</span> in tomato fruit at 5 days after breaker. (<b>C</b>) The relative expression of <span class="html-italic">SlGSGT2</span> in REM and GEM of tomato fruit injected with PVX/<span class="html-italic">pGSGT2</span> at 5 days after breaker. Three primer pairs are designed to detect the expression level of <span class="html-italic">SlGSGT2</span> by qRT-PCR. The primer information is listed in <a href="#app1-plants-13-02650" class="html-app">Table S1</a>. The values represent the means of three biological replicates, and the bars represent the standard deviation of the means. Lowercase letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05. REM: red exocarp and mesocarp; GEM: green exocarp and mesocarp.</p>
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<p>Biochemical characteristics of the ripe and non-ripe sectors of <span class="html-italic">SlGSGT2</span>-silenced fruit at 5 days after breaker. (<b>A</b>) pH, (<b>B</b>) soluble solids content, (<b>C</b>) lycopene content, (<b>D</b>) chlorophyll content, (<b>E</b>) flavonoid content, and (<b>F</b>) anthocyanin content. The values represent the means of three biological replicates, and the bars represent the standard deviation of the means. Lowercase letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05. REM: red exocarp and mesocarp; GEM: green exocarp and mesocarp.</p>
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<p>Relative expression of genes related to ethylene biosynthesis in the ripe and non-ripe sectors of <span class="html-italic">SlGSGT2</span>-silenced fruit at 5 days after breaker. The values represent the means of three biological replicates, and the bars represent the standard deviation of the means. Lowercase letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05. REM: red exocarp and mesocarp; GEM: green exocarp and mesocarp; ACS: 1-aminocyclopropanecarboxylic acid synthase; ACO: 1-aminocyclopropanecarboxylic acid oxidase.</p>
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<p>Relative expression of ripening-associated transcription factor genes in the ripe and non-ripe sectors of <span class="html-italic">SlGSGT2</span>-silenced fruit at 5 days after breaker. The values represent the means of three biological replicates, and the bars represent the standard deviation of the means. Lowercase letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05. REM: red exocarp and mesocarp; GEM: green exocarp and mesocarp.</p>
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<p>Relative expression of genes associated with carotenoid biosynthesis in the ripe and non-ripe sectors of <span class="html-italic">SlGSGT2</span>-silenced fruit at 5 days after breaker. The values represent the means of three biological replicates, and the bars represent the standard deviation of the means. Lowercase letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05. REM: red exocarp and mesocarp; GEM: green exocarp and mesocarp; PSY: Phytoene synthase; PDS: Phytoene desaturase; ZISO: Zeta-carotene isomerase; ZDS: Zeta-carotene desaturase; CRTISO: Carotenoid isomerase; β-LCY: Lycopene β-cyclase; ZEP: Zeaxanthin epoxidase; NCED: 9-cis-epoxycarotenoid dioxygenase; ε-LCY: Lycopene ε-cyclase; β-CRTR: β-carotene hydroxylase.</p>
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<p>Interaction between SlSPL-CNR and SlGSGT2. (<b>A</b>) Interaction between SlSPL-CNR and SlGSGT2 in the yeast two-hybrid system. DDO: SD/–Leu/–Trp double dropout; QDO: SD/–Ade/–His/–Leu/–Trp quadruple dropout; YPDA: yeast extract peptone dextrose adenine medium. a: positive control AH109/pGBKT7-53+pGADT7-T; b: negative control AH109; c: AH109/pGADT7+ pGBKT7; d: AH109/pGADT7-SlSPL-CNR+ pGBKT7-SlGSGT2; e: AH109/pGADT7- SlGSGT2+ pGBKT7-SlSPL-CNR; f: AH109/pGADT7-SlGSGT2+ pGBKT7; g: AH109/pGADT7+ pGBKT7-SlGSGT2. (<b>B</b>) The schematic representation of pGBKT7 and pGADT7 derived vectors used in the yeast two-hybrid system. Detailed vector information of pGADT7 or pGBKT7 can be found in the product manual.</p>
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18 pages, 4364 KiB  
Article
Impact of Chromosomal Fusion and Transposable Elements on the Genomic Evolution and Genetic Diversity of Ilex Species
by Zhenxiu Xu, Haikun Wei, Mingyue Li, Yingjie Qiu, Lei Li, Ke-Wang Xu and Zhonglong Guo
Plants 2024, 13(18), 2649; https://doi.org/10.3390/plants13182649 - 21 Sep 2024
Viewed by 1128
Abstract
The genus Ilex belongs to the sole family and is the single genus within the order Aquifoliales, exhibiting significant phenotypic diversity. However, the genetic differences underlying these phenotypic variations have rarely been studied. In this study, collinearity analyses of three Ilex genomes, Ilex [...] Read more.
The genus Ilex belongs to the sole family and is the single genus within the order Aquifoliales, exhibiting significant phenotypic diversity. However, the genetic differences underlying these phenotypic variations have rarely been studied. In this study, collinearity analyses of three Ilex genomes, Ilex latifolia Thunb., Ilex polyneura (Hand.-Mazz.) S. Y. Hu, and Ilex asprella Champ. ex Benth., indicated a recent fusion event contributing to the reduction of chromosomes in I. asprella. Comparative genome analyses showed slight differences in gene annotation among the three species, implying a minimal disruption of genes following chromosomal fusion in I. asprella. Comprehensive annotation of transposable elements (TEs) revealed that TEs constitute a significant portion of the Ilex genomes, with LTR transposons being predominant. TEs exhibited an inverse relationship with gene density, potentially influencing gene regulation and chromosomal architecture. TE insertions were shown to affect the conformation and binding sites of key genes such as 7-deoxyloganetin glucosyltransferase and transmembrane kinase (TMK) genes, highlighting potential functional impacts. The structural variations caused by TE insertions suggest significant roles in the evolutionary dynamics, leading to either loss or gain of gene function. This study underscores the importance of TEs in shaping the genomic landscape and evolutionary trajectories of Ilex species. Full article
(This article belongs to the Special Issue Genetic and Biological Diversity of Plants)
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<p>Chromosome number in <span class="html-italic">Ilex</span> and chromosome fusion in <span class="html-italic">I. asprella</span>. (<b>A</b>) Statistics of the chromosome number in representative species of <span class="html-italic">Ilex</span>. The photos from left to right indicate <span class="html-italic">I. crenata</span> Thunb. (x = 17), <span class="html-italic">I. opaca</span> Aiton and <span class="html-italic">I. verticillata</span> (L.) A. Gray (x = 18), <span class="html-italic">I. cornuta</span> Lindl. &amp; Paxton (x = 19), <span class="html-italic">I. decidua</span> Walter, <span class="html-italic">I. godajam</span> (Colebr.) Wall. ex Hook.f. and <span class="html-italic">I. pubescens</span> Hook. &amp; Arn. (x = 20), and <span class="html-italic">I. pedunculosa</span> (x = 60). (<b>B</b>) Collinearity plot showing the fusion of Chr1 in <span class="html-italic">I. asprella</span>.</p>
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<p>Comparative genomic analyses in three <span class="html-italic">Ilex</span> species. (<b>A</b>) Collinearity analysis in <span class="html-italic">I. latifolia</span>, <span class="html-italic">I. polyneura</span>, and <span class="html-italic">I. asprella</span>. The chromosome fusion in <span class="html-italic">I. asprella</span> is highlighted in blue. (<b>B</b>) The number of annotated protein-coding genes in corresponding chromosomes of <span class="html-italic">I. latifolia</span>, <span class="html-italic">I. polyneura</span>, and <span class="html-italic">I. asprella</span>. (<b>C</b>) Statistics of 58 transcription factor families in three <span class="html-italic">Ilex</span> species. Percentages in <span class="html-italic">I. latifolia</span>, <span class="html-italic">I. polyneura</span>, and <span class="html-italic">I. asprella</span> are marked in green, orange, and blue, respectively.</p>
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<p>Identification of TEs in three <span class="html-italic">Ilex</span> genomes. (<b>A</b>) Pie charts showing the total proportion of TEs in the genomes of <span class="html-italic">I. latifolia</span>, <span class="html-italic">I. polyneura</span>, and <span class="html-italic">I. asprella.</span> (<b>B</b>,<b>C</b>) Bar charts showing the proportion of TEs belonging to <span class="html-italic">Class I</span>, <span class="html-italic">Class II</span> (<b>B</b>), and each superfamily (<b>C</b>) in the three genomes.</p>
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<p>Distribution of protein-coding genes and TEs in genomes of three <span class="html-italic">Ilex</span> species. (<b>A</b>–<b>C</b>) Three circular plots represent the densities of distinct genomic features in <span class="html-italic">I. latifolia</span> (<b>A</b>), <span class="html-italic">I. polyneura</span> (<b>B</b>), and <span class="html-italic">I. asprella</span> (<b>C</b>). Layers of circular plots from outside to inside indicate (I) gene, (II) transposable elements, (III) terminal inverted repeat, (IV) long terminal repeat, and (V) LTR_<span class="html-italic">Gypsy</span>. The ideogram scale is in Mbp.</p>
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<p>Analysis of protein-coding genes potentially affected by TEs. (<b>A</b>) Number of protein-coding genes intersect with TEs. The solid and dashed rectangles indicate TEs intersect with gene bodies and promoters, respectively. Promoters are defined as the 2000 bps upstream of the transcriptional start site. (<b>B</b>) Proportion of genes which contain TEs in exons, introns, 5′ UTR, and 3′ UTR regions. (<b>C</b>,<b>D</b>) Number of TEs in distinct superfamilies which intersect with gene bodies (<b>C</b>) and promoters (<b>D</b>). (<b>E</b>) Number of predicted <span class="html-italic">cis</span>-regulatory elements caused by TE insertions in promoters. (<b>F</b>) The functional annotation of <span class="html-italic">cis</span>-regulatory elements caused by TE insertions in promoters. The normalized number is calculated by the number of one type of element divided by the total number of elements, then multiplied by 1000.</p>
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<p>Simulated docking structures of 7−deoxyloganetin glucosyltransferase with two small-molecule ligands, 7−deoxyloganetin and UDP−alpha−D−glucose. Protein structures of 7−deoxyloganetin glucosyltransferase in <span class="html-italic">I. asprella</span> (<b>A</b>)<span class="html-italic">, I. polyneura</span> (<b>B</b>), and <span class="html-italic">I. latifolia</span> (<b>C</b>) are indicated in green. Ball and stick structures with red, blue, and gray indicate 7-deoxyloganetin (<b>top</b>) and UDP−alpha−D−glucose (<b>bottom</b>). TEs belonging to <span class="html-italic">Gypsy</span> superfamily insert into the exons of <span class="html-italic">Ila08G000660.1</span> in <span class="html-italic">I. latifolia</span>. Δ<sup>i</sup>G (kcal/mol) indicates the binding free energy at the interface.</p>
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<p>Simulated binding structures of TMK acceptors and their donors. Three TMK proteins, in <span class="html-italic">I. polyneura</span> (<b>A</b>)<span class="html-italic">, I. latifolia</span> (<b>B</b>), and <span class="html-italic">I. asprella</span> (<b>C</b>), interactions with donors (AtMAK1, At4g33430) are predicted by AlphaFold3 [<a href="#B53-plants-13-02649" class="html-bibr">53</a>]. Green structures indicate TMK proteins, while blue structures indicate donors. TEs belonging to <span class="html-italic">CACTA</span> superfamily insert into the exons of <span class="html-italic">TMK</span> gene in <span class="html-italic">I. latifolia</span> and <span class="html-italic">I. asprella</span>. Δ<sup>i</sup>G (kcal/mol) indicates the binding free energy at the interface.</p>
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16 pages, 3963 KiB  
Article
Effect of Delayed Irrigation at the Jointing Stage on Nitrogen, Silicon Nutrition and Grain Yield of Winter Wheat in the North China Plain
by Hao Zheng, Jinyang Sun, Yueping Liang, Caiyun Cao, Yang Gao, Junpeng Zhang, Hongkai Dang and Chunlian Zheng
Plants 2024, 13(18), 2648; https://doi.org/10.3390/plants13182648 - 21 Sep 2024
Viewed by 976
Abstract
Water scarcity is a key limitation to winter wheat production in the North China Plain, and it is essential to explore the optimal timing of spring irrigation to optimize N and Si uptake as well as to safeguard yields. The aim of this [...] Read more.
Water scarcity is a key limitation to winter wheat production in the North China Plain, and it is essential to explore the optimal timing of spring irrigation to optimize N and Si uptake as well as to safeguard yields. The aim of this study was to systematically study the effect mechanism of nitrogen and silicon absorption of winter wheat on yield under spring irrigation and to provide a scientific basis for optimizing irrigation strategy during the growth period of winter wheat. In this experiment, the winter wheat ‘Heng 4399’ was used. Five irrigation periods, i.e., 0 d (CK), 5 d (AJ5), 10 d (AJ10), 15 d (AJ15), and 20 d (AJ20) after the jointing stage, were set up to evaluate the nitrogen (N) and silicon (Si) absorption and grain yield (GY). The results showed that delayed irrigation for 5–10 days at the jointing stage had increased the GY. With the delay of irrigation time, the N/Si content of the entire plant at the maturity period increased first and then decreased; among that, the maximum N contents appeared in AJ15 and AJ5 in 2015 and 2020, respectively, while the Si concentrations appeared in AJ5 and AJ10 in sequence. Compared with AJ15 and AJ20, the N accumulation of vegetative organs in AJ5 increased by 3.05~23.13% at the flowering stage, 14.12~40.12% after the flowering stage, and a 1.76~6.45% increase in the N distribution rate at maturity stage. A correlation analysis revealed that the GY was significantly and positively correlated with the N/Si accumulation at the anthesis and N translocation after the anthesis stage. In conclusion, under limited irrigation conditions, delaying watering for 5 to 10 days at the jointing stage can improve the nitrogen and silicon absorption and nutrient status of wheat plants and increase wheat yield. Full article
(This article belongs to the Special Issue Strategies to Improve Water-Use Efficiency in Plant Production)
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<p>Meteorological map of winter wheat growth period. Note: The subfigures (<b>a</b>,<b>b</b>) represent the daily rainfall and average temperature in 2014–2015 and 2019–20202, respectively. The subfigures (<b>c</b>,<b>d</b>) represent the daily cumulative solar radiation and relative humidity in 2014–2015 and 2019–2020, respectively.</p>
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<p>The N contents and accumulations in different wheat parts at the anthesis and maturity stage. Note: Values within columns followed by the same letter are statistically insignificant at the 0.05 level.</p>
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<p>The Si contents and accumulations in different wheat parts at the anthesis and maturity stage. Note: Values within columns followed by the same letter are statistically insignificant at the 0.05 level.</p>
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<p>Grain yield of winter wheat. Mean values in a separate column followed by similar letters were not significantly different at <span class="html-italic">p</span> &lt; 0.05. The values are the means ± SE (standard error).</p>
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<p>IUE of winter wheat. Mean values in a separate column followed by similar letters were not significantly different at <span class="html-italic">p</span> &lt; 0.05. The values are the means ± SE (standard error).</p>
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<p>The relationship between the yield and other studied parameters. (<b>a</b>) Correlation analysis between grain yield and N accumulation and translocation; (<b>b</b>) Correlation analysis between grain yield and silicon accumulation and translocation. Note: The intensity of color represents the significance of a variable. Blue represents a positive correlation, and red represents a negative correlation. *, **, *** significant at the 0.05, 0.01, and 0.001 probability levels, respectively. GY: grain yield; NAAA: N accumulation amount at anthesis; NAAM: N accumulation amount at maturity; NAAA<sub>leaf</sub>: N accumulation amount in leaf at anthesis; NAAM<sub>leaf</sub>: N accumulation amount in leaf at maturity; NAAAstem: N accumulation amount in stem and sheath at anthesis; NAAM<sub>stem</sub>: N accumulation amount in stem and sheath at maturity; NAAA<sub>spike</sub>: N accumulation amount in ear at anthesis; NAAM<sub>spike</sub>: N accumulation amount in ear at maturity; NAAA<sub>stem+ leaf</sub>: N accumulation amount in stem, sheath, and leaf at anthesis; NTA<sub>stem</sub>: N translocation amount from stem and sheath; NTAleaf: N translocation amount from leaf; NTAspike: N translocation and accumulation amount to the ear; NAA for 100 GY: N accumulation amount for per 100 kg grain yield construction; SiAAA: Si accumulation amount at anthesis; SiAAM: Si accumulation amount at maturity; SiAAA<sub>leaf</sub>: Si accumulation amount in leaf at anthesis; SiAAM<sub>leaf</sub>: Si accumulation amount in leaf at maturity; SiAAA<sub>stem</sub>: Si accumulation amount in stem and sheath at anthesis; SiAAM<sub>stem</sub>: Si accumulation amount in stem and sheath at maturity; SiAAAspike: Si accumulation amount in ear at anthesis; SiAAMspike: Si accumulation amount in ear at maturity; SiAAAM<sub>stem</sub>: Si accumulation amount in stem and sheath from anthesis to maturity; SiAAAM<sub>leaf</sub>: Si accumulation amount in leaf from anthesis to maturity; SiAAAM<sub>spike</sub>: Si accumulation amount in ear from anthesis to maturity; SiAA for 100 GY: Si accumulation amount for per 100 kg grain yield construction.</p>
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<p>The relationship between the yield and other studied parameters. (<b>a</b>) Correlation analysis between grain yield and N accumulation and translocation; (<b>b</b>) Correlation analysis between grain yield and silicon accumulation and translocation. Note: The intensity of color represents the significance of a variable. Blue represents a positive correlation, and red represents a negative correlation. *, **, *** significant at the 0.05, 0.01, and 0.001 probability levels, respectively. GY: grain yield; NAAA: N accumulation amount at anthesis; NAAM: N accumulation amount at maturity; NAAA<sub>leaf</sub>: N accumulation amount in leaf at anthesis; NAAM<sub>leaf</sub>: N accumulation amount in leaf at maturity; NAAAstem: N accumulation amount in stem and sheath at anthesis; NAAM<sub>stem</sub>: N accumulation amount in stem and sheath at maturity; NAAA<sub>spike</sub>: N accumulation amount in ear at anthesis; NAAM<sub>spike</sub>: N accumulation amount in ear at maturity; NAAA<sub>stem+ leaf</sub>: N accumulation amount in stem, sheath, and leaf at anthesis; NTA<sub>stem</sub>: N translocation amount from stem and sheath; NTAleaf: N translocation amount from leaf; NTAspike: N translocation and accumulation amount to the ear; NAA for 100 GY: N accumulation amount for per 100 kg grain yield construction; SiAAA: Si accumulation amount at anthesis; SiAAM: Si accumulation amount at maturity; SiAAA<sub>leaf</sub>: Si accumulation amount in leaf at anthesis; SiAAM<sub>leaf</sub>: Si accumulation amount in leaf at maturity; SiAAA<sub>stem</sub>: Si accumulation amount in stem and sheath at anthesis; SiAAM<sub>stem</sub>: Si accumulation amount in stem and sheath at maturity; SiAAAspike: Si accumulation amount in ear at anthesis; SiAAMspike: Si accumulation amount in ear at maturity; SiAAAM<sub>stem</sub>: Si accumulation amount in stem and sheath from anthesis to maturity; SiAAAM<sub>leaf</sub>: Si accumulation amount in leaf from anthesis to maturity; SiAAAM<sub>spike</sub>: Si accumulation amount in ear from anthesis to maturity; SiAA for 100 GY: Si accumulation amount for per 100 kg grain yield construction.</p>
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21 pages, 5341 KiB  
Article
Functional Identification and Regulatory Active Site Screening of the DfDXS Gene of Dryopteris fragrans
by Hanxu Zhao, Jiameng Su, Zhaoxuan Zhong, Tongyou Xiong, Weicong Dai, Dongrui Zhang and Ying Chang
Plants 2024, 13(18), 2647; https://doi.org/10.3390/plants13182647 - 21 Sep 2024
Viewed by 886
Abstract
Dryopteris fragrans (L.) Schott has anti-inflammatory and antioxidant properties, and terpenoids are important components of its active constituents. The methyl-D-erythritol 4-phosphate (MEP) pathway is one of the major pathways for the synthesis of terpene precursors in plants, and 1-deoxy-D-xylulose-5-phosphate synthase (DXS) is the [...] Read more.
Dryopteris fragrans (L.) Schott has anti-inflammatory and antioxidant properties, and terpenoids are important components of its active constituents. The methyl-D-erythritol 4-phosphate (MEP) pathway is one of the major pathways for the synthesis of terpene precursors in plants, and 1-deoxy-D-xylulose-5-phosphate synthase (DXS) is the first rate-limiting enzyme in this pathway. DXS has been shown to be associated with increased stress tolerance in plants. In this experiment, two DXS genes were extracted from the D. fragrans transcriptome and named DfDXS1 and DfDXS2. Based on phylogenetic tree and conserved motif analyses, DXS was shown to be highly conserved evolutionarily and its localization to chloroplasts was determined by subcellular localization. Prokaryotic expression results showed that the number and growth status of recombinant colonies were better than the control under 400 mM NaCl salt stress and 800 mM mannitol-simulated drought stress. In addition, the DfDXS1 and DfDXS2 transgenic tobacco plants showed improved resistance to drought and salt stress. DfDXS1 and DfDXS2 responded strongly to methyl jasmonate (MeJA) and PEG-mimicked drought stress following exogenous hormone and abiotic stress treatments of D. fragrans. The transcriptional active sites were investigated by dual luciferase and GUS staining assays, and the results showed that the STRE element (AGGGG), the ABRE element (ACGTGGC), and the MYC element (CATTTG) were the important transcriptional active sites in the promoters of the two DXS genes, which were closely associated with hormone response and abiotic stress. These results suggest that the DfDXS gene of D. fragrans plays an important role in hormone signaling and response to stress. This study provides a reference for analyzing the molecular mechanisms of stress tolerance in D. fragrans. Full article
(This article belongs to the Special Issue Isoprenoids: Metabolic Mechanisms, Bioactivity and Application)
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<p>Terpenoid biosynthesis pathway. DXS (marked in red), the first rate-limiting enzyme in the MEP pathway under focus.</p>
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<p>Evolutionary analyses between DfDXS and other species. (<b>A</b>) Phylogenetic tree analysis of the DXS gene family. DXS of the ferns, purple; DXS I, blue; DXS II, green; DXS III, grey. (<b>B</b>) Multiple sequence alignment of DXS protein. The red underline represents the binding site of thiamine pyrophosphate (TPP_DXS); the yellow underline represents the N-terminal domain of transketolase (Transket_pyr_3); and the blue underline represents the C-terminal domain of transketolase (Transketolase_C).</p>
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<p>Subcellular localization and prokaryotic expression of DfDXSs. (<b>A</b>) Subcellular localization of DfDXS1 and DfDXS2, Bar = 50 μm. (<b>B</b>) Growth status of recombinant bacteria and control bacteria under simulated stress, 0<sup>0</sup>~10<sup>−3</sup> represent the dilution gradients of <span class="html-italic">E. coli</span> liquid culture.</p>
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<p>Changes associated with the overexpression of <span class="html-italic">DfDXS1</span> and <span class="html-italic">DfDXS2</span> in transgenic tobacco under salt stress. (<b>A</b>) Comparison of the degree of leaf damage on day 7 after root irrigation treatment with 200 mM NaCl solution. Black arrows indicate the damaged parts of tobacco leaves, bar = 20 mm. (<b>B</b>–<b>E</b>) Physiological parameters of <span class="html-italic">DfDXS1/2</span> overexpressing transgenic tobacco plants under salt stress. An asterisk (*) in the figure indicates that the significant level is 0.05, two asterisks (**) indicate a significant level of 0.01.</p>
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<p>Changes associated with <span class="html-italic">DfDXS1</span>, <span class="html-italic">DfDXS2</span> transgenic tobacco under drought stress. (<b>A</b>) Phenotypic changes in tobacco treated with natural drought for 10 d compared to wild-type tobacco (WT), bar = 7 cm. (<b>B</b>–<b>E</b>) Physiological indices measured in transgenic tobacco plants overexpressing <span class="html-italic">DfDXS1</span>, <span class="html-italic">DfDXS2</span> under drought stress. An asterisk (*) in the figure indicates that the significant level is 0.05, two asterisks (**) indicate a significant level of 0.01.</p>
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<p>Expression patterns of <span class="html-italic">DfDXS1</span> and <span class="html-italic">DfDXS2</span> genes under different treatments. (<b>A</b>–<b>D</b>) Changes in the relative expression levels of <span class="html-italic">DfDXS1</span> and <span class="html-italic">DfDXS2</span> under different phytohormone treatments. (<b>E</b>–<b>H</b>) Changes in the relative expression levels of <span class="html-italic">DfDXS1</span> and <span class="html-italic">DfDXS2</span> under different stress treatments. An asterisk (*) in the figure indicates that the significant level is 0.05, two asterisks (**) indicate a significant level of 0.01, three asterisks (***) indicate that the significant level is 0.001, four asterisks.</p>
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<p>Truncation of the <span class="html-italic">DfDXS1/2</span> promoter and analysis of transcriptional activity. (<b>A</b>) Cloning of truncated fragments and prediction of cis-acting element distribution of <span class="html-italic">DfDXS1</span> gene promoter in <span class="html-italic">D. fragrans.</span> (<b>B</b>) Cloning of truncated fragments and prediction of cis-acting element distribution of <span class="html-italic">DfDXS2</span> gene promoter in <span class="html-italic">D. fragrans.</span> (<b>C</b>) Fluorescence response of truncated fragments of <span class="html-italic">DfDXS1/2</span> promoter of <span class="html-italic">D. fragrans</span> under different stresses. (<b>D</b>) GUS staining of truncated fragments of the <span class="html-italic">DfDXS1/2</span> promoter of <span class="html-italic">D. fragrans</span> under different stresses. The left part of C and D shows the positional distribution of the <span class="html-italic">DfDXS1/2</span> promoter truncation segments transiently transformed in tobacco leaves, where full denotes <span class="html-italic">Pro<sub>DfDXS1/2</sub></span>-full, Δ1 denotes <span class="html-italic">Pro<sub>DfDXS1/2</sub></span>-Δ1, Δ2 denotes <span class="html-italic">Pro<sub>DfDXS1/2</sub></span>-Δ2, Δ3 denotes <span class="html-italic">Pro<sub>DfDXS1/2</sub></span>-Δ3, and Δ4 denotes <span class="html-italic">Pro<sub>DfDXS1/2</sub></span>-Δ4.</p>
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<p>Heatmap of correlation between key enzyme genes of the MEP pathway and different gene modules of the transcriptome. The darker the color, the greater the correlation. DXS, 1-deoxy-D-xylulose-5-phosphate synthase. DXR, 1-Deoxy-d-xylulose-5-phosphate reductoisomerase. MCT, 2-C-methyl-D-erythritol-4-phosphate cytidylyltransferase. CMK, 4-diphosphocytidyl-2-C-methyl-D-erythritol kinase. MDS, 2-C-Methyl-D-erythritol-2,4-cyclodiphosphate synthase. HDS, hydroxide methyl enylamino 4-cyclodiphosphate synthase. HDR, hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate reductase.</p>
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<p>Binding sites and 3D structure prediction of <span class="html-italic">DfDXS1</span> cis-acting elements with transcription factors. (<b>A</b>) LG33.587 bonded to the ABRE assembly; (<b>B</b>,<b>C</b>) LG21.134 bonded to each of the two STRE assemblies; (<b>D</b>) LG15.289 bonded to the MYC assembly; and (<b>E</b>) LG.10.782 bonded to the MYC assembly.</p>
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20 pages, 15914 KiB  
Article
Genome-Wide Identification and Characterization of the HMGR Gene Family in Taraxacum kok-saghyz Provide Insights into Its Regulation in Response to Ethylene and Methyl Jsamonate Treatments
by Pingping Du, Huan He, Jiayin Wang, Lili Wang, Zhuang Meng, Xiang Jin, Liyu Zhang, Fei Wang, Hongbin Li and Quanliang Xie
Plants 2024, 13(18), 2646; https://doi.org/10.3390/plants13182646 - 21 Sep 2024
Cited by 1 | Viewed by 1263
Abstract
HMGR (3-hydroxy-3-methylglutaryl-CoA reductase) plays a crucial role as the first rate-limiting enzyme in the mevalonate (MVA) pathway, which is the upstream pathway of natural rubber biosynthesis. In this study, we carried out whole-genome identification of Taraxacum kok-saghyz (TKS), a novel rubber-producing alternative plant, [...] Read more.
HMGR (3-hydroxy-3-methylglutaryl-CoA reductase) plays a crucial role as the first rate-limiting enzyme in the mevalonate (MVA) pathway, which is the upstream pathway of natural rubber biosynthesis. In this study, we carried out whole-genome identification of Taraxacum kok-saghyz (TKS), a novel rubber-producing alternative plant, and obtained six members of the TkHMGR genes. Bioinformatic analyses were performed including gene structure, protein properties, chromosomal localization, evolutionary relationships, and cis-acting element analyses. The results showed that HMGR genes were highly conserved during evolution with a complete HMG-CoA reductase conserved domain and were closely related to Asteraceae plants during the evolutionary process. The α-helix is the most prominent feature of the secondary structure of the TkHMGR proteins. Collinearity analyses demonstrated that a whole-genome duplication (WGD) event and tandem duplication event play a key role in the expansion of this family and TkHMGR1 and TkHMGR6 have more homologous gene between other species. Cis-acting element analysis revealed that the TkHMGR gene family had a higher number of MYB-related, light-responsive, hormone-responsive elements. In addition, we investigated the expression patterns of family members induced by ethylene (ETH) and methyl jasmonate (MeJA), and their expression levels at different stages of T. kok-saghyz root development. Finally, subcellular localization results showed that six TkHMGR members were all located in the endoplasmic reticulum. In conclusion, the results of our study lay a certain theoretical basis for the subsequent improvement of rubber yield, molecular breeding of rubber-producing plants, and genetic improvement of T. kok-saghyz. Full article
(This article belongs to the Special Issue Bioinformatics and Functional Genomics in Modern Plant Science)
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<p>Phylogenetic relationship, conserved domain, motif analysis, and gene structure of the <span class="html-italic">TkHMGR</span> family members in <span class="html-italic">T. kok-saghyz</span>. (<b>A</b>) A phylogenetic tree based on the TkHMGR protein sequences was generated with MEGA 11.0 using the maximum likelihood (ML) method with 1000 bootstrap replications. (<b>B</b>) Predicted the distribution of conserved domains in TkHMGR proteins. (<b>C</b>) The top ten conserved motifs distribution of TkHMGR proteins; the color boxes represent different conserved motifs, as shown in the scheme on the lower right side of the figure. (<b>D</b>) The exon–intron structures of <span class="html-italic">TkHMGR</span> genes. (<b>E</b>) Three conserved motif logos including HMG-CoA binding sites and NADP(H) binding sites. Amino acids are represented by one-letter codes and presented in different colors.</p>
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<p>Multiple sequence alignment of the TkHMGR proteins. The secondary structural elements predicted with TkHMGR1 are shown above. Red box, white character represents strict identity; red character represents similarity in a group; blue frame represents similarity across groups. The η symbol refers to 3<sub>10</sub>-helixs; α-helixs and 3<sub>10</sub>-helixs are displayed as medium and small squiggles, respectively. β-strands are rendered as arrows; strict β-turns are denoted as TT letters. The orange line represents three different transmembrane helices. The blue and green boxes represent two HMG-CoA binding sites and two NADP(H) binding sites, respectively.</p>
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<p>Phylogenetic analysis of HMGR proteins in <span class="html-italic">T. mongolicum</span>, <span class="html-italic">T. kok-saghyz</span>, <span class="html-italic">A. thaliana</span>, <span class="html-italic">E. ulmoides</span>, <span class="html-italic">N. tabacum</span>, <span class="html-italic">H. annuus</span>, <span class="html-italic">H. brasiliensis</span>, <span class="html-italic">L. sativa</span>, <span class="html-italic">O. sativa</span>, and <span class="html-italic">Z. mays</span>. The tree was constructed with MEGA 11.0 using the maximum likelihood (ML) method with 1000 bootstrap replications.</p>
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<p>Collinearity analysis of <span class="html-italic">TkHMGR</span> genes. The red lines show the <span class="html-italic">TkHMGR</span> gene pairs replicated; the grey lines indicate collinear blocks across the whole genome. The innermost track of the Circos plot indicates the chromosome length and number. The second and third tracks indicate the density of genes on the corresponding chromosome; the gene density distribution of the TKS genome varies from 0 to 14, with an average of 4 genes per 100 kb. The outermost track represents the corresponding GC content of the whole genome.</p>
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<p>Collinearity analysis of <span class="html-italic">HMGR</span> genes between <span class="html-italic">T. kok-saghyz</span>, <span class="html-italic">A. thaliana</span>, <span class="html-italic">H. annuus</span>, <span class="html-italic">H. brasiliensis</span>, <span class="html-italic">L. sativa</span>, and <span class="html-italic">T. mongolicum</span>. The gray lines represent homologous gene pairs between TKS and other species. The highlighted red lines represent the collinear relationship of <span class="html-italic">HMGR</span> gene pairs.</p>
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<p>Predicted the cis-acting elements of the promoters 2000 bps upstream of <span class="html-italic">TkHMGR</span> genes. (<b>A</b>) The number of cis-acting elements in different classifications of each gene. (<b>B</b>) The total number of different cis-acting elements.</p>
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<p>Expression profiles of <span class="html-italic">TkHMGR</span> genes and the changes in proline, soluble sugar, and chlorophyll content under exogenous hormone treatment. (<b>A</b>) Expression levels in roots of six-month-old TKS treated with 100 μmol/L ETH. (<b>B</b>) Expression levels in leaves of six-month-old TKS treated with 100 μmol/L ETH. (<b>C</b>) Proline and soluble sugar content in 6-month-old TKS roots treated with ETH; chlorophyll content in 6-month-old TKS leaves treated with ETH. (<b>D</b>) Expression levels in roots of six-month-old TKS treated with 1 mmol/L MeJA. (<b>E</b>) Expression levels in leaves of six-month-old TKS treated with 1 mmol/L MeJA. (<b>F</b>) Proline and soluble sugar content in 6-month-old TKS roots treated with MeJA; chlorophyll content in 6-month-old TKS leaves treated with MeJA. Data are shown as the means ± SD of three independent biological repetitions using the 2<sup>−ΔΔCt</sup> method with <span class="html-italic">Tkβ-actin</span> as the internal standard for normalization. Asterisks represent significant differences via the Student’s <span class="html-italic">t</span>-test analysis compared with the control (* <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001, and **** <span class="html-italic">p</span> &lt; 0.0001). (<b>G</b>) The heatmap display of TKS roots from different developmental stages: 1 month old, 3 months old, 6 months old, 12 months old, and 18 months old based on transcript per million (TPM) values. Red indicates high expression levels, and white indicates low expression levels. The numbers on the box represent the TPM value.</p>
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<p>The subcellular localization of six TkHMGR proteins. The empty eGFP vector was used as the control. Endoplasmic reticulum (ER) marker was labeled with mCherry. The white line represents the region of interest in the merge field. Bar = 25 μm.</p>
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16 pages, 5598 KiB  
Article
Genome-Wide Identification and Characterization of MYB Transcription Factors in Sudan Grass under Drought Stress
by Qiuxu Liu, Yalin Xu, Xiangyan Li, Tiangang Qi, Bo Li, Hong Wang and Yongqun Zhu
Plants 2024, 13(18), 2645; https://doi.org/10.3390/plants13182645 - 21 Sep 2024
Viewed by 1185
Abstract
Sudan grass (Sorghum sudanense S.) is a warm-season annual grass with high yield, rich nutritional value, good regeneration, and tolerance to biotic and abiotic stresses. However, prolonged drought affects the yield and quality of Sudan grass. As one of the largest families [...] Read more.
Sudan grass (Sorghum sudanense S.) is a warm-season annual grass with high yield, rich nutritional value, good regeneration, and tolerance to biotic and abiotic stresses. However, prolonged drought affects the yield and quality of Sudan grass. As one of the largest families of multifunctional transcription factors in plants, MYB is widely involved in regulating plant growth and development, hormonal signaling, and stress responses at the gene transcription level. However, the regulatory role of MYB genes has not been well characterized in Sudan grass under abiotic stress. In this study, 113 MYB genes were identified in the Sudan grass genome and categorized into three groups by phylogenetic analysis. The promoter regions of SsMYB genes contain different cis-regulatory elements, which are involved in developmental, hormonal, and stress responses, and may be closely related to their diverse regulatory functions. In addition, collinearity analysis showed that the expansion of the SsMYB gene family occurred mainly through segmental duplications. Under drought conditions, SsMYB genes showed diverse expression patterns, which varied at different time points. Interaction networks of 74 SsMYB genes were predicted based on motif binding sites, expression correlations, and protein interactions. Heterologous expression showed that SsMYB8, SsMYB15, and SsMYB64 all significantly enhanced the drought tolerance of yeast cells. Meanwhile, the subcellular localization of all three genes is in the nucleus. Overall, this study provides new insights into the evolution and function of MYB genes and provides valuable candidate genes for breeding efforts in Sudan grass. Full article
(This article belongs to the Section Plant Response to Abiotic Stress and Climate Change)
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<p>Phylogenetic analysis of MYB proteins in Sudan grass, <span class="html-italic">Arabidopsis thaliana</span>, and <span class="html-italic">Sorghum bicolor</span>. Different MYB subgroups (1R-MYB, R2R3-MYB, and 3R-MYB) are indicated in different colors. Red dots represent members of the Sudan grass MYB family, with each subgroup represented by a different colored block. The subclasses were designated as previously reported [<a href="#B18-plants-13-02645" class="html-bibr">18</a>]. S1–S25 represent different subclasses of MYBs in <span class="html-italic">Arabidopsis</span> and classify <span class="html-italic">SsMYBs</span> of the same branch into the same subclass. The phylogenetic tree was constructed using the neighbor-joining (NJ) method with a bootstrap value of 1000.</p>
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<p>Phylogenetic tree, motif pattern, and gene structure analysis of the <span class="html-italic">MYB</span> gene family in Sudan grass. (<b>a</b>) Phylogenetic tree of the Sudan grass <span class="html-italic">MYB</span> gene family. (<b>b</b>) The 10 conserved MYB proteins are represented by different colored squares. (<b>c</b>) Characterization of the cis-acting elements in the promoter region of the <span class="html-italic">SsMYB</span> gene. (<b>d</b>) Exon-intron structure of the Sudan grass MYB proteins. The green frame represents the gene untranslated region (UTR), the yellow frame represents the gene exons, and the black lines represent the introns.</p>
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<p>Distribution of 113 <span class="html-italic">SsMYB</span> genes on 10 chromosomes. The scale indicates chromosome length.</p>
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<p>Distribution and collinearity analysis of MYBs in the Sudan grass genome. The blue line indicates the collinearity between the <span class="html-italic">SsMYBs</span>.</p>
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<p>Collinearity analysis of <span class="html-italic">MYB</span> genes between Sudan grass and sorghum. Gray lines represent covariance blocks between the Sudan grass and sorghum, and blue lines represent covariant <span class="html-italic">MYB</span> gene pairs.</p>
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<p>Expression levels of 70 <span class="html-italic">SsMYB</span> genes in the aboveground plant parts in response to drought stress. Gray frames indicate a lack of gene expression in the transcriptome data. DR: drought response; drought treatments: 6 h, 12 h, 24 h, 48 h, 72 h, 144 h.</p>
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<p>The interaction networks of 74 SsMYB proteins predicted based on the STRING database. The gray circles represent members of the <span class="html-italic">SsMYB</span> gene family, and the red circles represent other genes in Sudan grass.</p>
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<p>Overexpression of <span class="html-italic">SsMYB8</span>, <span class="html-italic">SsMYB15</span>, and <span class="html-italic">SsMYB64</span> improves drought tolerance in yeast. The growth of INSVC1 yeast transformed with pYES2-NTB containing <span class="html-italic">SsMYB8</span>, <span class="html-italic">SsMYB15</span>, and <span class="html-italic">SsMYB64</span> and empty vector pYES2-NTB. The left side indicates the concentration of different PEG3350 in SG-U medium. The top triangles indicate the OD values of the yeast, diluted tenfold as a gradient.</p>
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<p>Subcellular localization of pCAMBIA1302-GFP-<span class="html-italic">SsMYB8</span>, pCAMBIA1302-GFP-<span class="html-italic">SsMYB15</span>, and pCAMBIA1302-GFP-<span class="html-italic">SsMYB64</span> fusion proteins in leaf epidermal cells of <span class="html-italic">Tobacco benthamiana</span>. Leaf epidermal cells transformed with pCAMBIA1302-GFP were used as controls. Scale bar: 20 μm. Primers used for vector construction are listed in <a href="#app1-plants-13-02645" class="html-app">Table S5</a>.</p>
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14 pages, 715 KiB  
Article
Effects of Acmella radicans Invasion on Soil Seed Bank Community Characteristics in Different Habitats
by Xiaohan Wu, Kexin Yang, Fengping Zheng, Gaofeng Xu, Zewen Fan, David Roy Clements, Yunhai Yang, Shaosong Yang, Guimei Jin, Fudou Zhang and Shicai Shen
Plants 2024, 13(18), 2644; https://doi.org/10.3390/plants13182644 - 21 Sep 2024
Viewed by 897
Abstract
To examine the effects of the recent Acmella radicans invasion on plant community and diversity in invaded habitats, the composition, density, species richness, diversity indices, and evenness index of the soil seed bank community of two different habitats (wasteland and cultivated land) in [...] Read more.
To examine the effects of the recent Acmella radicans invasion on plant community and diversity in invaded habitats, the composition, density, species richness, diversity indices, and evenness index of the soil seed bank community of two different habitats (wasteland and cultivated land) in Yunnan Province, China, were analyzed through field sampling and greenhouse germination tests. A total of 28 species of plants belonging to 15 families and 28 genera, all annual herbs, were found in the soil seed bank. Seed densities and species number in the seed bank tended to be greater in April than in October; cultivated land also featured higher seed densities and species numbers compared to wasteland. With increased A. radicans cover, the seed bank population of A. radicans also significantly increased, but the seed bank populations of many other dominant species (e.g., Ageratum conyzoides and Gamochaeta pensylvanica) and native species (e.g., Laggera crispata and Poa annua) clearly declined. The germination of A. radicans seeds was concentrated during the period from the 4th to the 5th weeks. Vertically, the seed number of A. radicans was significantly different among the 0–5 cm, 5–10 cm and 10–20 cm layers that accounted for 80.7–90.6%, 9.4–16.1% and 0.0–3.2% of the total seed density in wasteland, respectively; and in cultivated land, A. radicans accounted for 56.8–64.9%, 26.7–31.8% and 8.1–13.5% of the total seed density, respectively. With reduced A. radicans cover, the species richness, Simpson index, Shannon–Wiener index, and Pielou indices of the weed community generally increased, and most diversity indices of weed communities in cultivated land were lower than in wasteland under the same cover of A. radicans. The results indicate that the invasion of A. radicans has negatively affected local weed community composition and reduced weed community diversity, and that these negative impacts in cultivated land may be enhanced by human disturbance. Our study was the first to elucidate the influence of A. radicans invasion on soil seed bank community characteristics in invaded habitats, providing a better understanding of its invasion and spread mechanisms in order to aid in developing a scientific basis for the prevention and control of this invader. Full article
(This article belongs to the Special Issue Plant Invasion 2023)
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<p>Percentage of invasive plants, native plants and <span class="html-italic">Acmella radicans</span> of the total density of soil weed communities within different habitats (CW = cover of wasteland and CC = cover of cultivated land).</p>
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<p>Percentage of soil seed distribution of <span class="html-italic">Acmella radicans</span> among different soil layers within different habitats (CW = cover of wasteland and CC = cover of cultivated land).</p>
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20 pages, 6666 KiB  
Article
Rhizofungus Aspergillus terreus Mitigates Heavy Metal Stress-Associated Damage in Triticum aestivum L.
by Naveen Dilawar, Muhammad Hamayun, Amjad Iqbal, Bokyung Lee, Sajid Ali, Ayaz Ahmad, Abdulwahed Fahad Alrefaei, Turki Kh. Faraj, Ho-Youn Kim and Anwar Hussain
Plants 2024, 13(18), 2643; https://doi.org/10.3390/plants13182643 - 21 Sep 2024
Viewed by 913
Abstract
Industrial waste and sewage deposit heavy metals into the soil, where they can remain for long periods. Although there are several methods to manage heavy metals in agricultural soil, microorganisms present a promising and effective solution for their detoxification. We isolated a rhizofungus, [...] Read more.
Industrial waste and sewage deposit heavy metals into the soil, where they can remain for long periods. Although there are several methods to manage heavy metals in agricultural soil, microorganisms present a promising and effective solution for their detoxification. We isolated a rhizofungus, Aspergillus terreus (GenBank Acc. No. KT310979.1), from Parthenium hysterophorus L., and investigated its growth-promoting and metal detoxification capabilities. The isolated fungus was evaluated for its ability to mitigate lead (25 and 75 ppm) and copper (100 and 200 ppm) toxicity in Triticum aestivum L. seedlings. The experiment utilized a completely randomized design with three replicates for each treatment. A. terreus successfully colonized the roots of wheat seedlings, even in the presence of heavy metals, and significantly enhanced plant growth. The isolate effectively alleviates lead and copper stress in wheat seedlings, as evidenced by increases in shoot length (142%), root length (98%), fresh weight (24%), dry weight (73%), protein content (31%), and sugar content (40%). It was observed that wheat seedlings possess a basic defense system against stress, but it was insufficient to support normal growth. Fungal inoculation strengthened the host’s defense system and reduced its exposure to toxic heavy metals. In treated seedlings, exposure to heavy metals significantly upregulated MT1 gene expression, which aided in metal detoxification, enhanced antioxidant defenses, and maintained metal homeostasis. A reduction in metal exposure was observed in several areas, including normalizing the activities of antioxidant enzymes that had been elevated by up to 67% following exposure to Pb (75 mg/kg) and Cu (200 mg/kg). Heavy metal exposure elevated antioxidant levels but also increased ROS levels by 86%. However, with Aspergillus terreus colonization, ROS levels stayed within normal ranges. This decrease in ROS was associated with reduced malondialdehyde (MDA) levels, enhanced membrane stability, and restored root architecture. In conclusion, rhizofungal colonization improved metal tolerance in seedlings by decreasing metal uptake and increasing the levels of metal-binding metallothionein proteins. Full article
(This article belongs to the Special Issue Role of Microbial Plant Biostimulants in Abiotic Stress Mitigation)
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<p>Assessment of the copper and lead tolerance potential of NB (<span class="html-italic">A. terreus</span>). The isolate was grown in shaking flasks (250 mL) containing 50 mL Czapek broth amended with different concentrations of Pb and Cu. Mean of triplicated data with standard error and letter labels for denoting significance are given (ANOVA-Duncan <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Colony morphologies on (<b>a</b>) a macroscopic and (<b>b</b>) a microscopic scale of the isolated rhizospheric fungi. (<b>c</b>) Phylogenetic tree based on ITS rDNA sequences of the rhizospheric fungal strain <span class="html-italic">A. terreus</span> was constructed.</p>
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<p>Release of soluble sugars and proteins by NB (<span class="html-italic">A. terreus</span>) fungus in response to varied amounts of lead acetate and copper sulfate stress. Data are the means of duplicates with standard error and letter labels denoting significance (ANOVA-Duncan <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>(<b>a</b>) Root length, shoot length, (<b>b</b>) fresh weight, and dry weight of <span class="html-italic">T. aestivum</span> L. in response to varied amounts of lead acetate and copper sulfate stress treated with NB (<span class="html-italic">A. terreus</span>). Data are the means of duplicates with standard error (Duncan test; <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>(<b>a</b>) Chlorophyll a, and (<b>b</b>) chlorophyll b of <span class="html-italic">T. aestivum</span> L. in response to varied amounts of lead acetate and copper sulfate stress treated with NB (<span class="html-italic">A. terreus</span>). Data are the means of duplicates with standard error (Duncan test; <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>(<b>a</b>) SOD, (<b>b</b>) POD, (<b>c</b>) CAT, and (<b>d</b>) electrolyte leakage of <span class="html-italic">T. aestivum</span> L. in response to varied amounts of lead acetate and copper sulfate stress treated with NB (<span class="html-italic">A. terreus</span>). Data are the means of duplicates with standard error (Duncan test; <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>(<b>a</b>) H<sub>2</sub>O<sub>2</sub> and (<b>b</b>) MDA content assessment of <span class="html-italic">T. aestivum</span> L. in response to varied amounts of lead acetate and copper sulfate stress treated with NB (<span class="html-italic">A. terreus</span>). Data are the means of duplicates with standard error (Duncan test; <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>(<b>a</b>) Total protein, and (<b>b</b>) sugar content assessment of <span class="html-italic">T. aestivum</span> L. in response to varied amounts of lead acetate and copper sulfate stress treated with NB (<span class="html-italic">A. terreus</span>). Data are the means of duplicates with standard error (Duncan test; <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Colonization of the rhizofungus NB (<span class="html-italic">A. terreus</span>) in the roots of <span class="html-italic">T. aestivum</span> L. exposed to different concentrations of Pb and Cu; (<b>a</b>) control, (<b>b</b>) NB (<span class="html-italic">A. terreus</span>), (<b>c</b>) NB + Pb 25 ppm, (<b>d</b>) NB + Pb 75 ppm, (<b>e</b>) NB + Cu 100 ppm, (<b>f</b>) NB + Cu 200 ppm, (<b>g</b>) NB + Pb 25Cu100 ppm, (<b>h</b>) NB + Pb75Cu200 ppm. Root sections were stained with lactophenol cotton blue and observed under a light microscope at 40× magnification.</p>
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<p>Role of NB (<span class="html-italic">A. terreus</span>) with lead acetate [Pb(C<sub>2</sub>H<sub>3</sub>O<sub>2</sub>)<sub>2</sub>] and copper sulfate [CuSO<sub>4</sub>] on (<b>a</b>) phytochelatin (PC1) and (<b>b</b>) metallothionein (MT1) gene expression in <span class="html-italic">T. aestivum</span> L. cultivated in soil polluted with Pb and Cu. Data are the means of duplicates with standard error (Duncan test; <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The scanning electron microscopy (SEM) picture of the root surface show the presence of strain <span class="html-italic">A. terreus</span> on it. (<b>A</b>) The root of <span class="html-italic">T. aestivum</span> plant without inoculation. (<b>B</b>) The fine structure of <span class="html-italic">T. aestivum</span> roots, subjected to both induced Pb and Cu stresses at the minutest level. (<b>C</b>) Hyphae of the <span class="html-italic">A. terreus</span> strain (the white arrows show the position). This activity was performed in Centralized Resource Laboratory (CRL), University of Peshawar.</p>
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<p>The scanning electron microscopy (SEM) picture of the root surface show the presence of strain <span class="html-italic">A. terreus</span> on it. (<b>A</b>) The root of <span class="html-italic">T. aestivum</span> plant without inoculation. (<b>B</b>) The fine structure of <span class="html-italic">T. aestivum</span> roots, subjected to both induced Pb and Cu stresses at the minutest level. (<b>C</b>) Hyphae of the <span class="html-italic">A. terreus</span> strain (the white arrows show the position). This activity was performed in Centralized Resource Laboratory (CRL), University of Peshawar.</p>
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12 pages, 2436 KiB  
Article
Identification of Salt-Stress-Responding Genes by Weighted Gene Correlation Network Analysis and Association Analysis in Wheat Leaves
by Linyi Qiao, Yijuan Li, Liujie Wang, Chunxia Gu, Shiyin Luo, Xin Li, Jinlong Yan, Chengda Lu, Zhijian Chang, Wei Gao and Xiaojun Zhang
Plants 2024, 13(18), 2642; https://doi.org/10.3390/plants13182642 - 21 Sep 2024
Cited by 1 | Viewed by 873
Abstract
The leaf is not only the main site of photosynthesis, but also an important organ reflecting plant salt tolerance. Discovery of salt-stress-responding genes in the leaf is of great significance for the molecular improvement of salt tolerance in wheat varieties. In this study, [...] Read more.
The leaf is not only the main site of photosynthesis, but also an important organ reflecting plant salt tolerance. Discovery of salt-stress-responding genes in the leaf is of great significance for the molecular improvement of salt tolerance in wheat varieties. In this study, transcriptome sequencing was conducted on the leaves of salt-tolerant wheat germplasm CH7034 seedlings at 0, 1, 6, 24, and 48 h after NaCl treatment. Based on weighted gene correlation network analysis of differentially expressed genes (DEGs) under salt stress, 12 co-expression modules were obtained, of which, 9 modules containing 4029 DEGs were related to the salt stress time-course. These DEGs were submitted to the Wheat Union database, and a total of 904,588 SNPs were retrieved from 114 wheat germplasms, distributed on 21 wheat chromosomes. Using the R language package and GAPIT program, association analysis was performed between 904,588 SNPs and leaf salt injury index of 114 wheat germplasms. The results showed that 30 single nucleotide polymorphisms (SNPs) from 15 DEGs were associated with salt tolerance. Then, nine candidate genes, including four genes (TaBAM, TaPGDH, TaGluTR, and TaAAP) encoding enzymes as well as five genes (TaB12D, TaS40, TaPPR, TaJAZ, and TaWRKY) encoding functional proteins, were identified by converting salt tolerance-related SNPs into Kompetitive Allele-Specifc PCR (KASP) markers for validation. Finally, interaction network prediction was performed on TaBAM and TaAAP, both belonging to the Turquoise module. Our results will contribute to a further understanding of the salt stress response mechanism in plant leaves and provide candidate genes and molecular markers for improving salt-tolerant wheat varieties. Full article
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<p>Differentially expressed genes (DEGs) under salt stress in the leaves of wheat strain CH7034. (<b>a</b>) The number of DEGs at 4 timepoints after 250 mmol/L NaCl treatment. (<b>b</b>) Venn diagram of DEGs.</p>
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<p>Weighted gene co-expression network analysis (WGCNA) for DEGs responding to salt stress in wheat leaves. (<b>a</b>) Cluster dendrogram and module colors of 4519 DEGs. (<b>b</b>) The number of DEGs contained in each module. (<b>c</b>) Heatmap for the relationships of modules and salt treatment time-courses. Each cell lists the correlation index and <span class="html-italic">p</span>-value in parentheses; * indicates <span class="html-italic">p</span> &lt; 0.05, ** indicates <span class="html-italic">p</span> &lt; 0.01, and **** indicates <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>Association analysis between salt-stress-response-module genes and salt-tolerance phenotype of wheat leaves. (<b>a</b>) Chromosome distribution of SNPs derived from target module genes. (<b>b</b>) Manhattan plot of association analysis between SNPs and leaf salt injury index of 114 wheat germplasms. The threshold is set to −log<sub>10</sub> (<span class="html-italic">p</span>) &gt; 4.</p>
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<p>KASP validation of candidate genes. LSI: leaf salt injury index; the bases listed on horizontal axis represent the binary genotypes of each KASP marker. ** indicates <span class="html-italic">p</span> &lt; 0.01, *** indicates <span class="html-italic">p</span> &lt; 0.001, and **** indicates <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>Predictive interaction network for <span class="html-italic">TaBAM</span> and <span class="html-italic">TaAAP</span> (<b>a</b>) and their transcriptional response to salt stress (<b>b</b>).</p>
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<p>The main GO enrichment terms of the Turquoise module. Terms related to oxidation–reduction or organic metabolism are displayed in bold.</p>
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29 pages, 7547 KiB  
Article
Transcriptomic and Phenotypical Analysis of the Physiological Plasticity of Chamaecyparis hodginsii Roots under Different Nutrient Environments and Adjacent Plant Competition
by Bingjun Li, Wenchen Chen, Yanmei Pan, Wenxiu Wu, Ying Zhang, Jundong Rong, Tianyou He, Liguang Chen and Yushan Zheng
Plants 2024, 13(18), 2641; https://doi.org/10.3390/plants13182641 - 21 Sep 2024
Viewed by 648
Abstract
Chamaecyparis hodginsii seedlings undergo significant changes during growth due to different nutrient environments and adjacent plant competition, which is evident in the physiological plasticity changes in their roots. Therefore, in this experiment, 20 one-year-old elite C. hodginsii family seedlings were selected as the [...] Read more.
Chamaecyparis hodginsii seedlings undergo significant changes during growth due to different nutrient environments and adjacent plant competition, which is evident in the physiological plasticity changes in their roots. Therefore, in this experiment, 20 one-year-old elite C. hodginsii family seedlings were selected as the test objects, and the different nutrient environments and adjacent plant competition environments in nature were artificially simulated. Four nutrient environments (N heterogeneous nutrient environment, P heterogeneous nutrient environment, K heterogeneous nutrient environment, and homogeneous environment) and three planting patterns (single plant, conspecific neighbor, and heterospecific neighbor) were set up to determine the differences in root physiological indexes and plasticity of different family seedlings, and the families and treatment combinations with higher comprehensive evaluation were selected. The transcriptome sequencing of fine roots of C. hodginsii under different treatments was performed to analyze the differentially expressed genes. The results showed that the root activity, antioxidant enzyme activity, and nutrient element content of C. hodginsii seedlings in the N and P heterogeneous environments were higher than those in the homogeneous nutrient environment, while there was no significant difference between the K heterogeneous nutrient environment and the homogeneous environment, but MDA content was higher than that in other nutrient environments. The root activity and antioxidant enzyme activity in the competitive patterns were generally higher than those in the single plant and reached the peak in the heterospecific neighbor. The root physiological plasticity index of line 490 was the highest, but the comprehensive evaluation of root physiological indexes of lines 539 and 535 was better. The pattern with the highest comprehensive evaluation score was P heterogeneous nutrient environment × heterospecific neighbor. The effects of the N and P heterogeneous nutrient environments on root transcriptome genes were similar, which significantly increased DNA transcription and regulatory factor activity, while K heterogeneous nutrient environment focused on the regulation of root enzyme activity. The heterogeneous nutrient environment induces the conduction of hormone signals in the roots of C. hodginsii and induces the synthesis of phenylpropanone. The biosynthesis of phenylpropanone in the roots of C. hodginsii will increase significantly under competitive patterns. In summary, the N and P heterogeneous nutrient environments and the heterospecific neighbor can improve the root physiological indexes of C. hodginsii families, and the root physiological indexes of lines 539 and 535 are the best. The nutrient environment and competition pattern mainly affect the root system to transmit hormone signals to regulate enzyme activity. Full article
(This article belongs to the Section Plant Molecular Biology)
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<p>Geographical location of the greenhouses in Fujian Agriculture and Forestry University. (Note: The blue part represents Fujian Province, the light green represents Fuzhou City, and the dark green represents Cangshan District.)</p>
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<p>A front view of the pot container.</p>
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<p>Differences in the root system activities of <span class="html-italic">C. hodginsii</span> family seedlings under different treatments. Note: Different uppercase letters represent significant differences in the indices of <span class="html-italic">C. hodginsii</span> seedlings in different nutrient environments under the same planting pattern (<span class="html-italic">p</span> &lt; 0.05). Different lowercase letters represent significant differences in the indices of <span class="html-italic">C. hodginsii</span> seedlings in different planting patterns under the same nutrient environments (<span class="html-italic">p</span> &lt; 0.05). HET-N, N heterogeneous nutrient environment; HET-P, P heterogeneous nutrient environment; HET-K, K heterogeneous nutrient environment; HOM, homogeneous environment; F-SP, single-plant pattern; F-CN, conspecific neighbor; F-MP, heterospecific neighbor. Error lines represent standard errors.</p>
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<p>Differences in antioxidant enzyme activities and MDA contents in the root systems of <span class="html-italic">C. hodginsii</span> seedlings under different treatments. Note: Different uppercase letters represent significant differences in the indices of <span class="html-italic">C. hodginsii</span> seedlings in different nutrient environments under the same planting pattern (<span class="html-italic">p</span> &lt; 0.05). Different lowercase letters represent significant differences in the indices of <span class="html-italic">C. hodginsii</span> seedlings in different planting patterns under the same nutrient environments (<span class="html-italic">p</span> &lt; 0.05). HET-N, N heterogeneous nutrient environment; HET-P, P heterogeneous nutrient environment; HET-K, K heterogeneous nutrient environment; HOM, homogeneous environment; F-SP, single-plant pattern; F-CN, conspecific neighbor; F-MP, heterospecific neighbor. Error lines represent standard errors.</p>
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<p>Nutrient content differences in the root system of <span class="html-italic">C. hodginsii</span> seedlings under different treatments. Note: Different uppercase letters represent significant differences in the indices of <span class="html-italic">C. hodginsii</span> seedlings in different nutrient environments under the same planting pattern (<span class="html-italic">p</span> &lt; 0.05). Different lowercase letters represent significant differences in the indices of <span class="html-italic">C. hodginsii</span> seedlings in different planting patterns under the same nutrient environments (<span class="html-italic">p</span> &lt; 0.05). HET-N, N heterogeneous nutrient environment; HET-P, P heterogeneous nutrient environment; HET-K, K heterogeneous nutrient environment; HOM, homogeneous environment; F-SP, single-plant pattern; F-CN, conspecific neighbor; F-MP, heterospecific neighbor. Error lines represent standard errors.</p>
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<p>Elemental stoichiometry characteristics of the root system of <span class="html-italic">C. hodginsii</span> seedlings under different treatments. Note: Different uppercase letters represent significant differences in the indices of <span class="html-italic">C. hodginsii</span> seedlings in different nutrient environments under the same planting pattern (<span class="html-italic">p</span> &lt; 0.05). Different lowercase letters represent significant differences in the indices of <span class="html-italic">C. hodginsii</span> seedlings in different planting patterns under the same nutrient environments (<span class="html-italic">p</span> &lt; 0.05). HET-N, N heterogeneous nutrient environment; HET-P, P heterogeneous nutrient environment; HET-K, K heterogeneous nutrient environment; HOM, homogeneous environment; F-SP, single-plant pattern; F-CN, conspecific neighbor; F-MP, heterospecific neighbor. Error lines represent standard errors.</p>
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<p>Cluster analysis of <span class="html-italic">C. hodginsii</span> families. Note: In the figure, the green part represents group I, the blue represents group II, and the red represents group III and group IV.</p>
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<p>Principal component analysis plot of physiological indicators of the <span class="html-italic">C. hodginsii</span> root system under different treatments.</p>
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<p>Distribution of differentially expressed genes in different comparison combinations.</p>
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<p>The GO bubble plot of the <span class="html-italic">C. hodginsii</span> root system in a heterogeneous nutrient environment. Note: The horizontal axis in the figure represents the ratio of DEGs annotated in the GO term to the total number of DEGs, while the vertical axis represents the GO term. The size of the dots represents the number of genes annotated in the GO term, and the red to purple color range represents the significance of the enrichment. The same applies below.</p>
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<p>The GO bubble plot of <span class="html-italic">C. hodginsii</span> in different planting patterns.</p>
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<p>The KEGG bubble plot of <span class="html-italic">C. hodginsii</span> under a heterogeneous nutrient environment.</p>
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<p>The KEGG bubble plot of <span class="html-italic">C. hodginsii</span> under planting patterns.</p>
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<p>qRT PCR validation of 12 candidate genes from the transcriptome of <span class="html-italic">C. hodginsii</span> roots.</p>
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23 pages, 10170 KiB  
Article
Comparative Analysis of Chemical Profiles and Biological Activities of Essential Oils Derived from Torreya grandis Arils and Leaves: In Vitro and In Silico Studies
by Pengfei Deng, Huiling Wang and Xiaoniu Xu
Plants 2024, 13(18), 2640; https://doi.org/10.3390/plants13182640 - 21 Sep 2024
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Abstract
Torreya grandis (T. grandis, Taxaceae) is a well-known nut tree species. Its fruit aril and leaves possess a unique aroma, making it an ideal natural raw material for extracting essential oils (EOs). This study aims to comprehensively compare the composition, biological [...] Read more.
Torreya grandis (T. grandis, Taxaceae) is a well-known nut tree species. Its fruit aril and leaves possess a unique aroma, making it an ideal natural raw material for extracting essential oils (EOs). This study aims to comprehensively compare the composition, biological activities, and pharmacological mechanism of EOs extracted from the arils (AEO) and leaves (LEO) of T. grandis. The results revealed that the chemical composition of the two EOs was highly consistent, with α-pinene and D-limonene as the main components. Both EOs significantly reduced cellular melanin production and inhibited tyrosinase activity in α-MSH-stimulated B16 cells (p < 0.05). AEO and LEO suppressed inflammatory responses in LPS-stimulated RAW 264.7 macrophages, significantly inhibiting cellular NO production and proinflammatory cytokines such as TNF-α and IL-6 (p < 0.05). A network pharmacology analysis reveals that AEO and LEO share similar molecular mechanisms and pharmacological pathways for treating skin pigmentation and inflammation. Regulating inflammatory cytokines may be a critical pathway for AEO and LEO in treating skin pigmentation. These findings suggest that AEO and LEO have potential for cosmetic applications. The leaves of T. grandis could be a valuable source of supplementary materials for producing T. grandis aril EO. Full article
(This article belongs to the Section Phytochemistry)
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Figure 1

Figure 1
<p>(<b>a</b>) Principal component analysis of components isolated from the samples of <span class="html-italic">Torreya grandis</span> aril (AEO) and leaves (LEO). (<b>b</b>) The difference in the percentages of the major components of AEO and LEO.</p>
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<p>Effects of AEO and LEO on (<b>a</b>) cellular tyrosinase activity and (<b>b</b>) melanin content in <span class="html-italic">α</span>-MSH-stimulated B16 cells. (<b>c</b>) The antioxidant efficacy of AEO and LEO was evaluated utilizing a <span class="html-italic">β</span>-carotene/linoleic acid bleaching assay. Effects of AEO and LEO on (<b>d</b>) NO synthesis, (<b>e</b>) IL-6 levels, and (<b>f</b>) TNF-<span class="html-italic">α</span> levels in LPS-activated RAW 264.7 macrophage cells. The results are expressed as mean and standard deviation (<span class="html-italic">n</span> = 3). Statistical data discrepancies were confirmed at <span class="html-italic">p</span> &lt; 0.05 and denoted by distinct lowercase letters in the graph.</p>
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<p>Compound–target interaction network of AEO and LEO with (<b>a</b>) skin pigmentation and (<b>b</b>) skin inflammation. Node size is relative to degree.</p>
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<p>Protein–protein interaction (PPI) network constructed by using STRING database. (<b>a</b>) Skin pigmentation-related PPI network of AEO. (<b>b</b>) Skin pigmentation-related PPI network of LEO. (<b>c</b>) Skin inflammation-related PPI network of AEO. (<b>d</b>) Skin inflammation-related PPI network of LEO. Nodes signify proteins, with colors ranging from pink to red indicating the extent of binding between them. Edge signifies protein–protein interaction.</p>
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<p>The interaction network of GO terms and KEGG pathways generated using ClueGo plugin in Cytoscape. (<b>a</b>) Skin pigmentation-related interaction network of AEO. (<b>b</b>) Skin pigmentation-related interaction network of LEO. (<b>c</b>) Skin inflammation-related interaction network of AEO. (<b>d</b>) Skin inflammation-related interaction network of LEO. Similar signaling terms are represented as a cluster by nodes of the same color. A node is involved in more than one cluster of terms if it contains different colors.</p>
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<p>Docking complexes of the main targets and their most strongly bound compositions. (<b>a</b>) TNF and cis-<span class="html-italic">β</span>-copaene, (<b>b</b>) STAT3 and (−)-globulol, (<b>c</b>) EGFR and (−)-globulol, (<b>d</b>) CASP3 and (−)-globulol, (<b>e</b>) HIF1A and <span class="html-italic">α</span>-pinene, (<b>f</b>) BCL2 and cis-<span class="html-italic">β</span>-copaene, and (<b>g</b>) NFKB1 and <span class="html-italic">α</span>-terpinyl acetate.</p>
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