[go: up one dir, main page]
More Web Proxy on the site http://driver.im/
You seem to have javascript disabled. Please note that many of the page functionalities won't work as expected without javascript enabled.
 
 
Sign in to use this feature.

Years

Between: -

Subjects

remove_circle_outline
remove_circle_outline
remove_circle_outline

Journals

Article Types

Countries / Regions

Search Results (2)

Search Parameters:
Keywords = GKK 1032B

Order results
Result details
Results per page
Select all
Export citation of selected articles as:
14 pages, 1046 KiB  
Article
Endophytic Microbes from Medicinal Plants in Fenghuang Mountain as a Source of Antibiotics
by Aiping Yang, Yu Hong, Fengjuan Zhou, Ling Zhang, Youjuan Zhu, Chang Wang, Yang Hu, Li Yu, Lihong Chen and Xiachang Wang
Molecules 2023, 28(17), 6301; https://doi.org/10.3390/molecules28176301 - 28 Aug 2023
Cited by 1 | Viewed by 1645
Abstract
One of the largest concerns with world health today is still antibiotic resistance, which is making it imperative to find efficient alternatives as soon as possible. It has been demonstrated that microbes are reliable sources for the creation of therapeutic antibiotics. This research [...] Read more.
One of the largest concerns with world health today is still antibiotic resistance, which is making it imperative to find efficient alternatives as soon as possible. It has been demonstrated that microbes are reliable sources for the creation of therapeutic antibiotics. This research intends to investigate the endophytic microorganisms from several medicinal plants in Fenghuang Mountain (Jiangsu Province, China) and to discover new antibiotics from their secondary metabolites. A total of 269 endophytic strains were isolated from nine distinct medicinal plants. Taxonomic analysis revealed that there were 20 distinct species among these endophytes, with Streptomyces being the most common genus. Three of the target strains were chosen for scale-up fermentation after preliminary screening of antibacterial activities and the metabolomics investigation using LC-MS. These strains were Penicillium sp. NX-S-6, Streptomyces sp. YHLB-L-2 and Streptomyces sp. ZLBB-S-6. Twenty-three secondary metabolites (123), including a new sorbicillin analogue (1), were produced as a result of antibacterial activity-guided isolation. Through spectroscopic analysis using MS and NMR, the structures of yield compounds were clarified. According to antibacterial data, S. aureus or B. subtilis were inhibited to varying degrees by sorrentanone (3), emodic acid (8), GKK1032 B (10), linoleic acid (14), toyocamycin (17) and quinomycin A (21). The most effective antimicrobial agent against S. aureus, B. subtilis, E. coli and A. baumannii was quinomycin A (21). In addition, quinomycin A showed strong antifungal activity against Aspergillus fumigatus, Cryptococcus neoformans, and two clinical isolated strains Aspergillus fumigatus #176 and #339, with MIC as 16, 4, 16 and 16 µg/mL, respectively. This is the first time that bioprospecting of actinobacteria and their secondary metabolites from medicinal plants in Fenghuang Mountain was reported. The finding demonstrates the potential of endophytic microbes in medical plants to produce a variety of natural products. Endophytic microbes will be an important source for new antibiotics. Full article
Show Figures

Figure 1

Figure 1
<p>Diversity analysis of 269 endophytic strains from nine medicinal plants.</p>
Full article ">Figure 2
<p><b>1</b>–<b>23</b> isolated from three endophytes <span class="html-italic">Penicillium</span> sp. NX-S-6, <span class="html-italic">Streptomyces</span> sp. YHLB-L-2 and <span class="html-italic">Streptomyces</span> sp. ZLBB-S-6.</p>
Full article ">Figure 3
<p>Key COSY, HMBC and NOESY correlations of <b>1</b>.</p>
Full article ">
23 pages, 2038 KiB  
Article
Chromone Derivatives and Other Constituents from Cultures of the Marine Sponge-Associated Fungus Penicillium erubescens KUFA0220 and Their Antibacterial Activity
by Decha Kumla, José A. Pereira, Tida Dethoup, Luis Gales, Joana Freitas-Silva, Paulo M. Costa, Michael Lee, Artur M. S. Silva, Nazim Sekeroglu, Madalena M. M. Pinto and Anake Kijjoa
Mar. Drugs 2018, 16(8), 289; https://doi.org/10.3390/md16080289 - 20 Aug 2018
Cited by 21 | Viewed by 6574
Abstract
A previously unreported chromene derivative, 1-hydroxy-12-methoxycitromycin (1c), and four previously undescribed chromone derivatives, including pyanochromone (3b), spirofuranochromone (4), 7-hydroxy-6-methoxy-4-oxo-3-[(1E)-3-oxobut-1-en-1-yl]-4H-chromene-5-carboxylic acid (5), a pyranochromone dimer (6) were isolated, together with [...] Read more.
A previously unreported chromene derivative, 1-hydroxy-12-methoxycitromycin (1c), and four previously undescribed chromone derivatives, including pyanochromone (3b), spirofuranochromone (4), 7-hydroxy-6-methoxy-4-oxo-3-[(1E)-3-oxobut-1-en-1-yl]-4H-chromene-5-carboxylic acid (5), a pyranochromone dimer (6) were isolated, together with thirteen known compounds: β-sitostenone, ergosterol 5,8-endoperoxide, citromycin (1a), 12-methoxycitromycin (1b), myxotrichin D (1d), 12-methoxycitromycetin (1e), anhydrofulvic acid (2a), myxotrichin C (2b), penialidin D (2c), penialidin F (3a), SPF-3059-30 (7), GKK1032B (8) and secalonic acid A (9), from cultures of the marine sponge- associated fungus Penicillium erubescens KUFA0220. Compounds 1ae, 2a, 3a, 4, 79, were tested for their antibacterial activity against Gram-positive and Gram-negative reference and multidrug-resistant strains isolated from the environment. Only 8 exhibited an in vitro growth inhibition of all Gram-positive bacteria whereas 9 showed growth inhibition of methicillin-resistant Staphyllococus aureus (MRSA). None of the compounds were active against Gram-negative bacteria tested. Full article
Show Figures

Graphical abstract

Graphical abstract
Full article ">Figure 1
<p>The structures of some secondary metabolites, isolated from cultures of the marine sponge-associated fungus <span class="html-italic">P. erubescens</span> KUFA 0220.</p>
Full article ">Figure 2
<p>The most stable APFD/6-311+G(2d,p) conformation of <b>3a</b> (C-2<span class="html-italic">R</span>). The asymmetric carbon is presented with the hydroxyl group facing straight down.</p>
Full article ">Figure 3
<p>The experimental (solid line, left axis) and simulated (dotted line, right axis) ECD spectra of 3a/C-2(<span class="html-italic">R</span>). The ECD experimental signal was very weak, requiring the use of 40 accumulations, increased digital integration time and post-acquisition noise filtering (moving mean).</p>
Full article ">Figure 4
<p>The formation of <b>3a</b>, <b>2b</b> and a pair of enantiomers of <b>3b</b> by nucleophilic addition of methanol to <b>2b</b>.</p>
Full article ">Figure 5
<p>The Ortep view of <b>4</b>.</p>
Full article ">Figure 6
<p>The Ortep view of <b>5</b>.</p>
Full article ">Figure 7
<p>The most stable APFD/6-31G conformation of <b>6</b>, presented with the absolute configuration found by spectrometric methods.</p>
Full article ">Figure 8
<p>The experimental (solid line, left axes) and simulated (dotted line, right axes) ECD spectra of four diastereoisomers of <b>6</b>. The best experimental-simulated fit belongs to the diastereoisomer with the absolute configuration 10<span class="html-italic">S</span>, 12<span class="html-italic">S</span>, 3′<span class="html-italic">S</span>, 15<span class="html-italic">S</span>. The theoretical ECD spectra of the enantiomers of the presented diastereoisomers are the exact inversions of the ones depicted here and do not fit the experimental data.</p>
Full article ">
Back to TopTop