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13 pages, 5044 KiB  
Article
Study on Smoke Characteristics in Cavern Complexes of Pumped-Storage Power Stations
by Peifeng Hu, Tong Xu, Chang Liu, Kai Wang, Fazheng Chong, Fengju Shang and Jiansong Wu
Fire 2024, 7(12), 453; https://doi.org/10.3390/fire7120453 - 2 Dec 2024
Viewed by 431
Abstract
The underground power houses of pumped-storage power stations (PSPSs) are highly complex, with interconnected and multidimensional structures, including various tunnels, such as the main and auxiliary power houses (MAPH), main transformer tunnel (MTT), tailrace gate tunnel (TGT), access tunnels (ATs), cable tunnels (CTs) [...] Read more.
The underground power houses of pumped-storage power stations (PSPSs) are highly complex, with interconnected and multidimensional structures, including various tunnels, such as the main and auxiliary power houses (MAPH), main transformer tunnel (MTT), tailrace gate tunnel (TGT), access tunnels (ATs), cable tunnels (CTs) etc. During intensive civil construction and electromechanical installation, fire risk becomes particularly prominent. Current research mainly examines fire incidents within individual tunnels, lacking comprehensive analyses of smoke spread across the entire cavern network. Therefore, in this study, a numerical model of a cavern complex in a PSPS was established to analyze smoke behavior and temperature distribution under various fire scenarios. The results indicated that when a fire occurred in the MAPH, the fire risk was relatively higher compared to fires in other places. Using the example of smoke spread from the MAPH to the MTT, the smoke spread process through key connecting caverns was analyzed. Initially, the temperature and velocity were stable, and the CTs and traffic cable tunnel in the auxiliary powerhouse (TCTAP) were the main smoke paths. After 7 min, the heat release rate (HRR) became stable, and CTs and ATs became the main paths for smoke spread, which could provide a reference for improving fire design in underground cavern systems. Full article
(This article belongs to the Special Issue Modeling, Experiment and Simulation of Tunnel Fire)
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Figure 1

Figure 1
<p>Geometry model of underground cavern group for PSPS.</p>
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<p>Schematic diagram of fire scenarios in MAPH: (<b>a</b>) front view; (<b>b</b>) side view.</p>
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<p>Smoke spread paths for different fire development stages at different fire source positions: (<b>a</b>) MAPH; (<b>b</b>) MTT; (<b>c</b>) TGT.</p>
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<p>Temperature characteristics of cavern groups at different fire development stages: fire in (<b>a</b>) MAPH; (<b>b</b>) MTT; (<b>c</b>) TGT.</p>
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<p>Smoke flow characteristics of cavern groups at different fire development stages: fire in (<b>a</b>) MAPH; (<b>b</b>) MTT; (<b>c</b>) TGT.</p>
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<p>Temperature distribution under ceiling in key caverns: (<b>a</b>) MAPH; (<b>b</b>) MTT.</p>
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<p>Temperature variations of ceiling in key connecting caverns: (<b>a</b>) CT; (<b>b</b>) TCTAPH; (<b>c</b>) AT.</p>
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<p>Variations in smoke flow velocity at the ceiling of key caverns: (<b>a</b>) MAPH; (<b>b</b>) MTT.</p>
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<p>Variations in Smoke Flow Velocity at the Ceiling of Key Connecting Caverns: (<b>a</b>) CT; (<b>b</b>) TCTAPH; (<b>c</b>) AT.</p>
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22 pages, 10755 KiB  
Article
Experimental Studies of Low-Reinforced Concrete Structures Containing Inter-Bay Construction Joints Strengthened with Prestressed Basalt Composite Reinforcements and External Transverse Reinforcements
by Oleg Rubin, Dmitry Kozlov, Anton Antonov and Amer Almasri
Buildings 2024, 14(11), 3594; https://doi.org/10.3390/buildings14113594 - 12 Nov 2024
Viewed by 614
Abstract
During the long-term operation of main run-of-river head powerhouses for hydroelectric power plants, technical changes that deteriorate the operational properties of their reinforced concrete structures can occur. Therefore, in order to substantiate the application of prestressed basalt composite reinforcements to strengthen reinforced concrete [...] Read more.
During the long-term operation of main run-of-river head powerhouses for hydroelectric power plants, technical changes that deteriorate the operational properties of their reinforced concrete structures can occur. Therefore, in order to substantiate the application of prestressed basalt composite reinforcements to strengthen reinforced concrete hydraulic structures in operation, a set of computational and experimental studies was carried out, taking into account their characteristic features. After 4 years of ageing, the serviceability and reliability of the beams with prestressed basalt composite reinforcements were demonstrated through stabilisation of the prestress losses and the values obtained for bearing capacity, deflection, and the width of the opening of the inter-bay construction joints and the deformations of the metal reinforcements and the basalt composite reinforcements. The bearing capacity of the investigated reinforced concrete beams reinforced with external transverse reinforcements was increased 1.4–2.5 times over that of the variants reinforced with longitudinal prestressed basal composite reinforcements. Furthermore, in this study, the impacts of static loads and seismic effects with a magnitude greater than 8 on the run-of-river hydroelectric power plant powerhouse were calculated based on dynamic design theory. Regarding applications to hydroelectric power plant structures and constructions, for which it is not always possible to determine the location of compressed or tensile zones during their operation nor under seismic action, our research results are suggestive of a reasonably positive effect. Full article
(This article belongs to the Section Building Structures)
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Figure 1

Figure 1
<p>Vertical section of the head powerhouse of a run-of-river HPP along the flow: (1) pier and (2) head wall of the powerhouse (shaded). Cross-section A-A shows (1) the piers, (2) the head wall of the powerhouse (shaded), and (3) the gate.</p>
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<p>Equipment for testing the reinforced concrete models.The 100-tonne power stand (the bottom part); The ENERPAC hydraulic power pumping station; A “CONER” hydraulic jack for tensioning the basalt composite reinforcements (the beam tensioning process is shown); Oil distributors.</p>
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<p>Prestress losses in reinforcements of different types (stresses are plotted vertically, in MPa).</p>
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<p>Maximum principal stresses in the structures of the HPP building under seismic action (<b>a</b>) in the upper head wall of the HPP building (MPa) under seismic action 2.62 s from the beginning of seismic action and (<b>b</b>) in the piers of the HPP building (MPa) 4.94 s from the beginning of seismic action.</p>
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<p>Design of prototype beams B1 and B2.</p>
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<p>Cracking behaviour in the experimental beams.</p>
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<p>Deflection plots of beam B1.</p>
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<p>Deflection plots of beam B2.</p>
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<p>Plots of the width of the opening of inter-bay joints in beam B1.</p>
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<p>Plots of the width of the opening of the inter-bay joints in beam B2.</p>
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<p>Plots of the deformation of the steel reinforcements in the inter-bay joints of beam B1 (×10<sup>−5</sup>).</p>
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<p>Plots of the deformation of steel reinforcements in the inter-bay joints of beam B2 (×10<sup>−5</sup>).</p>
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<p>Plots of the deformation of the basalt composite reinforcement in the inter-bay joints of beam B1 (×10<sup>−5</sup>).</p>
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<p>Plots of the deformation of basalt composite reinforcements in the inter-bay joints of beam B2 (×10<sup>−5</sup>).</p>
Full article ">Scheme 1
<p>Types and number of tests of experimental beams B1 and B2 in 2020 and in 2024. All beams were reinforced with a basic 2Ø12 longitudinal steel reinforcement of class A400 in the tensile zone, with a longitudinal reinforcement coefficient <math display="inline"><semantics> <mrow> <msub> <mrow> <mi mathvariant="sans-serif">μ</mi> </mrow> <mrow> <mi mathvariant="normal">s</mi> </mrow> </msub> </mrow> </semantics></math> = 0.0056; all beams also had two vertical inter-bay construction joints.</p>
Full article ">Scheme 1 Cont.
<p>Types and number of tests of experimental beams B1 and B2 in 2020 and in 2024. All beams were reinforced with a basic 2Ø12 longitudinal steel reinforcement of class A400 in the tensile zone, with a longitudinal reinforcement coefficient <math display="inline"><semantics> <mrow> <msub> <mrow> <mi mathvariant="sans-serif">μ</mi> </mrow> <mrow> <mi mathvariant="normal">s</mi> </mrow> </msub> </mrow> </semantics></math> = 0.0056; all beams also had two vertical inter-bay construction joints.</p>
Full article ">Scheme 1 Cont.
<p>Types and number of tests of experimental beams B1 and B2 in 2020 and in 2024. All beams were reinforced with a basic 2Ø12 longitudinal steel reinforcement of class A400 in the tensile zone, with a longitudinal reinforcement coefficient <math display="inline"><semantics> <mrow> <msub> <mrow> <mi mathvariant="sans-serif">μ</mi> </mrow> <mrow> <mi mathvariant="normal">s</mi> </mrow> </msub> </mrow> </semantics></math> = 0.0056; all beams also had two vertical inter-bay construction joints.</p>
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37 pages, 3352 KiB  
Review
Photosynthetic Electron Flows and Networks of Metabolite Trafficking to Sustain Metabolism in Photosynthetic Systems
by Neda Fakhimi and Arthur R. Grossman
Plants 2024, 13(21), 3015; https://doi.org/10.3390/plants13213015 - 28 Oct 2024
Viewed by 1176
Abstract
Photosynthetic eukaryotes have metabolic pathways that occur in distinct subcellular compartments. However, because metabolites synthesized in one compartment, including fixed carbon compounds and reductant generated by photosynthetic electron flows, may be integral to processes in other compartments, the cells must efficiently move metabolites [...] Read more.
Photosynthetic eukaryotes have metabolic pathways that occur in distinct subcellular compartments. However, because metabolites synthesized in one compartment, including fixed carbon compounds and reductant generated by photosynthetic electron flows, may be integral to processes in other compartments, the cells must efficiently move metabolites among the different compartments. This review examines the various photosynthetic electron flows used to generate ATP and fixed carbon and the trafficking of metabolites in the green alga Chlamydomomas reinhardtii; information on other algae and plants is provided to add depth and nuance to the discussion. We emphasized the trafficking of metabolites across the envelope membranes of the two energy powerhouse organelles of the cell, the chloroplast and mitochondrion, the nature and roles of the major mobile metabolites that move among these compartments, and the specific or presumed transporters involved in that trafficking. These transporters include sugar-phosphate (sugar-P)/inorganic phosphate (Pi) transporters and dicarboxylate transporters, although, in many cases, we know little about the substrate specificities of these transporters, how their activities are regulated/coordinated, compensatory responses among transporters when specific transporters are compromised, associations between transporters and other cellular proteins, and the possibilities for forming specific ‘megacomplexes’ involving interactions between enzymes of central metabolism with specific transport proteins. Finally, we discuss metabolite trafficking associated with specific biological processes that occur under various environmental conditions to help to maintain the cell’s fitness. These processes include C4 metabolism in plants and the carbon concentrating mechanism, photorespiration, and fermentation metabolism in algae. Full article
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Figure 1
<p>Photosynthetic and respiratory electron transport and their interactions. Linear photosynthetic electron transport (bottom) involves excitation of reaction centers, photosystem I and II, (PSI, PSII) and extraction of electrons from H<sub>2</sub>O by the PSII O<sub>2</sub> evolving complex. Extracted electrons pass through PSII reaction centers, the plastoquinone (PQ) pool, Cytochrome b<sub>6</sub>f (Cytb<sub>6</sub>f), plastocyanin (PC) and to PSI where they are used to generate reduced ferredoxin (FDX) and NADPH through the activity of Ferredoxin NADP<sup>+</sup> reductase (FNR); the NADPH and the ATP synthesized by the ATP synthase (fueled by the proton gradient across thylakoid membranes) and the NADPH are used to reduce CO<sub>2</sub> and drive metabolic processes in the cells. Reducing electrons generated on the acceptor side of PSI or PSII can be routed through AEF pathways: Cyclic electron flow occurs through both PGR5/PGRL1, and the NDA2 pathways. In the Mehler reaction, PSI-derived electrons are used to reduce O<sub>2</sub>, and the ROS generated (O<sub>2</sub><sup>−</sup> and H<sub>2</sub>O<sub>2</sub>) can be converted to H<sub>2</sub>O through superoxide dismutase and catalase/ascorbate peroxidase. In pseudocyclic electron flow (PCEF), electrons from PSI/FDX are transferred to the diiron proteins (FLV) to reduce O<sub>2</sub> to H<sub>2</sub>O. The plastoquinol terminal oxidase (PTOX) catalyzes the reduction of O<sub>2</sub> on the acceptor side of PSII. In chloroplast-to-mitochondria electron flow (CMEF), electrons are exported from the chloroplast to the mitochondrion through the function of OAA (or 2-oxoglutarate)/malate redox shuttles on both the chloroplast and mitochondria envelopes; reductant is shuttled between the compartments through the interconversion of malate/NAD(P)<sup>+</sup> to OAA/NAD(P)H. ***, Transporting triose-P out of chloroplasts is another potential avenue for delivering reductant to mitochondria. However, since there is still little reported evidence for that route of delivery, the extent to which it provides reductant to power mitochondrial respiration is uncertain. The electrons released from these reductants are used to drive oxidative phosphorylation in mitochondria (top) through either cytochrome oxidase (complex IV) or alternative oxidases (AOXs), generating additional ATP. ICEM, inner chloroplast envelope membrane; OCEM, outer chloroplast envelope membrane; IMM, inner mitochondrion membrane; OMM, outer mitochondrion membrane. Representation of the photosynthetic electron transport chain was modified from Grossman in [<a href="#B18-plants-13-03015" class="html-bibr">18</a>]. Created with <a href="http://BioRender.com" target="_blank">BioRender.com</a>.</p>
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<p>Overview of characterized and uncharacterized major fixed carbon and reductant transporters on inner chloroplast and mitochondrial envelope membranes. (<b>A</b>) Transporters on the chloroplast envelope in <span class="html-italic">Chlamydomonas</span> are divided into two major groups: sugar-P/phosphate transporters, including GPTs, TPTs, and PPTs, which transport both fixed carbon and reductants, and dicarboxylate transporters, which mainly shuttle reductants. Based on Doebbe et al. [<a href="#B19-plants-13-03015" class="html-bibr">19</a>], there might also be a hexose transporter on the chloroplast envelope, although the specificity and the mechanism of transport have not been elucidated. While the substrates transported are indicated, many of these bidirectional sugar-P transporters can use multiple substrates (and counter-substrate); Pi is considered a preferred counter-substrate. (<b>B</b>) Transporters on the mitochondrial inner membrane of plants, with analogous proteins in <span class="html-italic">Chlamydomonas</span>), include di- and tricarboxylate transporters. Most of the metabolites translocated across the mitochondria membrane are associated with the TCA cycle. Reductant imported into the mitochondria can drive oxidative phosphorylation. CCPs (two in <span class="html-italic">Chlamydomonas</span>) are mitochondrial transporters that increase in abundance (transcript level) under low CO<sub>2</sub> conditions, but their functions are yet to be determined. Dark gray indicates that some transporters from this category have been characterized in <span class="html-italic">Chlamydomonas</span>, while light gray indicates that the transporter has not yet been characterized; the presence of these transporters on the mitochondrial envelope of <span class="html-italic">Chlamydomonas</span> and their contribution to its metabolism are predicted from information derived from plant system. DIC, dicarboxylate translocator on the mitochondrial envelope; DiT, dicarboxylate translocator on the chloroplast envelope; DTC, tricarboxylate translocator; GPT, glucose 6-phosphate/phosphate transporter; HK, hexokinase; HXT, hexose transporter; MDH, malate dehydrogenase; PPT, phosphoenol pyruvate/phosphate transporter; TPT, triose-phosphate/phosphate transporter; DOXP/MEP, 1-deoxyxylulose 5-phosphate/2-C-methylerythritol 4-phosphate pathway; TCA, tricarboxylic acid cycle; AA, amino acid; ATP, adenosine triphosphate; Asp, aspartate; CO<sub>2</sub>, carbon dioxide; DHAP, dihydroxyacetone phosphate; E4P, D-erythrose 4-phosphate; Glc, glucose; Glc1P, glucose 1-phosphate; Glc6P, glucose 6-phosphate; G3P, glyceraldehyde-3-phosphate; Glu, glutamate; 3-PGA, 3-phosphoglyceric acid; NAD(P)(H), nicotinamide adenine dinucleotide (phosphate); OAA, oxaloacetate; 2-OG, 2-oxoglutarate; PEP, phosphoenol pyruvate; Pi, inorganic phosphate; RuBP, ribulose 1,5-bisphosphate; Ru5P, ribose-5-phosphate; ICEM, inner chloroplast envelope membrane; OCEM, outer chloroplast envelope membrane; IMM, inner mitochondrion membrane; OMM, outer mitochondrion membrane. Created with <a href="http://BioRender.com" target="_blank">BioRender.com</a>.</p>
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<p>Metabolite transport required for various metabolic processes in the cell. (<b>A</b>) CO<sub>2</sub>-concentrating mechanism in a NADP-malic enzyme type C4 plant, such as sugarcane [adapted with some modifications from [<a href="#B156-plants-13-03015" class="html-bibr">156</a>]]. (<b>B</b>) Trafficking of Ci across the plasma membrane and to the pyrenoid. CO<sub>2</sub> either directly diffuses across the plasma membrane or is transported by LCI1. It can also be converted to bicarbonate by the activity of CAH1 and transported by HLA3, LCIA, and BSTs through the plasma membrane, chloroplast envelope, and thylakoid membranes, respectively. In the thylakoids that penetrate the pyrenoid, the bicarbonate is converted to CO<sub>2</sub> through the activity of CAH3, and then fixed by Rubisco. The components and their locations in the cell are based on studies with <span class="html-italic">Chlamydomonas</span> [<a href="#B157-plants-13-03015" class="html-bibr">157</a>]. (<b>C</b>) Putative metabolite transport required for photorespiration in <span class="html-italic">Chlamydomonas</span>. Transporters responsible for metabolite transport at the chloroplast and mitochondrial envelope membranes; most of these transporters have not yet been identified in <span class="html-italic">Chlamydomonas</span> (except for ammonium transporter, AMT). (<b>D</b>) Fermentation in <span class="html-italic">Chlamydomonas</span>. Glycerol, lactate, CO<sub>2</sub>, H<sub>2</sub>, acetate, ethanol, and formate are fermentative end-products. The succinate-producing pathway (reverse TCA cycle) is not shown. Gray arrows in the cytosol indicate omitted steps under fermentative conditions. The ethanol pathway in mitochondria has been shown only at the activity level, so it is indicated in gray. Transporters responsible for metabolite transport at the chloroplast envelope membrane and mitochondria membrane are not yet characterized [adapted from <span class="html-italic">Chlamydomonas</span> Source Book [<a href="#B158-plants-13-03015" class="html-bibr">158</a>]]. AAT1, alanine aminotransferase; ACK, acetate kinase; ADH, alcohol dehydrogenase; AGT, alanine-glyoxylate transaminase; AldDH, aldehyde dehydrogenase; BST, bestrophin; CAH, carbonic anhydrase; DLDH1, dihydrolipoyl dehydrogenase; EPYC1, essential pyrenoid component 1; FDX, ferredoxin; GCSH/P/T, glycine cleavage system, H-protein/P-protein/T-protein; GPDH, glycerol-3-phosphate dehydrogenase; GPP, glycerol-3-phosphate phosphatase; GYD, glycolate dehydrogenase; HPR, hydroxypyruvate reductase; HYDA, FeFe hydrogenase; LCI, low-CO<sub>2</sub> inducible protein; LDH1, lactate dehydrogenase 1; MME, malic enzyme; PDC3, pyruvate decarboxylase; PEPC, phosphoenolpyruvate carboxylase; PFL1, pyruvate formate lyase 1; PFR1, pyruvate ferredoxin oxidoreductase; PGP, phosphoglycolate phosphatase; PPDK, pyruvate phosphate dikinase; PAT, phosphate acetyltransferase; Rubisco, ribulose-1,5-bisphosphate carboxylase/oxygenase; SGA1, serine glyoxylate aminotransferase; SHMT, serine hydroxymethyltransferase; AcAld, acetaldehyde; AcCoA, acetyl coenzyme A; CO<sub>2</sub>, carbon dioxide; DHAP, dihydroxyacetone phosphate; ETOH, ethanol; Glc6P, glucose 6-phosphate; G3P, glyceraldehyde-3-phosphate; GP, glycerol-3-phosphate; H<sub>2</sub>, hydrogen; HCO<sub>3</sub><sup>−</sup>, bicarbonate; NH<sub>3</sub>, ammonium; NADPH, reduced nicotinamide adenine dinucleotide phosphate; O<sub>2</sub>, oxygen; OAA, oxaloacetate; PEP, phosphoenolpyruvate; 3-PGA, 3-phosphoglyceric acid; Pi, inorganic phosphate; RuBP, ribulose 1,5-bisphosphate. ICEM, inner chloroplast envelope membrane; OCEM, outer chloroplast envelope membrane. Created with <a href="http://BioRender.com" target="_blank">BioRender.com</a>.</p>
Full article ">Figure 3 Cont.
<p>Metabolite transport required for various metabolic processes in the cell. (<b>A</b>) CO<sub>2</sub>-concentrating mechanism in a NADP-malic enzyme type C4 plant, such as sugarcane [adapted with some modifications from [<a href="#B156-plants-13-03015" class="html-bibr">156</a>]]. (<b>B</b>) Trafficking of Ci across the plasma membrane and to the pyrenoid. CO<sub>2</sub> either directly diffuses across the plasma membrane or is transported by LCI1. It can also be converted to bicarbonate by the activity of CAH1 and transported by HLA3, LCIA, and BSTs through the plasma membrane, chloroplast envelope, and thylakoid membranes, respectively. In the thylakoids that penetrate the pyrenoid, the bicarbonate is converted to CO<sub>2</sub> through the activity of CAH3, and then fixed by Rubisco. The components and their locations in the cell are based on studies with <span class="html-italic">Chlamydomonas</span> [<a href="#B157-plants-13-03015" class="html-bibr">157</a>]. (<b>C</b>) Putative metabolite transport required for photorespiration in <span class="html-italic">Chlamydomonas</span>. Transporters responsible for metabolite transport at the chloroplast and mitochondrial envelope membranes; most of these transporters have not yet been identified in <span class="html-italic">Chlamydomonas</span> (except for ammonium transporter, AMT). (<b>D</b>) Fermentation in <span class="html-italic">Chlamydomonas</span>. Glycerol, lactate, CO<sub>2</sub>, H<sub>2</sub>, acetate, ethanol, and formate are fermentative end-products. The succinate-producing pathway (reverse TCA cycle) is not shown. Gray arrows in the cytosol indicate omitted steps under fermentative conditions. The ethanol pathway in mitochondria has been shown only at the activity level, so it is indicated in gray. Transporters responsible for metabolite transport at the chloroplast envelope membrane and mitochondria membrane are not yet characterized [adapted from <span class="html-italic">Chlamydomonas</span> Source Book [<a href="#B158-plants-13-03015" class="html-bibr">158</a>]]. AAT1, alanine aminotransferase; ACK, acetate kinase; ADH, alcohol dehydrogenase; AGT, alanine-glyoxylate transaminase; AldDH, aldehyde dehydrogenase; BST, bestrophin; CAH, carbonic anhydrase; DLDH1, dihydrolipoyl dehydrogenase; EPYC1, essential pyrenoid component 1; FDX, ferredoxin; GCSH/P/T, glycine cleavage system, H-protein/P-protein/T-protein; GPDH, glycerol-3-phosphate dehydrogenase; GPP, glycerol-3-phosphate phosphatase; GYD, glycolate dehydrogenase; HPR, hydroxypyruvate reductase; HYDA, FeFe hydrogenase; LCI, low-CO<sub>2</sub> inducible protein; LDH1, lactate dehydrogenase 1; MME, malic enzyme; PDC3, pyruvate decarboxylase; PEPC, phosphoenolpyruvate carboxylase; PFL1, pyruvate formate lyase 1; PFR1, pyruvate ferredoxin oxidoreductase; PGP, phosphoglycolate phosphatase; PPDK, pyruvate phosphate dikinase; PAT, phosphate acetyltransferase; Rubisco, ribulose-1,5-bisphosphate carboxylase/oxygenase; SGA1, serine glyoxylate aminotransferase; SHMT, serine hydroxymethyltransferase; AcAld, acetaldehyde; AcCoA, acetyl coenzyme A; CO<sub>2</sub>, carbon dioxide; DHAP, dihydroxyacetone phosphate; ETOH, ethanol; Glc6P, glucose 6-phosphate; G3P, glyceraldehyde-3-phosphate; GP, glycerol-3-phosphate; H<sub>2</sub>, hydrogen; HCO<sub>3</sub><sup>−</sup>, bicarbonate; NH<sub>3</sub>, ammonium; NADPH, reduced nicotinamide adenine dinucleotide phosphate; O<sub>2</sub>, oxygen; OAA, oxaloacetate; PEP, phosphoenolpyruvate; 3-PGA, 3-phosphoglyceric acid; Pi, inorganic phosphate; RuBP, ribulose 1,5-bisphosphate. ICEM, inner chloroplast envelope membrane; OCEM, outer chloroplast envelope membrane. Created with <a href="http://BioRender.com" target="_blank">BioRender.com</a>.</p>
Full article ">
16 pages, 2098 KiB  
Article
Mitochondrial Abundance and Function Differ Across Muscle Within Species
by Con-Ning Yen, Jocelyn S. Bodmer, Jordan C. Wicks, Morgan D. Zumbaugh, Michael E. Persia, Tim H. Shi and David E. Gerrard
Metabolites 2024, 14(10), 553; https://doi.org/10.3390/metabo14100553 - 16 Oct 2024
Viewed by 880
Abstract
Background: Mitochondria are considered the powerhouse of cells, and skeletal muscle cells are no exception. However, information regarding muscle mitochondria from different species is limited. Methods: Different muscles from cattle, pigs and chickens were analyzed for mitochondrial DNA (mtDNA), protein and [...] Read more.
Background: Mitochondria are considered the powerhouse of cells, and skeletal muscle cells are no exception. However, information regarding muscle mitochondria from different species is limited. Methods: Different muscles from cattle, pigs and chickens were analyzed for mitochondrial DNA (mtDNA), protein and oxygen consumption. Results: Bovine oxidative muscle mitochondria contain greater mtDNA (p < 0.05), protein (succinate dehydrogenase, SDHA, p < 0.01; citrate synthase, CS, p < 0.01; complex I, CI, p < 0.05), and oxygen consumption (p < 0.01) than their glycolytic counterpart. Likewise, porcine oxidative muscle contains greater mtDNA (p < 0.01), mitochondrial proteins (SDHA, p < 0.05; CS, p < 0.001; CI, p < 0.01) and oxidative phosphorylation capacity (OXPHOS, p < 0.05) in comparison to glycolytic muscle. However, avian oxidative skeletal muscle showed no differences in absolute mtDNA, SDHA, CI, complex II, lactate dehydrogenase, or glyceraldehyde 3 phosphate dehydrogenase compared to their glycolytic counterpart. Even so, avian mitochondria isolated from oxidative muscles had greater OXPHOS capacity (p < 0.05) than glycolytic muscle. Conclusions: These data show avian mitochondria function is independent of absolute mtDNA content and protein abundance, and argue that multiple levels of inquiry are warranted to determine the wholistic role of mitochondria in skeletal muscle. Full article
(This article belongs to the Special Issue Unlocking the Mysteries of Muscle Metabolism in the Animal Sciences)
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Figure 1

Figure 1
<p>(<b>A</b>,<b>D</b>,<b>G</b>) Absolute mitochondrial DNA (mtDNA) number in glycolytic and oxidative muscles. (<b>B</b>,<b>E</b>,<b>H</b>) Relative mtDNA compared to genomic DNA (2 <sup>−∆CT</sup>) in glycolytic and oxidative muscles. (<b>C</b>,<b>F</b>,<b>I</b>) Fold change (2 <sup>−∆∆CT</sup>) of mtDNA in oxidative compared to the glycolytic muscle type. (<b>A</b>–<b>C</b>) Bovine (<span class="html-italic">n</span> = 6) and (<b>D</b>–<b>F</b>) porcine (<span class="html-italic">n</span> = 6) muscle mtDNA content from <span class="html-italic">longissimus lumborum</span> (LL) and <span class="html-italic">masseter</span> (MS). (<b>G</b>–<b>I</b>) Avian muscle (<span class="html-italic">n</span> = 6) mtDNA content in <span class="html-italic">pectoralis major</span> (PM) and <span class="html-italic">quadriceps femoris</span> (QF). All values are displayed as least square means followed by standard error bars. Significance is denoted as * <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.</p>
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<p>Oxidative protein abundance from whole muscle in bovine (<b>A</b>–<b>D</b>), porcine (<b>E</b>–<b>H</b>), and avian (<b>I</b>–<b>L</b>). Bovine (<span class="html-italic">n</span> = 6) and porcine (<span class="html-italic">n</span> = 6) muscle protein content from <span class="html-italic">longissimus lumborum</span> (LL) and <span class="html-italic">masseter</span> (MS). Avian (<span class="html-italic">n</span> = 6) muscle protein content in <span class="html-italic">pectoralis major</span> (PM) and <span class="html-italic">quadriceps femoris</span> (QF). Oxidative protein abundance of (<b>A</b>,<b>E</b>,<b>I</b>) succinate dehydrogenase (SDHA), (<b>B</b>,<b>F</b>,<b>J</b>) citrate synthase (CS), and (<b>C</b>,<b>G</b>,<b>K</b>) voltage-dependent anion channel (VDAC). (<b>D</b>,<b>H</b>,<b>L</b>) Representative Western blot images of SDHA, CS, VDAC, and total protein stain (Ponceau S). All values are displayed as least square means followed by standard error bars. Significance is denoted as * <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.</p>
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<p>Glycolytic protein abundance from whole muscle in bovine (<b>A</b>–<b>C</b>), porcine (<b>D</b>–<b>F</b>), and avian (<b>G</b>–<b>I</b>). Bovine (<span class="html-italic">n</span> = 6) and porcine (<span class="html-italic">n</span> = 6) muscle protein content from <span class="html-italic">longissimus lumborum</span> (LL) and <span class="html-italic">masseter</span> (MS). Avian muscle (<span class="html-italic">n</span> = 6) protein content in <span class="html-italic">pectoralis major</span> (PM) and <span class="html-italic">quadriceps femoris</span> (QF). Glycolytic enzyme protein abundance of (<b>A</b>,<b>D</b>,<b>G</b>) glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and (<b>B</b>,<b>E</b>,<b>H</b>) lactate dehydrogenase (LDHA). (<b>C</b>,<b>F</b>,<b>I</b>) Representative Western blot images of GAPDH, LDHA, and total protein stain (Ponceau S). All values are displayed as least square means followed by standard error bars. Significance is denoted as ** <span class="html-italic">p</span> &lt; 0.01 and *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Mitochondrial protein abundance in glycolytic and oxidative muscles from bovine (<b>A</b>–<b>C</b>), porcine (<b>D</b>–<b>F</b>), and avian (<b>G</b>–<b>I</b>) mitochondria enriched fractions. Bovine (<span class="html-italic">n</span> = 6) and porcine (<span class="html-italic">n</span> = 6) mitochondrial protein content from <span class="html-italic">longissimus lumborum</span> (LL) and <span class="html-italic">masseter</span> (MS) muscles. Avian (<span class="html-italic">n</span> = 6) mitochondrial protein content from <span class="html-italic">pectoralis major</span> (PM) and <span class="html-italic">quadriceps femoris</span> (QF) muscles. (<b>A</b>,<b>D</b>,<b>G</b>) Mitochondrial proteins abundance of complex I (CI, NDUFB8) and (<b>B</b>,<b>E</b>,<b>H</b>) complex II (CII, SDHB) and (<b>C</b>,<b>F</b>,<b>I</b>) voltage dependent anion channel (VDAC). (<b>J</b>) Representative Western blot images of complex I, complex II, complex III, complex V, VDAC, and total protein stain (Ponceau S). All values are displayed as least square means followed by standard error bars. Significance is denoted as † <span class="html-italic">p =</span> 0.08, * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Oxygen consumption rate of mitochondria isolated from (<b>A</b>,<b>D</b>) bovine (<span class="html-italic">n</span> = 6) and (<b>B</b>,<b>E</b>) porcine (<span class="html-italic">n</span> = 6) <span class="html-italic">longissimus lumborum</span> (LL) and <span class="html-italic">masseter</span> (MS) and (<b>C</b>,<b>F</b>) avian (<span class="html-italic">n</span> = 8) <span class="html-italic">pectoralis major</span> (PM) and <span class="html-italic">quadriceps femoris</span> (QF) muscles under saturating concentrations of pyruvate/malate (PyM; <b>A</b>–<b>C</b>) and succinate/rotenone (SR; <b>D</b>–<b>F</b>) substrates. Baseline represents basal respiration of isolated mitochondria with substrates. OXPHOS capacity is ADP (5 mM) stimulated respiration. Proton leak is determined with 2 µM oligomycin. Maximal respiration is achieved with the uncoupler FCCP (4 µM). All values are displayed as least square means followed by standard error bars. Significance is denoted as * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Oxygen consumption rate of mitochondria isolated from (<b>A</b>,<b>D</b>) bovine (<span class="html-italic">n</span> = 6) and (<b>B</b>,<b>E</b>) porcine (<span class="html-italic">n</span> = 6) <span class="html-italic">longissimus lumborum</span> (LL) and <span class="html-italic">masseter</span> (MS) and (<b>C</b>,<b>F</b>) avian <span class="html-italic">pectoralis major</span> (PM, <span class="html-italic">n</span> = 10) and <span class="html-italic">quadriceps femoris</span> (QF, <span class="html-italic">n</span> = 9) muscles under saturating concentrations of glutamate/malate (GM; <b>A</b>–<b>C</b>) and palmitoyl-carnitine/malate (PCM; <b>D</b>–<b>F</b>) substrates. Baseline represents basal respiration of isolated mitochondria with substrates. OXPHOS capacity is ADP (5 mM) stimulated respiration. Proton leak is determined with 2 µM oligomycin. Maximal respiration is achieved with the uncoupler FCCP (4 µM). All values are displayed as least square means followed by standard error bars. Significance is denoted as * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001.</p>
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17 pages, 4510 KiB  
Article
A Comparative Study for Evaluating the Groundwater Inflow and Drainage Effect of Jinzhai Pumped Storage Power Station, China
by Jian Wu, Zhifang Zhou, Hao Wang, Bo Chen and Jinguo Wang
Appl. Sci. 2024, 14(19), 9123; https://doi.org/10.3390/app14199123 - 9 Oct 2024
Viewed by 658
Abstract
Various hydrogeological problems like groundwater inflow, water table drawdown, and water pressure redistribution may be encountered in the construction of hydraulic projects. How to accurately predict the occurrence of groundwater inflow and assess the drainage effect during construction are still challenging problems for [...] Read more.
Various hydrogeological problems like groundwater inflow, water table drawdown, and water pressure redistribution may be encountered in the construction of hydraulic projects. How to accurately predict the occurrence of groundwater inflow and assess the drainage effect during construction are still challenging problems for engineering designers. Taking the Jinzhai pumped storage power station (JPSPS) of China as an example, this paper aims to use different methods to calculate the water inflow rates of an underground powerhouse and evaluate the drainage effect caused by tunnel inflow during construction. The methods consist of the analytical formulas, the site groundwater rating (SGR) method, and the Signorini type variational inequality formulation. The results show that the analytical methods considering stable water table may overestimate the water inflow rates of caverns in drained conditions, whereas the SGR method with available hydro-geological parameters obtains a qualitative hazard assessment in the preliminary phase. The numerical solutions provide more precise and reliable values of groundwater inflow considering complex geological structures and seepage control measures. Moreover, the drainage effects, including a seepage-free surface, pore water pressure redistribution, and hydraulic gradient, have been accurately evaluated using various numerical synthetic cases. Specifically, the faults intersecting on underground caverns and drainage structures significantly change the groundwater flow regime around caverns. This comparative study can not only exactly identify the capabilities of the methods for cavern inflow in drained conditions, but also can comprehensively evaluate the drainage effect during cavern construction. Full article
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<p>Schematic diagram of Jinzhai pumped storage power station: (<b>a</b>) geological map and (<b>b</b>) location.</p>
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<p>Geological cross section along the diversion tunnel #1 alignment.</p>
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<p>Stereographic plot of faults and joints around the underground powerhouse. The red line represents the fault, and the black line represents the joint. The bule breakpoint line represents the axis of the underground powerhouse. The number represents the group number of the joints.</p>
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<p>Groundwater fluctuation during the construction: (<b>a</b>) monitoring boreholes around the underground powerhouse and (<b>b</b>) monitoring boreholes along with the upper reservoir and diversion tunnels.</p>
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<p>Measured hydraulic conductivity with Lugeon tests (707 tests): (<b>a</b>) frequency distribution of Lugeon values and (<b>b</b>) relationship between Lugeon values and depth.</p>
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<p>Circular tunnel with stable water table: <span class="html-italic">Q</span>, groundwater inflow; <span class="html-italic">l</span>, the depth from the ground surface; <span class="html-italic">h</span>, water head; <span class="html-italic">H</span>, the thickness of the aquifer; <span class="html-italic">r</span>, tunnel radius; <span class="html-italic">K</span>, permeability of rock mass.</p>
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<p>Circular tunnel with lowered water table in drained conditions.</p>
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<p>Two-dimensional finite-element model of underground powerhouse along the diversion tunnel #1 alignment considering different weathered zones and structures.</p>
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<p>Water inflow rates of underground powerhouse calculated by various methods [<a href="#B3-applsci-14-09123" class="html-bibr">3</a>,<a href="#B8-applsci-14-09123" class="html-bibr">8</a>,<a href="#B9-applsci-14-09123" class="html-bibr">9</a>,<a href="#B10-applsci-14-09123" class="html-bibr">10</a>,<a href="#B31-applsci-14-09123" class="html-bibr">31</a>,<a href="#B33-applsci-14-09123" class="html-bibr">33</a>,<a href="#B34-applsci-14-09123" class="html-bibr">34</a>].</p>
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<p>Water head distributions of underground powerhouse in various working conditions: (<b>a</b>) Case 1, (<b>b</b>) Case 2, (<b>c</b>) Case 3, and (<b>d</b>) Case 4.</p>
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<p>Comparison between various methods and monitoring data of water table drawdown [<a href="#B3-applsci-14-09123" class="html-bibr">3</a>,<a href="#B34-applsci-14-09123" class="html-bibr">34</a>].</p>
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<p>Water pressure distribution around the underground powerhouse in numerical Case 2.</p>
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<p>Hydraulic gradient of seepage field in numerical Case 2, and the blue arrow represents the groundwater flow direction.</p>
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18 pages, 622 KiB  
Review
Mitochondrial Dysfunction in Systemic Lupus Erythematosus: Insights and Therapeutic Potential
by Anastasia V. Poznyak, Nikolay A. Orekhov, Alexey V. Churov, Irina A. Starodubtseva, Dmitry F. Beloyartsev, Tatiana I. Kovyanova, Vasily N. Sukhorukov and Alexander N. Orekhov
Diseases 2024, 12(9), 226; https://doi.org/10.3390/diseases12090226 - 23 Sep 2024
Cited by 1 | Viewed by 1768
Abstract
Systemic lupus erythematosus (SLE) is a complex autoimmune disorder characterized by the presence of various serum autoantibodies and multi-system effects, predominantly affecting young female patients. The pathogenesis of SLE involves a combination of genetic factors, environmental triggers, and pathogen invasions that disrupt immune [...] Read more.
Systemic lupus erythematosus (SLE) is a complex autoimmune disorder characterized by the presence of various serum autoantibodies and multi-system effects, predominantly affecting young female patients. The pathogenesis of SLE involves a combination of genetic factors, environmental triggers, and pathogen invasions that disrupt immune cell activation, leading to the release of autoantibodies and chronic inflammation. Mitochondria, as the primary cellular powerhouses, play a crucial role in SLE development through their control of energy generation, reactive oxygen species (ROS) production, and cellular apoptotic pathways. Dysregulation of mitochondrial structure and function can contribute to the immune dysregulation, oxidative stress, and inflammation seen in SLE. Recent research has highlighted the impact of mitochondrial dysfunction on various immune cells involved in SLE pathogenesis, such as T-lymphocytes, B-lymphocytes, neutrophils, and plasmacytoid dendritic cells. Mitochondrial dysfunction in these immune cells leads to increased ROS production, disrupted mitophagy, and alterations in energy metabolism, contributing to immune dysregulation and inflammation. Moreover, genetic variations in mitochondrial DNA (mtDNA) and abnormalities in mitochondrial dynamics have been linked to the pathogenesis of SLE, exacerbating oxidative stress and immune abnormalities. Targeting mitochondrial function has emerged as a promising therapeutic approach for SLE. Drugs such as sirolimus, N-acetylcysteine, coenzyme Q10, and metformin have shown potential in restoring mitochondrial homeostasis, reducing oxidative stress, and modulating immune responses in SLE. These agents have demonstrated efficacy in preclinical models and clinical studies by improving disease activity, reducing autoantibody titers, and ameliorating organ damage in SLE patients. In conclusion, this review underscores the critical role of mitochondria in the pathogenesis of SLE and the potential of targeting mitochondrial dysfunction as a novel therapeutic strategy for improving outcomes in SLE patients. Further investigation into the mechanisms underlying mitochondrial involvement in SLE and the development of targeted mitochondrial therapies hold promise for advancing SLE treatment and enhancing patient care. Full article
(This article belongs to the Special Issue Treatment Strategies and Immune Responses in Rheumatic Diseases)
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<p>Scheme of complex role of mitochondria dysfunction components in the SLE.</p>
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16 pages, 7055 KiB  
Article
Stability Study and Strengthening Strategy of Spiral Case-Encased Concrete Structure of Pumped Storage Power Station
by Yun Zhao, Xiji Li, Yonggang Lu, Haiyang Dong, Chuanzhen Sun and Zhengwei Wang
Water 2024, 16(18), 2687; https://doi.org/10.3390/w16182687 - 21 Sep 2024
Viewed by 766
Abstract
With the development of global hydropower, the scale of hydropower stations is increasing, and the operating conditions are becoming more complex, so the stable operation of hydropower stations is very important. The vibration of the turbine unit will cause resonance in the powerhouse, [...] Read more.
With the development of global hydropower, the scale of hydropower stations is increasing, and the operating conditions are becoming more complex, so the stable operation of hydropower stations is very important. The vibration of the turbine unit will cause resonance in the powerhouse, and the structural stability of the powerhouse will be affected. Many scholars pay attention to the stability of the turbine unit operation, and there are few studies on the powerhouse of the hydropower station. Therefore, this paper relies on the Weifang Hydropower Station project to study key issues such as the tensile strength of concrete and how to arrange steel bars to increase the structural stability by changing the material properties through FEA. Three schemes are designed to evaluate the safety of the powerhouse structure when the turbine unit is running through the safety factor. Our findings indicate that the stress variation patterns observed on the inner surface of the powerhouse remain consistent across different operating scenarios. Notably, along the spiral line of the worm section, we observed that the stress levels on the vertical loop line decrease gradually with increasing distance from the inlet. Conversely, stress concentrations arise near the inlet and the tongue. Additionally, it has been noted that the likelihood of concrete cracking increases significantly at the tongue region. Full article
(This article belongs to the Special Issue Hydrodynamic Science Experiments and Simulations)
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<p>Plant and unit structure model diagram.</p>
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<p>Plant unit final assembly model diagram.</p>
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<p>Steel bar layout diagram.</p>
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<p>Mohr diagram and failure envelopes.</p>
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<p>Vertical section of concrete b area.</p>
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<p>Stress distribution of vertical section in concrete b area (load rejection condition).</p>
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<p>Stress distribution of vertical section in concrete b area (maximum head pumping condition under pump condition).</p>
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<p>Stress distribution of vertical section in concrete b area (rated condition of turbine).</p>
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<p>Horizontal section of concrete b area. The section distribution is illustrated in (<b>a</b>), while (<b>b</b>) shows the stress ex-tracted from the curve of the inner surface of the concrete, extending from the inlet to the end of the tongue. The volute is analyzed along the symmetrical sections on both sides of the central hori-zontal plane.</p>
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<p>Horizontal section of concrete b area (load rejection condition).</p>
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<p>Horizontal section of concrete b area (maximum head pumping condition of pump condition).</p>
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<p>Horizontal section of concrete b area (rated condition of turbine).</p>
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<p>Fatigue analysis of concrete zone B without reinforcement under different perspectives. (<b>a</b>–<b>d</b>) provide a comprehensive view of the cracking on the inner surface of the concrete.</p>
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<p>The deformation of concrete and volute in three schemes.</p>
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<p>Three schemes of the concrete and volute stress diagram.</p>
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<p>Concrete point analysis diagram.</p>
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<p>Three schemes of safety factor distribution of the concrete b area.</p>
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15 pages, 675 KiB  
Review
The Complex and Changing Genus Bacillus: A Diverse Bacterial Powerhouse for Many Applications
by Ximena Blanco Crivelli, Cecilia Cundon, María Paz Bonino, Mariana Soledad Sanin and Adriana Bentancor
Bacteria 2024, 3(3), 256-270; https://doi.org/10.3390/bacteria3030017 - 2 Sep 2024
Viewed by 2418
Abstract
For years, the Bacillus genus has encompassed a heterogeneous group of individuals whose main common trait was their ability to sporulate in the presence of oxygen. This criterion has been revised, resulting in the reclassification of several species into new genera and to [...] Read more.
For years, the Bacillus genus has encompassed a heterogeneous group of individuals whose main common trait was their ability to sporulate in the presence of oxygen. This criterion has been revised, resulting in the reclassification of several species into new genera and to a redefinition of the characteristics of the members of this taxon. Currently, the species of the genus are grouped into the Subtilis clade and the Cereus clade. The former, called Bacillus sensu stricto, initially composed of B. subtilis, B. licheniformis, B. pumilus, and B. amyloliquefaciens, has subsequently incorporated new species related to these. The Cereus clade, Bacillus cereus sensu lato, consists of pathogenic species (B. anthracis, B. cereus, and B. thuringiensis) as well as others of significance in agriculture and industry. Furthermore, identifying these individuals remains complex, requiring alternatives to 16S rRNA sequencing. The ability to form spores resistant to stressful conditions provides a significant advantage over other genera, with observable differences in sporulation rates and spore structure among different species. Additionally, Bacillus spp. are known for their capacity to produce antimicrobial substances, lytic enzymes, and volatile organic compounds, each with diverse applications. Some species are even used as probiotics. This review delves into aspects related to the taxonomy and identification of microorganisms belonging to the genus Bacillus, which often present challenges. The aim is to provide a comprehensive overview of the topic. In addition, it highlights the characteristics and applications of the genus, emphasizing its importance in biotechnology and microbiology. Full article
21 pages, 2817 KiB  
Article
Measurement and Evaluation of the Modernization Development Level of Higher Education in China: Based on Panel Data Analysis of 31 Provinces from 2012 to 2022
by Qingqing Liang and Fang Yin
Sustainability 2024, 16(17), 7250; https://doi.org/10.3390/su16177250 - 23 Aug 2024
Viewed by 1046
Abstract
The scale and quality of higher education are key indicators of a country’s development level and its potential for future growth. This study utilizes literature analysis and the core functions of higher education institutions to construct an evaluation index system for the modernization [...] Read more.
The scale and quality of higher education are key indicators of a country’s development level and its potential for future growth. This study utilizes literature analysis and the core functions of higher education institutions to construct an evaluation index system for the modernization level of higher education in China, using data from 2012 to 2022. The results reveal the following: (1) From 2012 to 2022, the modernization level of higher education across China’s 31 provinces generally increased, despite some fluctuations. Beijing consistently maintained the highest level of modernization, while Hainan demonstrated the fastest growth rate. (2) The modernization level of higher education exhibited uneven distribution across the provinces: eleven provinces were at a low level, eight at a moderate level, eight at a relatively high level, and four at a high level. (3) The development level of higher education modernization shows a clear correlation with geographic location and economic development, characterized by a distinct ‘high in the east, low in the west’ pattern. (4) There is a urgent need to enhance the internationalization of higher education development in China. (5) The overall index of higher education development in China displayed a slow decline with fluctuations from 2012 to 2022, reflecting ongoing efforts toward balanced development across the 31 provinces and cities. The most significant disparities in higher education development remain between the western and eastern regions. Full article
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<p>Driving forces of Chinese-style higher education modernization development.</p>
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<p>The interactive mechanism between higher education modernization and high-quality economic development.</p>
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<p>Overall trends in the modernization development level of higher education in 31 provinces in China, 2012–2022.</p>
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<p>Radar chart illustrating the average annual growth rates of higher education modernization development levels.</p>
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<p>Hierarchical map of modernization development in higher education across 31 provinces of China from 2012 to 2022.</p>
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<p>Radar chart of average “input–output” indicators of high-quality higher education in 31 provinces in China, 2012–2022.</p>
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<p>Radar chart of average equity index of higher education in 31 provinces in China, 2012–2022.</p>
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<p>Radar chart of average social service indicator in 31 provinces in China, 2012–2022.</p>
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<p>Radar chart of average internationalization indicators of higher education in 31 provinces in China, 2012–2022.</p>
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<p>Radar chart of average informatization index of higher education in 31 provinces in China, 2012–2022.</p>
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30 pages, 7368 KiB  
Article
The Phylogenetic Relationships of Major Lizard Families Using Mitochondrial Genomes and Selection Pressure Analyses in Anguimorpha
by Lemei Zhan, Yuxin Chen, Jingyi He, Zhiqiang Guo, Lian Wu, Kenneth B. Storey, Jiayong Zhang and Danna Yu
Int. J. Mol. Sci. 2024, 25(15), 8464; https://doi.org/10.3390/ijms25158464 - 2 Aug 2024
Viewed by 1778
Abstract
Anguimorpha, within the order Squamata, represents a group with distinct morphological and behavioral characteristics in different ecological niches among lizards. Within Anguimorpha, there is a group characterized by limb loss, occupying lower ecological niches, concentrated within the subfamily Anguinae. Lizards with limbs and [...] Read more.
Anguimorpha, within the order Squamata, represents a group with distinct morphological and behavioral characteristics in different ecological niches among lizards. Within Anguimorpha, there is a group characterized by limb loss, occupying lower ecological niches, concentrated within the subfamily Anguinae. Lizards with limbs and those without exhibit distinct locomotor abilities when adapting to their habitats, which in turn necessitate varying degrees of energy expenditure. Mitochondria, known as the metabolic powerhouses of cells, play a crucial role in providing approximately 95% of an organism’s energy. Functionally, mitogenomes (mitochondrial genomes) can serve as a valuable tool for investigating potential adaptive evolutionary selection behind limb loss in reptiles. Due to the variation of mitogenome structures among each species, as well as its simple genetic structure, maternal inheritance, and high evolutionary rate, the mitogenome is increasingly utilized to reconstruct phylogenetic relationships of squamate animals. In this study, we sequenced the mitogenomes of two species within Anguimorpha as well as the mitogenomes of two species in Gekkota and four species in Scincoidea. We compared these data with the mitogenome content and evolutionary history of related species. Within Anguimorpha, between the mitogenomes of limbless and limbed lizards, a branch-site model analysis supported the presence of 10 positively selected sites: Cytb protein (at sites 183 and 187), ND2 protein (at sites 90, 155, and 198), ND3 protein (at site 21), ND5 protein (at sites 12 and 267), and ND6 protein (at sites 72 and 119). These findings suggested that positive selection of mitogenome in limbless lizards may be associated with the energy requirements for their locomotion. Additionally, we acquired data from 205 mitogenomes from the NCBI database. Bayesian inference (BI) and Maximum Likelihood (ML) trees were constructed using the 13 mitochondrial protein-coding genes (PCGs) and two rRNAs (12S rRNA and 16S rRNA) from 213 mitogenomes. Our phylogenetic tree and the divergence time estimates for Squamata based on mitogenome data are consistent with results from previous studies. Gekkota was placed at the root of Squamata in both BI and ML trees. However, within the Toxicofera clade, due to long-branch attraction, Anguimorpha and (Pleurodonta + (Serpentes + Acrodonta)) were closely related groupings, which might indicate errors and also demonstrate that mitogenome-based phylogenetic trees may not effectively resolve long-branch attraction issues. Additionally, we reviewed the origin and diversification of Squamata throughout the Mesozoic era, suggesting that Squamata originated in the Late Triassic (206.05 Mya), with the diversification of various superfamilies occurring during the Cretaceous period. Future improvements in constructing squamate phylogenetic relationships using mitogenomes will rely on identifying snake and acrodont species with slower evolutionary rates, ensuring comprehensive taxonomic coverage of squamate diversity, and increasing the number of genes analyzed. Full article
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<p>Mitogenome map of eight species in this study. The outermost two circles depict the gene map (PCGs, rRNAs, tRNAs, and D-loop region) and genes; the outer circle is encoded by the majority strand, the second circle is encoded by the minority strand, and the tRNAs are all denoted by abbreviations. The black circle represents GC content, whereas the circles are composed of green, and violet represent GC skew.</p>
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<p>The relative synonymous codon usage (RSCU) of the mitogenomes of eight species in this study. The X-axis displays all the utilized codons, including various combinations of synonymous codons, where each codon is depicted with a distinct color. The Y-axis presents the corresponding RSCU values in a list format. Different codons are shown in the different colors.</p>
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<p>BI tree constructed with 13 protein-coding genes (the first and the second codons) and two rRNAs (12S rRNA and 16S rRNA) based on 213 datasets. Summary of the relationships between higher-level branches of squamate reptiles estimated in this study, with numbers at the nodes indicating bootstrap support values (the full tree is presented in <a href="#ijms-25-08464-f004" class="html-fig">Figure 4</a>, <a href="#ijms-25-08464-f005" class="html-fig">Figure 5</a> and <a href="#ijms-25-08464-f006" class="html-fig">Figure 6</a>). The same color displayed on both sides of the figure represents the same clade in the phylogeny.</p>
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<p>The left side is the skeleton version of 213 mitogenomes, and the right side shows an enlarged view of the corresponding branch on the left side, which is distinguished by different colors. Species-level squamate phylogeny Part A. To illustrate clearly, the complete species-level tree of Squamata in BI tree was divided into three parts: A, B, and C. For Part B and C, please see the next legend.</p>
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<p>Species-level squamate phylogeny Part B. For Part C, please see the next legend.</p>
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<p>Species-level squamate phylogeny Part C.</p>
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<p>Evolutionary timescale within Squamata based on phylogenetic analyses. Median-divergence times are provided above every node, and the seven fossil calibration points used are marked in the figure. The scale data are from million years ago (Mya), and the geological timescale is shown at the bottom of the chronogram.</p>
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27 pages, 2090 KiB  
Review
Flavonoids: Antioxidant Powerhouses and Their Role in Nanomedicine
by Mehak Zahra, Heidi Abrahamse and Blassan P. George
Antioxidants 2024, 13(8), 922; https://doi.org/10.3390/antiox13080922 - 29 Jul 2024
Cited by 2 | Viewed by 5392
Abstract
This study emphasizes the critical role of antioxidants in protecting human health by counteracting the detrimental effects of oxidative stress induced by free radicals. Antioxidants—found in various forms such as vitamins, minerals, and the phytochemicals abundant in fruits and vegetables—neutralize free radicals by [...] Read more.
This study emphasizes the critical role of antioxidants in protecting human health by counteracting the detrimental effects of oxidative stress induced by free radicals. Antioxidants—found in various forms such as vitamins, minerals, and the phytochemicals abundant in fruits and vegetables—neutralize free radicals by stabilizing them through electron donation. Specifically, flavonoid compounds are highlighted as robust defenders, addressing oxidative stress and inflammation to avert chronic illnesses like cancer, cardiovascular diseases, and neurodegenerative diseases. This research explores the bioactive potential of flavonoids, shedding light on their role not only in safeguarding health, but also in managing conditions such as diabetes, cancer, cardiovascular diseases, and neurodegenerative diseases. This review highlights the novel integration of South African-origin flavonoids with nanotechnology, presenting a cutting-edge strategy to improve drug delivery and therapeutic outcomes. This interdisciplinary approach, blending traditional wisdom with contemporary techniques, propels the exploration of flavonoid-mediated nanoparticles toward groundbreaking pharmaceutical applications, promising revolutionary advancements in healthcare. This collaborative synergy between traditional knowledge and modern science not only contributes to human health, but also underscores a significant step toward sustainable and impactful biomedical innovations, aligning with principles of environmental conservation. Full article
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<p>The role and functional significance of flavonoids: an illustrated overview.</p>
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<p>Flavonoids prevent oxidative stress-related diseases.</p>
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<p>The targets of flavonoids in inflammatory processes.</p>
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<p>Flavonoid targets in the extrinsic and intrinsic apoptosis pathways: key molecules and signaling cascades.</p>
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19 pages, 602 KiB  
Article
The Influence of New Quality Productive Forces on High-Quality Agricultural Development in China: Mechanisms and Empirical Testing
by Li Lin, Tianyu Gu and Yi Shi
Agriculture 2024, 14(7), 1022; https://doi.org/10.3390/agriculture14071022 - 27 Jun 2024
Cited by 9 | Viewed by 4405
Abstract
Advancing the construction and application of new quality productive forces is an essential prerequisite for achieving high-quality agricultural development and expediting the establishment of agricultural powerhouses. This study aims to elucidate the internal mechanisms through which new quality productivity contributes to high-quality agricultural [...] Read more.
Advancing the construction and application of new quality productive forces is an essential prerequisite for achieving high-quality agricultural development and expediting the establishment of agricultural powerhouses. This study aims to elucidate the internal mechanisms through which new quality productivity contributes to high-quality agricultural development and to explore practical pathways for enhancing agricultural quality through its promotion. Utilizing panel data spanning 2012 to 2021 from 30 provinces and municipalities in mainland China, the entropy method is employed to gauge levels of new quality productivity and high-quality agricultural development. Additionally, employing research methodologies including SYS-GMM and threshold effect models, this study empirically investigates how the advancement of new quality productivity influences high-quality agricultural development. Our research reveals the following key findings: (1) The development of new quality productive forces significantly enhances high-quality agricultural development, exhibiting a heterogeneous distribution pattern favoring the “eastern region > western region > central region” and “northern region > southern region”. (2) New quality productive forces can bolster the level of high-quality agricultural development by fostering innovation, coordination, openness, and shared development within its subsystems. However, they may impede progress by inhibiting improvements in green development within the subsystems. (3) The results of the threshold effect test demonstrate that the promotion effect of the development of new quality productive forces on high-quality agricultural development escalates with the level of high-quality agricultural development. Specifically, as the level of high-quality agricultural development exceeds the first threshold value of 0.1502, the promotion effect becomes significant; crossing the second threshold value of 0.2010 further amplifies this effect. This paper’s primary marginal contribution involves empirically analyzing the potential nonlinear effects of advancing new quality productivity in enhancing the level of high-quality agricultural development. This enriches empirical research on how new quality productivity fosters the development of high-quality agriculture. Full article
(This article belongs to the Section Agricultural Economics, Policies and Rural Management)
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<p>Trends in high-quality agricultural development and new qualitative productivity changes (2012–2021).</p>
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36 pages, 3676 KiB  
Review
Building Information Modelling in Hydropower Infrastructures: Design, Engineering and Management Perspectives
by Jigme Wangchuk, Saeed Banihashemi, Hamidreza Abbasianjahromi and Maxwell Fordjour Antwi-Afari
Infrastructures 2024, 9(7), 98; https://doi.org/10.3390/infrastructures9070098 - 25 Jun 2024
Cited by 1 | Viewed by 2017
Abstract
Building Information Modelling (BIM) has emerged as a transformative force in the construction industry, gaining traction within the hydropower sector. This study critically examines the adoption and application of BIM throughout the entire lifecycle of hydropower projects, addressing a notable gap in existing [...] Read more.
Building Information Modelling (BIM) has emerged as a transformative force in the construction industry, gaining traction within the hydropower sector. This study critically examines the adoption and application of BIM throughout the entire lifecycle of hydropower projects, addressing a notable gap in existing research, to encompass a holistic approach to the management and resilience of these critical infrastructures. The objective is to delineate the comprehensive range of BIM applications, use cases, and adoption, integrating technologies including Digital Twin, UAV, GIS, and simulation tools, across components of hydropower projects. Employing a systematic search paired with a critical review of the selected literature, this study meticulously evaluates significant contributions in this domain. Through thematic analysis, the multifaceted utility of BIM in hydropower structures, including an in-depth evaluation of its current adoption within the industry, is presented. This encompasses an analysis of both benefits and challenges inherent in BIM implementation for hydropower infrastructures. This study is a significant contribution to understanding how BIM can be leveraged to enhance the resilience of hydropower infrastructures. It provides a comprehensive view of BIM’s applications, challenges, and future potential, guiding stakeholders in adopting strategies that ensure these structures withstand, adapt, and recover from disruptions while maintaining sustainable and efficient operations. Full article
(This article belongs to the Special Issue Smart Construction in Infrastructure Project Development)
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<p>The PRISMA flow diagram of the study.</p>
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<p>Research trend from 2013 to 2023.</p>
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<p>Theoretical framework of the study.</p>
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<p>Literature distribution of BIM in hydropower infrastructures.</p>
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<p>BIM-Hydropower literature distribution by country.</p>
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<p>Evolution model of BIM-hydropower infrastructures.</p>
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<p>The knowledge gaps and future research framework for BIM-hydropower infrastructures.</p>
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19 pages, 2499 KiB  
Review
Current Developments and Future Directions in Energy-Efficient Buildings from the Perspective of Building Construction Materials and Enclosure Systems
by Rahman Azari, Ehsan Kamel and Ali M. Memari
Buildings 2024, 14(7), 1921; https://doi.org/10.3390/buildings14071921 - 23 Jun 2024
Cited by 1 | Viewed by 1959
Abstract
The need to design buildings in compliance with the Paris Agreement goal requirements is urgent, and architects and engineers need to consider energy use and operational and embodied carbon requirements in doing so. Building envelopes will be an important element in the next [...] Read more.
The need to design buildings in compliance with the Paris Agreement goal requirements is urgent, and architects and engineers need to consider energy use and operational and embodied carbon requirements in doing so. Building envelopes will be an important element in the next generation of high-performance buildings and there have been significant advancements in recent years to develop building envelopes that help mitigate the building carbon emissions through energy-conserving low-embodied carbon or carbon-sequestering solutions. The key objective of this article is to present an overview of the state-of-the-art in the field of energy-efficient low-carbon buildings with a focus on envelope systems. This article provides a survey of the literature on energy use and carbon emissions of the United States building stock, presents recent advancements in energy-conserving building envelopes, and highlights reuse–reduce–sequester strategies that mitigate the embodied carbon of buildings. As materials are critical in reducing the energy consumption and carbon emissions of buildings, this paper also presents developments on diverse materials and building envelope solutions that have been effective in creating high-performance buildings, from insulation materials to phase-change materials and aerogels. Finally, the characteristics of a selected number of progressive net-zero-energy guidelines such as Passive House Institute (PHI) standards, Passive House Institute US (Phius) standards, the PowerHouse standard, and the BENG standard are discussed. The findings of this work highlight the increased focus on the design, construction, and engineering strategies that aim to mitigate the carbon emissions of buildings based on a holistic whole-life carbon mitigation approach. Full article
(This article belongs to the Special Issue Energy Efficiency and Carbon Neutrality in Buildings)
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<p>The life cycle of construction and its carbon footprint.</p>
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<p>Share of buildings in global energy and process emissions in 2021.</p>
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<p>A schematic overview of the reviewed building envelope energy conservation measures.</p>
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<p>A visual representation of software and tools frequency in energy modeling research for building envelope energy conservation measures.</p>
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18 pages, 1910 KiB  
Review
Lipid Droplet–Mitochondria Contacts in Health and Disease
by Hongjun Fan and Yanjie Tan
Int. J. Mol. Sci. 2024, 25(13), 6878; https://doi.org/10.3390/ijms25136878 - 22 Jun 2024
Cited by 6 | Viewed by 3438
Abstract
The orchestration of cellular metabolism and redox balance is a complex, multifaceted process crucial for maintaining cellular homeostasis. Lipid droplets (LDs), once considered inert storage depots for neutral lipids, are now recognized as dynamic organelles critical in lipid metabolism and energy regulation. Mitochondria, [...] Read more.
The orchestration of cellular metabolism and redox balance is a complex, multifaceted process crucial for maintaining cellular homeostasis. Lipid droplets (LDs), once considered inert storage depots for neutral lipids, are now recognized as dynamic organelles critical in lipid metabolism and energy regulation. Mitochondria, the powerhouses of the cell, play a central role in energy production, metabolic pathways, and redox signaling. The physical and functional contacts between LDs and mitochondria facilitate a direct transfer of lipids, primarily fatty acids, which are crucial for mitochondrial β-oxidation, thus influencing energy homeostasis and cellular health. This review highlights recent advances in understanding the mechanisms governing LD–mitochondria interactions and their regulation, drawing attention to proteins and pathways that mediate these contacts. We discuss the physiological relevance of these interactions, emphasizing their role in maintaining energy and redox balance within cells, and how these processes are critical in response to metabolic demands and stress conditions. Furthermore, we explore the pathological implications of dysregulated LD–mitochondria interactions, particularly in the context of metabolic diseases such as obesity, diabetes, and non-alcoholic fatty liver disease, and their potential links to cardiovascular and neurodegenerative diseases. Conclusively, this review provides a comprehensive overview of the current understanding of LD–mitochondria interactions, underscoring their significance in cellular metabolism and suggesting future research directions that could unveil novel therapeutic targets for metabolic and degenerative diseases. Full article
(This article belongs to the Special Issue New Players in the Research of Oxidative Stress and Cancer)
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<p>Composition and metabolic process of lipid droplets: LDs are unique cellular organelles composed of a monolayer of phospholipids surrounding a core of neutral lipids (triglycerides, cholesterol, sterols). They originate from the endoplasmic reticulum, initially accumulating as lens-like structures in the ER membrane and ultimately released into the cytoplasm via budding. Free LDs grow through fusion or autonomous growth, leading to the formation of mature LDs. The surface of LDs contains lipolytic enzymes, activated during starvation, which hydrolyze neutral lipids into fatty acids. Additionally, LDs can be targeted and broken down by autophagolysosomes, releasing fatty acids that undergo beta-oxidation in mitochondria to provide energy. TAG: Triacylglycerol; DAG: Diacylglycerol; MAG: Monoacylglycerol; ATGL: Adipose triglyceride lipase; HSL: Hormone-sensitive lipase; MGL: Monoacylglycerol lipase.</p>
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<p>Mechanisms of Mitochondria–LD Interaction. (1) PLIN5 and FATP4 interaction: The C-terminal structural domain of PLIN5 interacts with FATP4, enhancing the connections between LDs and mitochondria. Starvation triggers the phosphorylation of PLIN5, leading to lipolysis and the release of fatty acids from LDs into mitochondria. These fatty acids are then converted to fatty acyl-CoAs for oxidation. (2) ARFRP1 and SNAP23 recruitment: ARFRP1 recruits SNAP23 to a site near the LD, promoting LD–mitochondria interactions and facilitating LD amplification. (3) MIGA2 linkage: The mitochondrial outer membrane protein MIGA2 links mitochondria to LD proteins, enabling efficient lipid storage within the LD. (4) Mfn2 and Hsc70/PLIN1 complex formation: Mitochondria-localized Mfn2 and LD-localized Hsc70 or PLIN1 form a complex at the mitochondria–LD membrane contact site. This complex tethers mitochondria to the LD, facilitating the transfer of fatty acids from LDs to mitochondria for β-oxidation.</p>
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<p>Role of LD–Mitochondria Interaction in Diverse Diseases. (1) Type 2 diabetes: Excessive storage of lipid droplets (LDs) in skeletal muscle is a hallmark of type 2 diabetes. High-intensity interval training (HIIT) exercise alters the size, subcellular distribution, and mitochondrial content of LDs, improving the deficiency of intramuscular LDs. (2) Viral replication: The ORF6 protein inserts into the LD lipid monolayer through its two amphipathic helices. It interacts with endoplasmic reticulum (ER) membrane proteins BAP31 and USE1 to mediate the formation of ER–LD contacts. Additionally, ORF6 connects mitochondria to LDs by interacting with the SAM complex in the mitochondrial outer membrane, promoting cellular lipolysis and LD biogenesis, reprogramming lipid fluxes, and facilitating viral replication. (3) Astrocyte reactivity: When fatty acid load exceeds the oxidative phosphorylation (OxPhos) capacity of astrocytes, elevated acetyl-CoA levels induce astrocyte reactivity by enhancing STAT3 acetylation and activation. (4) Fatty acid utilization in skeletal muscle: In rat skeletal muscle cells, the energy sensor AMPK increases the GTP-binding activity of Rab8a, facilitating LD–mitochondria interactions by binding to PLIN5 under starvation conditions. The assembly of the Rab8a-PLIN5 tethering complex recruits ATGL, mobilizing and transferring long-chain fatty acids (LCFAs) from LDs to mitochondria for β-oxidation. Rab8a deficiency in a mouse model impairs fatty acid utilization and reduces exercise endurance. The arrows mean decrease or increase.</p>
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