Variation in energy metabolism structure of microbial community during bioleaching chalcopyrites with different iron-sulfur ratios

2021 ◽  
Vol 28 (7) ◽  
pp. 2022-2036
Author(s):  
Yu Yang ◽  
Zhen-yu Zhu ◽  
Ting-ting Hu ◽  
Meng-jun Zhang ◽  
Guan-zhou Qiu
2020 ◽  
Vol 56 (80) ◽  
pp. 11989-11992
Author(s):  
Sebastian A. Sanden ◽  
Ruiqin Yi ◽  
Masahiko Hara ◽  
Shawn E. McGlynn

Thioesters and peptide ligated [Fe–S] clusters can be synthesized simultaneously from thioacetic acid in an aqueous one-pot reaction.


2020 ◽  
Vol 56 (94) ◽  
pp. 14920-14920
Author(s):  
Sebastian A. Sanden ◽  
Ruiqin Yi ◽  
Masahiko Hara ◽  
Shawn E. McGlynn

Correction for ‘Simultaneous synthesis of thioesters and iron–sulfur clusters in water: two universal components of energy metabolism’ by Sebastian A. Sanden et al., Chem. Commun., 2020, 56, 11989–11992, DOI: 10.1039/D0CC07078A.


2021 ◽  
Vol 7 (8) ◽  
pp. eabf0717
Author(s):  
Florian A. Schober ◽  
David Moore ◽  
Ilian Atanassov ◽  
Marco F. Moedas ◽  
Paula Clemente ◽  
...  

Induction of the one-carbon cycle is an early hallmark of mitochondrial dysfunction and cancer metabolism. Vital intermediary steps are localized to mitochondria, but it remains unclear how one-carbon availability connects to mitochondrial function. Here, we show that the one-carbon metabolite and methyl group donor S-adenosylmethionine (SAM) is pivotal for energy metabolism. A gradual decline in mitochondrial SAM (mitoSAM) causes hierarchical defects in fly and mouse, comprising loss of mitoSAM-dependent metabolites and impaired assembly of the oxidative phosphorylation system. Complex I stability and iron-sulfur cluster biosynthesis are directly controlled by mitoSAM levels, while other protein targets are predominantly methylated outside of the organelle before import. The mitoSAM pool follows its cytosolic production, establishing mitochondria as responsive receivers of one-carbon units. Thus, we demonstrate that cellular methylation potential is required for energy metabolism, with direct relevance for pathophysiology, aging, and cancer.


Horticulturae ◽  
2021 ◽  
Vol 7 (6) ◽  
pp. 151
Author(s):  
Hongfei Li ◽  
Fang Song ◽  
Qiang Xu ◽  
Shu’ang Peng ◽  
Zhiyong Pan ◽  
...  

The plant rhizosphere microbiome is known to play a vital role in plant health by competing with pathogens or inducing plant resistance. This study aims to investigate rhizosphere microorganisms responsive to a devastating citrus disease caused by ‘Candidatus Liberibacter asiaticus’ (CLas) infection, by using 16S rRNA sequencing and metagenome technologies. The results show that 30 rhizosphere and 14 root bacterial genera were significantly affected by CLas infection, including 9 plant resistance-associated bacterial genera. Among these, Amycolatopsis, Sphingopyxis, Chryseobacterium, Flavobacterium, Ralstonia, Stenotrophomonas, Duganella, and Streptacidiphilus were considerably enriched in CLas-infected roots, while Rhizobium was significantly decreased. Metagenome analysis revealed that the abundance of genes involved in carbohydrate metabolism, such as glycolysis, starch and sucrose metabolism, amino sugar and nucleotide sugar metabolism, was significantly reduced in the CLas-infected citrus rhizosphere microbial community. Likewise, the abundance of genes involved in phosphoinositide signaling and phosphoinositide metabolism, which play important roles in energy metabolism (such as carbohydrate metabolism and lipid metabolism), was also decreased in the CLas-infected samples. Taken together, our results indicate that CLas infection could affect the resistance potential and energy metabolism of the citrus rhizosphere microbial community, which may help us to understand the rhizosphere responses to plant disease and thus facilitate the development and application of antagonistic microorganism products in citrus industry.


2018 ◽  
Author(s):  
Joana Thiel ◽  
James Byrne ◽  
Andreas Kappler ◽  
Bernhard Schink ◽  
Michael Pester

AbstractThe exergonic reaction of FeS with H2S to form FeS2(pyrite) and H2was postulated to have operated as an early form of energy metabolism on primordial Earth. Since the Archean, sedimentary pyrite formation played a major role in the global iron and sulfur cycles, with direct impact on the redox chemistry of the atmosphere. To date, pyrite formation was considered a purely geochemical reaction. Here, we present microbial enrichment cultures, which grew with FeS, H2S, and CO2as their sole substrates to produce FeS2and CH4. Cultures grew over periods of three to eight months to cell densities of up to 2–9×106cells mL−1. Transformation of FeS with H2S to FeS2was followed by57Fe Mössbauer spectroscopy and showed a clear biological temperature profile with maximum activity at 28°C and decreasing activities towards 4°C and 60°C. CH4was formed concomitantly with FeS2and exhibited the same temperature dependence. Addition of either penicillin or 2-bromoethanesulfonate inhibited both FeS2and CH4production, indicating a syntrophic coupling of pyrite formation to methanogenesis. This hypothesis was supported by a 16S rRNA gene-based phylogenetic analysis, which identified at least one archaeal and five bacterial species. The archaeon was closely related to the hydrogenotrophic methanogenMethanospirillum stamsiiwhile the bacteria were most closely related to sulfate-reducingDeltaproteobacteria, as well as unculturedFirmicutesandActinobacteria. We identified a novel type of microbial metabolism able to conserve energy from FeS transformation to FeS2, which may serve as a model for a postulated primordial iron-sulfur world.Significance statementPyrite is the most abundant iron-sulfur mineral in sediments. Over geological times, its burial controlled oxygen levels in the atmosphere and sulfate concentrations in seawater. Its formation in sediments is so far considered a purely geochemical process that is at most indirectly supported by microbial activity. We show that lithotrophic microorganisms can directly transform FeS and H2S to FeS2and use this exergonic reaction as a novel form of energy metabolism that is syntrophically coupled to methanogenesis. Our results provide insights into a syntrophic relationship that could sustain part of the deep biosphere and lend support to the iron-sulfur-world theory that postulated FeS transformation to FeS2as a key energy-delivering reaction for life to emerge.


2021 ◽  
Author(s):  
Suprokash Koner ◽  
Jung-Sheng Chen ◽  
Bing-Mu Hsu ◽  
Chao-Wen Tan ◽  
Cheng-Wei Fan ◽  
...  

Abstract Microbially induced calcium carbonate precipitation (MICP), a widespread biochemical process involving heterotopic bacterial communities, generally occurs in organic matter-rich environments. Limestone caves, whose oligotrophic conditions result from the absence of sunlight, are considered an extreme environment. In such environments, bacteria have the potential to form calcium carbonate. In this study, the microbial community diversity and taxonomical structure outside and inside a limestone cave was investigated with their community-level carbon source by fingerprinting and functional metabolic pathway prediction using 16S rRNA amplicon sequencing analysis. The Biolog EcoPlate™ assay revealed that microbes from outside the cave were metabolically highly active, resulting in a rising carbon source utilization rate curve. Conversely, the microbial community within the cave was not very active in consuming the carbon substrates of Biolog EcoPlate™. Although major carbon sources were found to be used by microbial communities both inside and outside the cave, the microbial utilization rate of carbon bacteria inside was much lower than for bacteria outside the cave. The taxonomic classification of microbial diversity using 16S rRNA metagenomic analysis revealed eight predominant bacterial phyla associated with both sampling areas: Proteobacteria, Acidobacteria, Actinobacteria, Planctomycetes, Nitrospirae, Chloroflexi, Gemmatimonadetes, and Cyanobacteria. Among these, Planctomycetes, Proteobacteria, Cyanobacteria, and Nitrospirae were predominantly associated with external cave samples, whereas Acidobacteria, Actinobacteria, Chloroflexi, and Gemmatimonadetes were associated with internal cave samples. Functional prediction analysis showed that bacterial communities both inside and outside the cave were functionally involved in the metabolism of carbohydrates, amino acids, other amino acid, lipids, xenobiotic compounds, energy metabolism, and environmental information processing. However, the amino acid and carbohydrate metabolic pathways were predominantly linked to the external cave samples, while xenobiotic compounds, lipids, other amino acids, and energy metabolism were associated with internal cave samples. Overall, a positive correlation was observed between Biolog EcoPlate™ assay carbon utilization and metagenomically observed metabolic function.


2021 ◽  
Vol 9 (8) ◽  
pp. 1789
Author(s):  
Suprokash Koner ◽  
Jung-Sheng Chen ◽  
Bing-Mu Hsu ◽  
Chao-Wen Tan ◽  
Cheng-Wei Fan ◽  
...  

Carbon utilization of bacterial communities is a key factor of the biomineralization process in limestone-rich curst areas. An efficient carbon catabolism of the microbial community is associated with the availability of carbon sources in such an ecological niche. As cave environments promote oligotrophic (carbon source stress) situations, the present study investigated the variations of different carbon substrate utilization patterns of soil and rock microbial communities between outside and inside cave environments in limestone-rich crust topography by Biolog EcoPlate™ assay and categorized their taxonomical structure and predicted functional metabolic pathways based on 16S rRNA amplicon sequencing. Community level physiological profiling (CLPP) analysis by Biolog EcoPlate™ assay revealed that microbes from outside of the cave were metabolically active and had higher carbon source utilization rate than the microbial community inside the cave. 16S rRNA amplicon sequence analysis demonstrated, among eight predominant bacterial phylum Planctomycetes, Proteobacteria, Cyanobacteria, and Nitrospirae were predominantly associated with outside-cave samples, whereas Acidobacteria, Actinobacteria, Chloroflexi, and Gemmatimonadetes were associated with inside-cave samples. Functional prediction showed bacterial communities both inside and outside of the cave were functionally involved in the metabolism of carbohydrates, amino acids, lipids, xenobiotic compounds, energy metabolism, and environmental information processing. However, the amino acid and carbohydrate metabolic pathways were predominantly linked to the outside-cave samples, while xenobiotic compounds, lipids, other amino acids, and energy metabolism were associated with inside-cave samples. Overall, a positive correlation was observed between Biolog EcoPlate™ assay carbon utilization and the abundance of functional metabolic pathways in this study.


Author(s):  
W.A. Jacob ◽  
R. Hertsens ◽  
A. Van Bogaert ◽  
M. De Smet

In the past most studies of the control of energy metabolism focus on the role of the phosphorylation potential ATP/ADP.Pi on the regulation of respiration. Studies using NMR techniques have demonstrated that the concentrations of these compounds for oxidation phosphorylation do not change appreciably throughout the cardiac cycle and during increases in cardiac work. Hence regulation of energy production by calcium ions, present in the mitochondrial matrix, has been the object of a number of recent studies.Three exclusively intramitochondnal dehydrogenases are key enzymes for the regulation of oxidative metabolism. They are activated by calcium ions in the low micromolar range. Since, however, earlier estimates of the intramitochondnal calcium, based on equilibrium thermodynamic considerations, were in the millimolar range, a physiological correlation was not evident. The introduction of calcium-sensitive probes fura-2 and indo-1 made monitoring of free calcium during changing energy metabolism possible. These studies were performed on isolated mitochondria and extrapolation to the in vivo situation is more or less speculative.


2020 ◽  
Vol 48 (2) ◽  
pp. 399-409
Author(s):  
Baizhen Gao ◽  
Rushant Sabnis ◽  
Tommaso Costantini ◽  
Robert Jinkerson ◽  
Qing Sun

Microbial communities drive diverse processes that impact nearly everything on this planet, from global biogeochemical cycles to human health. Harnessing the power of these microorganisms could provide solutions to many of the challenges that face society. However, naturally occurring microbial communities are not optimized for anthropogenic use. An emerging area of research is focusing on engineering synthetic microbial communities to carry out predefined functions. Microbial community engineers are applying design principles like top-down and bottom-up approaches to create synthetic microbial communities having a myriad of real-life applications in health care, disease prevention, and environmental remediation. Multiple genetic engineering tools and delivery approaches can be used to ‘knock-in' new gene functions into microbial communities. A systematic study of the microbial interactions, community assembling principles, and engineering tools are necessary for us to understand the microbial community and to better utilize them. Continued analysis and effort are required to further the current and potential applications of synthetic microbial communities.


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