Metabolic transcriptional analysis on copper tolerance in moderate thermophilic bioleaching microorganism Acidithiobacillus caldus
Bioleaching, an alternative environmental smelting technology, typically uses high concentrations of heavy metal ions, especially in the subsequent phase, due to metal ion accumulation from the mineral. In this study, we analyzed the overall response of the bioleaching microorganism Acidithiobacillu...
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description | Bioleaching, an alternative environmental smelting technology, typically uses high concentrations of heavy metal ions, especially in the subsequent phase, due to metal ion accumulation from the mineral. In this study, we analyzed the overall response of the bioleaching microorganism
Acidithiobacillus caldus
to copper stress through physiological and transcriptomic analyses. Scanning electron microscopy results showed higher extracellular polymeric substances secretion and cell aggregation under copper stress. Intracellular levels of glutamic acid, glycine and cysteine increased, favoring the synthesis of glutathione for maintenance of the oxidation–reduction state. GSH, during copper stress conditions, the activity of GSH-PX and CAT increased, resulting in reduced oxidative damage while maintaining stable intracellular pH. Higher unsaturated and cyclopropane fatty acid levels resulted in increased membrane fluidity and compactness and decreased ATP levels to support the energy requirements for stress resistance. Initially, H
+
-ATPase activity increased to provide energy for proton output and decreased later at higher copper ion stress. From transcriptome analysis, 140 genes were differentially expressed under low copper stress (1 g/L), while 250 genes exhibited altered transcriptional levels at higher copper stress (3 g/L). These differentially expressed genes were involved primarily in metabolic pathways such as energy metabolism, two-component systems, amino acid metabolism, and signal transduction. The Sox family cluster gene cluster involved in the conversion of thiosulfate to sulfate was upregulated in the sulfur metabolism pathway. In the oxidative phosphorylation pathway, genes participating in the synthesis of NADH oxidoreductase and cytochrome c oxidase,
nuoL
,
cyoABD
(
cyoA
,
cyoB
and
cyoD
) and
cydAB
(
cydA
and
cydB
), were downregulated. The TCS element
ompR
, closely associated with the osmotic pressure, exhibited active response, while Cu
2+
efflux system gene
cusRS
was upregulated. In the amino acid metabolism, the
glnA
involved in nitrogen fixation was upregulated and promoted the synthesis of glutamine synthetase for reducing excessive oxidative stress. This study provides new insights into the mechanism underlying
A. caldus
response to heavy-metal ion stress under harsh bioleaching conditions. |
doi_str_mv | 10.1007/s10295-019-02247-6 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2317604444</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2344268715</sourcerecordid><originalsourceid>FETCH-LOGICAL-c412t-d0c21cf446927a3bfd9b058f9cb79ba0861535497147f785eb78ad0edcaf6cfe3</originalsourceid><addsrcrecordid>eNp9kTtPHDEUha0oUSALf4AispQmzRDb48dMiRAhSKA0SW3ZHs-ukWc8sT0FLb-cu1kgUgpc-CF_91zdcxA6o-ScEqK-FUpYLxpC-4YwxlUj36FjypVshGjFe7i3UjWCt-IIfSrlnhAilGIf0VFLleg4bY_R452vxqYYHK7ZzMXlsNSQZhOxge2hhILTjF1aFp9xTdED5TwOM57SAI_qcd35PKVlF_YqNgBj3C7MWzwFl1PKWzOHMuELF4ZQdyFZ40KMa8HOxGEtJ-jDaGLxp8_nBv3-fvXr8kdz-_P65vLitnGcstoMxDHqRs5lz5Rp7Tj0lohu7J1VvTWkkxSm5r0CB0bVCW9VZwbiB2dG6UbfbtDXg-6S05_Vl6qnUJyP0cw-rUUzcEUSDgvQL_-h92nN4Mee4pzJTkGzDWIHCqYsJftRLzlMJj9oSvQ-IX1ISENC-m9CWkLR52fp1U5-eC15iQSA9gAU-Jq3Pv_r_YbsE8Tun3Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2344268715</pqid></control><display><type>article</type><title>Metabolic transcriptional analysis on copper tolerance in moderate thermophilic bioleaching microorganism Acidithiobacillus caldus</title><source>MEDLINE</source><source>Oxford Journals Open Access Collection</source><source>Springer Nature - Complete Springer Journals</source><creator>Feng, Shoushuai ; Hou, Shaoxiang ; Cui, Yaquan ; Tong, Yanjun ; Yang, Hailin</creator><creatorcontrib>Feng, Shoushuai ; Hou, Shaoxiang ; Cui, Yaquan ; Tong, Yanjun ; Yang, Hailin</creatorcontrib><description>Bioleaching, an alternative environmental smelting technology, typically uses high concentrations of heavy metal ions, especially in the subsequent phase, due to metal ion accumulation from the mineral. In this study, we analyzed the overall response of the bioleaching microorganism
Acidithiobacillus caldus
to copper stress through physiological and transcriptomic analyses. Scanning electron microscopy results showed higher extracellular polymeric substances secretion and cell aggregation under copper stress. Intracellular levels of glutamic acid, glycine and cysteine increased, favoring the synthesis of glutathione for maintenance of the oxidation–reduction state. GSH, during copper stress conditions, the activity of GSH-PX and CAT increased, resulting in reduced oxidative damage while maintaining stable intracellular pH. Higher unsaturated and cyclopropane fatty acid levels resulted in increased membrane fluidity and compactness and decreased ATP levels to support the energy requirements for stress resistance. Initially, H
+
-ATPase activity increased to provide energy for proton output and decreased later at higher copper ion stress. From transcriptome analysis, 140 genes were differentially expressed under low copper stress (1 g/L), while 250 genes exhibited altered transcriptional levels at higher copper stress (3 g/L). These differentially expressed genes were involved primarily in metabolic pathways such as energy metabolism, two-component systems, amino acid metabolism, and signal transduction. The Sox family cluster gene cluster involved in the conversion of thiosulfate to sulfate was upregulated in the sulfur metabolism pathway. In the oxidative phosphorylation pathway, genes participating in the synthesis of NADH oxidoreductase and cytochrome c oxidase,
nuoL
,
cyoABD
(
cyoA
,
cyoB
and
cyoD
) and
cydAB
(
cydA
and
cydB
), were downregulated. The TCS element
ompR
, closely associated with the osmotic pressure, exhibited active response, while Cu
2+
efflux system gene
cusRS
was upregulated. In the amino acid metabolism, the
glnA
involved in nitrogen fixation was upregulated and promoted the synthesis of glutamine synthetase for reducing excessive oxidative stress. This study provides new insights into the mechanism underlying
A. caldus
response to heavy-metal ion stress under harsh bioleaching conditions.</description><identifier>ISSN: 1367-5435</identifier><identifier>EISSN: 1476-5535</identifier><identifier>DOI: 10.1007/s10295-019-02247-6</identifier><identifier>PMID: 31758413</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Acidithiobacillus - drug effects ; Acidithiobacillus - metabolism ; Adenosine triphosphatase ; Amino acids ; Bacterial leaching ; Biochemistry ; Bioinformatics ; Biomedical and Life Sciences ; Biotechnology ; Cell aggregation ; Copper ; Copper - metabolism ; Copper - pharmacology ; Cyclopropane ; Cysteine - metabolism ; Cytochrome-c oxidase ; Cytochromes ; Efflux ; Energy metabolism ; Energy requirements ; Environmental Microbiology - Original Paper ; Fatty acids ; Fluidity ; Gene expression ; Gene Expression Profiling ; Genes ; Genetic Engineering ; Glutamate-ammonia ligase ; Glutamic acid ; Glutamine ; Glutathione ; Glycine ; H+-transporting ATPase ; Heavy metals ; Inorganic Chemistry ; Ion accumulation ; Leaching ; Life Sciences ; Membrane fluidity ; Metabolic Networks and Pathways ; Metabolism ; Metal concentrations ; Metal ions ; Microbiology ; Microorganisms ; Nicotinamide adenine dinucleotide ; Nitrogen fixation ; Nitrogenation ; Osmosis ; Osmotic pressure ; Oxidation ; Oxidation-Reduction ; Oxidative phosphorylation ; Oxidative stress ; Oxidoreductase ; Phosphorylation ; Scanning electron microscopy ; Signal transduction ; Smelting ; Sulfates - metabolism ; Sulfur ; Synthesis ; Thiosulfates ; Transcription</subject><ispartof>Journal of industrial microbiology & biotechnology, 2020, Vol.47 (1), p.21-33</ispartof><rights>Society for Industrial Microbiology and Biotechnology 2019</rights><rights>Journal of Industrial Microbiology & Biotechnology is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-d0c21cf446927a3bfd9b058f9cb79ba0861535497147f785eb78ad0edcaf6cfe3</citedby><cites>FETCH-LOGICAL-c412t-d0c21cf446927a3bfd9b058f9cb79ba0861535497147f785eb78ad0edcaf6cfe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10295-019-02247-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10295-019-02247-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31758413$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Feng, Shoushuai</creatorcontrib><creatorcontrib>Hou, Shaoxiang</creatorcontrib><creatorcontrib>Cui, Yaquan</creatorcontrib><creatorcontrib>Tong, Yanjun</creatorcontrib><creatorcontrib>Yang, Hailin</creatorcontrib><title>Metabolic transcriptional analysis on copper tolerance in moderate thermophilic bioleaching microorganism Acidithiobacillus caldus</title><title>Journal of industrial microbiology & biotechnology</title><addtitle>J Ind Microbiol Biotechnol</addtitle><addtitle>J Ind Microbiol Biotechnol</addtitle><description>Bioleaching, an alternative environmental smelting technology, typically uses high concentrations of heavy metal ions, especially in the subsequent phase, due to metal ion accumulation from the mineral. In this study, we analyzed the overall response of the bioleaching microorganism
Acidithiobacillus caldus
to copper stress through physiological and transcriptomic analyses. Scanning electron microscopy results showed higher extracellular polymeric substances secretion and cell aggregation under copper stress. Intracellular levels of glutamic acid, glycine and cysteine increased, favoring the synthesis of glutathione for maintenance of the oxidation–reduction state. GSH, during copper stress conditions, the activity of GSH-PX and CAT increased, resulting in reduced oxidative damage while maintaining stable intracellular pH. Higher unsaturated and cyclopropane fatty acid levels resulted in increased membrane fluidity and compactness and decreased ATP levels to support the energy requirements for stress resistance. Initially, H
+
-ATPase activity increased to provide energy for proton output and decreased later at higher copper ion stress. From transcriptome analysis, 140 genes were differentially expressed under low copper stress (1 g/L), while 250 genes exhibited altered transcriptional levels at higher copper stress (3 g/L). These differentially expressed genes were involved primarily in metabolic pathways such as energy metabolism, two-component systems, amino acid metabolism, and signal transduction. The Sox family cluster gene cluster involved in the conversion of thiosulfate to sulfate was upregulated in the sulfur metabolism pathway. In the oxidative phosphorylation pathway, genes participating in the synthesis of NADH oxidoreductase and cytochrome c oxidase,
nuoL
,
cyoABD
(
cyoA
,
cyoB
and
cyoD
) and
cydAB
(
cydA
and
cydB
), were downregulated. The TCS element
ompR
, closely associated with the osmotic pressure, exhibited active response, while Cu
2+
efflux system gene
cusRS
was upregulated. In the amino acid metabolism, the
glnA
involved in nitrogen fixation was upregulated and promoted the synthesis of glutamine synthetase for reducing excessive oxidative stress. This study provides new insights into the mechanism underlying
A. caldus
response to heavy-metal ion stress under harsh bioleaching conditions.</description><subject>Acidithiobacillus - drug effects</subject><subject>Acidithiobacillus - metabolism</subject><subject>Adenosine triphosphatase</subject><subject>Amino acids</subject><subject>Bacterial leaching</subject><subject>Biochemistry</subject><subject>Bioinformatics</subject><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>Cell aggregation</subject><subject>Copper</subject><subject>Copper - metabolism</subject><subject>Copper - pharmacology</subject><subject>Cyclopropane</subject><subject>Cysteine - metabolism</subject><subject>Cytochrome-c oxidase</subject><subject>Cytochromes</subject><subject>Efflux</subject><subject>Energy metabolism</subject><subject>Energy requirements</subject><subject>Environmental Microbiology - Original Paper</subject><subject>Fatty acids</subject><subject>Fluidity</subject><subject>Gene expression</subject><subject>Gene Expression Profiling</subject><subject>Genes</subject><subject>Genetic Engineering</subject><subject>Glutamate-ammonia ligase</subject><subject>Glutamic acid</subject><subject>Glutamine</subject><subject>Glutathione</subject><subject>Glycine</subject><subject>H+-transporting ATPase</subject><subject>Heavy metals</subject><subject>Inorganic Chemistry</subject><subject>Ion accumulation</subject><subject>Leaching</subject><subject>Life Sciences</subject><subject>Membrane fluidity</subject><subject>Metabolic Networks and Pathways</subject><subject>Metabolism</subject><subject>Metal concentrations</subject><subject>Metal ions</subject><subject>Microbiology</subject><subject>Microorganisms</subject><subject>Nicotinamide adenine dinucleotide</subject><subject>Nitrogen fixation</subject><subject>Nitrogenation</subject><subject>Osmosis</subject><subject>Osmotic pressure</subject><subject>Oxidation</subject><subject>Oxidation-Reduction</subject><subject>Oxidative phosphorylation</subject><subject>Oxidative stress</subject><subject>Oxidoreductase</subject><subject>Phosphorylation</subject><subject>Scanning electron microscopy</subject><subject>Signal transduction</subject><subject>Smelting</subject><subject>Sulfates - metabolism</subject><subject>Sulfur</subject><subject>Synthesis</subject><subject>Thiosulfates</subject><subject>Transcription</subject><issn>1367-5435</issn><issn>1476-5535</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kTtPHDEUha0oUSALf4AispQmzRDb48dMiRAhSKA0SW3ZHs-ukWc8sT0FLb-cu1kgUgpc-CF_91zdcxA6o-ScEqK-FUpYLxpC-4YwxlUj36FjypVshGjFe7i3UjWCt-IIfSrlnhAilGIf0VFLleg4bY_R452vxqYYHK7ZzMXlsNSQZhOxge2hhILTjF1aFp9xTdED5TwOM57SAI_qcd35PKVlF_YqNgBj3C7MWzwFl1PKWzOHMuELF4ZQdyFZ40KMa8HOxGEtJ-jDaGLxp8_nBv3-fvXr8kdz-_P65vLitnGcstoMxDHqRs5lz5Rp7Tj0lohu7J1VvTWkkxSm5r0CB0bVCW9VZwbiB2dG6UbfbtDXg-6S05_Vl6qnUJyP0cw-rUUzcEUSDgvQL_-h92nN4Mee4pzJTkGzDWIHCqYsJftRLzlMJj9oSvQ-IX1ISENC-m9CWkLR52fp1U5-eC15iQSA9gAU-Jq3Pv_r_YbsE8Tun3Q</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Feng, Shoushuai</creator><creator>Hou, Shaoxiang</creator><creator>Cui, Yaquan</creator><creator>Tong, Yanjun</creator><creator>Yang, Hailin</creator><general>Springer International Publishing</general><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7QR</scope><scope>7T7</scope><scope>7WY</scope><scope>7WZ</scope><scope>7X7</scope><scope>7XB</scope><scope>87Z</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FL</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BEZIV</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FRNLG</scope><scope>FYUFA</scope><scope>F~G</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K60</scope><scope>K6~</scope><scope>K9.</scope><scope>L.-</scope><scope>LK8</scope><scope>M0C</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQBIZ</scope><scope>PQBZA</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>2020</creationdate><title>Metabolic transcriptional analysis on copper tolerance in moderate thermophilic bioleaching microorganism Acidithiobacillus caldus</title><author>Feng, Shoushuai ; Hou, Shaoxiang ; Cui, Yaquan ; Tong, Yanjun ; Yang, Hailin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-d0c21cf446927a3bfd9b058f9cb79ba0861535497147f785eb78ad0edcaf6cfe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Acidithiobacillus - drug effects</topic><topic>Acidithiobacillus - metabolism</topic><topic>Adenosine triphosphatase</topic><topic>Amino acids</topic><topic>Bacterial leaching</topic><topic>Biochemistry</topic><topic>Bioinformatics</topic><topic>Biomedical and Life Sciences</topic><topic>Biotechnology</topic><topic>Cell aggregation</topic><topic>Copper</topic><topic>Copper - metabolism</topic><topic>Copper - pharmacology</topic><topic>Cyclopropane</topic><topic>Cysteine - metabolism</topic><topic>Cytochrome-c oxidase</topic><topic>Cytochromes</topic><topic>Efflux</topic><topic>Energy metabolism</topic><topic>Energy requirements</topic><topic>Environmental Microbiology - Original Paper</topic><topic>Fatty acids</topic><topic>Fluidity</topic><topic>Gene expression</topic><topic>Gene Expression Profiling</topic><topic>Genes</topic><topic>Genetic Engineering</topic><topic>Glutamate-ammonia ligase</topic><topic>Glutamic acid</topic><topic>Glutamine</topic><topic>Glutathione</topic><topic>Glycine</topic><topic>H+-transporting ATPase</topic><topic>Heavy metals</topic><topic>Inorganic Chemistry</topic><topic>Ion accumulation</topic><topic>Leaching</topic><topic>Life Sciences</topic><topic>Membrane fluidity</topic><topic>Metabolic Networks and Pathways</topic><topic>Metabolism</topic><topic>Metal concentrations</topic><topic>Metal ions</topic><topic>Microbiology</topic><topic>Microorganisms</topic><topic>Nicotinamide adenine dinucleotide</topic><topic>Nitrogen fixation</topic><topic>Nitrogenation</topic><topic>Osmosis</topic><topic>Osmotic pressure</topic><topic>Oxidation</topic><topic>Oxidation-Reduction</topic><topic>Oxidative phosphorylation</topic><topic>Oxidative stress</topic><topic>Oxidoreductase</topic><topic>Phosphorylation</topic><topic>Scanning electron microscopy</topic><topic>Signal transduction</topic><topic>Smelting</topic><topic>Sulfates - metabolism</topic><topic>Sulfur</topic><topic>Synthesis</topic><topic>Thiosulfates</topic><topic>Transcription</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Feng, Shoushuai</creatorcontrib><creatorcontrib>Hou, Shaoxiang</creatorcontrib><creatorcontrib>Cui, Yaquan</creatorcontrib><creatorcontrib>Tong, Yanjun</creatorcontrib><creatorcontrib>Yang, Hailin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Chemoreception Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>ABI/INFORM Collection</collection><collection>ABI/INFORM Global (PDF only)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ABI/INFORM Global (Alumni Edition)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ABI/INFORM Collection (Alumni Edition)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Business Premium Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Business Premium Collection (Alumni)</collection><collection>Health Research Premium Collection</collection><collection>ABI/INFORM Global (Corporate)</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Business Collection (Alumni Edition)</collection><collection>ProQuest Business Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ABI/INFORM Professional Advanced</collection><collection>ProQuest Biological Science Collection</collection><collection>ABI/INFORM Global</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Business</collection><collection>ProQuest One Business (Alumni)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of industrial microbiology & biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Feng, Shoushuai</au><au>Hou, Shaoxiang</au><au>Cui, Yaquan</au><au>Tong, Yanjun</au><au>Yang, Hailin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolic transcriptional analysis on copper tolerance in moderate thermophilic bioleaching microorganism Acidithiobacillus caldus</atitle><jtitle>Journal of industrial microbiology & biotechnology</jtitle><stitle>J Ind Microbiol Biotechnol</stitle><addtitle>J Ind Microbiol Biotechnol</addtitle><date>2020</date><risdate>2020</risdate><volume>47</volume><issue>1</issue><spage>21</spage><epage>33</epage><pages>21-33</pages><issn>1367-5435</issn><eissn>1476-5535</eissn><abstract>Bioleaching, an alternative environmental smelting technology, typically uses high concentrations of heavy metal ions, especially in the subsequent phase, due to metal ion accumulation from the mineral. In this study, we analyzed the overall response of the bioleaching microorganism
Acidithiobacillus caldus
to copper stress through physiological and transcriptomic analyses. Scanning electron microscopy results showed higher extracellular polymeric substances secretion and cell aggregation under copper stress. Intracellular levels of glutamic acid, glycine and cysteine increased, favoring the synthesis of glutathione for maintenance of the oxidation–reduction state. GSH, during copper stress conditions, the activity of GSH-PX and CAT increased, resulting in reduced oxidative damage while maintaining stable intracellular pH. Higher unsaturated and cyclopropane fatty acid levels resulted in increased membrane fluidity and compactness and decreased ATP levels to support the energy requirements for stress resistance. Initially, H
+
-ATPase activity increased to provide energy for proton output and decreased later at higher copper ion stress. From transcriptome analysis, 140 genes were differentially expressed under low copper stress (1 g/L), while 250 genes exhibited altered transcriptional levels at higher copper stress (3 g/L). These differentially expressed genes were involved primarily in metabolic pathways such as energy metabolism, two-component systems, amino acid metabolism, and signal transduction. The Sox family cluster gene cluster involved in the conversion of thiosulfate to sulfate was upregulated in the sulfur metabolism pathway. In the oxidative phosphorylation pathway, genes participating in the synthesis of NADH oxidoreductase and cytochrome c oxidase,
nuoL
,
cyoABD
(
cyoA
,
cyoB
and
cyoD
) and
cydAB
(
cydA
and
cydB
), were downregulated. The TCS element
ompR
, closely associated with the osmotic pressure, exhibited active response, while Cu
2+
efflux system gene
cusRS
was upregulated. In the amino acid metabolism, the
glnA
involved in nitrogen fixation was upregulated and promoted the synthesis of glutamine synthetase for reducing excessive oxidative stress. This study provides new insights into the mechanism underlying
A. caldus
response to heavy-metal ion stress under harsh bioleaching conditions.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>31758413</pmid><doi>10.1007/s10295-019-02247-6</doi><tpages>13</tpages></addata></record> |
fulltext | fulltext |
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ispartof | Journal of industrial microbiology & biotechnology, 2020, Vol.47 (1), p.21-33 |
issn | 1367-5435 1476-5535 |
language | eng |
recordid | cdi_proquest_miscellaneous_2317604444 |
source | MEDLINE; Oxford Journals Open Access Collection; Springer Nature - Complete Springer Journals |
subjects | Acidithiobacillus - drug effects Acidithiobacillus - metabolism Adenosine triphosphatase Amino acids Bacterial leaching Biochemistry Bioinformatics Biomedical and Life Sciences Biotechnology Cell aggregation Copper Copper - metabolism Copper - pharmacology Cyclopropane Cysteine - metabolism Cytochrome-c oxidase Cytochromes Efflux Energy metabolism Energy requirements Environmental Microbiology - Original Paper Fatty acids Fluidity Gene expression Gene Expression Profiling Genes Genetic Engineering Glutamate-ammonia ligase Glutamic acid Glutamine Glutathione Glycine H+-transporting ATPase Heavy metals Inorganic Chemistry Ion accumulation Leaching Life Sciences Membrane fluidity Metabolic Networks and Pathways Metabolism Metal concentrations Metal ions Microbiology Microorganisms Nicotinamide adenine dinucleotide Nitrogen fixation Nitrogenation Osmosis Osmotic pressure Oxidation Oxidation-Reduction Oxidative phosphorylation Oxidative stress Oxidoreductase Phosphorylation Scanning electron microscopy Signal transduction Smelting Sulfates - metabolism Sulfur Synthesis Thiosulfates Transcription |
title | Metabolic transcriptional analysis on copper tolerance in moderate thermophilic bioleaching microorganism Acidithiobacillus caldus |
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