Ferric Uptake Regulator Provides a New Strategy for Acidophile Adaptation to Acidic Ecosystems
Acidophiles play a dominant role in driving elemental cycling in natural acid mine drainage (AMD) habitats and exhibit important application value in bioleaching and bioremediation. Acidity is an inevitable environmental stress and a key factor that affects the survival of acidophiles in their acidi...
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creator | Chen, Xian-Ke Li, Xiao-Yan Ha, Yi-Fan Lin, Jian-Qiang Liu, Xiang-Mei Pang, Xin Lin, Jian-Qun Chen, Lin-Xu |
description | Acidophiles play a dominant role in driving elemental cycling in natural acid mine drainage (AMD) habitats and exhibit important application value in bioleaching and bioremediation. Acidity is an inevitable environmental stress and a key factor that affects the survival of acidophiles in their acidified natural habitats; however, the regulatory strategies applied by acidophilic bacteria to withstand low pH are unclear. We identified the significance of the ferric uptake regulator (Fur) in acidophiles adapting to acidic environments and discovered that Fur is ubiquitous as well as highly conserved in acidophilic bacteria. Mutagenesis of the
gene of
, a prototypical acidophilic sulfur-oxidizing bacterium found in AMD, revealed that Fur is required for the acid resistance of this acidophilic bacterium. Phenotypic characterization, transcriptome sequencing (RNA-seq), mutagenesis, and biochemical assays indicated that the
ferric uptake regulator (AcFur) is involved in extreme acid resistance by regulating the expression of several key genes of certain cellular activities, such as iron transport, biofilm formation, sulfur metabolism, chemotaxis, and flagellar biosynthesis. Finally, a Fur-dependent acid resistance regulatory strategy in
was proposed to illustrate the ecological behavior of acidophilic bacteria under low pH. This study provides new insights into the adaptation strategies of acidophiles to AMD ecosystems and will promote the design and development of engineered biological systems for the environmental adaptation of acidophiles.
This study advances our understanding of the acid tolerance mechanism of
, identifies the key
gene responsible for acid resistance, and elucidates the correlation between
and acid resistance, thus contributing to an understanding of the ecological behavior of acidophilic bacteria. These findings provide new insights into the acid resistance process in
species, thereby promoting the study of the environmental adaptation of acidophilic bacteria and the design of engineered biological systems. |
doi_str_mv | 10.1128/AEM.00268-20 |
format | Article |
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gene of
, a prototypical acidophilic sulfur-oxidizing bacterium found in AMD, revealed that Fur is required for the acid resistance of this acidophilic bacterium. Phenotypic characterization, transcriptome sequencing (RNA-seq), mutagenesis, and biochemical assays indicated that the
ferric uptake regulator (AcFur) is involved in extreme acid resistance by regulating the expression of several key genes of certain cellular activities, such as iron transport, biofilm formation, sulfur metabolism, chemotaxis, and flagellar biosynthesis. Finally, a Fur-dependent acid resistance regulatory strategy in
was proposed to illustrate the ecological behavior of acidophilic bacteria under low pH. This study provides new insights into the adaptation strategies of acidophiles to AMD ecosystems and will promote the design and development of engineered biological systems for the environmental adaptation of acidophiles.
This study advances our understanding of the acid tolerance mechanism of
, identifies the key
gene responsible for acid resistance, and elucidates the correlation between
and acid resistance, thus contributing to an understanding of the ecological behavior of acidophilic bacteria. These findings provide new insights into the acid resistance process in
species, thereby promoting the study of the environmental adaptation of acidophilic bacteria and the design of engineered biological systems.</description><identifier>ISSN: 0099-2240</identifier><identifier>EISSN: 1098-5336</identifier><identifier>DOI: 10.1128/AEM.00268-20</identifier><identifier>PMID: 32245756</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Acid mine drainage ; Acid resistance ; Acidification ; Acidithiobacillus - genetics ; Acidithiobacillus - physiology ; Acidity ; Acidophilic bacteria ; Acids ; Adaptation ; Adaptation, Biological - genetics ; Amino Acid Sequence ; Bacteria ; Bacterial leaching ; Bacterial Proteins - chemistry ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Biofilms ; Bioremediation ; Biosynthesis ; Chemotaxis ; Ecosystem ; Environmental Microbiology ; Environmental stress ; Ferric Compounds - metabolism ; Flagella ; Gene expression ; Gene sequencing ; Hydrogen-Ion Concentration ; Leaching ; Metabolism ; Mine drainage ; Mining ; Mutagenesis ; Oxidation ; pH effects ; Repressor Proteins - chemistry ; Repressor Proteins - genetics ; Repressor Proteins - metabolism ; Ribonucleic acid ; RNA ; Sequence Alignment ; Spotlight ; Sulfur</subject><ispartof>Applied and environmental microbiology, 2020-05, Vol.86 (11)</ispartof><rights>Copyright © 2020 Chen et al.</rights><rights>Copyright American Society for Microbiology Jun 2020</rights><rights>Copyright © 2020 Chen et al. 2020 Chen et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-3170ca6594bb56fae4e49699b199d7079fd092b3d05453112534951398038c833</citedby><cites>FETCH-LOGICAL-c478t-3170ca6594bb56fae4e49699b199d7079fd092b3d05453112534951398038c833</cites><orcidid>0000-0002-2908-184X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7237784/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7237784/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32245756$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Xian-Ke</creatorcontrib><creatorcontrib>Li, Xiao-Yan</creatorcontrib><creatorcontrib>Ha, Yi-Fan</creatorcontrib><creatorcontrib>Lin, Jian-Qiang</creatorcontrib><creatorcontrib>Liu, Xiang-Mei</creatorcontrib><creatorcontrib>Pang, Xin</creatorcontrib><creatorcontrib>Lin, Jian-Qun</creatorcontrib><creatorcontrib>Chen, Lin-Xu</creatorcontrib><title>Ferric Uptake Regulator Provides a New Strategy for Acidophile Adaptation to Acidic Ecosystems</title><title>Applied and environmental microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>Acidophiles play a dominant role in driving elemental cycling in natural acid mine drainage (AMD) habitats and exhibit important application value in bioleaching and bioremediation. Acidity is an inevitable environmental stress and a key factor that affects the survival of acidophiles in their acidified natural habitats; however, the regulatory strategies applied by acidophilic bacteria to withstand low pH are unclear. We identified the significance of the ferric uptake regulator (Fur) in acidophiles adapting to acidic environments and discovered that Fur is ubiquitous as well as highly conserved in acidophilic bacteria. Mutagenesis of the
gene of
, a prototypical acidophilic sulfur-oxidizing bacterium found in AMD, revealed that Fur is required for the acid resistance of this acidophilic bacterium. Phenotypic characterization, transcriptome sequencing (RNA-seq), mutagenesis, and biochemical assays indicated that the
ferric uptake regulator (AcFur) is involved in extreme acid resistance by regulating the expression of several key genes of certain cellular activities, such as iron transport, biofilm formation, sulfur metabolism, chemotaxis, and flagellar biosynthesis. Finally, a Fur-dependent acid resistance regulatory strategy in
was proposed to illustrate the ecological behavior of acidophilic bacteria under low pH. This study provides new insights into the adaptation strategies of acidophiles to AMD ecosystems and will promote the design and development of engineered biological systems for the environmental adaptation of acidophiles.
This study advances our understanding of the acid tolerance mechanism of
, identifies the key
gene responsible for acid resistance, and elucidates the correlation between
and acid resistance, thus contributing to an understanding of the ecological behavior of acidophilic bacteria. These findings provide new insights into the acid resistance process in
species, thereby promoting the study of the environmental adaptation of acidophilic bacteria and the design of engineered biological systems.</description><subject>Acid mine drainage</subject><subject>Acid resistance</subject><subject>Acidification</subject><subject>Acidithiobacillus - genetics</subject><subject>Acidithiobacillus - physiology</subject><subject>Acidity</subject><subject>Acidophilic bacteria</subject><subject>Acids</subject><subject>Adaptation</subject><subject>Adaptation, Biological - genetics</subject><subject>Amino Acid Sequence</subject><subject>Bacteria</subject><subject>Bacterial leaching</subject><subject>Bacterial Proteins - chemistry</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Biofilms</subject><subject>Bioremediation</subject><subject>Biosynthesis</subject><subject>Chemotaxis</subject><subject>Ecosystem</subject><subject>Environmental Microbiology</subject><subject>Environmental stress</subject><subject>Ferric Compounds - metabolism</subject><subject>Flagella</subject><subject>Gene expression</subject><subject>Gene sequencing</subject><subject>Hydrogen-Ion Concentration</subject><subject>Leaching</subject><subject>Metabolism</subject><subject>Mine drainage</subject><subject>Mining</subject><subject>Mutagenesis</subject><subject>Oxidation</subject><subject>pH effects</subject><subject>Repressor Proteins - chemistry</subject><subject>Repressor Proteins - genetics</subject><subject>Repressor Proteins - metabolism</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Sequence Alignment</subject><subject>Spotlight</subject><subject>Sulfur</subject><issn>0099-2240</issn><issn>1098-5336</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUclOwzAQtRAIynLjjCxxJWUSL7EvSFVVFqksYrliOYlTAmldbAfUv8e0BcFppHlv3ryZh9BhCv00zcTpYHTdB8i4SDLYQL0UpEgYIXwT9QCkTLKMwg7a9f4VAChwsY12SGyynPEeej43zjUlfpoH_WbwvZl0rQ7W4TtnP5rKeKzxjfnED8HpYCYLXEdsUDaVnb80rcGDSsfJ0NgZDnYJRLFRaf3CBzP1-2ir1q03B-u6h57OR4_Dy2R8e3E1HIyTkuYiJCTNodScSVoUjNfaUEMll7JIpaxyyGVdgcwKUgGjjMSzGaGSpUQKIKIUhOyhs5XuvCumpirNLPpt1dw1U-0WyupG_UdmzYua2A-VZyTPBY0Cx2sBZ98744N6tZ2bRc8q_o9LzlgGkXWyYpXOeu9M_bshBfWdhoppqGUaakk_-uvql_zzfvIFULyEaQ</recordid><startdate>20200519</startdate><enddate>20200519</enddate><creator>Chen, Xian-Ke</creator><creator>Li, Xiao-Yan</creator><creator>Ha, Yi-Fan</creator><creator>Lin, Jian-Qiang</creator><creator>Liu, Xiang-Mei</creator><creator>Pang, Xin</creator><creator>Lin, Jian-Qun</creator><creator>Chen, Lin-Xu</creator><general>American Society for Microbiology</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>7QL</scope><scope>7QO</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2908-184X</orcidid></search><sort><creationdate>20200519</creationdate><title>Ferric Uptake Regulator Provides a New Strategy for Acidophile Adaptation to Acidic Ecosystems</title><author>Chen, Xian-Ke ; 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Acidity is an inevitable environmental stress and a key factor that affects the survival of acidophiles in their acidified natural habitats; however, the regulatory strategies applied by acidophilic bacteria to withstand low pH are unclear. We identified the significance of the ferric uptake regulator (Fur) in acidophiles adapting to acidic environments and discovered that Fur is ubiquitous as well as highly conserved in acidophilic bacteria. Mutagenesis of the
gene of
, a prototypical acidophilic sulfur-oxidizing bacterium found in AMD, revealed that Fur is required for the acid resistance of this acidophilic bacterium. Phenotypic characterization, transcriptome sequencing (RNA-seq), mutagenesis, and biochemical assays indicated that the
ferric uptake regulator (AcFur) is involved in extreme acid resistance by regulating the expression of several key genes of certain cellular activities, such as iron transport, biofilm formation, sulfur metabolism, chemotaxis, and flagellar biosynthesis. Finally, a Fur-dependent acid resistance regulatory strategy in
was proposed to illustrate the ecological behavior of acidophilic bacteria under low pH. This study provides new insights into the adaptation strategies of acidophiles to AMD ecosystems and will promote the design and development of engineered biological systems for the environmental adaptation of acidophiles.
This study advances our understanding of the acid tolerance mechanism of
, identifies the key
gene responsible for acid resistance, and elucidates the correlation between
and acid resistance, thus contributing to an understanding of the ecological behavior of acidophilic bacteria. These findings provide new insights into the acid resistance process in
species, thereby promoting the study of the environmental adaptation of acidophilic bacteria and the design of engineered biological systems.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>32245756</pmid><doi>10.1128/AEM.00268-20</doi><orcidid>https://orcid.org/0000-0002-2908-184X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acid mine drainage Acid resistance Acidification Acidithiobacillus - genetics Acidithiobacillus - physiology Acidity Acidophilic bacteria Acids Adaptation Adaptation, Biological - genetics Amino Acid Sequence Bacteria Bacterial leaching Bacterial Proteins - chemistry Bacterial Proteins - genetics Bacterial Proteins - metabolism Biofilms Bioremediation Biosynthesis Chemotaxis Ecosystem Environmental Microbiology Environmental stress Ferric Compounds - metabolism Flagella Gene expression Gene sequencing Hydrogen-Ion Concentration Leaching Metabolism Mine drainage Mining Mutagenesis Oxidation pH effects Repressor Proteins - chemistry Repressor Proteins - genetics Repressor Proteins - metabolism Ribonucleic acid RNA Sequence Alignment Spotlight Sulfur |
title | Ferric Uptake Regulator Provides a New Strategy for Acidophile Adaptation to Acidic Ecosystems |
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