Global transcriptome analysis of the tetrachloroethene-dechlorinating bacterium Desulfitobacterium hafniense Y51 in the presence of various electron donors and terminal electron acceptors

Desulfitobacterium hafniense Y51 is a dechlorinating bacterium that encodes an unusually large set of O-demethylase paralogs and specialized respiratory systems including specialized electron donors and acceptors. To use this organism in bioremediation of tetrachloroethene (PCE) or trichloroethene (...

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Veröffentlicht in:Journal of industrial microbiology & biotechnology 2012-02, Vol.39 (2), p.255-268
Hauptverfasser: Peng, Xue, Yamamoto, Shogo, Vertès, Alain A, Keresztes, Gabor, Inatomi, Ken-ichi, Inui, Masayuki, Yukawa, Hideaki
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container_title Journal of industrial microbiology & biotechnology
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creator Peng, Xue
Yamamoto, Shogo
Vertès, Alain A
Keresztes, Gabor
Inatomi, Ken-ichi
Inui, Masayuki
Yukawa, Hideaki
description Desulfitobacterium hafniense Y51 is a dechlorinating bacterium that encodes an unusually large set of O-demethylase paralogs and specialized respiratory systems including specialized electron donors and acceptors. To use this organism in bioremediation of tetrachloroethene (PCE) or trichloroethene (TCE) pollution, expression patterns of its 5,060 genes were determined under different conditions using 60-mer probes in DNA microarrays. PCE, TCE, fumarate, nitrate, and dimethyl sulfoxide (DMSO) respiration all sustain the growth of strain Y51. Global transcriptome analyses were thus performed using various electron donor and acceptor couples (respectively, pyruvate and either fumarate, TCE, nitrate, or DMSO, and vanillate/fumarate). When TCE is used as terminal electron acceptor, resulting in its detoxification, a series of electron carriers comprising a cytochrome bd-type quinol oxidase (DSY4055-4056), a ferredoxin (DSY1451), and four Fe–S proteins (DSY1626, DSY1629, DSY0733, DSY3309) are upregulated, suggesting that the products of these genes are involved in PCE oxidoreduction. Interestingly, the PCE dehalogenase cluster (pceABCT) is constitutively expressed in the media tested, with pceT being upregulated and pceC downregulated in pyruvate/TCE-containing medium. In addition, another dehalogenation enzyme (DSY1155 coding for a putative chlorophenol reductive dehalogenase), is induced 225-fold in that medium, despite not being involved in PCE respiration. Remarkably since the reducing equivalents formed during pyruvate conversion to acetyl-CoA are channeled to electron acceptors including halogenated compounds, pyruvate induces expression of a pyruvate:ferredoxin oxidoreductase. This study paves the way to understanding the physiology of D. hafniense, optimizing this microbe as a bioremediation agent, and designing bioarray sensors to monitor the presence of dechlorinating organisms in the environment.
doi_str_mv 10.1007/s10295-011-1023-7
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To use this organism in bioremediation of tetrachloroethene (PCE) or trichloroethene (TCE) pollution, expression patterns of its 5,060 genes were determined under different conditions using 60-mer probes in DNA microarrays. PCE, TCE, fumarate, nitrate, and dimethyl sulfoxide (DMSO) respiration all sustain the growth of strain Y51. Global transcriptome analyses were thus performed using various electron donor and acceptor couples (respectively, pyruvate and either fumarate, TCE, nitrate, or DMSO, and vanillate/fumarate). When TCE is used as terminal electron acceptor, resulting in its detoxification, a series of electron carriers comprising a cytochrome bd-type quinol oxidase (DSY4055-4056), a ferredoxin (DSY1451), and four Fe–S proteins (DSY1626, DSY1629, DSY0733, DSY3309) are upregulated, suggesting that the products of these genes are involved in PCE oxidoreduction. Interestingly, the PCE dehalogenase cluster (pceABCT) is constitutively expressed in the media tested, with pceT being upregulated and pceC downregulated in pyruvate/TCE-containing medium. In addition, another dehalogenation enzyme (DSY1155 coding for a putative chlorophenol reductive dehalogenase), is induced 225-fold in that medium, despite not being involved in PCE respiration. Remarkably since the reducing equivalents formed during pyruvate conversion to acetyl-CoA are channeled to electron acceptors including halogenated compounds, pyruvate induces expression of a pyruvate:ferredoxin oxidoreductase. 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Psychology ; gene expression ; Gene Expression Profiling ; gene expression regulation ; Genes ; Genetic Engineering ; Genomes ; Halogenated compounds ; Halogenation ; Hydrogen ; Inorganic Chemistry ; Iron-Sulfur Proteins - genetics ; Iron-Sulfur Proteins - metabolism ; Laboratories ; Life Sciences ; microarray technology ; Microbiology ; Nitrates ; Original Paper ; Oxidants - metabolism ; Oxidation-Reduction ; Oxidoreductases - genetics ; Oxidoreductases - metabolism ; Oxidoreductases, O-Demethylating - genetics ; Oxidoreductases, O-Demethylating - metabolism ; Physiology ; pollution ; Proteins ; pyruvate synthase ; pyruvic acid ; Respiration ; Respiratory system ; Soil contamination ; Studies ; Succinate Dehydrogenase - genetics ; Succinate Dehydrogenase - metabolism ; Tetrachloroethylene ; Tetrachloroethylene - metabolism ; Transcriptome ; transcriptomics ; Trichloroethylene - metabolism ; Water Pollutants, Chemical - metabolism</subject><ispartof>Journal of industrial microbiology &amp; biotechnology, 2012-02, Vol.39 (2), p.255-268</ispartof><rights>Society for Industrial Microbiology 2011</rights><rights>2015 INIST-CNRS</rights><rights>Society for Industrial Microbiology and Biotechnology 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-f7b3b3c3bc40412359061d65eda0aca87420114a9b0df13d41e427f5105a14b3</citedby><cites>FETCH-LOGICAL-c499t-f7b3b3c3bc40412359061d65eda0aca87420114a9b0df13d41e427f5105a14b3</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/s10295-011-1023-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10295-011-1023-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=25613509$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21861158$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Peng, Xue</creatorcontrib><creatorcontrib>Yamamoto, Shogo</creatorcontrib><creatorcontrib>Vertès, Alain A</creatorcontrib><creatorcontrib>Keresztes, Gabor</creatorcontrib><creatorcontrib>Inatomi, Ken-ichi</creatorcontrib><creatorcontrib>Inui, Masayuki</creatorcontrib><creatorcontrib>Yukawa, Hideaki</creatorcontrib><title>Global transcriptome analysis of the tetrachloroethene-dechlorinating bacterium Desulfitobacterium hafniense Y51 in the presence of various electron donors and terminal electron acceptors</title><title>Journal of industrial microbiology &amp; biotechnology</title><addtitle>J Ind Microbiol Biotechnol</addtitle><addtitle>J Ind Microbiol Biotechnol</addtitle><description>Desulfitobacterium hafniense Y51 is a dechlorinating bacterium that encodes an unusually large set of O-demethylase paralogs and specialized respiratory systems including specialized electron donors and acceptors. To use this organism in bioremediation of tetrachloroethene (PCE) or trichloroethene (TCE) pollution, expression patterns of its 5,060 genes were determined under different conditions using 60-mer probes in DNA microarrays. PCE, TCE, fumarate, nitrate, and dimethyl sulfoxide (DMSO) respiration all sustain the growth of strain Y51. Global transcriptome analyses were thus performed using various electron donor and acceptor couples (respectively, pyruvate and either fumarate, TCE, nitrate, or DMSO, and vanillate/fumarate). When TCE is used as terminal electron acceptor, resulting in its detoxification, a series of electron carriers comprising a cytochrome bd-type quinol oxidase (DSY4055-4056), a ferredoxin (DSY1451), and four Fe–S proteins (DSY1626, DSY1629, DSY0733, DSY3309) are upregulated, suggesting that the products of these genes are involved in PCE oxidoreduction. Interestingly, the PCE dehalogenase cluster (pceABCT) is constitutively expressed in the media tested, with pceT being upregulated and pceC downregulated in pyruvate/TCE-containing medium. In addition, another dehalogenation enzyme (DSY1155 coding for a putative chlorophenol reductive dehalogenase), is induced 225-fold in that medium, despite not being involved in PCE respiration. Remarkably since the reducing equivalents formed during pyruvate conversion to acetyl-CoA are channeled to electron acceptors including halogenated compounds, pyruvate induces expression of a pyruvate:ferredoxin oxidoreductase. 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Psychology</subject><subject>gene expression</subject><subject>Gene Expression Profiling</subject><subject>gene expression regulation</subject><subject>Genes</subject><subject>Genetic Engineering</subject><subject>Genomes</subject><subject>Halogenated compounds</subject><subject>Halogenation</subject><subject>Hydrogen</subject><subject>Inorganic Chemistry</subject><subject>Iron-Sulfur Proteins - genetics</subject><subject>Iron-Sulfur Proteins - metabolism</subject><subject>Laboratories</subject><subject>Life Sciences</subject><subject>microarray technology</subject><subject>Microbiology</subject><subject>Nitrates</subject><subject>Original Paper</subject><subject>Oxidants - metabolism</subject><subject>Oxidation-Reduction</subject><subject>Oxidoreductases - genetics</subject><subject>Oxidoreductases - metabolism</subject><subject>Oxidoreductases, O-Demethylating - genetics</subject><subject>Oxidoreductases, O-Demethylating - metabolism</subject><subject>Physiology</subject><subject>pollution</subject><subject>Proteins</subject><subject>pyruvate synthase</subject><subject>pyruvic acid</subject><subject>Respiration</subject><subject>Respiratory system</subject><subject>Soil contamination</subject><subject>Studies</subject><subject>Succinate Dehydrogenase - genetics</subject><subject>Succinate Dehydrogenase - metabolism</subject><subject>Tetrachloroethylene</subject><subject>Tetrachloroethylene - metabolism</subject><subject>Transcriptome</subject><subject>transcriptomics</subject><subject>Trichloroethylene - metabolism</subject><subject>Water Pollutants, Chemical - metabolism</subject><issn>1367-5435</issn><issn>1476-5535</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</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>eNp9ks9u1DAQxiMEon_gAbiAhVRxCtixHSfHqkBBqsSBcuAUTZzJrivHXuwEqc_GyzHbLKzEgZPHnt_MfJrPRfFC8LeCc_MuC161uuRClBTJ0jwqToUydam11I8plrUptZL6pDjL-Y5zro2pnhYnlWhqIXRzWvy69rEHz-YEIdvkdnOckEEAf59dZnFk8xbZjJS3Wx9TRLoHLAd8uLoAswsb1oOdMbllYu8xL350czw-bWEMDkNG9l0L5sJDy13CjMHifsRPSC4umaFHO6cY2BBDTJlkDDQ6TTTFH5NgLZLMlJ8VT0bwGZ8fzvPi9uOH26tP5c2X689XlzelVW07l6PpZS-t7K3iSlRSt7wWQ61xAA4WGqMq2qCCtufDKOSgBKrKjFpwDUL18rx4s7bdpfhjwTx3k8sWvYeApLprq7pptKobIl__Q97FJZF4goSRVV2pmiCxQjbFnBOO3S65CdJ9J3i3t7Vbbe1IVLe3tTNU8_LQeOknHP5W_PGRgIsDANmCH8lN6_KR07WQmrfEVSuXKRU2mI4K_zf91Vo0Quxgk6jxt6-0M0UfSrWNbuVvuZ3IBA</recordid><startdate>20120201</startdate><enddate>20120201</enddate><creator>Peng, Xue</creator><creator>Yamamoto, Shogo</creator><creator>Vertès, Alain A</creator><creator>Keresztes, Gabor</creator><creator>Inatomi, Ken-ichi</creator><creator>Inui, Masayuki</creator><creator>Yukawa, Hideaki</creator><general>Springer-Verlag</general><general>Springer</general><general>Oxford University Press</general><scope>FBQ</scope><scope>IQODW</scope><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>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>7QO</scope></search><sort><creationdate>20120201</creationdate><title>Global transcriptome analysis of the tetrachloroethene-dechlorinating bacterium Desulfitobacterium hafniense Y51 in the presence of various electron donors and terminal electron acceptors</title><author>Peng, Xue ; Yamamoto, Shogo ; Vertès, Alain A ; Keresztes, Gabor ; Inatomi, Ken-ichi ; Inui, Masayuki ; Yukawa, Hideaki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c499t-f7b3b3c3bc40412359061d65eda0aca87420114a9b0df13d41e427f5105a14b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>acetyl coenzyme A</topic><topic>Analysis</topic><topic>Animals</topic><topic>Bacteria</topic><topic>Biochemistry</topic><topic>Biodegradation, Environmental</topic><topic>Bioinformatics</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Bioremediation</topic><topic>Biotechnology</topic><topic>Chemical engineering</topic><topic>Chlorophenol</topic><topic>dehalogenation</topic><topic>Desulfitobacterium - genetics</topic><topic>Desulfitobacterium - growth &amp; development</topic><topic>Desulfitobacterium - metabolism</topic><topic>Desulfitobacterium hafniense</topic><topic>Detoxification</topic><topic>dimethyl sulfoxide</topic><topic>DNA probes</topic><topic>Electrons</topic><topic>Fundamental and applied biological sciences. 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biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Peng, Xue</au><au>Yamamoto, Shogo</au><au>Vertès, Alain A</au><au>Keresztes, Gabor</au><au>Inatomi, Ken-ichi</au><au>Inui, Masayuki</au><au>Yukawa, Hideaki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Global transcriptome analysis of the tetrachloroethene-dechlorinating bacterium Desulfitobacterium hafniense Y51 in the presence of various electron donors and terminal electron acceptors</atitle><jtitle>Journal of industrial microbiology &amp; biotechnology</jtitle><stitle>J Ind Microbiol Biotechnol</stitle><addtitle>J Ind Microbiol Biotechnol</addtitle><date>2012-02-01</date><risdate>2012</risdate><volume>39</volume><issue>2</issue><spage>255</spage><epage>268</epage><pages>255-268</pages><issn>1367-5435</issn><eissn>1476-5535</eissn><abstract>Desulfitobacterium hafniense Y51 is a dechlorinating bacterium that encodes an unusually large set of O-demethylase paralogs and specialized respiratory systems including specialized electron donors and acceptors. To use this organism in bioremediation of tetrachloroethene (PCE) or trichloroethene (TCE) pollution, expression patterns of its 5,060 genes were determined under different conditions using 60-mer probes in DNA microarrays. PCE, TCE, fumarate, nitrate, and dimethyl sulfoxide (DMSO) respiration all sustain the growth of strain Y51. Global transcriptome analyses were thus performed using various electron donor and acceptor couples (respectively, pyruvate and either fumarate, TCE, nitrate, or DMSO, and vanillate/fumarate). When TCE is used as terminal electron acceptor, resulting in its detoxification, a series of electron carriers comprising a cytochrome bd-type quinol oxidase (DSY4055-4056), a ferredoxin (DSY1451), and four Fe–S proteins (DSY1626, DSY1629, DSY0733, DSY3309) are upregulated, suggesting that the products of these genes are involved in PCE oxidoreduction. Interestingly, the PCE dehalogenase cluster (pceABCT) is constitutively expressed in the media tested, with pceT being upregulated and pceC downregulated in pyruvate/TCE-containing medium. In addition, another dehalogenation enzyme (DSY1155 coding for a putative chlorophenol reductive dehalogenase), is induced 225-fold in that medium, despite not being involved in PCE respiration. Remarkably since the reducing equivalents formed during pyruvate conversion to acetyl-CoA are channeled to electron acceptors including halogenated compounds, pyruvate induces expression of a pyruvate:ferredoxin oxidoreductase. This study paves the way to understanding the physiology of D. hafniense, optimizing this microbe as a bioremediation agent, and designing bioarray sensors to monitor the presence of dechlorinating organisms in the environment.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>21861158</pmid><doi>10.1007/s10295-011-1023-7</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record>
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1476-5535
language eng
recordid cdi_proquest_miscellaneous_926885468
source Oxford Journals Open Access Collection; MEDLINE; Springer Nature - Complete Springer Journals
subjects acetyl coenzyme A
Analysis
Animals
Bacteria
Biochemistry
Biodegradation, Environmental
Bioinformatics
Biological and medical sciences
Biomedical and Life Sciences
Bioremediation
Biotechnology
Chemical engineering
Chlorophenol
dehalogenation
Desulfitobacterium - genetics
Desulfitobacterium - growth & development
Desulfitobacterium - metabolism
Desulfitobacterium hafniense
Detoxification
dimethyl sulfoxide
DNA probes
Electrons
Fundamental and applied biological sciences. Psychology
gene expression
Gene Expression Profiling
gene expression regulation
Genes
Genetic Engineering
Genomes
Halogenated compounds
Halogenation
Hydrogen
Inorganic Chemistry
Iron-Sulfur Proteins - genetics
Iron-Sulfur Proteins - metabolism
Laboratories
Life Sciences
microarray technology
Microbiology
Nitrates
Original Paper
Oxidants - metabolism
Oxidation-Reduction
Oxidoreductases - genetics
Oxidoreductases - metabolism
Oxidoreductases, O-Demethylating - genetics
Oxidoreductases, O-Demethylating - metabolism
Physiology
pollution
Proteins
pyruvate synthase
pyruvic acid
Respiration
Respiratory system
Soil contamination
Studies
Succinate Dehydrogenase - genetics
Succinate Dehydrogenase - metabolism
Tetrachloroethylene
Tetrachloroethylene - metabolism
Transcriptome
transcriptomics
Trichloroethylene - metabolism
Water Pollutants, Chemical - metabolism
title Global transcriptome analysis of the tetrachloroethene-dechlorinating bacterium Desulfitobacterium hafniense Y51 in the presence of various electron donors and terminal electron acceptors
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