XacR - a novel transcriptional regulator of D-xylose and L-arabinose catabolism in the haloarchaeon Haloferax volcanii
Summary The haloarchaeon Haloferax volcanii degrades D‐xylose and L‐arabinose via oxidative pathways to α‐ketoglutarate. The genes involved in these pathways are clustered and were transcriptionally upregulated by both D‐xylose and L‐arabinose suggesting a common regulator. Adjacent to the gene clus...
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Veröffentlicht in: | Environmental microbiology 2015-05, Vol.17 (5), p.1663-1676 |
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description | Summary
The haloarchaeon Haloferax volcanii degrades D‐xylose and L‐arabinose via oxidative pathways to α‐ketoglutarate. The genes involved in these pathways are clustered and were transcriptionally upregulated by both D‐xylose and L‐arabinose suggesting a common regulator. Adjacent to the gene cluster, a putative IclR‐like transcriptional regulator, HVO_B0040, was identified. It is shown that HVO_B0040, designated xacR, encodes an activator of both D‐xylose and L‐arabinose catabolism: in ΔxacR cells, transcripts of genes involved in pentose catabolism could not be detected; transcript formation could be recovered by complementation, indicating XacR dependent transcriptional activation. Upstream activation promoter regions and nucleotide sequences that were essential for XacR‐mediated activation of pentose‐specific genes were identified by in vivo deletion and scanning mutagenesis. Besides its activator function XacR acted as repressor of its own synthesis: xacR deletion resulted in an increase of xacR promoter activity. A palindromic sequence was identified at the operator site of xacR promoter, and mutation of this sequence also resulted in an increase and thus derepression of xacR promoter activity. It is concluded that the palindromic sequence represents the binding site of XacR as repressor. This is the first report of a transcriptional regulator of pentose catabolism in the domain of archaea. |
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The haloarchaeon Haloferax volcanii degrades D‐xylose and L‐arabinose via oxidative pathways to α‐ketoglutarate. The genes involved in these pathways are clustered and were transcriptionally upregulated by both D‐xylose and L‐arabinose suggesting a common regulator. Adjacent to the gene cluster, a putative IclR‐like transcriptional regulator, HVO_B0040, was identified. It is shown that HVO_B0040, designated xacR, encodes an activator of both D‐xylose and L‐arabinose catabolism: in ΔxacR cells, transcripts of genes involved in pentose catabolism could not be detected; transcript formation could be recovered by complementation, indicating XacR dependent transcriptional activation. Upstream activation promoter regions and nucleotide sequences that were essential for XacR‐mediated activation of pentose‐specific genes were identified by in vivo deletion and scanning mutagenesis. Besides its activator function XacR acted as repressor of its own synthesis: xacR deletion resulted in an increase of xacR promoter activity. A palindromic sequence was identified at the operator site of xacR promoter, and mutation of this sequence also resulted in an increase and thus derepression of xacR promoter activity. It is concluded that the palindromic sequence represents the binding site of XacR as repressor. This is the first report of a transcriptional regulator of pentose catabolism in the domain of archaea.</description><identifier>ISSN: 1462-2912</identifier><identifier>EISSN: 1462-2920</identifier><identifier>DOI: 10.1111/1462-2920.12603</identifier><identifier>PMID: 25141768</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Amino Acid Sequence ; Arabinose - metabolism ; Bacteriology ; Base Sequence ; Binding Sites - genetics ; Carbohydrate Metabolism - genetics ; DNA, Archaeal - analysis ; DNA, Archaeal - genetics ; Gene Expression Regulation, Archaeal ; Genes ; Haloferax volcanii - genetics ; Haloferax volcanii - metabolism ; Inverted Repeat Sequences - genetics ; Ketoglutaric Acids - metabolism ; Molecular Sequence Data ; Oxidation-Reduction ; Promoter Regions, Genetic - genetics ; Sequence Alignment ; Sequence Analysis, DNA ; Sequence Deletion - genetics ; Transcription, Genetic - genetics ; Transcriptional Activation - genetics ; Xylose - metabolism</subject><ispartof>Environmental microbiology, 2015-05, Vol.17 (5), p.1663-1676</ispartof><rights>2014 Society for Applied Microbiology and John Wiley & Sons Ltd</rights><rights>2014 Society for Applied Microbiology and John Wiley & Sons Ltd.</rights><rights>Copyright © 2015 Society for Applied Microbiology and John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2F1462-2920.12603$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2F1462-2920.12603$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25141768$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Johnsen, Ulrike</creatorcontrib><creatorcontrib>Sutter, Jan-Moritz</creatorcontrib><creatorcontrib>Schulz, Anne-Christine</creatorcontrib><creatorcontrib>Tästensen, Julia-Beate</creatorcontrib><creatorcontrib>Schönheit, Peter</creatorcontrib><title>XacR - a novel transcriptional regulator of D-xylose and L-arabinose catabolism in the haloarchaeon Haloferax volcanii</title><title>Environmental microbiology</title><addtitle>Environ Microbiol</addtitle><description>Summary
The haloarchaeon Haloferax volcanii degrades D‐xylose and L‐arabinose via oxidative pathways to α‐ketoglutarate. The genes involved in these pathways are clustered and were transcriptionally upregulated by both D‐xylose and L‐arabinose suggesting a common regulator. Adjacent to the gene cluster, a putative IclR‐like transcriptional regulator, HVO_B0040, was identified. It is shown that HVO_B0040, designated xacR, encodes an activator of both D‐xylose and L‐arabinose catabolism: in ΔxacR cells, transcripts of genes involved in pentose catabolism could not be detected; transcript formation could be recovered by complementation, indicating XacR dependent transcriptional activation. Upstream activation promoter regions and nucleotide sequences that were essential for XacR‐mediated activation of pentose‐specific genes were identified by in vivo deletion and scanning mutagenesis. Besides its activator function XacR acted as repressor of its own synthesis: xacR deletion resulted in an increase of xacR promoter activity. A palindromic sequence was identified at the operator site of xacR promoter, and mutation of this sequence also resulted in an increase and thus derepression of xacR promoter activity. It is concluded that the palindromic sequence represents the binding site of XacR as repressor. This is the first report of a transcriptional regulator of pentose catabolism in the domain of archaea.</description><subject>Amino Acid Sequence</subject><subject>Arabinose - metabolism</subject><subject>Bacteriology</subject><subject>Base Sequence</subject><subject>Binding Sites - genetics</subject><subject>Carbohydrate Metabolism - genetics</subject><subject>DNA, Archaeal - analysis</subject><subject>DNA, Archaeal - genetics</subject><subject>Gene Expression Regulation, Archaeal</subject><subject>Genes</subject><subject>Haloferax volcanii - genetics</subject><subject>Haloferax volcanii - metabolism</subject><subject>Inverted Repeat Sequences - genetics</subject><subject>Ketoglutaric Acids - metabolism</subject><subject>Molecular Sequence Data</subject><subject>Oxidation-Reduction</subject><subject>Promoter Regions, Genetic - genetics</subject><subject>Sequence Alignment</subject><subject>Sequence Analysis, DNA</subject><subject>Sequence Deletion - genetics</subject><subject>Transcription, Genetic - genetics</subject><subject>Transcriptional Activation - genetics</subject><subject>Xylose - metabolism</subject><issn>1462-2912</issn><issn>1462-2920</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9UU1PAjEQbYxGET17M008r26_9uNoEMEENRoV46WZ3e1KtWyxXRD-vUWUXmbe9L1J5j2ETkh8TsK7IDyhEc1pgDSJ2Q7qbCe7257QA3To_Ucck5Sl8T46oIJwkiZZBy1eoXzEEQbc2IUyuHXQ-NLpWattAwY79T430FqHbY2vouXKWK8wNBUeReCg0M0al9BCYY32U6wb3E4UnoCx4MoJKNvgYQC1crDEC2tKaLQ-Qns1GK-O_2oXPV_3n3rDaHQ_uOldjiLNspxFRSEEMKVIzghUUPFKlFma8ioDTrI6iYWqC8opy-u8LkpRqJRzQoFz4HXFE9ZFZ5u9M2e_5sq38sPOXTjMS5KkIliYZyywTv9Y82KqKjlzegpuJf9tCgSxIXxro1bbfxLLdQpy7bNcey5_U5D925vfJuiijU77Vi23OnCfMglRCDm-G8i30fjl7iGsGbIffaSI4A</recordid><startdate>201505</startdate><enddate>201505</enddate><creator>Johnsen, Ulrike</creator><creator>Sutter, Jan-Moritz</creator><creator>Schulz, Anne-Christine</creator><creator>Tästensen, Julia-Beate</creator><creator>Schönheit, Peter</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QH</scope><scope>7QL</scope><scope>7ST</scope><scope>7T7</scope><scope>7TN</scope><scope>7U9</scope><scope>7UA</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H94</scope><scope>H95</scope><scope>H97</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><scope>SOI</scope></search><sort><creationdate>201505</creationdate><title>XacR - a novel transcriptional regulator of D-xylose and L-arabinose catabolism in the haloarchaeon Haloferax volcanii</title><author>Johnsen, Ulrike ; Sutter, Jan-Moritz ; Schulz, Anne-Christine ; Tästensen, Julia-Beate ; Schönheit, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i3893-bb55a3ee1931adad4d5c8774d8a418f605efb24239f9fbc5be74412a44a4fd463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Amino Acid Sequence</topic><topic>Arabinose - metabolism</topic><topic>Bacteriology</topic><topic>Base Sequence</topic><topic>Binding Sites - genetics</topic><topic>Carbohydrate Metabolism - genetics</topic><topic>DNA, Archaeal - analysis</topic><topic>DNA, Archaeal - genetics</topic><topic>Gene Expression Regulation, Archaeal</topic><topic>Genes</topic><topic>Haloferax volcanii - genetics</topic><topic>Haloferax volcanii - metabolism</topic><topic>Inverted Repeat Sequences - genetics</topic><topic>Ketoglutaric Acids - metabolism</topic><topic>Molecular Sequence Data</topic><topic>Oxidation-Reduction</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>Sequence Alignment</topic><topic>Sequence Analysis, DNA</topic><topic>Sequence Deletion - genetics</topic><topic>Transcription, Genetic - genetics</topic><topic>Transcriptional Activation - genetics</topic><topic>Xylose - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Johnsen, Ulrike</creatorcontrib><creatorcontrib>Sutter, Jan-Moritz</creatorcontrib><creatorcontrib>Schulz, Anne-Christine</creatorcontrib><creatorcontrib>Tästensen, Julia-Beate</creatorcontrib><creatorcontrib>Schönheit, Peter</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Aqualine</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Oceanic Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Water Resources Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><jtitle>Environmental microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Johnsen, Ulrike</au><au>Sutter, Jan-Moritz</au><au>Schulz, Anne-Christine</au><au>Tästensen, Julia-Beate</au><au>Schönheit, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>XacR - a novel transcriptional regulator of D-xylose and L-arabinose catabolism in the haloarchaeon Haloferax volcanii</atitle><jtitle>Environmental microbiology</jtitle><addtitle>Environ Microbiol</addtitle><date>2015-05</date><risdate>2015</risdate><volume>17</volume><issue>5</issue><spage>1663</spage><epage>1676</epage><pages>1663-1676</pages><issn>1462-2912</issn><eissn>1462-2920</eissn><abstract>Summary
The haloarchaeon Haloferax volcanii degrades D‐xylose and L‐arabinose via oxidative pathways to α‐ketoglutarate. The genes involved in these pathways are clustered and were transcriptionally upregulated by both D‐xylose and L‐arabinose suggesting a common regulator. Adjacent to the gene cluster, a putative IclR‐like transcriptional regulator, HVO_B0040, was identified. It is shown that HVO_B0040, designated xacR, encodes an activator of both D‐xylose and L‐arabinose catabolism: in ΔxacR cells, transcripts of genes involved in pentose catabolism could not be detected; transcript formation could be recovered by complementation, indicating XacR dependent transcriptional activation. Upstream activation promoter regions and nucleotide sequences that were essential for XacR‐mediated activation of pentose‐specific genes were identified by in vivo deletion and scanning mutagenesis. Besides its activator function XacR acted as repressor of its own synthesis: xacR deletion resulted in an increase of xacR promoter activity. A palindromic sequence was identified at the operator site of xacR promoter, and mutation of this sequence also resulted in an increase and thus derepression of xacR promoter activity. It is concluded that the palindromic sequence represents the binding site of XacR as repressor. This is the first report of a transcriptional regulator of pentose catabolism in the domain of archaea.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>25141768</pmid><doi>10.1111/1462-2920.12603</doi><tpages>14</tpages></addata></record> |
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subjects | Amino Acid Sequence Arabinose - metabolism Bacteriology Base Sequence Binding Sites - genetics Carbohydrate Metabolism - genetics DNA, Archaeal - analysis DNA, Archaeal - genetics Gene Expression Regulation, Archaeal Genes Haloferax volcanii - genetics Haloferax volcanii - metabolism Inverted Repeat Sequences - genetics Ketoglutaric Acids - metabolism Molecular Sequence Data Oxidation-Reduction Promoter Regions, Genetic - genetics Sequence Alignment Sequence Analysis, DNA Sequence Deletion - genetics Transcription, Genetic - genetics Transcriptional Activation - genetics Xylose - metabolism |
title | XacR - a novel transcriptional regulator of D-xylose and L-arabinose catabolism in the haloarchaeon Haloferax volcanii |
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