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Biosynthesis of the biomarker okenone: χ-ring formation
Purple sulfur bacteria (PSB) mainly occur in anoxic aquatic and benthic environments, where they play important roles in cycling carbon and sulfur. Many PSB characteristically produce the unique keto‐carotenoid, okenone, which is important not only for its light absorption and photoprotection proper...
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Published in: | Geobiology 2012-05, Vol.10 (3), p.205-215 |
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description | Purple sulfur bacteria (PSB) mainly occur in anoxic aquatic and benthic environments, where they play important roles in cycling carbon and sulfur. Many PSB characteristically produce the unique keto‐carotenoid, okenone, which is important not only for its light absorption and photoprotection properties but also because of its diagenesis product, okenane, which is a biomarker for ancient sediments derived from anoxic environments. The specific methylation pattern of the χ‐ring of okenane is unlikely to be formed by diagenetic processes and should therefore reflect an enzymatic activity from okenone biosynthesis. This study describes two enzymes that produce the χ‐ring of okenone, the only structural element of okenone preserved in okenane. Genes encoding enzymes of carotenogenesis were identified in the draft genome sequence of an okenone‐producing PSB, Thiodictyon sp. strain CAD16. Two divergently transcribed genes encoded a CrtY‐type lycopene cyclase and a CrtU/CruE‐type γ‐carotene desaturase/methyltransferase. Expression of crtY in Escherichia coli showed that this gene encoded a lycopene cyclase that produced γ‐carotene as the only product. Although the sequence of the γ‐carotene desaturase/methyltransferase was more similar to CrtU sequences of green sulfur bacteria than to CruE sequences of cyanobacteria, expression of the crtU gene in Chlorobaculum tepidum showed that the enzyme produced carotenoids with χ‐rings rather than φ‐rings. Phylogenetic analysis of the carotene desaturase/methyltransferases revealed that enzymes capable of converting β‐rings to χ‐rings have independently evolved at least two times. These results indicate that it probably will not be possible to deduce the activity of carotene desaturase/methyltransferases solely from sequence data. |
doi_str_mv | 10.1111/j.1472-4669.2011.00297.x |
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A.</creator><creatorcontrib>VOGL, K. ; BRYANT, D. A.</creatorcontrib><description>Purple sulfur bacteria (PSB) mainly occur in anoxic aquatic and benthic environments, where they play important roles in cycling carbon and sulfur. Many PSB characteristically produce the unique keto‐carotenoid, okenone, which is important not only for its light absorption and photoprotection properties but also because of its diagenesis product, okenane, which is a biomarker for ancient sediments derived from anoxic environments. The specific methylation pattern of the χ‐ring of okenane is unlikely to be formed by diagenetic processes and should therefore reflect an enzymatic activity from okenone biosynthesis. This study describes two enzymes that produce the χ‐ring of okenone, the only structural element of okenone preserved in okenane. Genes encoding enzymes of carotenogenesis were identified in the draft genome sequence of an okenone‐producing PSB, Thiodictyon sp. strain CAD16. Two divergently transcribed genes encoded a CrtY‐type lycopene cyclase and a CrtU/CruE‐type γ‐carotene desaturase/methyltransferase. Expression of crtY in Escherichia coli showed that this gene encoded a lycopene cyclase that produced γ‐carotene as the only product. Although the sequence of the γ‐carotene desaturase/methyltransferase was more similar to CrtU sequences of green sulfur bacteria than to CruE sequences of cyanobacteria, expression of the crtU gene in Chlorobaculum tepidum showed that the enzyme produced carotenoids with χ‐rings rather than φ‐rings. Phylogenetic analysis of the carotene desaturase/methyltransferases revealed that enzymes capable of converting β‐rings to χ‐rings have independently evolved at least two times. These results indicate that it probably will not be possible to deduce the activity of carotene desaturase/methyltransferases solely from sequence data.</description><identifier>ISSN: 1472-4677</identifier><identifier>EISSN: 1472-4669</identifier><identifier>DOI: 10.1111/j.1472-4669.2011.00297.x</identifier><identifier>PMID: 22070388</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Biomarkers - metabolism ; Biosynthetic Pathways - genetics ; Carotenoids - biosynthesis ; Chlorobi - genetics ; Chromatiaceae - enzymology ; Chromatiaceae - genetics ; Chromatiaceae - metabolism ; Cloning, Molecular ; Cyanobacteria ; DNA, Bacterial - chemistry ; DNA, Bacterial - genetics ; Escherichia coli ; Escherichia coli - genetics ; Gene Expression ; Intramolecular Lyases - genetics ; Methyltransferases - genetics ; Molecular Sequence Data ; Oxidoreductases - genetics ; Phylogeny ; Sequence Analysis, DNA ; Sequence Homology, Amino Acid</subject><ispartof>Geobiology, 2012-05, Vol.10 (3), p.205-215</ispartof><rights>2011 Blackwell Publishing Ltd</rights><rights>2011 Blackwell Publishing Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4387-81dcfd41afe9f3cfac70412439e33a87bbc1551edd31880e6c828ee9b9d301893</citedby><cites>FETCH-LOGICAL-c4387-81dcfd41afe9f3cfac70412439e33a87bbc1551edd31880e6c828ee9b9d301893</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22070388$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>VOGL, K.</creatorcontrib><creatorcontrib>BRYANT, D. A.</creatorcontrib><title>Biosynthesis of the biomarker okenone: χ-ring formation</title><title>Geobiology</title><addtitle>Geobiology</addtitle><description>Purple sulfur bacteria (PSB) mainly occur in anoxic aquatic and benthic environments, where they play important roles in cycling carbon and sulfur. Many PSB characteristically produce the unique keto‐carotenoid, okenone, which is important not only for its light absorption and photoprotection properties but also because of its diagenesis product, okenane, which is a biomarker for ancient sediments derived from anoxic environments. The specific methylation pattern of the χ‐ring of okenane is unlikely to be formed by diagenetic processes and should therefore reflect an enzymatic activity from okenone biosynthesis. This study describes two enzymes that produce the χ‐ring of okenone, the only structural element of okenone preserved in okenane. Genes encoding enzymes of carotenogenesis were identified in the draft genome sequence of an okenone‐producing PSB, Thiodictyon sp. strain CAD16. Two divergently transcribed genes encoded a CrtY‐type lycopene cyclase and a CrtU/CruE‐type γ‐carotene desaturase/methyltransferase. Expression of crtY in Escherichia coli showed that this gene encoded a lycopene cyclase that produced γ‐carotene as the only product. Although the sequence of the γ‐carotene desaturase/methyltransferase was more similar to CrtU sequences of green sulfur bacteria than to CruE sequences of cyanobacteria, expression of the crtU gene in Chlorobaculum tepidum showed that the enzyme produced carotenoids with χ‐rings rather than φ‐rings. Phylogenetic analysis of the carotene desaturase/methyltransferases revealed that enzymes capable of converting β‐rings to χ‐rings have independently evolved at least two times. These results indicate that it probably will not be possible to deduce the activity of carotene desaturase/methyltransferases solely from sequence data.</description><subject>Biomarkers - metabolism</subject><subject>Biosynthetic Pathways - genetics</subject><subject>Carotenoids - biosynthesis</subject><subject>Chlorobi - genetics</subject><subject>Chromatiaceae - enzymology</subject><subject>Chromatiaceae - genetics</subject><subject>Chromatiaceae - metabolism</subject><subject>Cloning, Molecular</subject><subject>Cyanobacteria</subject><subject>DNA, Bacterial - chemistry</subject><subject>DNA, Bacterial - genetics</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Gene Expression</subject><subject>Intramolecular Lyases - genetics</subject><subject>Methyltransferases - genetics</subject><subject>Molecular Sequence Data</subject><subject>Oxidoreductases - genetics</subject><subject>Phylogeny</subject><subject>Sequence Analysis, DNA</subject><subject>Sequence Homology, Amino Acid</subject><issn>1472-4677</issn><issn>1472-4669</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqNkctOAjEUhhujEUVfwcxONzP2tDO0NW6ECJIQ3GhM2DRzOaPlMsUpRHgCH89XsgiyNHbTP-n3n6ZfCQmARuDX9TiCWLAwbrVUxChARClTIlodkJP9weE-C9Egp86NPRQnHI5JgzEqKJfyhMi2sW5dLd7QGRfYMvApyIydpfUE68BOsLIV3gRfn2FtqtegtPUsXRhbnZGjMp06PN_tTfLcvX_qPISDx16_czcI85hLEUoo8rKIIS1RlTwv01zQGFjMFXKeSpFlOSQJYFFwkJJiK5dMIqpMFZyCVLxJLrdz57V9X6Jb6JlxOU6naYV26bRSnINgSeLJqz9JYAwgThIpPSq3aF5b52os9bw2_slrDVRvDOux3sjTG5F6Y1j_GNYrX73Y3bLMZljsi79KPXC7BT7MFNf_Hqx77b4Pvh5u68YtcLWv--_QLcFFol-GPd0ZsS4bqJEe8m8qDpgw</recordid><startdate>201205</startdate><enddate>201205</enddate><creator>VOGL, K.</creator><creator>BRYANT, D. A.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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>7TN</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>7X8</scope></search><sort><creationdate>201205</creationdate><title>Biosynthesis of the biomarker okenone: χ-ring formation</title><author>VOGL, K. ; BRYANT, D. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4387-81dcfd41afe9f3cfac70412439e33a87bbc1551edd31880e6c828ee9b9d301893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Biomarkers - metabolism</topic><topic>Biosynthetic Pathways - genetics</topic><topic>Carotenoids - biosynthesis</topic><topic>Chlorobi - genetics</topic><topic>Chromatiaceae - enzymology</topic><topic>Chromatiaceae - genetics</topic><topic>Chromatiaceae - metabolism</topic><topic>Cloning, Molecular</topic><topic>Cyanobacteria</topic><topic>DNA, Bacterial - chemistry</topic><topic>DNA, Bacterial - genetics</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Gene Expression</topic><topic>Intramolecular Lyases - genetics</topic><topic>Methyltransferases - genetics</topic><topic>Molecular Sequence Data</topic><topic>Oxidoreductases - genetics</topic><topic>Phylogeny</topic><topic>Sequence Analysis, DNA</topic><topic>Sequence Homology, Amino Acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>VOGL, K.</creatorcontrib><creatorcontrib>BRYANT, D. A.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oceanic Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>MEDLINE - Academic</collection><jtitle>Geobiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>VOGL, K.</au><au>BRYANT, D. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biosynthesis of the biomarker okenone: χ-ring formation</atitle><jtitle>Geobiology</jtitle><addtitle>Geobiology</addtitle><date>2012-05</date><risdate>2012</risdate><volume>10</volume><issue>3</issue><spage>205</spage><epage>215</epage><pages>205-215</pages><issn>1472-4677</issn><eissn>1472-4669</eissn><abstract>Purple sulfur bacteria (PSB) mainly occur in anoxic aquatic and benthic environments, where they play important roles in cycling carbon and sulfur. Many PSB characteristically produce the unique keto‐carotenoid, okenone, which is important not only for its light absorption and photoprotection properties but also because of its diagenesis product, okenane, which is a biomarker for ancient sediments derived from anoxic environments. The specific methylation pattern of the χ‐ring of okenane is unlikely to be formed by diagenetic processes and should therefore reflect an enzymatic activity from okenone biosynthesis. This study describes two enzymes that produce the χ‐ring of okenone, the only structural element of okenone preserved in okenane. Genes encoding enzymes of carotenogenesis were identified in the draft genome sequence of an okenone‐producing PSB, Thiodictyon sp. strain CAD16. Two divergently transcribed genes encoded a CrtY‐type lycopene cyclase and a CrtU/CruE‐type γ‐carotene desaturase/methyltransferase. Expression of crtY in Escherichia coli showed that this gene encoded a lycopene cyclase that produced γ‐carotene as the only product. Although the sequence of the γ‐carotene desaturase/methyltransferase was more similar to CrtU sequences of green sulfur bacteria than to CruE sequences of cyanobacteria, expression of the crtU gene in Chlorobaculum tepidum showed that the enzyme produced carotenoids with χ‐rings rather than φ‐rings. Phylogenetic analysis of the carotene desaturase/methyltransferases revealed that enzymes capable of converting β‐rings to χ‐rings have independently evolved at least two times. These results indicate that it probably will not be possible to deduce the activity of carotene desaturase/methyltransferases solely from sequence data.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>22070388</pmid><doi>10.1111/j.1472-4669.2011.00297.x</doi><tpages>11</tpages></addata></record> |
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subjects | Biomarkers - metabolism Biosynthetic Pathways - genetics Carotenoids - biosynthesis Chlorobi - genetics Chromatiaceae - enzymology Chromatiaceae - genetics Chromatiaceae - metabolism Cloning, Molecular Cyanobacteria DNA, Bacterial - chemistry DNA, Bacterial - genetics Escherichia coli Escherichia coli - genetics Gene Expression Intramolecular Lyases - genetics Methyltransferases - genetics Molecular Sequence Data Oxidoreductases - genetics Phylogeny Sequence Analysis, DNA Sequence Homology, Amino Acid |
title | Biosynthesis of the biomarker okenone: χ-ring formation |
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