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Bioconversion of C20- and C22-polyunsaturated fatty acids into 9S,15S- and 11S,17S-dihydroxy fatty acids by Escherichia coli expressing double-oxygenating 9S-lipoxygenase from Sphingopyxis macrogoltabida
Double-oxygenating lipoxygenase (LOX) converted C20- and C22-polyunsaturated fatty acids (PUFAs) into C20 dihydroxy fatty acids (DiHFAs) as inflammatory mediators and C22 DiHFAs as specialized pro-resolving mediators, which are involved in the resolution of inflammation and infection in humans, and...
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Published in: | Journal of bioscience and bioengineering 2022-07, Vol.134 (1), p.14-20 |
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description | Double-oxygenating lipoxygenase (LOX) converted C20- and C22-polyunsaturated fatty acids (PUFAs) into C20 dihydroxy fatty acids (DiHFAs) as inflammatory mediators and C22 DiHFAs as specialized pro-resolving mediators, which are involved in the resolution of inflammation and infection in humans, and their isomers, respectively. However, the quantitative bioconversion of C20- and C22-PUFAs into 9S,15S- and 11S,17S-DiHFAs has been not attempted to date, respectively. Here, we performed the efficient quantitative production of 9S,15S- and 11S,17S-DiHFAs by Escherichia coli expressing 9S-LOX from Sphingopyxis macrogoltabida. The optimal bioconversion conditions of the C20 PUFA arachidonic acid or the C22-PUFA docosahexaenoic acid were pH 8.5, 35 °C, 6 mM substrate, and 5 g dry cells/L for C20 PUFAs or 7 g dry cells/L for C22-PUFAs, respectively. Under these conditions, E. coli expressing double-oxygenating 9S-LOX from S. macrogoltabida converted arachidonic acid, eicosapentaenoic acid, docosapentaenoic acidn-3, and docosahexaenoic acid into 5.85 mM 9S,15S-dihydroxyeicosatetraenoic acid, 5.79 mM 9S,15S-dihydroxyeicosapentaenoic acid, 5.89 mM 11S,17S-hydroxydocosapentaenoic acidn-3, and 5.24 mM 11S,17S-dihydroxydocosahexaenoic acid in 40, 30, 50, and 60 min, with conversion yields of 97.5%, 96.5%, 98.1%, and 87.3%; and volumetric productivities of 8.78, 11.6, 7.07, and 5.24 mM/h, respectively. To date, these are the highest concentrations, conversion yields, and volumetric productivities reported in the bioconversion of C20- and C22-PUFAs into DiHFAs. |
doi_str_mv | 10.1016/j.jbiosc.2022.04.001 |
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However, the quantitative bioconversion of C20- and C22-PUFAs into 9S,15S- and 11S,17S-DiHFAs has been not attempted to date, respectively. Here, we performed the efficient quantitative production of 9S,15S- and 11S,17S-DiHFAs by Escherichia coli expressing 9S-LOX from Sphingopyxis macrogoltabida. The optimal bioconversion conditions of the C20 PUFA arachidonic acid or the C22-PUFA docosahexaenoic acid were pH 8.5, 35 °C, 6 mM substrate, and 5 g dry cells/L for C20 PUFAs or 7 g dry cells/L for C22-PUFAs, respectively. Under these conditions, E. coli expressing double-oxygenating 9S-LOX from S. macrogoltabida converted arachidonic acid, eicosapentaenoic acid, docosapentaenoic acidn-3, and docosahexaenoic acid into 5.85 mM 9S,15S-dihydroxyeicosatetraenoic acid, 5.79 mM 9S,15S-dihydroxyeicosapentaenoic acid, 5.89 mM 11S,17S-hydroxydocosapentaenoic acidn-3, and 5.24 mM 11S,17S-dihydroxydocosahexaenoic acid in 40, 30, 50, and 60 min, with conversion yields of 97.5%, 96.5%, 98.1%, and 87.3%; and volumetric productivities of 8.78, 11.6, 7.07, and 5.24 mM/h, respectively. To date, these are the highest concentrations, conversion yields, and volumetric productivities reported in the bioconversion of C20- and C22-PUFAs into DiHFAs.</description><identifier>ISSN: 1389-1723</identifier><identifier>EISSN: 1347-4421</identifier><identifier>DOI: 10.1016/j.jbiosc.2022.04.001</identifier><identifier>PMID: 35466059</identifier><language>eng</language><publisher>Japan: Elsevier B.V</publisher><subject>9S-Lipoxygenase ; C20 9S,15S-dihydroxy fatty acids ; C22 11S,17S-dihydroxy fatty acids ; Double oxygenation ; Sphingopyxis macrogoltabida</subject><ispartof>Journal of bioscience and bioengineering, 2022-07, Vol.134 (1), p.14-20</ispartof><rights>2022 The Society for Biotechnology, Japan</rights><rights>Copyright © 2022 The Society for Biotechnology, Japan. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c292t-22c1e0e31bd88b06fbed4e2223eed6943b837c72b37c366d2fb7cb5c75c5d9d83</citedby><cites>FETCH-LOGICAL-c292t-22c1e0e31bd88b06fbed4e2223eed6943b837c72b37c366d2fb7cb5c75c5d9d83</cites><orcidid>0000-0002-6886-7589 ; 0000-0002-3787-7514</orcidid></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/35466059$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oh, Chae-Won</creatorcontrib><creatorcontrib>Kim, Seong-Eun</creatorcontrib><creatorcontrib>Lee, Jin</creatorcontrib><creatorcontrib>Oh, Deok-Kun</creatorcontrib><title>Bioconversion of C20- and C22-polyunsaturated fatty acids into 9S,15S- and 11S,17S-dihydroxy fatty acids by Escherichia coli expressing double-oxygenating 9S-lipoxygenase from Sphingopyxis macrogoltabida</title><title>Journal of bioscience and bioengineering</title><addtitle>J Biosci Bioeng</addtitle><description>Double-oxygenating lipoxygenase (LOX) converted C20- and C22-polyunsaturated fatty acids (PUFAs) into C20 dihydroxy fatty acids (DiHFAs) as inflammatory mediators and C22 DiHFAs as specialized pro-resolving mediators, which are involved in the resolution of inflammation and infection in humans, and their isomers, respectively. However, the quantitative bioconversion of C20- and C22-PUFAs into 9S,15S- and 11S,17S-DiHFAs has been not attempted to date, respectively. Here, we performed the efficient quantitative production of 9S,15S- and 11S,17S-DiHFAs by Escherichia coli expressing 9S-LOX from Sphingopyxis macrogoltabida. The optimal bioconversion conditions of the C20 PUFA arachidonic acid or the C22-PUFA docosahexaenoic acid were pH 8.5, 35 °C, 6 mM substrate, and 5 g dry cells/L for C20 PUFAs or 7 g dry cells/L for C22-PUFAs, respectively. Under these conditions, E. coli expressing double-oxygenating 9S-LOX from S. macrogoltabida converted arachidonic acid, eicosapentaenoic acid, docosapentaenoic acidn-3, and docosahexaenoic acid into 5.85 mM 9S,15S-dihydroxyeicosatetraenoic acid, 5.79 mM 9S,15S-dihydroxyeicosapentaenoic acid, 5.89 mM 11S,17S-hydroxydocosapentaenoic acidn-3, and 5.24 mM 11S,17S-dihydroxydocosahexaenoic acid in 40, 30, 50, and 60 min, with conversion yields of 97.5%, 96.5%, 98.1%, and 87.3%; and volumetric productivities of 8.78, 11.6, 7.07, and 5.24 mM/h, respectively. To date, these are the highest concentrations, conversion yields, and volumetric productivities reported in the bioconversion of C20- and C22-PUFAs into DiHFAs.</description><subject>9S-Lipoxygenase</subject><subject>C20 9S,15S-dihydroxy fatty acids</subject><subject>C22 11S,17S-dihydroxy fatty acids</subject><subject>Double oxygenation</subject><subject>Sphingopyxis macrogoltabida</subject><issn>1389-1723</issn><issn>1347-4421</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kctu1DAUhiMEoqXwBgh5yQIHX3KZbJDoqBSkSiwCa8uXkxmPkjjYTjV5Rl4KRxkqsWHjy_H3-9j6suwtJTkltPp4yk_KuqBzRhjLSZETQp9l15QXNS4KRp-v612Dac34VfYqhFMCalLTl9kVL4uqImVznf2-tU678RF8sG5ErkN7RjCSo0kLhifXL_MYZJy9jGBQJ2NckNTWBGTH6FDTfqBluwUoTZu6xcYeF-PdefkHVwu6C_oI3uqjlUi73iI4Tx5CsOMBGTerHnBKHWCUcS01Le7tdKkEQJ13A2qnYzpz03K2AQ1Se3dwfZTKGvk6e9HJPsCby3yT_fxy92P_FT98v_-2__yANWtYxIxpCgQ4VWa3U6TqFJgCGGMcwFRNwdWO17pmKo28qgzrVK1VqetSl6YxO36Tvd_unbz7NUOIYrBBQ9_LEdwcBKvKkiYpfEWLDU3vDMFDJyZvB-kXQYlYNYqT2DSKVaMghUiWUuzdpcOsBjBPob_eEvBpAyD989GCF0FbGDUY60FHYZz9f4c_lG-zlQ</recordid><startdate>20220701</startdate><enddate>20220701</enddate><creator>Oh, Chae-Won</creator><creator>Kim, Seong-Eun</creator><creator>Lee, Jin</creator><creator>Oh, Deok-Kun</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6886-7589</orcidid><orcidid>https://orcid.org/0000-0002-3787-7514</orcidid></search><sort><creationdate>20220701</creationdate><title>Bioconversion of C20- and C22-polyunsaturated fatty acids into 9S,15S- and 11S,17S-dihydroxy fatty acids by Escherichia coli expressing double-oxygenating 9S-lipoxygenase from Sphingopyxis macrogoltabida</title><author>Oh, Chae-Won ; Kim, Seong-Eun ; Lee, Jin ; Oh, Deok-Kun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c292t-22c1e0e31bd88b06fbed4e2223eed6943b837c72b37c366d2fb7cb5c75c5d9d83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>9S-Lipoxygenase</topic><topic>C20 9S,15S-dihydroxy fatty acids</topic><topic>C22 11S,17S-dihydroxy fatty acids</topic><topic>Double oxygenation</topic><topic>Sphingopyxis macrogoltabida</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oh, Chae-Won</creatorcontrib><creatorcontrib>Kim, Seong-Eun</creatorcontrib><creatorcontrib>Lee, Jin</creatorcontrib><creatorcontrib>Oh, Deok-Kun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of bioscience and bioengineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oh, Chae-Won</au><au>Kim, Seong-Eun</au><au>Lee, Jin</au><au>Oh, Deok-Kun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bioconversion of C20- and C22-polyunsaturated fatty acids into 9S,15S- and 11S,17S-dihydroxy fatty acids by Escherichia coli expressing double-oxygenating 9S-lipoxygenase from Sphingopyxis macrogoltabida</atitle><jtitle>Journal of bioscience and bioengineering</jtitle><addtitle>J Biosci Bioeng</addtitle><date>2022-07-01</date><risdate>2022</risdate><volume>134</volume><issue>1</issue><spage>14</spage><epage>20</epage><pages>14-20</pages><issn>1389-1723</issn><eissn>1347-4421</eissn><abstract>Double-oxygenating lipoxygenase (LOX) converted C20- and C22-polyunsaturated fatty acids (PUFAs) into C20 dihydroxy fatty acids (DiHFAs) as inflammatory mediators and C22 DiHFAs as specialized pro-resolving mediators, which are involved in the resolution of inflammation and infection in humans, and their isomers, respectively. However, the quantitative bioconversion of C20- and C22-PUFAs into 9S,15S- and 11S,17S-DiHFAs has been not attempted to date, respectively. Here, we performed the efficient quantitative production of 9S,15S- and 11S,17S-DiHFAs by Escherichia coli expressing 9S-LOX from Sphingopyxis macrogoltabida. The optimal bioconversion conditions of the C20 PUFA arachidonic acid or the C22-PUFA docosahexaenoic acid were pH 8.5, 35 °C, 6 mM substrate, and 5 g dry cells/L for C20 PUFAs or 7 g dry cells/L for C22-PUFAs, respectively. Under these conditions, E. coli expressing double-oxygenating 9S-LOX from S. macrogoltabida converted arachidonic acid, eicosapentaenoic acid, docosapentaenoic acidn-3, and docosahexaenoic acid into 5.85 mM 9S,15S-dihydroxyeicosatetraenoic acid, 5.79 mM 9S,15S-dihydroxyeicosapentaenoic acid, 5.89 mM 11S,17S-hydroxydocosapentaenoic acidn-3, and 5.24 mM 11S,17S-dihydroxydocosahexaenoic acid in 40, 30, 50, and 60 min, with conversion yields of 97.5%, 96.5%, 98.1%, and 87.3%; and volumetric productivities of 8.78, 11.6, 7.07, and 5.24 mM/h, respectively. To date, these are the highest concentrations, conversion yields, and volumetric productivities reported in the bioconversion of C20- and C22-PUFAs into DiHFAs.</abstract><cop>Japan</cop><pub>Elsevier B.V</pub><pmid>35466059</pmid><doi>10.1016/j.jbiosc.2022.04.001</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-6886-7589</orcidid><orcidid>https://orcid.org/0000-0002-3787-7514</orcidid></addata></record> |
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subjects | 9S-Lipoxygenase C20 9S,15S-dihydroxy fatty acids C22 11S,17S-dihydroxy fatty acids Double oxygenation Sphingopyxis macrogoltabida |
title | Bioconversion of C20- and C22-polyunsaturated fatty acids into 9S,15S- and 11S,17S-dihydroxy fatty acids by Escherichia coli expressing double-oxygenating 9S-lipoxygenase from Sphingopyxis macrogoltabida |
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