Structural analysis of conjugated linoleic acid produced by Lactobacillus plantarum, and factors affecting isomer production
An isomer of the conjugated linoleic acid (CLA) produced from linoleic acid by Lactobacillus plantarum was identified as cis-9,trans-11-octadecadienoic acid by proton nuclear magnetic resonance spectroscopy. Together with earlier results, we concluded that the bacterium produces two CLA isomers, cis...
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| Veröffentlicht in: | Bioscience, biotechnology, and biochemistry biotechnology, and biochemistry, 2003-01, Vol.67 (1), p.179-182 |
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| container_title | Bioscience, biotechnology, and biochemistry |
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| creator | Kishino, S. (Kyoto Univ. (Japan)) Ogawa, J Ando, A Iwashita, T Fujita, T Kawashima, H Shimizu, S |
| description | An isomer of the conjugated linoleic acid (CLA) produced from linoleic acid by Lactobacillus plantarum was identified as cis-9,trans-11-octadecadienoic acid by proton nuclear magnetic resonance spectroscopy. Together with earlier results, we concluded that the bacterium produces two CLA isomers, cis-9,trans-11- and trans-9,trans-11-octadecadienoic acid from linoleic acid. The addition of L-serine, glucose, AgNO
3
, or NaCl to the reaction mixture reduced production of the latter. |
| doi_str_mv | 10.1271/bbb.67.179 |
| format | Article |
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3
, or NaCl to the reaction mixture reduced production of the latter.</description><identifier>ISSN: 0916-8451</identifier><identifier>EISSN: 1347-6947</identifier><identifier>DOI: 10.1271/bbb.67.179</identifier><identifier>PMID: 12619692</identifier><language>eng</language><publisher>Tokyo: Japan Society for Bioscience, Biotechnology, and Agrochemistry</publisher><subject>Biological and medical sciences ; CHEMICAL STRUCTURE ; conjugated linoleic acid ; Culture Media ; Enzyme Inhibitors - pharmacology ; Fatty Acids - chemistry ; Fundamental and applied biological sciences. Psychology ; Glucose - pharmacology ; Isomerism ; ISOMERIZATION ; lactic acid bacteria ; Lactobacillus - chemistry ; Lactobacillus - drug effects ; Lactobacillus - metabolism ; LACTOBACILLUS PLANTARUM ; LINOLEIC ACID ; Linoleic Acid - biosynthesis ; Linoleic Acid - chemistry ; Magnetic Resonance Spectroscopy ; Mass Spectrometry ; Serine - pharmacology ; Silver Nitrate - pharmacology ; Sodium Chloride - pharmacology</subject><ispartof>Bioscience, biotechnology, and biochemistry, 2003-01, Vol.67 (1), p.179-182</ispartof><rights>2003 by Japan Society for Bioscience, Biotechnology, and Agrochemistry 2003</rights><rights>2003 INIST-CNRS</rights><rights>Copyright Japan Science and Technology Agency 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c566t-159ebd923758622c1caf534f6eb065729746b7b699e0afa8832ed2a3ff18e4753</citedby><cites>FETCH-LOGICAL-c566t-159ebd923758622c1caf534f6eb065729746b7b699e0afa8832ed2a3ff18e4753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14882380$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12619692$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kishino, S. (Kyoto Univ. (Japan))</creatorcontrib><creatorcontrib>Ogawa, J</creatorcontrib><creatorcontrib>Ando, A</creatorcontrib><creatorcontrib>Iwashita, T</creatorcontrib><creatorcontrib>Fujita, T</creatorcontrib><creatorcontrib>Kawashima, H</creatorcontrib><creatorcontrib>Shimizu, S</creatorcontrib><title>Structural analysis of conjugated linoleic acid produced by Lactobacillus plantarum, and factors affecting isomer production</title><title>Bioscience, biotechnology, and biochemistry</title><addtitle>Biosci Biotechnol Biochem</addtitle><description>An isomer of the conjugated linoleic acid (CLA) produced from linoleic acid by Lactobacillus plantarum was identified as cis-9,trans-11-octadecadienoic acid by proton nuclear magnetic resonance spectroscopy. Together with earlier results, we concluded that the bacterium produces two CLA isomers, cis-9,trans-11- and trans-9,trans-11-octadecadienoic acid from linoleic acid. The addition of L-serine, glucose, AgNO
3
, or NaCl to the reaction mixture reduced production of the latter.</description><subject>Biological and medical sciences</subject><subject>CHEMICAL STRUCTURE</subject><subject>conjugated linoleic acid</subject><subject>Culture Media</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Fatty Acids - chemistry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glucose - pharmacology</subject><subject>Isomerism</subject><subject>ISOMERIZATION</subject><subject>lactic acid bacteria</subject><subject>Lactobacillus - chemistry</subject><subject>Lactobacillus - drug effects</subject><subject>Lactobacillus - metabolism</subject><subject>LACTOBACILLUS PLANTARUM</subject><subject>LINOLEIC ACID</subject><subject>Linoleic Acid - biosynthesis</subject><subject>Linoleic Acid - chemistry</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Mass Spectrometry</subject><subject>Serine - pharmacology</subject><subject>Silver Nitrate - pharmacology</subject><subject>Sodium Chloride - pharmacology</subject><issn>0916-8451</issn><issn>1347-6947</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUurFDEQhRtRvOPVjXslILoQe8z7sZSLTwYU1HVTnU6GDOnOmHQjA_54M0zLBRGEQODkq1OVOk3zmOAtoYq87vt-K9WWKHOn2RDGVSsNV3ebDTZEtpoLctU8KOWAcRUEud9cESqJkYZuml9f57zYeckQEUwQTyUUlDyyaTose5jdgGKYUnTBIrBhQMechsVWuT-hHdg59VWOcSnoGGGaIS_jq-o0IH9-zAWB987OYdqjUNLo8uowhzQ9bO55iMU9Wu_r5vu7t99uPrS7z-8_3rzZtVZIObdEGNcPhjIltKTUEgteMO6l67EUihrFZa96aYzD4EFrRt1AgXlPtONKsOvmxcW3tv6xuDJ3YyjWxTqwS0vpFMOaMEz_CxKtMdXiDD77CzykJdf9VYZzwwXHmFXq5YWyOZWSne-OOYyQTx3B3Tm6rkbXSdXV6Cr8dLVc-tENt-iaVQWerwAUC9FnmGwotxzXmjKNKycuXJh8yiP8TDkO3QynmPKfIvbPAZ5c6jykDva5Yp--0PqPekRdzm8S471j</recordid><startdate>200301</startdate><enddate>200301</enddate><creator>Kishino, S. 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Together with earlier results, we concluded that the bacterium produces two CLA isomers, cis-9,trans-11- and trans-9,trans-11-octadecadienoic acid from linoleic acid. The addition of L-serine, glucose, AgNO
3
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| source | J-STAGE Free; Oxford University Press Journals All Titles (1996-Current); MEDLINE; Freely Accessible Japanese Titles; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Free Full-Text Journals in Chemistry |
| subjects | Biological and medical sciences CHEMICAL STRUCTURE conjugated linoleic acid Culture Media Enzyme Inhibitors - pharmacology Fatty Acids - chemistry Fundamental and applied biological sciences. Psychology Glucose - pharmacology Isomerism ISOMERIZATION lactic acid bacteria Lactobacillus - chemistry Lactobacillus - drug effects Lactobacillus - metabolism LACTOBACILLUS PLANTARUM LINOLEIC ACID Linoleic Acid - biosynthesis Linoleic Acid - chemistry Magnetic Resonance Spectroscopy Mass Spectrometry Serine - pharmacology Silver Nitrate - pharmacology Sodium Chloride - pharmacology |
| title | Structural analysis of conjugated linoleic acid produced by Lactobacillus plantarum, and factors affecting isomer production |
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