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Quantitative effects of unsaturated fatty acids in microbial mutants : VII. Influence of the acetylenic bond location on the effectiveness of acyl chains

dc.contributor.authorLands, William E. M.en_US
dc.contributor.authorOhlrogge, John B.en_US
dc.contributor.authorRobinson, John R.en_US
dc.contributor.authorSacks, Roger W.en_US
dc.contributor.authorBarve, John A.en_US
dc.contributor.authorGunstone, Frank D.en_US
dc.date.accessioned2006-04-07T17:12:19Z
dc.date.available2006-04-07T17:12:19Z
dc.date.issued1977-03-25en_US
dc.identifier.citationLands, William E. M., Ohlrogge, John B., Robinson, John R., Sacks, Roger W., Barve, John A., Gunstone, Frank D. (1977/03/25)."Quantitative effects of unsaturated fatty acids in microbial mutants : VII. Influence of the acetylenic bond location on the effectiveness of acyl chains." Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism 486(3): 451-461. <http://hdl.handle.net/2027.42/22954>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T1X-47F715C-9D/2/9eb43a2909e2cc05ae2511f4d48bee72en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/22954
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=322722&dopt=citationen_US
dc.description.abstractThe ability of a series of 18 carbon acetylenic fatty acids to fulfill the unsaturated fatty acid requirements of Escherichia coli and Saccharomyces cerevisiae was investigated. Despite their high melting points (&gt;40[deg]C), several isomers of the acetylenic fatty acids were as efficient or more efficient in supporting growth than the analogous fatty acid having a cis-double bond.The efficiencies of the different positional isomers in supporting cell proliferation varied from essentially 0 cells per fmol for the 2-5 and 13-17 isomers to high values when the acetylenic bond was near the center of the chain: e.g. 45 E. coli and 5.5 S. cerevisiae cells/fmol for the 10 isomer. A striking ineffectiveness of the 9 isomer was observed with E. coli. The 7, 8 and 10 isomers were at least 10-fold more efficient than any of the other positional isomers in supporting the growth of E. coli. In contrast, the 9 isomer was among the most effective acetylenic fatty acids tested with the yeast mutant.Chromatographic analysis of the extracted lipids indicated that each of the acetylenic isomers tested (except [Delta]2 and [Delta]3) could be esterified by the prokaryotic and eukaryotic microorganisms. The content of unsaturated plus cyclopropane acids observed when growth ceased in E. coli cultures supplemented with growth-limiting concentrations of the acetylenic fatty acids ranged from approx. 15 mol% for the 8 isomer to approx. 35 mol% for the 14 and 17 isomers. The 8-11 isomers were observed to be esterified predominantly at the two position in phosphatidylethanolamine of E. coli and in phosphatidylcholine of S. cerevisiae.en_US
dc.format.extent957389 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleQuantitative effects of unsaturated fatty acids in microbial mutants : VII. Influence of the acetylenic bond location on the effectiveness of acyl chainsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumThe Department of Biological Chemistry, The University of Michigan, Ann Arbor, Mich. 48109, U.S.A.en_US
dc.contributor.affiliationumThe Department of Biological Chemistry, The University of Michigan, Ann Arbor, Mich. 48109, U.S.A.en_US
dc.contributor.affiliationumThe Department of Biological Chemistry, The University of Michigan, Ann Arbor, Mich. 48109, U.S.A.en_US
dc.contributor.affiliationumThe Department of Biological Chemistry, The University of Michigan, Ann Arbor, Mich. 48109, U.S.A.en_US
dc.contributor.affiliationotherDepartment of Chemistry, St. Andrews University, St. Andrews, U.K.en_US
dc.contributor.affiliationotherDepartment of Chemistry, St. Andrews University, St. Andrews, U.K.en_US
dc.identifier.pmid322722en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/22954/1/0000521.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0005-2760(77)90095-9en_US
dc.identifier.sourceBiochimica et Biophysica Actaen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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