Synthesis in vitro of very long chain fatty acids in Vibrio sp. strain ABE-1 |
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Authors: | Naoki Morita Nobuhiro Okajima Masaru Gotoh Hideyuki Hayashi Hidetoshi Okuyama Shoji Sasaki |
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Affiliation: | (1) Department of Biology, Faculty of Science, Hokkaido University, 060 Sapporo, Japan;(2) Research Laboratory of Honen Corporation, Totsuka-ku, 245 Yokohama, Japan;(3) Department of Environmental Chemistry, Faculty of Pharmaceutical Science, Higashi Nippon Gakuen University, 061-02 Tobetsu, Hokkaido, Japan |
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Abstract: | The activity of fatty acid synthetase (FAS) from Vibrio sp. strain ABE-1 required the presence of acyl carrier protein and was completely inhibited by thiolactomycin, an inhibitor specific for a type II FAS. These observations indicate that this enzyme is a type II FAS. Analysis by gas-liquid chromotography of the reaction products synthesized in vitro from [2-14C]malonyl-CoA by the partially purified FAS revealed, in addition to 16-and 18-carbon fatty acids which are normal constituents of this bacterium, the presence of fatty acids with very long chains. These fatty acids were identified as saturated and mono-unsaturated fatty acids with 20 up to as many as 30 carbon atoms. The longest fatty acids normally found in this bacterium contain 18-carbon atoms. These results suggest that the FAS from Vibrio sp. strain ABE-1 has potentially the ability to synthesize fatty acids with very long chains.Abbreviations ACP acyl carrier protein - FAME fatty acid methyl ester - FAS fatty acid synthetase - FID flame ionization detection - GLC gas-liquid chromatography - TLC thin-layer chromatography - In designations of fatty acids, such as 16:0, 16:1, etc the colon separates the number that denotes the number of carbon atoms and the number that denotes the number of double bonds, respectively, in the molecule - 16:0-CoA CoA ester of 16:0 |
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Keywords: | Fatty acids synthetase Very long chain fatty acids Psychrophilic bacteria Vibrio sp |
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