Alpha-oxidation of long-chain unsaturated fatty acids in the marine green alga Ulva pertusa

When long-chain unsaturated fatty acids such as oleic, linoleic, and linolenic acid were incubated with crude enzymes from the marine green alga Ulva pertusa, the corresponding (R)-2-hydroperoxy acids were formed with a high enantiomeric excess (>99%).

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Veröffentlicht in:Bioscience, biotechnology, and biochemistry biotechnology, and biochemistry, 2000-12, Vol.64 (12), p.2680-2681
Hauptverfasser: Akakabe, Y. (Yamaguchi Univ. (Japan). Faculty of Agriculture), Matsui, K, Kajiwara, T
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container_title Bioscience, biotechnology, and biochemistry
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creator Akakabe, Y. (Yamaguchi Univ. (Japan). Faculty of Agriculture)
Matsui, K
Kajiwara, T
description When long-chain unsaturated fatty acids such as oleic, linoleic, and linolenic acid were incubated with crude enzymes from the marine green alga Ulva pertusa, the corresponding (R)-2-hydroperoxy acids were formed with a high enantiomeric excess (>99%).
doi_str_mv 10.1271/bbb.64.2680
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source J-STAGE Free; MEDLINE; Oxford University Press Journals All Titles (1996-Current); Open Access Titles of Japan; EZB-FREE-00999 freely available EZB journals; Free Full-Text Journals in Chemistry
subjects 2-hydroperoxy acid
Bioconversions. Hemisynthesis
Biological and medical sciences
Biotechnology
CHLOROPHYCEAE
Chlorophyta - metabolism
Chromatography, High Pressure Liquid
Enzymes - isolation & purification
Enzymes - metabolism
Fatty Acids, Unsaturated - chemistry
Fatty Acids, Unsaturated - metabolism
Fundamental and applied biological sciences. Psychology
green alga
linoleic acid
linolenic acid
long-chain fatty acid
Marine
Methods. Procedures. Technologies
Molecular Structure
oleic acid
OXIDATION
Oxidation-Reduction
Stereoisomerism
Ulva pertusa
UNSATURATED FATTY ACIDS
α-oxidation
title Alpha-oxidation of long-chain unsaturated fatty acids in the marine green alga Ulva pertusa
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