Microbial conversions of alkanes and fatty acids

Abstract Alkanes are attacked readily by a wide variety of microorganisms. The most frequently encountered mode of oxidation is for one of the terminal methyl groups to be oxidized, through the alkanol, then the alkanal, to the corresponding fatty acid. Alkanes may be attacked subterminally also, an...

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Published in:Journal of the American Oil Chemists' Society
Main Author: Ratledge, Colin
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 1984
Subjects:
Online Access:http://dx.doi.org/10.1007/bf02678812
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spelling crwiley:10.1007/bf02678812 2024-06-02T08:14:54+00:00 Microbial conversions of alkanes and fatty acids Ratledge, Colin 1984 http://dx.doi.org/10.1007/bf02678812 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1007%2FBF02678812 https://onlinelibrary.wiley.com/doi/full/10.1007/BF02678812 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Journal of the American Oil Chemists' Society volume 61, issue 2, page 447-453 ISSN 0003-021X 1558-9331 journal-article 1984 crwiley https://doi.org/10.1007/bf02678812 2024-05-03T11:18:02Z Abstract Alkanes are attacked readily by a wide variety of microorganisms. The most frequently encountered mode of oxidation is for one of the terminal methyl groups to be oxidized, through the alkanol, then the alkanal, to the corresponding fatty acid. Alkanes may be attacked subterminally also, and various ketones as well as the corresponding secondary alcohols can be produced. Subsequent degradation of these ketones occurs via introduction of oxygen into the chain to give a corresponding ester, which is then hydrolyzed to give a primary alkanol 2 carbon atoms shorter than the original alkane. The fatty acids arising by either route of oxidation, or by gratuitous introduction to the microbial system, may be oxidized by: (a) β‐oxidation to give a number of acetyl‐CoA units—intermediates of the process cannot be isolated from this pathway due to the tightly coupled nature of the substrates to the enzymes; (b) α‐oxidation; or (c) oxidation at the other end of the molecule. In the latter case, ω‐ and ω—1‐hydroxyfatty acids can be produced. ω‐Hydroxyfatty acids are subsequently oxidized to give dicarboxylic acids, which can be isolated, sometimes in high yield, by use of appropriate microbial mutants lacking in certain of the key metabolizing enzymes. With some yeasts, the fatty acids, including the ω‐hydroxyfatty acids, can be esterified to various sugars to give a series of glycolipids. In some cases, wax esters are formed between fatty acid and alkanol; these wax esters can include diunsaturated molecules having a close chemical similarity to those of sperm whale and jojoba oils. Various recent innovations have occurred using isolated enzyme systems which can be used in transesterification reactions to convert cheap triacylglycerols into high value added commodities such as cocoa butter. Article in Journal/Newspaper Sperm whale Wiley Online Library Journal of the American Oil Chemists' Society 61 2 447 453
institution Open Polar
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language English
description Abstract Alkanes are attacked readily by a wide variety of microorganisms. The most frequently encountered mode of oxidation is for one of the terminal methyl groups to be oxidized, through the alkanol, then the alkanal, to the corresponding fatty acid. Alkanes may be attacked subterminally also, and various ketones as well as the corresponding secondary alcohols can be produced. Subsequent degradation of these ketones occurs via introduction of oxygen into the chain to give a corresponding ester, which is then hydrolyzed to give a primary alkanol 2 carbon atoms shorter than the original alkane. The fatty acids arising by either route of oxidation, or by gratuitous introduction to the microbial system, may be oxidized by: (a) β‐oxidation to give a number of acetyl‐CoA units—intermediates of the process cannot be isolated from this pathway due to the tightly coupled nature of the substrates to the enzymes; (b) α‐oxidation; or (c) oxidation at the other end of the molecule. In the latter case, ω‐ and ω—1‐hydroxyfatty acids can be produced. ω‐Hydroxyfatty acids are subsequently oxidized to give dicarboxylic acids, which can be isolated, sometimes in high yield, by use of appropriate microbial mutants lacking in certain of the key metabolizing enzymes. With some yeasts, the fatty acids, including the ω‐hydroxyfatty acids, can be esterified to various sugars to give a series of glycolipids. In some cases, wax esters are formed between fatty acid and alkanol; these wax esters can include diunsaturated molecules having a close chemical similarity to those of sperm whale and jojoba oils. Various recent innovations have occurred using isolated enzyme systems which can be used in transesterification reactions to convert cheap triacylglycerols into high value added commodities such as cocoa butter.
format Article in Journal/Newspaper
author Ratledge, Colin
spellingShingle Ratledge, Colin
Microbial conversions of alkanes and fatty acids
author_facet Ratledge, Colin
author_sort Ratledge, Colin
title Microbial conversions of alkanes and fatty acids
title_short Microbial conversions of alkanes and fatty acids
title_full Microbial conversions of alkanes and fatty acids
title_fullStr Microbial conversions of alkanes and fatty acids
title_full_unstemmed Microbial conversions of alkanes and fatty acids
title_sort microbial conversions of alkanes and fatty acids
publisher Wiley
publishDate 1984
url http://dx.doi.org/10.1007/bf02678812
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1007%2FBF02678812
https://onlinelibrary.wiley.com/doi/full/10.1007/BF02678812
genre Sperm whale
genre_facet Sperm whale
op_source Journal of the American Oil Chemists' Society
volume 61, issue 2, page 447-453
ISSN 0003-021X 1558-9331
op_rights http://onlinelibrary.wiley.com/termsAndConditions#vor
op_doi https://doi.org/10.1007/bf02678812
container_title Journal of the American Oil Chemists' Society
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container_start_page 447
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