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Identification and characterization of new Δ-17 fatty acid desaturases
ω-3 fatty acid desaturase is a key enzyme for the biosynthesis of ω-3 polyunsaturated fatty acids via the oxidative desaturase/elongase pathways. Here we report the identification of three ω-3 desaturases from oomycetes, Pythium aphanidermatum, Phytophthora sojae, and Phytophthora ramorum. These new...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer-Verlag
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3570762/ https://www.ncbi.nlm.nih.gov/pubmed/22639141 http://dx.doi.org/10.1007/s00253-012-4068-2 |
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author | Xue, Zhixiong He, Hongxian Hollerbach, Dieter Macool, Daniel J. Yadav, Narendra S. Zhang, Hongxiang Szostek, Bogdan Zhu, Quinn |
author_facet | Xue, Zhixiong He, Hongxian Hollerbach, Dieter Macool, Daniel J. Yadav, Narendra S. Zhang, Hongxiang Szostek, Bogdan Zhu, Quinn |
author_sort | Xue, Zhixiong |
collection | PubMed |
description | ω-3 fatty acid desaturase is a key enzyme for the biosynthesis of ω-3 polyunsaturated fatty acids via the oxidative desaturase/elongase pathways. Here we report the identification of three ω-3 desaturases from oomycetes, Pythium aphanidermatum, Phytophthora sojae, and Phytophthora ramorum. These new ω-3 desaturases share 55 % identity at the amino acid level with the known Δ-17 desaturase of Saprolegnia diclina, and about 31 % identity with the bifunctional Δ-12/Δ-15 desaturase of Fusarium monoliforme. The three enzymes were expressed in either wild-type or codon optimized form in an engineered arachidonic acid producing strain of Yarrowia lipolytica to study their activity and substrate specificity. All three were able to convert the ω-6 arachidonic acid to the ω-3 eicosapentanoic acid, with a substrate conversion efficiency of 54–65 %. These enzymes have a broad ω-6 fatty acid substrate spectrum, including both C18 and C20 ω-6 fatty acids although they prefer the C20 substrates, and have strong Δ-17 desaturase activity but weaker Δ-15 desaturase activity. Thus, they belong to the Δ-17 desaturase class. Unlike the previously identified bifunctional Δ-12/Δ-15 desaturase from F. monoliforme, they lack Δ-12 desaturase activity. The newly identified Δ-17 desaturases could use fatty acids in both acyl-CoA and phospholipid fraction as substrates. The identification of these Δ-17 desaturases provides a set of powerful new tools for genetic engineering of microbes and plants to produce ω-3 fatty acids, such as eicosapentanoic acid and docosahexanoic acid, at high levels. |
format | Online Article Text |
id | pubmed-3570762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-35707622013-02-14 Identification and characterization of new Δ-17 fatty acid desaturases Xue, Zhixiong He, Hongxian Hollerbach, Dieter Macool, Daniel J. Yadav, Narendra S. Zhang, Hongxiang Szostek, Bogdan Zhu, Quinn Appl Microbiol Biotechnol Biotechnologically Relevant Enzymes and Proteins ω-3 fatty acid desaturase is a key enzyme for the biosynthesis of ω-3 polyunsaturated fatty acids via the oxidative desaturase/elongase pathways. Here we report the identification of three ω-3 desaturases from oomycetes, Pythium aphanidermatum, Phytophthora sojae, and Phytophthora ramorum. These new ω-3 desaturases share 55 % identity at the amino acid level with the known Δ-17 desaturase of Saprolegnia diclina, and about 31 % identity with the bifunctional Δ-12/Δ-15 desaturase of Fusarium monoliforme. The three enzymes were expressed in either wild-type or codon optimized form in an engineered arachidonic acid producing strain of Yarrowia lipolytica to study their activity and substrate specificity. All three were able to convert the ω-6 arachidonic acid to the ω-3 eicosapentanoic acid, with a substrate conversion efficiency of 54–65 %. These enzymes have a broad ω-6 fatty acid substrate spectrum, including both C18 and C20 ω-6 fatty acids although they prefer the C20 substrates, and have strong Δ-17 desaturase activity but weaker Δ-15 desaturase activity. Thus, they belong to the Δ-17 desaturase class. Unlike the previously identified bifunctional Δ-12/Δ-15 desaturase from F. monoliforme, they lack Δ-12 desaturase activity. The newly identified Δ-17 desaturases could use fatty acids in both acyl-CoA and phospholipid fraction as substrates. The identification of these Δ-17 desaturases provides a set of powerful new tools for genetic engineering of microbes and plants to produce ω-3 fatty acids, such as eicosapentanoic acid and docosahexanoic acid, at high levels. Springer-Verlag 2012-05-27 2013 /pmc/articles/PMC3570762/ /pubmed/22639141 http://dx.doi.org/10.1007/s00253-012-4068-2 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Biotechnologically Relevant Enzymes and Proteins Xue, Zhixiong He, Hongxian Hollerbach, Dieter Macool, Daniel J. Yadav, Narendra S. Zhang, Hongxiang Szostek, Bogdan Zhu, Quinn Identification and characterization of new Δ-17 fatty acid desaturases |
title | Identification and characterization of new Δ-17 fatty acid desaturases |
title_full | Identification and characterization of new Δ-17 fatty acid desaturases |
title_fullStr | Identification and characterization of new Δ-17 fatty acid desaturases |
title_full_unstemmed | Identification and characterization of new Δ-17 fatty acid desaturases |
title_short | Identification and characterization of new Δ-17 fatty acid desaturases |
title_sort | identification and characterization of new δ-17 fatty acid desaturases |
topic | Biotechnologically Relevant Enzymes and Proteins |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3570762/ https://www.ncbi.nlm.nih.gov/pubmed/22639141 http://dx.doi.org/10.1007/s00253-012-4068-2 |
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