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Deciphering and engineering the polyunsaturated fatty acid synthase pathway from eukaryotic microorganisms

Polyunsaturated fatty acids (PUFAs) are important nutrients that play important roles in human health. In eukaryotes, PUFAs can be de novo synthesized through two independent biosynthetic pathways: the desaturase/elongase pathway and the PUFA synthase pathway. Among them, PUFAs synthesized through t...

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Autores principales: Guo, Pengfei, Dong, Liang, Wang, Fangzhong, Chen, Lei, Zhang, Weiwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9702510/
https://www.ncbi.nlm.nih.gov/pubmed/36452206
http://dx.doi.org/10.3389/fbioe.2022.1052785
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author Guo, Pengfei
Dong, Liang
Wang, Fangzhong
Chen, Lei
Zhang, Weiwen
author_facet Guo, Pengfei
Dong, Liang
Wang, Fangzhong
Chen, Lei
Zhang, Weiwen
author_sort Guo, Pengfei
collection PubMed
description Polyunsaturated fatty acids (PUFAs) are important nutrients that play important roles in human health. In eukaryotes, PUFAs can be de novo synthesized through two independent biosynthetic pathways: the desaturase/elongase pathway and the PUFA synthase pathway. Among them, PUFAs synthesized through the PUFA synthase pathway typically have few byproducts and require fewer reduction equivalents. In the past 2 decades, numerous studies have been carried out to identify, analyze and engineer PUFA synthases from eukaryotes. These studies showed both similarities and differences between the eukaryotic PUFA synthase pathways and those well studied in prokaryotes. For example, eukaryotic PUFA synthases contain the same domain types as those in prokaryotic PUFA synthases, but the number and arrangement of several domains are different; the basic functions of same-type domains are similar, but the properties and catalytic activities of these domains are somewhat different. To further utilize the PUFA synthase pathway in microbial cell factories and improve the productivity of PUFAs, many challenges still need to be addressed, such as incompletely elucidated PUFA synthesis mechanisms and the difficult genetic manipulation of eukaryotic hosts. In this review, we provide an updated introduction to the eukaryotic PUFA synthase pathway, summarize the functions of domains and propose the possible mechanisms of the PUFA synthesis process, and then provide future research directions to further elucidate and engineer the eukaryotic PUFA synthase pathway for the maximal benefits of humans.
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spelling pubmed-97025102022-11-29 Deciphering and engineering the polyunsaturated fatty acid synthase pathway from eukaryotic microorganisms Guo, Pengfei Dong, Liang Wang, Fangzhong Chen, Lei Zhang, Weiwen Front Bioeng Biotechnol Bioengineering and Biotechnology Polyunsaturated fatty acids (PUFAs) are important nutrients that play important roles in human health. In eukaryotes, PUFAs can be de novo synthesized through two independent biosynthetic pathways: the desaturase/elongase pathway and the PUFA synthase pathway. Among them, PUFAs synthesized through the PUFA synthase pathway typically have few byproducts and require fewer reduction equivalents. In the past 2 decades, numerous studies have been carried out to identify, analyze and engineer PUFA synthases from eukaryotes. These studies showed both similarities and differences between the eukaryotic PUFA synthase pathways and those well studied in prokaryotes. For example, eukaryotic PUFA synthases contain the same domain types as those in prokaryotic PUFA synthases, but the number and arrangement of several domains are different; the basic functions of same-type domains are similar, but the properties and catalytic activities of these domains are somewhat different. To further utilize the PUFA synthase pathway in microbial cell factories and improve the productivity of PUFAs, many challenges still need to be addressed, such as incompletely elucidated PUFA synthesis mechanisms and the difficult genetic manipulation of eukaryotic hosts. In this review, we provide an updated introduction to the eukaryotic PUFA synthase pathway, summarize the functions of domains and propose the possible mechanisms of the PUFA synthesis process, and then provide future research directions to further elucidate and engineer the eukaryotic PUFA synthase pathway for the maximal benefits of humans. Frontiers Media S.A. 2022-11-14 /pmc/articles/PMC9702510/ /pubmed/36452206 http://dx.doi.org/10.3389/fbioe.2022.1052785 Text en Copyright © 2022 Guo, Dong, Wang, Chen and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Guo, Pengfei
Dong, Liang
Wang, Fangzhong
Chen, Lei
Zhang, Weiwen
Deciphering and engineering the polyunsaturated fatty acid synthase pathway from eukaryotic microorganisms
title Deciphering and engineering the polyunsaturated fatty acid synthase pathway from eukaryotic microorganisms
title_full Deciphering and engineering the polyunsaturated fatty acid synthase pathway from eukaryotic microorganisms
title_fullStr Deciphering and engineering the polyunsaturated fatty acid synthase pathway from eukaryotic microorganisms
title_full_unstemmed Deciphering and engineering the polyunsaturated fatty acid synthase pathway from eukaryotic microorganisms
title_short Deciphering and engineering the polyunsaturated fatty acid synthase pathway from eukaryotic microorganisms
title_sort deciphering and engineering the polyunsaturated fatty acid synthase pathway from eukaryotic microorganisms
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9702510/
https://www.ncbi.nlm.nih.gov/pubmed/36452206
http://dx.doi.org/10.3389/fbioe.2022.1052785
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