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用于在[具体环境未给出]中特异性生产芽孢杆菌素同工型的支链氨基酸途径的生物信息学建模与代谢工程

Bioinformatics Modelling and Metabolic Engineering of the Branched Chain Amino Acid Pathway for Specific Production of Mycosubtilin Isoforms in .

作者信息

Guez Jean-Sébastien, Coucheney Françoise, Guy Joany, Béchet Max, Fontanille Pierre, Chihib Nour-Eddine, Niehren Joachim, Coutte François, Jacques Philippe

机构信息

Institut Pascal, Clermont Auvergne INP, CNRS, Université Clermont Auvergne, F-63000 Clermont-Ferrand, France.

Équipe Métabolites Secondaires d'Origine Microbienne, Institut Charles Viollette, UMRt BioEcoAgro 1158-INRAE, Université de Lille, F-59000 Lille, France.

出版信息

Metabolites. 2022 Jan 24;12(2):107. doi: 10.3390/metabo12020107.

DOI:10.3390/metabo12020107
PMID:35208182
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8877110/
Abstract

Mycosubtilin belongs to the family of lipopeptides. Different isoforms with various antifungal activities can be obtained according to the length and the isomery of the fatty acid. In this work, the activities of the mycosubtilin isoforms were first studied against the pathogen , revealing the high activity of the -C17 isoform. Modification of the mycosubtilin isoform patterns during cultures of the natural strain ATCC 6633 was then investigated through amino acid feeding experiments. In parallel, single-gene knockouts and single-gene overexpression, leading to the overproduction of the -C15 fatty acid chains, were predicted using informatics tools which provide logical reasoning with formal models of reaction networks. In this way, it was predicted that the single overexpression of the gene as well as the single knockout of the gene may lead to the overproduction of -C15 fatty acid chains. For the first time, it has been demonstrated that overexpression of helps to enhance the furniture of odd fatty acids leading to a favored mycosubtilin -C17 production pattern (+41%). Alternatively, a knock-out mutant led to a higher furniture of even fatty acids, leading to a favored mycosubtilin -C16 production pattern (+180%). These results showed that increased selective synthesis of particular isoforms of mycosubtilin through metabolic engineering is feasible, disclosing the interest of these approaches for future development of lipopeptide-producing strains.

摘要

抗霉枯草菌素属于脂肽家族。根据脂肪酸的长度和异构情况,可以获得具有不同抗真菌活性的不同异构体。在这项工作中,首先研究了抗霉枯草菌素异构体对病原体的活性,结果表明-C17异构体具有高活性。然后通过氨基酸添加实验研究了天然菌株ATCC 6633培养过程中抗霉枯草菌素异构体模式的变化。同时,使用能为反应网络的形式模型提供逻辑推理的信息学工具,预测了导致-C15脂肪酸链过量产生的单基因敲除和单基因过表达情况。通过这种方式,预测出基因的单过表达以及基因的单敲除可能会导致-C15脂肪酸链的过量产生。首次证明,的过表达有助于增强奇数脂肪酸的合成,从而有利于抗霉枯草菌素-C17的产生模式(提高41%)。另外,一个基因敲除突变体导致偶数脂肪酸的合成增加,从而有利于抗霉枯草菌素-C16的产生模式(提高180%)。这些结果表明,通过代谢工程增加抗霉枯草菌素特定异构体的选择性合成是可行的,这揭示了这些方法在未来脂肽生产菌株开发中的价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4578/8877110/dc1ab9c8c159/metabolites-12-00107-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4578/8877110/1d1f43bf600d/metabolites-12-00107-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4578/8877110/bb088181d1e6/metabolites-12-00107-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4578/8877110/7e2a9f693c82/metabolites-12-00107-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4578/8877110/ee4413cafe39/metabolites-12-00107-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4578/8877110/f835cd728389/metabolites-12-00107-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4578/8877110/88e3b4d7b536/metabolites-12-00107-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4578/8877110/8398527c4b3e/metabolites-12-00107-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4578/8877110/dc1ab9c8c159/metabolites-12-00107-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4578/8877110/1d1f43bf600d/metabolites-12-00107-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4578/8877110/bb088181d1e6/metabolites-12-00107-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4578/8877110/7e2a9f693c82/metabolites-12-00107-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4578/8877110/ee4413cafe39/metabolites-12-00107-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4578/8877110/f835cd728389/metabolites-12-00107-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4578/8877110/88e3b4d7b536/metabolites-12-00107-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4578/8877110/8398527c4b3e/metabolites-12-00107-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4578/8877110/dc1ab9c8c159/metabolites-12-00107-g008.jpg

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