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

Metabolites

Équipe Métabolites Spécialisés d'Origine Microbienne, UMRt BioEcoAgro 1158-INRAE, TERRA Teaching and Research Centre, MiPI, Gembloux Agro-Bio Tech, Université de Liège, B-5030 Gembloux, Belgium.

Published: January 2022

AI Article Synopsis

  • * The study explored how amino acid feeding impacts the mycosubtilin isoforms produced by the natural strain ATCC 6633 and used informatics tools to predict changes in fatty acid production through gene modification.
  • * Results indicated that overexpressing certain genes can increase -C17 production by 41%, while knocking out others boosts -C16 production by 180%, highlighting the potential of metabolic engineering to optimize lipopeptide production.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8877110PMC
http://dx.doi.org/10.3390/metabo12020107DOI Listing

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