Genetic engineering of the branched fatty acid metabolic pathway of Bacillus subtilis for the overproduction of surfactin C 14 isoform

• Published in: Biotechnology journal 2017-07, Vol.12 (7)
• Main Authors: Dhali, Debarun, Coutte, François, Arias, Anthony Argüelles, Auger, Sandrine, Bidnenko, Vladimir, Chataigné, Gabrielle, Lalk, Michael, Niehren, Joachim, de Sousa, Joana, Versari, Cristian, Jacques, Philippe
• Format: Article
• Language: English
• Subjects: Bacillus subtilis - genetics; Bacillus subtilis - growth & development; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Chromatography, Liquid; Fatty Acids - biosynthesis; Gas Chromatography-Mass Spectrometry; Gene Deletion; Genetic Engineering; Lipopeptides - genetics; Lipopeptides - metabolism; Metabolic Networks and Pathways; Operon; Protein Isoforms - metabolism; Tandem Mass Spectrometry
• ISSN: 1860-6768; 1860-7314
• DOI: 10.1002/biot.201600574

Surfactin, a lipopeptide produced by Bacillus subtilis, is one of the most powerful biosurfactants known. This molecule consists of a cyclic heptapeptide linked to a β-hydroxy fatty acid chain. The isomery and the length of the fatty acid (FA) chain are responsible for the surfactin's activities. In this study, the gene codY, which encode for the global transcriptional regulator and the gene lpdV, located in the bkd operon (lpdV, bkdAA, bkdAB and bkdB genes), which is responsible for the last step of the branched chain amino acid (BCAA) degradation in acyl-CoA were deleted. The influence of these deletions on the quantitative and qualitative surfactin production was analysed. The surfactin production was quantified by RP-HPLC and the surfactin isoforms were characterized using LC-MS-MS and GC-MS analysis. The results obtained in the mutants showed an enhancement of surfactin specific production by a factor of 5.8 for the codY mutant and 1.4 for lpdV mutant. Moreover qualitative analysis of the lpdV mutant reveals that it mainly produced surfactin C isoform (2 fold more than the wild type) with linear FA chain. Complete analysis of the extracellular metabolites using H quantitative NMR reveals a reduced production of acetoin in this mutant. This work demonstrates for the first time an original approach to overproduce specifically surfactin with C FA chain.