Surger Maximilian J, Angelov Angel, Stier Philipp, Übelacker Maria, Liebl Wolfgang
Department of Microbiology, Technical University of Munich, Munich, Germany.
Front Microbiol. 2018 Mar 12;9:374. doi: 10.3389/fmicb.2018.00374. eCollection 2018.
naturally produces alkenes, unsaturated aliphatic hydrocarbons, and represents a promising host to produce hydrocarbons as constituents of biofuels and lubricants. In this work, we identify the genes for key enzymes of the branched-chain amino acid catabolism in , whose first metabolic steps lead also to the formation of primer molecules for branched-chain fatty acid and olefin biosynthesis, and demonstrate how these genes can be used to manipulate the production of specific olefins in this organism. We constructed mutants of several gene candidates involved in the branched-chain amino acid metabolism or its regulation and investigated the resulting changes in the cellular fatty acid and olefin profiles by GC/MS. The gene cluster encoding the components of the branched-chain α-keto acid dehydrogenase (BCKD) complex was identified by deletion and promoter exchange mutagenesis. Overexpression of the BCKD gene cluster resulted in about threefold increased olefin production whereas deletion of the cluster led to a drastic reduction in branched-chain fatty acid content and a complete loss of olefin production. The specificities of the acyl-CoA dehydrogenases of the branched amino acid degradation pathways were deduced from the fatty acid and olefin profiles of the respective deletion mutant strains. In addition, growth experiments with branched amino acids as the only nitrogen source were carried out with the mutants in order to confirm our annotations. Both the deletion mutant of the BCKD complex, responsible for the further degradation of all three branched-chain amino acids, as well as the deletion mutant of the proposed isovaleryl-CoA dehydrogenase (specific for leucine degradation) were not able to grow on leucine in contrast to the parental strain. In conclusion, our experiments allow the unambigous assignment of specific functions to the genes for key enzymes of the branched-chain amino acid metabolism of . We also show how this knowledge can be used to engineer the isomeric composition and the chain lengths of the olefins produced by this organism.
天然产生烯烃、不饱和脂肪烃,是一种有潜力的宿主,可用于生产作为生物燃料和润滑剂成分的碳氢化合物。在这项工作中,我们鉴定了[具体生物名称未给出]中支链氨基酸分解代谢关键酶的基因,其最初的代谢步骤也导致了支链脂肪酸和烯烃生物合成引物分子的形成,并展示了如何利用这些基因来操纵该生物体中特定烯烃的生产。我们构建了参与支链氨基酸代谢或其调控的几个候选基因的突变体,并通过气相色谱/质谱法研究了细胞脂肪酸和烯烃谱的变化。通过缺失和启动子交换诱变鉴定了编码支链α-酮酸脱氢酶(BCKD)复合物组分的基因簇。BCKD基因簇的过表达导致烯烃产量增加约三倍,而该基因簇的缺失导致支链脂肪酸含量急剧降低且烯烃生产完全丧失。从各个缺失突变体菌株的脂肪酸和烯烃谱推断出支链氨基酸降解途径中酰基辅酶A脱氢酶的特异性。此外,用突变体进行了以支链氨基酸作为唯一氮源的生长实验,以证实我们的注释。与亲本菌株相比,负责所有三种支链氨基酸进一步降解的BCKD复合物缺失突变体以及拟议的异戊酰辅酶A脱氢酶(特异性用于亮氨酸降解)缺失突变体均不能在亮氨酸上生长。总之,我们的实验明确了[具体生物名称未给出]支链氨基酸代谢关键酶基因的特定功能。我们还展示了如何利用这些知识来设计该生物体产生的烯烃的异构体组成和链长。