Department of Biological Sciences, Indian Institute of Science Education and Research (IISER) Mohali, SAS Nagar, Punjab, India.
Curr Genet. 2021 Aug;67(4):573-582. doi: 10.1007/s00294-021-01178-z. Epub 2021 Mar 19.
Long-chain fatty acids (LCFAs) are a tremendous source of metabolic energy, an essential component of membranes, and important effector molecules that regulate a myriad of cellular processes. As an energy-rich nutrient source, the role of LCFAs in promoting bacterial survival and infectivity is well appreciated. LCFA degradation generates a large number of reduced cofactors that may confer redox stress; therefore, it is imperative to understand how bacteria deal with this paradoxical situation. Although the LCFA utilization pathway has been studied in great detail, especially in Escherichia coli, where the earliest studies date back to the 1960s, the interconnection of LCFA degradation with bacterial stress responses remained largely unexplored. Recent work in E. coli shows that LCFA degradation induces oxidative stress and also impedes oxidative protein folding. Importantly, both issues arise due to the insufficiency of ubiquinone, a lipid-soluble electron carrier in the electron transport chain. However, to maintain redox homeostasis, bacteria induce sophisticated cellular responses. Here, we review these findings in light of our current knowledge of the LCFA metabolic pathway, metabolism-induced oxidative stress, the process of oxidative protein folding, and stress combat mechanisms. We discuss probable mechanisms for the activation of defense players during LCFA metabolism and the likely feedback imparted by them. We suggest that besides defending against intrinsic stresses, LCFA-mediated upregulation of stress response pathways primes bacteria to adapt to harsh external environments. Collectively, the interplay between LCFA metabolism and stress responses is likely an important factor that underlies the success of LCFA-utilizing bacteria in the host.
长链脂肪酸 (LCFAs) 是代谢能量的巨大来源,是膜的必需组成部分,也是调节众多细胞过程的重要效应分子。作为一种富含能量的营养源,LCFAs 促进细菌存活和感染性的作用得到了很好的认识。LCFA 降解会产生大量的还原辅因子,可能会引起氧化还原应激;因此,了解细菌如何应对这种矛盾的情况至关重要。尽管 LCFAs 的利用途径已经得到了深入研究,特别是在大肠杆菌中,最早的研究可以追溯到 20 世纪 60 年代,但 LCFAs 降解与细菌应激反应的相互联系在很大程度上仍未得到探索。最近在大肠杆菌中的研究表明,LCFA 降解会诱导氧化应激,同时也会阻碍氧化蛋白折叠。重要的是,这两个问题都是由于电子传递链中脂溶性电子载体泛醌的不足引起的。然而,为了维持氧化还原平衡,细菌会诱导复杂的细胞反应。在这里,我们根据当前对 LCFAs 代谢途径、代谢诱导的氧化应激、氧化蛋白折叠过程以及应激应对机制的认识,综述了这些发现。我们讨论了在 LCFAs 代谢过程中防御因子激活的可能机制,以及它们可能带来的反馈。我们认为,除了抵御内在应激外,LCFA 介导的应激反应途径的上调使细菌能够适应恶劣的外部环境。总之,LCFA 代谢与应激反应之间的相互作用可能是 LCFAs 利用细菌在宿主中成功的重要因素。