Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, 161 Cathedral Street, Glasgow G4 0RE, UK.
Department of Biology, Edge Hill University, St Helens Road, Ormskirk, Lancashire L39 4QP, UK.
Environ Microbiol Rep. 2018 Jun;10(3):231-238. doi: 10.1111/1758-2229.12629. Epub 2018 Apr 6.
The increase in availability of actinobacterial whole genome sequences has revealed huge numbers of specialised metabolite biosynthetic gene clusters, encoding a range of bioactive molecules such as antibiotics, antifungals, immunosuppressives and anticancer agents. Yet the majority of these clusters are not expressed under standard laboratory conditions in rich media. Emerging data from studies of specialised metabolite biosynthesis suggest that the diversity of regulatory mechanisms is greater than previously thought and these act at multiple levels, through a range of signals such as nutrient limitation, intercellular signalling and competition with other organisms. Understanding the regulation and environmental cues that lead to the production of these compounds allows us to identify the role that these compounds play in their natural habitat as well as provide tools to exploit this untapped source of specialised metabolites for therapeutic uses. Here, we provide an overview of novel regulatory mechanisms that act in physiological, global and cluster-specific regulatory manners on biosynthetic pathways in Actinobacteria and consider these alongside their ecological and evolutionary implications.
放线菌全基因组序列可用性的增加揭示了大量专门代谢物生物合成基因簇,这些基因簇编码了一系列生物活性分子,如抗生素、抗真菌药、免疫抑制剂和抗癌剂。然而,在丰富培养基的标准实验室条件下,大多数这些簇都没有表达。专门代谢物生物合成研究的新数据表明,调节机制的多样性比以前认为的要大,这些机制在多个层面上发挥作用,通过一系列信号,如营养限制、细胞间信号和与其他生物的竞争。了解导致这些化合物产生的调控和环境线索,使我们能够确定这些化合物在其自然栖息地中所扮演的角色,并为利用这种未开发的专门代谢物资源提供治疗用途的工具。在这里,我们概述了放线菌中生理、全局和簇特异性调节方式作用于生物合成途径的新型调节机制,并考虑了它们的生态和进化意义。