Cruz-Bautista Rodrigo, Zelarayan-Agüero Augusto, Ruiz-Villafán Beatriz, Escalante-Lozada Adelfo, Rodríguez-Sanoja Romina, Sánchez Sergio
Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad Universitaria, 04510, Mexico City, Mexico.
Departamento de Ingeniería Celular y Biocatálisis, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Ave. Universidad 2001, 62210, Cuernavaca, Mexico.
Appl Microbiol Biotechnol. 2024 Apr 24;108(1):306. doi: 10.1007/s00253-024-13136-z.
The Streptomyces genus comprises Gram-positive bacteria known to produce over two-thirds of the antibiotics used in medical practice. The biosynthesis of these secondary metabolites is highly regulated and influenced by a range of nutrients present in the growth medium. In Streptomyces coelicolor, glucose inhibits the production of actinorhodin (ACT) and undecylprodigiosin (RED) by a process known as carbon catabolite repression (CCR). However, the mechanism mediated by this carbon source still needs to be understood. It has been observed that glucose alters the transcriptomic profile of this actinobacteria, modifying different transcriptional regulators, including some of the one- and two-component systems (TCSs). Under glucose repression, the expression of one of these TCSs SCO6162/SCO6163 was negatively affected. We aimed to study the role of this TCS on secondary metabolite formation to define its influence in this general regulatory process and likely establish its relationship with other transcriptional regulators affecting antibiotic biosynthesis in the Streptomyces genus. In this work, in silico predictions suggested that this TCS can regulate the production of the secondary metabolites ACT and RED by transcriptional regulation and protein-protein interactions of the transcriptional factors (TFs) with other TCSs. These predictions were supported by experimental procedures such as deletion and complementation of the TFs and qPCR experiments. Our results suggest that in the presence of glucose, the TCS SCO6162/SCO6163, named GarR/GarS, is an important negative regulator of the ACT and RED production in S. coelicolor. KEY POINTS: • GarR/GarS is a TCS with domains for signal transduction and response regulation • GarR/GarS is an essential negative regulator of the ACT and RED production • GarR/GarS putatively interacts with and regulates activators of ACT and RED.
链霉菌属包含革兰氏阳性菌,已知其能产生超过三分之二用于医学实践的抗生素。这些次生代谢产物的生物合成受到高度调控,并受到生长培养基中一系列营养物质的影响。在天蓝色链霉菌中,葡萄糖通过一种称为碳分解代谢物阻遏(CCR)的过程抑制放线紫红素(ACT)和十一烷基灵菌红素(RED)的产生。然而,这种碳源介导的机制仍有待了解。据观察,葡萄糖会改变这种放线菌的转录组图谱,改变不同的转录调节因子,包括一些单组分和双组分系统(TCSs)。在葡萄糖阻遏下,这些TCSs之一SCO6162/SCO6163的表达受到负面影响。我们旨在研究这个TCS在次生代谢产物形成中的作用,以确定其在这个一般调控过程中的影响,并可能建立其与影响链霉菌属抗生素生物合成的其他转录调节因子的关系。在这项工作中,计算机模拟预测表明,这个TCS可以通过转录调节以及转录因子(TFs)与其他TCSs的蛋白质-蛋白质相互作用来调节次生代谢产物ACT和RED的产生。这些预测得到了诸如TFs的缺失和互补以及qPCR实验等实验程序的支持。我们的结果表明,在葡萄糖存在的情况下,名为GarR/GarS的TCS SCO6162/SCO6163是天蓝色链霉菌中ACT和RED产生的重要负调节因子。要点:• GarR/GarS是一个具有信号转导和反应调节结构域的TCS • GarR/GarS是ACT和RED产生的必需负调节因子 • GarR/GarS可能与ACT和RED的激活剂相互作用并对其进行调节