PsrA is a novel regulator contributes to antibiotic synthesis, bacterial virulence, cell motility and extracellular polysaccharides production in Serratia marcescens
Year: 2021
Type: article
Abstract: Serratia marcescens is a Gram-negative bacterium of the Enterobacteriaceae family that can produce numbers of biologically active secondary metabolites. However, our understanding of the regulatory mechanisms behind secondary metabolites biosynthesis in S. marcescens remains limited. In this study, we identified an uncharacterized LysR family transcriptional regulator, encoding gene BVG90_12635, here we named psrA, that positively controlled prodigiosin synthesis in S. marcescens. This phenotype corresponded to PsrA positive control of transcriptional of the prodigiosin-associated pig operon by directly binding to a regulatory binding site (RBS) and an activating binding site (ABS) in the promoter region of the pig operon. We demonstrated that L-proline is an effector for the PsrA, which enhances the binding affinity of PsrA to its target promoters. Using transcriptomics and further experiments, we show that PsrA indirectly regulates pleiotropic phenotypes, including serrawettin W1 biosynthesis, extracellular polysaccharide production, biofilm formation, swarming motility and T6SS-mediated antibacterial activity in S. marcescens. Collectively, this study proposes that PsrA is a novel regulator that contributes to antibiotic synthesis, bacterial virulence, cell motility and extracellular polysaccharides production in S. marcescens and provides important clues for future studies exploring the function of the PsrA and PsrA-like proteins which are widely present in many other bacteria.
Source: Nucleic Acids Research
DOI: 10.1093/nar/gkab1186
Authors: Xuewei Pan, Mi Tang, Jiajia You, Tolbert Osire, Changhao Sun, Weilai Fu, Ganfeng Yi, Taowei Yang, Shang-Tian Yang, Zhiming Rao
Institutions: Jiangnan University, The Ohio State University
Language: English
Subfield: Biotechnology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $3,800
Funders: National Natural Science Foundation of China, China Postdoctoral Science Foundation, Government of Jiangsu Province, Natural Science Foundation of Jiangsu Province, Jiangsu Planned Projects for Postdoctoral Research Funds, National Key Research and Development Program of China, Project 211, Fundamental Research Funds for the Central Universities
Awards: G1313489940, G1382579305, G1422126724, G1471083644, G1719990679, G2078253599, G2861522142, G317084139, G3210934364, G3647688764, G422170960, G4671492311, G4676424518, G4935962909, LysR家族转录因子LrpG影响温度调控粘质沙雷氏菌合成灵菌红素的分子机理研究, G5056432137, G5176082798, 通过重构胞内氧化还原反应平衡路径选择性强化乙偶姻和2,3-丁二醇合成效率的分子机制, G5811846755, G5932131938, G6063614250, G6091959227, G6243057627, G6367471778, G6652965904, G6738784746, G725769962, G7633810554, G8265704819, G8375954940, G8764037402, G8791523754, G8892636586, G8901236909, G8906533199
OpenAlex ID: W4200291068
