Suzuki-Minakuchi Chiho, Hirotani Ryusuke, Shintani Masaki, Takeda Toshiharu, Takahashi Yurika, Matsui Kazuhiro, Vasileva Delyana, Yun Choong-Soo, Okada Kazunori, Yamane Hisakazu, Nojiri Hideaki
Biotechnology Research Center, The University of Tokyo, Tokyo, Japan.
Biotechnology Research Center, The University of Tokyo, Tokyo, Japan Japan Collection of Microorganisms, RIKEN BioResource Center, Ibaraki, Japan Department of Applied Chemistry and Biochemical Engineering, Graduate School of Engineering, Shizuoka University, Hamamatsu, Japan.
Appl Environ Microbiol. 2015 Apr;81(8):2869-80. doi: 10.1128/AEM.00023-15. Epub 2015 Feb 13.
Nucleoid-associated proteins (NAPs), which fold bacterial DNA and influence gene transcription, are considered to be global transcriptional regulators of genes on both plasmids and the host chromosome. Incompatibility P-7 group plasmid pCAR1 carries genes encoding three NAPs: H-NS family protein Pmr, NdpA-like protein Pnd, and HU-like protein Phu. In this study, the effects of single or double disruption of pmr, pnd, and phu were assessed in host Pseudomonas putida KT2440. When pmr and pnd or pmr and phu were simultaneously disrupted, both the segregational stability and the structural stability of pCAR1 were markedly decreased, suggesting that Pmr, Pnd, and Phu act as plasmid-stabilizing factors in addition to their established roles in replication and partition systems. The transfer frequency of pCAR1 was significantly decreased in these double mutants. The segregational and structural instability of pCAR1 in the double mutants was recovered by complementation of pmr, whereas no recovery of transfer deficiency was observed. Comprehensive phenotype comparisons showed that the host metabolism of carbon compounds, which was reduced by pCAR1 carriage, was restored by disruption of the NAP gene(s). Transcriptome analyses of mutants indicated that transcription of genes for energy production, conversion, inorganic ion transport, and metabolism were commonly affected; however, how their products altered the phenotypes of mutants was not clear. The findings of this study indicated that Pmr, Pnd, and Phu act synergistically to affect pCAR1 replication, maintenance, and transfer, as well as to alter the host metabolic phenotype.
类核相关蛋白(NAPs)可折叠细菌DNA并影响基因转录,被认为是质粒和宿主染色体上基因的全局转录调节因子。不相容性P-7群质粒pCAR1携带编码三种NAPs的基因:H-NS家族蛋白Pmr、NdpA样蛋白Pnd和HU样蛋白Phu。在本研究中,评估了pmr、pnd和phu单基因或双基因缺失对宿主恶臭假单胞菌KT2440的影响。当pmr和pnd或pmr和phu同时缺失时,pCAR1的分离稳定性和结构稳定性均显著降低,这表明Pmr、Pnd和Phu除了在复制和分配系统中已确定的作用外,还作为质粒稳定因子发挥作用。在这些双突变体中,pCAR1的转移频率显著降低。通过pmr的互补可恢复双突变体中pCAR1的分离和结构不稳定性,而未观察到转移缺陷的恢复。综合表型比较表明,pCAR1携带导致降低的宿主碳化合物代谢通过NAP基因的缺失得以恢复。突变体的转录组分析表明,能量产生、转化、无机离子运输和代谢相关基因的转录普遍受到影响;然而,其产物如何改变突变体的表型尚不清楚。本研究结果表明,Pmr、Pnd和Phu协同作用,影响pCAR1的复制、维持和转移,以及改变宿主代谢表型。