Kannan T R, Musatovova Oxana, Gowda Pramod, Baseman Joel B
Department of Microbiology and Immunology, The University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Drive, San Antonio, TX 78229-3900, USA.
Infect Immun. 2008 Nov;76(11):5082-92. doi: 10.1128/IAI.00698-08. Epub 2008 Sep 8.
Mycoplasma pneumoniae accounts for 20 to 30% of all community-acquired pneumonia and has been associated with other airway pathologies, including asthma, and a range of extrapulmonary manifestations. Although the entire genomic sequence of M. pneumoniae has been completed, the functions of many of these genes in mycoplasma physiology are unknown. In this study, we focused on clpB, a well-known heat shock gene in other bacteria, to examine its role in mycoplasma growth. Transcriptional and translational analyses of heat shock in M. pneumoniae indicated that clpB is significantly upregulated, reinforcing its status as a critical responder to heat stress. Interestingly, M. pneumoniae ClpB does not use dual translational start points for ClpB synthesis, like other ClpB-characterized bacteria. Biochemical characterization of purified M. pneumoniae recombinant ClpB revealed casein- and lysine-independent ATPase activity and DnaK-DnaJ-GrpE-dependent chaperone activity. An M. pneumoniae mini-Tn4001-integrated, clpB-null mutant was impaired in its ability to replicate under permissive growth conditions, demonstrating the growth-promoting status of ClpB.
肺炎支原体占所有社区获得性肺炎的20%至30%,并与包括哮喘在内的其他气道疾病以及一系列肺外表现有关。尽管肺炎支原体的全基因组序列已经完成,但这些基因在支原体生理学中的许多功能尚不清楚。在本研究中,我们聚焦于clpB(其他细菌中一种著名的热休克基因),以研究其在支原体生长中的作用。对肺炎支原体热休克的转录和翻译分析表明,clpB显著上调,强化了其作为热应激关键应答者的地位。有趣的是,与其他已鉴定ClpB的细菌不同,肺炎支原体ClpB在合成ClpB时不使用双翻译起始点。纯化的肺炎支原体重组ClpB的生化特性显示其具有不依赖酪蛋白和赖氨酸的ATP酶活性以及依赖DnaK-DnaJ-GrpE的伴侣活性。一个整合了肺炎支原体mini-Tn4001的clpB缺失突变体在允许的生长条件下复制能力受损,证明了ClpB对生长的促进作用。