Suppr超能文献

负责响应厌氧状态协同调节光捕获和反应中心基因表达的一种传感激酶的鉴定及分子遗传学特征分析

Identification and molecular genetic characterization of a sensor kinase responsible for coordinately regulating light harvesting and reaction center gene expression in response to anaerobiosis.

作者信息

Mosley C S, Suzuki J Y, Bauer C E

机构信息

Department of Biology, Indiana University, Bloomington 47405.

出版信息

J Bacteriol. 1994 Dec;176(24):7566-73. doi: 10.1128/jb.176.24.7566-7573.1994.

Abstract

Our laboratory recently demonstrated that anaerobic induction of light harvesting and reaction center structural gene expression involved a trans-acting factor, RegA, which exhibits sequence similarity to the class of prokaryotic sensory transduction proteins known as response regulators (M. W. Sganga and C. E. Bauer, Cell 68:945-954, 1992). In this study, we performed a screen for additional genes involved in inducing anaerobic expression of light harvesting and reaction center structural genes. This search resulted in the isolation of four strains that were shown by complementation and marker rescue analysis to harbor mutations allelic to the originally described regA mutation and one strain with a mutation found to be linked but nonallelic to regA. Sequence analysis indicated that this additional gene, regB, codes for a polypeptide that exhibits sequence similarity to the prokaryotic family of histidine sensor kinases. Analysis of photosynthesis gene expression in regB mutants indicates that the disruption of regB results in a phenotype that is very similar to that described for regA mutants, namely, a failure to trans activate anaerobic expression of the puf, puh, and puc operons. In analogy to other prokaryotic sensory transduction systems, we propose that RegB functions as a membrane-spanning sensor kinase that controls the anaerobic phosphorylation state of RegA, which in turn controls the induction of light harvesting and reaction center structural genes.

摘要

我们实验室最近证明,光捕获和反应中心结构基因表达的厌氧诱导涉及一种反式作用因子RegA,它与一类被称为应答调节因子的原核生物感觉转导蛋白具有序列相似性(M. W. Sganga和C. E. Bauer,《细胞》68:945 - 954,1992)。在本研究中,我们对参与诱导光捕获和反应中心结构基因厌氧表达的其他基因进行了筛选。这项搜索导致分离出四个菌株,通过互补和标记拯救分析表明它们携带与最初描述的regA突变等位的突变,以及一个菌株,其突变被发现与regA连锁但不等位。序列分析表明,这个额外的基因regB编码一种与原核生物组氨酸传感器激酶家族具有序列相似性的多肽。对regB突变体中光合作用基因表达的分析表明,regB的破坏导致一种与regA突变体所描述的非常相似的表型,即不能反式激活puf、puh和puc操纵子的厌氧表达。类似于其他原核生物感觉转导系统,我们提出RegB作为一种跨膜传感器激酶发挥作用,它控制RegA的厌氧磷酸化状态,而RegA又反过来控制光捕获和反应中心结构基因的诱导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7396/197214/ca4609ab42f0/jbacter00042-0170-a.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验