Hodson Christopher T C, Lewin Allison, Hederstedt Lars, Le Brun Nick E
Centre for Molecular and Structural Biochemistry, School of Chemical Sciences and Pharmacy, University of East Anglia, Norwich NR4 7TJ, United Kingdon.
J Bacteriol. 2008 Jul;190(13):4697-705. doi: 10.1128/JB.00145-08. Epub 2008 May 2.
ResA is an extracytoplasmic membrane-bound thiol-disulfide oxidoreductase required for cytochrome c maturation in Bacillus subtilis. Previous biochemical and structural studies have revealed that the active-site cysteinyls cycle between oxidized and reduced states with a low reduction potential and that, upon reduction, a hydrophobic cavity forms close to the active site. Here we report in vivo studies of ResA-deficient B. subtilis complemented with a series of ResA variants. Using a range of methods to analyze the cellular cytochrome c content, we demonstrated (i) that the N-terminal transmembrane segment of ResA serves principally to anchor the protein to the cytoplasmic membrane but also plays a role in mediating the activity of the protein; (ii) that the active-site cysteines are important for cytochrome c maturation activity; (iii) that Pro141, which forms part of the hydrophobic cavity and which adopts a cis conformation, plays an important role in protein stability; (iv) that Glu80, which lies at the base of the hydrophobic cavity, is important for cytochrome c maturation activity; and, finally, (v) that Pro141 and Glu80 ResA mutant variants promote selective maturation of low levels of one c-type cytochrome, subunit II of the cytochrome c oxidase caa(3), indicating that this apocytochrome is distinct from the other three endogenous c-type cytochromes of B. subtilis.
ResA是一种胞外膜结合硫醇-二硫键氧化还原酶,是枯草芽孢杆菌中细胞色素c成熟所必需的。先前的生化和结构研究表明,活性位点的半胱氨酸残基以低还原电位在氧化态和还原态之间循环,并且在还原时,靠近活性位点会形成一个疏水腔。在此,我们报告了对缺乏ResA的枯草芽孢杆菌用一系列ResA变体进行互补的体内研究。通过使用一系列方法分析细胞色素c的含量,我们证明:(i)ResA的N端跨膜片段主要起到将蛋白质锚定到细胞质膜的作用,但也在介导蛋白质的活性中发挥作用;(ii)活性位点的半胱氨酸对细胞色素c成熟活性很重要;(iii)构成疏水腔一部分且呈顺式构象的Pro141在蛋白质稳定性中起重要作用;(iv)位于疏水腔底部的Glu80对细胞色素c成熟活性很重要;最后,(v)Pro141和Glu80 ResA突变变体促进细胞色素c氧化酶caa(3)的一个c型细胞色素亚基II低水平的选择性成熟,这表明这种脱辅基细胞色素与枯草芽孢杆菌的其他三种内源性c型细胞色素不同。