Page M Dudley, Ferguson Stuart J
Department of Biochemistry, University of Oxford, South Parks Road, Oxford, OX1 3QU, UK, and Oxford Centre for Molecular Sciences, New Chemistry Building, South Parks Road, Oxford, OX1 3QT, UK1.
Microbiology (Reading). 1999 Nov;145 ( Pt 11):3047-3057. doi: 10.1099/00221287-145-11-3047.
Each of the Paracoccus denitrificans genes in the c-type cytochrome biogenesis gene cluster ccmABCDG, plus the two flanking genes ORF117 and hisH, were individually disrupted by omega insertion. Resultant phenotypes were restored to the wild-type by complementation from a set of plasmids. All of the ccm genes, but neither ORF117 nor hisH, were required for c-type cytochrome biogenesis; only ccmG was also implicated in the biosynthesis of cytochrome aa3. Disruption of ccmC or ccmG resulted in failure to grow on rich media, but disruption of ccmA, ccmB or ccmD did not. The ccmC mutant, but not the ccmA, ccmB or ccmD mutants, also exhibited the increased sensitivity to growth inhibition by oxidized thiol compounds previously observed for the ccmG mutant. In contrast to the ccmG mutant, however, growth of the ccmC mutant on rich media could not be restored by DTT. Siderophore biosynthesis and/or secretion by P. denitrificans was also attenuated by disruption of ccmC and ccmG but not of ccmA, ccmB or ccmD. These results indicate that CcmC can function independently of CcmA, CcmB and CcmD despite other evidence that these gene products form an ATP-binding cassette (ABC)-type-transporter with the subunit composition (CcmA)2-CcmB-CcmC or (CcmA)2-CcmB-CcmC-CcmD, and also suggest a possible link between the functions of CcmC and CcmG.
通过ω插入分别破坏了反硝化副球菌c型细胞色素生物合成基因簇ccmABCDG中的每个基因,以及两个侧翼基因ORF117和hisH。通过一组质粒的互补作用,使所得表型恢复为野生型。c型细胞色素生物合成需要所有的ccm基因,但不需要ORF117和hisH;只有ccmG也参与细胞色素aa3的生物合成。破坏ccmC或ccmG导致在丰富培养基上无法生长,但破坏ccmA、ccmB或ccmD则不会。ccmC突变体,而不是ccmA、ccmB或ccmD突变体,也表现出对氧化硫醇化合物生长抑制的敏感性增加,这与之前在ccmG突变体中观察到的情况相同。然而,与ccmG突变体不同的是,DTT无法恢复ccmC突变体在丰富培养基上的生长。反硝化副球菌的铁载体生物合成和/或分泌也因ccmC和ccmG的破坏而减弱,但ccmA、ccmB或ccmD的破坏则不会。这些结果表明,尽管有其他证据表明这些基因产物与亚基组成(CcmA)2-CcmB-CcmC或(CcmA)2-CcmB-CcmC-CcmD形成ATP结合盒(ABC)型转运体,但CcmC可以独立于CcmA、CcmB和CcmD发挥作用,并且还表明CcmC和CcmG的功能之间可能存在联系。