Sylvestre M, Sirois M, Hurtubise Y, Bergeron J, Ahmad D, Shareck F, Barriault D, Guillemette I, Juteau J M
Institut National de la Recherche Scientifique, INRS-Santé, Université du Québec, Pointe-Claire, Canada.
Gene. 1996 Oct 3;174(2):195-202. doi: 10.1016/0378-1119(96)00039-x.
In a previous work, all three components of Comamonas testosteroni B-356 biphenyl (BPH)/chlorobiphenyls (PCBs) dioxygenase (dox) have been purified and characterized. They include an iron-sulphur protein (ISPBPH) which is the terminal oxygenase composed of two subunits (encoded by bphA and bphE), a ferredoxin (FERBPH) encoded by bphF and a reductase (REDBPH) encoded by bphG. bphG Is not located in the neighbourhood of bphAEF in B-356. We are reporting the cloning of B-356-bphG and the sequencing of B-356-BPH dox genes. Comparative analysis of the genes provided genetic evidence showing that two BPH dox lineages have emerged in Gram-negative bacteria. The main features of the lineage that includes B-356 are the location of bphG outside the bph gene cluster and the structure of REDBPH which is very distinct from all other aryl dioxygenase-reductases.
在之前的一项研究中,睾丸酮丛毛单胞菌B-356联苯(BPH)/氯代联苯(PCBs)双加氧酶(dox)的所有三个组分均已得到纯化和表征。它们包括一种铁硫蛋白(ISPBPH),它是由两个亚基(由bphA和bphE编码)组成的末端加氧酶、由bphF编码的铁氧还蛋白(FERBPH)以及由bphG编码的还原酶(REDBPH)。在B-356中,bphG并不位于bphAEF附近。我们在此报告B-356-bphG的克隆以及B-356-BPH双加氧酶基因的测序。对这些基因的比较分析提供了遗传学证据,表明革兰氏阴性菌中出现了两个BPH双加氧酶谱系。包括B-356在内的该谱系的主要特征是bphG位于bph基因簇之外,以及REDBPH的结构与所有其他芳基双加氧酶还原酶非常不同。