Brandão Pedro F B, Clapp Justin P, Bull Alan T
Research School of Biosciences, University of Kent, Canterbury, Kent CT2 7NJ, United Kingdom.
Appl Environ Microbiol. 2003 Oct;69(10):5754-66. doi: 10.1128/AEM.69.10.5754-5766.2003.
A molecular screening approach was developed in order to amplify the genomic region that codes for the alpha- and beta-subunits of the nitrile hydratase (NHase) enzyme in rhodococci. Specific PCR primers were designed for the NHase genes from a collection of nitrile-degrading actinomycetes, but amplification was successful only with strains identified as Rhodococcus erythropolis. A hydratase PCR product was also obtained from R. erythropolis DSM 43066(T), which did not grow on nitriles. Southern hybridization of other members of the nitrile-degrading bacterial collection resulted in no positive signals other than those for the R. erythropolis strains used as positive controls. PCR-restriction fragment length polymorphism-single-strand conformational polymorphism (PRS) analysis of the hydratases in the R. erythropolis strains revealed unique patterns that mostly correlated with distinct geographical sites of origin. Representative NHases were sequenced, and they exhibited more than 92.4% similarity to previously described NHases. The phylogenetic analysis and deduced amino acid sequences suggested that the novel R. erythropolis enzymes belonged to the iron-type NHase family. Some different residues in the translated sequences were located near the residues involved in the stabilization of the NHase active site, suggesting that the substitutions could be responsible for the different enzyme activities and substrate specificities observed previously in this group of actinomycetes. A similar molecular screening analysis of the amidase gene was performed, and a correlation between the PRS patterns and the geographical origins identical to the correlation found for the NHase gene was obtained, suggesting that there was coevolution of the two enzymes in R. erythropolis. Our findings indicate that the NHase and amidase genes present in geographically distinct R. erythropolis strains are not globally mixed.
为了扩增编码红球菌腈水合酶(NHase)α和β亚基的基因组区域,开发了一种分子筛选方法。针对一组腈降解放线菌的NHase基因设计了特异性PCR引物,但仅对鉴定为红平红球菌的菌株扩增成功。从红平红球菌DSM 43066(T)也获得了水合酶PCR产物,该菌株不能在腈类物质上生长。对腈降解细菌集合的其他成员进行Southern杂交,除用作阳性对照的红平红球菌菌株外,未产生阳性信号。对红平红球菌菌株中的水合酶进行PCR-限制性片段长度多态性-单链构象多态性(PRS)分析,揭示了独特的模式,这些模式大多与不同的地理起源地点相关。对代表性的NHase进行了测序,它们与先前描述的NHase表现出超过92.4%的相似性。系统发育分析和推导的氨基酸序列表明,新的红平红球菌酶属于铁型NHase家族。翻译序列中的一些不同残基位于参与NHase活性位点稳定的残基附近,这表明这些取代可能是导致先前在这组放线菌中观察到的不同酶活性和底物特异性的原因。对酰胺酶基因进行了类似的分子筛选分析,获得了与NHase基因相同的PRS模式与地理起源之间的相关性,这表明红平红球菌中这两种酶存在共同进化。我们的研究结果表明,地理上不同的红平红球菌菌株中存在的NHase和酰胺酶基因并非全球混合。