Koper Teresa E, El-Sheikh Amal F, Norton Jeanette M, Klotz Martin G
Departments of Biology, Utah State University, Logan, Utah 84322-4820, USA.
Appl Environ Microbiol. 2004 Apr;70(4):2342-8. doi: 10.1128/AEM.70.4.2342-2348.2004.
Many but not all ammonia-oxidizing bacteria (AOB) produce urease (urea amidohydrolase, EC 3.5.1.5) and are capable of using urea for chemolithotrophic growth. We sequenced the urease operons from two AOB, the beta-proteobacterium Nitrosospira sp. strain NpAV and the gamma-proteobacterium Nitrosococcus oceani. In both organisms, all seven urease genes were contiguous: the three structural urease genes ureABC were preceded and succeeded by the accessory genes ureD and ureEFG, respectively. Green fluorescent protein reporter gene fusions revealed that the ure genes were under control of a single operon promoter upstream of the ureD gene in Nitrosococcus oceani. Southern analyses revealed two copies of ureC in the Nitrosospira sp. strain NpAV genome, while a single copy of the ure operon was detected in the genome of Nitrosococcus oceani. The ureC gene encodes the alpha subunit protein containing the active site and conserved nickel binding ligands; these conserved regions were suitable primer targets for obtaining further ureC sequences from additional AOB. In order to develop molecular tools for detecting the ureolytic ecotype of AOB, ureC genes were sequenced from several beta-proteobacterial AOB. Pairwise identity values ranged from 80 to 90% for the UreC peptides of AOB within a subdivision. UreC sequences deduced from AOB urease genes and available UreC sequences in the public databases were used to construct alignments and make phylogenetic inferences. The UreC proteins from beta-proteobacterial AOB formed a distinct monophyletic group. Unexpectedly, the peptides from AOB did not group most closely with the UreC proteins from other beta-proteobacteria. Instead, it appears that urease in beta-proteobacterial autotrophic ammonia oxidizers is the product of divergent evolution in the common ancestor of gamma- and beta-proteobacteria that was initiated before their divergence during speciation. Sequence motifs conserved for the proteobacteria and variable regions possibly discriminatory for ureC from beta-proteobacterial AOB were identified for future use in environmental analysis of ureolytic AOB. These gene sequences are the first publicly available for ure genes from autotrophic AOB.
许多但并非所有的氨氧化细菌(AOB)都能产生脲酶(尿素酰胺水解酶,EC 3.5.1.5),并能够利用尿素进行化能无机营养生长。我们对两种AOB的脲酶操纵子进行了测序,这两种AOB分别是β-变形菌亚纲的亚硝化螺菌属菌株NpAV和γ-变形菌亚纲的海洋亚硝化球菌。在这两种微生物中,所有七个脲酶基因都是连续的:三个结构脲酶基因ureABC的前后分别是辅助基因ureD和ureEFG。绿色荧光蛋白报告基因融合显示,在海洋亚硝化球菌中,脲酶基因受ureD基因上游单个操纵子启动子的控制。Southern分析显示,亚硝化螺菌属菌株NpAV基因组中有两个ureC拷贝,而在海洋亚硝化球菌基因组中检测到单个脲酶操纵子拷贝。ureC基因编码含有活性位点和保守镍结合配体的α亚基蛋白;这些保守区域是从其他AOB获取更多ureC序列的合适引物靶点。为了开发检测AOB尿素分解生态型的分子工具,我们对几种β-变形菌亚纲AOB的ureC基因进行了测序。同一分类中的AOB的脲酶C肽的成对同一性值在80%至90%之间。从AOB脲酶基因推导的UreC序列和公共数据库中可用的UreC序列被用于构建比对并进行系统发育推断。β-变形菌亚纲AOB的UreC蛋白形成了一个独特的单系群。出乎意料的是,AOB的肽与其他β-变形菌的UreC蛋白并非最紧密地聚在一起。相反,β-变形菌自养氨氧化菌中的脲酶似乎是γ-和β-变形菌共同祖先中趋异进化的产物,这种进化在物种形成过程中它们分化之前就已开始。确定了变形菌中保守的序列基序以及可能对β-变形菌亚纲AOB的ureC具有鉴别作用的可变区域,以供未来用于尿素分解AOB的环境分析。这些基因序列是自养AOB脲酶基因首次公开可用的序列。