Graduate School of Environmental Health Sciences, Azabu University, 1-17-71, Fuchinobe, Chuo-ku Sagamihara, 252-5201, Japan.
Folia Microbiol (Praha). 2011 Mar;56(2):159-65. doi: 10.1007/s12223-011-0020-6. Epub 2011 Mar 24.
When recombinant plasmid DNA from a genomic DNA library and inverse PCR products of Campylobacter sputorum biovar paraureolyticus LMG17591 strain were analyzed, an approximate 6.5-kb pair region, encoding a urease gene operon, was identified. Within the operon, seven closely spaced and putative open reading frames for ureG, ureH(D), ureA, ureB, ureC, ureE, and ureF were detected in order. A possible overlap was detected between ureG and ureH(D), ureH(D) and ureA, and ureE and ureF. In addition, two putative promoter structures, probable ribosome-binding sites and a putative ρ-independent transcriptional terminator structure were identified. The urease gene operon transcription in the cells was confirmed by the reverse transcription-PCR analysis. A neighbor-joining tree constructed based on the nucleotide sequence information of urease genes showed that C. sputorum biovar paraureolyticus formed a cluster with Arcobacter butzleri, urease-positive thermophilic Campylobacter and some Helicobacter spp., separating those from the other urease-producing bacteria, suggesting a commonly shared ancestry among these organisms.
当分析来自基因组 DNA 文库的重组质粒 DNA 和弯曲杆菌属副溶血性亚种 LMG17591 菌株的反向 PCR 产物时,鉴定出一个大约 6.5kb 对的区域,该区域编码一个脲酶基因操纵子。在操纵子中,按顺序检测到七个紧密间隔且假定的开放阅读框,用于 ureG、ureH(D)、ureA、ureB、ureC、ureE 和 ureF。在 ureG 和 ureH(D)、ureH(D)和 ureA 以及 ureE 和 ureF 之间检测到可能的重叠。此外,还鉴定了两个假定的启动子结构、可能的核糖体结合位点和一个假定的 ρ 独立转录终止子结构。通过逆转录-PCR 分析证实了细胞中脲酶基因的转录。基于脲酶基因的核苷酸序列信息构建的邻接树表明,副溶血性弯曲杆菌与 Arcobacter butzleri、产脲酶的嗜热弯曲杆菌和一些 Helicobacter spp. 形成一个聚类,与其他产脲酶的细菌分离,表明这些生物体之间存在共同的祖先。