Mulrooney S B, Hausinger R P
Department of Biochemistry, Michigan State University, East Lansing 48824.
J Bacteriol. 1990 Oct;172(10):5837-43. doi: 10.1128/jb.172.10.5837-5843.1990.
A 4.8-kilobase-pair region of cloned DNA encoding the genes of the Klebsiella aerogenes urease operon has been sequenced. Six closely spaced open reading frames were found: ureA (encoding a peptide of 11.1 kilodaltons [kDa]), ureB (11.7-kDa peptide), ureC (60.3-kDa peptide), ureE (17.6-kDa peptide), ureF (25.2-kDa peptide), and ureG (21.9-kDa peptide). Immediately after the ureG gene is a putative rho-dependent transcription terminator. The three subunits of the nickel-containing enzyme are encoded by ureA, ureB, and ureC based on protein structural studies and sequence homology to jack bean urease. Potential roles for ureE, ureF, and ureG were explored by deleting these accessory genes from the operon. The deletion mutant produced inactive urease, which was partially purified and found to have the same subunit stoichiometry and native size as the active enzyme but which contained no significant levels of nickel. The three accessory genes were able to activate apo-urease in vivo when they were cloned into a compatible expression vector and cotransformed into cells carrying the plasmid containing ureA, ureB, and ureC. Thus, one or more of the ureE, ureF, or ureG gene products are involved in nickel incorporation into urease.
已对编码产气克雷伯菌脲酶操纵子基因的一段4.8千碱基对的克隆DNA区域进行了测序。发现了6个紧密排列的开放阅读框:ureA(编码11.1千道尔顿[kDa]的肽)、ureB(11.7-kDa肽)、ureC(60.3-kDa肽)、ureE(17.6-kDa肽)、ureF(25.2-kDa肽)和ureG(21.9-kDa肽)。在ureG基因之后紧接着是一个假定的依赖于rho的转录终止子。根据蛋白质结构研究以及与刀豆脲酶的序列同源性,含镍酶的三个亚基由ureA、ureB和ureC编码。通过从操纵子中删除这些辅助基因来探索ureE、ureF和ureG的潜在作用。缺失突变体产生无活性的脲酶,该脲酶经过部分纯化后,发现其亚基化学计量和天然大小与活性酶相同,但不含显著水平的镍。当将这三个辅助基因克隆到一个相容的表达载体中并共转化到携带含有ureA、ureB和ureC质粒的细胞中时,它们能够在体内激活脱辅基脲酶。因此,ureE、ureF或ureG基因产物中的一个或多个参与了镍掺入脲酶的过程。