Neyrolles O, Ferris S, Behbahani N, Montagnier L, Blanchard A
Unité d'Oncologie Virale, Institut Pasteur, Paris, France.
J Bacteriol. 1996 Feb;178(3):647-55. doi: 10.1128/jb.178.3.647-655.1996.
Ureaplasma urealyticum is a pathogenic ureolytic mollicute which colonizes the urogenital tracts of humans. A genetic polymorphism between the two biotypes of U. urealyticum at the level of the urease genes was found. The urease gene cluster from a biotype 1 representative of U. urealyticum (serotype I) was cloned and sequenced. Seven genes were found, with ureA, ureB, and ureC encoding the structural subunits and ureE, ureF, ureG, and a truncated ureI) gene encoding accessory proteins. Urease expression was not obtained when the plasmid containing these genes was incorporated into an opal suppressor strain of Escherichia coli, although this enzymatic activity was found in the same E. coli strain transformed with pC6b, a plasmid with previously cloned urease genes from the U. urealyticum T960 strain of biotype 2 (serotype 8). Although there are 12 TGA triplets encoding tryptophan within urease genes, the level of expression obtained was comparable to the levels reported for other bacterial genes expressed in E. coli. Nested deletion experiments allowed us to demonstrate that ureD is necessary for urease activity whereas another open reading frame located downstream is not. The promoter for ureA and possibly other urease genes was identified for both serotypes.
解脲脲原体是一种致病性的解脲支原体,可定植于人类泌尿生殖道。在解脲脲原体的两种生物型之间,发现了脲酶基因水平上的遗传多态性。对解脲脲原体生物型1(血清型I)的一个代表菌株的脲酶基因簇进行了克隆和测序。发现了7个基因,其中ureA、ureB和ureC编码结构亚基,ureE、ureF、ureG和一个截短的ureI基因编码辅助蛋白。当将含有这些基因的质粒导入大肠杆菌的乳白抑制菌株时,未获得脲酶表达,尽管在用pC6b转化的同一大肠杆菌菌株中发现了这种酶活性,pC6b是一种含有先前从生物型2(血清型8)的解脲脲原体T960菌株克隆的脲酶基因的质粒。尽管脲酶基因中有12个编码色氨酸的TGA三联体,但获得的表达水平与在大肠杆菌中表达的其他细菌基因所报道的水平相当。嵌套缺失实验使我们能够证明ureD对脲酶活性是必需的,而位于下游的另一个开放阅读框则不是。确定了两种血清型的ureA启动子以及可能的其他脲酶基因启动子。