Gatermann S, Marre R
Institut für Medizinische Mikrobiologie, Medizinische Universität, Lübeck, Federal Republic of Germany.
Infect Immun. 1989 Oct;57(10):2998-3002. doi: 10.1128/iai.57.10.2998-3002.1989.
The urease gene of Staphylococcus saprophyticus CCM883 was cloned and expressed in Staphylococcus carnosus TM300. In vitro translation of the cloned DNA sequences revealed six polypeptides (of 70, 47, 29, 27, 20, and 17 kilodaltons) that were associated with enzyme activity. Introduction of the cloned genes into a urease-negative mutant of S. saprophyticus restored the virulence of this strain, confirming our previous suggestion (S. Gatermann, J. John, and R. Marre, Infect. Immun. 57:110-116, 1989) that this enzyme is a major virulence factor of the organism and contributes mainly to cystopathogenicity.
腐生葡萄球菌CCM883的脲酶基因被克隆并在肉葡萄球菌TM300中表达。对克隆的DNA序列进行体外翻译,发现有六种多肽(分子量分别为70、47、29、27、20和17千道尔顿)与酶活性相关。将克隆基因导入腐生葡萄球菌的脲酶阴性突变体后,该菌株的毒力得以恢复,这证实了我们之前的推测(S. Gatermann、J. John和R. Marre,《感染与免疫》57:110 - 116,1989年),即这种酶是该生物体的主要毒力因子,主要导致膀胱致病性。