Meziane-Cherif D, Badet-Denisot M A, Evers S, Courvalin P, Badet B
Groupe Biocatalyse & Régulation, Institut de Chimie des Substances Naturelles, CNRS, Gif-sur-Yvette, France.
FEBS Lett. 1994 Nov 7;354(2):140-2. doi: 10.1016/0014-5793(94)01096-x.
Acquired resistance to glycopeptides in enterococci is associated with the production of D-Alanine:D-Alanine ligase-related proteins. The VanA protein associated with high-level vancomycin and teicoplanin resistance (VanA phenotype) synthesizes a new peptidoglycan precursor, D-alanine-D-lactate, that has reduced glycopeptide affinity. Production of a similar protein, VanB, is induced in strains that display variable levels of vancomycin resistance but remain susceptible to teicoplanin (VanB phenotype). This paper describes the over-production, purification and characterization of VanB. Comparison of kinetic parameters of the two Van enzymes suggests that differences in catalytic efficiency could account, at least in part, for the various levels of vancomycin resistance.
肠球菌对糖肽类抗生素的获得性耐药与D-丙氨酸:D-丙氨酸连接酶相关蛋白的产生有关。与高水平万古霉素和替考拉宁耐药性相关的VanA蛋白(VanA表型)合成一种新的肽聚糖前体D-丙氨酸-D-乳酸,其对糖肽类抗生素的亲和力降低。在表现出不同水平万古霉素耐药性但仍对替考拉宁敏感的菌株(VanB表型)中可诱导产生一种类似的蛋白VanB。本文描述了VanB的过量表达、纯化及特性。对两种Van酶动力学参数的比较表明,催化效率的差异至少在一定程度上可以解释万古霉素耐药性的不同水平。