内酰胺酶活性及抑制作用测定。

Thammaiah Viswanatha, Laura Marrone, Valerie Goodfellow, Gary I Dmitrienko
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引用次数: 13

摘要

产生内酰胺酶的能力,无论是先天的还是后天的,能够水解内酰胺类抗生素中的内环肽键的酶,似乎是对这类抗生素不断增加的耐药性的主要原因。迄今为止,已经确定了四种不同的β -内酰胺酶,A、B、C和D。其中,A类、C类和D类酶在其催化机制中利用丝氨酸残基作为亲核试剂,而B类酶的功能依赖于Zn2+。人们一直在努力开发这些酶的有效抑制剂,以确保β -内酰胺类抗生素在临床医学中的疗效。本章关注的是评估β -内酰胺酶的催化活性的程序,作为筛选化合物抑制效力的一种手段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assays for beta-lactamase activity and inhibition.

The ability, either innate or acquired, to produce beta-lactamases, enzymes capable of hydrolyzing the endocyclic peptide bond in beta-lactam antibiotics, would appear to be a primary contributor to the ever-increasing incidences of resistance to this class of antibiotics. To date, four distinct classes, A, B, C, and D, of beta-lactamases have been identified. Of these, enzymes in classes A, C, and D utilize a serine residue as a nucleophile in their catalytic mechanism while class B members are Zn2+-dependent for their function. Efforts have been and still continue to be made toward the development of potent inhibitors of these enzymes as a means to ensure the efficacy of beta-lactam antibiotics in clinical medicine. This chapter concerns procedures for the evaluation of the catalytic activity of beta-lactamases as a means to screen compounds for their inhibitory potency.

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