Samraoui B, Sutton B J, Todd R J, Artymiuk P J, Waley S G, Phillips D C
Nature. 1986;320(6060):378-80. doi: 10.1038/320378a0.
beta-Lactam antibiotics--the penicillins, cephalosporins and related compounds--act by inhibiting enzymes that catalyse the final stages of the synthesis of bacterial cell walls. Recent crystallographic studies of representative enzymes are beginning to reveal the structural bases of antibiotic specificity and mechanism of action, while intensive efforts are being made to understand the beta-lactamase enzymes that are largely responsible for bacterial resistance to these antibiotics. It has been suggested that the beta-lactamases and beta-lactam target enzymes may be evolutionarily related and some similarity of amino-acid sequence around a common active-site serine residue supports this idea. We present here the first evidence from a comparison of three-dimensional structures in support of this hypothesis: the structure of beta-lactamase I from Bacillus cereus is similar to that of the penicillin-sensitive D-alanyl-D-alanine carboxypeptidase-transpeptidase from Streptomyces R61.
β-内酰胺抗生素(青霉素、头孢菌素及相关化合物)通过抑制催化细菌细胞壁合成最后阶段的酶发挥作用。近期对代表性酶的晶体学研究开始揭示抗生素特异性的结构基础及作用机制,同时人们正在深入研究主要导致细菌对这些抗生素产生耐药性的β-内酰胺酶。有人提出β-内酰胺酶和β-内酰胺靶标酶可能在进化上相关,围绕一个共同活性位点丝氨酸残基的氨基酸序列的某些相似性支持了这一观点。我们在此展示了来自三维结构比较的首个证据来支持这一假说:蜡样芽孢杆菌β-内酰胺酶I的结构与来自链霉菌R61的对青霉素敏感的D-丙氨酰-D-丙氨酸羧肽酶-转肽酶的结构相似。