期刊名称：Proceedings of the National Academy of Sciences
印刷版ISSN：0027-8424
电子版ISSN：1091-6490
出版年度：1998
卷号：95
期号：16
页码：9082-9086
DOI：10.1073/pnas.95.16.9082
语种：English
出版社：The National Academy of Sciences of the United States of America
摘要：The principal cause of bacterial resistance to penicillin and other {beta}-lactam antibiotics is the acquisition of plasmid-encoded {beta}-lactamases, enzymes that catalyze hydrolysis of the {beta}-lactam bond and render these antibiotics inactive. Clavulanic acid is a potent inhibitor of {beta}-lactamases and has proven clinically effective in combating resistant infections. Although clavulanic acid and penicillin share marked structural similarities, the biosyntheses of their bicyclic nuclei are wholly dissimilar. In contrast to the efficient iron-mediated oxidative cyclization of a tripeptide to isopenicillin N, the critical {beta}-lactam ring of clavulanic acid is demonstrated to form by intramolecular closure catalyzed by a new type of ATP/Mg2+-dependent enzyme, a {beta}-lactam synthetase ({beta}-LS). Insertional inactivation of its encoding gene in wild-type Streptomyces clavuligerus resulted in complete loss of clavulanic acid production and the accumulation of N2-(carboxyethyl)-L-arginine (CEA). Chemical complementation of this blocked mutant with authentic deoxyguanidinoproclavaminic acid (DGPC), the expected product of the {beta}-LS, restored clavulanic acid synthesis. Finally, overexpression of this gene gave the {beta}-LS, which was shown to mediate the conversion of CEA to DGPC in the presence of ATP/Mg2+. Primary amino acid sequence comparisons suggest that this mode of {beta}-lactam formation could be more widely spread in nature and mechanistically related to asparagine synthesis.
