Chin H S, Sim J, Sim T S
Department of Microbiology, Faculty of Medicine, National University of Singapore, 5 Science Drive 2, Singapore 117597, Singapore.
Biochem Biophys Res Commun. 2001 Sep 21;287(2):507-13. doi: 10.1006/bbrc.2001.5552.
Superimposition of deacetoxycephalosporin C synthase (DAOCS) and isopenicillin N synthase (IPNS) structures revealed that R74, R160, R266 and N304 are strategically located in the catalytic cavity of Streptomyces clavuligerus DAOCS (scDAOCS) and are crucial for orchestrating different substrates. Substitutions at these sites to a hydrophobic leucine residue were expected to stabilize the hydrophobic substrate bound state. Substantial improvements in the biotransformation of penicillin G, ampicillin and amoxicillin to their respective cephalosporin moieties were observed using the N304L mutant scDAOCS. Thus, our results have demonstrated the enhancement of scDAOCS activity via critical computational analysis and site-directed mutagenesis of endogenous ligands.
去乙酰氧基头孢菌素C合酶(DAOCS)和异青霉素N合酶(IPNS)结构的叠加显示,R74、R160、R266和N304位于克拉维链霉菌DAOCS(scDAOCS)的催化腔中,对协调不同底物至关重要。预期将这些位点替换为疏水性亮氨酸残基可稳定疏水性底物结合状态。使用N304L突变体scDAOCS观察到青霉素G、氨苄青霉素和阿莫西林向各自头孢菌素部分的生物转化有显著改善。因此,我们的结果通过对内源配体的关键计算分析和定点诱变证明了scDAOCS活性的增强。