Wu Xiao-Bin, Fan Ke-Qiang, Wang Qin-Hong, Yang Ke-Qian
State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, 100080, PR China.
FEMS Microbiol Lett. 2005 May 1;246(1):103-10. doi: 10.1016/j.femsle.2005.03.043.
Deacetoxy/deacetylcephalosporin C synthase (acDAOC/DACS) from Acremonium chrysogenum is a bifunctional enzyme that catalyzes both the ring-expansion of penicillin N to deacetoxycephalosporin C (DAOC) and the hydroxylation of the latter to deacetylcephalosporin C (DAC). Three residues N305, R307 and R308 located in close proximity to the C-terminus of acDAOC/DACS were each mutated to leucine. The N305L and R308L mutant acDAOC/DACSs showed significant improvement in their ability to convert penicillin analogs. R308 was identified for the first time as a critical residue for DAOC/DACS activity. Kinetic analyses of purified R308L enzyme indicated its improved catalytic efficiency is due to combined improvements of K(m) and k(cat). Comparative modeling of acDAOC/DACS supports the involvement of R308 in the formation of substrate-binding pocket.
来自产黄青霉的脱乙酰氧基/脱乙酰头孢菌素C合酶(acDAOC/DACS)是一种双功能酶,它既能催化青霉素N环扩展生成脱乙酰氧基头孢菌素C(DAOC),又能将后者羟基化生成脱乙酰头孢菌素C(DAC)。位于acDAOC/DACS C末端附近的三个残基N305、R307和R308分别突变为亮氨酸。N305L和R308L突变型acDAOC/DACS在转化青霉素类似物的能力上有显著提高。R308首次被确定为DAOC/DACS活性的关键残基。对纯化的R308L酶的动力学分析表明,其催化效率的提高归因于K(m)和k(cat)的共同改善。acDAOC/DACS的比较建模支持R308参与底物结合口袋的形成。