首页> 外文期刊>Enzyme and Microbial Technology >Inactivation of deacetoxycephalosporin C synthase in extracts of Streptomyces clavuligerus during bioconversion of penicillin G to deacetoxycephalosporin G
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Inactivation of deacetoxycephalosporin C synthase in extracts of Streptomyces clavuligerus during bioconversion of penicillin G to deacetoxycephalosporin G

机译:青霉素G转化为脱乙酰氧基头孢菌素G的过程中克拉维链霉菌提取物中的脱乙酰氧基头孢菌素C合酶失活

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摘要

By using cell-free extracts of Streptomyces clavuligerus containing deacetoxycephalosporin C synthase, we can convert penicillin G into deacetoxycephalosporin G. The degree of bioconversion was low (below 1% based on charged substrate) and decreased as substrate concentration was increased. Formation of product occurred during the first 2 h and then ceased. Addition of increasing levels of cofactors and/or substrate at the 2-h point did not result in more product. Preincubation of the crude extracts in the presence of ferrous ions plus either ascorbate or α-ketoglutarate led to complete loss of activity. Such inactivation could not be reversed by catalase, superoxide dismutase, mannitol, thiourea, dimethylsulfoxide, dithiothreitol, or β-mercaptoethanol.
机译:通过使用含有脱乙酰氧基头孢菌素C合酶的棒状链霉菌无细胞提取物,我们可以将青霉素G转化为脱乙酰氧基头孢菌素G。生物转化度低(基于带电荷的底物,低于1%),并且随着底物浓度的增加而降低。在最初的2小时内形成了产品,然后停止了。在2-h点添加增加水平的辅因子和/或底物不会导致更多的产物。在亚铁离子加抗坏血酸盐或α-酮戊二酸存在下,将粗提取物进行预培养会导致活性完全丧失。过氧化氢酶,超氧化物歧化酶,甘露醇,硫脲,二甲基亚砜,二硫苏糖醇或β-巯基乙醇不能逆转这种失活。

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