Suppr超能文献

非天然三肽δ-(D-α-氨基己二酰基)-L-半胱氨酰-D-缬氨酸向β-内酰胺抗生素的酶促转化

Enzymatic conversion of the unnatural tripeptide delta-(D-alpha-aminoadipyl)-L-cysteinyl-D-valine to beta-lactam antibiotics.

作者信息

Shen Y Q, Wolfe S, Demain A L

出版信息

J Antibiot (Tokyo). 1984 Sep;37(9):1044-8. doi: 10.7164/antibiotics.37.1044.

Abstract

Incubation of the unnatural tripeptide delta-(D-alpha-aminoadipyl)-L-cysteinyl-D-valine (DLD-ACV) with a partially purified extract of Cephalosporium acremonium resulted in the production of deacetoxycephalosporin C. The extract contained isopenicillin N synthetase (cyclase) and deacetoxycephalosporin C synthetase (expandase) but no penicillin epimerase activity, and was incubated aerobically in the presence of the components of the cyclase and expandase reaction mixtures (Fe++, ascorbate, dithiothreitol, alpha-ketoglutarate and ATP). The reaction was sensitive to penicillinase, indicating penicillin N to be an intermediate. However, when ring expansion was prevented by omission of alpha-ketoglutarate and ATP, no penicillin N was detected.

摘要

将非天然三肽δ-(D-α-氨基己二酰基)-L-半胱氨酰-D-缬氨酸(DLD-ACV)与顶头孢霉的部分纯化提取物一起温育,产生了去乙酰氧基头孢菌素C。该提取物含有异青霉素N合成酶(环化酶)和去乙酰氧基头孢菌素C合成酶(扩环酶),但没有青霉素差向异构酶活性,并且在环化酶和扩环酶反应混合物的组分(Fe++、抗坏血酸盐、二硫苏糖醇、α-酮戊二酸和ATP)存在的情况下进行需氧温育。该反应对青霉素酶敏感,表明青霉素N是中间体。然而,当通过省略α-酮戊二酸和ATP来阻止环扩展时,未检测到青霉素N。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验