Accellular synthesis of cephalosporins
    36.
    发明授权
    Accellular synthesis of cephalosporins 失效
    头孢菌素的细胞合成

    公开(公告)号:US4178210A

    公开(公告)日:1979-12-11

    申请号:US880036

    申请日:1978-03-17

    IPC分类号: C07D501/10 C12P35/00 C12D9/00

    CPC分类号: C12P35/00 Y10S435/926

    摘要: A cephalosporin antibiotic is produced from a precursor comprising the five membered thiazolidine ring and the .beta. lactam moiety characteristics of penicillins by contacting the precursor with a cell-free extract of Cephalosporium acremonium in the presence of ATP under conditions favoring high oxygen transfer. Preferably, an ATP regeneration system comprising a phosphate donor and a phosphotransferase enzyme is included in the reaction.

    摘要翻译: 通过在有利于高氧转移的条件下,在ATP存在下使前体与顶头孢霉的无细胞提取物接触,由包含五元噻唑烷环的前体和β-内酰胺部分特征产生头孢菌素抗生素。 优选地,包含磷酸供体和磷酸转移酶的ATP再生系统包括在反应中。