Biosynthesis of unnatural cephalosporins
    1.
    发明公开
    Biosynthesis of unnatural cephalosporins 失效
    生物合成on b b en en en。。。。。。

    公开(公告)号:EP0296641A2

    公开(公告)日:1988-12-28

    申请号:EP88200129.0

    申请日:1983-08-12

    摘要: A peptide precursor of the ACV (aminoadipyl-cysteinyl-valine) type, in which the valine moiety may be replaced by any readily available amino acid may be converted into a cephalosporin of the type
    where R, is H, lower alkyl or functionalized carboxylic group and R 2 is H or lower alkyl, by reacting the precursor with novel cyclase, epimerase and ring expansion enzymes isolated from a cell-free extract of a prokaryotic organism such as Streptomyces clavuligerus. The three novel enzymes may be immobilized separately or together on a suitable support medium and the conversion may be carried out in a continuous mode.

    摘要翻译: ACV(氨基己二酰基 - 半胱氨酰 - 缬氨酸)类型的肽前体,其中缬氨酸部分可被任何容易获得的氨基酸替代,可转化为类型的头孢菌素,其中R 1为H,低级烷基或官能化 羧酸基团,并且R 2是H或低级烷基,通过使前体与从原核生物例如Streptomyces clavuligerus的无细胞提取物分离的新型环化酶,差向异构酶和环扩增酶反应。 三种新型酶可以单独地或一起固定在合适的载体介质上,并且转化可以以连续模式进行。

    Biosynthesis of unnatural cephalosporins
    2.
    发明公开
    Biosynthesis of unnatural cephalosporins 失效
    非天然头孢菌素的生物合成

    公开(公告)号:EP0295724A3

    公开(公告)日:1990-04-18

    申请号:EP88200131.6

    申请日:1983-08-12

    摘要: A peptide precursor of the ACV (aminoadipyl-cysteinyl-valine) type, in which the valine moiety may be replaced by any readily available amino acid may be converted into a cephalosporin of the type
    where R 1 is H, lower alkyl or functionalized carboxylic group and R 2 is H or lower alkyl, by reacting the precursor with novel cyclase, epimerase and ring expansion enzymes isolated from a cell-free extract of a prokaryotic organism such as Streptomyces clavuligerus. The three novel enzymes may be immobilized separately or together on a suitable support medium and the conversion may be carried out in a continuous mode.

    摘要翻译: ACV(氨基己二酰 - 半胱氨酰 - 缬氨酸)类型的肽前体(其中缬氨酸部分可以被任何容易获得的氨基酸置换)可以转化为其中R1是H,低级烷基或官能化羧基类型的头孢菌素和 R2是H或低级烷基,通过使前体与从原核生物如链霉菌(Streptomyces clavuligerus)的无细胞提取物分离的新型环化酶,差向异构酶和环扩张酶反应。 三种新型酶可以分别或一起固定在合适的载体介质上,并且转化可以以连续模式进行。

    Biosynthesis of unnatural cephalosporins
    3.
    发明公开
    Biosynthesis of unnatural cephalosporins 失效
    非天然头孢菌素的生物合成

    公开(公告)号:EP0296641A3

    公开(公告)日:1990-06-20

    申请号:EP88200129.0

    申请日:1983-08-12

    摘要: A peptide precursor of the ACV (aminoadipyl-cysteinyl-valine) type, in which the valine moiety may be replaced by any readily available amino acid may be converted into a cephalosporin of the type
    where R, is H, lower alkyl or functionalized carboxylic group and R 2 is H or lower alkyl, by reacting the precursor with novel cyclase, epimerase and ring expansion enzymes isolated from a cell-free extract of a prokaryotic organism such as Streptomyces clavuligerus. The three novel enzymes may be immobilized separately or together on a suitable support medium and the conversion may be carried out in a continuous mode.

    摘要翻译: ACV(氨基己二酰 - 半胱氨酰 - 缬氨酸)类型的肽前体(其中缬氨酸部分可以被任何容易获得的氨基酸置换)可以转化为其中R1是H,低级烷基或官能化羧基类型的头孢菌素 R2是H或低级烷基,通过使前体与从原核生物如链霉菌(Streptomyces clavuligerus)的无细胞提取物分离的新型环化酶,差向异构酶和扩环酶反应。 三种新型酶可以分别或一起固定在合适的载体介质上,并且转化可以以连续模式进行。

    Biosynthesis of unnatural cephalosporins
    4.
    发明公开
    Biosynthesis of unnatural cephalosporins 失效
    联合化学品的生物化学

    公开(公告)号:EP0296642A3

    公开(公告)日:1990-04-11

    申请号:EP88200130.8

    申请日:1983-08-12

    摘要: A peptide precursor of the ACV (aminoadipyl-cysteinyl­valine) type, in which the valine moiety may be replaced by any readily available amino acid may be converted into a cephalosporin of the type
    where R₁ is H, lower alkyl or functionalized carboxylic group and R₂ is H or lower alkyl, by reacting the precursor with novel cyclase, epimerase and ring expansion enzymes isolated from a cell-free extract of a prokaryotic organism such as Streptomyces clavuligerus . The three novel enzymes may be immobilized separately or together on a suitable support medium and the conversion may be carried out in a continuous mode.

    摘要翻译: ACV(氨基己二酰基半胱氨酰缬氨酸)类型的肽前体,其中缬氨酸部分可被任何容易获得的氨基酸替代,可转化为类型的头孢菌素,其中R 1为H,低级烷基或官能化羧基,R 2 通过使前体与从原核生物例如链霉菌(Streptomyces clavuligerus)的无细胞提取物分离的新型环化酶,差向异构酶和环膨化酶反应而形成H或低级烷基。 三种新型酶可以单独地或一起固定在合适的载体介质上,并且转化可以以连续模式进行。

    Biosynthesis of unnatural cephalosporins
    5.
    发明公开
    Biosynthesis of unnatural cephalosporins 失效
    非天然头孢菌素的生物合成

    公开(公告)号:EP0296642A2

    公开(公告)日:1988-12-28

    申请号:EP88200130.8

    申请日:1983-08-12

    摘要: A peptide precursor of the ACV (aminoadipyl-cysteinyl­valine) type, in which the valine moiety may be replaced by any readily available amino acid may be converted into a cephalosporin of the type
    where R₁ is H, lower alkyl or functionalized carboxylic group and R₂ is H or lower alkyl, by reacting the precursor with novel cyclase, epimerase and ring expansion enzymes isolated from a cell-free extract of a prokaryotic organism such as Streptomyces clavuligerus . The three novel enzymes may be immobilized separately or together on a suitable support medium and the conversion may be carried out in a continuous mode.

    摘要翻译: ACV(氨基己二酰 - 半胱胺酰缬氨酸)类型的肽前体(其中缬氨酸部分可以被任何容易得到的氨基酸置换)可以转化为其中R 1是H,低级烷基或官能化羧基并且R 2是类型的头孢菌素 H或低级烷基,通过将前体与从原核生物如链霉菌(Streptomyces clavuligerus)的无细胞提取物分离的新型环化酶,差向异构酶和扩环酶反应。 三种新型酶可以分别或一起固定在合适的载体介质上,并且转化可以以连续模式进行。

    Biosynthesis of unnatural cephalosporins
    6.
    发明公开
    Biosynthesis of unnatural cephalosporins 失效
    生物合成Nichtbiogenen头孢菌素。

    公开(公告)号:EP0295724A2

    公开(公告)日:1988-12-21

    申请号:EP88200131.6

    申请日:1983-08-12

    摘要: A peptide precursor of the ACV (aminoadipyl-cysteinyl-valine) type, in which the valine moiety may be replaced by any readily available amino acid may be converted into a cephalosporin of the type
    where R 1 is H, lower alkyl or functionalized carboxylic group and R 2 is H or lower alkyl, by reacting the precursor with novel cyclase, epimerase and ring expansion enzymes isolated from a cell-free extract of a prokaryotic organism such as Streptomyces clavuligerus. The three novel enzymes may be immobilized separately or together on a suitable support medium and the conversion may be carried out in a continuous mode.

    摘要翻译: ACV(氨基己二酰基 - 半胱氨酰 - 缬氨酸)类型的肽前体,其中缬氨酸部分可被任何容易获得的氨基酸替代,可转化为类型的头孢菌素,其中R 1为H,低级烷基或官能化 羧酸基团,并且R 2是H或低级烷基,通过使前体与从原核生物例如Streptomyces clavuligerus的无细胞提取物分离的新型环化酶,差向异构酶和环扩增酶反应。 三种新型酶可以单独地或一起固定在合适的载体介质上,并且转化可以以连续模式进行。