8.
    发明专利
    未知

    公开(公告)号:NO932327D0

    公开(公告)日:1993-06-24

    申请号:NO932327

    申请日:1993-06-24

    Applicant: HOECHST AG

    Abstract: Bacterial strains are able to produce rhamnolipids which they release into the culture solution. On use of bacteria of the species Pseudomonas aeruginosa for the fermentation, these microorganisms synthesise rhamnolipids in a concentration of 70-120 g/l of culture solution. The L-rhamnose can be isolated from the culture solution directly by hydrolysis of the rhamnolipids, i.e. without an elaborate removal of the biomass and without isolation of the rhamnolipids before the hydrolysis.

    PROCESS FOR THE CLOSTRIPAIN-CATALYZED LINKAGE OF ARG-PRO AND ARG-B (B=PROTEINOGENOUS AND NON-PROTEINOGENOUS AMINO ACIDS) CONTAINING PEPTIDES

    公开(公告)号:CA2069199A1

    公开(公告)日:1992-11-24

    申请号:CA2069199

    申请日:1992-05-22

    Applicant: HOECHST AG

    Abstract: HOE 91/F 154 A process for the clostripain-catalyzed linkage of ArgPro and Arg-B (B = proteinogenous and non-proteinogenous amino acids) containing peptides The clostripain obtained from the culture filtrate from Clostridium histolyticum DSM 627 is employed for the linkage of arginine with amino-terminal protection or of peptides with amino-terminal protection and carboxylterminal arginine (acyl donor) to an amino acid or to a peptide with amino donor function. The enzyme can be obtained in high purity by alcohol precipitation and subsequent adsorption of the enzyme obtained from the alcohol-precipitated culture filtrate onto reactive dye and used for the linkage. The specific activity of clostripain is at least 80 U/mg. Clostripain catalyzes not only the abovementioned linkage of proteinogenous amino acids but also the linkage of a proteinogenous to a non-proteinogenous amino acid.

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