会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 12. 发明专利
    • DE3223874A1
    • 1983-01-20
    • DE3223874
    • 1982-06-25
    • TOYO JOZO KK
    • IMAMURA SHIGEYUKIMISAKI HIDEOISHIKAWA HIDEHIKOMATSUURA KAZUO
    • C12N9/02C12N9/10C12N9/88C12Q1/25C12N9/04C12N1/20C12Q1/60C12Q1/00C12Q1/32C12Q1/48G01N33/92
    • An enzyme having enoyl-CoA hydratase activity, 3-hydroxyacyl-CoA dehydrogenase activity and 3-ketoacyl-CoA thiolase activity, all in the same enzyme, is produced by culturing the microorganism strain Pseudomonas fragi B-0771 FERM-P No. 5701, and isolating the enzyme thus produced from the culture medium. Such an enzyme is useful in an assay method for a fatty acid component in a sample, which fatty acid is originally present in the sample or is liberated from a fatty acid ester in the sample, comprising: (a) converting the fatty acid to acyl-CoA; (b) converting the thus-produced acyl-CoA to dehydroacyl-CoA; (c) converting the thus-produced dehydroacyl-CoA to hydroxyacyl-CoA; (d) converting the thus-produced hydroxyacyl-CoA to ketoacyl-CoA; (e) converting the thus-produced ketoacyl-CoA to acyl-CoA; and measuring the detectable changes in the reaction mixture. A composition suitable for such lipid assay comprises ATP or GTP, CoASH, NAD, acyl-CoA synthetase activity, acyl-CoA oxidase activity, enoyl-CoA hydratase activity, 3-hydroxyacyl-CoA dehydrogenase activity, and 3-ketoacyl-CoA thiolase activity, wherein the last three activities are supplied by the new multi-active enzyme.
    • 18. 发明专利
    • FR2508487B1
    • 1986-06-27
    • FR8211073
    • 1982-06-24
    • TOYO JOZO KK
    • IMAMURA SHIGEYUKIMISAKI HIDEOISHIKAWA HIDEHIKOMATSUURA KAZUO
    • C12N9/02C12N9/10C12N9/88C12Q1/25C12Q1/26
    • An enzyme having enoyl-CoA hydratase activity, 3-hydroxyacyl-CoA dehydrogenase activity and 3-ketoacyl-CoA thiolase activity, all in the same enzyme, is produced by culturing the microorganism strain Pseudomonas fragi B-0771 FERM-P No. 5701, and isolating the enzyme thus produced from the culture medium. Such an enzyme is useful in an assay method for a fatty acid component in a sample, which fatty acid is originally present in the sample or is liberated from a fatty acid ester in the sample, comprising: (a) converting the fatty acid to acyl-CoA; (b) converting the thus-produced acyl-CoA to dehydroacyl-CoA; (c) converting the thus-produced dehydroacyl-CoA to hydroxyacyl-CoA; (d) converting the thus-produced hydroxyacyl-CoA to ketoacyl-CoA; (e) converting the thus-produced ketoacyl-CoA to acyl-CoA; and measuring the detectable changes in the reaction mixture. A composition suitable for such lipid assay comprises ATP or GTP, CoASH, NAD, acyl-CoA synthetase activity, acyl-CoA oxidase activity, enoyl-CoA hydratase activity, 3-hydroxyacyl-CoA dehydrogenase activity, and 3-ketoacyl-CoA thiolase activity, wherein the last three activities are supplied by the new multi-active enzyme.