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    • 34. 发明授权
    • Bacillus strains which produce HMG-CoA reductase inhibitors
    • 产生HMG-CoA还原酶抑制剂的芽孢杆菌菌株
    • US06468780B2
    • 2002-10-22
    • US09829080
    • 2001-04-10
    • Yutaka TakanoMasaru HasegawaHideo MoriKatsuhiko AndoKeiko OchiaiHiroaki MotoyamaAkio Ozaki
    • Yutaka TakanoMasaru HasegawaHideo MoriKatsuhiko AndoKeiko OchiaiHiroaki MotoyamaAkio Ozaki
    • C12N120
    • C12R1/07C12P7/62C12P17/06
    • Disclosed is a process for producing a compound represented by general formula (II-a): (wherein R1 represents a hydrogen atom, a substituted or unsubstituted alkyl group, or an alkali metal; and R2 represents a substituted or unsubstituted alkyl or aryl group) [hereinafter referred to as Compound (II-a)] or the lactone form of Compound (II-a) [hereinafter referred to as Compound (II-b)] which comprises subjecting a compound represented by general formula (I-a): (wherein R1 represents a hydrogen atom, a substituted or unsubstituted alkyl group, or an alkali metal; and R2 represents a substituted or unsubstituted alkyl or aryl group) [hereinafter referred to as Compound (I-a)] or the lactone form of Compound (I-a) [hereinafter referred to as Compound (I-b)] to the action of an enzyme source derived from a microorganism belonging to the genus Bacillus and capable of converting Compound (I-a) or Compound (I-b) into Compound (II-a) or Compound (II-b) in a reaction mixture to form Compound (II-a) or Compound (II-b) in the reaction mixture, and recovering Compound (II-a) or Compound (II-b) from the reaction mixture.
    • 公开了一种制备由通式(II-a)表示的化合物的方法:其中R 1表示氢原子,取代或未取代的烷基或碱金属; R 2表示取代或未取代的烷基或芳基) [化学式(II-a)]或化合物(II-a)的内酯形式[以下称为化合物(II-b)]] [其中包括使通式(Ia)表示的化合物 R1表示氢原子,取代或未取代的烷基或碱金属; R2表示取代或未取代的烷基或芳基)[以下称为化合物(Ia)]或化合物(Ia)的内酯形式[ (Ia)或化合物(Ib)转化为化合物(II-a)或化合物(II-a)的酶源的作用,以下称为化合物(Ib) b)在反应混合物中形成化合物(II -a)或化合物(II-b),并从反应混合物中回收化合物(II-a)或化合物(II-b)。
    • 36. 发明授权
    • Process for producing trans-4-hydroxy-L-proline
    • 制备反式-4-羟基-L-脯氨酸的方法
    • US06242231B1
    • 2001-06-05
    • US09104382
    • 1998-06-25
    • Akio OzakiHideo MoriTakeshi ShibasakiKatsuhiko AndoShigeru Chiba
    • Akio OzakiHideo MoriTakeshi ShibasakiKatsuhiko AndoShigeru Chiba
    • C12N902
    • C12N9/0071C12P13/24C12Y114/11002
    • An industrially applicable process for producing trans-4-hydroxy-L-proline, which is useful as a raw material for medicines or as an additive to foods. In the process, L-proline is converted into trans-4-hydroxy-L-proline in the presence of an enzyme source which is derived from a microorganism belonging to the genus Dactylosporangium, Amycolatopsis or Streptomyces and which catalyzes the hydroxylation of L-proline into trans-4-hydroxy-L-proline, a divalent iron ion and 2-ketoglutaric acid, in an aqueous medium, and the produced trans-4-hydroxy-L-proline is collected from the aqueous medium. Also provided is a novel enzyme L-proline-4-hydroxylase which is useful for the process, a gene of L-proline-4-hydroxylase which is useful for the process, a transformant containing the gene, and a process for producing L-proline-4-hydroxylase using the transformant. In addition, provided is a process for producing L-proline-4-hydroxylase using the transformant which contains the gene and has a reinforced proline biosynthesis activity.
    • 用于生产反式-4-羟基-L-脯氨酸的工业上适用的方法,其可用作药物的原料或作为食品的添加剂。 在此过程中,L-脯氨酸在衍生自属于Dactylosporangium,Amycolatopsis或Streptomyces属的微生物的酶源的存在下转化成反式-4-羟基-L-脯氨酸,其催化L-脯氨酸的羟基化 在水性介质中转化成反式-4-羟基-L-脯氨酸,二价铁离子和2-酮戊二酸,从水性介质中收集生成的反式-4-羟基-L-脯氨酸。 还提供了可用于该方法的新型L-脯氨酸-4-羟化酶,可用于该方法的L-脯氨酸-4-羟化酶的基因,含有该基因的转化体的基因, 脯氨酸-4-羟化酶。 此外,提供了使用含有该基因并具有增强的脯氨酸生物合成活性的转化体生产L-脯氨酸-4-羟化酶的方法。
    • 37. 发明授权
    • Method for quantitative determination of 1,5-anhydroglucitol
    • 1,5-脱水葡萄糖醇定量测定方法
    • US6153419A
    • 2000-11-28
    • US930709
    • 1997-10-16
    • Kazuo AisakaSakae TazoeKatsuhiko AndoKeiko Ochiai
    • Kazuo AisakaSakae TazoeKatsuhiko AndoKeiko Ochiai
    • C12N9/24C12Q1/34C12Q1/48
    • C12Q1/34C12N9/2402C12Q1/48C12Y302/01028G01N2333/355G01N2333/924Y10S435/872
    • The present invention relates to a method for quantitative determination of 1,5-anhydroglucitol in a sample, which comprises mixing the sample and an enzyme having activity that is inhibited by 1,5-anhydroglucitol in a concentration-dependent manner, and measuring the activity of the enzyme; and a reagent for quantitative determination of 1,5-anhydroglucitol which comprises an enzyme having activity that is inhibited by 1,5-anhydroglucitol in a concentration-dependent manner, a substrate for the enzyme, and a reagent for quantitative determination of a product formed by the enzyme activity. The present invention also relates to novel trehalase having a Ki value of 0.33 mM or less for 1,5-anhydroglucitol; and a process for producing novel trehalase having the above-mentioned physicochemical properties, which comprises culturing in a medium a microorganism belonging to the genus Nocardia and capable of producing the trehalase, and recovering the trehalase from the culture.
    • PCT No.PCT / JP97 / 00440 Sec。 371日期:1997年10月16日 102(e)1997年10月16日PCT PCT 1997年2月19日PCT公布。 公开号WO97 / 31103 日期:1997年8月28日本发明涉及一种样品中1,5-脱水葡萄糖醇的定量测定方法,该方法包括以浓度依赖性方式将样品与具有1,5-脱水葡萄糖醇抑制活性的酶 ,并测定酶的活性; 以及用于定量测定1,5-脱水葡萄糖醇的试剂,该试剂含有以浓度依赖性方式被1,5-脱水葡萄糖醇抑制的活性的酶,酶底物和定量产物形成试剂 通过酶活性。 本发明还涉及1,5-脱水葡萄糖醇的Ki值为0.33mM以下的新型海藻糖酶; 以及具有上述物理化学性质的新型海藻糖酶的制造方法,其包括在培养基中培养属于诺卡氏菌属的微生物并能够生产海藻糖酶,并从培养物中回收海藻糖酶的方法。