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MUTANASE-PRODUCING MICROORGANISM AND MUTANASE

机译:产生诱变酶的微生物和诱变酶

摘要

PURPOSE: To obtain a new mutanase having excellent suppressing effect on the formation of dental plaque and sufficiently stably miscible to form a product of a composition for oral cavity application. ;CONSTITUTION: Bacillus sp. RM1 strain (FERM P-14836) is cultured and the objective mutanase is collected from the culture product. The mutanase has high activity to decompose the α-1,3-glucoside bond of mutan and optimum working condition of pH4 and 60°C, stably keeps its activity at pH4-10 and ≤60°C and has a molecular weight of about 150,000 by SDS-polyacrylamide gel electrophoresis. The activity of the enzyme is inhibited by mercury, silver, trivalent iron and p-chloromercury benzoic acid. A synergistic plaque-removing effect can be achieved by the combined use of the enzyme with dextranase.;COPYRIGHT: (C)1996,JPO
机译:用途:获得一种新型的变色酶,其对牙菌斑的形成具有极佳的抑制作用,并且具有足够的稳定性,可混溶以形成口腔用组合物的产品。 ;组成:芽孢杆菌培养RM1菌株(FERM P-14836),并从培养产物中收集目标突变酶。诱变酶具有很高的分解穆坦α-1,3-葡糖苷键的活性,在pH4和60°C的最佳工作条件下均可稳定地在pH4-10和≤60°C下保持活性,分子量约为150,000通过SDS-聚丙烯酰胺凝胶电泳。该酶的活性受到汞,银,三价铁和对氯汞苯甲酸的抑制。将该酶与葡聚糖酶联合使用可达到协同的去除斑块的作用。; COPYRIGHT:(C)1996,JPO

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