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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. M7 strain (FERM P-14835) 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 pH4.5 and 50°C, stably keeps its activity at pH4-10 and ≤50°C and has a molecular weight of about 160,000 by SDS-polyacrylamide gel electrophoresis. The activity of the enzyme is inhibited by mercury, silver and p-chloromercury benzoic acid. The enzyme exhibits extremely excellent plaque-removing effect even by the single use.;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M7菌株(FERM P-14835),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pH4.5和50°C的最佳工作条件下均可稳定地在pH4-10和≤50°C下保持活性,分子量为通过SDS-聚丙烯酰胺凝胶电泳可得到约160,000。汞,银和对氯汞苯甲酸会抑制酶的活性。即使一次使用,该酶也具有极好的去斑效果。; COPYRIGHT:(C)1996,JPO

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