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11 Bacillus subtilis EK11 strain and process for preparation of protopectinase using the same

机译:11枯草芽孢杆菌EK11菌株及其制备原果胶酶的方法

摘要

PURPOSE: A Bacillus subtilis EK11 strain and a method for producing protopectinase therefrom are provided, thereby the protopectinase can be mass-produced. CONSTITUTION: The Bacillus subtilis EK11 (KCTC 8986P) strain is isolated by the steps of: treating a mother strain, Bacillus subtilis IFO12113, with nitrosoguanidine for 40 minutes; spreading the mutant strain on an LB agar medium containing 1.5% of arabinogalactan; incubating it and first selecting a strain from colonies forming a transparent ring therearound; incubating the selected strain in a medium containing 1% of glucose, 0.2% of (NH4)2SO4, 1.4% of KH2PO4, 0.6% of K2HPO4, 0.1% of Na3-citrate2H2O, and 0.02% of MgSO4H2O; and second selecting a strain having a high protopectinase productivity by measuring the activity of protopectinase and identifying it as Bacillus subtilis EK11 (KCTC 8986P). The protopectinase is produced by incubating Bacillus subtilis EK11 (KCTC 8986P) in a medium containing 0.7% of corn starch, 0.3% of yeast extract, 1.4% of KH2PO4, 0.6% of K2HPO4, 0.02% of MgSO4 H2O and 0.1% of Na3-citrate2H2O.
机译:目的:提供枯草芽孢杆菌EK11菌株和由其产生原果胶酶的方法,从而可以大量生产原果胶酶。组成:枯草芽孢杆菌EK11(KCTC 8986P)菌株通过以下步骤分离:用亚硝基胍处理母菌株枯草芽孢杆菌IFO12113 40分钟;将突变菌株传播到含有1.5%阿拉伯半乳聚糖的LB琼脂培养基上;温育它,并首先从在其周围形成透明环的菌落中选择菌株;在含有1%的葡萄糖,0.2%的(NH4)2SO4、1.4%的KH2PO4、0.6%的K2HPO4、0.1%的Na3-柠檬酸盐2H2O和0.02%的MgSO4H2O的培养基中孵育所选菌株;其次,通过测量原果胶酶的活性并将其鉴定为枯草芽孢杆菌EK11(KCTC 8986P),选择具有高原果胶酶生产率的菌株。原果胶酶是通过将枯草芽孢杆菌EK11(KCTC 8986P)在含有0.7%玉米淀粉,0.3%酵母提取物,1.4%KH2PO4、0.6%K2HPO4、0.02%MgSO4 H2O和0.1%Na3-的培养基中孵育而产生的柠檬酸盐2 H 2O。

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