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Methods for obtaining active mutanase preparations from Paenibacillus curdlanolyticus

机译:从解脂巴氏芽孢杆菌获得活性诱变酶制剂的方法

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The strain Paenibacillus curdlanolyticus MP-1 was used to obtain mutan-hydrolyzing enzymes. Different methods of precipitation and concentration of the post culture liquid were tested. All these methods produced satisfactory results in regard to the overall activity of mutanase and yielded active preparations of the enzyme. The best precipitation was obtained with propanol -98% of the initial enzyme activity was preserved with a purification of 2-fold. Salting out with ammonium sulfate at 50% saturation gave mutanase recovery of 77% and a purification of around 2-fold. Ultrafiltration yielded an about 10-fold concentrated preparation of the enzyme with a yield of 98%. Lyophilization and concentration of the culture broth (in the range from 5 to 20 times) in a vacuum evaporator yielded active crude preparations with mutanase recovery of 97%.
机译:用枯草芽孢杆菌MP-1菌株获得水解穆坦的酶。测试了不同的沉淀方法和后培养液浓度。所有这些方法均在诱变酶的总体活性方面产生了令人满意的结果,并产生了该酶的活性制剂。用丙醇可获得最佳沉淀-原始酶活性的98%保留2倍纯化。用饱和度为50%的硫酸铵盐析,可得到77%的突变酶回收率和约2倍的纯化率。超滤产生酶的约10倍浓缩制剂,产率为98%。在真空蒸发器中冻干和浓缩培养液(5至20倍)可得到活性粗制物,其诱变酶的回收率为97%。

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