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Formation of glycosidases in batch and continuous culture of Bacteroides fragilis.

机译:分批和连续培养脆弱拟杆菌的糖苷酶的形成。

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Nine strains of bacteroides fragilis were cultivated in stirred fermentors and tested for their ability to produce glycosidases. B. fragilis subsp. vulgatus B70 was used for optimizing the production of glycosidases. The highest bacterial yield was obtained in proteose peptone-yeast extract medium. The optimum pH for maximal bacterial yield was 7.0, and the optimum temperature for growth was 37 degrees C. The formation of glycosidases was optimal between pH 6.5 and 7.5, and the optimum temperature for synthesis of glycosidases was between 33 and 37 degrees C. Culture under controlled conditions in fermentors gave more reproducible production of glycosidases than static cultures in bottles. The strain was also grown in continuous culture at a dilution rate of 0.1 liter/h at pH 7.0 and 37 degrees C with a yield of 2.0 mg of dry weight per ml in the complex medium. The formation of glycosidases remained constant during the entire continuous process.
机译:在搅拌的发酵罐中培养了九种脆弱类细菌,并测试了它们产生糖苷酶的能力。脆弱的B.亚种寻常型B70用于优化糖苷酶的生产。在蛋白p-酵母提取物培养基中获得最高的细菌产量。最大细菌产量的最佳pH为7.0,最适生长温度为37摄氏度。糖苷酶的形成在pH 6.5至7.5之间最佳,糖苷酶合成的最佳温度在33至37摄氏度之间。在受控条件下,发酵罐中的糖苷酶生产要比瓶中的静态培养物重现。菌株还以0.1升/小时的稀释率在pH 7.0和37摄氏度下以连续培养的方式生长,在复杂培养基中每毫升干重为2.0毫克。在整个连续过程中,糖苷酶的形成保持恒定。

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