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析因设计在优化肺炎克雷伯菌AS-22产环糊精糖基转移酶中的应用。

Application of factorial designs for optimization of cyclodextrin glycosyltransferase production from Klebsiella pneumoniae pneumoniae AS-22.

作者信息

Gawande B N, Patkar A Y

机构信息

Chemical Engineering Division, National Chemical Laboratory, Pune 411 008, India.

出版信息

Biotechnol Bioeng. 1999 Jul 20;64(2):168-73.

Abstract

Production of cyclodextrin glycosyltransferase (CGTase) from Klebsiella pneumoniae pneumoniae AS-22 was optimized in shake flasks using a statistical experimental design approach. Effect of various components in the basal medium, like carbon, nitrogen, phosphorus, and mineral sources as well as initial pH and temperature, were tested on enzyme production. The optimum concentrations of the selected media components were determined using statistical experimental designs. Two level fractional factorial designs in five variables, namely, dextrin, peptone, yeast extract, ammonium dihydrogen orthophosphate, and magnesium sulphate concentrations were constructed. The optimum medium composition thus found consisted of 49.3 g/L dextrin, 20.6 g/L peptone, 18.3 g/L yeast extract, 6.7 g/L ammonium dihydrogen orthophosphate, and 0.5 g/L magnesium sulphate. The maximum CGTase activity obtained was 21.4 U/mL in 28 h of incubation. The cell growth and CGTase production profiles were studied with the optimized medium in shake flasks and in 1-L fermenters. It was observed that the enzyme production was growth associated both in shake flask and in fermenter, although it was slower in shake flask. The maximum CGTase activity obtained in the fermenter was 32.5 U/mL in 16 h. The optimized medium resulted in about 9-fold increase in the enzyme activity as compared to that obtained in the basal medium in shake flask as well as in fermenter.

摘要

采用统计实验设计方法,在摇瓶中对肺炎克雷伯菌肺炎亚种AS-22产环糊精糖基转移酶(CGTase)的条件进行了优化。测试了基础培养基中各种成分,如碳源、氮源、磷源、矿物质来源以及初始pH值和温度对酶产量的影响。使用统计实验设计确定所选培养基成分的最佳浓度。构建了五个变量的两水平部分因子设计,这五个变量分别是糊精、蛋白胨、酵母提取物、磷酸二氢铵和硫酸镁的浓度。由此发现的最佳培养基组成包括49.3 g/L糊精、20.6 g/L蛋白胨、18.3 g/L酵母提取物、6.7 g/L磷酸二氢铵和0.5 g/L硫酸镁。在培养28 h时获得的最大CGTase活性为21.4 U/mL。在摇瓶和1-L发酵罐中使用优化后的培养基研究了细胞生长和CGTase产生情况。观察到,无论是在摇瓶还是在发酵罐中,酶的产生都与细胞生长相关,尽管在摇瓶中速度较慢。在发酵罐中16 h时获得的最大CGTase活性为32.5 U/mL。与在摇瓶和发酵罐的基础培养基中获得的酶活性相比,优化后的培养基使酶活性提高了约9倍。

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