Production of Milk-Clotting Protease from Bacillus subtilis

被引:24
|
作者
Dutt, Kakoli [1 ]
Gupta, Pritesh [1 ]
Saran, Saurabh [1 ]
Misra, Swati [1 ]
Saxena, Rajendra Kumar [1 ]
机构
[1] Univ Delhi, Dept Microbiol, New Delhi 110021, India
关键词
Milk clotting protease; Response surface methodology; Solid-state fermentation; Biphasic system; ALKALINE PROTEASE; CULTURE-CONDITIONS; ENZYME; OPTIMIZATION; ENHANCEMENT;
D O I
10.1007/s12010-008-8504-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
An indigenous Bacillus subtilis strain isolated from soil was found to be a potent milk-clotting protease (mcp) producer. Production optimized using response surface methodology (RSM) yielded 1,190 U/ml of enzyme in medium containing 6% fructose, 1% casein, 0.3% NH4NO3, 10 MM CaCl2, pH 6.0 and inoculated with 3% inoculuill and incubated at 250 rpm for 72 h. Solid-state fermentation resulted in 1,080 and 952.3 U/gds of milk-clotting protease using soybean meal and rice bran, respectively, with higher proteolytic values of 18.97 and 9.1 IU/gds. Production in a biphasic system using an overlay of RSM-optimized medium on solid layer of 6% fructose and 1% casein with 1.5% agar resulted in significant enzyme production. Maximum mcp was obtained using a biphasic system where solid: liquid ratio of 3.0 resulted in a final yield of 1,276.65 U/ml with a yield index of 1.80 as compared to static liquid culture. However, significant increase or difference was noted as compared to yield obtained after RSM. This is the first report on the use of RSM for production of mcp from a bacterial species.
引用
收藏
页码:761 / 772
页数:12
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