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纳豆激酶高活性菌株BN-05鉴定及发酵工艺优化
引用本文:王常苏,孙晓彤,余洁,高冰. 纳豆激酶高活性菌株BN-05鉴定及发酵工艺优化[J]. 中国酿造, 2014, 0(1): 91-95
作者姓名:王常苏  孙晓彤  余洁  高冰
作者单位:[1]武汉轻工大学生物与制药工程学院,湖北武汉430023 [2]武汉鑫宏食品酿造科研所,湖北武汉430051
摘    要:对分离的纳豆激酶高活性菌株BN-05进行了初步鉴定,并对其固态发酵产纳豆激酶的工艺条件进行了优化,旨在提高纳豆激酶的含量。通过形态和分子生物学鉴定BN-05为枯草芽孢杆菌属菌株,优化后发酵工艺参数:大豆破碎度为2,发酵温度为36℃,接种量为5.5%,葡萄糖添加量为2.5%。在优化条件下,BN-05通过固态发酵纳豆激酶活力达到(4 715.26±103.23)IU/g湿黄豆,比之前优化提高137%。

关 键 词:枯草芽孢杆菌属  纳豆激酶  固态发酵  酶活力

Identification of nattokinase high activity strain BN-05 and optimization of the fermentation technology
WANG Changsu,SUN Xiaotong,YU Jie,GAO Bing. Identification of nattokinase high activity strain BN-05 and optimization of the fermentation technology[J]. China Brewing, 2014, 0(1): 91-95
Authors:WANG Changsu  SUN Xiaotong  YU Jie  GAO Bing
Affiliation:1.Schnol of Biological and Pharmaceucal Engineenng, Wuhan Polytechnic University, Wuhan 430023, China; 2.Xinhong InsO'tute of Food and Brewing, Wuhan 430051, China)
Abstract:Nattokinase high activity strain BN-05 was preliminarily identified and the nattokinase prodution technology with solid-substrate fermenta- tion was optimized in order to improve the content of nattokinase. BN-05 was determined as Bacillus subtilis by morphological and molecular identi- fication. The optimum condition of technology was as follows: degree of soybean fragmentation 2, fermentation temperature 36~C, inoculum 5.5% and glucose addition 2.5 %. At the optimizing conditions, the activity of nattokinase fermented by BN-05 could reach (4 715.26 ~ 103.23 ) 1U/g (wet weight), which was 137% times of the former culture conditions.
Keywords:Bacillus subtilis  nattokinase  solid-substrate fermentation  enzyme activity
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