食品科学

• 生物工程 • 上一篇    下一篇

纳豆激酶高产菌株的选育及固态发酵技术

张 杰1,葛武鹏1,*,陈 瑛2,张 悦3,刘李婷3   

  1. 1.西北农林科技大学食品科学与工程学院,陕西 杨凌 712100;2.陕西省质量技术监督局,陕西 西安 710068;
    3.陕西省产品质量监督检验研究院,陕西 西安 710068
  • 出版日期:2016-02-15 发布日期:2016-02-26

Strain Improvement of Bacillus subtilis for Enhanced Production of Nattokinase and Optimization of Solid-State Fermentation Conditions

ZHANG Jie1, GE Wupeng1,*, CHEN Ying2, ZHANG Yue3, LIU Liting3   

  1. 1. College of Food Science and Engineering, Northwest A&F University, Yangling 712100, China;
    2. Shaanxi Bureau of Quality and Technical Supervision, Xi’an 710068, China;
    3. Shaanxi Product Quality Supervision and Inspection Research Institute, Xi’an 710068, China
  • Online:2016-02-15 Published:2016-02-26

摘要:

以枯草芽孢杆菌为出发菌株,选用超声波和紫外线进行诱变处理,根据致死率、突变率与诱变剂量的关系选择合适的诱变剂量,以筛选高产纳豆激酶的优势菌株。实验表明:最佳诱变条件为:超声波45 kHz、280 W,时间60 min,紫外线照射距离30 cm,时间120 s。经多次初筛、复筛,选育出一株命名为BSCZ-4的优势菌株,其纳豆激酶酶活力为原始菌株的1.96 倍。对该菌种进行连续20 代培养,测得其溶解圈直径稳定在18~19 mm之间,表明该突变株遗传特性稳定。并采用Box-Behnken响应曲面法优化其固态发酵工艺条件,结果为:魔芋精粉添加量5%、接种量8%,34 ℃发酵24 h,纳豆激酶活力可达(4 087.83±93.75) U/g。

关键词: 诱变, 枯草芽孢杆菌, 响应面, 工艺

Abstract:

In this study, the nattokinase-producing capacity of Bacillus subtilis subsp. subtilis BS21076 was improved by
sequential mutagenization with ultrasonic followed by UV light at the appropriate doses determined according to death
and mutation rates. The optimal mutation conditions of strain BS21076 were established as 60 min ultrasonic treatment at
45 kHz and 280 W followed by 120 s UV irradiation at a distance of 30 cm. A high nattokinase-producing mutant strain
named BSCZ-4, producing 1.96 times higher nattokinase than BS21076, was obtained after several rounds of primary and
secondary screening. After 20 consecutive passages, the diameter of the zone of dissolution produced by BSCZ-4 remained
stable in the range of 18–19 mm, suggesting good genetic stability. Using Box-Behnken response surface methodology,
the optimal culture conditions for the enhanced production of nattokinase by BSCZ-4 in solid-state fermentation were
determined as addition of 5% konjac power to the culture medium, an inoculum size of 8%, and 24 h culture at 34 ℃,
resulting in a nattokinase activity of (4 087.83 ± 93.75) U/g.

Key words: mutation, Bacillus subtilis, response surface methodology, process

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