Literature DB >> 17914859

Medium optimization for the production of recombinant nattokinase by Bacillus subtilis using response surface methodology.

Po Ting Chen1, Chung-Jen Chiang, Yun-Peng Chao.   

Abstract

Nattokinase is a potent fibrinolytic enzyme with the potential for fighting cardiovascular diseases. Most recently, a new Bacillus subtilis/Escherichia coli (B. subtilis/E. coli) shuttle vector has been developed to achieve stable production of recombinant nattokinase in B. subtilis (Chen; et al. 2007, 23, 808-813). With this developed B. subtilis strain, the design of an optimum but cost-effective medium for high-level production of recombinant nattokinase was attempted by using response surface methodology. On the basis of the Plackett-Burman design, three critical medium components were selected. Subsequently, the optimum combination of selected factors was investigated by the Box-Behnken design. As a result, it gave the predicted maximum production of recombinant nattokinase with 71 500 CU/mL for shake-flask cultures when the concentrations of soybean hydrolysate, potassium phosphate, and calcium chloride in medium were at 6.100, 0.415, and 0.015%, respectively. This was further verified by a duplicated experiment. Moreover, the production scheme based on the optimum medium was scaled up in a fermenter. The batch fermentation of 3 L was carried out by controlling the condition at 37 degrees C and dissolved oxygen reaching 20% of air saturation level while the fermentation pH was initially set at 8.5. Without the need for controlling the broth pH, recombinant nattokinase production with a yield of 77 400 CU/mL (corresponding to 560 mg/L) could be obtained in the culture broth within 24 h. In particular, the recombinant B. subtilis strain was found fully stable at the end of fermentation when grown on the optimum medium. Overall, it indicates the success of this experimental design approach in formulating a simple and cost-effective medium, which provides the developed strain with sufficient nutrient supplements for stable and high-level production of recombinant nattokinase in a fermenter.

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Year:  2007        PMID: 17914859     DOI: 10.1021/bp070109b

Source DB:  PubMed          Journal:  Biotechnol Prog        ISSN: 1520-6033


  4 in total

1.  Optimization of Douchi fibrinolytic enzyme production by statistical experimental methods.

Authors:  Xu Zhang; Luo-Jia Yun; Liang-Bin Peng; Yi Lu; Kun-Peng Ma; Fei Tang
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2013-02-08

2.  Efficient expression of nattokinase in Bacillus licheniformis: host strain construction and signal peptide optimization.

Authors:  Xuetuan Wei; Yinhua Zhou; Jingbang Chen; Dongbo Cai; Dan Wang; Gaofu Qi; Shouwen Chen
Journal:  J Ind Microbiol Biotechnol       Date:  2014-12-05       Impact factor: 3.346

Review 3.  Nattokinase: An Oral Antithrombotic Agent for the Prevention of Cardiovascular Disease.

Authors:  Yunqi Weng; Jian Yao; Sawyer Sparks; Kevin Yueju Wang
Journal:  Int J Mol Sci       Date:  2017-02-28       Impact factor: 5.923

Review 4.  The potential role of ischaemia-reperfusion injury in chronic, relapsing diseases such as rheumatoid arthritis, Long COVID, and ME/CFS: evidence, mechanisms, and therapeutic implications.

Authors:  Douglas B Kell; Etheresia Pretorius
Journal:  Biochem J       Date:  2022-08-31       Impact factor: 3.766

  4 in total

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