文献类型：期刊文献

英文题名：Enhancement of alkaline protease production in recombinant Bacillus licheniformis by response surface methodology

作者：Zhang, Ying[1];Hu, Jingmin[1];Zhang, Qing[2];Cai, Dongbo[2];Chen, Shouwen[2];Wang, Yonghong[1]

机构：[1]East China Univ Sci & Technol, State Key Lab Bioreactor Engn, 130 Meilong Rd,POB 329, Shanghai 20037, Peoples R China;[2]Hubei Univ, Microbial Technol Ctr Hubei Prov Coll Life Sci, State Key Lab Biocatalysis & Enzyme Engn Environm, Wuhan, Peoples R China

年份：2023

卷号：10

期号：1

外文期刊名：BIORESOURCES AND BIOPROCESSING

收录：;EI(收录号：20231814036554);WOS:【SCI-EXPANDED(收录号:WOS:000979057000001)】；

基金：This work was financially supported by the National Key Research Development Program of China (2021YFC2100205).

语种：英文

外文关键词：Alkaline protease; Recombinant Bacillus licheniformis; Medium optimization; Response surface methodology

摘要：Alkaline protease is widely used in the food, detergent, and pharmaceutical industries because of its comparatively great hydrolysis ability and alkali tolerance. To improve the ability of the recombinant Bacillus licheniformis to produce alkaline protease, single-factor experiments and response surface methodology (RSM) were utilized to determine and develop optimal culture conditions. The results showed that three factors (corn starch content, soybean meal content, and initial medium pH) had significant effects on alkaline protease production (P < 0.05), as determined through the Plackett-Burman design. The maximum enzyme activity was observed with an optimal medium composition by central composite design (CCD): corn starch, 92.3 g/L; soybean meal, 35.8 g/L; and initial medium pH, 9.58. Under these optimum conditions, the alkaline protease activity of strain BL10::aprE was 15,435.1 U/mL, 82% higher than that in the initial fermentation medium. To further investigate the application of the optimum fermentation medium, the overexpressed strain BL10::aprE/pHYaprE was cultured using the optimized medium to achieve an enzyme activity of 39,233.6 U/mL. The present study achieved the highest enzyme activity of alkaline protease by B. licheniformis at the shake-flask fermentation level, which has important application value for large-scale production.