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Optimization of fermentation conditions for surfactin production by B. subtilis YPS-32

莎梵婷 发酵 拉伤 食品科学 枯草芽孢杆菌 产量(工程) 谷氨酸 化学 生物 生物化学 细菌 材料科学 氨基酸 遗传学 解剖 冶金
作者
Yingjun Zhou,Xiaoxue Yang,Qing Li,Zheng Peng,Jianghua Li,Juan Zhang
出处
期刊:BMC Microbiology [BioMed Central]
卷期号:23 (1): 117-117 被引量:33
标识
DOI:10.1186/s12866-023-02838-5
摘要

Abstract Background Surfactin produced by microbial fermentation has attracted increasing attention because of its low toxicity and excellent antibacterial activity. However, its application is greatly limited by high production costs and low yield. Therefore, it is important to produce surfactin efficiently while reducing the cost. In this study, B . subtilis strain YPS-32 was used as a fermentative strain for the production of surfactin, and the medium and culture conditions for the fermentation of B . subtilis YPS-32 for surfactin production were optimized. Results First, Landy 1 medium was screened as the basal medium for surfactin production by B . subtilis strain YPS-32. Then, using single-factor optimization, the optimal carbon source for surfactin production by B . subtilis YPS-32 strain was determined to be molasses, nitrogen sources were glutamic acid and soybean meal, and inorganic salts were KCl, K 2 HPO 4 , MgSO 4 , and Fe 2 (SO 4 ) 3 . Subsequently, using Plackett-Burman design, MgSO 4 , time (h) and temperature (°C) were identified as the main effect factors. Finally, Box-Behnken design were performed on the main effect factors to obtain optimal fermentation conditions: temperature of 42.9 °C, time of 42.8 h, MgSO 4 = 0.4 g·L − 1 . This modified Landy medium was predicted to be an optimal fermentation medium: molasses 20 g·L − 1 , glutamic acid 15 g·L − 1 , soybean meal 4.5 g·L − 1 , KCl 0.375 g·L − 1 , K 2 HPO 4 0.5 g·L − 1 , Fe 2 (SO 4 ) 3 1.725 mg·L − 1 , MgSO 4 0.4 g·L − 1 . Using the modified Landy medium, the yield of surfactin reached 1.82 g·L − 1 at pH 5.0, 42.9 ℃, and 2% inoculum for 42.8 h, which was 2.27-fold higher than that of the Landy 1 medium in shake flask fermentation. Additionally, under these optimal process conditions, further fermentation was carried out at the 5 L fermenter level by foam reflux method, and at 42.8 h of fermentation, surfactin reached a maximum yield of 2.39 g·L − 1 , which was 2.96-fold higher than that of the Landy 1 medium in 5 L fermenter. Conclusion In this study, the fermentation process of surfactin production by B . subtilis YPS-32 was improved by using a combination of single-factor tests and response surface methodology for test optimization, which laid the foundation for its industrial development and application.
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