Duan Peifeng, You Jiajia, Xu Meijuan, Yang Taowei, Shao Minglong, Zhang Xian, Rao Zhiming
Key Laboratory of Industrial Biotechnology of Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi 214122, Jiangsu, China.
Sheng Wu Gong Cheng Xue Bao. 2020 Sep 25;36(9):1918-1928. doi: 10.13345/j.cjb.190588.
2-O-α-D-glu-copyranosyl-sn-glycerol is a high value-added product with prospective application in food, cosmetics, health products and pharmaceutical industries. However, industrial scale of 2-O-α-D-glu-copyranosyl-sn-glycerol has not yet been applied in China, and there are few related reports on 2-O-α-D-glu-copyranosyl-sn-glycerol synthesis. The purpose of this experiment is to develop a method for catalyzing the synthesis of food-grade 2-O-α-D-glu-copyranosyl-sn-glycerol using whole cells of "Generally Recognized as Safe" (GRAS) recombinant Bacillus subtilis. In our work, a recombinant B. subtilis 168/pMA5-gtfA that heterologously expressing Leuconostoc mesenteroides sucrose phosphorylase was constructed and used as a whole-cell catalyst to synthesize 2-O-α-D-glu-copyranosyl-sn-glycerol. Optimizing the culture temperature, time and whole cell transformation conditions has increased the yield of 2-O-α-D-glu-copyranosyl-sn-glycerol. The results showed that 1.43 U/mL of sucrose phosphorylase was achieved in B. subtilis 168/pMA5-gtfA after culturing for 20 h at 30 °C in fermentation medium. The highest conversion rate reached 75.1%, and the yield of 2-O-α-D-glu-copyranosyl-sn-glycerol was 189.3 g/L with an average transformation rate of 15.6 mmol/(L·h) after 48 hours whole-cell transformation with the sucrose concentration of 1 mol/L and the glycerol concentration of 2.5 mol/L at 30 °C, OD₆₀₀ 40 and pH 7.0. This is the highest yield of 2-O-α-D-glu-copyranosyl-sn-glycerol synthesized catalytically by recombinant B. subtilis that was ever reported, and this study provides the theoretical and experimental basis for the industrial production and application of 2-O-α-D-glucopyranosyl-sn-glycerol.
2-O-α-D-吡喃葡萄糖基-sn-甘油是一种具有高附加值的产品,在食品、化妆品、保健品和制药行业具有潜在应用价值。然而,2-O-α-D-吡喃葡萄糖基-sn-甘油的工业化规模在中国尚未得到应用,关于其合成的相关报道也很少。本实验的目的是开发一种利用“一般认为安全”(GRAS)重组枯草芽孢杆菌全细胞催化合成食品级2-O-α-D-吡喃葡萄糖基-sn-甘油的方法。在我们的工作中,构建了异源表达肠膜明串珠菌蔗糖磷酸化酶的重组枯草芽孢杆菌168/pMA5-gtfA,并将其用作全细胞催化剂来合成2-O-α-D-吡喃葡萄糖基-sn-甘油。通过优化培养温度、时间和全细胞转化条件,提高了2-O-α-D-吡喃葡萄糖基-sn-甘油的产量。结果表明,在发酵培养基中于30℃培养20小时后,枯草芽孢杆菌168/pMA5-gtfA中蔗糖磷酸化酶的活性达到1.43 U/mL。在30℃、OD₆₀₀为40、pH为7.0的条件下,以1 mol/L的蔗糖浓度和2.5 mol/L的甘油浓度进行48小时全细胞转化后,最高转化率达到75.1%,2-O-α-D-吡喃葡萄糖基-sn-甘油的产量为189.3 g/L,平均转化速率为15.6 mmol/(L·h)。这是迄今为止报道的重组枯草芽孢杆菌催化合成2-O-α-D-吡喃葡萄糖基-sn-甘油的最高产量,本研究为2-O-α-D-吡喃葡萄糖基-sn-甘油的工业化生产和应用提供了理论和实验依据。