School of Marine and Bioengineering, Yancheng Institute of Technology, Yancheng 224051, PR China.
School of Marine and Bioengineering, Yancheng Institute of Technology, Yancheng 224051, PR China; State Key Laboratory of Materials-Oriented Chemical Engineering, College of Food Science and Light Industry, Nanjing Tech University, Nanjing 211816, PR China.
Bioresour Technol. 2018 Aug;261:272-278. doi: 10.1016/j.biortech.2018.04.036. Epub 2018 Apr 11.
The present study describes the use of metabolic engineering to achieve the production of R,R-2,3-butanediol (R,R-2,3-BD) of ultra-high optical purity (>99.99%). To this end, the diacetyl reductase (DAR) gene (dud A) of Paenibacillus polymyxa ZJ-9 was knocked out via homologous recombination between the genome and the previously constructed targeting vector pRN5101-L'C in a process based on homologous single-crossover. PCR verification confirmed the successful isolation of the dud A gene disruption mutant P. polymyxa ZJ-9-△dud A. Moreover, fermentation results indicated that the optical purity of R,R-2,3-BD increased from about 98% to over 99.99%, with a titer of 21.62 g/L in Erlenmeyer flasks. The latter was further increased to 25.88 g/L by fed-batch fermentation in a 5-L bioreactor.
本研究描述了利用代谢工程实现超高光学纯度 (>99.99%)的 R,R-2,3-丁二醇 (R,R-2,3-BD) 的生产。为此,通过基因组与先前构建的靶向载体 pRN5101-L'C 之间的同源单交换,敲除了多粘类芽孢杆菌 ZJ-9 的二乙酰还原酶 (DAR) 基因 (dud A)。PCR 验证证实成功分离了 dud A 基因敲除突变体 P. polymyxa ZJ-9-△dud A。此外,发酵结果表明,R,R-2,3-BD 的光学纯度从约 98%提高到 99.99%以上,在摇瓶中的产量为 21.62 g/L。通过在 5 L 生物反应器中进行分批补料发酵,后者进一步提高到 25.88 g/L。