Zheng Yu, Zhao Li, Zhang Jianguo, Zhang Haiyi, Ma Xingyuan, Wei Dongzhi
State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, PR China.
J Biosci Bioeng. 2008 May;105(5):508-12. doi: 10.1263/jbb.105.508.
As a valuable chemical, 1,3-propanediol (1,3-PD) could be biosynthesized by glycerol fermentation. However, no natural microorganisms that could directly convert glucose into 1,3-PD have been found so far. In this work, genes coding for two enzymes, glycerol-3-phosphate dehydrogenase (GPD, EC 1.1.1.8) and glycerol-3-phosphatase (GPP, EC 3.1.3.21), which were responsible for glycerol production, were organized into the plasmid pUC18K under control of the respective lac promoters. Two recombinant proteins were expressed successfully in wild-type Klebsiella pneumoniae. A glycerol concentration of 6.8 g l(-1) was obtained in flask culture. When glucose was exhausted, dihydroxyacetone was added and medium pH was adjusted to 7.0, and then a 1,3-PD concentration of 0.58 g l(-1) was achieved with engineered K. pneumoniae from glucose.
作为一种有价值的化学品,1,3 - 丙二醇(1,3 - PD)可通过甘油发酵生物合成。然而,目前尚未发现能直接将葡萄糖转化为1,3 - PD的天然微生物。在这项工作中,编码负责甘油生产的两种酶,即甘油 - 3 - 磷酸脱氢酶(GPD,EC 1.1.1.8)和甘油 - 3 - 磷酸酶(GPP,EC 3.1.3.21)的基因,在各自的lac启动子控制下被构建到质粒pUC18K中。两种重组蛋白在野生型肺炎克雷伯菌中成功表达。在摇瓶培养中获得了6.8 g l(-1)的甘油浓度。当葡萄糖耗尽时,添加二羟基丙酮并将培养基pH值调至7.0,然后利用工程化的肺炎克雷伯菌从葡萄糖中获得了0.58 g l(-1)的1,3 - PD浓度。