Ingram L O, Conway T, Clark D P, Sewell G W, Preston J F
Department of Microbiology and Cell Science, University of Florida, Gainesville 32611.
Appl Environ Microbiol. 1987 Oct;53(10):2420-5. doi: 10.1128/aem.53.10.2420-2425.1987.
The genes encoding essential enzymes of the fermentative pathway for ethanol production in Zymomonas mobilis, an obligately ethanologenic bacterium, were inserted into Escherichia coli under the control of a common promoter. Alcohol dehydrogenase II and pyruvate decarboxylase from Z. mobilis were expressed at high levels in E. coli, resulting in increased cell growth and the production of ethanol as the principal fermentation product from glucose. These results demonstrate that it is possible to change the fermentation products of an organism, such as E. coli, by the addition of genes encoding appropriate enzymes which form an alternative system for the regeneration of NAD+.
运动发酵单胞菌是一种专性产乙醇细菌,其编码乙醇发酵途径中必需酶的基因在一个共同启动子的控制下被插入到大肠杆菌中。运动发酵单胞菌的乙醇脱氢酶II和丙酮酸脱羧酶在大肠杆菌中高水平表达,导致细胞生长增加,并产生乙醇作为葡萄糖发酵的主要产物。这些结果表明,通过添加编码合适酶的基因来改变生物体(如大肠杆菌)的发酵产物是可能的,这些酶形成了一个用于NAD⁺再生的替代系统。