Department of Microbiology and Cell Science and Department of Immunology and Medical Microbiology, University of Florida, Gainesville, Florida 32611.
Appl Environ Microbiol. 1988 Feb;54(2):397-404. doi: 10.1128/aem.54.2.397-404.1988.
The expression of Zymomonas mobilis genes encoding pyruvate decarboxylase and alcohol dehydrogenase II in Escherichia coli converted this organism from the production of organic acids to the production of ethanol. Ethanol was produced during both anaerobic and aerobic growth. The extent to which these ethanologenic enzymes were expressed correlated with the extent of ethanol production. The replacement of organic acids with ethanol as a metabolic product during aerobic and anaerobic growth resulted in dramatic increases in final cell density, indicating that these acids (and the associated decline in pH) are more damaging than the production of ethanol. Of the plasmids examined, the best plasmid for growth and ethanol production expressed pyruvate decarboxylase and alcohol dehydrogenase II at levels of 6.5 and 2.5 IU/mg of total cell protein, respectively.
运动发酵单胞菌编码丙酮酸脱羧酶和醇脱氢酶 II 的基因在大肠杆菌中的表达使该生物从有机酸的生产转变为乙醇的生产。在厌氧和需氧生长过程中都产生了乙醇。这些乙醇生物合成酶的表达程度与乙醇产量的程度相关。在需氧和厌氧生长过程中,用乙醇代替有机酸作为代谢产物,最终细胞密度显著增加,表明这些酸(以及相关的 pH 值下降)比乙醇的产生更具破坏性。在所检查的质粒中,用于生长和乙醇生产的最佳质粒分别以 6.5 和 2.5 IU/mg 总细胞蛋白的水平表达丙酮酸脱羧酶和醇脱氢酶 II。