Underwood S A, Buszko M L, Shanmugam K T, Ingram L O
Institute of Food and Agricultural Sciences, Department of Microbiology and Cell Science, University of Florida, Gainesville, FL 32611, USA.
Appl Environ Microbiol. 2002 Mar;68(3):1071-81. doi: 10.1128/AEM.68.3.1071-1081.2002.
Previous studies have shown that high levels of complex nutrients (Luria broth or 5% corn steep liquor) were necessary for rapid ethanol production by the ethanologenic strain Escherichia coli KO11. Although this strain is prototrophic, cell density and ethanol production remained low in mineral salts media (10% xylose) unless complex nutrients were added. The basis for this nutrient requirement was identified as a regulatory problem created by metabolic engineering of an ethanol pathway. Cells must partition pyruvate between competing needs for biosynthesis and regeneration of NAD(+). Expression of low-K(m) Zymomonas mobilis pdc (pyruvate decarboxylase) in KO11 reduced the flow of pyruvate carbon into native fermentation pathways as desired, but it also restricted the flow of carbon skeletons into the 2-ketoglutarate arm of the tricarboxylic acid pathway (biosynthesis). In mineral salts medium containing 1% corn steep liquor and 10% xylose, the detrimental effect of metabolic engineering was substantially reduced by addition of pyruvate. A similar benefit was also observed when acetaldehyde, 2-ketoglutarate, or glutamate was added. In E. coli, citrate synthase links the cellular abundance of NADH to the supply of 2-ketoglutarate for glutamate biosynthesis. This enzyme is allosterically regulated and inhibited by high NADH concentrations. In addition, citrate synthase catalyzes the first committed step in 2-ketoglutarate synthesis. Oxidation of NADH by added acetaldehyde (or pyruvate) would be expected to increase the activity of E. coli citrate synthase and direct more carbon into 2-ketoglutarate, and this may explain the stimulation of growth. This hypothesis was tested, in part, by cloning the Bacillus subtilis citZ gene encoding an NADH-insensitive citrate synthase. Expression of recombinant citZ in KO11 was accompanied by increases in cell growth and ethanol production, which substantially reduced the need for complex nutrients.
先前的研究表明,高水平的复合营养物质(鲁氏肉汤或5%玉米浆)对于产乙醇菌株大肠杆菌KO11快速生产乙醇是必需的。尽管该菌株是原养型的,但在矿物盐培养基(10%木糖)中,除非添加复合营养物质,细胞密度和乙醇产量仍然很低。这种营养需求的基础被确定为乙醇途径代谢工程产生的一个调控问题。细胞必须在生物合成和NAD⁺再生的竞争需求之间分配丙酮酸。在KO11中表达低Kₘ的运动发酵单胞菌pdc(丙酮酸脱羧酶)按预期减少了丙酮酸碳进入天然发酵途径的流量,但同时也限制了碳骨架进入三羧酸途径(生物合成)的2-酮戊二酸分支。在含有1%玉米浆和10%木糖的矿物盐培养基中,添加丙酮酸可大幅降低代谢工程的有害影响。添加乙醛、2-酮戊二酸或谷氨酸时也观察到了类似的益处。在大肠杆菌中,柠檬酸合酶将细胞内NADH的丰度与用于谷氨酸生物合成的2-酮戊二酸供应联系起来。该酶受到变构调节,高浓度NADH会抑制它。此外,柠檬酸合酶催化2-酮戊二酸合成中的第一个关键步骤。添加的乙醛(或丙酮酸)对NADH的氧化预计会增加大肠杆菌柠檬酸合酶的活性,并将更多碳导向2-酮戊二酸,这可能解释了对生长的刺激作用。通过克隆编码对NADH不敏感的柠檬酸合酶的枯草芽孢杆菌citZ基因,对这一假设进行了部分验证。在KO11中表达重组citZ伴随着细胞生长和乙醇产量的增加,这大大减少了对复合营养物质的需求。