Isar Jasmine, Agarwal Lata, Saran Saurabh, Gupta Pritesh, Saxena Rajendra Kumar
Department of Microbiology, University of Delhi South Campus, New Delhi, India.
Can J Microbiol. 2006 Sep;52(9):893-902. doi: 10.1139/w06-034.
The effect of process optimization on succinic acid production by Escherichia coli W3110 and on enzymes involved in the reverse tricarboxylic acid cycle was studied. Approximately, 7.02 g L-1 of succinic acid was produced in 60 h at pH 7.0 in 500 mL anaerobic bottles containing 300 mL of the medium, wherein the sucrose concentration was 2.5%, the ratio of tryptone to ammonium hydrogen phosphate was 1:1, and the concentration of magnesium carbon ate was 1.5%. When these optimized fermentation conditions were employed in a 10 L bioreactor, 11.2 g L-1 of succinic acid was produced in 48 h. This is a 10-fold increase in succinic acid production from the initial titer of 0.94 g L-1. This clearly indicates the importance of process optimization, where by manipulating the media composition and production conditions, a remarkable increase in the production of the desired biomolecule can be obtained. The production of succinic acid is a multi-step reaction through the reverse tricarboxylic acid cycle. A linear relationship was observed between succinic acid production and the enzyme activities. The enzyme activities were found to increase in the order phospho-enol-pyruvate carboxylase<malate dehydrogenase<fumarase<fumarate reductase. The activity of phospho-enol-pyruvate carboxykinase was also estimated. Results indicate that this enzyme was not a very active participant in the production of succinic acid, since it catalyzes the phosphorylation of oxaloacetic acid to yield phospho-enol-pyruvate.
研究了工艺优化对大肠杆菌W3110琥珀酸产量以及参与反向三羧酸循环的酶的影响。在含有300 mL培养基的500 mL厌氧瓶中,于pH 7.0条件下培养60 h,大约产生了7.02 g L-1的琥珀酸,其中蔗糖浓度为2.5%,胰蛋白胨与磷酸氢铵的比例为1:1,碳酸镁浓度为1.5%。当在10 L生物反应器中采用这些优化的发酵条件时,48 h内产生了11.2 g L-1的琥珀酸。这是从初始滴度0.94 g L-1的琥珀酸产量增加了约10倍。这清楚地表明了工艺优化的重要性,即通过控制培养基组成和生产条件,可以显著提高所需生物分子的产量。琥珀酸的产生是通过反向三羧酸循环的多步反应。观察到琥珀酸产量与酶活性之间存在线性关系。发现酶活性按磷酸烯醇丙酮酸羧化酶<苹果酸脱氢酶<延胡索酸酶<延胡索酸还原酶的顺序增加。还估计了磷酸烯醇丙酮酸羧激酶的活性。结果表明,该酶在琥珀酸产生过程中不是非常活跃的参与者,因为它催化草酰乙酸磷酸化生成磷酸烯醇丙酮酸。