Ponce Elizabeth, García Mauricio, Muñoz Maria Enriqueta
Centro de Investigación Científica y de Educación Superior de Ensenada (CICESE), Dept. Of Marine Biotechnology, Km 107 Carretera Tijuana-Ensenada, C.P. 22860 Ensenada, B.C., Mexico.
Can J Microbiol. 2005 Nov;51(11):975-82. doi: 10.1139/w05-101.
The activity of the enzymes of the central metabolic pathways has been the subject of intensive analysis; however, the Entner-Doudoroff (ED) pathway has only recently begun to attract attention. The metabolic response to edd gene knockout in Escherichia coli JM101 and PTS- Glc+ was investigated in gluconate and glucose batch cultures and compared with other pyruvate kinase and PTS mutants previously constructed. Even though the specific growth rates between the strain carrying the edd gene knockout and its parent JM101 and PTS- Glc+ edd and its parent PTS- Glc+ were very similar, reproducible changes in the specific consumption rates and biomass yields were obtained when grown on glucose. These results support the participation of the ED pathway not only on gluconate metabolism but on other metabolic and biochemical processes in E. coli. Despite that gluconate is a non-PTS carbohydrate, the PTS- Glc+ and derived strains showed important reductions in the specific growth and gluconate consumption rates. Moreover, the overall activity of the ED pathway on gluconate resulted in important increments in PTS- Glc+ and PTS- Glc+ pykF mutants. Additional results obtained with the pykA pykF mutant indicate the important contribution of the pyruvate kinase enzymes to pyruvate synthesis and energy production in both carbon sources.
中心代谢途径中酶的活性一直是深入分析的对象;然而,Entner-Doudoroff(ED)途径直到最近才开始受到关注。在葡萄糖酸盐和葡萄糖分批培养中,研究了大肠杆菌JM101和PTS-Glc+中edd基因敲除后的代谢反应,并与先前构建的其他丙酮酸激酶和PTS突变体进行了比较。尽管携带edd基因敲除的菌株与其亲本JM101以及PTS-Glc+ edd与其亲本PTS-Glc+之间的比生长速率非常相似,但在以葡萄糖为碳源生长时,比消耗速率和生物量产量出现了可重复的变化。这些结果支持ED途径不仅参与葡萄糖酸盐代谢,还参与大肠杆菌中的其他代谢和生化过程。尽管葡萄糖酸盐是一种非PTS碳水化合物,但PTS-Glc+及其衍生菌株的比生长速率和葡萄糖酸盐消耗速率显著降低。此外,ED途径对葡萄糖酸盐的总体活性导致PTS-Glc+和PTS-Glc+ pykF突变体有显著增加。用pykA pykF突变体获得的其他结果表明,丙酮酸激酶酶在两种碳源中对丙酮酸合成和能量产生有重要贡献。