Lan Jie, Newman Elaine B
Biology Department, Concordia University, 1455 de Maisonneuve Avenue, Montreal, Quebec H3G 1M8, Canada.
Res Microbiol. 2003 Apr;154(3):191-7. doi: 10.1016/S0923-2508(03)00032-9.
Escherichia coli strains with mutations in 3 genes coding for redox functions--torA, nuoM and glpC--are able to grow with pyruvate as carbon source, but are not able to use a combination of serine, glycine and leucine as carbon source, unlike the parent strain which uses either. All three mutants are able to produce and activate L-serine deaminase (L-SD) when grown in glucose minimal medium, and thus should be able to convert serine to pyruvate and grow on it. We suggest that activation of L-SD involves specific chemical reactions, perhaps building an Fe-S cluster. Mutant cells can carry out the necessary reaction to activate L-SD when grown in glucose minimal medium but apparently cannot do so when grown in SGL medium.
在编码氧化还原功能的3个基因(torA、nuoM和glpC)中发生突变的大肠杆菌菌株能够以丙酮酸作为碳源生长,但不能使用丝氨酸、甘氨酸和亮氨酸的组合作为碳源,这与能使用其中任何一种的亲本菌株不同。当在葡萄糖基本培养基中生长时,所有这三个突变体都能够产生并激活L-丝氨酸脱氨酶(L-SD),因此应该能够将丝氨酸转化为丙酮酸并以此生长。我们认为L-SD的激活涉及特定的化学反应,也许是构建一个铁硫簇。突变细胞在葡萄糖基本培养基中生长时能够进行激活L-SD所需的反应,但在SGL培养基中生长时显然无法做到这一点。