Monticello D J, Hadioetomo R S, Costilow R N
J Gen Microbiol. 1984 Feb;130(2):309-18. doi: 10.1099/00221287-130-2-309.
Preliminary studies demonstrated that Clostridium sporogenes synthesized isoleucine by a pathway not involving threonine or threonine dehydratase. Radiotracer experiments with cells grown in a defined carbohydrate-free medium showed that radioactivity from [U-14C]serine, [3-14C]pyruvate, [14C]NaHCO3 and [1-], [2-] and [3-14C]propionate was incorporated into isoleucine. Conversely, there was no detectable incorporation of 14C into isoleucine during growth with [U-14C]glutamate, [U-14C]threonine, [U-14C]valine, [U-14C]leucine or [U-14C]methionine. Crude extracts of the bacteria grown in a minimal medium contained levels of alpha-acetohydroxyacid synthase activities comparable to those in Escherichia coli K12 grown in minimal medium. Stepwise degradation of isoleucine obtained from C. sporogenes grown in the presence of specifically-labelled precursors indicated that C. sporogenes can make isoleucine via the reductive carboxylation of propionate to yield alpha-oxobutyrate, which is metabolized to isoleucine in the classical fashion. Isoleucine was also formed by C. sporogenes via the reductive carboxylation of alpha-methylbutyrate to alpha-oxo-beta-methylvalerate.
初步研究表明,生孢梭菌通过一条不涉及苏氨酸或苏氨酸脱水酶的途径合成异亮氨酸。对在限定的无碳水化合物培养基中生长的细胞进行的放射性示踪实验表明,来自[U-14C]丝氨酸、[3-14C]丙酮酸、[14C]碳酸氢钠以及[1-]、[2-]和[3-14C]丙酸的放射性被掺入到异亮氨酸中。相反,在用[U-14C]谷氨酸、[U-14C]苏氨酸、[U-14C]缬氨酸、[U-14C]亮氨酸或[U-14C]甲硫氨酸培养期间,未检测到14C掺入到异亮氨酸中。在基本培养基中生长的细菌的粗提取物中,α-乙酰乳酸合酶活性水平与在基本培养基中生长的大肠杆菌K12中的活性水平相当。对在存在特异性标记前体的情况下生长的生孢梭菌所获得的异亮氨酸进行逐步降解表明,生孢梭菌可通过丙酸还原羧化生成α-氧代丁酸,然后以经典方式将其代谢为异亮氨酸来合成异亮氨酸。生孢梭菌还可通过α-甲基丁酸还原羧化生成α-氧代-β-甲基戊酸来形成异亮氨酸。