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大肠杆菌K12中甲硫氨酸生物合成的调控:对类似物抗性突变体的深入研究

Control of methionine biosynthesis in Escherichia coli K12: a closer study with analogue-resistant mutants.

作者信息

Chattopadhyay M K, Ghosh A K, Sengupta S

机构信息

Department of Applied Biochemistry, Indian Institute of Chemical Biology, Calcutta.

出版信息

J Gen Microbiol. 1991 Mar;137(3):685-91. doi: 10.1099/00221287-137-3-685.

Abstract

Control of methionine biosynthesis in Escherichia coli K12 was reinvestigated by using methionine-analogue-resistant mutants. Norleucine (NL) and alpha-methylmethionine (MM) were found to inhibit methionine biosynthesis directly whereas ethionine (Et) competitively inhibited methionine utilization. Adenosylation of Et to generate S-adenosylethionine (AdoEt) by cell-free enzyme from E. coli K12 was demonstrated. Tolerance of increasing concentrations of NL by E. coli K12 mutants is expressed serially as phenotypes NLR, NLREtR, NLRMMR and finally NLREtRMMR. All spontaneous NLR mutants had a metK mutation, whereas NTG-induced mutants had mutations in both the metK and metJ genes. The kinetics of methionine adenosylation by the E. coli K12 cell-free enzyme were found to be similar to those reported for the yeast enzyme, showing the typical lag phase at low methionine concentration and disappearance of this phase when AdoMet was included in the incubation mixture. NL extended the lag phase, and lowered the rate of subsequent methionine adenosylation, but did not affect the shortening of the lag phase of adenosylation by AdoMet.

摘要

通过使用抗甲硫氨酸类似物的突变体,对大肠杆菌K12中甲硫氨酸生物合成的调控进行了重新研究。发现正亮氨酸(NL)和α-甲基甲硫氨酸(MM)直接抑制甲硫氨酸生物合成,而乙硫氨酸(Et)竞争性抑制甲硫氨酸的利用。证明了大肠杆菌K12的无细胞酶将Et腺苷化生成S-腺苷乙硫氨酸(AdoEt)。大肠杆菌K12突变体对不断增加浓度的NL的耐受性依次表现为NLR、NLREtR、NLRMMR和最终的NLREtRMMR表型。所有自发的NLR突变体都有metK突变,而NTG诱导的突变体在metK和metJ基因中都有突变。发现大肠杆菌K12无细胞酶进行甲硫氨酸腺苷化的动力学与报道的酵母酶相似,在低甲硫氨酸浓度下显示出典型的延迟期,当在孵育混合物中加入AdoMet时该期消失。NL延长了延迟期,并降低了随后甲硫氨酸腺苷化的速率,但不影响AdoMet缩短腺苷化延迟期的作用。

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