Montie D B, Montie T C
J Bacteriol. 1975 Oct;124(1):296-306. doi: 10.1128/jb.124.1.296-306.1975.
Yersinia pestis TJW, an avirulent wild-type strain, requires phenylalanine and methionine for growth. It was of interest to examine and define the methionine transport system because of this requirement. The methionine system showed saturation kinetics with a Km for transport of approximately 9 times 10(-7) M. After 8 s of methionine transport, essentially all of the methionine label appeared in S-adenosyl-L-methionine (SAM) as detected in ethanol extracts. Small amounts of free methionine was detected intracellularly after 1 min of transport. Addition of glucose increased significantly the amount of intracellular methionine at 1 min. A series of SAM metabolic products was detected after 90 s to 5 min of transport including: 5'-thiomethyladenosine, homoserine lactone, S-adenosyl homoserine, and a fluorescent methyl receptor compound. Results from assays for SAM synthetase in spheroplast fractions showed a small (16%) but significant portion of synthetase associated with the membrane. However, most of the enzyme activity was associated with the cytoplasmic fraction. Methionine transport was characterized by a high degree of stereospecificity. No competition occurred from structurally unrelated amino acids. Although uptake was inhibited by uncoupling and sulfhydryl reagents, no efflux was observed. Results using energy inhibitors on unstarved and starved cells showed that respiratory inhibitors such as potassium cyanide (KCN) and amytal were most effective, and that arsenate was least effective. KCN plus arsenate completely blocked utilization of energy derived from glucose, and KCN completely blocked utilization of energy deived from D-lactate. The data indicate that methionine transport in Y. pestis is linked to the trapping of methionine in SAM. The results further suggest that this transport system can be classified as a permease-bound system where transport is coupled to an energized membrane state and to respiration.
鼠疫耶尔森氏菌TJW是一种无毒野生型菌株,生长需要苯丙氨酸和蛋氨酸。鉴于这种需求,研究并确定蛋氨酸转运系统很有意义。蛋氨酸系统呈现饱和动力学,转运的Km约为9×10⁻⁷M。在蛋氨酸转运8秒后,如在乙醇提取物中检测到的那样,基本上所有的蛋氨酸标记物都出现在S-腺苷-L-蛋氨酸(SAM)中。转运1分钟后,细胞内检测到少量游离蛋氨酸。添加葡萄糖显著增加了1分钟时细胞内蛋氨酸的量。在转运90秒至5分钟后检测到一系列SAM代谢产物,包括:5'-硫代甲基腺苷、高丝氨酸内酯、S-腺苷高丝氨酸和一种荧光甲基受体化合物。对原生质球组分中SAM合成酶的测定结果表明,有一小部分(16%)但显著比例的合成酶与膜相关。然而,大多数酶活性与细胞质组分相关。蛋氨酸转运具有高度的立体特异性。结构不相关的氨基酸不会产生竞争。虽然摄取受到解偶联剂和巯基试剂的抑制,但未观察到外流。对未饥饿和饥饿细胞使用能量抑制剂的结果表明,呼吸抑制剂如氰化钾(KCN)和阿米妥最有效,而砷酸盐最无效。KCN加砷酸盐完全阻断了源自葡萄糖的能量利用,KCN完全阻断了源自D-乳酸的能量利用。数据表明,鼠疫耶尔森氏菌中的蛋氨酸转运与蛋氨酸在SAM中的捕获有关。结果进一步表明,这种转运系统可归类为一种通透酶结合系统,其中转运与活跃的膜状态和呼吸相关。