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有证据表明,阻遏机制可对大肠杆菌K-12的苏氨酸、亮氨酸和异亮氨酸操纵子施加调控。

Evidence that repression mechanisms can exert control over the thr, leu, and ilv operons of Escherichia coli K-12.

作者信息

Johnson D I, Somerville R L

出版信息

J Bacteriol. 1983 Jul;155(1):49-55. doi: 10.1128/jb.155.1.49-55.1983.

Abstract

Mutants of Escherichia coli K-12 resistant to either the threonine analog DL-alpha-amino-beta-hydroxyvaleric acid or the leucine analog 5',5',5'-trifluoro-DL-leucine were isolated. One DL-alpha-amino-beta-hydroxyvaleric acid-resistant mutant strain, designated SP572, constitutively expressed the thr and ilv operons. The mutant allele, avr-16, was localized between trpR and the thr operon at min 0. The wildtype allele of avr-16, designated ileR, is trans dominant. One 5',5',5'-trifluoro-DL-leucine-resistant mutant strain, designated FLR9, expressed the leu and ilv operons constitutively. The mutant allele, flr-9, is linked to entA at min 13. The constitutive expression of the thr, leu, and ilv operons in mutants avr-16 and flr-9 was partly reversed in cells harboring a plasmid, which leads to elevated levels of the trpR gene product, the Trp aporepressor protein. Operator-like sequences situated upstream from the transcription startpoints of the thr, leu, and ilv operons are plausible candidates for targets of systems of repressor-operator control functioning in parallel with attenuation.

摘要

分离出了对苏氨酸类似物DL-α-氨基-β-羟基戊酸或亮氨酸类似物5',5',5'-三氟-DL-亮氨酸具有抗性的大肠杆菌K-12突变体。一株对DL-α-氨基-β-羟基戊酸具有抗性的突变菌株,命名为SP572,组成型表达thr和ilv操纵子。突变等位基因avr-16定位于0分钟处的trpR和thr操纵子之间。avr-16的野生型等位基因,命名为ileR,是反式显性的。一株对5',5',5'-三氟-DL-亮氨酸具有抗性的突变菌株,命名为FLR9,组成型表达leu和ilv操纵子。突变等位基因flr-9与13分钟处的entA相连。在携带质粒的细胞中,avr-16和flr-9突变体中thr、leu和ilv操纵子的组成型表达部分被逆转,该质粒导致trpR基因产物(色氨酸无辅基阻遏蛋白)水平升高。位于thr、leu和ilv操纵子转录起始点上游的类操纵序列是与衰减并行发挥作用的阻遏物-操纵子控制系统靶标的合理候选者。

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