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亮氨酸-3顺反子在粗糙脉孢菌异亮氨酸和缬氨酸生物合成酶合成调控中的作用。

Role of the leu-3 cistron in the regulation of the synthesis of isoleucine and valine biosynthetic enzymes of Neurospora.

作者信息

Olshan A R, Gross S R

出版信息

J Bacteriol. 1974 May;118(2):374-84. doi: 10.1128/jb.118.2.374-384.1974.

Abstract

The production by Neurospora of the enzymes of isoleucine and valine synthesis in response to specific end product-derived signals depends upon the presence of an effective leu-3 regulatory product and its effector alpha-isopropylmalate (alpha-IPM). In leu-3(+) strains, threonine deaminase production is repressed as a function of available isoleucine, acetohydroxy acid synthetase as a function of valine, and the isomeroreductase and dihydroxy acid dehydratase as a function of isoleucine and leucine. In the absence of an effective leu-3 regulatory product, alpha-isopropylmalate, or both, the production of isoleucine and valine biosynthetic enzymes is fixed at or near fully repressed levels even under conditions of severe end product limitation. Thus, in addition to its involvement in the regulation of expression of the three structural genes of leucine synthesis, the leu-3 alpha-IPM regulatory product is necessary for full expression of at least four genes specifying the structure of the enzymes of isoleucine and valine synthesis. It is suggested that the leu-3 alpha-IPM regulatory element may facilitate transcription of the genetically dispersed cistrons either by imposing specificity on ribonucleic acid polymerase for structurally similar promoters adjacent to each of the cistrons or by "opening" promoters after interaction with nearly identical stretches of deoxyribonucleic acid near each of the structural genes.

摘要

粗糙脉孢菌响应特定终产物衍生信号合成异亮氨酸和缬氨酸的酶,这取决于有效亮氨酸3调控产物及其效应物α-异丙基苹果酸(α-IPM)的存在。在亮氨酸3(+)菌株中,苏氨酸脱氨酶的合成作为可用异亮氨酸的函数被抑制,乙酰羟酸合成酶作为缬氨酸的函数被抑制,而异构还原酶和二羟基酸脱水酶作为异亮氨酸和亮氨酸的函数被抑制。在没有有效亮氨酸3调控产物、α-异丙基苹果酸或两者的情况下,即使在终产物严重受限的条件下,异亮氨酸和缬氨酸生物合成酶的合成也固定在或接近完全抑制的水平。因此,除了参与亮氨酸合成的三个结构基因表达的调控外,亮氨酸3α-IPM调控产物对于至少四个指定异亮氨酸和缬氨酸合成酶结构的基因的完全表达也是必需的。有人提出,亮氨酸3α-IPM调控元件可能通过对与每个顺反子相邻的结构相似启动子的核糖核酸聚合酶施加特异性,或通过与每个结构基因附近几乎相同的脱氧核糖核酸片段相互作用后“打开”启动子,来促进基因分散的顺反子的转录。

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