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粗糙脉孢菌中色氨酸生物合成途径中间反应的体内调节。

In vivo regulation of intermediate reactions in the pathway of tryptophan biosynthesis in Neurospora crassa.

作者信息

Lester G

出版信息

J Bacteriol. 1968 Nov;96(5):1768-73. doi: 10.1128/jb.96.5.1768-1773.1968.

Abstract

The in vivo regulation of intermediate reactions in the pathway of tryptophan synthesis in Neurospora crassa was examined in a double mutant (tr-2, tr-3) which lacks the functions of the first and last enzymes in the pathway from chorismic acid to tryptophan. The double mutant can convert anthranilic acid to indole and indole-3-glycerol, and the production of these indolyl compounds by germinated conidia was used to estimate the activity of the intermediate enzymes in the pathway. Indole-synthesizing activity was maximal in germinated conidia obtained from cultures in which the levels of l-tryptophan were growth-limiting; the formation of this activity was markedly repressed when the levels of l-tryptophan exceeded those required for maximal growth. d-, 5-methyl-dl-, and 6-methyl-dl-tryptophan were less effective than l-tryptophan, and 4-methyl-dl-tryptophan, tryptamine, and indole-3-acetic acid were ineffective in repressing the formation of indole-synthesizing activity; anthranilic acid stimulated the formation of indole-synthesizing activity. Preformed indole-synthesizing activity was strongly and specifically inhibited by low levels of l-tryptophan; several related compounds were ineffective as inhibitors. These results suggest that, in addition to repression, an end product feedback inhibition mechanism is operative on an intermediate enzyme(s) in tryptophan biosynthesis. The relation of these results to other in vivo and in vitro studies and to general aspects of the regulation of tryptophan biosynthesis in N. crassa are discussed.

摘要

在一种双突变体(tr-2,tr-3)中研究了粗糙脉孢菌色氨酸合成途径中间反应的体内调节,该双突变体缺乏从分支酸到色氨酸途径中第一种和最后一种酶的功能。双突变体可以将邻氨基苯甲酸转化为吲哚和吲哚-3-甘油,并且用萌发分生孢子产生这些吲哚化合物来估计该途径中中间酶的活性。吲哚合成活性在从l-色氨酸水平限制生长的培养物中获得的萌发分生孢子中最大;当l-色氨酸水平超过最大生长所需水平时,这种活性的形成受到明显抑制。d-、5-甲基-dl-和6-甲基-dl-色氨酸的抑制效果不如l-色氨酸,而4-甲基-dl-色氨酸、色胺和吲哚-3-乙酸在抑制吲哚合成活性的形成方面无效;邻氨基苯甲酸刺激吲哚合成活性的形成。预先形成的吲哚合成活性受到低水平l-色氨酸的强烈且特异性抑制;几种相关化合物作为抑制剂无效。这些结果表明,除了阻遏作用外,一种终产物反馈抑制机制作用于色氨酸生物合成途径中的一种中间酶。讨论了这些结果与其他体内和体外研究以及与粗糙脉孢菌色氨酸生物合成调节的一般方面的关系。

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