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粗糙脉孢菌中的色氨酸转运。II. 代谢控制。

Tryptophan transport in Neurospora crassa. II. Metabolic control.

作者信息

Wiley W R, Matchett W H

出版信息

J Bacteriol. 1968 Mar;95(3):959-66. doi: 10.1128/jb.95.3.959-966.1968.

Abstract

The rate of tryptophan transport in Neurospora is regulated by the intracellular pool of tryptophan. When cells were shifted from growth in minimal medium to tryptophan-containing medium for 10 min, there was a 50% reduction in the rate of tryptophan transport. Intracellular tryptophan pools derived from indole were equally effective in reducing the rate of transport as externally supplied tryptophan. The regulatory influence of tryptophan on the transport system appears to be a property of all the amino acids transported by the tryptophan transport site or sites. Lysine and glutamic acid are not transported by the tryptophan transport site or sites and are ineffective in the regulation of tryptophan uptake. Continued protein synthesis is required for the maintenance of a functional tryptophan transport system. The half-life of the transport system, estimated by inhibiting protein synthesis with cycloheximide, was about 15 min. Turnover of the system occurred at 30 C but not at 4 C, suggesting that the breakdown of the system is enzymatically mediated. It was inferred that the rate of tryptophan transport in Neurospora is modulated through the maintenance of a delicate balance between the synthesis and breakdown of some component of the transport system.

摘要

粗糙脉孢菌中色氨酸的转运速率受细胞内色氨酸池的调节。当细胞从在基本培养基中生长转移至含色氨酸的培养基中培养10分钟时,色氨酸的转运速率降低了50%。源自吲哚的细胞内色氨酸池在降低转运速率方面与外源供应的色氨酸同样有效。色氨酸对转运系统的调节作用似乎是色氨酸转运位点所转运的所有氨基酸的共同特性。赖氨酸和谷氨酸不由色氨酸转运位点转运,对色氨酸摄取的调节无效。维持功能性色氨酸转运系统需要持续的蛋白质合成。用环己酰亚胺抑制蛋白质合成来估计,转运系统的半衰期约为15分钟。该系统在30℃时发生周转,但在4℃时不发生,这表明该系统的分解是由酶介导的。据推测,粗糙脉孢菌中色氨酸的转运速率是通过维持转运系统某些组分合成与分解之间的微妙平衡来调节的。

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本文引用的文献

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PHYSIOLOGICAL CHANNELING OF TRYPTOPHAN IN NEUROSPORA CRASSA.粗糙脉孢菌中色氨酸的生理通道
Biochim Biophys Acta. 1964 Apr 4;86:91-9. doi: 10.1016/0304-4165(64)90162-x.
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Studies on the mechanism of the tryptophan synthetase reaction.色氨酸合成酶反应机制的研究。
Biochim Biophys Acta. 1962 Aug 13;62:279-93. doi: 10.1016/0006-3002(62)90041-0.

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