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粗糙脉孢菌中精氨酸限制对酶合成的抑制作用。

Depression of enzyme synthesis in response to arginine limitation in Neurospora crassa.

作者信息

Flint H J, Dible S, Kacser H

出版信息

J Gen Microbiol. 1985 Nov;131(11):2891-900. doi: 10.1099/00221287-131-11-2891.

DOI:10.1099/00221287-131-11-2891
PMID:2936866
Abstract

Ornithine carbamoyltransferase and argininosuccinase, two enzymes involved in arginine synthesis, are regulated by cross-pathway amino acid control in Neurospora and show derepression in response to limitation of any one of a number of amino acids. The effects of varying the severity of arginine limitation upon the synthesis of these enzymes, in mycelial cultures of an arginine auxotrophic strain, are reported here. Depression occurred at arginine concentrations sufficient to allow normal rates of protein accumulation, leading to increases of not more than fourfold in the absolute rate of enzyme synthesis. On the other hand, differential rates of enzyme synthesis increased progressively up to 20-fold or more under extreme conditions of arginine limitation that also limit net protein synthesis. The major part of the derepression response thus occurred at arginine concentrations that allowed low net rates of protein synthesis. The physiological significance of this is not yet understood. Our evidence suggests that these responses were mediated entirely through the cross-pathway control system, and may not be untypical (allowing for variations in magnitude) of depression resulting through this mechanism in Neurospora.

摘要

鸟氨酸氨甲酰基转移酶和精氨琥珀酸酶是参与精氨酸合成的两种酶,在粗糙脉孢菌中受交叉途径氨基酸控制的调节,并且在多种氨基酸中的任何一种受到限制时会表现出阻遏解除。本文报道了在精氨酸营养缺陷型菌株的菌丝体培养物中,改变精氨酸限制的严重程度对这些酶合成的影响。在足以使蛋白质积累达到正常速率的精氨酸浓度下出现了抑制作用,导致酶合成的绝对速率增加不超过四倍。另一方面,在同样限制净蛋白质合成的极端精氨酸限制条件下,酶合成的差异速率逐渐增加至20倍或更多。因此,阻遏解除反应的主要部分发生在允许低净蛋白质合成速率的精氨酸浓度下。其生理意义尚不清楚。我们的证据表明,这些反应完全是通过交叉途径控制系统介导的,并且对于粗糙脉孢菌中通过这种机制导致的抑制作用(考虑到幅度的变化)可能并非不典型。

相似文献

1
Depression of enzyme synthesis in response to arginine limitation in Neurospora crassa.粗糙脉孢菌中精氨酸限制对酶合成的抑制作用。
J Gen Microbiol. 1985 Nov;131(11):2891-900. doi: 10.1099/00221287-131-11-2891.
2
Cross-pathway control of ornithine carbamoyltransferase synthesis in Neurospora crassa.粗糙脉孢菌中鸟氨酸氨甲酰基转移酶合成的跨途径调控
J Gen Microbiol. 1982 Jul;128(7):1503-7. doi: 10.1099/00221287-128-7-1503.
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General control of arginine biosynthetic enzymes in Neurospora crassa.粗糙脉孢菌中精氨酸生物合成酶的总体调控
J Gen Microbiol. 1981 May;124(1):129-40. doi: 10.1099/00221287-124-1-129.
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Cross-pathway regulation: tryptophan-mediated control of histidine and arginine biosynthetic enzymes in Neurospora crassa.交叉途径调控:粗糙脉孢菌中色氨酸介导的组氨酸和精氨酸生物合成酶的控制
J Bacteriol. 1974 Sep;119(3):889-92. doi: 10.1128/jb.119.3.889-892.1974.
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Cross-pathway regulation: histidine-mediated control of histidine, tryptophan, and arginine biosynthetic enzymes in Neurospora crassa.跨途径调控:粗糙脉孢菌中组氨酸介导的对组氨酸、色氨酸和精氨酸生物合成酶的控制
J Bacteriol. 1974 Sep;119(3):893-98. doi: 10.1128/jb.119.3.893-898.1974.
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Control of the flux to arginine in Neurospora crassa: de-repression of the last three enzymes of the arginine pathway.粗糙脉孢菌中精氨酸通量的调控:精氨酸途径最后三种酶的去阻遏作用
J Mol Biol. 1974 Aug 5;87(2):303-16. doi: 10.1016/0022-2836(74)90151-x.
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Organization and control in the arginine biosynthetic pathway of Neurospora.粗糙脉孢菌精氨酸生物合成途径中的组织与调控
J Bacteriol. 1975 Jul;123(1):196-202. doi: 10.1128/jb.123.1.196-202.1975.
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Effect of chloramphenicol and ethidium bromide on the level of ornithine carbamoyltransferase in Neurospora crassa.
J Bacteriol. 1986 May;166(2):679-82. doi: 10.1128/jb.166.2.679-682.1986.
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Control of the flux in the arginine pathway of Neurospora crassa. Modulations of enzyme activity and concentration.粗糙脉孢菌精氨酸途径中通量的控制。酶活性和浓度的调节。
Biochem J. 1981 Nov 15;200(2):231-46. doi: 10.1042/bj2000231.
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Inhibition of aminoacyl-transfer ribonucleic acid synthetases and the regulation of amino acid biosynthetic enzymes in Neurospora crassa.粗糙脉孢菌中氨酰基转移核糖核酸合成酶的抑制作用及氨基酸生物合成酶的调控
J Bacteriol. 1977 Mar;129(3):1303-12. doi: 10.1128/jb.129.3.1303-1312.1977.

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Cloning of the arg-12 gene of Neurospora crassa and regulation of its transcript via cross-pathway amino acid control.粗糙脉孢菌arg-12基因的克隆及其转录通过跨途径氨基酸控制的调节。
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Compartmental and regulatory mechanisms in the arginine pathways of Neurospora crassa and Saccharomyces cerevisiae.
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