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鸟氨酸转氨甲酰酶的体外合成

In vitro synthesis of ornithine transcarbamylase.

作者信息

Dohi M, Inouye H, Kikuchi A, Gorini L

出版信息

J Biochem. 1978 Dec;84(6):1389-99. doi: 10.1093/oxfordjournals.jbchem.a132261.

Abstract

An in vitro system for the synthesis of ornithine transcarbamylase (OTCase) was established using iS-30 extract from E. coli MDS6-2(lambda) and DNA of a lambda transducing phage carrying argI and argF genes. This in vitro synthesis was completely dependent on the additon of DNA, and was sensitive to chloramphenicol and rifampicin. Radioisotopic analysis confirmed that the synthesized enzyme catalyzes the carbamylation of ornithine to citrulline. In the in vitro system the repression and derepression of OTCase synthesis could be observed by mixing iS-30 extracts prepared from argR+ and argR- cells. A remarkable maturation effect could be observed for the FFF enzyme, but not for the III enzyme. This system is considered to reflect the in vivo situation, and should therefore be useful for investigations on the regulation of OTCase synthesis in vivo.

摘要

利用大肠杆菌MDS6 - 2(λ)的iS - 30提取物和携带argI和argF基因的λ转导噬菌体的DNA,建立了一种用于合成鸟氨酸转氨甲酰酶(OTCase)的体外系统。这种体外合成完全依赖于DNA的添加,并且对氯霉素和利福平敏感。放射性同位素分析证实,合成的酶催化鸟氨酸氨甲酰化生成瓜氨酸。在体外系统中,通过混合从argR⁺和argR⁻细胞制备的iS - 30提取物,可以观察到OTCase合成的阻遏和去阻遏。对于FFF酶可以观察到显著的成熟效应,但对于III酶则没有。该系统被认为反映了体内情况,因此对于研究体内OTCase合成的调控应该是有用的。

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