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植物线粒体抗氰交替氧化酶的调控。参与α-酮酸刺激和亚基间二硫键形成的半胱氨酸残基的鉴定。

Regulation of the cyanide-resistant alternative oxidase of plant mitochondria. Identification of the cysteine residue involved in alpha-keto acid stimulation and intersubunit disulfide bond formation.

作者信息

Rhoads D M, Umbach A L, Sweet C R, Lennon A M, Rauch G S, Siedow J N

机构信息

Developmental, Cell, and Molecular Biology/Botany Department, Duke University, Durham, North Carolina 27708-1000, USA.

出版信息

J Biol Chem. 1998 Nov 13;273(46):30750-6. doi: 10.1074/jbc.273.46.30750.

Abstract

The cyanide-resistant alternative oxidase of plant mitochondria is a homodimeric protein whose activity can be regulated by a redox-sensitive intersubunit sulfhydryl/disulfide system and by alpha-keto acids. After determining that the Arabidopsis alternative oxidase possesses the redox-sensitive sulfhydryl/disulfide system, site-directed mutagenesis of an Arabidopsis cDNA clone was used to individually change the two conserved Cys residues, Cys-128 and Cys-78, to Ala. Using diamide oxidation and chemical cross-linking of the protein expressed in Escherichia coli, Cys-78 was shown to be: 1) the Cys residue involved in the sulfhydryl/disulfide system; and 2) not required for subunit dimerization. The C128A mutant was stimulated by pyruvate, while the C78A mutant protein had little activity and displayed no stimulation by pyruvate. Mutating Cys-78 to Glu produced an active enzyme which was insensitive to pyruvate, consistent with alpha-keto acid activation occurring through a thiohemiacetal. These results indicate that Cys-78 serves as both the regulatory sulfhydryl/disulfide and the site of activation by alpha-keto acids. In light of these results, the previously observed effects of sulfhydryl reagents on the alternative oxidase of isolated soybean mitochondria were re-examined and were found to be in agreement with a single sulfhydryl residue being the site both of alpha-keto acid activation and of the regulatory sulfhydryl/disulfide system.

摘要

植物线粒体中对氰化物不敏感的交替氧化酶是一种同型二聚体蛋白,其活性可由氧化还原敏感的亚基间巯基/二硫键系统以及α-酮酸调节。在确定拟南芥交替氧化酶具有氧化还原敏感的巯基/二硫键系统后,利用拟南芥cDNA克隆的定点诱变技术,将两个保守的半胱氨酸残基Cys-128和Cys-78分别突变为丙氨酸。通过对大肠杆菌中表达的蛋白进行二酰胺氧化和化学交联,结果表明Cys-78:1)是参与巯基/二硫键系统的半胱氨酸残基;2)不是亚基二聚化所必需的。C128A突变体受到丙酮酸的刺激,而C78A突变体蛋白活性很低,且不受丙酮酸刺激。将Cys-78突变为谷氨酸产生了一种对丙酮酸不敏感的活性酶,这与通过硫代半缩醛发生的α-酮酸激活一致。这些结果表明,Cys-78既是调节性巯基/二硫键,也是α-酮酸激活的位点。鉴于这些结果,对之前观察到的巯基试剂对分离的大豆线粒体交替氧化酶的影响进行了重新研究,发现与单一巯基残基是α-酮酸激活位点和调节性巯基/二硫键系统位点的情况一致。

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