Laboratoire mixte Centre National de la Recherche Scientifique/Rhône-Poulenc UMR-41, Rhône-Poulenc Agrochimie, 14-20 rue Pierre Baizet, 69263 Lyon, France.
Plant Physiol. 1992 Jun;99(2):450-5. doi: 10.1104/pp.99.2.450.
Mitochondria from green pea (Pisum sativum) leaves were purified free of peroxisomes and chlorophyll contamination and examined for their biotin content. The bulk of the bound biotin detected in plant mitochondria was shown to be associated with the matrix space to a concentration of about 13 micromolar, and no free biotin was detected. Western blot analysis of mitochondrial polypeptides using horseradish peroxidase-labeled streptavidin revealed a unique biotin-containing polypeptide with a molecular weight of 76,000. This polypeptide was implicated as being the biotinylated subunit of 3-methylcrotonyl-coenzyme A (CoA) carboxylase. Fractionation of pea leaf protoplasts demonstrated that this enzyme activity was located largely in mitochondria. The 3-methylcrotonyl-CoA carboxylase activity was latent when assayed in isotonic media. The majority of the enzyme activity was found in the soluble matrix of mitochondria. Maximal 3-methylcrotonyl-CoA carboxylase activity was found at pH 8.3 in the presence of Mg(2+). Kinetic constants (apparent K(m) values) for the enzyme substrates were: 3-methylcrotonyl-CoA, 0.05 millimolar; ATP, 0.16 millimolar; HCO(3) (-), 2.2 millimolar. The involvement of 3-methylcrotonyl-CoA carboxylase in the leucine degradation pathway in plant mitochondria is proposed.
从绿豆(豌豆)叶片中纯化的线粒体,不含过氧化物酶体和叶绿素污染,并检测其生物素含量。植物线粒体中检测到的大部分结合生物素与基质空间结合,浓度约为 13 微摩尔,未检测到游离生物素。使用辣根过氧化物酶标记的链霉亲和素对线粒体多肽进行的 Western blot 分析显示,存在一种独特的含生物素的多肽,分子量为 76000。该多肽被认为是 3-甲基巴豆酰辅酶 A(CoA)羧化酶的生物素化亚基。豌豆叶片原生质体的分级分离表明,这种酶活性主要位于线粒体中。在等渗介质中测定时,3-甲基巴豆酰 CoA 羧化酶活性处于潜伏状态。该酶的大部分活性存在于线粒体的可溶性基质中。在 pH8.3 下存在 Mg(2+)时,发现最大的 3-甲基巴豆酰 CoA 羧化酶活性。该酶底物的动力学常数(表观 Km 值)为:3-甲基巴豆酰 CoA,0.05 毫摩尔;ATP,0.16 毫摩尔;HCO(3) (-),2.2 毫摩尔。提出 3-甲基巴豆酰 CoA 羧化酶参与植物线粒体中亮氨酸降解途径。