Studart-Guimarães Claudia, Gibon Yves, Frankel Nicolás, Wood Craig C, Zanor María Inés, Fernie Alisdair R, Carrari Fernando
Max-Planck Institute for Molecular Plant Physiology, Am Mühlenberg 1, 14476 Golm, Germany.
Plant Mol Biol. 2005 Nov;59(5):781-91. doi: 10.1007/s11103-005-1004-1.
Despite the central importance of the TCA cycle in plant metabolism not all of the genes encoding its constituent enzymes have been functionally identified. In yeast, the heterodimeric protein succinyl CoA ligase is encoded for by two single-copy genes. Here we report the isolation of two tomato cDNAs coding for alpha- and one coding for the beta-subunit of succinyl CoA ligase. These three cDNAs were used to complement the respective Saccharomyces cerevisiae mutants deficient in the alpha- and beta-subunit, demonstrating that they encode functionally active polypeptides. The genes encoding for the subunits were expressed in all tissues, but most strongly in floral and leaf tissues, with equivalent expression of the two alpha-subunit genes being expressed to equivalent levels in all tissues. In all instances GFP fusion expression studies confirmed an expected mitochondrial location of the proteins encoded. Following the development of a novel assay to measure succinyl CoA ligase activity, in the direction of succinate formation, the evaluation of the maximal catalytic activities of the enzyme in a range of tissues revealed that these paralleled those of mRNA levels. We also utilized this assay to perform a preliminary characterisation of the regulatory properties of the enzyme suggesting allosteric control of this enzyme which may regulate flux through the TCA cycle in a manner consistent with its position therein.
尽管三羧酸循环在植物代谢中至关重要,但并非所有编码其组成酶的基因都已被功能鉴定。在酵母中,异二聚体蛋白琥珀酰辅酶A连接酶由两个单拷贝基因编码。本文我们报道了两个编码琥珀酰辅酶A连接酶α亚基的番茄cDNA和一个编码β亚基的番茄cDNA的分离。这三个cDNA用于互补酿酒酵母中缺乏α亚基和β亚基的相应突变体,证明它们编码具有功能活性的多肽。编码这些亚基的基因在所有组织中均有表达,但在花和叶组织中表达最强,两个α亚基基因在所有组织中的表达水平相当。在所有情况下,绿色荧光蛋白融合表达研究均证实了所编码蛋白质预期的线粒体定位。在开发了一种用于测量琥珀酰辅酶A连接酶活性(向琥珀酸形成方向)的新测定方法后,对一系列组织中该酶的最大催化活性进行评估发现,这些活性与mRNA水平平行。我们还利用该测定方法对该酶的调节特性进行了初步表征,表明该酶存在变构调节,这可能以与其在三羧酸循环中的位置一致的方式调节通过三羧酸循环的通量。