Brondijk T H, Durand R, van der Giezen M, Gottschal J C, Prins R A, Fèvre M
Laboratoire de Biologie Cellulaire Fongique, CNRS UMR 5534, Université Lyon I, Villeurbanne, France.
Mol Gen Genet. 1996 Dec 13;253(3):315-23. doi: 10.1007/pl00008598.
A clone containing a Neocallimastix frontalis cDNA assumed to encode the beta subunit of succinyl-CoA synthetase (SCSB) was identified by sequence homology with prokaryotic and eukaryotic counter-parts. An open reading frame of 1311 bp was found. The deduced 437 amino acid sequence showed a high degree of identity to the beta-succinyl-CoA synthetase of Escherichia coli (46%), the mitochondrial beta-succinyl-CoA synthetase from pig (48%) and the hydrogenosomal beta-succinyl-CoA synthetase from Trichomonas vaginalis (49%). The G + C content of the succinyl-CoA synthetase coding sequence (43.8%) was considerably higher than that of the 5' (14.8%) and 3' (13.3%) non-translated flanking sequences, as has been observed for other genes from N. frontalis. The codon usage pattern was biased, with only 34 codons used and a strong preference for a pyrimidine (T) in the third positions of the codons. The coding sequence of the beta-succinyl-CoA synthetase cDNA was cloned in an E. coli expression vector encoding a 6(His) tag. The recombinant protein was purified by affinity binding and used to produce polyclonal antibodies. The anti-succinyl-CoA synthetase serum recognized a 45 kDa protein from a N. frontalis fraction enriched for hydrogenosomes and similar polypeptides in two related anaerobic fungi, Piromyces rhizinflata (45 kDa) and Caecomyces communis (47 kDa). Immunocytochemical experiments suggest that succinyl-CoA synthetase is located in the hydrogenosomal matrix. Staining for SCS activity in native electrophoretic gels revealed a band with an apparent molecular weight of approximately 330 kDa. The C-terminus of the succinyl-CoA synthetase sequence was devoid of the typical targeting signals identified so far in microbody proteins, indicating that N. frontalis uses a different signal for sorting SCSB into hydrogenosomes. Based on comparisons with other proteins we propose a putative N-terminal targeting signal for succinyl-CoA synthetase of N. frontalis that shows some of the features of mitochondrial targeting sequences.
通过与原核生物和真核生物对应物的序列同源性,鉴定出一个含有假定编码琥珀酰辅酶A合成酶(SCSB)β亚基的额叶新丽鞭毛虫cDNA的克隆。发现了一个1311 bp的开放阅读框。推导的437个氨基酸序列与大肠杆菌的β-琥珀酰辅酶A合成酶(46%)、猪的线粒体β-琥珀酰辅酶A合成酶(48%)和阴道毛滴虫的氢化酶体β-琥珀酰辅酶A合成酶(49%)具有高度同一性。琥珀酰辅酶A合成酶编码序列的G + C含量(43.8%)明显高于5'非翻译侧翼序列(14.8%)和3'非翻译侧翼序列(13.3%),这与额叶新丽鞭毛虫的其他基因情况一致。密码子使用模式存在偏向性,仅使用了34个密码子,且在密码子的第三位强烈偏好嘧啶(T)。β-琥珀酰辅酶A合成酶cDNA的编码序列被克隆到一个编码6×组氨酸标签的大肠杆菌表达载体中。重组蛋白通过亲和结合进行纯化,并用于制备多克隆抗体。抗琥珀酰辅酶A合成酶血清识别来自额叶新丽鞭毛虫富含氢化酶体的组分中的一种45 kDa蛋白,以及两种相关厌氧真菌——根状梨形鞭毛虫(45 kDa)和普通腔囊霉(47 kDa)中的类似多肽。免疫细胞化学实验表明琥珀酰辅酶A合成酶位于氢化酶体基质中。在天然电泳凝胶上对SCS活性进行染色,显示出一条表观分子量约为330 kDa的条带。琥珀酰辅酶A合成酶序列的C末端没有迄今在微体蛋白中鉴定出的典型靶向信号,这表明额叶新丽鞭毛虫使用不同的信号将SCSB分选到氢化酶体中。基于与其他蛋白质的比较,我们提出了额叶新丽鞭毛虫琥珀酰辅酶A合成酶假定的N末端靶向信号,其具有线粒体靶向序列的一些特征。