Saavedra Lira E, Robinson O, Pérez Montfort R
Departamento de Microbiología, Instituto de Fisiología Celular, UNAM, México, DF.
Arch Med Res. 1992;23(2):39-40.
We isolated a clone from a lambda gt11 cDNA library of E. histolytica, subcloned its insert in the vector pTZ18R and sequenced it by the method of Sanger. Sequence comparison with Genbank and of the corresponding amino acid sequence with the NBRF/PIR data bank using the FastA program, showed homologies between 54.9 and 58.5% for the nucleotides and between 48.6 and 49.4% for the amino acids with pyruvate, orthophosphate dikinases from maize, Flaveria trinervia and Bacteroides symbiosus. The sequence obtained for E. histolytica represents about 20% of the complete gene or protein sequence.
我们从溶组织内阿米巴的λgt11 cDNA文库中分离出一个克隆,将其插入片段亚克隆到载体pTZ18R中,并采用桑格法进行测序。使用FastA程序将核苷酸序列与Genbank进行比较,将相应的氨基酸序列与NBRF/PIR数据库进行比较,结果表明,溶组织内阿米巴与玉米、三脉黄菀和共生拟杆菌的丙酮酸、正磷酸二激酶的核苷酸同源性在54.9%至58.5%之间,氨基酸同源性在48.6%至49.4%之间。溶组织内阿米巴获得的序列约占完整基因或蛋白质序列的20%。