Cournoyer B, Watanabe S, Vivian A
Department of Biological Sciences, University of the West of England, Bristol BS16 1QY, UK.
Biochim Biophys Acta. 1998 Apr 29;1397(2):161-8. doi: 10.1016/s0167-4781(98)00020-7.
A tellurite-resistance genetic determinant was isolated from the pea blight pathogen Pseudomonas syringae pathovar pisi by a shotgun strategy involving a tellurite-selective screening in Escherichia coli. A 1.65 kb tellurite resistance insert was obtained and analysed. It harbours a single complete and functional ORF encoding a deduced protein of 24, 445 Da. The deduced AA sequence shows significant similarities with the complete human thiopurine methyltransferase enzyme, a methyltransferase from Synechocystis and a methyltransferase-like sequence from Bordetella pertussis. The encoded thiopurine methyltransferase activity was demonstrated using a radiochemical microassay for the methylation of 6-mercaptopurine. This gene was detected in most P. syringae legume pathogens.
通过在大肠杆菌中进行亚碲酸盐选择性筛选的鸟枪法策略,从豌豆疫病病原体丁香假单胞菌豌豆致病变种中分离出了一个抗亚碲酸盐遗传决定因素。获得了一个1.65 kb的抗亚碲酸盐插入片段并进行了分析。它包含一个单一的完整且功能性的开放阅读框,编码一个推导分子量为24445 Da的蛋白质。推导的氨基酸序列与完整的人硫嘌呤甲基转移酶、来自集胞藻的一种甲基转移酶以及百日咳博德特氏菌的一个类甲基转移酶序列具有显著相似性。使用放射性化学微量测定法检测6-巯基嘌呤的甲基化,证明了所编码的硫嘌呤甲基转移酶活性。在大多数丁香假单胞菌豆科病原体中都检测到了这个基因。