O'Dwyer Karen, Watts Joseph M, Biswas Sanjoy, Ambrad Jennifer, Barber Michael, Brulé Hervé, Petit Chantal, Holmes David J, Zalacain Magdalena, Holmes Walter M
Microbial, Musculoskeletal and Proliferative Diseases CEDD, GlaxoSmithKline, Collegeville, Pennsylvania 19426, USA.
J Bacteriol. 2004 Apr;186(8):2346-54. doi: 10.1128/JB.186.8.2346-2354.2004.
Down-regulation of expression of trmD, encoding the enzyme tRNA (guanosine-1)-methyltransferase, has shown that this gene is essential for growth of Streptococcus pneumoniae. The S. pneumoniae trmD gene has been isolated and expressed in Escherichia coli by using a His-tagged T7 expression vector. Recombinant protein has been purified, and its catalytic and physical properties have been characterized. The native enzyme displays a molecular mass of approximately 65,000 Da, suggesting that streptococcal TrmD is a dimer of two identical subunits. In fact, this characteristic can be extended to several other TrmD orthologs, including E. coli TrmD. Kinetic studies show that the streptococcal enzyme utilizes a sequential mechanism. Binding of tRNA by gel mobility shift assays gives a dissociation constant of 22 nM for one of its substrates, tRNA(Leu)(CAG). Other heterologous nonsubstrate tRNA species, like, tRNA (Thr)(GGT), tRNA(Phe), and tRNA (Ala)(TGC), bind the enzyme with similar affinities, suggesting that tRNA specificity is achieved via a postbinding event(s).
编码tRNA(鸟苷-1)-甲基转移酶的trmD表达下调已表明该基因对肺炎链球菌的生长至关重要。肺炎链球菌trmD基因已通过使用His标签的T7表达载体在大肠杆菌中分离并表达。重组蛋白已被纯化,其催化和物理性质已被表征。天然酶的分子量约为65,000 Da,表明链球菌TrmD是由两个相同亚基组成的二聚体。事实上,这一特性也适用于其他几种TrmD直系同源物,包括大肠杆菌TrmD。动力学研究表明,链球菌酶采用顺序机制。通过凝胶迁移率变动分析测定,其一种底物tRNA(Leu)(CAG)与tRNA的结合解离常数为22 nM。其他异源非底物tRNA种类,如tRNA(Thr)(GGT)、tRNA(Phe)和tRNA(Ala)(TGC),与该酶的结合亲和力相似,这表明tRNA特异性是通过结合后事件实现的。