Title of article :
Elongation Factor Ts ofChlamydia trachomatis:Structure of the Gene and Properties of the Protein
Author/Authors :
Zhang، نويسنده , , You-xun and Tao، نويسنده , , Jun and Zhou، نويسنده , , Min and Meng، نويسنده , , Qin and Zhang، نويسنده , , Li and Shen، نويسنده , , Li and Klein، نويسنده , , Rachel and Miller، نويسنده , , David L.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 1997
Abstract :
A putative structural gene cluster containing four open reading frames (ORFs) located downstream of theomp1gene ofChlamydia trachomatismouse pneumonitis (MoPn) was cloned and sequenced. A GenBank survey indicated that the identified cluster is similar to therpsB-tsf-pyrH(smbA)-frrregion ofEscherichia coli.The second ORF was 846 bp encoding a 282-amino-acid polypeptide with a calculatedMr30,824. Alignment of this deduced protein sequence andE. colielongation factor Ts (EF-Ts, product oftsf) demonstrated 34% identity and an additional 14% similarity. The putative chlamydialtsfgene was expressed inE. colias a nonfusion protein and as a 6× His-tagged fusion protein. By SDS–PAGE analysis, the molecular weights of the nonfusion recombinant protein and a protein of chlamydial elementary bodies (EBs), which was recognized by monoclonal antibodies derived from the nonfusion recombinant protein, are 34 kDa. The purified recombinant 6× His-tagged fusion protein increased the rate of GDP exchange with bothChlamydiaandE. colielongation factor Tu (EF-Tu). These data show that the second gene of the identified cluster istsf.Unlike EF-Ts from any other species, its activity was comparable to that ofE. coliEF-Ts in exchange reaction withE. coliEF-Tu.
Keywords :
GDP exchange , 6× His-tagged fusion protein , C. trachomatis , E. coli , EF-Ts , EF-Tu
Journal title :
Archives of Biochemistry and Biophysics
Journal title :
Archives of Biochemistry and Biophysics