The heterotrimeric Thermus thermophilus Asp-tRNAAsn amidotransferase can also generate Gln-tRNAGln

被引:38
作者
Becker, HD
Min, B
Jacobi, C
Raczniak, G
Pelaschier, J
Roy, H
Klein, S
Kern, D
Söll, D
机构
[1] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
[2] Inst Microbiol & Genet, Gottingen Genom Lab, D-37077 Gottingen, Germany
[3] CNRS, Inst Biol Mol & Cellulaire, F-67084 Strasbourg, France
[4] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06511 USA
关键词
aminoacyl-tRNA; tRNA-dependent amidation; Thermus thermophilus; tRNA specificity;
D O I
10.1016/S0014-5793(00)01697-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tlermas thermophilus strain HB8 is known to have a heterodimeric aspartyl-tRNA(Asn) amidotransferase (Asp-AdT) capable of forming Asn-tRNA(Asn) [Becker, H.D. and Kern, D. (1998) Proc. Natl, Acad. Sci. USA 95, 12832-12837]. Here we show that, like other bacteria, T. thermophilus possesses the canonical set of amidotransferase (AdT) genes (gatA, gatB and gatC). We cloned and sequenced these genes, and constructed an artificial operon for overexpression in Escherichia coli of the thermophilic holoenzyme. The overproduced T. thermophilus AdT can generate Gln-tRNA(Gln) as well as Asn-tRNA(Asn). Thus, the T. thermophilus tRNA-dependent AdT is a dual-specific Asp/ Glu-AdT resembling other bacterial AdTs. In addition, rye observed that removal of the 44 carboxy-terminal amino acids of the GatA subunit only inhibits the Asp-AdT activity, leaving the Glu-AdT activity of the mutant AdT unaltered: this shows that Asp-AdT and Glu-AdT activities can be mechanistically separated. (C) 2000 Federation of European Biochemical Societies, Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:140 / 144
页数:5
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