The heterotrimeric Thermus thermophilus Asp‐tRNAAsn amidotransferase can also generate Gln‐tRNAGln
Open Access
- 3 July 2000
- journal article
- Published by Wiley in FEBS Letters
- Vol. 476 (3) , 140-144
- https://doi.org/10.1016/s0014-5793(00)01697-5
Abstract
Thermus thermophilus strain HB8 is known to have a heterodimeric aspartyl‐tRNAAsn amidotransferase (Asp‐AdT) capable of forming Asn‐tRNAAsn [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‐tRNAGln as well as Asn‐tRNAAsn. Thus, the T. thermophilus tRNA‐dependent AdT is a dual‐specific Asp/Glu‐AdT resembling other bacterial AdTs. In addition, we 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.Keywords
This publication has 9 references indexed in Scilit:
- Thermus thermophilus Contains an Eubacterial and an Archaebacterial Aspartyl-tRNA Synthetase,Biochemistry, 2000
- Thermus thermophilus : A link in evolution of the tRNA-dependent amino acid amidation pathwaysProceedings of the National Academy of Sciences, 1998
- Glutamyl-tRNA Gln amidotransferase in Deinococcus radiodurans may be confined to asparagine biosynthesisProceedings of the National Academy of Sciences, 1998
- Glu-tRNA Gln amidotransferase: A novel heterotrimeric enzyme required for correct decoding of glutamine codons during translationProceedings of the National Academy of Sciences, 1997
- tRNA-dependent asparagine formationNature, 1996
- Gene for a novel tRNA species that accepts L-serine and cotranslationally inserts selenocysteineNature, 1988
- High guanine plus cytosine content in the third letter of codons of an extreme thermophile. DNA sequence of the isopropylmalate dehydrogenase of Thermus thermophilus.Journal of Biological Chemistry, 1984
- Transfer RNA as a cofactor coupling amino acid synthesis with that of protein.Proceedings of the National Academy of Sciences, 1968
- Formylation of Escherichia coli Methionyl-sRNACold Spring Harbor Symposia on Quantitative Biology, 1966