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J. Biol. Chem., Vol. 265, Issue 14, 8059-8064, 05, 1990
Purification and functional characterization of the Glu-tRNA(Gln) amidotransferase from Chlamydomonas reinhardtii
D Jahn, YC Kim, Y Ishino, MW Chen and D Soll
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06511.
The formation of glutaminyl-tRNA (Gln-tRNA) in Bacilli, chloroplasts, and
mitochondria occurs in a two-step reaction. This involves misacylation of
tRNA(Gln) with glutamate by glutamyl-tRNA synthetase and subsequent
amidation of Glu-tRNA(Gln) to the correctly acylated Gln- tRNA(Gln) by a
specific amidotransferase (Schon, A., Kannangara, C. G., Gough, S., and
Soll, D. (1988) Nature 331, 187-190). Here we demonstrate the existence of
this pathway in green algae and describe the purification of the
Glu-tRNA(Gln) amidotransferase from Chlamydomonas reinhardtii. The purified
enzyme showed an Mr of approximately 120,000 when analyzed by glycerol
gradient sedimentation and gel filtration. An apparent Mr of 63,000 of the
denatured protein was demonstrated by electrophoresis on sodium dodecyl
sulfate- polyacrylamide gels. This indicates that the enzyme possesses an
alpha 2 structure. The substrate for the purified enzyme is Glu-tRNA(Gln)
but not Glu-tRNA(Glu). The enzyme requires ATP, Mg2+, and an amide donor
for the conversion. Acceptable amide donors are glutamine, asparagine, and
ammonia. Blocking of the glutamine-dependent reaction by alkylation of the
protein with 6-diazo-5-oxonorleucine did not inhibit the ammonia- dependent
reaction, suggesting that the enzyme has separate glutamine and ammonia
binding sites. As suggested by Wilcox (Wilcox, M. (1969) Eur. J. Biochem.
11, 405-412) the amidation reaction may involve glutamyl-phosphate
formation, since ATP is cleaved to ADP when the enzyme is incubated with
Glu-tRNA(Gln) and ATP. In common with other glutamine amidotransferases,
the enzyme also possesses low glutaminase activity. The purified
Glu-tRNA(Gln) amidotransferase forms a stable complex with Glu-tRNA(Gln) in
the presence of ATP and Mg2+ but in the absence of the amide donor as
determined by gradient centrifugation.

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Copyright © 1990 by the American Society for Biochemistry and Molecular Biology.
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