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PMID: 3281834 Published · ppublish English Journal Article

Isoleucyl-tRNA synthetase from baker's yeast and from Escherichia coli MRE 600. Discrimination of 20 amino acids in aminoacylation of tRNA(Ile)-C-C-A.

European journal of biochemistry ·Vol. 173 ·No. 1 ·1988-04-05 ·Pages 27-34

Freist W, Sternbach H, Cramer F

Abstract

For discrimination between isoleucine and 19 other amino acids by isoleucyl-tRNA synthetase from baker's yeast and from Escherichia coli MRE 600, discrimination factors D have been determined from kcat and Km values in amino-acylation of cognate tRNA(Ile)-C-C-A. Factors D are also products of initial discrimination factors I' and proof-reading factors II'; D = I' II'. Factors II' were calculated from AMP formation stoichiometries and factors I' as quotients of D and II'; I' = D/II'. II' is considered as a product of a pre- and post-transfer proof-reading factor (II' = II1II2), I' as a product of initial discrimination factors I1 and I2 which are due to two steps of initial discrimination. With the yeast enzyme the highest accuracy is achieved in discrimination between isoleucine and valine (D = 38,000); other D values in a high range (10,000-20,000) are observed for Gly, Ser, Thr, Leu and Met; the lowest factors D belong to Cys, Asp, Asn and Trp (300-700); the remaining amino acids are discriminated with medium D values (1000-10,000). Discrimination factors D observed for isoleucyl-tRNA synthetase from E. coli are on average 2-3 times higher than for the yeast enzyme. Highest values were found in discrimination against Gly, Ala and Val (60,000-72,000), the lowest values for Cys, Arg and Trp (600-3000); the other amino acids exhibit D values between 20,000 and 50,000. Initial discrimination factors can be related to hydrophobic interaction forces between the substrates and the enzyme; a hypothetical model of the amino acid binding site is discussed.

MeSH Terms
Acylation Adenosine Monophosphate/biosynthesis Amides/metabolism Amino Acids/metabolism Amino Acyl-tRNA Synthetases/metabolism Energy Metabolism Escherichia coli/enzymology Hydrolysis Isoleucine-tRNA Ligase/metabolism Protein Conformation Saccharomyces cerevisiae/enzymology Substrate Specificity
Chemicals
Amides Amino Acids Adenosine Monophosphate Amino Acyl-tRNA Synthetases Isoleucine-tRNA Ligase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Freist W
Abteilung Chemie, Max-Planck-Institut, Göttingen, Federal Republic of Germany.
Sternbach H
Cramer F
Article Info
Journal
European journal of biochemistry
Abbr.
Eur J Biochem
ISSN
0014-2956
Published
1988-04-05
Pages
27-34
Language
English
Region
England
NLM ID
0107600
Subset
IM
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