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PMID: 8349709 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The anticodon and discriminator base are important for aminoacylation of Escherichia coli tRNA(Asn).

The Journal of biological chemistry ·Vol. 268 ·No. 24 ·1993-08-25 ·Pages 18335-9

Li S, Pelka H, Schulman LH

Abstract

A gel shift assay that distinguishes the aminoacylated form from the deacylated form of tRNAs was used to study the requirements for aminoacylation of Escherichia coli tRNA(Asn) in vivo. tRNA(Asn) derivatives containing single base changes in their anticodons or discriminator bases were constructed, and the extent of in vivo aminoacylation was determined directly. Substitution of U35 with C35 or U36 with C36 abolished aminoacylation of the tRNA. Substitution of G34 with C34 converted tRNA(Asn) into a lysine acceptor. Thus, each of the anticodon nucleotides are important for aminoacylation of tRNA(Asn). Substitution of discriminator base G73 with A73 affected the extent of aminoacylation in vivo indicating that the discriminator base also contributes to aminoacylation of tRNA(Asn).

MeSH Terms
Acylation Anticodon/metabolism Base Sequence Blotting, Northern Escherichia coli/metabolism Lysine/metabolism Molecular Sequence Data Mutagenesis Nucleic Acid Conformation Oligonucleotide Probes Plasmids RNA, Transfer, Asn/genetics,isolation & purification,metabolism
Chemicals
Anticodon Oligonucleotide Probes RNA, Transfer, Asn Lysine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Li S
Department of Developmental Biology and Cancer, Albert Einstein College of Medicine, Bronx, New York 10461.
Pelka H
Schulman L H
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1993-08-25
Pages
18335-9
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIGMS NIH HHS · GM16995-23 · United States
NIGMS NIH HHS · GM17151 · United States
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