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A novel lysine-substituted nucleoside in the first position of the anticodon of minor isoleucine tRNA from Escherichia coli
- Source :
- Scopus-Elsevier
- Publication Year :
- 1988
- Publisher :
- Elsevier BV, 1988.
-
Abstract
- A minor species of isoleucine tRNA (tRNA(minor Ile)) specific to the codon AUA has been isolated from Escherichia coli B and a modified nucleoside N+ has been found in the first position of the anticodon (Harada, F., and Nishimura, S. (1974) Biochemistry 13, 300-307). In the present study, tRNA(minor Ile)) was purified from E. coli A19, and nucleoside N+ was prepared, by high-performance liquid chromatography, in an amount (0.6) A260 units) sufficient for the determination of chemical structures. By 400 MHz 1H NMR analysis, nucleoside N+ was found to have a pyrimidine moiety and a lysine moiety, the epsilon amino group of which was involved in the linkage between these two moieties. From the NMR analysis together with mass spectrometry, the structure of nucleoside N+ was determined as 4-amino-2-(N6-lysino)-1-(beta-D-ribofuranosyl)pyrimidinium ("lysidine"), which was confirmed by chemical synthesis. Lysidine is a novel type of modified cytidine with a lysine moiety and has one positive charge. Probably because of such a unique structure, lysidine in the first position of anticodon recognizes adenosine but not guanosine in the third position of codon.
- Subjects :
- Pyrimidine
Stereochemistry
General Chemical Engineering
Lysine
Molecular Sequence Data
Guanosine
Biology
medicine.disease_cause
Biochemistry
Mass Spectrometry
chemistry.chemical_compound
RNA, Transfer
medicine
Anticodon
Escherichia coli
Moiety
Agmatidine
RNA, Transfer, Ile
Molecular Biology
Isoleucine tRNA
Base Sequence
Nucleosides
Cytidine
General Chemistry
Cell Biology
RNA, Transfer, Amino Acid-Specific
Kinetics
chemistry
Transfer RNA
Nucleic Acid Conformation
Lysidine
Nucleoside
Subjects
Details
- ISSN :
- 00219258
- Volume :
- 263
- Database :
- OpenAIRE
- Journal :
- Journal of Biological Chemistry
- Accession number :
- edsair.doi.dedup.....39a355df9d5eea417b860c6c436bf08a
- Full Text :
- https://doi.org/10.1016/s0021-9258(19)76533-8