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Title: Ribosomal synthesis of polylysine from individual lysyl-tRNA/sup Lys/ in the absence of a template

Journal Article · · Dokl. Biochem. (Engl. Transl.); (United States)
OSTI ID:5856593

Earlier studies showed that ribosomes of Escherichia coli, in the absence of a template, can synthesize oligolysine, using lysyl-tRNA as a substrate. The authors present results on the use of preparations of individual lysyl-tRNA/sup Lys/ and phenylalanyl-tRNA/sup Phe/ in a system of templateless peptide synthesis. For these studies, the authors used ribosomes of E. coli MRE 600, washed four times with 1 M NH/sub 4/Cl with 10 MM MgCl/sub 2/. The purified ribosomes were stored at -70/sup 0/C in standard buffer, containing 20 mM Tris-HCl, 100 mM NH/sub 4/Cl, 10 mM MgCl/sub 2/, 0.1 mM ethylenediamine tetraacetate (EDTA), and 10% glycerin, pH/sub 37/sup 0/C/7.6. A preparation of (/sup 14/C)lysyl-tRNA/sup Lys/ was produced by affinity chromatography on immobilized factor EF-T/sub u/ from Thermus thermophilus HB8. The elongation factor EF-T/sub u/ from T. thermophilus and immobilized on BrCN-activated Sepharose 4B. The initial preparation of total tRNA of E. coli, enzymatically acylated by (/sup 14/C)lysine (348 Ci/mole, Amersham), was produced as described earlier. The degree of aminoacylation was 52-59 pmoles (/sup 14/C)lysine per unit of A/sub 260/ of tRNA.

Research Organization:
Protein Institute, Pushchino, USSR
OSTI ID:
5856593
Journal Information:
Dokl. Biochem. (Engl. Transl.); (United States), Vol. 289:1-6; Other Information: Translated from Dokl. Akad. Nauk SSSR; 289: No.3, 725-728(Jul 1986)
Country of Publication:
United States
Language:
English