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T Blumenthal

Publications and source records attributed to T Blumenthal.

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Phage Q-beta ribonucleic acid replicase. Subunit relationships determined by intramolecular cross-linking.

Phage Qbeta replicase is composed of four subunits of molecular weights 70,000, 65,000, 45,000, and 35,000. Treatment of the enzyme with protein cross-linking reagents results in formation of three covalently bound complexes of molecular weights 215,000, 135,000, and 80,000. Analysis of the two larger complexes formed by cross-linking with a reversible cross-linker (methyl-4-mercaptobutyrimidate) demonstrates that the 215,000 molecular weight complex is composed of one each of the replicase subunits, while the 135,000 molecular weight complex is composed of the two larger subunits. The 80,000 molecular weight complex was shown to be made up of the two smaller subunits by cross-linking these two subunits in the absence of the larger pair. Increasing ionic strength stabilizes the large complex at the expense of the two smaller complexes. The presence of stoichiometric amounts of Qbeta RNA during cross-linking dramatically reduces formation of the large complex; other natural and synthetic RNAs reduce the formation of this complex to a lesser extent.

Butyrates↗

Bacteriophage Q replicase contains the protein biosynthesis elongation factors EF Tu and EF Ts.

The enzyme, Qbeta replicase, responsible for the replication of the RNA of Escherichia coli pahge Qbeta, is composed of four nonidentical subunits, three of which, I, III, and IV, are coded for by the bacterial genome, while subunit II is phage-specific. SUBUNIT IV IS SHOWN TO BE IDENTICAL TO THE PROTEIN SYNTHESIS ELONGATION FACTOR EF TS BY THE FOLLOWING CRITERIA: coelectrophoresis on polyacrylamide gels in sodium dodecyl sulfate and in urea buffers, identity of the first seven amino acids at the amino-terminus, precipitation of sub-unit IV by anti-EF T-factor serum, and stimulation of EF Tu-GDP exchange by subunit IV. Subunit III is shown to be identical to the protein synthesis elongation factor EF Tu by the following criteria: coelectrophoresis on sodium dodecyl sulfate gels, precipitation of EF Tu by anti-Qbeta replicase serum, binding of guanine nucleotides, and binding of phenylalanyl-tRNA. In addition, Qbeta replicase activity can be reconstituted from subunits I and II with EF Tu and EF Ts.

Acrylamides↗