Abstract
This communication describes the methods for the purification of the elongation factor G from B. subtilis cells and the characterization of its activity by a direct means using 3H labeled puromycin and 'natural' peptidyl tRNA molecules. The application of this method to the analysis of a temperature sensitive mutant blocked in protein synthesis is discussed.
Original language | English |
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Title of host publication | AMER.SOC.MICROBIOL.,WASHINGTON |
Pages | 194-201 |
Number of pages | 8 |
State | Published - 1976 |