Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.451692
Title: Purification of Semliki Forest virus RNA-dependent RNA polymerase
Author: Clewley, Jonathan P.
ISNI:       0000 0001 3559 0061
Awarding Body: University of Warwick
Current Institution: University of Warwick
Date of Award: 1976
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Abstract:
Replicase activity was found in the cytoplasm of the infected cell and, after removal of nuclei, the replication complex was characterized by isopycnic sucrose gradient centrifugation. A membranous band at 35% (w/w) sucrose contained replicase activity and was the site of RNA synthesis. At 1 3/4 hr post-infection the replicase was associated with input virion RNA but not input virion proteins. Replicase present in the post-nuclear supernatant was competent to synthesize all forms of virus-specific RNA found in the infected cell. However, on further purification there was a loss of the production of discrete single- stranded RNA in vitro. This loss was probably caused by endogenous ribonuclease activity and disruption of the replication complex. Recovery of the replicase rich band from isopycnic gradients allowed it to be analysed on linear sucrose gradients. The replication complex had an S-value of 250 which, on nonionic detergent treatment, was converted to a 25S structure. The replicase activity of this 25S complex was specifically bound to an oligo(dT)- cellulose column bearing attached 42S virion RNA. Analysis of the polypeptides eluted off in the fractions having replicase activity showed that there were only 3 labelled bands visible on polyacrylamide gels. Two of these comigrated with two non-structural virus polypeptides identified in infected cells. The third polypeptide of the purified replicase preparation (MW 40,000 daltons) is probably a host protein. Material from mock- infected cells purified exactly as the replicase contained only the 40,000 dalton protein. It is therefore concluded that SFV replicase contains 2 virus-specific polypeptides which have MWs of 90,000 and 63,000 daltons.
Supervisor: Not available Sponsor: Science Research Council
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.451692  DOI: Not available
Keywords: Q Science (General) ; QP Physiology
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