Escherichia coli merodiploids with altered ratios of episomal to chromosomal RNA polymerase activity
β Scribed by Tittawella, Ivor P. B.
- Publisher
- Springer
- Year
- 1981
- Tongue
- English
- Weight
- 440 KB
- Volume
- 184
- Category
- Article
- ISSN
- 0026-8925
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β¦ Synopsis
Starting with an E. coli merodiploid strain (rpoB + (rifS)/rpoB-(rifR)) containing equal amounts of rifampicin-sensitive and resistant RNA polymerase activities, mutants were isolated that had a disproportionately high ratio of the rifampicin-resistant enzyme activityβ’ With one strain it is shown that the mutation responsible for this phenotype is closely linked to the rifR (rpoB-) allele.
The enzyme RNA polymerase is responsible for most if not all RNA synthesis in E. coli. The RNA polymerase subunits e, ~, /~', and ~r, which occur in the stoichiometry ~2flfl'ff in the complete enzyme (holoenzyme) are encoded in the genes rpoA (72 rain on the chromosome), rpoB (89.5 min), rpoC (89.5 rain), and rpoD (66 rain), respectively (Scaife 1976;Lathe 1978;Yura and Ishihama 1979;Bachmann and Low 1980). rpoB and rpoC share an operon with the ribosomal protein genes rplJ and rplL,
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π SIMILAR VOLUMES
A temperature shift-up accompanied by a reduction in RNA polymerase activity in Escherichia coli causes an increased rate of initiation leading to a 1.7- to 2.2-fold increase in chromosome copy number. A temperature shift-up without a reduction in polymerase activity induces only a transient non-sch
Bacteria with specific temperature sensitive lethal mutations in the gene for the beta' subunit of RNA polymerase synthesize both the beta and beta' subunits at a several fold higher rate at 42 degrees C than wild-type cells relative to total protein. Synthesis of the alpha and sigma subunits procee
tained from Worthington (Freehold, N. J.). Wheat germ DNA topoisomerase was purified in our laboratory according to a procedure to be published elsewhere (W. Dynan. J. Jendrisak. D. Hager. and R. Burgess, unpublished procedure). Wheat cu-amylase was provided by R. Boston and plasmid pBR322 DNA was t