Abstract |
Several mutants of Rhodopseudomonas sphaeroides defective in the derepression of the enzyme ribulose 1,5-bisphosphate carboxylase have been isolated by using the unstable Tn5 vectors pJB4JI and pRK340. Transpositional insertion mutants obtained with pJB4JI were demonstrated to be incapable of increasing ribulose 1,5-bisphosphate carboxylase/ oxygenase levels when grown on butyrate- bicarbonate medium or under conditions of carbon starvation, whereas the wild-type strain increased activity four- to eightfold. When the wild-type strain was starved for carbon in the presence of chloramphenicol, no derepression was observed. Crude extracts from mutant and wild-type strains had distinct and consistent differences in protein content as observed by sodium dodecyl sulfate- polyacrylamide gel electrophoresis. Chromatographic evidence indicated that mutants were defective in the regulation of only one of the two forms of ribulose 1,5-bisphosphate carboxylase/ oxygenase synthesized by R. sphaeroides.
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Authors | K E Weaver, F R Tabita |
Journal | Journal of bacteriology
(J Bacteriol)
Vol. 156
Issue 2
Pg. 507-15
(Nov 1983)
ISSN: 0021-9193 [Print] United States |
PMID | 6313604
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- DNA Transposable Elements
- Ribulose-Bisphosphate Carboxylase
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Topics |
- Conjugation, Genetic
- DNA Transposable Elements
- Genetic Vectors
- Kinetics
- Mutation
- Plasmids
- Rhodobacter sphaeroides
(enzymology, genetics, growth & development)
- Ribulose-Bisphosphate Carboxylase
(genetics)
- Species Specificity
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