Abstract
recB and/or recC deficiency in Escherichia coli K-12 is indirectly suppressed in the presence of sbcA - mutations. Such strains remain genotypically recB and/or recC deficient but become recombination proficient and resistant to ultraviolet light. Barbour et al. (1970) showed that strains carrying sbcA - mutations contained increased levels of an ATP-independent DNase. Since the product of the recB-recC genes (exonuclease V) is a multifunctional DNase that requires ATP for the hydrolysis of double-stranded DNA (Goldmark and Linn, 1972), characterization of the ATP-independent nuclease found in sbcA - strains might provide an important clue to the in vivo function of the recB-recC gene products.
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References
Barbour, S. D., H. Nagaishi, A. Templin and A. J. Clark. 1970. Biochemical and genetic studies of recombination proficiency in Escherichia coli II. Rec + revertants caused by indirect suppression of rec - mutations. Proc. Nat. Acad. Sci. U.S.A. 67: 128.
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Templin, A., S. R. Kushner and A. J. Clark. 1972. Genetic analysis of mutations indirectly suppressing recB and recC mutations. Genetics 72: 205.
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© 1974 Plenum Press, New York
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Kushner, S.R., Nagaishi, H., Clark, A.J. (1974). Isolation of the Enzyme Associated with the sbcA Indirect Suppressor. In: Grell, R.F. (eds) Mechanisms in Recombination. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-2133-0_13
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DOI: https://doi.org/10.1007/978-1-4684-2133-0_13
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