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GENETIC CONTROL OF NEAR‐UV (300–400nm) SENSITIVITY INDEPENDENT OF THE recA GENE IN STRAINS OF ESCHERICHIA COLI K12
Author(s) -
Tuveson R. W.,
Jonas Richard B.
Publication year - 1979
Publication title -
photochemistry and photobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.818
H-Index - 131
eISSN - 1751-1097
pISSN - 0031-8655
DOI - 10.1111/j.1751-1097.1979.tb07197.x
Subject(s) - escherichia coli , biology , allele , gene , transduction (biophysics) , auxotrophy , genetics , recombination , microbiology and biotechnology , biophysics
— Stationary cells of isogenic pairs of Escherichia coli K12 strains presumably differing only in the recA function have been inactivated with near‐UV (300–400 nm) radiation. Based on near‐UV inactivation kinetics, the strains can be divided into two discrete categories in which near‐UV sensitivity does not necessarily correlate with far‐UV sensitivity conferred by two different recA alleles. Lack of overlap between near‐UV and far‐UV ( recA ) sensitivity can be explained hy assuming that a different chromosomal gene ( nur ) controls near‐UV sensitivity. Support for this hypothesis comes from a mating experiment in which four selected recombinants, isogenic with respect to auxotrophic markers, were identified exhibiting all four possible combinations of far‐UV ( recA 1 vs recA + ) and near‐UV sensitivity ( nur vs nur + ). Transduction with phase P1 has shown that introduction of the recA 1 allele into a recA + recipient does not affect the near‐UV sensitivity of the recipient. Additional matings together with transduction experiments suggest that the nur gene is located at a position on the E. coli linkage map clearly separable from recA (minute 58).