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Journal of Bacteriology, July 2001, p. 4374-4381, Vol. 183, No. 14
Mikrobiologie/Biotechnologie,
Universität Tübingen, Auf der Morgenstelle 28, D-72076
Tübingen, Germany
Received 27 December 2000/Accepted 9 April 2001
In contrast to recA of other bacteria, the
recA gene of Streptomyces lividans has
been described as indispensable for viability (G. Muth, D. Frese, A. Kleber, and W. Wohlleben, Mol. Gen. Genet. 255:420-428,
1997.). Therefore, a closer analysis of this gene was performed to
detect possible unique features distinguishing the
Streptomyces RecA protein from the well-characterized
Escherichia coli RecA protein. The S. lividans
recA gene restored UV resistance and recombination activity of an
E. coli recA mutant. Also, transcriptional regulation was
similar to that of E. coli recA. Gel retardation experiments showed that S. lividans recA is also under
control of the Streptomyces SOS repressor LexA. The
S. lividans recA gene could be replaced only by
simultaneously expressing a plasmid encoded recA copy.
Surprisingly, the recA expression plasmid could subsequently be eliminated using an incompatible plasmid without the
loss of viability. Besides being UV sensitive and recombination deficient, all the mutants were blocked in sporulation. Genetic complementation restored UV resistance and recombination activity but
did not affect the sporulation defect. This indicated that all the
recA mutants had suffered from an additional mutation, which might allow toleration of a recA deficiency.
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.14.4374-4381.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Evidence that an Additional Mutation Is Required To
Tolerate Insertional Inactivation of the Streptomyces lividans
recA Gene
*
Corresponding author. Mailing address:
Mikrobiologie/Biotechnologie, Universität Tübingen, Auf der
Morgenstelle 28, D-72076 Tübingen, Germany. Phone: 49 7071 2974637 or 49 7071 2976945. Fax: 49 7071 295979. E-mail:
gmuth{at}biotech.uni-tuebingen.de.
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