Applied and Environmental Microbiology, April 2001, p. 1405-1411, Vol. 67, No. 4
Department of Plant Pathology and
Microbiology, Texas A&M University, College Station, Texas 77843-2132
Received 14 November 2000/Accepted 9 January 2001
Based on nucleotide sequence homology with the Escherichia
coli photolyase gene (phr), the phr
sequence of Pseudomonas aeruginosa PAO1 was identified from
the genome sequence, amplified by PCR, cloned, and shown to complement
a known phr mutation following expression in
Escherichia coli SY2. Stable, insertional phr
mutants containing a tetracycline resistance gene cassette were
constructed in P. aeruginosa PAO1 and P. syringae pv. syringae FF5 by homologous recombination and
sucrose-mediated counterselection. These mutants showed a decrease in
survival compared to the wild type of as much as 19-fold after
irradiation at UV-B doses of 1,000 to 1,550 J m
0099-2240/01/$04.00+0 DOI: 10.1128/AEM.67.4.1405-1411.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Construction and Analysis of Photolyase Mutants of
Pseudomonas aeruginosa and Pseudomonas syringae:
Contribution of Photoreactivation, Nucleotide Excision Repair, and
Mutagenic DNA Repair to Cell Survival and Mutability following Exposure
to UV-B Radiation
2 followed
by a recovery period under photoreactivating conditions. A phr
uvrA mutant of P. aeruginosa PAO1 was markedly
sensitive to UV-B irradiation exhibiting a decrease in survival of 6 orders of magnitude following a UV-B dose of 250 J m
2.
Complementation of the phr mutations in P. aeruginosa PAO1 and P. syringae pv. syringae FF5
using the cloned phr gene from strain PAO1 resulted in a
restoration of survival following UV-B irradiation and recovery under
photoreactivating conditions. The UV-B survival of the phr
mutants could also be complemented by the P. syringae mutagenic DNA repair determinant rulAB. Assays for
increases in the frequency of spontaneous rifampin-resistant mutants in
UV-B-irradiated strains containing rulAB indicated that
significant UV-B mutability (up to a 51-fold increase compared to a
nonirradiated control strain) occurred even in the wild-type PAO1
background in which rulAB only enhanced the UV-B survival
by 2-fold under photoreactivating conditions. The frequency of
occurrence of spontaneous nalidixic acid-resistant mutants in the PAO1
uvrA and uvrA phr backgrounds complemented with
rulAB were 3.8 × 10
5 and 2.1 × 10
3, respectively, following a UV-B dose of 1,550 J
m
2. The construction and characterization of
phr mutants in the present study will facilitate the
determination of the roles of light and dark repair systems in
organisms exposed to solar radiation in their natural habitats.
*
Corresponding author. Mailing address: Department of
Plant Pathology and Microbiology, Texas A&M University, 2132 TAMU,
College Station, TX 77843-2132. Phone: (979) 862-7518. Fax: (979)
845-6483. E-mail: gsundin{at}acs.tamu.edu.
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