TY - JOUR
T1 - Microbial sensors of ultraviolet radiation based on recA'::Lux fusions
AU - Rosen, Rachel
AU - Davidov, Yaakov
AU - LaRossa, Robert A.
AU - Belkin, Shimshon
PY - 2000
Y1 - 2000
N2 - Escherichia coli strains containing plasmid-borne fusions of the recA promoter-operator region to the Vibrio fischeri lux genes were previously shown to increase their luminescence in the presence of DNA damage hazards, and thus to be useful for genotoxicant detection. The present study expands previous work by demonstrating and investigating the luminescent response of these strains to ultraviolet radiation. Several genetic variants of the basic recA'::lux design were examined, including a tolC modification of membrane efflux capacity, a chromosomal integration of the recA'::lux fusion, a different lux reporter (Photorhabdus luminescens instead of V. fischeri, allowing the assay to be run at 37°C), and a different host bacterium (Salmonella typhimurium instead of E. coli). Generally, two modifications provided the fastest responses: the use of the S. typhimurium host or the P. luminescens lux reporter. Highest sensitivity, however, was demonstrated in an E. coli strain in which a single copy of the V. fischeri lux fusion was integrated into the bacterial chromosome.
AB - Escherichia coli strains containing plasmid-borne fusions of the recA promoter-operator region to the Vibrio fischeri lux genes were previously shown to increase their luminescence in the presence of DNA damage hazards, and thus to be useful for genotoxicant detection. The present study expands previous work by demonstrating and investigating the luminescent response of these strains to ultraviolet radiation. Several genetic variants of the basic recA'::lux design were examined, including a tolC modification of membrane efflux capacity, a chromosomal integration of the recA'::lux fusion, a different lux reporter (Photorhabdus luminescens instead of V. fischeri, allowing the assay to be run at 37°C), and a different host bacterium (Salmonella typhimurium instead of E. coli). Generally, two modifications provided the fastest responses: the use of the S. typhimurium host or the P. luminescens lux reporter. Highest sensitivity, however, was demonstrated in an E. coli strain in which a single copy of the V. fischeri lux fusion was integrated into the bacterial chromosome.
KW - Bioluminescence
KW - DNA damage
KW - Escherichia coli
KW - Genotoxicity
KW - Microbialbiosensors
KW - Photorhabdus luminescens
KW - SOS response
KW - Salmonella typhimurium
KW - UV irradiation
KW - Vibrio fischeri
UR - http://www.scopus.com/inward/record.url?scp=0034529667&partnerID=8YFLogxK
U2 - 10.1385/ABAB:89:2-3:151
DO - 10.1385/ABAB:89:2-3:151
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 11209459
AN - SCOPUS:0034529667
SN - 0273-2289
VL - 89
SP - 151
EP - 160
JO - Applied Biochemistry and Biotechnology
JF - Applied Biochemistry and Biotechnology
IS - 2-3
ER -