TY - JOUR
T1 - Increased UV sensitivity of Escherichia coli cells after introduction of foreign photolyase genes
AU - Kobayashi, Takayasu
AU - Takao, Masashi
AU - Oikawa, Atsushi
AU - Yasui, Akira
N1 - Funding Information:
We thank Dr. K. Yamamoto for helpful suggestions and providing us with E. coli mutants. This work was supported by a grant-in-aid for scientific research on priority area 'The Molecular Mechanism of Photoreception', No. 62621001, from the Ministry of Education, Science and Culture of Japan to A.Y.
PY - 1990/7
Y1 - 1990/7
N2 - High-expression plasmids for photolyase (phr) genes from the bacteria Escherichia coli, Anacystis nidulans, Streptomyces griseus and Halobacterium halobium and the yeast Saccharomyces cerevisiae were constructed and introduced into E. coli phr recA cells. As previously reported, all introduced phr genes provided the host cells with photoreactivation-repair activity and the introduced E. coli phr gene rendered the host cells more UV-resistant in the dark. E. coli cells harboring foreign phr genes, however, were found to be more sensitive to UV light in the dark than cells containing the vector plasmid only. These differences in UV sensitivity in the dark disappeared when the host cells had an additional mutation, uvrA, suggesting that the foreign photolyases inhibited the E. coli excision-repair system.
AB - High-expression plasmids for photolyase (phr) genes from the bacteria Escherichia coli, Anacystis nidulans, Streptomyces griseus and Halobacterium halobium and the yeast Saccharomyces cerevisiae were constructed and introduced into E. coli phr recA cells. As previously reported, all introduced phr genes provided the host cells with photoreactivation-repair activity and the introduced E. coli phr gene rendered the host cells more UV-resistant in the dark. E. coli cells harboring foreign phr genes, however, were found to be more sensitive to UV light in the dark than cells containing the vector plasmid only. These differences in UV sensitivity in the dark disappeared when the host cells had an additional mutation, uvrA, suggesting that the foreign photolyases inhibited the E. coli excision-repair system.
KW - Evolution
KW - Excision repair
KW - Photolyase
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U2 - 10.1016/0921-8777(90)90029-5
DO - 10.1016/0921-8777(90)90029-5
M3 - Article
C2 - 2114539
AN - SCOPUS:0025306994
SN - 0921-8777
VL - 236
SP - 27
EP - 34
JO - Mutation Research - DNA Repair
JF - Mutation Research - DNA Repair
IS - 1
ER -