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Active DNA photolyase encoded by a baculovirus from the insect Chrysodeixis chalcites.

Authors :
van Oers MM
Lampen MH
Bajek MI
Vlak JM
Eker AP
Source :
DNA repair [DNA Repair (Amst)] 2008 Aug 02; Vol. 7 (8), pp. 1309-18. Date of Electronic Publication: 2008 Jun 10.
Publication Year :
2008

Abstract

The genome of Chrysodeixis chalcites nucleopolyhedrovirus (ChchNPV) contains two open reading frames, Cc-phr1 and Cc-phr2, which encode putative class II CPD-DNA photolyases. CPD-photolyases repair UV-induced pyrimidine cyclobutane dimers using visible light as an energy source. Expression of Cc-phr2 provided photolyase deficient Escherichia coli cells with photoreactivating activity indicating that Cc-phr2 encodes an active photolyase. In contrast, Cc-phr1 did not rescue the photolyase deficiency. Cc-phr2 was overexpressed in E. coli and the resulting photolyase was purified till apparent homogeneity. Spectral measurements indicated the presence of FAD, but a second chromophore appeared to be absent. Recombinant Cc-phr2 photolyase was found to bind specifically F0 (8-hydroxy-7,8-didemethyl-5-deazariboflavin), which is an antenna chromophore present in various photolyases.. After reconstitution, FAD and F0 were present in approximately equimolar amounts. In reconstituted photolyase the F0 chromophore is functionally active as judged from the increase in the in vitro repair activity. This study demonstrates for the first time that a functional photolyase is encoded by an insect virus, which may have implications for the design of a new generation of baculoviruses with improved performance in insect pest control.

Details

Language :
English
ISSN :
1568-7864
Volume :
7
Issue :
8
Database :
MEDLINE
Journal :
DNA repair
Publication Type :
Academic Journal
Accession number :
18547877
Full Text :
https://doi.org/10.1016/j.dnarep.2008.04.013