ライフサイエンスコーパス: photoreactivation

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1 S. acidocaldarius cells with visible light (photoreactivation).

2 3'-thymines; this process can be reversed by photoreactivation.

3 ore for all photolyases and is essential for photoreactivation.

4 enes (phr1 and phr2) implicated only phr2 in photoreactivation.

5 ich is similar to the expression profile for photoreactivation activity in plants.

6 plasmids carrying M. xanthus phrA rescue the photoreactivation activity of an irradiated strain of Es

7 mutant of Escherichia coli and thus confers photoreactivation activity.

8 d chromophore is considered nonessential for photoreactivation because DNA photolyase bound to only F

9 Mutation spectra obtained with and without photoreactivation by CPD photolyase indicated that the r

10 The mutant frequency in the cII gene after photoreactivation by CPD photolyase was reduced from 127

11 nd that this deficiency, as well as the phr1 photoreactivation deficiency, could be rescued by transf

12 Overexpression of PHR2 photolyase in a photoreactivation-deficient mutant, phr1, results in a l

13 phr1 is a photoreactivation-deficient strain of Chlamydomonas.

14 The important issue of photoreactivation DNA repair in plants has become even m

15 homologue in FPV suggests the presence of a photoreactivation DNA repair pathway.

16 dimers from the UV-damaged DNA by enzymatic photoreactivation has little effect on the affinity of N

17 gene encodes an FO synthase and that optimal photoreactivation in Chlamydomonas requires FO, a molecu

18 ion of PHR1 increases the rate and extent of photoreactivation in vivo, demonstrating that the damage

19 in DNA and repairs them in a process called photoreactivation in which blue light is used to initiat

20 s are repaired both through a dimer-specific photoreactivation mechanism and through a less efficient

21 med uvr2 and uvr3, that are defective in the photoreactivation of CPDs and 6-4 products, respectively

22 Mutation of phr abolishes photoreactivation of UV-induced killing, whereas mutatio

23 in bacteria, plants, and animals, including photoreactivation, plant development, and circadian phot

24 cerevisiae histone acetyltransferase Gcn5 in photoreactivation (PR) and nucleotide excision repair (N

25 by exposure to UV sunlight, is repaired in a photoreactivation process, which is essential to maintai

26 In the lacI gene the mutant frequency after photoreactivation repair of CPDs was reduced from 148 x

27 e beta, and an NAD+-dependent DNA ligase), a photoreactivation repair pathway (cyclobutane pyrimidine

28 e light photoreceptors) do not contribute to photoreactivation repair, at least in the case of Arabid

29 Whereas photoreactivation results indeed hint at the latter poss

30 ection of UV-treated pRSVcat with or without photoreactivation revealed that his cells, like XP cells

31 noncovalently bound chromophores to catalyze photoreactivation, the blue light-dependent repair of DN

32 In addition to photoreactivation, three other putative repair mechanism

33 In addition, photoreactivation was used to specifically remove CPDs,

34 Photoreactivation with (6-4) photolyase did not lower th

35 This cleavage is completely reversed by photoreactivation with E. coli UV photolyase, further de

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