Chemistry Reference
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Table 12 . 26. Product yields ( G values, unit: of 10 −7 mol J −1 ) of differently hydrated DNA
γ -irradiated under N 2 . (Swarts et al. 1996)
Product
Γ
= 2.5
Γ
= 10.3
Γ
= 13.2
Γ
= 24.4
Γ
= 32.8
8-oxo-G
1.0
0.81
0.84
0.72
0.69
FAPY-G
0.12
0.21
0.13
0.081
0.16
Gua
0.12
0.079
0.08
0.095
0.094
8-oxo-A
0.014
0.015
0.018
0.013
0.014
FAPY-A
0.005
0.008
0.004
0.012
0.022
2-OH-Ade
0.006
0.004
0.005
0.01
0.01
Ade
0. 21
0.13
0.14
0.16
0.17
5-OH-Ura
0.014
0.007
0.003
0.011
0.016
5-OH-Cyt
0.004
0.001
0.002
0.008
0.007
5,6-diOH-Ura
0.004
0.003
0.004
0.006
0.005
5-OH-Hyd
0.019
0.008
0.004
0.002
0.003
Cy t
0. 21
0.14
0.13
0.13
0.15
5,6-diOHThy
0.26
0.67
0.51
0.11
0.093
5-OHMe-Ura
0.05
0.027
0.022
0.035
0.03
5-OH-5,6diHThy
0.022
0.015
0.013
0.004
0.007
Tg
0.007
0.003
0.011
0.007
0.013
5-OH-5-Me-Hyd
0.017
0.006
0.001
0.003
0.004
Thy
0.019
0.12
0.13
0.17
0.20
lower the free Gua yield, as is indeed observed. The results of a detailed prod-
uct study are compiled in Table 12.26 (for H 2 and dihydropyrimidine yields as a
function of the water content see Falcone et al. 2005).
As SSBs are concerned, data are available on single crystals of dsODNs of dif-
ferent composition (Debije et al. 2001; Razskazovskiy et al. 2003a, 2003b). There
is little base sequence specificity and preference of 5
-cleavage.
Although there is a certain span for G (SSB) among the various systems studied
((
-cleavage vs 3
10 −7 mol J −1 ), these data clearly point to the importance of SSB for-
mation by the direct effect.
In the presence of electron scavengers such as iodoacetamide, electron-gain
centers are transformed into alkyl-type radicals which preferentially abstract a
0.4
1.4)
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