Radiation Research 2004-04-01

Qualitative and quantitative analyses of the decomposition products that arise from the exposure of thymine to monochromatic ultrasoft X rays and 60Co gamma rays in the solid state.

Ken Akamatsu, Kentaro Fujii, Akinari Yokoya

Index: Radiat. Res. 161(4) , 442-50, (2004)

Full Text: HTML

Abstract

HPLC analyses of condensed thymine irradiated with monochromatic synchrotron ultrasoft X rays in the energy region around nitrogen and oxygen K-shell edges were performed. Cobalt-60 gamma rays were used as a reference radiation. The radiation chemical dose response of each separated thymine decomposition product was also determined. Uracil (U), 5-(hydroxymethyl)uracil (HMU), 5,6-dihydrothymine (DHT), 5-formyluracil (foU) and four main unknown products were found in the HPLC chromatogram of the sample irradiated with ultrasoft X rays in vacuo. Similar spectra of the products were also found in the gamma-ray experiment; however, some unknown products that appeared after elution of the thymine peak were significantly larger than those in the ultrasoft X- ray experiment. This result indicates the difference in radiation quality. The G value of DHT produced by gamma radiation was 10 times larger than those produced by the ultrasoft X- ray photons with energies of 395 and 407 eV corresponding to below and on the nitrogen K-shell edge, respectively. This result suggests that the differences in the photon energy and/ or in the energy spectra of the secondary electron between ultrasoft X rays and gamma rays are causing differences in the process of the radiation chemistry. Moreover, the yields of all the thymine decomposition products induced by 538 eV photons (oxygen K-shell edge) were significantly smaller than those induced by photons around the nitrogen K-shell edge. The K-shell excitation of oxygen in thymine may efficiently promote the production of small thymine fragments susceptible to desorption from the sample.


Related Compounds

  • 5-Formyluracil
  • 5-Hydroxymethylura...

Related Articles:

Role of the Escherichia coli and human DNA glycosylases that remove 5-formyluracil from DNA in the prevention of mutations.

2001-03-01

[J. Radiat. Res. 42(1) , 11-9, (2001)]

Repair of the mutagenic DNA oxidation product, 5-formyluracil.

2003-02-03

[DNA Repair (Amst.) 2(2) , 199-210, (2003)]

Nucleotide excision repair of 5-formyluracil in vitro is enhanced by the presence of mismatched bases.

2004-03-16

[Biochemistry 43(10) , 2682-7, (2004)]

Mammalian 5-formyluracil-DNA glycosylase. 2. Role of SMUG1 uracil-DNA glycosylase in repair of 5-formyluracil and other oxidized and deaminated base lesions.

2003-05-06

[Biochemistry 42(17) , 5003-12, (2003)]

Induction of T --> G and T --> A transversions by 5-formyluracil in mammalian cells.

2002-01-15

[Mutat. Res. 513(1-2) , 213-22, (2002)]

More Articles...