Published April 2009 | Version v1
Journal article

Radical intermediates generated in the reactions of L-arginine with hydroxyl radical and sulfate radical anion: A pulse radiolysis study

  • 1. Department of Energy and Hydrocarbon Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 615-8510 (Japan)
  • 2. Research Institute of Advanced Technology, University of Osaka Prefecture, Osaka 599-8570 (Japan)

Description

Reactions of L-arginine (Arg) with hydroxyl radical (·OH) and sulfate radical anion (SO4-·) were kinetically investigated by the pulse radiolysis technique. Hydrogen abstraction from Arg by ·OH afforded redox chemically oxidizing, neutral, and reducing carbon-centered Arg radicals. Kinetic properties of the radicals indicated that the reducing species might include the δ-C-centered Arg radical and CO2 radical anion. Similar transient spectra were observed in the SO4-· reaction with Arg, suggesting direct oxidation at the guanidino group is less likely

Availability note (English)

Available from http://dx.doi.org/10.1016/j.radphyschem.2009.01.005

Additional details

Identifiers

DOI
10.1016/j.radphyschem.2009.01.005;
PII
S0969-806X(09)00018-8;

Publishing Information

Journal Title
Radiation Physics and Chemistry (1993)
Journal Volume
78
Journal Issue
4
Journal Page Range
p. 256-260
ISSN
0969-806X
CODEN
RPCHDM

Optional Information

Copyright
Copyright (c) 2009 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.