N-Bromosuccinimide assisted oxidation of hydrophobic tetrapeptide sequences of elastin: A mechanistic study

Linge Gowda, N. S. and Kumara, M. N. and Channe Gowda, D. and Rangappa, K. S. and Made Gowda, N. M. (2007) N-Bromosuccinimide assisted oxidation of hydrophobic tetrapeptide sequences of elastin: A mechanistic study. Journal of Molecular Catalysis A: Chemical, 269 (1). 225 - 233. ISSN 1381-1169

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Official URL: https://doi.org/10.1016/j.molcata.2007.01.019

Abstract

The repeating sequences of elastin, glycyl–glycyl–alanyl–proline (GGAP) glycyl–glycyl–isoleucyl–proline (GGIP) and more hydrophobic glycyl–glycyl–phenylalanyl–proline (GGPP), were synthesized by classical solution phase methods and characterized. The kinetics of oxidation of tetrapeptides (TPs) and their constituent amino acids (AAs) by N-bromosuccinimide (NBS) was studied in the presence of perchlorate ions in acidic medium at 28°C. The reaction was followed spectrophotometrically at λmax=240nm. The reactions follow identical kinetics, being first order each in NBS, AA and TP. No effect on the rate of H+, reduction product succinimide and ionic strength was observed. Effects of dielectric constant of the medium and the added anions such as chloride and perchlorate were studied. Activation parameters have been computed. The oxidation products of the reaction were isolated and characterized. The proposed mechanism is consistent with the experimental results. An apparent correlation was noted between the rate of oxidation and the hydrophobicity of AAs and TPs.

Item Type: Article
Uncontrolled Keywords: Amino acids, Tetra peptide sequences, Elastin, Oxidation, -Bromosuccinimide
Subjects: C Chemical Science > Chemistry
Divisions: Department of > Chemistry
Depositing User: C Swapna Library Assistant
Date Deposited: 16 Sep 2019 09:47
Last Modified: 18 Sep 2019 11:31
URI: http://eprints.uni-mysore.ac.in/id/eprint/8168

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