http://hdl.handle.net/20.500.12128/8650
Title: | The influence of heavy water as a solvent on the spontaneous oscillatory reactions of [alpha]-amino acids |
Authors: | Godziek, Agnieszka Łągiewka, Anna Kowalska, Teresa Sajewicz, Mieczysław |
Keywords: | dynamics of spontaneous peptidization; a-amino acids; heavy water; turbidimetry; mass spectrometry |
Issue Date: | 2018 |
Citation: | Reaction Kinetics, Mechanisms and Catalysis, Vol. 123 no. 1 (2018), s. 141-153 |
Abstract: | In our earlier investigations, we have discovered that a-amino acids dissolved in water or aqueous-organic solvents undergo spontaneous oscillatory chiral inversion and oscillatory peptidization in parallel, and the dynamics of these processes strongly depends on the chemical structure of a given amino acid, physicochemical characteristics of a solvent used, ambient temperature, etc. The aim of this study was to perform a preliminary reconnaissance on the possible impact of D2O on the dynamics of spontaneous behavior of the selected test aamino acids (L-Phe, L-His, L-Pro and L-Cys) stored at 25 ± 0.5 C for the period of 1 week. As the measuring techniques, turbidimetry in continuous registration mode and mass spectrometry were employed. For the sake of comparison, the analogous results were presented for the discussed a-amino acids dissolved in the aqueous organic solvents and originally published elsewhere. Based on a comparison of the turbidimetric fingerprints, the dynamics of the turbidity changes in heavy water have proved rather moderate. Mass spectrometric results provided a confirmatory evidence witnessing to rather negligible peptide yields in heavy water. Thus, turbidimetric and mass spectrometric data have served as complementary proofs of a considerable hampering of spontaneous peptidization of a-amino acids in D2O. |
URI: | http://hdl.handle.net/20.500.12128/8650 |
DOI: | 10.1007/s11144-017-1221-z |
ISSN: | 1878-5190 |
Appears in Collections: | Artykuły (WNŚiT) |
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Godziek_The_influence_of_heavy_water.pdf | 1 MB | Adobe PDF | View/Open |
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