Observation of complex formation between L-histidine and heterocyclic compounds in water and aqueous buffer solution using calorimetric and spectroscopic methods

被引:12
|
作者
Tyunina, Elena Yu [1 ]
Badelin, Valentin G. [1 ]
Mezhevoi, Igor N. [1 ]
机构
[1] Russian Acad Sci, GA Krestov Inst Solut Chem, Akad Skaya St 1, Ivanovo 153045, Russia
关键词
L-Histidine; Uracil; Nicotinic acid; Aqueous solution; Buffer solution; Enthalpy of dissolution; Complex formation; Thermodynamic parameters; GUANIDINE-HYDROCHLORIDE SOLUTIONS; NUCLEIC-ACID BASES; ALPHA-AMINO-ACIDS; NICOTINIC-ACID; THERMODYNAMIC CHARACTERISTICS; PHOSPHATE BUFFER; STACKING INTERACTIONS; AMINOBENZOIC ACID; L-PHENYLALANINE; ENTHALPIES;
D O I
10.1016/j.molliq.2019.01.092
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Interactions between the aromatic amino acid (L-histidine) and heterocyclic ligands (uracil, nicotinic acid) in pure water (pH 5.4) and in aqueous buffer solutions (pH 7.4) were studied by calorimetry and UV-vis spectroscopy. Stability constants (IgK(c)) and thermodynamic parameters of complex formation (Delta(c)G, Delta H-c, Delta S-c) have been calculated and presented in a table. The buffer solution was found to be a more suitable medium for complex formation between L-histidine (His) and uracil (Ura) and nicotinic acid (NA), since the amino acid forms more stable complexes with them in the buffer than in pure water: IgK(pH7.4)>IgK(pH5.4). It was shown that the complexes of NA with the His are mainly enthalpically stabilized, while those of Ura with His are stabilized by both enthalpic and entropic contributions to the free Gibbs energy for both buffer solution and pure water. The data obtained reveal the presence of complexes between His and ligands (Ura, NA) with 1:1 and 1:2 stoichiometry, respectively, for pure water and buffer solution. (C) 2019 Elsevier B.V. All rights reserved.
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页码:505 / 511
页数:7
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