Microcalorimetric studies of the effects of MgCl2 concentrations and pH on the adsorption of DNA on montmorillonite, kaolinite and goethite

被引:59
作者
Cai, P [1 ]
Huang, QY [1 ]
Zhang, XW [1 ]
机构
[1] Huazhong Agr Univ, Coll Resources & Environm, State Key Lab Agr Microbiol, Wuhan 430070, Peoples R China
基金
中国国家自然科学基金;
关键词
microcalorimetry; thermodynamic parameters; adsorption; DNA; minerals;
D O I
10.1016/j.clay.2005.11.004
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
This study attempted to comprehend the interaction mechanisms between DNA and the common minerals in soil such as montmorillonite, kaolinite and goethite at various environmental conditions. The effects of MgCl2 concentrations (0, 1, 10 and 60 mM) and pH (3.0, 5.0, 7.0 and 9.0) on the adsorption of DNA on the examined minerals were investigated by the equilibrium adsorption and direct measurement of adsorption enthalpies. The adsorption isotherms fitted by the Langmuirian model revealed that the maximum capacities and affinities of DNA adsorption on minerals increased with MgCl2 concentrations and decrease of pH. No DNA was adsorbed on montmorillonite at pH 9.0. The values of DNA adsorption enthalpies (Delta H-ads) ranged from -0.3 to 4.9 kJ g(-1) at different systems. The Delta H-ads values decreased with increasing MgCl2 concentrations and decreasing pH. The adsorption of DNA on montmorillonite, kaolinite and goethite was an exothermic reaction (-0.3<Delta H-ads<-0.1 kJ g(-1)) at 60 mM MgCl2 and pH 3.0, suggesting a more significant electrostatic attraction in the adsorption process. In contrast, DNA adsorption on minerals became endothermic (0.1 < Delta H-ads<4.9 kJ g(-1)) at 0-10 mM MgCl2 and pH 5.0-9.0 and dehydration effects were considered as the dominant driving forces for DNA adsorption on minerals. The thermodynamic parameters presented in this study have important implications for clarifying the binding mechanisms between DNA and mineral particles in soil and associated environments. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:147 / 152
页数:6
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