针铁矿
吸附
X射线光电子能谱
化学
傅里叶变换红外光谱
动力学
DNA
磷酸盐
化学工程
无机化学
物理化学
有机化学
生物化学
量子力学
物理
工程类
作者
Michael P. Schmidt,Carmen Enid Martı́nez
出处
期刊:Langmuir
[American Chemical Society]
日期:2017-07-21
卷期号:33 (34): 8525-8532
被引量:38
标识
DOI:10.1021/acs.langmuir.7b01911
摘要
DNA fate in soil plays an important role in the cycling of genetic information in the environment. Adsorption onto mineral surfaces has great impact on this function. This study probes the kinetics, equilibrium behavior and bonding mechanisms associated with adsorption of DNA onto goethite, a common soil mineral. Surface sensitive ATR-FTIR and XPS approaches are applied to directly characterize the DNA-goethite interface. Adsorption kinetics follow a pseudo-first-order model, suggesting adsorption rate is surface limited. Adsorption rate constants increase with DNA concentration, ranging from 3.29 × 10-3 to 3.55 × 10-1 min-1. Equilibrium adsorption, as monitored by ATR-FTIR and XPS, follows the Langmuir model, with a high affinity of DNA for goethite observed (K = 1.25 × 103 and 9.48 × 102 mL/mg for ATR-FTIR and XPS, respectively). ATR-FTIR and XPS characterization of the structure of surface adsorbed DNA demonstrates inner-sphere coordination between backbone phosphate groups of DNA and goethite. Furthermore, adsorbed DNA retains a B-form, suggesting the DNA helix adsorbs on goethite without degradation or alteration to helical structure, despite binding of backbone phosphate groups. This work advances our understanding of the environmental behavior of DNA by characterizing the mechanism of adsorption onto a prominent soil mineral.
科研通智能强力驱动
Strongly Powered by AbleSci AI