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Characterization of the Adsorption of Nucleic Acid Bases onto Ferrihydrite via Fourier Transform Infrared and Surface-Enhanced Raman Spectroscopy and X-ray Diffractometry

机译:傅立叶变换红外和表面增强拉曼光谱及X射线衍射法表征铁酸铁上的核酸碱基吸附

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摘要

Minerals could have played an important role in concentration, protection, and polymerization of biomolecules. Although iron is the fourth most abundant element in Earth's crust, there are few works in the literature that describe the use of iron oxide-hydroxide in prebiotic chemistry experiments. In the present work, the interaction of adenine, thymine, and uracil with ferrihydrite was studied under conditions that resemble those of prebiotic Earth. At acidic pH, anions in artificial seawater decreased the pH at the point of zero charge (pHpzc) of ferrihydrite; and at basic pH, cations increased the pHpzc. The adsorption of nucleic acid bases onto ferrihydrite followed the order adenine uracil>thymine. Adenine adsorption peaked at neutral pH; however, for thymine and uracil, adsorption increased with increasing pH. Electrostatic interactions did not appear to play an important role on the adsorption of nucleic acid bases onto ferrihydrite. Adenine adsorption onto ferrihydrite was higher in distilled water compared to artificial seawater. After ferrihydrite was mixed with artificial seawaters or nucleic acid bases, X-ray diffractograms and Fourier transform infrared spectra did not show any change. Surface-enhanced Raman spectroscopy showed that the interaction of adenine with ferrihydrite was not pH-dependent. In contrast, the interactions of thymine and uracil with ferrihydrite were pH-dependent such that, at basic pH, thymine and uracil lay flat on the surface of ferrihydrite, and at acidic pH, thymine and uracil were perpendicular to the surface. Ferrihydrite adsorbed much more adenine than thymine; thus adenine would have been better protected against degradation by hydrolysis or UV radiation on prebiotic Earth. Key Words: FerrihydriteNucleic acid basesSeawaterAdsorptionPrebiotic chemistry. Astrobiology 15, 728-738.
机译:矿物质可能在生物分子的浓缩,保护和聚合中发挥了重要作用。尽管铁是地壳中含量第四高的元素,但文献中很少有文献描述过氧化铁-氢氧化铁在益生元化学实验中的使用。在目前的工作中,在类似于益生元地球的条件下研究了腺嘌呤,胸腺嘧啶和尿嘧啶与水铁矿的相互作用。在酸性pH值下,人造海水中的阴离子会在亚铁水合物的零电荷(pHpzc)时降低pH值。在碱性pH下,阳离子会增加pHpzc。核酸碱基在亚铁酸盐上的吸附遵循腺嘌呤尿嘧啶>胸腺嘧啶的顺序。腺嘌呤的吸附在中性pH达到峰值。然而,对于胸腺嘧啶和尿嘧啶,吸附随着pH值的增加而增加。静电相互作用在核酸碱基吸附到亚铁水合物上似乎没有发挥重要作用。与人造海水相比,蒸馏水中的腺嘌呤吸附在亚铁酸盐上的吸附率更高。将水铁矿与人造海水或核酸碱基混合后,X射线衍射图和傅立叶变换红外光谱未显示任何变化。表面增强拉曼光谱表明,腺嘌呤与水铁矿的相互作用不依赖于pH。相反,胸腺嘧啶和尿嘧啶与三水铁矿的相互作用是pH依赖性的,使得在碱性pH下,胸腺嘧啶和尿嘧啶平放在三水铁矿的表面上,而在酸性pH下,胸腺嘧啶和尿嘧啶垂直于该表面。水铁矿吸附的腺嘌呤比胸腺嘧啶多。因此,本来就可以更好地保护腺嘌呤,使其免受益生元地球上的水解或紫外线辐射降解。关键词:水铁矿核酸碱海水吸附益生元化学。天体生物学15,728-738。

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  • 来源
    《Astrobiology》 |2015年第9期|728-738|共11页
  • 作者单位

    Univ Estadual Londrina, Dept Quim CCE, Lab Quim Prebiot, BR-86051990 Londrina, PR, Brazil.;

    Univ Estadual Londrina, Dept Quim CCE, Lab Quim Prebiot, BR-86051990 Londrina, PR, Brazil.;

    Univ Estadual Londrina, Dept Quim CCE, Lab Quim Prebiot, BR-86051990 Londrina, PR, Brazil.;

    Univ Estadual Londrina, Dept Fis CCE, BR-86051990 Londrina, PR, Brazil.;

    Univ Estadual Maringa, Dept Agron CCA, Maringa, Parana, Brazil.;

    Univ Estadual Londrina, Dept Ciencias Fisiol CCB, BR-86051990 Londrina, PR, Brazil.;

    Univ Estadual Londrina, Dept Quim CCE, Lab Quim Prebiot, BR-86051990 Londrina, PR, Brazil.;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 13:06:38

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