使用傅立叶变换红外光谱(FTIR)研究镉诱导的 Padina tetrastromatica (Hauck) 变化。

Analytical Chemistry Insights Pub Date : 2008-10-15
Lisette D'Souza, Prabha Devi, Divya M P Shridhar, Chandrakant G Naik
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引用次数: 0

摘要

本研究的目的是通过傅立叶变换红外技术(FTIR),采用新陈代谢指纹图谱的方法,了解四溴褐藻(Padina tetrastromatica (Hauck))化学结构的变化。研究中的这种海洋棕色藻类在两种不同的环境条件下生长:在自然海水中(P. tetrastromatica (c))和在添加了 50 ppm 镉的海水中(P. tetrastromatica (t)),在实验室中生长三周。在中红外区域(4000-400 cm(-1))的第二衍生物红外光谱被用来区分和识别四带喙藻(c)中存在的各种官能团。接触镉后,P. tetrastromatica(t)积累了 412 ppm 的镉,并在中红外吸收区显示出带结构的扰动。四色菊(未处理和已处理)红外波段光谱特征的变化表明,镉离子与羟基、氨基、羰基和磷酸官能团结合。这可归因于以下特定波段的出现。未经处理的 P. tetrastromatica(c)在 3666 厘米(-1)处出现一条带,而经镉处理的 P. tetrastromatica(t)在 3560 厘米(-1)处出现一条带,这分别是由于非键合和键合 O-H 所致。同样,在经 Cd 处理的 P. tetrastromatica(t)中,非键合 N-H 在 3500 cm(-1) 和 3450 cm(-1) 处出现两条 N-H 伸缩振动带,在 1577 cm(-1) 处出现一条 N-H 弯曲振动带;而在经 Cd 处理的 P. tetrastromatica(t)中,在 3350 cm(-1) 处出现一条键合 N-H 伸缩振动强带,在 1571 cm(-1) 处出现一条弯曲振动强带。未经处理的 P. tetrastromatica(c)在 1764 厘米(-1)处出现一条带,而经镉处理的 P. tetrastromatica(t)则在 1760 厘米(-1)处出现一条带,这表明酯羰基的参与。镉处理后,对照样品中 1710 厘米(-1)处的条带强度急剧下降,表明 COOH 的羰基参与了金属螯合。未经处理的四色菊(c)和经镉处理的四色菊(t)在 1224 厘米(-1)处的条带表明磷酰参与了金属结合。本文还讨论了其他一些明显的此类变化。根据我们的观察,傅立叶变换红外技术被证明是检测海洋环境中金属污染物镉引起的结构变化和可能的结合位点的有效工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Use of Fourier Transform Infrared (FTIR) spectroscopy to study cadmium-induced changes in Padina tetrastromatica (Hauck).

The aim of this study is to adopt the approach of metabolic fingerprinting through the use of Fourier Transform Infrared (FTIR) technique to understand changes in the chemical structure in Padina tetrastromatica (Hauck). The marine brown alga under study was grown in two different environmental conditions; in natural seawater (P. tetrastromatica (c)) and in seawater suplemented with 50 ppm of cadmium (P. tetrastromatica (t)) for a three-week period in the laboratory. The second derivative, IR specrum in the mid-infrared region (4000-400 cm(-1)) was used for discriminating and identifying various functional groups present in P. tetrastromatica (c). On exposure to Cd, P. tetrastromatica (t) accumulated 412 ppm of Cd and showed perturbation in the band structure in the mid-IR absorption region. Variation in spectral features of the IR bands of P. tetrastromatica (untreated and treated) suggests that cadmium ions bind to hydroxyl, amino, carbonyl and phosphoryl functionalities. This was attributable to the presence of the following specific bands. A band at 3666 cm(-1) in untreated P. tetrastromatica (c) while a band at 3560 cm(-1) in Cd-treated P. tetrastromatica (t) due to non bonded and bonded O-H respectively. Similarly, non bonded N-H for P. tetrastromatica (c) showed two bands at 3500 cm(-1) and 3450 cm(-1) due to the N-H stretching vibrations and a band at 1577 cm(-1) due to N-H bending vibrations, while an intense band at 3350 cm(-1) due to bonded N-H stretching vibrations and at 1571 cm(-1) due to bending vibrations was observed for Cd-treated P. tetrastromatica (t). Involvement of ester carbonyl group is characterized by the presence of a band at 1764 cm(-1) in untreated P. tetrastromatica (c) while the Cd-treated P. tetrastromatica (t) showed the band at 1760 cm(-1). The intensity of the band at 1710 cm(-1) in the control samples decreased drastically after cadmium treatment indicating carbonyl of COOH to be involved in metal chelation. A band at 1224 cm(-1) for untreated P. tetrastromatica (c) and at 1220 cm(-1) for Cd-treated P. tetrastromatica (t) is indicative of the involvement of phosphoryl group in metal binding. Several other such changes were also evident and discussed in this paper. Based on our observation, FTIR technique proves to be an efficient tool for detecting structural changes and probable binding sites induced by the presence of a metal pollutant, cadmium, in the marine environment.

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