D'Souza Lisette, Devi Prabha, Shridhar Divya M P, Naik Chandrakant G
Bioorganic Chemistry laboratory, National Institute of Oceanography, Dona Paula Goa, 403 004, India.
Anal Chem Insights. 2008 Oct 15;3:135-43.
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.
本研究的目的是采用傅里叶变换红外(FTIR)技术的代谢指纹图谱方法,以了解四列藻(Hauck)化学结构的变化。所研究的海洋褐藻在两种不同的环境条件下生长;在天然海水中(四列藻(c))以及在添加了50 ppm镉的海水中(四列藻(t)),在实验室中培养三周。利用中红外区域(4000 - 400 cm⁻¹)的二阶导数红外光谱来鉴别和识别四列藻(c)中存在的各种官能团。暴露于镉后,四列藻(t)积累了412 ppm的镉,并在中红外吸收区域的能带结构中表现出扰动。四列藻(未处理和处理过的)红外波段光谱特征的变化表明镉离子与羟基、氨基、羰基和磷酰基官能团结合。这归因于以下特定波段的存在。未处理的四列藻(c)在3666 cm⁻¹处有一个波段,而镉处理过的四列藻(t)在3560 cm⁻¹处有一个波段,分别归因于未键合和键合的O - H。同样,四列藻(c)的未键合N - H由于N - H伸缩振动在3500 cm⁻¹和3450 cm⁻¹处有两个波段,由于N - H弯曲振动在1577 cm⁻¹处有一个波段,而镉处理过的四列藻(t)观察到由于键合N - H伸缩振动在3350 cm⁻¹处有一个强波段以及由于弯曲振动在1571 cm⁻¹处有一个波段。酯羰基的参与特征是未处理的四列藻(c)在1764 cm⁻¹处有一个波段,而镉处理过的四列藻(t)在1760 cm⁻¹处有该波段。镉处理后,对照样品中1710 cm⁻¹处波段的强度急剧下降,表明COOH的羰基参与了金属螯合。未处理的四列藻(c)在1224 cm⁻¹处以及镉处理过的四列藻(t)在1220 cm⁻¹处的一个波段表明磷酰基参与了金属结合。本文还明显观察到并讨论了其他几个此类变化。基于我们的观察,FTIR技术被证明是检测海洋环境中金属污染物镉的存在所引起的结构变化和可能的结合位点的有效工具。