Biosorption mechanisms of Cu(II) by extracellular polymeric substances from Bacillus subtilis
Biosorption mechanisms of Cu(II) by extracellular polymeric substances (EPS) from Bacillus subtilis were investigated using a combination of batch experiments, attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy, isothermal titration calorimetry (ITC), and X-ray absorption...
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Published in | Chemical geology Vol. 386; pp. 143 - 151 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
29.10.2014
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Abstract | Biosorption mechanisms of Cu(II) by extracellular polymeric substances (EPS) from Bacillus subtilis were investigated using a combination of batch experiments, attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy, isothermal titration calorimetry (ITC), and X-ray absorption fine structure (XAFS) spectroscopy. A three discrete site non-electrostatic model fit the potentiometric titration data best, with the pKa values of 4.12±0.12, 6.60±0.06, and 9.09±0.03, and site concentrations of 4.81±0.62×10−3, 2.16±0.14×10−3, and 2.87±0.21×10−3mol per gram dry mass of EPS, respectively. The ATR–FTIR results confirmed the presence of the functional groups with above pKa values within the EPS molecules, and indicated that Cu(II) binding onto the EPS involves either phosphoryl or carboxyl sites, or both. The calculated enthalpies and entropies of Cu(II) adsorption onto EPS suggest that Cu(II) binds with anionic oxygen-bearing ligands and forms inner-sphere complexes with the EPS functional groups. The XAFS results were consistent with inner-sphere binding of Cu(II) by carboxyl sites with 2.03 C atoms at distance of 2.96Å in the second shell, which further suggests that the carboxyl groups are the dominant sites for Cu(II) adsorption by EPS at pH5.0, and that a five-membered chelate ring structure is the most likely binding environment for Cu(II) bound to EPS. The molecular binding mechanisms obtained in this study will add fundamental knowledge of understanding the fate of heavy metals in natural environments.
•Bacterial EPS has a considerable potential for binding metals.•Cu(II) binds with anionic oxygen-bearing ligands and forms inner-sphere complexes with the EPS.•The carboxyl groups are the dominant adsorption sites at pH5.0.•The five-membered chelate ring structure is the most likely binding environment for Cu(II) bound to EPS. |
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AbstractList | Biosorption mechanisms of Cu(II) by extracellular polymeric substances (EPS) from Bacillus subtilis were investigated using a combination of batch experiments, attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy, isothermal titration calorimetry (ITC), and X-ray absorption fine structure (XAFS) spectroscopy. A three discrete site non-electrostatic model fit the potentiometric titration data best, with the pKa values of 4.12±0.12, 6.60±0.06, and 9.09±0.03, and site concentrations of 4.81±0.62×10−3, 2.16±0.14×10−3, and 2.87±0.21×10−3mol per gram dry mass of EPS, respectively. The ATR–FTIR results confirmed the presence of the functional groups with above pKa values within the EPS molecules, and indicated that Cu(II) binding onto the EPS involves either phosphoryl or carboxyl sites, or both. The calculated enthalpies and entropies of Cu(II) adsorption onto EPS suggest that Cu(II) binds with anionic oxygen-bearing ligands and forms inner-sphere complexes with the EPS functional groups. The XAFS results were consistent with inner-sphere binding of Cu(II) by carboxyl sites with 2.03 C atoms at distance of 2.96Å in the second shell, which further suggests that the carboxyl groups are the dominant sites for Cu(II) adsorption by EPS at pH5.0, and that a five-membered chelate ring structure is the most likely binding environment for Cu(II) bound to EPS. The molecular binding mechanisms obtained in this study will add fundamental knowledge of understanding the fate of heavy metals in natural environments.
•Bacterial EPS has a considerable potential for binding metals.•Cu(II) binds with anionic oxygen-bearing ligands and forms inner-sphere complexes with the EPS.•The carboxyl groups are the dominant adsorption sites at pH5.0.•The five-membered chelate ring structure is the most likely binding environment for Cu(II) bound to EPS. Biosorption mechanisms of Cu(II) by extracellular polymeric substances (EPS) from Bacillus subtilis were investigated using a combination of batch experiments, attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy, isothermal titration calorimetry (ITC), and X-ray absorption fine structure (XAFS) spectroscopy. A three discrete site non-electrostatic model fit the potentiometric titration data best, with the pK a values of 4.12 plus or minus 0.12, 6.60 plus or minus 0.06, and 9.09 plus or minus 0.03, and site concentrations of 4.81 plus or minus 0.6210-3, 2.16 plus or minus 0.1410-3, and 2.87 plus or minus 0.2110-3 mol per gram dry mass of EPS, respectively. The ATR-FTIR results confirmed the presence of the functional groups with above pK a values within the EPS molecules, and indicated that Cu(II) binding onto the EPS involves either phosphoryl or carboxyl sites, or both. The calculated enthalpies and entropies of Cu(II) adsorption onto EPS suggest that Cu(II) binds with anionic oxygen-bearing ligands and forms inner-sphere complexes with the EPS functional groups. The XAFS results were consistent with inner-sphere binding of Cu(II) by carboxyl sites with 2.03 C atoms at distance of 2.96Aa in the second shell, which further suggests that the carboxyl groups are the dominant sites for Cu(II) adsorption by EPS at pH5.0, and that a five-membered chelate ring structure is the most likely binding environment for Cu(II) bound to EPS. The molecular binding mechanisms obtained in this study will add fundamental knowledge of understanding the fate of heavy metals in natural environments. |
Author | Cai, Peng Yang, Shanshan Xue, Aifang Fang, Linchuan Huang, Qiaoyun |
Author_xml | – sequence: 1 givenname: Linchuan surname: Fang fullname: Fang, Linchuan organization: State Key Laboratory of Soil Erosion and Dryland Farming on the Loess Plateau, Northwest A&F University, Yangling 712100, China – sequence: 2 givenname: Shanshan surname: Yang fullname: Yang, Shanshan organization: State Key Laboratory of Agricultural Microbiology, College of Resources and Environment, Huazhong Agricultural University, Wuhan 430070, China – sequence: 3 givenname: Qiaoyun surname: Huang fullname: Huang, Qiaoyun organization: State Key Laboratory of Agricultural Microbiology, College of Resources and Environment, Huazhong Agricultural University, Wuhan 430070, China – sequence: 4 givenname: Aifang surname: Xue fullname: Xue, Aifang organization: College of Science, Huazhong Agricultural University, Wuhan 430070, China – sequence: 5 givenname: Peng surname: Cai fullname: Cai, Peng email: cp@mail.hzau.edu.cn organization: State Key Laboratory of Agricultural Microbiology, College of Resources and Environment, Huazhong Agricultural University, Wuhan 430070, China |
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SubjectTerms | Adsorption ATR-FTIR Bacillus subtilis Binding Cu(II) Entropy EPS Fine structure Functional groups ITC Spectroscopy XAFS |
Title | Biosorption mechanisms of Cu(II) by extracellular polymeric substances from Bacillus subtilis |
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