TY - JOUR
T1 - Differential ultraviolet-visible absorbance spectra for characterizing metal ions binding onto extracellular polymeric substances in different mixed microbial cultures
AU - Yin, Cuiqin
AU - Meng, Fangang
AU - Meng, Yabing
AU - Chen, Guang Hao
N1 - Publisher Copyright:
© 2016 Elsevier Ltd.
PY - 2016/9/1
Y1 - 2016/9/1
N2 - Ultraviolet-visible (UV-vis) absorbance spectra was adopted to quantify the binding of major metal ions (e.g., Na(I), Ca((II)), Fe(III), Cu(II), and Pb(II)) on extracellular polymeric substances (EPSs) extracted from different mixed cultures. The results showed that the differential absorbance spectra (DAS) provided discernible features for revealing the changes in optical properties of EPSs induced by metals, i.e., the intensity of DAS increased largely with incrementally increased metal concentrations (Fe(III), Cu(II), and Pb(II)). It can be assumed attributable to the changes in the conformations and inter-chromophores of the EPS biomolecules. In addition, the changes in spectral parameters of DSlope325-375 (spectral slope in the range of wavelengths 325-375 nm) and DA300 (differential absorbance at 300 nm) were found to be closely related to the amounts of metals bound onto all extracted EPSs, particularly for Fe(III) and Cu(II). The decreased SR (the ratio of slope275-295 to slope350-400) of the EPS solutions after dosage of metals suggested increased molecular weight or size of the EPS biomolecules. Deconvolution of the DAS yielded six Gaussian bands, which were present in all of the EPS samples with various metals. Moreover, the relative contributions of different Gaussian bands in the DAS were determined by the nature of EPS-metal ions interactions good correlated with the covalent-bonding index. This study concluded that DAS and selected spectral parameters (DA300, DSlope325-375 and SR) can be used to successfully characterize the binding of metals onto EPS at environmentally relevant concentrations.
AB - Ultraviolet-visible (UV-vis) absorbance spectra was adopted to quantify the binding of major metal ions (e.g., Na(I), Ca((II)), Fe(III), Cu(II), and Pb(II)) on extracellular polymeric substances (EPSs) extracted from different mixed cultures. The results showed that the differential absorbance spectra (DAS) provided discernible features for revealing the changes in optical properties of EPSs induced by metals, i.e., the intensity of DAS increased largely with incrementally increased metal concentrations (Fe(III), Cu(II), and Pb(II)). It can be assumed attributable to the changes in the conformations and inter-chromophores of the EPS biomolecules. In addition, the changes in spectral parameters of DSlope325-375 (spectral slope in the range of wavelengths 325-375 nm) and DA300 (differential absorbance at 300 nm) were found to be closely related to the amounts of metals bound onto all extracted EPSs, particularly for Fe(III) and Cu(II). The decreased SR (the ratio of slope275-295 to slope350-400) of the EPS solutions after dosage of metals suggested increased molecular weight or size of the EPS biomolecules. Deconvolution of the DAS yielded six Gaussian bands, which were present in all of the EPS samples with various metals. Moreover, the relative contributions of different Gaussian bands in the DAS were determined by the nature of EPS-metal ions interactions good correlated with the covalent-bonding index. This study concluded that DAS and selected spectral parameters (DA300, DSlope325-375 and SR) can be used to successfully characterize the binding of metals onto EPS at environmentally relevant concentrations.
KW - Extracellular polymeric substances
KW - Gaussian bands
KW - Metal ions
KW - Ultraviolet-visible absorbance spectra
UR - https://www.webofscience.com/wos/woscc/full-record/WOS:000380417800033
UR - https://openalex.org/W2410722148
UR - https://www.scopus.com/pages/publications/84974849179
U2 - 10.1016/j.chemosphere.2016.05.089
DO - 10.1016/j.chemosphere.2016.05.089
M3 - Journal Article
C2 - 27300774
SN - 0045-6535
VL - 159
SP - 267
EP - 274
JO - Chemosphere
JF - Chemosphere
ER -