In pH 3.8 acetic acid-sodium acetate （HAC-NaAC） buffer solution, laccase exhibited a strong catalytic effect on the H2O2 oxidation of I- to form I2, and I2 combined with excess I- to form I3- that reacted with catio...In pH 3.8 acetic acid-sodium acetate （HAC-NaAC） buffer solution, laccase exhibited a strong catalytic effect on the H2O2 oxidation of I- to form I2, and I2 combined with excess I- to form I3- that reacted with cationic surfactants of tetradecyl dimethylbenzyl ammonium chloride （TDMAC） to produce the （TDMAC-I3）n association complex particles, which exhibited a strong resonance scattering （RS） peak at 468 nm. Under the chosen conditions, as the concentration of laccase activity increased, the RS intensity at 468 nm （1468 nm） increased linearly. The increased RS intensity A1468 nm was linear to laccase activity in the range of 0.08-0.96 U/mL, with a regression equation of △1468 nm =88.8 U-1.9, and a detection limit of 0.02 U/mL laccase. This proposed method was applied to detect laccase activity in waste water, with satisfactory results.展开更多
基金Project supported by the National Natural Science Foundation of China （Nos. 20865002, 20965002）, the Research Funds of Key Laboratory of Ecology of Rare and Endangered Species and Environmental Protection （Guangxi Normal University）, Ministry of Education （No. 10012018）.
文摘In pH 3.8 acetic acid-sodium acetate （HAC-NaAC） buffer solution, laccase exhibited a strong catalytic effect on the H2O2 oxidation of I- to form I2, and I2 combined with excess I- to form I3- that reacted with cationic surfactants of tetradecyl dimethylbenzyl ammonium chloride （TDMAC） to produce the （TDMAC-I3）n association complex particles, which exhibited a strong resonance scattering （RS） peak at 468 nm. Under the chosen conditions, as the concentration of laccase activity increased, the RS intensity at 468 nm （1468 nm） increased linearly. The increased RS intensity A1468 nm was linear to laccase activity in the range of 0.08-0.96 U/mL, with a regression equation of △1468 nm =88.8 U-1.9, and a detection limit of 0.02 U/mL laccase. This proposed method was applied to detect laccase activity in waste water, with satisfactory results.
