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作 者:Peng Zhang Philippe Van Cappellen Kunfu Pi Songhu Yuan
机构地区:[1]State Key Laboratory of Biogeology and Environmental Geology,China University of Geosciences,68 Jincheng Street,East Lake High-Tech Development Zone,Wuhan,Hubei 430078,China [2]Ecohydrology Research Group,Water Institute and Department of Earth and Environmental Sciences,University of Waterloo,Waterloo,Ontario N2L 3G1,Canada [3]Hubei Key Laboratory of Yangtze Catchment Environmental Aquatic Science,School of Environmental Studies,China University of Geosciences,68 Jincheng Street,East Lake High-Tech Development Zone,Wuhan,Hubei 430078,China
出 处:《Fundamental Research》2022年第2期208-217,共10页自然科学基础研究(英文版)
基 金:Natural Sciences and Engineering Research Council of Canada(Strategic Project STPGP 494652-16);the This work was financially supported by the Canada Excellence Research Chair(CERC)program;the National Natural Science Foundation of China(Grants No.41907169,42025703);the Fundamental Research Funds for the Central Universities,China University of Geosciences(Wuhan)(Grant No.CUG2106364).
摘 要:Flavins and siderophores secreted by various plants,fungi and bacteria under iron(Fe)deficient conditions play important roles in the biogeochemical cycling of Fe in the environment.Although the mechanisms of flavin and siderophore mediated Fe(Ⅱ)reduction and dissolution under anoxic conditions have been widely studied,the influence of these compounds on Fe(ID)oxidation under oxic conditions is still unclear.In this study,we investi-gated the kinetics of aqueous Fe(Ⅱ)(17.8μM)oxidation by O_(2)at pH 5-7 in the presence of riboflavin(oxidized(RBF)and reduced(RBFH_(2)))and desferrioxamine B(DFOB)as representative flavins and siderophores,respec-tively.Results showed that the addition of RBF/RBFH_(2)or DFOB markedly accelerates the oxidation of aqueous Fe(Ⅱ)by O_(2).For instance,at pH 6,the rate of Fe(Ⅱ)oxidation was enhanced 20-70 times when 10μM RBFH_(2)was added.The mechanisms responsible for the accelerated Fe(Ⅰ)oxidation are related to the redox reactivity and complexation ability of RBFH_(2),RBF and DFOB.While RBFH_(2)does not readily complex Fe(Ⅰ)/Fe(Ⅱ),it can activate O_(2)and generate reactive oxygen species,which then rapidly oxidize Fe(Ⅱ).In contrast,both RBF and DFOB do not reduce O_(2)but react with Fe(Ⅱ)to form RBF/DFOB-complexed Fe(Ⅱ),which in turn accelerates Fe(Ⅰ)oxidation.Furthermore,the lower standard reduction potential of the Fe(Ⅰ)-DFOB complex,compared to the Fe(Ⅰ)-RBF complex,correlates with a higher oxidation rate constant for the Fe(Ⅰ)-DFOB complex.Our study reveals an overlooked catalytic role of flavins and siderophores that may contribute to Fe(Ⅱ)/Fe(Ⅱ)cycling at oxic-anoxic interfaces.
关 键 词:RIBOFLAVIN Desferrioxamine B Ferrous iron Abiotic oxidation OXYGEN
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