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Effect of arsenate contamination on free, immobilized and soil alkaline phosphatases: activity, kinetics and thermodynamics
Author(s) -
Wang Z. Q.,
Li Y. B.,
Tan X. P.,
He W. X.,
Xie W.,
Megharaj M.,
Wei G. H.
Publication year - 2017
Publication title -
european journal of soil science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.244
H-Index - 111
eISSN - 1365-2389
pISSN - 1351-0754
DOI - 10.1111/ejss.12397
Subject(s) - arsenate , chemistry , arsenic , alkaline phosphatase , gibbs free energy , michaelis–menten kinetics , mixed inhibition , arsenite , phosphatase , inorganic chemistry , enzyme assay , non competitive inhibition , enzyme , biochemistry , organic chemistry , thermodynamics , physics
Summary Soil alkaline phosphatase plays a vital role in phosphorus cycling in the soil ecosystem. Arsenic, an ecotoxic element, affects the normal function of phosphatase in the soil environment. To understand the effects of arsenic on phosphatase, the activity, kinetic and thermodynamic characteristics were investigated systematically following the addition of arsenate to free soluble, clay‐immobilized alkaline phosphatase ( ALP ) and soil ALP . The results showed that the ALP activity was strongly inhibited by arsenate. The Michaelis constant K m increased linearly with increasing arsenate concentration, indicating a decrease in affinity of the enzyme for the substrate. The inhibition constant K i increased after the ALP was immobilized on montmorillonite and goethite. Thermodynamic properties such as activation energy, activation enthalpy, Gibbs activation free energy and activation entropy increased when arsenate was added, which suggests that more energy is required to form the activated molecule and the enzyme–substrate complex. The reaction was less spontaneous and the enzyme–substrate complex was less ordered. Immobilization of the ALP on minerals reduced the variation in kinetic and thermodynamic properties in the presence of arsenate, indicating that immobilization provided protection from arsenate stress. Arsenate toxicity to soil ALP was affected markedly by soil texture. The results suggest that the type of arsenate inhibition on free soluble ALP was competitive inhibition, whereas for immobilized and soil ALPs , the inhibition was competitive or mixed inhibition depending on the mineral or soil property. Highlights Alkaline phosphatase ( ALP ) activity was inhibited by arsenate. The kinetic and thermodynamic properties of ALP were changed in the presence of arsenate. Arsenate inhibition on free, mineral‐immobilized ALP and soil ALP was different. ALP immobilization on minerals reduced arsenate toxicity to ALP .