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Using a combination of high-performance ion chromatography analysis and kinetic studies, the pathway of dephosphorylation of myo-inositol hexakisphosphate by the phytases purified from faba bean and lupine seeds, respectively, was established. The data demonstrate that the legume seed phytases under investigation dephosphorylate myo-inositol hexakisphosphate in a stereospecific way. The phytase from faba bean seeds and the phytase LP2 from lupine seeds degrade phytate by sequential removal of phosphate groups via D-Ins(1,2,3,5,6)P(5), D-Ins(1,2,5,6)P(4), D-Ins(1,2,6)P(3), and D-Ins(1,2)P(2) to finally Ins(2)P, whereas the phytases LP11 and LP12 from lupine seeds generate the final degradation product Ins(2)P via D-Ins(1,2,4,5,6)P(5), D-Ins(1,2,5,6)P(4), D-Ins(1,2,6)P(3), and D-Ins(1,2)P(2).
6-Phytase, info:eu-repo/classification/ddc/660, 660, Phytic Acid, ddc:660, Hydrolysis, Phytate degradation, Myo-inositol phosphate isomers, Fabaceae, Hydrogen-Ion Concentration, Lupine, Kinetics, Chemical engineering, Seeds, Faba bean, Phosphorylation, Legume phytase
6-Phytase, info:eu-repo/classification/ddc/660, 660, Phytic Acid, ddc:660, Hydrolysis, Phytate degradation, Myo-inositol phosphate isomers, Fabaceae, Hydrogen-Ion Concentration, Lupine, Kinetics, Chemical engineering, Seeds, Faba bean, Phosphorylation, Legume phytase
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