Add time:07/24/2019         Source:sciencedirect.com

Using a combination of high-performance ion chromatography analysis and kinetic studies, the stereospecificity of myo-inositol hexakisphosphate dephosphorylation by the phytate-degrading enzyme P2 of Escherichia coli was established. High-performance ion chromatography revealed that the phytate-degrading enzyme P2 of E. coli degrades myo-inositol hexakisphosphate by stepwise dephosphorylation via d/l-Ins(1,2,3,4,5)P5, d/l-Ins(2,3,4,5)P4, d/l-Ins(2,4,5)P3 or d/l-Ins(1,2,4)P3, d/l-Ins(1,2)P2 or Ins(2,5)P2 or d/l-Ins(4,5)P2 to finally Ins(2)P or Ins(5)P. Kinetic parameters for myo-inositol pentakisphosphate hydrolysis by E. coli and wheat phytase, respectively, showed that the myo-inositol pentakisphosphate intermediate produced either by the phytate-degrading enzyme of wheat or E. coli are not identical. The absolute configuration of the myo-inositol pentakisphosphate isomer produced by the E. coli enzyme was determined by taking into consideration that wheat phytase produces predominantly the d-Ins(1,2,3,5,6)P5 isomer (Lim, P.E., Tate, M.E., 1973. The phytases: II. Properties of phytase fraction F1 and F2 from wheat bran and the myo-inositol phosphates produced by fraction F2. Biochim. Biophys. Acta 302, 326–328). The data demonstrate that the phytate-degrading enzyme P2 of E. coli dephosphorylates myo-inositol hexakisphosphate in a stereospecific way by sequential removal of phosphate groups via d-Ins(1,2,3,4,5)P5, d-Ins(2,3,4,5)P4, d-Ins(2,4,5)P3, Ins(2,5)P2 to finally Ins(2)P (notation 6/1/3/4/5).

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