Phytase and acid phosphatase activities were measured in extracts from roots of 14- to 22- day old seedlings of a range of temperate pasture species that were grown aseptically in sand culture. Phytase activity from roots of phosphorus- (P-)-deficient Trifolium subterraneum L. was characterised. Activity was enhanced by 40% when extracts were passed through Sephadex G-25, and increased by a further 20–30% with the addition of either 1 mМ EDTA or 5 mМ cysteine to assay solutions. The optimum temperature for phytase activity was 50°C and the optimum pH was 5.3. When compared with phosphatase activity measured in the roots of T. subterraneum , phytase activity exhibited narrower pH and temperature optima, and was also more strongly inhibited by Co2+, Zn2+ and AsO42− ions. Significantly, for the five pasture species examined, phytase activity was less than 5% of the total acid phosphatase activity in extracts of plant roots. Measured phytase activity ranged between 0.13 and 1.7 nkat g–1 root fresh wt and was enhanced under P-deficient relative to P-sufficient growth conditions in all of the pasture species with the exception of Trifolium repens L., for which the K m constant for activity was 50% lower in P-deficient plants. When expressed on a root fresh wt basis, increases in phytase activity of ~1.25-fold were observed for extracts from T. subterraneum and Medicago polymorpha L., and of up to 3.3-fold for Danthonia richardsonii A.B. Cashmore and Phalaris aquatica L. Increases in acid phosphatase activity with P deficiency were less evident. Between 3.1% and 4.3% only of the total phytase activity measured in root extracts was eluted from intact roots into 0.1 М NaCl.
No takes yet. Share an insight, caveat, or question.
Hayes et al. (1999) studied this question.