Aspergillus ficuum phytase activity is inhibited by cereal grain components.

PLoS One

Department of Molecular Biology and Genetics, Research Center Flakkebjerg, Aarhus University, Slagelse, Denmark.

Published: September 2017

AI Article Synopsis

  • The study reveals that grain components from barley, rice, wheat, and maize can inhibit Aspergillus ficuum phytase, with the inhibition showing a dose-dependent relationship and differing significantly across cereal species and cultivars.* -
  • F. graminearum infected wheat grains exhibit the highest inhibition of phytase activity, with the greatest effect found in grain protein extracts (GPE) from these infected samples compared to non-infected ones.* -
  • The research identifies a 30-35 kDa protein purified from barley that inhibits phytase activity, and suggests that the inhibition mechanism involves aspartic protease activity, as evidenced by the effect of pepstatin A in reversing the inhibition.*

Article Abstract

In the current study, we report for the first time that grain components of barley, rice, wheat and maize can inhibit the activity of Aspergillus ficuum phytase. The phytase inhibition is dose dependent and varies significantly between cereal species, between cultivars of barley and cultivars of wheat and between Fusarium graminearum infected and non-infected wheat grains. The highest endpoint level of phytase activity inhibition was 90%, observed with grain protein extracts (GPE) from F. graminearum infected wheat. Wheat GPE from grains infected with F. graminearum inhibits phytase activity significantly more than GPE from non-infected grains. For four barley cultivars studied, the IC50 value ranged from 0.978 ± 0.271 to 3.616 ± 0.087 mg×ml-1. For two non-infected wheat cultivars investigated, the IC50 values were varying from 2.478 ± 0.114 to 3.038 ± 0.097 mg×ml-1. The maize and rice cultivars tested gaveIC50 values on 0.983 ± 0.205 and 1.972 ± 0.019 mg×ml-1, respectively. After purifying the inhibitor from barley grains via Superdex G200, an approximately 30-35 kDa protein was identified. No clear trend for the mechanism of inhibition could be identified via Michaelis-Menten kinetics and Lineweaver-Burk plots. However, testing of the purified phytase inhibitor together with the A. ficuum phytase and the specific protease inhibitors pepstatin A, E64, EDTA and PMSF revealed that pepstatin A repealed the phytase inhibition. This indicates that the observed inhibition of A. ficuum phytase by cereal grain extracts is caused by protease activity of the aspartic proteinase type.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5417552PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0176838PLOS

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