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Comparison of methods used to measure polyphenol oxidase in wheat.
D. VAZQUEZ (1,2), B.
Watts (1), F. Townley-Smith (3), O. Lukow (3), and N. Ames (3). (1) Dept. Foods and Nutrition, University
of Manitoba, Winnipeg, MB, Canada; (2) INIA, La Estanzuela, Uruguay; (3) Cereal Research Center,
Winnipeg, MB, Canada.
Polyphenol Oxidase (PPO) has been implicated in enzymatic browning of wheat end products during
processing or storage. This discoloration makes products less acceptable to consumers. The aim of this
research was to identify a rapid, reliable method of measuring PPO activity for application in wheat
breeding experiments. Methods for PPO activity were tested on two sets of white wheats, one set consisting
of 27 samples of 6 classes, the second of 56 double haploid lines obtained from a cross of a white by red
wheats, and 8 checks, grown in four locations. PPO activity was measured by an oxygen consumption rate
method, and by two absorbance assay methods. One spectrophotometric assay method used an aqueous
extract; the other the whole kernel. Catechol and tyrosine were used as substrates. Results for the oxygen
consumption method and for assays performed using whole kernels, showed better results than for assays
carried out on extracts. Correlation coefficients between PPO methods were determined for each set of
samples. Results were correlated with dough discoloration data.