A Simple and Rapid Test for Assessment of Endosperm Protein Modification During Malting*

A simple test has been developed for the quantitation of endosperm protein modification in malts. Barley meals or ground malts were extracted with a suitable solvent and the clarified hordein extract diluted into an appropriate precipitant. Of a variety of extractants and precipitants investigated, 1M urea-1% (v/v) mercaptoethanol and 1M sodium chloride were respectively found to be most suitable. Under these conditions a turbid suspension forms; the turbidity of extracts decreased progressively during malting. Turbidity was due to selective precipitation of a specific group of “B” hordeins. In an analysis of nine varieties differing in malting qualities, a significant correlation between the reduction in extract turbidity and cell wall modification (Calcofluor staining) was observed at 48 hours' malting. In addition, for each variety examined, protein modification occurred about one day before carbohydrate modification. Analysis of commercial malts and several samples of selected cultivars from regional trials found good correlations between malt turbidities and percent malt extract and Kolbach index. The test is rapid (10–90 mins) and can be used to screen large numbers of samples; since it is simpler than alpha—amino nitrogen or Kolbach index determination, it may be of use in analysis of malts for protein modification.