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Plant Physiology 71:229-234 (1983)
© 1983 American Society of Plant Biologists

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Articles

Specific Determination of {alpha}-Amylase Activity in Crude Plant Extracts Containing {beta}-Amylase 1

Douglas C. Doehlert2 and Stanley H. Duke3

Department of Agronomy, University of Wisconsin, Madison, Wisconsin 53706

The specific measurement of {alpha}-amylase activity in crude plant extracts is difficult because of the presence of {beta}-amylases which directly interfere with most assay methods. Methods compared in this study include heat treatment at 70°C for 20 min, HgCl2 treatment, and the use of the {alpha}-amylase specific substrate starch azure. In comparing alfalfa (Medicago sativa L.), soybeans (Glycine max [L.] Merr.), and malted barley (Hordeum vulgare L.), the starch azure assay was the only satisfactory method for all tissues. While {beta}-amylase can liberate no color alone, over 10 International units per milliliter {beta}-amylase activity has a stimulatory effect on the rate of color release. This stimulation becomes constant (about 4-fold) at {beta}-amylase activities over 1,000 International units per milliliter. Two starch azure procedures were developed to eliminate {beta}-amylase interference: (a) the dilution procedure, the serial dilution of samples until {beta}-amylase levels are below levels that interfere; (b) the {beta}-amylase saturation procedure, addition of exogenous {beta}-amylase to increase endogenous {beta}-amylase activity to saturating levels. Both procedures yield linear calibrations up to 0.3 International units per milliliter. These two procedures produced statistically identical results with most tissues, but not for all tissues. Differences between the two methods with some plant tissues was attributed to inaccuracy with the dilution procedure in tissues high in {beta}-amylase activity or inhibitory effects of the commercial {beta}-amylase. The {beta}-amylase saturation procedure was found to be preferable with most species. The heat treatment was satisfactory only for malted barley, as {alpha}-amylases in alfalfa and soybeans are heat labile. Whereas HgCl2 proved to be a potent inhibitor of {beta}-amylase activity at concentrations of 10 to 100 micromolar, these concentrations also partially inhibited {alpha}-amylase in barley malt. The reported {alpha}-amylase activities in crude enzyme extracts from a number of plant species are apparently the first specific measurements reported for any plant tissues other than germinating cereals.


2 Present address: United States Department of Agriculture/Agricultural Research Service, Plant Science Research, 3127 Ligon Road, North Carolina State University, Raleigh, NC 27650.

3 To whom reprint requests should be addressed.

1 Supported by the College of Agricultural and Life Sciences, University of Wisconsin-Madison.







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Copyright © 1983 by the American Society of Plant Biologists