Plant Physiol. Journal of Pharmacology and Experimental Therapeutics
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Plant Physiology 74:324-328 (1984)
© 1984 American Society of Plant Biologists

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Articles

A Debranching Enzyme Deficiency in Endosperms of the Sugary-1 Mutants of Maize 1

David Pan and Oliver E. Nelson

Department of Genetics, University of Wisconsin, Madison, Wisconsin 53706

Many of the sugary-1 mutants of maize (Zea mays L.) have the highly branched water-soluble polysaccharide, phytoglycogen, in quantities equal to or greater than starch as an endosperm storage product in mature seeds. We find that all sugary mutants investigated are deficient in debranching enzyme [{alpha}-(1, 6)-glucosidase] activity in endosperm tissue 23 days postpollination and suggest that this deficiency is the primary biochemical lesion leading to phytoglycogen accumulation in sugary endosperms. This would indicate that the amylopectin component of starch depends on an equilibrium between the activities of branching enzymes introducing {alpha}-1,6 branch points into the linear {alpha}-1,4 glucans and debranching enzymes. The debranching enzyme activities from nonsugary endosperms can be separated into three peaks on a hydroxyapatite column. The sugary endosperm extracts lack one of these peaks of activity while the other two fractions have much reduced activity. The embryos of developing seeds (23 days after pollination) from both sugary and nonsugary genotypes have equivalent debranching activity. The debranching enzyme activity of developing endosperms is proportional to the number of copies (0 to 3) of the nonmutant (Su) allele present suggesting that the Su allele may be the structural gene for this debranching enzyme, although this is not definitive. This identification of debranching enzyme activity as being the biochemical lesion in sugary endosperms is consistent with several previous observations on the mutant.


1 Supported by the College of Agriculture and Life Sciences, University of Wisconsin-Madison and by Department of Energy Contract No. DE-AC02-82ER12031. Paper No. 2670 from the Department of Genetics.




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