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Characterization of SU1 Isoamylase, a Determinant of Storage Starch Structure in Maize1
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AbstractFunction of the maize (Zea mays) gene sugary1 (su1) is required for normal starch biosynthesis in endosperm. Homozygoussu1- mutant endosperms accumulate a highly branched polysaccharide, phytoglycogen, at the expense of the normal branched component of starch, amylopectin. These data suggest that both branched polysaccharides share a common precursor, and that the product of thesu1 gene, designated SU1, participates in kernel starch biosynthesis. SU1 is similar in sequence to α-(1→6) glucan hydrolases (starch-debranching enzymes [DBEs]). Specific antibodies were produced and used to demonstrate that SU1 is a 79-kD protein that accumulates in endosperm coincident with the time of starch biosynthesis. Nearly full-length SU1 was expressed inEscherichia coli and purified to apparent homogeneity. Two biochemical assays confirmed that SU1 hydrolyzes α-(1→6) linkages in branched polysaccharides. Determination of the specific activity of SU1 toward various substrates enabled its classification as an isoamylase. Previous studies had shown, however, thatsu1- mutant endosperms are deficient in a different type of DBE, a pullulanase (or R enzyme). Immunoblot analyses revealed that both SU1 and a protein detected by antibodies specific for the rice (Oryza sativa) R enzyme are missing fromsu1- mutant kernels. These data support the hypothesis that DBEs are directly involved in starch biosynthesis.
Oxford University Press (OUP)
Title: Characterization of SU1 Isoamylase, a Determinant of Storage Starch Structure in Maize1
Description:
AbstractFunction of the maize (Zea mays) gene sugary1 (su1) is required for normal starch biosynthesis in endosperm.
Homozygoussu1- mutant endosperms accumulate a highly branched polysaccharide, phytoglycogen, at the expense of the normal branched component of starch, amylopectin.
These data suggest that both branched polysaccharides share a common precursor, and that the product of thesu1 gene, designated SU1, participates in kernel starch biosynthesis.
SU1 is similar in sequence to α-(1→6) glucan hydrolases (starch-debranching enzymes [DBEs]).
Specific antibodies were produced and used to demonstrate that SU1 is a 79-kD protein that accumulates in endosperm coincident with the time of starch biosynthesis.
Nearly full-length SU1 was expressed inEscherichia coli and purified to apparent homogeneity.
Two biochemical assays confirmed that SU1 hydrolyzes α-(1→6) linkages in branched polysaccharides.
Determination of the specific activity of SU1 toward various substrates enabled its classification as an isoamylase.
Previous studies had shown, however, thatsu1- mutant endosperms are deficient in a different type of DBE, a pullulanase (or R enzyme).
Immunoblot analyses revealed that both SU1 and a protein detected by antibodies specific for the rice (Oryza sativa) R enzyme are missing fromsu1- mutant kernels.
These data support the hypothesis that DBEs are directly involved in starch biosynthesis.
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