Rice Endosperm Starch Phosphorylase (Pho1) Assembles with Disproportionating Enzyme (Dpe1) to Form a Protein Complex That Enhances Synthesis of Malto-oligosaccharides

• Published in: The Journal of biological chemistry Vol. 291; no. 38; pp. 19994 - 20007
• Main Authors: Hwang, Seon-Kap, Koper, Kaan, Satoh, Hikaru, Okita, Thomas W.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 16-09-2016; Elsevier; American Society for Biochemistry and Molecular Biology
• Subjects: D-enzyme; disproportionating enzyme; Endosperm - enzymology; Endosperm - genetics; glycosyltransferase; metabolism; Multienzyme Complexes - genetics; Multienzyme Complexes - metabolism; Oligosaccharides - genetics; Oligosaccharides - metabolism; Oryza - enzymology; Oryza - genetics; phosphorylase; Plant Biology; protein complex; protein-protein interaction; rice endosperm; starch phosphorylase; Starch Phosphorylase - genetics; Starch Phosphorylase - metabolism; starch synthesis; D-enzyme; starch phosphorylase; disproportionating enzyme; glycosyltransferase; rice endosperm; starch synthesis; metabolism; protein-protein interaction; protein complex; phosphorylase
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M116.735449

Starch synthesis in cereal grain endosperm is dependent on the concerted actions of many enzymes. The starch plastidial phosphorylase (Pho1) plays an important role in the initiation of starch synthesis and in the maturation of starch granule in developing rice seeds. Prior evidence has suggested that the rice enzyme, OsPho1, may have a physical/functional interaction with other starch biosynthetic enzymes. Pulldown experiments showed that OsPho1 as well as OsPho1 devoid of its L80 region, a peptide unique to higher plant phosphorylases, captures disproportionating enzyme (OsDpe1). Interaction of the latter enzyme form with OsDpe1 indicates that the putative regulatory L80 is not responsible for multienzyme assembly. This heterotypic enzyme complex, determined at a molar ratio of 1:1, was validated by reciprocal co-immunoprecipitation studies of native seed proteins and by co-elution chromatographic and co-migration electrophoretic patterns of these enzymes in rice seed extracts. The OsPho1-OsDpe1 complex utilized a broader range of substrates for enhanced synthesis of larger maltooligosaccharides than each individual enzyme and significantly elevated the substrate affinities of OsPho1 at 30 °C. Moreover, the assembly with OsDpe1 enables OsPho1 to utilize products of transglycosylation reactions involving G1 and G3, sugars that it cannot catalyze directly.