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Amylopectin biosynthetic enzymes from developing rice seed form enzymatically active protein complexes
- Source :
- Journal of Experimental Botany
- Publication Year :
- 2015
-
Abstract
- Highlight Starch biosynthetic enzymes in rice endosperm are physically associated with each other and form enzymatically active multiple protein–protein complexes, several of which were common to cereals while others were unique.<br />Amylopectin is a highly branched, organized cluster of glucose polymers, and the major component of rice starch. Synthesis of amylopectin requires fine co-ordination between elongation of glucose polymers by soluble starch synthases (SSs), generation of branches by branching enzymes (BEs), and removal of misplaced branches by debranching enzymes (DBEs). Among the various isozymes having a role in amylopectin biosynthesis, limited numbers of SS and BE isozymes have been demonstrated to interact via protein–protein interactions in maize and wheat amyloplasts. This study investigated whether protein–protein interactions are also found in rice endosperm, as well as exploring differences between species. Gel permeation chromatography of developing rice endosperm extracts revealed that all 10 starch biosynthetic enzymes analysed were present at larger molecular weights than their respective monomeric sizes. SSIIa, SSIIIa, SSIVb, BEI, BEIIb, and PUL co-eluted at mass sizes >700kDa, and SSI, SSIIa, BEIIb, ISA1, PUL, and Pho1 co-eluted at 200–400kDa. Zymogram analyses showed that SSI, SSIIIa, BEI, BEIIa, BEIIb, ISA1, PUL, and Pho1 eluted in high molecular weight fractions were active. Comprehensive co-immunoprecipitation analyses revealed associations of SSs–BEs, and, among BE isozymes, BEIIa–Pho1, and pullulanase-type DBE–BEI interactions. Blue-native-PAGE zymogram analyses confirmed the glucan-synthesizing activity of protein complexes. These results suggest that some rice starch biosynthetic isozymes are physically associated with each other and form active protein complexes. Detailed analyses of these complexes will shed light on the mechanisms controlling the unique branch and cluster structure of amylopectin, and the physicochemical properties of starch.
- Subjects :
- 0106 biological sciences
Physiology
Starch
Amylopectin
Plant Science
Biology
01 natural sciences
Isozyme
Endosperm
Gel permeation chromatography
03 medical and health sciences
chemistry.chemical_compound
Protein Interaction Mapping
Immunoprecipitation
Amyloplast
Protein Interaction Domains and Motifs
Glucans
starch synthesis
030304 developmental biology
Plant Proteins
2. Zero hunger
chemistry.chemical_classification
0303 health sciences
Molecular mass
rice
starch
digestive, oral, and skin physiology
food and beverages
Oryza
glucan
Isoenzymes
Enzyme
protein–protein interaction
chemistry
Biochemistry
Chromatography, Gel
010606 plant biology & botany
Research Paper
Subjects
Details
- ISSN :
- 14602431
- Volume :
- 66
- Issue :
- 15
- Database :
- OpenAIRE
- Journal :
- Journal of experimental botany
- Accession number :
- edsair.doi.dedup.....8e61e67447ceb1363a116393728f6692