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PROTEIN TARGETING TO STARCH Is Required for Localising GRANULE-BOUND STARCH SYNTHASE to Starch Granules and for Normal Amylose Synthesis in Arabidopsis
- Source :
- PLoS Biology, 13 (2), PLoS Biology, Vol 13, Iss 2, p e1002080 (2015), PLOS Biology
- Publication Year :
- 2015
- Publisher :
- PLOS, 2015.
-
Abstract
- The domestication of starch crops underpinned the development of human civilisation, yet we still do not fully understand how plants make starch. Starch is composed of glucose polymers that are branched (amylopectin) or linear (amylose). The amount of amylose strongly influences the physico-chemical behaviour of starchy foods during cooking and of starch mixtures in non-food manufacturing processes. The GRANULE-BOUND STARCH SYNTHASE (GBSS) is the glucosyltransferase specifically responsible for elongating amylose polymers and was the only protein known to be required for its biosynthesis. Here, we demonstrate that PROTEIN TARGETING TO STARCH (PTST) is also specifically required for amylose synthesis in Arabidopsis. PTST is a plastidial protein possessing an N-terminal coiled coil domain and a C-terminal carbohydrate binding module (CBM). We discovered that Arabidopsis ptst mutants synthesise amylose-free starch and are phenotypically similar to mutants lacking GBSS. Analysis of granule-bound proteins showed a dramatic reduction of GBSS protein in ptst mutant starch granules. Pull-down assays with recombinant proteins in vitro, as well as immunoprecipitation assays in planta, revealed that GBSS physically interacts with PTST via a coiled coil. Furthermore, we show that the CBM domain of PTST, which mediates its interaction with starch granules, is also required for correct GBSS localisation. Fluorescently tagged Arabidopsis GBSS, expressed either in tobacco or Arabidopsis leaves, required the presence of Arabidopsis PTST to localise to starch granules. Mutation of the CBM of PTST caused GBSS to remain in the plastid stroma. PTST fulfils a previously unknown function in targeting GBSS to starch. This sheds new light on the importance of targeting biosynthetic enzymes to sub-cellular sites where their action is required. Importantly, PTST represents a promising new gene target for the biotechnological modification of starch composition, as it is exclusively involved in amylose synthesis.<br />PLoS Biology, 13 (2)<br />ISSN:1544-9173<br />ISSN:1545-7885
- Subjects :
- 0106 biological sciences
Starch
QH301-705.5
01 natural sciences
General Biochemistry, Genetics and Molecular Biology
03 medical and health sciences
chemistry.chemical_compound
Amylose
Arabidopsis
Biology (General)
030304 developmental biology
0303 health sciences
General Immunology and Microbiology
biology
General Neuroscience
food and beverages
biology.organism_classification
Plastid stroma
Chloroplast
Biochemistry
chemistry
Amylopectin
biology.protein
Carbohydrate-binding module
General Agricultural and Biological Sciences
Starch synthase
010606 plant biology & botany
Subjects
Details
- Language :
- English
- ISSN :
- 15449173 and 15457885
- Database :
- OpenAIRE
- Journal :
- PLoS Biology, 13 (2), PLoS Biology, Vol 13, Iss 2, p e1002080 (2015), PLOS Biology
- Accession number :
- edsair.doi.dedup.....75be7c94209d01cf76c2494a14646b55