Cargando…

Biosynthesis and Regulation of Wheat Amylose and Amylopectin from Proteomic and Phosphoproteomic Characterization of Granule-binding Proteins

Waxy starch has an important influence on the qualities of breads. Generally, grain weight and yield in waxy wheat (Triticum aestivum L.) are significantly lower than in bread wheat. In this study, we performed the first proteomic and phosphoproteomic analyses of starch granule-binding proteins by c...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Guan-Xing, Zhou, Jian-Wen, Liu, Yan-Lin, Lu, Xiao-Bing, Han, Cai-Xia, Zhang, Wen-Ying, Xu, Yan-Hao, Yan, Yue-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015113/
https://www.ncbi.nlm.nih.gov/pubmed/27604546
http://dx.doi.org/10.1038/srep33111
_version_ 1782452385516355584
author Chen, Guan-Xing
Zhou, Jian-Wen
Liu, Yan-Lin
Lu, Xiao-Bing
Han, Cai-Xia
Zhang, Wen-Ying
Xu, Yan-Hao
Yan, Yue-Ming
author_facet Chen, Guan-Xing
Zhou, Jian-Wen
Liu, Yan-Lin
Lu, Xiao-Bing
Han, Cai-Xia
Zhang, Wen-Ying
Xu, Yan-Hao
Yan, Yue-Ming
author_sort Chen, Guan-Xing
collection PubMed
description Waxy starch has an important influence on the qualities of breads. Generally, grain weight and yield in waxy wheat (Triticum aestivum L.) are significantly lower than in bread wheat. In this study, we performed the first proteomic and phosphoproteomic analyses of starch granule-binding proteins by comparing the waxy wheat cultivar Shannong 119 and the bread wheat cultivar Nongda 5181. These results indicate that reduced amylose content does not affect amylopectin synthesis, but it causes significant reduction of total starch biosynthesis, grain size, weight and grain yield. Two-dimensional differential in-gel electrophoresis identified 40 differentially expressed protein (DEP) spots in waxy and non-waxy wheats, which belonged mainly to starch synthase (SS) I, SS IIa and granule-bound SS I. Most DEPs involved in amylopectin synthesis showed a similar expression pattern during grain development, suggesting relatively independent amylose and amylopectin synthesis pathways. Phosphoproteome analysis of starch granule-binding proteins, using TiO(2) microcolumns and LC-MS/MS, showed that the total number of phosphoproteins and their phosphorylation levels in ND5181 were significantly higher than in SN119, but proteins controlling amylopectin synthesis had similar phosphorylation levels. Our results revealed the lack of amylose did not affect the expression and phosphorylation of the starch granule-binding proteins involved in amylopectin biosynthesis.
format Online
Article
Text
id pubmed-5015113
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-50151132016-09-12 Biosynthesis and Regulation of Wheat Amylose and Amylopectin from Proteomic and Phosphoproteomic Characterization of Granule-binding Proteins Chen, Guan-Xing Zhou, Jian-Wen Liu, Yan-Lin Lu, Xiao-Bing Han, Cai-Xia Zhang, Wen-Ying Xu, Yan-Hao Yan, Yue-Ming Sci Rep Article Waxy starch has an important influence on the qualities of breads. Generally, grain weight and yield in waxy wheat (Triticum aestivum L.) are significantly lower than in bread wheat. In this study, we performed the first proteomic and phosphoproteomic analyses of starch granule-binding proteins by comparing the waxy wheat cultivar Shannong 119 and the bread wheat cultivar Nongda 5181. These results indicate that reduced amylose content does not affect amylopectin synthesis, but it causes significant reduction of total starch biosynthesis, grain size, weight and grain yield. Two-dimensional differential in-gel electrophoresis identified 40 differentially expressed protein (DEP) spots in waxy and non-waxy wheats, which belonged mainly to starch synthase (SS) I, SS IIa and granule-bound SS I. Most DEPs involved in amylopectin synthesis showed a similar expression pattern during grain development, suggesting relatively independent amylose and amylopectin synthesis pathways. Phosphoproteome analysis of starch granule-binding proteins, using TiO(2) microcolumns and LC-MS/MS, showed that the total number of phosphoproteins and their phosphorylation levels in ND5181 were significantly higher than in SN119, but proteins controlling amylopectin synthesis had similar phosphorylation levels. Our results revealed the lack of amylose did not affect the expression and phosphorylation of the starch granule-binding proteins involved in amylopectin biosynthesis. Nature Publishing Group 2016-09-08 /pmc/articles/PMC5015113/ /pubmed/27604546 http://dx.doi.org/10.1038/srep33111 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Chen, Guan-Xing
Zhou, Jian-Wen
Liu, Yan-Lin
Lu, Xiao-Bing
Han, Cai-Xia
Zhang, Wen-Ying
Xu, Yan-Hao
Yan, Yue-Ming
Biosynthesis and Regulation of Wheat Amylose and Amylopectin from Proteomic and Phosphoproteomic Characterization of Granule-binding Proteins
title Biosynthesis and Regulation of Wheat Amylose and Amylopectin from Proteomic and Phosphoproteomic Characterization of Granule-binding Proteins
title_full Biosynthesis and Regulation of Wheat Amylose and Amylopectin from Proteomic and Phosphoproteomic Characterization of Granule-binding Proteins
title_fullStr Biosynthesis and Regulation of Wheat Amylose and Amylopectin from Proteomic and Phosphoproteomic Characterization of Granule-binding Proteins
title_full_unstemmed Biosynthesis and Regulation of Wheat Amylose and Amylopectin from Proteomic and Phosphoproteomic Characterization of Granule-binding Proteins
title_short Biosynthesis and Regulation of Wheat Amylose and Amylopectin from Proteomic and Phosphoproteomic Characterization of Granule-binding Proteins
title_sort biosynthesis and regulation of wheat amylose and amylopectin from proteomic and phosphoproteomic characterization of granule-binding proteins
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015113/
https://www.ncbi.nlm.nih.gov/pubmed/27604546
http://dx.doi.org/10.1038/srep33111
work_keys_str_mv AT chenguanxing biosynthesisandregulationofwheatamyloseandamylopectinfromproteomicandphosphoproteomiccharacterizationofgranulebindingproteins
AT zhoujianwen biosynthesisandregulationofwheatamyloseandamylopectinfromproteomicandphosphoproteomiccharacterizationofgranulebindingproteins
AT liuyanlin biosynthesisandregulationofwheatamyloseandamylopectinfromproteomicandphosphoproteomiccharacterizationofgranulebindingproteins
AT luxiaobing biosynthesisandregulationofwheatamyloseandamylopectinfromproteomicandphosphoproteomiccharacterizationofgranulebindingproteins
AT hancaixia biosynthesisandregulationofwheatamyloseandamylopectinfromproteomicandphosphoproteomiccharacterizationofgranulebindingproteins
AT zhangwenying biosynthesisandregulationofwheatamyloseandamylopectinfromproteomicandphosphoproteomiccharacterizationofgranulebindingproteins
AT xuyanhao biosynthesisandregulationofwheatamyloseandamylopectinfromproteomicandphosphoproteomiccharacterizationofgranulebindingproteins
AT yanyueming biosynthesisandregulationofwheatamyloseandamylopectinfromproteomicandphosphoproteomiccharacterizationofgranulebindingproteins