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Proteomic profiling of cellulase-aid-extracted membrane proteins for functional identification of cellulose synthase complexes and their potential associated- components in cotton fibers

Cotton fibers are an excellent model for understanding of cellulose biosynthesis in higher plants. In this study, we determined a high cellulose biosynthesis activity in vitro by optimizing biochemical reaction conditions in cotton fibers. By adding a commercial cellulase enzyme into fibers extracti...

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Autores principales: Li, Ao, Wang, Ruyi, Li, Xianliang, Liu, Mingyong, Fan, Jian, Guo, Kai, Luo, Bing, Chen, Tingting, Feng, Shengqiu, Wang, Yanting, Wang, Bingrui, Peng, Liangcai, Xia, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872218/
https://www.ncbi.nlm.nih.gov/pubmed/27192945
http://dx.doi.org/10.1038/srep26356
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author Li, Ao
Wang, Ruyi
Li, Xianliang
Liu, Mingyong
Fan, Jian
Guo, Kai
Luo, Bing
Chen, Tingting
Feng, Shengqiu
Wang, Yanting
Wang, Bingrui
Peng, Liangcai
Xia, Tao
author_facet Li, Ao
Wang, Ruyi
Li, Xianliang
Liu, Mingyong
Fan, Jian
Guo, Kai
Luo, Bing
Chen, Tingting
Feng, Shengqiu
Wang, Yanting
Wang, Bingrui
Peng, Liangcai
Xia, Tao
author_sort Li, Ao
collection PubMed
description Cotton fibers are an excellent model for understanding of cellulose biosynthesis in higher plants. In this study, we determined a high cellulose biosynthesis activity in vitro by optimizing biochemical reaction conditions in cotton fibers. By adding a commercial cellulase enzyme into fibers extraction process, we extracted markedly higher levels of GhCESA1 and GhCESA8 proteins and observed an increase in β-1,4-glucan and β-1,3-glucan products in vitro. LC-MS/MS analysis of anti-GhCESA8-immunoprecipitated proteins showed that 19 proteins could be found in three independent experiments including four CESAs (GhCESA1,2,7,8), five well-known non-CESA proteins, one callose synthase (CALS) and nine novel proteins. Notably, upon the cellulase treatment, four CESAs, one CALS and four novel proteins were measured at relatively higher levels by calculating total peptide counts and distinct peptide numbers, indicating that the cellulase-aid-extracted proteins most likely contribute to the increase in β-glucan products in vitro. These results suggest that the cellulase treatment may aid to release active cellulose synthases complexes from growing glucan chains and make them more amenable to extraction. To our knowledge, it is the first time report about the functional identification of the potential proteins that were associated with plant cellulose and callose synthases complexes by using the cellulase-aided protein extraction.
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spelling pubmed-48722182016-06-01 Proteomic profiling of cellulase-aid-extracted membrane proteins for functional identification of cellulose synthase complexes and their potential associated- components in cotton fibers Li, Ao Wang, Ruyi Li, Xianliang Liu, Mingyong Fan, Jian Guo, Kai Luo, Bing Chen, Tingting Feng, Shengqiu Wang, Yanting Wang, Bingrui Peng, Liangcai Xia, Tao Sci Rep Article Cotton fibers are an excellent model for understanding of cellulose biosynthesis in higher plants. In this study, we determined a high cellulose biosynthesis activity in vitro by optimizing biochemical reaction conditions in cotton fibers. By adding a commercial cellulase enzyme into fibers extraction process, we extracted markedly higher levels of GhCESA1 and GhCESA8 proteins and observed an increase in β-1,4-glucan and β-1,3-glucan products in vitro. LC-MS/MS analysis of anti-GhCESA8-immunoprecipitated proteins showed that 19 proteins could be found in three independent experiments including four CESAs (GhCESA1,2,7,8), five well-known non-CESA proteins, one callose synthase (CALS) and nine novel proteins. Notably, upon the cellulase treatment, four CESAs, one CALS and four novel proteins were measured at relatively higher levels by calculating total peptide counts and distinct peptide numbers, indicating that the cellulase-aid-extracted proteins most likely contribute to the increase in β-glucan products in vitro. These results suggest that the cellulase treatment may aid to release active cellulose synthases complexes from growing glucan chains and make them more amenable to extraction. To our knowledge, it is the first time report about the functional identification of the potential proteins that were associated with plant cellulose and callose synthases complexes by using the cellulase-aided protein extraction. Nature Publishing Group 2016-05-19 /pmc/articles/PMC4872218/ /pubmed/27192945 http://dx.doi.org/10.1038/srep26356 Text en Copyright © 2016, Macmillan Publishers Limited 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
Li, Ao
Wang, Ruyi
Li, Xianliang
Liu, Mingyong
Fan, Jian
Guo, Kai
Luo, Bing
Chen, Tingting
Feng, Shengqiu
Wang, Yanting
Wang, Bingrui
Peng, Liangcai
Xia, Tao
Proteomic profiling of cellulase-aid-extracted membrane proteins for functional identification of cellulose synthase complexes and their potential associated- components in cotton fibers
title Proteomic profiling of cellulase-aid-extracted membrane proteins for functional identification of cellulose synthase complexes and their potential associated- components in cotton fibers
title_full Proteomic profiling of cellulase-aid-extracted membrane proteins for functional identification of cellulose synthase complexes and their potential associated- components in cotton fibers
title_fullStr Proteomic profiling of cellulase-aid-extracted membrane proteins for functional identification of cellulose synthase complexes and their potential associated- components in cotton fibers
title_full_unstemmed Proteomic profiling of cellulase-aid-extracted membrane proteins for functional identification of cellulose synthase complexes and their potential associated- components in cotton fibers
title_short Proteomic profiling of cellulase-aid-extracted membrane proteins for functional identification of cellulose synthase complexes and their potential associated- components in cotton fibers
title_sort proteomic profiling of cellulase-aid-extracted membrane proteins for functional identification of cellulose synthase complexes and their potential associated- components in cotton fibers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872218/
https://www.ncbi.nlm.nih.gov/pubmed/27192945
http://dx.doi.org/10.1038/srep26356
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