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Proteome Analysis of Potato Starch Reveals the Presence of New Starch Metabolic Proteins as Well as Multiple Protease Inhibitors
Starch bound proteins mainly include enzymes from the starch biosynthesis pathway. Recently, new functions in starch molecular assembly or active protein targeting were also proposed for starch associated proteins. The potato genome sequence reveals 77 loci encoding starch metabolizing enzymes with...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6013586/ https://www.ncbi.nlm.nih.gov/pubmed/29963063 http://dx.doi.org/10.3389/fpls.2018.00746 |
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author | Helle, Stanislas Bray, Fabrice Verbeke, Jérémy Devassine, Stéphanie Courseaux, Adeline Facon, Maud Tokarski, Caroline Rolando, Christian Szydlowski, Nicolas |
author_facet | Helle, Stanislas Bray, Fabrice Verbeke, Jérémy Devassine, Stéphanie Courseaux, Adeline Facon, Maud Tokarski, Caroline Rolando, Christian Szydlowski, Nicolas |
author_sort | Helle, Stanislas |
collection | PubMed |
description | Starch bound proteins mainly include enzymes from the starch biosynthesis pathway. Recently, new functions in starch molecular assembly or active protein targeting were also proposed for starch associated proteins. The potato genome sequence reveals 77 loci encoding starch metabolizing enzymes with the identification of previously unknown putative isoforms. Here we show by bottom-up proteomics that most of the starch biosynthetic enzymes in potato remain associated with starch even after washing with SDS or protease treatment of the granule surface. Moreover, our study confirmed the presence of PTST1 (Protein Targeting to Starch), ESV1 (Early StarVation1) and LESV (Like ESV), that have recently been identified in Arabidopsis. In addition, we report on the presence of a new isoform of starch synthase, SS6, containing both K-X-G-G-L catalytic motifs. Furthermore, multiple protease inhibitors were also identified that are cleared away from starch by SDS and thermolysin treatments. Our results indicate that SS6 may play a yet uncharacterized function in starch biosynthesis and open new perspectives both in understanding storage starch metabolism as well as breeding improved potato lines. |
format | Online Article Text |
id | pubmed-6013586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60135862018-06-29 Proteome Analysis of Potato Starch Reveals the Presence of New Starch Metabolic Proteins as Well as Multiple Protease Inhibitors Helle, Stanislas Bray, Fabrice Verbeke, Jérémy Devassine, Stéphanie Courseaux, Adeline Facon, Maud Tokarski, Caroline Rolando, Christian Szydlowski, Nicolas Front Plant Sci Plant Science Starch bound proteins mainly include enzymes from the starch biosynthesis pathway. Recently, new functions in starch molecular assembly or active protein targeting were also proposed for starch associated proteins. The potato genome sequence reveals 77 loci encoding starch metabolizing enzymes with the identification of previously unknown putative isoforms. Here we show by bottom-up proteomics that most of the starch biosynthetic enzymes in potato remain associated with starch even after washing with SDS or protease treatment of the granule surface. Moreover, our study confirmed the presence of PTST1 (Protein Targeting to Starch), ESV1 (Early StarVation1) and LESV (Like ESV), that have recently been identified in Arabidopsis. In addition, we report on the presence of a new isoform of starch synthase, SS6, containing both K-X-G-G-L catalytic motifs. Furthermore, multiple protease inhibitors were also identified that are cleared away from starch by SDS and thermolysin treatments. Our results indicate that SS6 may play a yet uncharacterized function in starch biosynthesis and open new perspectives both in understanding storage starch metabolism as well as breeding improved potato lines. Frontiers Media S.A. 2018-06-15 /pmc/articles/PMC6013586/ /pubmed/29963063 http://dx.doi.org/10.3389/fpls.2018.00746 Text en Copyright © 2018 Helle, Bray, Verbeke, Devassine, Courseaux, Facon, Tokarski, Rolando and Szydlowski. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Helle, Stanislas Bray, Fabrice Verbeke, Jérémy Devassine, Stéphanie Courseaux, Adeline Facon, Maud Tokarski, Caroline Rolando, Christian Szydlowski, Nicolas Proteome Analysis of Potato Starch Reveals the Presence of New Starch Metabolic Proteins as Well as Multiple Protease Inhibitors |
title | Proteome Analysis of Potato Starch Reveals the Presence of New Starch Metabolic Proteins as Well as Multiple Protease Inhibitors |
title_full | Proteome Analysis of Potato Starch Reveals the Presence of New Starch Metabolic Proteins as Well as Multiple Protease Inhibitors |
title_fullStr | Proteome Analysis of Potato Starch Reveals the Presence of New Starch Metabolic Proteins as Well as Multiple Protease Inhibitors |
title_full_unstemmed | Proteome Analysis of Potato Starch Reveals the Presence of New Starch Metabolic Proteins as Well as Multiple Protease Inhibitors |
title_short | Proteome Analysis of Potato Starch Reveals the Presence of New Starch Metabolic Proteins as Well as Multiple Protease Inhibitors |
title_sort | proteome analysis of potato starch reveals the presence of new starch metabolic proteins as well as multiple protease inhibitors |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6013586/ https://www.ncbi.nlm.nih.gov/pubmed/29963063 http://dx.doi.org/10.3389/fpls.2018.00746 |
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