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Engineering α-amylase levels in wheat grain suggests a highly sophisticated level of carbohydrate regulation during development
Wheat starch degradation requires the synergistic action of different amylolytic enzymes. Our spatio-temporal study of wheat α-amylases throughout grain development shows that AMY3 is the most abundant isoform compared with the other known α-amylases. Endosperm-specific over-expression of AMY3 resul...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4157717/ https://www.ncbi.nlm.nih.gov/pubmed/25053646 http://dx.doi.org/10.1093/jxb/eru299 |
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author | Whan, Alex Dielen, Anne-Sophie Mieog, Jos Bowerman, Andrew F. Robinson, Hannah M. Byrne, Keren Colgrave, Michelle Larkin, Philip J. Howitt, Crispin A. Morell, Matthew K. Ral, Jean-Philippe |
author_facet | Whan, Alex Dielen, Anne-Sophie Mieog, Jos Bowerman, Andrew F. Robinson, Hannah M. Byrne, Keren Colgrave, Michelle Larkin, Philip J. Howitt, Crispin A. Morell, Matthew K. Ral, Jean-Philippe |
author_sort | Whan, Alex |
collection | PubMed |
description | Wheat starch degradation requires the synergistic action of different amylolytic enzymes. Our spatio-temporal study of wheat α-amylases throughout grain development shows that AMY3 is the most abundant isoform compared with the other known α-amylases. Endosperm-specific over-expression of AMY3 resulted in an increase of total α-amylase activity in harvested grains. Unexpectedly, increased activity did not have a significant impact on starch content or composition but led to an increase of soluble carbohydrate (mainly sucrose) in dry grain. In AMY3 overexpression lines (A3OE), germination was slightly delayed and triacylglycerol (TAG) content was increased in the endosperm of mature grain. Despite increased AMY3 transcript and protein content throughout grain development, alterations of α-amylase activity and starch granule degradation were not detected until grain maturation, suggesting a post-translational inhibition of α-amylase activity in the endosperm during the starch filling period. These findings show unexpected effects of a high level of α-amylase on grain development and composition, notably in carbon partitioning and TAG accumulation, and suggest the presence of a hitherto unknown regulatory pathway during grain filling. |
format | Online Article Text |
id | pubmed-4157717 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-41577172014-09-10 Engineering α-amylase levels in wheat grain suggests a highly sophisticated level of carbohydrate regulation during development Whan, Alex Dielen, Anne-Sophie Mieog, Jos Bowerman, Andrew F. Robinson, Hannah M. Byrne, Keren Colgrave, Michelle Larkin, Philip J. Howitt, Crispin A. Morell, Matthew K. Ral, Jean-Philippe J Exp Bot Research Paper Wheat starch degradation requires the synergistic action of different amylolytic enzymes. Our spatio-temporal study of wheat α-amylases throughout grain development shows that AMY3 is the most abundant isoform compared with the other known α-amylases. Endosperm-specific over-expression of AMY3 resulted in an increase of total α-amylase activity in harvested grains. Unexpectedly, increased activity did not have a significant impact on starch content or composition but led to an increase of soluble carbohydrate (mainly sucrose) in dry grain. In AMY3 overexpression lines (A3OE), germination was slightly delayed and triacylglycerol (TAG) content was increased in the endosperm of mature grain. Despite increased AMY3 transcript and protein content throughout grain development, alterations of α-amylase activity and starch granule degradation were not detected until grain maturation, suggesting a post-translational inhibition of α-amylase activity in the endosperm during the starch filling period. These findings show unexpected effects of a high level of α-amylase on grain development and composition, notably in carbon partitioning and TAG accumulation, and suggest the presence of a hitherto unknown regulatory pathway during grain filling. Oxford University Press 2014-10 2014-07-22 /pmc/articles/PMC4157717/ /pubmed/25053646 http://dx.doi.org/10.1093/jxb/eru299 Text en © The Author 2014. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Whan, Alex Dielen, Anne-Sophie Mieog, Jos Bowerman, Andrew F. Robinson, Hannah M. Byrne, Keren Colgrave, Michelle Larkin, Philip J. Howitt, Crispin A. Morell, Matthew K. Ral, Jean-Philippe Engineering α-amylase levels in wheat grain suggests a highly sophisticated level of carbohydrate regulation during development |
title | Engineering α-amylase levels in wheat grain suggests a highly sophisticated level of carbohydrate regulation during development |
title_full | Engineering α-amylase levels in wheat grain suggests a highly sophisticated level of carbohydrate regulation during development |
title_fullStr | Engineering α-amylase levels in wheat grain suggests a highly sophisticated level of carbohydrate regulation during development |
title_full_unstemmed | Engineering α-amylase levels in wheat grain suggests a highly sophisticated level of carbohydrate regulation during development |
title_short | Engineering α-amylase levels in wheat grain suggests a highly sophisticated level of carbohydrate regulation during development |
title_sort | engineering α-amylase levels in wheat grain suggests a highly sophisticated level of carbohydrate regulation during development |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4157717/ https://www.ncbi.nlm.nih.gov/pubmed/25053646 http://dx.doi.org/10.1093/jxb/eru299 |
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