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Exploring natural genetic variation in tomato sucrose synthases on the basis of increased kinetic properties
Sucrose synthase (SuSy) is one key enzyme directly hydrolyzing sucrose to supply substrates for plant metabolism, and is considered to be a biomarker for plant sink strength. Improvement in plant sink strength could lead to enhanced plant growth and yield. Cultivated tomatoes are known to have a nar...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6205638/ https://www.ncbi.nlm.nih.gov/pubmed/30372500 http://dx.doi.org/10.1371/journal.pone.0206636 |
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author | Dinh, Quy-Dung Finkers, Richard Westphal, Adrie H. van Dongen, Walter M. A. M. Visser, Richard G. F. Trindade, Luisa M. |
author_facet | Dinh, Quy-Dung Finkers, Richard Westphal, Adrie H. van Dongen, Walter M. A. M. Visser, Richard G. F. Trindade, Luisa M. |
author_sort | Dinh, Quy-Dung |
collection | PubMed |
description | Sucrose synthase (SuSy) is one key enzyme directly hydrolyzing sucrose to supply substrates for plant metabolism, and is considered to be a biomarker for plant sink strength. Improvement in plant sink strength could lead to enhanced plant growth and yield. Cultivated tomatoes are known to have a narrow genetic diversity, which hampers further breeding for novel and improved traits in new cultivars. In this study, we observed limited genetic variation in SuSy1, SuSy3 and SuSy4 in 53 accessions of cultivated tomato and landraces, but identified a wealth of genetic diversity in 32 accessions of related wild species. The variation in the deduced amino acid sequences was grouped into 23, 22, and 17 distinct haplotypes for SuSy1/3/4, respectively. Strikingly, all known substrate binding sites were highly conserved, as well as most of the phosphorylation sites except in SuSy1. Two SuSy1 and three SuSy3 protein variants were heterologously expressed to study the effect of the amino acid changes on enzyme kinetic properties, i.e. maximal sucrose hydrolyzing capacity (V(max)), affinity for sucrose (K(m)), and catalytic efficiency (V(max)/K(m)) at 25°C and 16°C. SuSy1-haplotype#3 containing phosphorylation site Ser-16 did not have an improvement in the kinetic properties compared to the reference SuSy1-haplotype#1 containing Arg-16. Meanwhile SuSy3-haplotype#9 from a wild accession, containing four amino acid changes S53A, S106I, E727D and K741E, showed an increase in V(max)/K(m) at 16°C compared to the reference SuSy3-haplotype#1. This study demonstrates that SuSy kinetic properties can be enhanced by exploiting natural variation, and the potential of this enzyme to improve sucrose metabolism and eventually sink strength in planta. |
format | Online Article Text |
id | pubmed-6205638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-62056382018-11-19 Exploring natural genetic variation in tomato sucrose synthases on the basis of increased kinetic properties Dinh, Quy-Dung Finkers, Richard Westphal, Adrie H. van Dongen, Walter M. A. M. Visser, Richard G. F. Trindade, Luisa M. PLoS One Research Article Sucrose synthase (SuSy) is one key enzyme directly hydrolyzing sucrose to supply substrates for plant metabolism, and is considered to be a biomarker for plant sink strength. Improvement in plant sink strength could lead to enhanced plant growth and yield. Cultivated tomatoes are known to have a narrow genetic diversity, which hampers further breeding for novel and improved traits in new cultivars. In this study, we observed limited genetic variation in SuSy1, SuSy3 and SuSy4 in 53 accessions of cultivated tomato and landraces, but identified a wealth of genetic diversity in 32 accessions of related wild species. The variation in the deduced amino acid sequences was grouped into 23, 22, and 17 distinct haplotypes for SuSy1/3/4, respectively. Strikingly, all known substrate binding sites were highly conserved, as well as most of the phosphorylation sites except in SuSy1. Two SuSy1 and three SuSy3 protein variants were heterologously expressed to study the effect of the amino acid changes on enzyme kinetic properties, i.e. maximal sucrose hydrolyzing capacity (V(max)), affinity for sucrose (K(m)), and catalytic efficiency (V(max)/K(m)) at 25°C and 16°C. SuSy1-haplotype#3 containing phosphorylation site Ser-16 did not have an improvement in the kinetic properties compared to the reference SuSy1-haplotype#1 containing Arg-16. Meanwhile SuSy3-haplotype#9 from a wild accession, containing four amino acid changes S53A, S106I, E727D and K741E, showed an increase in V(max)/K(m) at 16°C compared to the reference SuSy3-haplotype#1. This study demonstrates that SuSy kinetic properties can be enhanced by exploiting natural variation, and the potential of this enzyme to improve sucrose metabolism and eventually sink strength in planta. Public Library of Science 2018-10-29 /pmc/articles/PMC6205638/ /pubmed/30372500 http://dx.doi.org/10.1371/journal.pone.0206636 Text en © 2018 Dinh et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Dinh, Quy-Dung Finkers, Richard Westphal, Adrie H. van Dongen, Walter M. A. M. Visser, Richard G. F. Trindade, Luisa M. Exploring natural genetic variation in tomato sucrose synthases on the basis of increased kinetic properties |
title | Exploring natural genetic variation in tomato sucrose synthases on the basis of increased kinetic properties |
title_full | Exploring natural genetic variation in tomato sucrose synthases on the basis of increased kinetic properties |
title_fullStr | Exploring natural genetic variation in tomato sucrose synthases on the basis of increased kinetic properties |
title_full_unstemmed | Exploring natural genetic variation in tomato sucrose synthases on the basis of increased kinetic properties |
title_short | Exploring natural genetic variation in tomato sucrose synthases on the basis of increased kinetic properties |
title_sort | exploring natural genetic variation in tomato sucrose synthases on the basis of increased kinetic properties |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6205638/ https://www.ncbi.nlm.nih.gov/pubmed/30372500 http://dx.doi.org/10.1371/journal.pone.0206636 |
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