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Characterization of purple acid phosphatases involved in extracellular dNTP utilization in Stylosanthes

Stylo (Stylosanthes spp.) is a pasture legume predominant in tropical and subtropical areas, where low phosphorus (P) availability is a major constraint for plant growth. Therefore, stylo might exhibit superior utilization of the P pool on acid soils, particularly organic P. However, little is known...

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Autores principales: Liu, Pan-Dao, Xue, Ying-Bin, Chen, Zhi-Jian, Liu, Guo-Dao, Tian, Jiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5301924/
https://www.ncbi.nlm.nih.gov/pubmed/27194738
http://dx.doi.org/10.1093/jxb/erw190
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author Liu, Pan-Dao
Xue, Ying-Bin
Chen, Zhi-Jian
Liu, Guo-Dao
Tian, Jiang
author_facet Liu, Pan-Dao
Xue, Ying-Bin
Chen, Zhi-Jian
Liu, Guo-Dao
Tian, Jiang
author_sort Liu, Pan-Dao
collection PubMed
description Stylo (Stylosanthes spp.) is a pasture legume predominant in tropical and subtropical areas, where low phosphorus (P) availability is a major constraint for plant growth. Therefore, stylo might exhibit superior utilization of the P pool on acid soils, particularly organic P. However, little is known about mechanisms of inorganic phosphate (Pi) acquisition employed by stylo. In this study, the utilization of extracellular deoxy-ribonucleotide triphosphate (dNTP) and the underlying physiological and molecular mechanisms were examined for two stylo genotypes with contrasting P efficiency. Results showed that the P-efficient genotype, TPRC2001-1, was superior to the P-inefficient genotype, Fine-stem, when using dNTP as the sole P source. This was reflected by a higher dry weight and total P content for TPRC2001-1 than for Fine-stem, which was correlated with higher root-associated acid phosphatase (APase) activities in TPRC2001-1 under low P conditions. Subsequently, three PAP members were cloned from TPRC2001-1: SgPAP7, SgPAP10, and SgPAP26. Expression levels of these three SgPAPs were up-regulated by Pi starvation in stylo roots. Furthermore, there was a higher abundance of transcripts of SgPAP7 and SgPAP10 in TPRC2001-1 than in Fine-stem. Subcellular localization analysis demonstrated that these three SgPAPs were localized on the plasma membrane. Overexpression of these three SgPAPs could result in significantly increased root-associated APase activities, and thus extracellular dNTP utilization in bean hairy roots. Taken together, the results herein suggest that SgPAP7, SgPAP10, and SgPAP26 may differentially contribute to root-associated APase activities, and thus control extracellular dNTP utilization in stylo.
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spelling pubmed-53019242017-02-16 Characterization of purple acid phosphatases involved in extracellular dNTP utilization in Stylosanthes Liu, Pan-Dao Xue, Ying-Bin Chen, Zhi-Jian Liu, Guo-Dao Tian, Jiang J Exp Bot Research Paper Stylo (Stylosanthes spp.) is a pasture legume predominant in tropical and subtropical areas, where low phosphorus (P) availability is a major constraint for plant growth. Therefore, stylo might exhibit superior utilization of the P pool on acid soils, particularly organic P. However, little is known about mechanisms of inorganic phosphate (Pi) acquisition employed by stylo. In this study, the utilization of extracellular deoxy-ribonucleotide triphosphate (dNTP) and the underlying physiological and molecular mechanisms were examined for two stylo genotypes with contrasting P efficiency. Results showed that the P-efficient genotype, TPRC2001-1, was superior to the P-inefficient genotype, Fine-stem, when using dNTP as the sole P source. This was reflected by a higher dry weight and total P content for TPRC2001-1 than for Fine-stem, which was correlated with higher root-associated acid phosphatase (APase) activities in TPRC2001-1 under low P conditions. Subsequently, three PAP members were cloned from TPRC2001-1: SgPAP7, SgPAP10, and SgPAP26. Expression levels of these three SgPAPs were up-regulated by Pi starvation in stylo roots. Furthermore, there was a higher abundance of transcripts of SgPAP7 and SgPAP10 in TPRC2001-1 than in Fine-stem. Subcellular localization analysis demonstrated that these three SgPAPs were localized on the plasma membrane. Overexpression of these three SgPAPs could result in significantly increased root-associated APase activities, and thus extracellular dNTP utilization in bean hairy roots. Taken together, the results herein suggest that SgPAP7, SgPAP10, and SgPAP26 may differentially contribute to root-associated APase activities, and thus control extracellular dNTP utilization in stylo. Oxford University Press 2016-07 2016-05-18 /pmc/articles/PMC5301924/ /pubmed/27194738 http://dx.doi.org/10.1093/jxb/erw190 Text en © The Author 2016. 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
Liu, Pan-Dao
Xue, Ying-Bin
Chen, Zhi-Jian
Liu, Guo-Dao
Tian, Jiang
Characterization of purple acid phosphatases involved in extracellular dNTP utilization in Stylosanthes
title Characterization of purple acid phosphatases involved in extracellular dNTP utilization in Stylosanthes
title_full Characterization of purple acid phosphatases involved in extracellular dNTP utilization in Stylosanthes
title_fullStr Characterization of purple acid phosphatases involved in extracellular dNTP utilization in Stylosanthes
title_full_unstemmed Characterization of purple acid phosphatases involved in extracellular dNTP utilization in Stylosanthes
title_short Characterization of purple acid phosphatases involved in extracellular dNTP utilization in Stylosanthes
title_sort characterization of purple acid phosphatases involved in extracellular dntp utilization in stylosanthes
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5301924/
https://www.ncbi.nlm.nih.gov/pubmed/27194738
http://dx.doi.org/10.1093/jxb/erw190
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