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Overexpression of PtDXS Enhances Stress Resistance in Poplars.

Identifieur interne : 000939 ( Main/Corpus ); précédent : 000938; suivant : 000940

Overexpression of PtDXS Enhances Stress Resistance in Poplars.

Auteurs : Hui Wei ; Ali Movahedi ; Chen Xu ; Weibo Sun ; Amir Almasi Zadeh Yaghuti ; Pu Wang ; Dawei Li ; Qiang Zhuge

Source :

RBID : pubmed:30987184

English descriptors

Abstract

1-Deoxy-d-xylulose-5-phosphate synthase (DXS) is the rate-limiting enzyme in the plastidial methylerythritol phosphate pathway (MEP). In this study, PtDXS (XM_024607716.1) was isolated from Populus trichocarpa. A bioinformatics analysis revealed that PtDXS had high homology with the DXSs of other plant species. PtDXS expression differed among plant tissues and was highest in young leaves and lowest in roots. The recombinant protein was produced in Escherichia coli BL21 (DE3), purified, and its activity evaluated. The purified protein was capable of catalyzing the formation of 1-deoxy-d-xylulose-5-phosphate (DXP) from glyceraldehyde-3-phosphate and pyruvate. A functional color assay in E. coli harboring pAC-BETA indicated that PtDXS encodes a functional protein involved in the biosynthesis of isoprenoid precursors. The treatment of P. trichocarpa seedlings with 200 μM abscisic acid (ABA), 200 mM NaCl, 10% polyethylene glycol6000, and 2 mM H₂O₂ resulted in increased expression of PtDXS. The ABA and gibberellic acid contents of the transgenic lines (Poplar Nanlin 895) were higher than wild types, suggesting that DXS is important in terpenoid biosynthesis. Overexpression of PtDXS enhanced resistance to S. populiperda infection. Furthermore, the transgenic lines showed decreased feeding by Micromelalopha troglodyta, supporting the notion that PtDXS is a key enzyme in terpenoid biosynthesis.

DOI: 10.3390/ijms20071669
PubMed: 30987184
PubMed Central: PMC6479640

Links to Exploration step

pubmed:30987184

Le document en format XML

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<term>Sequence Analysis, Protein (MeSH)</term>
<term>Sodium Chloride (pharmacology)</term>
<term>Stress, Physiological (drug effects)</term>
<term>Stress, Physiological (genetics)</term>
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<front>
<div type="abstract" xml:lang="en">1-Deoxy-d-xylulose-5-phosphate synthase (DXS) is the rate-limiting enzyme in the plastidial methylerythritol phosphate pathway (MEP). In this study,
<i>PtDXS</i>
(XM_024607716.1) was isolated from
<i>Populus trichocarpa</i>
. A bioinformatics analysis revealed that
<i>PtDXS</i>
had high homology with the
<i>DXS</i>
s of other plant species.
<i>PtDXS</i>
expression differed among plant tissues and was highest in young leaves and lowest in roots. The recombinant protein was produced in
<i>Escherichia coli</i>
BL21 (DE3), purified, and its activity evaluated. The purified protein was capable of catalyzing the formation of 1-deoxy-d-xylulose-5-phosphate (DXP) from glyceraldehyde-3-phosphate and pyruvate. A functional color assay in
<i>E</i>
.
<i>coli</i>
harboring pAC-BETA indicated that
<i>PtDXS</i>
encodes a functional protein involved in the biosynthesis of isoprenoid precursors. The treatment of
<i>P</i>
.
<i>trichocarpa</i>
seedlings with 200 μM abscisic acid (ABA), 200 mM NaCl, 10% polyethylene glycol
<sub>6000</sub>
, and 2 mM H₂O₂ resulted in increased expression of
<i>PtDXS</i>
. The ABA and gibberellic acid contents of the transgenic lines (Poplar Nanlin 895) were higher than wild types, suggesting that DXS is important in terpenoid biosynthesis. Overexpression of
<i>PtDXS</i>
enhanced resistance to
<i>S</i>
.
<i>populiperda</i>
infection. Furthermore, the transgenic lines showed decreased feeding by
<i>Micromelalopha troglodyta</i>
, supporting the notion that PtDXS is a key enzyme in terpenoid biosynthesis.</div>
</front>
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<DateCompleted>
<Year>2019</Year>
<Month>07</Month>
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<DateRevised>
<Year>2020</Year>
<Month>02</Month>
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<ArticleTitle>Overexpression of
<i>PtDXS</i>
Enhances Stress Resistance in Poplars.</ArticleTitle>
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<ELocationID EIdType="doi" ValidYN="Y">10.3390/ijms20071669</ELocationID>
<Abstract>
<AbstractText>1-Deoxy-d-xylulose-5-phosphate synthase (DXS) is the rate-limiting enzyme in the plastidial methylerythritol phosphate pathway (MEP). In this study,
<i>PtDXS</i>
(XM_024607716.1) was isolated from
<i>Populus trichocarpa</i>
. A bioinformatics analysis revealed that
<i>PtDXS</i>
had high homology with the
<i>DXS</i>
s of other plant species.
<i>PtDXS</i>
expression differed among plant tissues and was highest in young leaves and lowest in roots. The recombinant protein was produced in
<i>Escherichia coli</i>
BL21 (DE3), purified, and its activity evaluated. The purified protein was capable of catalyzing the formation of 1-deoxy-d-xylulose-5-phosphate (DXP) from glyceraldehyde-3-phosphate and pyruvate. A functional color assay in
<i>E</i>
.
<i>coli</i>
harboring pAC-BETA indicated that
<i>PtDXS</i>
encodes a functional protein involved in the biosynthesis of isoprenoid precursors. The treatment of
<i>P</i>
.
<i>trichocarpa</i>
seedlings with 200 μM abscisic acid (ABA), 200 mM NaCl, 10% polyethylene glycol
<sub>6000</sub>
, and 2 mM H₂O₂ resulted in increased expression of
<i>PtDXS</i>
. The ABA and gibberellic acid contents of the transgenic lines (Poplar Nanlin 895) were higher than wild types, suggesting that DXS is important in terpenoid biosynthesis. Overexpression of
<i>PtDXS</i>
enhanced resistance to
<i>S</i>
.
<i>populiperda</i>
infection. Furthermore, the transgenic lines showed decreased feeding by
<i>Micromelalopha troglodyta</i>
, supporting the notion that PtDXS is a key enzyme in terpenoid biosynthesis.</AbstractText>
</Abstract>
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<Affiliation>Jiangsu Provincial Key Construction Laboratory of Special Biomass Resource Utilization, Nanjing Xiaozhuang University, Nanjing 211171, China. xuchenidea@hotmail.com.</Affiliation>
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</AffiliationInfo>
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<Affiliation>Co-Innovation Center for Sustainable Forestry in Southern China, Key Laboratory of Forest Genetics & Biotechnology, Ministry of Education, College of Biology and the Environment, Nanjing Forestry University, Nanjing 210037, China. 18705155218@163.com.</Affiliation>
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<AffiliationInfo>
<Affiliation>Co-Innovation Center for Sustainable Forestry in Southern China, Key Laboratory of Forest Genetics & Biotechnology, Ministry of Education, College of Biology and the Environment, Nanjing Forestry University, Nanjing 210037, China. dwli@njfu.edu.cn.</Affiliation>
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