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231224s2013 xx |||||o 00| ||eng c |
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|a 10.1016/j.plaphy.2013.10.009
|2 doi
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|a pubmed24n0773.xml
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|a (DE-627)NLM232023875
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|a (NLM)24161755
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|a (PII)S0981-9428(13)00355-0
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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| 100 |
1 |
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|a Camillo, Luciana Rodrigues
|e verfasserin
|4 aut
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| 245 |
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|a Tc-cAPX, a cytosolic ascorbate peroxidase of Theobroma cacao L. engaged in the interaction with Moniliophthora perniciosa, the causing agent of witches' broom disease
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|c 2013
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 29.07.2014
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|a Date Revised 30.09.2020
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2013 The Authors. Published by Elsevier Masson SAS.. All rights reserved.
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|a The level of hydrogen peroxide (H2O2) in plants signalizes the induction of several genes, including that of ascorbate peroxidase (APX-EC 1.11.1.11). APX isoenzymes play a central role in the elimination of intracellular H2O2 and contribute to plant responses to diverse stresses. During the infection process in Theobroma cacao by Moniliophthora perniciosa oxidative stress is generated and the APX action recruited from the plant. The present work aimed to characterize the T. cacao APX involved in the molecular interaction of T. cacao-M. perniciosa. The peroxidase activity was analyzed in protein extracts from cocoa plants infected by M. perniciosa and showed the induction of peroxidases like APX in resistant cocoa plants. The cytosolic protein of T. cacao (GenBank: ABR68691.2) was phylogenetically analyzed in relation to other peroxidases from the cocoa genome and eight genes encoding APX proteins with conserved domains were also analyzed. The cDNA from cytosolic APX was cloned in pET28a and the recombinant protein expressed and purified (rTc-cAPX). The secondary structure of the protein was analyzed by Circular Dichroism (CD) displaying high proportion of α-helices when folded. The enzymatic assay shows stable activity using ascorbate and guaiacol as an electron donor for H2O2 reduction. The pH 7.5 is the optimum for enzyme activity. Chromatographic analysis suggests that rTc-cAPX is a homodimer in solution. Results indicate that the rTc-cAPX is correctly folded, stable and biochemically active. The purified rTc-cAPX presented biotechnological potential and is adequate for future structural and functional studies
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Ascorbate peroxidase-related (APX-R)
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|a Enzyme activity
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|a Enzyme characterization
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|a Hydrogen peroxide
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|a Oxidative stress
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|a Peroxidase
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|a Recombinant protein
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|a DNA, Complementary
|2 NLM
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| 650 |
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|a Plant Proteins
|2 NLM
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| 650 |
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|a Recombinant Proteins
|2 NLM
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| 650 |
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|a Hydrogen Peroxide
|2 NLM
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| 650 |
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|a BBX060AN9V
|2 NLM
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| 650 |
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|a Ascorbate Peroxidases
|2 NLM
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| 650 |
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|a EC 1.11.1.11
|2 NLM
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| 700 |
1 |
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|a Filadelfo, Ciro Ribeiro
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Monzani, Paulo Sérgio
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Corrêa, Ronan Xavier
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Gramacho, Karina Peres
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Micheli, Fabienne
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Pirovani, Carlos Priminho
|e verfasserin
|4 aut
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| 773 |
0 |
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|i Enthalten in
|t Plant physiology and biochemistry : PPB
|d 1991
|g 73(2013) vom: 01. Dez., Seite 254-65
|w (DE-627)NLM098178261
|x 1873-2690
|7 nnns
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| 773 |
1 |
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|g volume:73
|g year:2013
|g day:01
|g month:12
|g pages:254-65
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|u http://dx.doi.org/10.1016/j.plaphy.2013.10.009
|3 Volltext
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|a GBV_ILN_350
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|a AR
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|d 73
|j 2013
|b 01
|c 12
|h 254-65
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