Cargando…
HPLC Analysis and Biochemical Characterization of LOX from Eschscholtzia californica Cham.
Background: Plant lipoxygenases (LOXs, EC 1.13.11.12) are involved in lipid degradation, regulation of growth and development, senescence, and defence reactions. LOX represents the starting enzyme of the octadecanoid pathway. The aim of the work was to purify LOX from California poppy (Eschscholtzia...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150234/ https://www.ncbi.nlm.nih.gov/pubmed/29113053 http://dx.doi.org/10.3390/molecules22111899 |
_version_ | 1783356948770455552 |
---|---|
author | Kollárová, Renáta Holková, Ivana Rauová, Drahomíra Bálintová, Barbora Mikuš, Peter Obložinský, Marek |
author_facet | Kollárová, Renáta Holková, Ivana Rauová, Drahomíra Bálintová, Barbora Mikuš, Peter Obložinský, Marek |
author_sort | Kollárová, Renáta |
collection | PubMed |
description | Background: Plant lipoxygenases (LOXs, EC 1.13.11.12) are involved in lipid degradation, regulation of growth and development, senescence, and defence reactions. LOX represents the starting enzyme of the octadecanoid pathway. The aim of the work was to purify LOX from California poppy (Eschscholtzia californica Cham.), to determine its biochemical properties and to identify and quantify the products of LOX reaction with unsaturated fatty acids. Methods: LOX from California poppy seedlings was purified by hydrophobic chromatography (Phenyl-Sepharose CL-4B) and by ion-exchange chromatography (Q-Sepharose). The isolated LOX was incubated with linoleic acid used as a substrate. The HPLC experiments were performed with the Agilent Technologies 1050 series HPLC system. For the preparative separation of a mixture of hydroxy fatty acids from the sample matrix, the RP-HPLC method was used (column 120-5 Nucleosil C18). Then, the NP-HPLC analysis (separation, identification, and determination) of hydroxy fatty acid isomers was carried out on a Zorbax Rx-SIL column. Results: The purified LOX indicates the presence of a nontraditional plant enzyme with dual positional specificity (a ratio of 9- and 13-hydroperoxide products 1:1), a relative molecular mass of 85 kDa, a pH optimum of 6.5, an increasing activity stimulation by CaCl(2) till 2 mM, and a high substrate reactivity to linoleic acid with kinetic values of K(M) 2.6 mM and V(max) 3.14 μM/min/mg. Conclusions: For the first time, the LOX from California poppy seedlings was partially purified and the biochemical properties of the enzyme were analyzed. A dual positional specificity of the LOX found from California poppy seedlings is in agreement with the results obtained for LOXs isolated from other Papaveraceaes. A 1:1 ratio of 9-/13-HODE is attractive for the simultaneous investigation of both biotic stress responses (indicated by the 9-HODE marker) and the biosynthesis of jasmonic acid and jasmonates (indicated by the 13-HODE marker). |
format | Online Article Text |
id | pubmed-6150234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61502342018-11-13 HPLC Analysis and Biochemical Characterization of LOX from Eschscholtzia californica Cham. Kollárová, Renáta Holková, Ivana Rauová, Drahomíra Bálintová, Barbora Mikuš, Peter Obložinský, Marek Molecules Article Background: Plant lipoxygenases (LOXs, EC 1.13.11.12) are involved in lipid degradation, regulation of growth and development, senescence, and defence reactions. LOX represents the starting enzyme of the octadecanoid pathway. The aim of the work was to purify LOX from California poppy (Eschscholtzia californica Cham.), to determine its biochemical properties and to identify and quantify the products of LOX reaction with unsaturated fatty acids. Methods: LOX from California poppy seedlings was purified by hydrophobic chromatography (Phenyl-Sepharose CL-4B) and by ion-exchange chromatography (Q-Sepharose). The isolated LOX was incubated with linoleic acid used as a substrate. The HPLC experiments were performed with the Agilent Technologies 1050 series HPLC system. For the preparative separation of a mixture of hydroxy fatty acids from the sample matrix, the RP-HPLC method was used (column 120-5 Nucleosil C18). Then, the NP-HPLC analysis (separation, identification, and determination) of hydroxy fatty acid isomers was carried out on a Zorbax Rx-SIL column. Results: The purified LOX indicates the presence of a nontraditional plant enzyme with dual positional specificity (a ratio of 9- and 13-hydroperoxide products 1:1), a relative molecular mass of 85 kDa, a pH optimum of 6.5, an increasing activity stimulation by CaCl(2) till 2 mM, and a high substrate reactivity to linoleic acid with kinetic values of K(M) 2.6 mM and V(max) 3.14 μM/min/mg. Conclusions: For the first time, the LOX from California poppy seedlings was partially purified and the biochemical properties of the enzyme were analyzed. A dual positional specificity of the LOX found from California poppy seedlings is in agreement with the results obtained for LOXs isolated from other Papaveraceaes. A 1:1 ratio of 9-/13-HODE is attractive for the simultaneous investigation of both biotic stress responses (indicated by the 9-HODE marker) and the biosynthesis of jasmonic acid and jasmonates (indicated by the 13-HODE marker). MDPI 2017-11-04 /pmc/articles/PMC6150234/ /pubmed/29113053 http://dx.doi.org/10.3390/molecules22111899 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kollárová, Renáta Holková, Ivana Rauová, Drahomíra Bálintová, Barbora Mikuš, Peter Obložinský, Marek HPLC Analysis and Biochemical Characterization of LOX from Eschscholtzia californica Cham. |
title | HPLC Analysis and Biochemical Characterization of LOX from Eschscholtzia californica Cham. |
title_full | HPLC Analysis and Biochemical Characterization of LOX from Eschscholtzia californica Cham. |
title_fullStr | HPLC Analysis and Biochemical Characterization of LOX from Eschscholtzia californica Cham. |
title_full_unstemmed | HPLC Analysis and Biochemical Characterization of LOX from Eschscholtzia californica Cham. |
title_short | HPLC Analysis and Biochemical Characterization of LOX from Eschscholtzia californica Cham. |
title_sort | hplc analysis and biochemical characterization of lox from eschscholtzia californica cham. |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150234/ https://www.ncbi.nlm.nih.gov/pubmed/29113053 http://dx.doi.org/10.3390/molecules22111899 |
work_keys_str_mv | AT kollarovarenata hplcanalysisandbiochemicalcharacterizationofloxfromeschscholtziacalifornicacham AT holkovaivana hplcanalysisandbiochemicalcharacterizationofloxfromeschscholtziacalifornicacham AT rauovadrahomira hplcanalysisandbiochemicalcharacterizationofloxfromeschscholtziacalifornicacham AT balintovabarbora hplcanalysisandbiochemicalcharacterizationofloxfromeschscholtziacalifornicacham AT mikuspeter hplcanalysisandbiochemicalcharacterizationofloxfromeschscholtziacalifornicacham AT oblozinskymarek hplcanalysisandbiochemicalcharacterizationofloxfromeschscholtziacalifornicacham |