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Simultaneous determination of protoporphyrin IX and magnesium protoporphyrin IX in Arabidopsis thaliana and Camellia sinensis using UPLC-MS/MS

BACKGROUNDS: Insertion of Mg(2+) into protoporphyrin IX (PPIX) to produce magnesium-protoporphyrin IX (Mg-PPIX) was the first step toward chlorophyll biosynthesis, which not only imparts plants green pigmentation but underpins photosynthesis. Plants that blocked the conversion of PPIX to Mg-PPIX dis...

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Autores principales: Zhang, Chenyu, Ma, Chunlei, Zhu, Li, Yao, Mingzhe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10061815/
https://www.ncbi.nlm.nih.gov/pubmed/36998023
http://dx.doi.org/10.1186/s13007-023-01008-y
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author Zhang, Chenyu
Ma, Chunlei
Zhu, Li
Yao, Mingzhe
author_facet Zhang, Chenyu
Ma, Chunlei
Zhu, Li
Yao, Mingzhe
author_sort Zhang, Chenyu
collection PubMed
description BACKGROUNDS: Insertion of Mg(2+) into protoporphyrin IX (PPIX) to produce magnesium-protoporphyrin IX (Mg-PPIX) was the first step toward chlorophyll biosynthesis, which not only imparts plants green pigmentation but underpins photosynthesis. Plants that blocked the conversion of PPIX to Mg-PPIX displayed yellowish or albino-lethal phenotypes. However, the lack of systematic study of the detection method and the metabolic difference between species have caused the research on chloroplast retrograde signaling controversial for a long time. RESULTS: An advanced and sensitive UPLC-MS/MS strategy for determining PPIX and Mg-PPIX was established in two metabolic different plants, Arabidopsis thaliana (Columbia-0) and Camellia sinensis var. sinensis. Two metabolites could be extracted by 80% acetone (v/v) and 20% 0.1 M NH(4)OH (v/v) without hexane washing. Since the Mg-PPIX could be substantially de-metalized into PPIX in acidic conditions, analysis was carried out by UPLC-MS/MS with 0.1% ammonia (v/v) and 0.1% ammonium acetonitrile (v/v) as mobile phases using negative ion multiple reaction monitoring modes. Interestingly, it could be easier to monitor these two compounds in dehydrated samples rather than in fresh samples. Validation was performed in spiked samples and mean recoveries ranged from 70.5 to 916%, and the intra-day and inter-day variations were less than 7.5 and 10.9%, respectively. The limit of detection was 0.01 mg·kg(− 1) and the limit of quantification was 0.05 mg·kg(− 1). The contents of PPIX (1.67 ± 0.12 mg·kg(− 1)) and Mg-PPIX (3.37 ± 0.10 mg·kg(− 1)) in tea were significantly higher than in Arabidopsis (PPIX: 0.05 ± 0.02 mg·kg(− 1); Mg-PPIX: 0.08 ± 0.01 mg·kg(− 1)) and they were only detected in the leaf. CONCLUSIONS: Our study establishes a universal and reliable method for determining PPIX and Mg-PPIX in two plants using UPLC-MS/MS. This procedure will facilitate studying chlorophyll metabolism and natural chlorophyll production.
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spelling pubmed-100618152023-03-31 Simultaneous determination of protoporphyrin IX and magnesium protoporphyrin IX in Arabidopsis thaliana and Camellia sinensis using UPLC-MS/MS Zhang, Chenyu Ma, Chunlei Zhu, Li Yao, Mingzhe Plant Methods Methodology BACKGROUNDS: Insertion of Mg(2+) into protoporphyrin IX (PPIX) to produce magnesium-protoporphyrin IX (Mg-PPIX) was the first step toward chlorophyll biosynthesis, which not only imparts plants green pigmentation but underpins photosynthesis. Plants that blocked the conversion of PPIX to Mg-PPIX displayed yellowish or albino-lethal phenotypes. However, the lack of systematic study of the detection method and the metabolic difference between species have caused the research on chloroplast retrograde signaling controversial for a long time. RESULTS: An advanced and sensitive UPLC-MS/MS strategy for determining PPIX and Mg-PPIX was established in two metabolic different plants, Arabidopsis thaliana (Columbia-0) and Camellia sinensis var. sinensis. Two metabolites could be extracted by 80% acetone (v/v) and 20% 0.1 M NH(4)OH (v/v) without hexane washing. Since the Mg-PPIX could be substantially de-metalized into PPIX in acidic conditions, analysis was carried out by UPLC-MS/MS with 0.1% ammonia (v/v) and 0.1% ammonium acetonitrile (v/v) as mobile phases using negative ion multiple reaction monitoring modes. Interestingly, it could be easier to monitor these two compounds in dehydrated samples rather than in fresh samples. Validation was performed in spiked samples and mean recoveries ranged from 70.5 to 916%, and the intra-day and inter-day variations were less than 7.5 and 10.9%, respectively. The limit of detection was 0.01 mg·kg(− 1) and the limit of quantification was 0.05 mg·kg(− 1). The contents of PPIX (1.67 ± 0.12 mg·kg(− 1)) and Mg-PPIX (3.37 ± 0.10 mg·kg(− 1)) in tea were significantly higher than in Arabidopsis (PPIX: 0.05 ± 0.02 mg·kg(− 1); Mg-PPIX: 0.08 ± 0.01 mg·kg(− 1)) and they were only detected in the leaf. CONCLUSIONS: Our study establishes a universal and reliable method for determining PPIX and Mg-PPIX in two plants using UPLC-MS/MS. This procedure will facilitate studying chlorophyll metabolism and natural chlorophyll production. BioMed Central 2023-03-30 /pmc/articles/PMC10061815/ /pubmed/36998023 http://dx.doi.org/10.1186/s13007-023-01008-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology
Zhang, Chenyu
Ma, Chunlei
Zhu, Li
Yao, Mingzhe
Simultaneous determination of protoporphyrin IX and magnesium protoporphyrin IX in Arabidopsis thaliana and Camellia sinensis using UPLC-MS/MS
title Simultaneous determination of protoporphyrin IX and magnesium protoporphyrin IX in Arabidopsis thaliana and Camellia sinensis using UPLC-MS/MS
title_full Simultaneous determination of protoporphyrin IX and magnesium protoporphyrin IX in Arabidopsis thaliana and Camellia sinensis using UPLC-MS/MS
title_fullStr Simultaneous determination of protoporphyrin IX and magnesium protoporphyrin IX in Arabidopsis thaliana and Camellia sinensis using UPLC-MS/MS
title_full_unstemmed Simultaneous determination of protoporphyrin IX and magnesium protoporphyrin IX in Arabidopsis thaliana and Camellia sinensis using UPLC-MS/MS
title_short Simultaneous determination of protoporphyrin IX and magnesium protoporphyrin IX in Arabidopsis thaliana and Camellia sinensis using UPLC-MS/MS
title_sort simultaneous determination of protoporphyrin ix and magnesium protoporphyrin ix in arabidopsis thaliana and camellia sinensis using uplc-ms/ms
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10061815/
https://www.ncbi.nlm.nih.gov/pubmed/36998023
http://dx.doi.org/10.1186/s13007-023-01008-y
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