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Spectral Characteristics Related to Chemical Substructures and Structures Indicative of Organic Precursors from Fulvic Acids in Sediments by NMR and HPLC-ESI-MS

The aim of this work was to determine Fulvic Acids (FAs) in sediments to better know their composition at the molecular level and to propose substructures and structures of organic precursors. The sediment samples were obtained from a priority area for the conservation of ecosystems and biodiversity...

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Autores principales: López-Martínez, Verónica Gisela, Guerrero-Álvarez, Jorge A., Ronderos-Lara, José Gustavo, Murillo-Tovar, Mario Alfonso, Solá-Pérez, Jorge Ernesto, León-Rivera, Ismael, Saldarriaga-Noreña, Hugo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8272027/
https://www.ncbi.nlm.nih.gov/pubmed/34279390
http://dx.doi.org/10.3390/molecules26134051
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author López-Martínez, Verónica Gisela
Guerrero-Álvarez, Jorge A.
Ronderos-Lara, José Gustavo
Murillo-Tovar, Mario Alfonso
Solá-Pérez, Jorge Ernesto
León-Rivera, Ismael
Saldarriaga-Noreña, Hugo
author_facet López-Martínez, Verónica Gisela
Guerrero-Álvarez, Jorge A.
Ronderos-Lara, José Gustavo
Murillo-Tovar, Mario Alfonso
Solá-Pérez, Jorge Ernesto
León-Rivera, Ismael
Saldarriaga-Noreña, Hugo
author_sort López-Martínez, Verónica Gisela
collection PubMed
description The aim of this work was to determine Fulvic Acids (FAs) in sediments to better know their composition at the molecular level and to propose substructures and structures of organic precursors. The sediment samples were obtained from a priority area for the conservation of ecosystems and biodiversity in Mexico. FAs were extracted and purified using modifications to the International Humic Substances Society method. The characterization was carried out by 1D and 2D nuclear magnetic resonance (NMR) and high-performance liquid chromatography-electrospray ionization-mass spectrometry (HPLC-ESI-MS) in positive (ESI(+)) and negative (ESI(−)) modes. Twelve substructures were proposed by the COSY and HSQC experiments, correlating with compounds likely belonging to lignin derivatives obtained from soils as previously reported. The analysis of spectra obtained by HPLC-ESI-MS indicated likely presence of compounds chemically similar to that of the substructures elucidated by NMR. FAs studied are mainly constituted by carboxylic acids, hydroxyl, esters, vinyls, aliphatics, substituted aromatic rings, and amines, presenting structures related to organic precursors, such as lignin derivatives and polysaccharides.
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spelling pubmed-82720272021-07-11 Spectral Characteristics Related to Chemical Substructures and Structures Indicative of Organic Precursors from Fulvic Acids in Sediments by NMR and HPLC-ESI-MS López-Martínez, Verónica Gisela Guerrero-Álvarez, Jorge A. Ronderos-Lara, José Gustavo Murillo-Tovar, Mario Alfonso Solá-Pérez, Jorge Ernesto León-Rivera, Ismael Saldarriaga-Noreña, Hugo Molecules Article The aim of this work was to determine Fulvic Acids (FAs) in sediments to better know their composition at the molecular level and to propose substructures and structures of organic precursors. The sediment samples were obtained from a priority area for the conservation of ecosystems and biodiversity in Mexico. FAs were extracted and purified using modifications to the International Humic Substances Society method. The characterization was carried out by 1D and 2D nuclear magnetic resonance (NMR) and high-performance liquid chromatography-electrospray ionization-mass spectrometry (HPLC-ESI-MS) in positive (ESI(+)) and negative (ESI(−)) modes. Twelve substructures were proposed by the COSY and HSQC experiments, correlating with compounds likely belonging to lignin derivatives obtained from soils as previously reported. The analysis of spectra obtained by HPLC-ESI-MS indicated likely presence of compounds chemically similar to that of the substructures elucidated by NMR. FAs studied are mainly constituted by carboxylic acids, hydroxyl, esters, vinyls, aliphatics, substituted aromatic rings, and amines, presenting structures related to organic precursors, such as lignin derivatives and polysaccharides. MDPI 2021-07-02 /pmc/articles/PMC8272027/ /pubmed/34279390 http://dx.doi.org/10.3390/molecules26134051 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
López-Martínez, Verónica Gisela
Guerrero-Álvarez, Jorge A.
Ronderos-Lara, José Gustavo
Murillo-Tovar, Mario Alfonso
Solá-Pérez, Jorge Ernesto
León-Rivera, Ismael
Saldarriaga-Noreña, Hugo
Spectral Characteristics Related to Chemical Substructures and Structures Indicative of Organic Precursors from Fulvic Acids in Sediments by NMR and HPLC-ESI-MS
title Spectral Characteristics Related to Chemical Substructures and Structures Indicative of Organic Precursors from Fulvic Acids in Sediments by NMR and HPLC-ESI-MS
title_full Spectral Characteristics Related to Chemical Substructures and Structures Indicative of Organic Precursors from Fulvic Acids in Sediments by NMR and HPLC-ESI-MS
title_fullStr Spectral Characteristics Related to Chemical Substructures and Structures Indicative of Organic Precursors from Fulvic Acids in Sediments by NMR and HPLC-ESI-MS
title_full_unstemmed Spectral Characteristics Related to Chemical Substructures and Structures Indicative of Organic Precursors from Fulvic Acids in Sediments by NMR and HPLC-ESI-MS
title_short Spectral Characteristics Related to Chemical Substructures and Structures Indicative of Organic Precursors from Fulvic Acids in Sediments by NMR and HPLC-ESI-MS
title_sort spectral characteristics related to chemical substructures and structures indicative of organic precursors from fulvic acids in sediments by nmr and hplc-esi-ms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8272027/
https://www.ncbi.nlm.nih.gov/pubmed/34279390
http://dx.doi.org/10.3390/molecules26134051
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