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Conformational Behavior, Topographical Features, and Antioxidant Activity of Partly De-Esterified Arabinoxylans

This study aimed to investigate the effect of arabinoxylans (AX) partial de-esterification with feruloyl esterase on the polysaccharide conformational behavior, topographical features, and antioxidant activity. After enzyme treatment, the ferulic acid (FA) content in AX was reduced from 7.30 to 5.48...

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Autores principales: De Anda-Flores, Yubia, Carvajal-Millan, Elizabeth, Lizardi-Mendoza, Jaime, Rascon-Chu, Agustin, Tanori-Cordova, Judith, Martínez-López, Ana Luisa, Burgara-Estrella, Alexel J., Pedroza-Montero, Martin R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8398917/
https://www.ncbi.nlm.nih.gov/pubmed/34451333
http://dx.doi.org/10.3390/polym13162794
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author De Anda-Flores, Yubia
Carvajal-Millan, Elizabeth
Lizardi-Mendoza, Jaime
Rascon-Chu, Agustin
Tanori-Cordova, Judith
Martínez-López, Ana Luisa
Burgara-Estrella, Alexel J.
Pedroza-Montero, Martin R.
author_facet De Anda-Flores, Yubia
Carvajal-Millan, Elizabeth
Lizardi-Mendoza, Jaime
Rascon-Chu, Agustin
Tanori-Cordova, Judith
Martínez-López, Ana Luisa
Burgara-Estrella, Alexel J.
Pedroza-Montero, Martin R.
author_sort De Anda-Flores, Yubia
collection PubMed
description This study aimed to investigate the effect of arabinoxylans (AX) partial de-esterification with feruloyl esterase on the polysaccharide conformational behavior, topographical features, and antioxidant activity. After enzyme treatment, the ferulic acid (FA) content in AX was reduced from 7.30 to 5.48 µg FA/mg polysaccharide, and the molecule registered a small reduction in radius of gyration (RG), hydrodynamic radius (Rh), characteristic ratio (C∞), and persistence length (q). A slight decrease in α and a small increase in K constants in the Mark–Houwink–Sakurada equation for partially de-esterified AX (FAX) suggested a reduction in molecule structural rigidity and a more expanded coil conformation, respectively, in relation to AX. Fourier transform infrared spectroscopy spectra of AX and FAX presented a pattern characteristic for this polysaccharide. Atomic force microscopy topographic analysis of FAX showed a more regular surface without larger hollows in relation to AX. The antioxidant activity of FAX, compared to AX, was reduced by 30 and 41% using both 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid) (ABTS(+)) and 1,1-diphenyl-2-picryl-hydrazyl (DPPH) methods, respectively. These results suggest that feruloyl esterase treatment of AX could offer a strategy to tailor AX chains conformation, morphological features, and antioxidant activity, impacting the development of advanced biomaterials for biomedical and pharmaceutical applications.
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spelling pubmed-83989172021-08-29 Conformational Behavior, Topographical Features, and Antioxidant Activity of Partly De-Esterified Arabinoxylans De Anda-Flores, Yubia Carvajal-Millan, Elizabeth Lizardi-Mendoza, Jaime Rascon-Chu, Agustin Tanori-Cordova, Judith Martínez-López, Ana Luisa Burgara-Estrella, Alexel J. Pedroza-Montero, Martin R. Polymers (Basel) Communication This study aimed to investigate the effect of arabinoxylans (AX) partial de-esterification with feruloyl esterase on the polysaccharide conformational behavior, topographical features, and antioxidant activity. After enzyme treatment, the ferulic acid (FA) content in AX was reduced from 7.30 to 5.48 µg FA/mg polysaccharide, and the molecule registered a small reduction in radius of gyration (RG), hydrodynamic radius (Rh), characteristic ratio (C∞), and persistence length (q). A slight decrease in α and a small increase in K constants in the Mark–Houwink–Sakurada equation for partially de-esterified AX (FAX) suggested a reduction in molecule structural rigidity and a more expanded coil conformation, respectively, in relation to AX. Fourier transform infrared spectroscopy spectra of AX and FAX presented a pattern characteristic for this polysaccharide. Atomic force microscopy topographic analysis of FAX showed a more regular surface without larger hollows in relation to AX. The antioxidant activity of FAX, compared to AX, was reduced by 30 and 41% using both 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid) (ABTS(+)) and 1,1-diphenyl-2-picryl-hydrazyl (DPPH) methods, respectively. These results suggest that feruloyl esterase treatment of AX could offer a strategy to tailor AX chains conformation, morphological features, and antioxidant activity, impacting the development of advanced biomaterials for biomedical and pharmaceutical applications. MDPI 2021-08-20 /pmc/articles/PMC8398917/ /pubmed/34451333 http://dx.doi.org/10.3390/polym13162794 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 Communication
De Anda-Flores, Yubia
Carvajal-Millan, Elizabeth
Lizardi-Mendoza, Jaime
Rascon-Chu, Agustin
Tanori-Cordova, Judith
Martínez-López, Ana Luisa
Burgara-Estrella, Alexel J.
Pedroza-Montero, Martin R.
Conformational Behavior, Topographical Features, and Antioxidant Activity of Partly De-Esterified Arabinoxylans
title Conformational Behavior, Topographical Features, and Antioxidant Activity of Partly De-Esterified Arabinoxylans
title_full Conformational Behavior, Topographical Features, and Antioxidant Activity of Partly De-Esterified Arabinoxylans
title_fullStr Conformational Behavior, Topographical Features, and Antioxidant Activity of Partly De-Esterified Arabinoxylans
title_full_unstemmed Conformational Behavior, Topographical Features, and Antioxidant Activity of Partly De-Esterified Arabinoxylans
title_short Conformational Behavior, Topographical Features, and Antioxidant Activity of Partly De-Esterified Arabinoxylans
title_sort conformational behavior, topographical features, and antioxidant activity of partly de-esterified arabinoxylans
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8398917/
https://www.ncbi.nlm.nih.gov/pubmed/34451333
http://dx.doi.org/10.3390/polym13162794
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