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Oligochitosan Synthesized by Cunninghamella elegans, a Fungus from Caatinga (The Brazilian Savanna) Is a Better Antioxidant than Animal Chitosan

Animal chitosan (Chit-A) is gaining more acceptance in daily activities. It is used in a range of products from food supplements for weight loss to even raw materials for producing nanoparticles and hydrogel drug carriers; however, it has low antioxidant activity. Fungal oligochitosan (OChit-F) was...

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Autores principales: Paiva, Weslley Souza, de Souza Neto, Francisco Ernesto, Queiroz, Moacir Fernandes, Batista, Lucas Alighieri Neves Costa, Rocha, Hugo Alexandre Oliveira, de Lima Batista, Anabelle Camarotti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8747077/
https://www.ncbi.nlm.nih.gov/pubmed/35011403
http://dx.doi.org/10.3390/molecules27010171
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author Paiva, Weslley Souza
de Souza Neto, Francisco Ernesto
Queiroz, Moacir Fernandes
Batista, Lucas Alighieri Neves Costa
Rocha, Hugo Alexandre Oliveira
de Lima Batista, Anabelle Camarotti
author_facet Paiva, Weslley Souza
de Souza Neto, Francisco Ernesto
Queiroz, Moacir Fernandes
Batista, Lucas Alighieri Neves Costa
Rocha, Hugo Alexandre Oliveira
de Lima Batista, Anabelle Camarotti
author_sort Paiva, Weslley Souza
collection PubMed
description Animal chitosan (Chit-A) is gaining more acceptance in daily activities. It is used in a range of products from food supplements for weight loss to even raw materials for producing nanoparticles and hydrogel drug carriers; however, it has low antioxidant activity. Fungal oligochitosan (OChit-F) was identified as a potential substitute for Chit-A. Cunninghamella elegans is a fungus found in the Brazilian savanna (Caatinga) that produces OligoChit-F, which is a relatively poorly studied compound. In this study, 4 kDa OChit-F with a 76% deacetylation degree was extracted from C. elegans. OChit-F showed antioxidant activity similar to that of Chit-A in only one in vitro test (copper chelation) but exhibited higher activity than that of Chit-A in three other tests (reducing power, hydroxyl radical scavenging, and iron chelation). These results indicate that OChit-F is a better antioxidant than Chit-A. In addition, Chit-A significantly increased the formation of calcium oxalate crystals in vitro, particularly those of the monohydrate (COM) type; however, OChit-F had no effect on this process in vitro. In summary, OChit-F had higher antioxidant activity than Chit-A and did not induce the formation of CaOx crystals. Thus, OChit-F can be used as a Chit-A substitute in applications affected by oxidative stress.
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spelling pubmed-87470772022-01-11 Oligochitosan Synthesized by Cunninghamella elegans, a Fungus from Caatinga (The Brazilian Savanna) Is a Better Antioxidant than Animal Chitosan Paiva, Weslley Souza de Souza Neto, Francisco Ernesto Queiroz, Moacir Fernandes Batista, Lucas Alighieri Neves Costa Rocha, Hugo Alexandre Oliveira de Lima Batista, Anabelle Camarotti Molecules Article Animal chitosan (Chit-A) is gaining more acceptance in daily activities. It is used in a range of products from food supplements for weight loss to even raw materials for producing nanoparticles and hydrogel drug carriers; however, it has low antioxidant activity. Fungal oligochitosan (OChit-F) was identified as a potential substitute for Chit-A. Cunninghamella elegans is a fungus found in the Brazilian savanna (Caatinga) that produces OligoChit-F, which is a relatively poorly studied compound. In this study, 4 kDa OChit-F with a 76% deacetylation degree was extracted from C. elegans. OChit-F showed antioxidant activity similar to that of Chit-A in only one in vitro test (copper chelation) but exhibited higher activity than that of Chit-A in three other tests (reducing power, hydroxyl radical scavenging, and iron chelation). These results indicate that OChit-F is a better antioxidant than Chit-A. In addition, Chit-A significantly increased the formation of calcium oxalate crystals in vitro, particularly those of the monohydrate (COM) type; however, OChit-F had no effect on this process in vitro. In summary, OChit-F had higher antioxidant activity than Chit-A and did not induce the formation of CaOx crystals. Thus, OChit-F can be used as a Chit-A substitute in applications affected by oxidative stress. MDPI 2021-12-28 /pmc/articles/PMC8747077/ /pubmed/35011403 http://dx.doi.org/10.3390/molecules27010171 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
Paiva, Weslley Souza
de Souza Neto, Francisco Ernesto
Queiroz, Moacir Fernandes
Batista, Lucas Alighieri Neves Costa
Rocha, Hugo Alexandre Oliveira
de Lima Batista, Anabelle Camarotti
Oligochitosan Synthesized by Cunninghamella elegans, a Fungus from Caatinga (The Brazilian Savanna) Is a Better Antioxidant than Animal Chitosan
title Oligochitosan Synthesized by Cunninghamella elegans, a Fungus from Caatinga (The Brazilian Savanna) Is a Better Antioxidant than Animal Chitosan
title_full Oligochitosan Synthesized by Cunninghamella elegans, a Fungus from Caatinga (The Brazilian Savanna) Is a Better Antioxidant than Animal Chitosan
title_fullStr Oligochitosan Synthesized by Cunninghamella elegans, a Fungus from Caatinga (The Brazilian Savanna) Is a Better Antioxidant than Animal Chitosan
title_full_unstemmed Oligochitosan Synthesized by Cunninghamella elegans, a Fungus from Caatinga (The Brazilian Savanna) Is a Better Antioxidant than Animal Chitosan
title_short Oligochitosan Synthesized by Cunninghamella elegans, a Fungus from Caatinga (The Brazilian Savanna) Is a Better Antioxidant than Animal Chitosan
title_sort oligochitosan synthesized by cunninghamella elegans, a fungus from caatinga (the brazilian savanna) is a better antioxidant than animal chitosan
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8747077/
https://www.ncbi.nlm.nih.gov/pubmed/35011403
http://dx.doi.org/10.3390/molecules27010171
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