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Enzyme-Functionalized Cellulose Beads as a Promising Antimicrobial Material

[Image: see text] The extensive use of antibiotics over the last decades is responsible for the emergence of multidrug-resistant (MDR) microorganisms that are challenging health care systems worldwide. The use of alternative antimicrobial materials could mitigate the selection of new MDR strains by...

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Autores principales: Califano, Davide, Patenall, Bethany Lee, Kadowaki, Marco A.S., Mattia, Davide, Scott, Janet L., Edler, Karen J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884000/
https://www.ncbi.nlm.nih.gov/pubmed/33404227
http://dx.doi.org/10.1021/acs.biomac.0c01536
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author Califano, Davide
Patenall, Bethany Lee
Kadowaki, Marco A.S.
Mattia, Davide
Scott, Janet L.
Edler, Karen J.
author_facet Califano, Davide
Patenall, Bethany Lee
Kadowaki, Marco A.S.
Mattia, Davide
Scott, Janet L.
Edler, Karen J.
author_sort Califano, Davide
collection PubMed
description [Image: see text] The extensive use of antibiotics over the last decades is responsible for the emergence of multidrug-resistant (MDR) microorganisms that are challenging health care systems worldwide. The use of alternative antimicrobial materials could mitigate the selection of new MDR strains by reducing antibiotic overuse. This paper describes the design of enzyme-based antimicrobial cellulose beads containing a covalently coupled glucose oxidase from Aspergillus niger (GOx) able to release antimicrobial concentrations of hydrogen peroxide (H(2)O(2)) (≈ 1.8 mM). The material preparation was optimized to obtain the best performance in terms of mechanical resistance, shelf life, and H(2)O(2) production. As a proof of concept, agar inhibition halo assays (Kirby-Bauer test) against model pathogens were performed. The two most relevant factors affecting the bead functionalization process were the degree of oxidation and the pH used for the enzyme binding process. Slightly acidic conditions during the functionalization process (pH 6) showed the best results for the GOx/cellulose system. The functionalized beads inhibited the growth of all the microorganisms assayed, confirming the release of sufficient antimicrobial levels of H(2)O(2). The maximum inhibition efficiency was exhibited toward Pseudomonas aeruginosa (P. aeruginosa) and Escherichia coli (E. coli), although significant inhibitory effects toward methicillin-resistant Staphylococcus aureus (MRSA) and S. aureus were also observed. These enzyme-functionalized cellulose beads represent an inexpensive, sustainable, and biocompatible antimicrobial material with potential use in many applications, including the manufacturing of biomedical products and additives for food preservation.
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spelling pubmed-78840002021-02-16 Enzyme-Functionalized Cellulose Beads as a Promising Antimicrobial Material Califano, Davide Patenall, Bethany Lee Kadowaki, Marco A.S. Mattia, Davide Scott, Janet L. Edler, Karen J. Biomacromolecules [Image: see text] The extensive use of antibiotics over the last decades is responsible for the emergence of multidrug-resistant (MDR) microorganisms that are challenging health care systems worldwide. The use of alternative antimicrobial materials could mitigate the selection of new MDR strains by reducing antibiotic overuse. This paper describes the design of enzyme-based antimicrobial cellulose beads containing a covalently coupled glucose oxidase from Aspergillus niger (GOx) able to release antimicrobial concentrations of hydrogen peroxide (H(2)O(2)) (≈ 1.8 mM). The material preparation was optimized to obtain the best performance in terms of mechanical resistance, shelf life, and H(2)O(2) production. As a proof of concept, agar inhibition halo assays (Kirby-Bauer test) against model pathogens were performed. The two most relevant factors affecting the bead functionalization process were the degree of oxidation and the pH used for the enzyme binding process. Slightly acidic conditions during the functionalization process (pH 6) showed the best results for the GOx/cellulose system. The functionalized beads inhibited the growth of all the microorganisms assayed, confirming the release of sufficient antimicrobial levels of H(2)O(2). The maximum inhibition efficiency was exhibited toward Pseudomonas aeruginosa (P. aeruginosa) and Escherichia coli (E. coli), although significant inhibitory effects toward methicillin-resistant Staphylococcus aureus (MRSA) and S. aureus were also observed. These enzyme-functionalized cellulose beads represent an inexpensive, sustainable, and biocompatible antimicrobial material with potential use in many applications, including the manufacturing of biomedical products and additives for food preservation. American Chemical Society 2021-01-06 2021-02-08 /pmc/articles/PMC7884000/ /pubmed/33404227 http://dx.doi.org/10.1021/acs.biomac.0c01536 Text en © 2021 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Califano, Davide
Patenall, Bethany Lee
Kadowaki, Marco A.S.
Mattia, Davide
Scott, Janet L.
Edler, Karen J.
Enzyme-Functionalized Cellulose Beads as a Promising Antimicrobial Material
title Enzyme-Functionalized Cellulose Beads as a Promising Antimicrobial Material
title_full Enzyme-Functionalized Cellulose Beads as a Promising Antimicrobial Material
title_fullStr Enzyme-Functionalized Cellulose Beads as a Promising Antimicrobial Material
title_full_unstemmed Enzyme-Functionalized Cellulose Beads as a Promising Antimicrobial Material
title_short Enzyme-Functionalized Cellulose Beads as a Promising Antimicrobial Material
title_sort enzyme-functionalized cellulose beads as a promising antimicrobial material
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884000/
https://www.ncbi.nlm.nih.gov/pubmed/33404227
http://dx.doi.org/10.1021/acs.biomac.0c01536
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