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Optimizing and purifying extracellular amylase from soil bacteria to inhibit clinical biofilm-forming bacteria

BACKGROUND: Bacterial biofilms have become a major threat to human health. The objective of this study was to isolate amylase-producing bacteria from soil to determine the overall inhibition of certain pathogenic bacterial biofilms. METHODS: We used serial dilution and the streaking method to obtain...

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Autores principales: Elamary, Rokaia, Salem, Wesam M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643558/
https://www.ncbi.nlm.nih.gov/pubmed/33194439
http://dx.doi.org/10.7717/peerj.10288
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author Elamary, Rokaia
Salem, Wesam M.
author_facet Elamary, Rokaia
Salem, Wesam M.
author_sort Elamary, Rokaia
collection PubMed
description BACKGROUND: Bacterial biofilms have become a major threat to human health. The objective of this study was to isolate amylase-producing bacteria from soil to determine the overall inhibition of certain pathogenic bacterial biofilms. METHODS: We used serial dilution and the streaking method to obtain a total of 75 positive amylase isolates. The starch-agar plate method was used to screen the amylolytic activities of these isolates, and we used morphological and biochemical methods to characterize the isolates. Optimal conditions for amylase production and purification using Sephadex G-200 and SDS-PAGE were monitored. We screened these isolates’ antagonistic activities and the purified amylase against pathogenic and multi-drug-resistant human bacteria using the agar disk diffusion method. Some standard antibiotics were controlled according to their degree of sensitivity. Finally, we used spectrophotometric methods to screen the antibiofilm 24 and 48 h after application of filtering and purifying enzymes in order to determine its efficacy at human pathogenic bacteria. RESULTS: The isolated Bacillus species were Bacillus megaterium (26.7%), Bacillus subtilis (16%), Bacillus cereus (13.3%), Bacillus thuringiesis (10.7%), Bacillus lentus (10.7%), Bacillus mycoides (5.3%), Bacillus alvei (5.3%), Bacillus polymyxa (4%), Bacillus circulans (4%), and Micrococcus roseus (4%). Interestingly, all isolates showed a high antagonism to target pathogens. B. alevi had the highest recorded activity (48 mm) and B. polymyxa had the lowest recorded activity (12 mm) against Staphylococcus aureus (MRSA) and Escherichia coli, respectively. On the other hand, we detected no antibacterial activity for purified amylase. The supernatant of the isolated amylase-producing bacteria and its purified amylase showed significant inhibition for biofilm: 93.7% and 78.8%, respectively. This suggests that supernatant and purified amylase may be effective for clinical and environmental biofilm control. DISCUSSION: Our results showed that soil bacterial isolates such as Bacillus sp. supernatant and its purified amylase are good antibiofilm tools that can inhibit multidrug-resistant former strains. They could be beneficial for pharmaceutical use. While purified amylase was effective as an antibiofilm, the isolated supernatant showed better results.
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spelling pubmed-76435582020-11-12 Optimizing and purifying extracellular amylase from soil bacteria to inhibit clinical biofilm-forming bacteria Elamary, Rokaia Salem, Wesam M. PeerJ Biotechnology BACKGROUND: Bacterial biofilms have become a major threat to human health. The objective of this study was to isolate amylase-producing bacteria from soil to determine the overall inhibition of certain pathogenic bacterial biofilms. METHODS: We used serial dilution and the streaking method to obtain a total of 75 positive amylase isolates. The starch-agar plate method was used to screen the amylolytic activities of these isolates, and we used morphological and biochemical methods to characterize the isolates. Optimal conditions for amylase production and purification using Sephadex G-200 and SDS-PAGE were monitored. We screened these isolates’ antagonistic activities and the purified amylase against pathogenic and multi-drug-resistant human bacteria using the agar disk diffusion method. Some standard antibiotics were controlled according to their degree of sensitivity. Finally, we used spectrophotometric methods to screen the antibiofilm 24 and 48 h after application of filtering and purifying enzymes in order to determine its efficacy at human pathogenic bacteria. RESULTS: The isolated Bacillus species were Bacillus megaterium (26.7%), Bacillus subtilis (16%), Bacillus cereus (13.3%), Bacillus thuringiesis (10.7%), Bacillus lentus (10.7%), Bacillus mycoides (5.3%), Bacillus alvei (5.3%), Bacillus polymyxa (4%), Bacillus circulans (4%), and Micrococcus roseus (4%). Interestingly, all isolates showed a high antagonism to target pathogens. B. alevi had the highest recorded activity (48 mm) and B. polymyxa had the lowest recorded activity (12 mm) against Staphylococcus aureus (MRSA) and Escherichia coli, respectively. On the other hand, we detected no antibacterial activity for purified amylase. The supernatant of the isolated amylase-producing bacteria and its purified amylase showed significant inhibition for biofilm: 93.7% and 78.8%, respectively. This suggests that supernatant and purified amylase may be effective for clinical and environmental biofilm control. DISCUSSION: Our results showed that soil bacterial isolates such as Bacillus sp. supernatant and its purified amylase are good antibiofilm tools that can inhibit multidrug-resistant former strains. They could be beneficial for pharmaceutical use. While purified amylase was effective as an antibiofilm, the isolated supernatant showed better results. PeerJ Inc. 2020-11-02 /pmc/articles/PMC7643558/ /pubmed/33194439 http://dx.doi.org/10.7717/peerj.10288 Text en ©2020 Elamary and Salem https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Biotechnology
Elamary, Rokaia
Salem, Wesam M.
Optimizing and purifying extracellular amylase from soil bacteria to inhibit clinical biofilm-forming bacteria
title Optimizing and purifying extracellular amylase from soil bacteria to inhibit clinical biofilm-forming bacteria
title_full Optimizing and purifying extracellular amylase from soil bacteria to inhibit clinical biofilm-forming bacteria
title_fullStr Optimizing and purifying extracellular amylase from soil bacteria to inhibit clinical biofilm-forming bacteria
title_full_unstemmed Optimizing and purifying extracellular amylase from soil bacteria to inhibit clinical biofilm-forming bacteria
title_short Optimizing and purifying extracellular amylase from soil bacteria to inhibit clinical biofilm-forming bacteria
title_sort optimizing and purifying extracellular amylase from soil bacteria to inhibit clinical biofilm-forming bacteria
topic Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643558/
https://www.ncbi.nlm.nih.gov/pubmed/33194439
http://dx.doi.org/10.7717/peerj.10288
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