Bacterial Biofilm Degradation Using Extracellular Enzymes Produced by Penicillium janthinellum EU2D-21 under Submerged Fermentation
Autor: | Anil Kumar Nagraj, Digambar Gokhale |
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Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Enzyme complex Protease biology Chemistry Pseudomonas aeruginosa medicine.medical_treatment 030106 microbiology Biofilm 04 agricultural and veterinary sciences General Medicine Cellulase medicine.disease_cause biology.organism_classification 040401 food science Microbiology 03 medical and health sciences 0404 agricultural biotechnology Extracellular polymeric substance medicine biology.protein Escherichia coli Bacteria |
Zdroj: | Advances in Microbiology. :687-698 |
ISSN: | 2165-3410 2165-3402 |
DOI: | 10.4236/aim.2018.89046 |
Popis: | Bacterial biofilms are the bacterial aggregates that are embedded in the self-produced matrix of extracellular polymeric substances (EPS) that cause persistent bacterial infections posing significant medical challenges. They are recalcitrant to antibiotics and host defenses which make the treatments difficult and costly. Penicillium janthinellum mutant EU2D-21 was found to produce extracellular enzyme complex (amylase, cellulase, protease) under submerged fermentation. Maximum specific enzyme activities were found to be 3.04 IU/mg, 2.61 IU/mg and 3.39 IU/mg for alpha-amylase, cellulase and protease respectively, after 8 days of incubation at 30˚C. We evaluated the enzyme complex for its ability to target and degrade the biofilms of different bacteria. We found that it degraded biofilms of Escherichia coli (85.5%), Salmonella enterica (79.72%), Pseudomonas aeruginosa (88.76%) and Staphyloccus aureus (87.42%) within 1 h of incubation at 50˚C. The scanning electron microscopy (SEM), quantitation of biofilm removal assay and Crystal violet assay demonstrated that the enzyme complex detached the biofilm exo-polysaccharide matrix and bacteria from the cell surface. These results illustrate the feasibility and benefits of using this enzyme complex as anti-biofilm therapeutics to eradicate biofilms. This can also be used as a promising strategy to improve treatment of multidrug resistant bacterial infections. |
Databáze: | OpenAIRE |
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