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Evaluation of Antibacterial Mechanism of Action, Tyrosinase Inhibition, and Photocatalytic Degradation Potential of Sericin-Based Gold Nanoparticles

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dc.contributor.authorDas, Gitishree-
dc.contributor.authorPatra, Jayanta Kumar-
dc.date.accessioned2024-09-26T12:02:04Z-
dc.date.available2024-09-26T12:02:04Z-
dc.date.issued2023-05-
dc.identifier.issn1661-6596-
dc.identifier.issn1422-0067-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/24970-
dc.description.abstractIn recent times, numerous natural materials have been used for the fabrication of gold nanoparticles (AuNPs). Natural resources used for the synthesis of AuNPs are more environment friendly than chemical resources. Sericin is a silk protein that is discarded during the degumming process for obtaining silk. The current research used sericin silk protein waste materials as the reducing agent for the manufacture of gold nanoparticles (SGNPs) by a one-pot green synthesis method. Further, the antibacterial effect and antibacterial mechanism of action, tyrosinase inhibition, and photocatalytic degradation potential of these SGNPs were evaluated. The SGNPs displayed positive antibacterial activity (8.45-9.58 mm zone of inhibition at 50 mu g/disc) against all six tested foodborne pathogenic bacteria, namely, Enterococcus feacium DB01, Staphylococcus aureus ATCC 13565, Listeria monocytogenes ATCC 33090, Escherichia coli O157:H7 ATCC 23514, Aeromonas hydrophila ATCC 7966, and Pseudomonas aeruginosa ATCC 27583. The SGNPs also exhibited promising tyrosinase inhibition potential, with 32.83% inhibition at 100 mu g/mL concentration as compared to 52.4% by Kojic acid, taken as a reference standard compound. The SGNPs also displayed significant photocatalytic degradation effects, with 44.87% methylene blue dye degradation after 5 h of incubation. Moreover, the antibacterial mode of action of the SGNPs was also investigated against E. coli and E. feacium, and the results show that due to the small size of the nanomaterials, they could have adhered to the surface of the bacterial pathogens, and could have released more ions and dispersed in the bacterial cell wall surrounding environment, thereby disrupting the cell membrane and ROS production, and subsequently penetrating the bacterial cells, resulting in lysis or damage to the cell by the process of structural damage to the membrane, oxidative stress, and damage to the DNA and bacterial proteins. The overall outcome of the current investigation concludes the positive effects of the obtained SGNPs and their prospective applications as a natural antibacterial agent in cosmetics, environmental, and foodstuff industries, and for the management of environmental contagion.-
dc.format.extent16-
dc.language영어-
dc.language.isoENG-
dc.publisherMDPI-
dc.titleEvaluation of Antibacterial Mechanism of Action, Tyrosinase Inhibition, and Photocatalytic Degradation Potential of Sericin-Based Gold Nanoparticles-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/ijms24119477-
dc.identifier.scopusid2-s2.0-85161669328-
dc.identifier.wosid001005808600001-
dc.identifier.bibliographicCitationInternational Journal of Molecular Sciences, v.24, no.11, pp 1 - 16-
dc.citation.titleInternational Journal of Molecular Sciences-
dc.citation.volume24-
dc.citation.number11-
dc.citation.startPage1-
dc.citation.endPage16-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusGREEN SYNTHESIS-
dc.subject.keywordPlusNANOSTRUCTURES-
dc.subject.keywordPlusMELANOGENESIS-
dc.subject.keywordPlusANTIOXIDANT-
dc.subject.keywordPlusBIOLOGY-
dc.subject.keywordAuthorgold nanoparticles-
dc.subject.keywordAuthorsericin-
dc.subject.keywordAuthorantibacterial activity-
dc.subject.keywordAuthormechanism of action-
dc.subject.keywordAuthortyrosinase inhibition-
dc.subject.keywordAuthorphotocatalytic degradation-
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