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Enhancing the Thermo-Stability and Anti-Biofilm Activity of Alginate Lyase by Immobilization on Low Molecular Weight Chitosan Nanoparticles

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dc.contributor.authorLi, Shangyong-
dc.contributor.authorWang, Yanan-
dc.contributor.authorLi, Xiao-
dc.contributor.authorLee, Beom Suk-
dc.contributor.authorJung, Samil-
dc.contributor.authorLee, Myeong-Sok-
dc.date.available2021-02-22T05:45:49Z-
dc.date.issued2019-09-
dc.identifier.issn1661-6596-
dc.identifier.issn1422-0067-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/2849-
dc.description.abstractBacterial biofilm causes severe antibiotic resistance. An extracellular polymeric substance (EPS) is the main component in the bacterial biofilm. Alginate is a key EPS component in the biofilm of Pseudomonas aeruginosa and responsible for surface adhesion and stabilization of biofilm. Alginate lyase has emerged as an efficient therapeutic strategy targeting to degrade the alginate in the biofilm of P. aeruginosa. However, the application of this enzyme is limited by its poor stability. In this study, chitosan nanoparticles (CS-NPs) were synthesized using low molecular weight chitosan and alginate lyase Aly08 was immobilized on low molecular weight chitosan nanoparticles (AL-LMW-CS-NPs). As a result, the immobilization significantly enhanced the thermal stability and reusability of Aly08. In addition, compared with free Aly08, the immobilized AL-LMW-CS-NPs exhibited higher efficiency in inhibiting biofilm formation and interrupting the established mature biofilm of P. aeruginosa, which could reduce its biomass and thickness confirmed by confocal microscopy. Moreover, the biofilm disruption greatly increased the antibiotic sensitivity of P. aeruginosa. This research will contribute to the further development of alginate lyase as an anti-biofilm agent.-
dc.language영어-
dc.language.isoENG-
dc.publisherMDPI-
dc.titleEnhancing the Thermo-Stability and Anti-Biofilm Activity of Alginate Lyase by Immobilization on Low Molecular Weight Chitosan Nanoparticles-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/ijms20184565-
dc.identifier.scopusid2-s2.0-85072528485-
dc.identifier.wosid000489100500244-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v.20, no.18-
dc.citation.titleINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES-
dc.citation.volume20-
dc.citation.number18-
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.keywordPlusPSEUDOMONAS-AERUGINOSA-BIOFILMS-
dc.subject.keywordPlusANTIBIOTIC-RESISTANCE-
dc.subject.keywordAuthorimmobilization-
dc.subject.keywordAuthorchitosan nanoparticles-
dc.subject.keywordAuthoralginate lyase-
dc.subject.keywordAuthoranti-biofilm activity-
dc.subject.keywordAuthorantibiotics susceptibility-
dc.identifier.urlhttps://www.mdpi.com/1422-0067/20/18/4565-
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