DC Field | Value | Language |
---|---|---|
dc.contributor.author | Jeon, JR | - |
dc.contributor.author | Kim, JH | - |
dc.contributor.author | Chang, YS | - |
dc.date.accessioned | 2015-06-25T02:27:02Z | - |
dc.date.available | 2015-06-25T02:27:02Z | - |
dc.date.created | 2014-03-11 | - |
dc.date.issued | 2013-10 | - |
dc.identifier.issn | 2050-750X | - |
dc.identifier.other | 2015-OAK-0000029451 | en_US |
dc.identifier.uri | https://oasis.postech.ac.kr/handle/2014.oak/10982 | - |
dc.description.abstract | Versatile binding features of ortho-dihydroxyphenyl groups ubiquitously found in mussel adhesive proteins are inducible with polyphenolic moieties that are widespread in the plant kingdom, strongly supporting the idea that previously reported mussel-related material-independent adhesion is reproducible with plant-derived phenolics. Here, we directly demonstrate that material-independent coating action can be achieved by in vitro laccase-catalyzed polymerization of plant phenols. Deposition rates of polymeric products onto solid surfaces are superior to that of polydopamine, the known mussel-derived coating agent. The coated surfaces are robust against strong acid and salt. In addition, FTIR-ATR and analyses of bactericidal action, phenol content, charge-dependent sorption behavior, and free radical scavenging activity strongly indicate that the coating agents are structurally multiple hydroxyphenyl group-bearing polyaromatics. We finally demonstrate that hydroxyphenyl group bearing polymers act as either conjugation sites for proteins or chelating/reduction sites for metal ions, and also that co-deposition of functional organics during the enzymatic polymerization of plant phenols is feasible. Both immobilization results strongly suggest that coated layers by our products can lead to further surface functionalization. | - |
dc.description.statementofresponsibility | open | en_US |
dc.language | English | - |
dc.publisher | ROYAL SOC CHEMISTRY | - |
dc.relation.isPartOf | JOURNAL OF MATERIALS CHEMISTRY B | - |
dc.rights | BY_NC_ND | en_US |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/2.0/kr | en_US |
dc.title | Enzymatic polymerization of plant-derived phenols for material-independent and multifunctional coating | - |
dc.type | Article | - |
dc.contributor.college | 환경공학부 | en_US |
dc.identifier.doi | 10.1039/C3TB21161D | - |
dc.author.google | Jeon, JR | en_US |
dc.author.google | Kim, JH | en_US |
dc.author.google | Chang, YS | en_US |
dc.relation.volume | 1 | en_US |
dc.relation.issue | 47 | en_US |
dc.relation.startpage | 6501 | en_US |
dc.relation.lastpage | 6509 | en_US |
dc.contributor.id | 10086108 | en_US |
dc.relation.journal | JOURNAL OF MATERIALS CHEMISTRY B | en_US |
dc.relation.index | SCI급, SCOPUS 등재논문 | en_US |
dc.relation.sci | SCI | en_US |
dc.collections.name | Journal Papers | en_US |
dc.type.rims | ART | - |
dc.identifier.bibliographicCitation | JOURNAL OF MATERIALS CHEMISTRY B, v.1, no.47, pp.6501 - 6509 | - |
dc.identifier.wosid | 000327259400003 | - |
dc.date.tcdate | 2019-01-01 | - |
dc.citation.endPage | 6509 | - |
dc.citation.number | 47 | - |
dc.citation.startPage | 6501 | - |
dc.citation.title | JOURNAL OF MATERIALS CHEMISTRY B | - |
dc.citation.volume | 1 | - |
dc.contributor.affiliatedAuthor | Chang, YS | - |
dc.identifier.scopusid | 2-s2.0-84887793518 | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.wostc | 29 | - |
dc.description.scptc | 29 | * |
dc.date.scptcdate | 2018-10-274 | * |
dc.type.docType | Article | - |
dc.subject.keywordPlus | SURFACE-CHEMISTRY | - |
dc.subject.keywordPlus | MUSSEL | - |
dc.subject.keywordPlus | IMMOBILIZATION | - |
dc.subject.keywordPlus | POLYPHENOLS | - |
dc.subject.keywordPlus | OXIDATION | - |
dc.subject.keywordPlus | GROWTH | - |
dc.relation.journalWebOfScienceCategory | Materials Science, Biomaterials | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Materials Science | - |
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