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dc.contributor.authorPark, Jong-Min-
dc.contributor.authorKim, Jo-Il-
dc.contributor.authorNoh, Joo-Yoon-
dc.contributor.authorKim, Mira-
dc.contributor.authorKang, Min-Jung-
dc.contributor.authorPyun, Jae-Chul-
dc.date.accessioned2024-01-20T02:04:43Z-
dc.date.available2024-01-20T02:04:43Z-
dc.date.created2021-09-01-
dc.date.issued2017-02-
dc.identifier.issn0141-0229-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/123124-
dc.description.abstractMany kinds of susceptibility test for P-lactam antibiotics have been used to determine the antibiotic resistance of bacterial strains. Here, a sensitive antibiotic susceptibility test was presented by using a specialized reaction tool for laser desorption/ionization time-of-flight mass spectrometry (LDI-TOF MS) based on parylene-matrix chip. The p-lactamase assay was carried out in a specialized reaction tool by (1) concentrating the bacterial strain and (2) incubating the bacteria with penicillin-G. The parylene-matrix chip was produced by deposition of a partially porous parylene-N thin film on a dried organic matrix array, and the products of p-lactamase reaction in the low range of mass-to-charge ratio (m/z< 500) could be effectively analyzed by using a parylene-matrix chip. The sensing parameters were compared with conventional chromogenic antibiotic susceptibility test for beta-lactam antibiotics. Finally, LDI-TOF MS with a specialized reaction tool and parylene-matrix chip could achieve a limit of detection as low as 600 cells/spot for penicillin-G. (C) 2016 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE INC-
dc.subjectFLIGHT MASS-SPECTROMETRY-
dc.subjectAUTODISPLAYED Z-DOMAINS-
dc.subjectCOLI OUTER-MEMBRANE-
dc.subjectBACTERIAL SUSCEPTIBILITY-
dc.subjectSPR BIOSENSOR-
dc.subjectE. COLI-
dc.subjectIMMOBILIZATION-
dc.subjectIMMUNOASSAY-
dc.subjectLAYER-
dc.subjectFILM-
dc.titleHypersensitive antibiotic susceptibility test based on a beta-lactamase assay with a parylene-matrix chip-
dc.typeArticle-
dc.identifier.doi10.1016/j.enzmictec.2016.11.008-
dc.description.journalClass1-
dc.identifier.bibliographicCitationENZYME AND MICROBIAL TECHNOLOGY, v.97, pp.90 - 96-
dc.citation.titleENZYME AND MICROBIAL TECHNOLOGY-
dc.citation.volume97-
dc.citation.startPage90-
dc.citation.endPage96-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000393542300011-
dc.identifier.scopusid2-s2.0-84999750737-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.type.docTypeArticle-
dc.subject.keywordPlusFLIGHT MASS-SPECTROMETRY-
dc.subject.keywordPlusAUTODISPLAYED Z-DOMAINS-
dc.subject.keywordPlusCOLI OUTER-MEMBRANE-
dc.subject.keywordPlusBACTERIAL SUSCEPTIBILITY-
dc.subject.keywordPlusSPR BIOSENSOR-
dc.subject.keywordPlusE. COLI-
dc.subject.keywordPlusIMMOBILIZATION-
dc.subject.keywordPlusIMMUNOASSAY-
dc.subject.keywordPlusLAYER-
dc.subject.keywordPlusFILM-
dc.subject.keywordAuthorLaser desorption/ionization time-of-flight mass spectrometry (LDI-TOF MS)-
dc.subject.keywordAuthorParylene-matrix chip-
dc.subject.keywordAuthorAntibiotic susceptibility test-
dc.subject.keywordAuthorbeta-lactamase-
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