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dc.contributor.author조경숙*
dc.contributor.author이은희*
dc.date.accessioned2016-08-28T12:08:09Z-
dc.date.available2016-08-28T12:08:09Z-
dc.date.issued2009*
dc.identifier.issn0254-8704*
dc.identifier.otherOAK-5348*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/220128-
dc.description.abstractRhodococcus sp. EH831 is a microbial species that can degrade volatile organic compounds. We optimized a method for monitoring quantitative real-time PCR (qRT-PCR) of EH831 that was incorporated into a polyurethane (PU) biofilter. When the genomic DNA of EH831 was directly extracted from a PU sample with immobilized EH831, the recovery efficiency was very low due to DNA absorption into the PU. DNA amplification during PCR was also inhibited by PU impurities. Therefore, a pre-treatment step was necessary. We successfully recovered cells from the PU by squeezing the matrix, adding sterilized water, and vortexing. The recovery efficiency ranged from 105 to 144%, and there was no statistically significant difference. We designed a novel TaqMan probe for EH831 and demonstrated its high specificity for EH831. The detection range for EH831 was 105-1011 CFU ml-1. The method described in this study can be used to investigate the relationship between quantitative analysis of Rhodococcus sp. EH831 and PU biofilter performance. © Triveni Enterprises, Lucknow (India).*
dc.languageEnglish*
dc.titleApplication of quantitative real-time PCR for quantification of Rhodococcus sp. EH831 in a polyurethane biofilter*
dc.typeArticle*
dc.relation.issue1*
dc.relation.volume30*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage155*
dc.relation.lastpage159*
dc.relation.journaltitleJournal of Environmental Biology*
dc.identifier.wosidWOS:000262706900025*
dc.identifier.scopusid2-s2.0-59349102118*
dc.author.googleLee E.H.*
dc.author.googleCho K.S.*
dc.author.googleRyu H.W.*
dc.contributor.scopusid조경숙(7403957095)*
dc.contributor.scopusid이은희(55773710100;56141882500)*
dc.date.modifydate20240322131338*
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공과대학 > 환경공학과 > Journal papers
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