Please use this identifier to cite or link to this item: https://doi.org/10.1128/AEM.02576-08
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dc.titleHierarchical oligonucleotide primer extension as a time- and cost-effective approach for quantitative determination of Bifidobacterium spp. in Infant feces
dc.contributor.authorHong, P.-Y.
dc.contributor.authorYap, G.C.
dc.contributor.authorLee, B.W.
dc.contributor.authorChua, K.Y.
dc.contributor.authorLiu, W.-T.
dc.date.accessioned2014-10-08T08:32:27Z
dc.date.available2014-10-08T08:32:27Z
dc.date.issued2009-04
dc.identifier.citationHong, P.-Y., Yap, G.C., Lee, B.W., Chua, K.Y., Liu, W.-T. (2009-04). Hierarchical oligonucleotide primer extension as a time- and cost-effective approach for quantitative determination of Bifidobacterium spp. in Infant feces. Applied and Environmental Microbiology 75 (8) : 2573-2576. ScholarBank@NUS Repository. https://doi.org/10.1128/AEM.02576-08
dc.identifier.issn00992240
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/87517
dc.description.abstractThe Bifidobacterium spp. present in 10 infant fecal samples (4 from infants with eczema and 6 from healthy infants) were quantified with both hierarchical oligonucleotide primer extension (HOPE) and fluorescence in situ hybridization-flow cytometry. The relative abundances of Bifidobacterium longum and B. catenulatum with respect to the total bifidobacteria had a poor correlation (ρ, 0.208), presumably due to differences in primer specificity and the level of hybridization stringency of both methods. In contrast, the relative abundances of organisms of the genus Bifidobacterium against the total amplified 16S rRNA genes and those of B. adolescentis, B. bifidum, and B. breve against the genus Bifidobacterium exhibited a good statistical correlation (ρ, >0.783; P value,
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1128/AEM.02576-08
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentDIVISION OF ENVIRONMENTAL SCIENCE & ENGG
dc.description.doi10.1128/AEM.02576-08
dc.description.sourcetitleApplied and Environmental Microbiology
dc.description.volume75
dc.description.issue8
dc.description.page2573-2576
dc.description.codenAEMID
dc.identifier.isiut000264936800039
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