Specific PCR assay for a tannin-tolerant Selenomonas ruminantium isolate, derived from helicase coding sequences

Sequences from a tannin-tolerant Selenomonas ruminantium isolate (EAT2) that hydrolyzes gallic acid were identified. Two exhibited identity to helicases with a wide phylogenetic distribution. PCR amplification by using primers from one helicase gene detected 2,000 to 5,000 EAT2 genome equivalents bu...

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Detalles Bibliográficos
Autores principales: Bishop, Richard P., Obura, M., Odongo, D., Odenyo, A.A.
Formato: Journal Article
Lenguaje:Inglés
Publicado: American Society for Microbiology 2004
Materias:
Acceso en línea:https://hdl.handle.net/10568/35306
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author Bishop, Richard P.
Obura, M.
Odongo, D.
Odenyo, A.A.
author_browse Bishop, Richard P.
Obura, M.
Odenyo, A.A.
Odongo, D.
author_facet Bishop, Richard P.
Obura, M.
Odongo, D.
Odenyo, A.A.
author_sort Bishop, Richard P.
collection Repository of Agricultural Research Outputs (CGSpace)
description Sequences from a tannin-tolerant Selenomonas ruminantium isolate (EAT2) that hydrolyzes gallic acid were identified. Two exhibited identity to helicases with a wide phylogenetic distribution. PCR amplification by using primers from one helicase gene detected 2,000 to 5,000 EAT2 genome equivalents but did not amplify total gastrointestinal microbial DNA of nine other ungulate species.
format Journal Article
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language Inglés
publishDate 2004
publishDateRange 2004
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publisherStr American Society for Microbiology
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spelling CGSpace353062024-08-27T12:27:43Z Specific PCR assay for a tannin-tolerant Selenomonas ruminantium isolate, derived from helicase coding sequences Bishop, Richard P. Obura, M. Odongo, D. Odenyo, A.A. animal diseases genetics ecology food science biotechnology Sequences from a tannin-tolerant Selenomonas ruminantium isolate (EAT2) that hydrolyzes gallic acid were identified. Two exhibited identity to helicases with a wide phylogenetic distribution. PCR amplification by using primers from one helicase gene detected 2,000 to 5,000 EAT2 genome equivalents but did not amplify total gastrointestinal microbial DNA of nine other ungulate species. 2004-05 2014-04-14T10:55:54Z 2014-04-14T10:55:54Z Journal Article https://hdl.handle.net/10568/35306 en Open Access American Society for Microbiology Bishop, R., Obura, M., Odongo, D. and Odenyo, A. 2004. Specific PCR assay for a tannin-tolerant Selenomonas ruminantium isolate, derived from helicase coding sequences. Applied and Environmental Microbiology 70(5):3180-3182.
spellingShingle animal diseases
genetics
ecology
food science
biotechnology
Bishop, Richard P.
Obura, M.
Odongo, D.
Odenyo, A.A.
Specific PCR assay for a tannin-tolerant Selenomonas ruminantium isolate, derived from helicase coding sequences
title Specific PCR assay for a tannin-tolerant Selenomonas ruminantium isolate, derived from helicase coding sequences
title_full Specific PCR assay for a tannin-tolerant Selenomonas ruminantium isolate, derived from helicase coding sequences
title_fullStr Specific PCR assay for a tannin-tolerant Selenomonas ruminantium isolate, derived from helicase coding sequences
title_full_unstemmed Specific PCR assay for a tannin-tolerant Selenomonas ruminantium isolate, derived from helicase coding sequences
title_short Specific PCR assay for a tannin-tolerant Selenomonas ruminantium isolate, derived from helicase coding sequences
title_sort specific pcr assay for a tannin tolerant selenomonas ruminantium isolate derived from helicase coding sequences
topic animal diseases
genetics
ecology
food science
biotechnology
url https://hdl.handle.net/10568/35306
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