16S rDNA analysis of bacterial diversity in three fractions of cow rumen

examined using a PCR-based approach. 16S rDNA sequenceswere amplified and cloned from thre fractions of rumen(solid, fluid, and epithelium) that are likely to representdiferent bacterial niches. A total of 113 clones weresequenced, and similarities to known 16S rDNA sequenceswere examined. About 47....

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Veröffentlicht in:Journal of microbiology and biotechnology 2006, 16(1), , pp.92-101
Hauptverfasser: CHO, Soo Jeong, KYE MAN CHO, HAN DAE YUN, EUN CHULE SHIN, WOO JIN LIM, SU YOUNG HONG, BYOUNG ROCK CHOI, JUNG MI KANG, SUN MI LEE, YONG HEE KIM, KIM, Hoon
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Zusammenfassung:examined using a PCR-based approach. 16S rDNA sequenceswere amplified and cloned from thre fractions of rumen(solid, fluid, and epithelium) that are likely to representdiferent bacterial niches. A total of 113 clones weresequenced, and similarities to known 16S rDNA sequenceswere examined. About 47.8% of the sequences had 90-97%similarity to 16S rDNA database sequences. Furthermore, about62.2% of the sequences were 98-100% similar to 16S rDNAdatabase sequences. For the remaining 6.1%, the similarityinfer the makeup of the bacterial comunities in the differentrumen fractions. The Cytophaga-Flexibacter-Bacteroides group(CFB, 67.5%), low G+C Gram-positive bacteria (LGCGPB,30%), and Proteobacteria (2.5%) were represented in therumen fluid clone set; LGCGPB (75.7%), CFB (10.8%),Proteobacteria (5.4%), high G+C Gram-positive bacteria(HGCGPB, 5.4%), and Spirochaetes (2.7%) were representedin the rumen solid clone set; and the CFB group (94.4%) andclone set. These findings sugest that the rumen fluid, solid,and epithelium suport diferent microbial populations thatmay play specific roles in rumen function. KCI Citation Count: 30
ISSN:1017-7825