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Applied and Environmental Microbiology, April 2004, p. 2172-2179, Vol. 70, No. 4
0099-2240/04/$08.00+0     DOI: 10.1128/AEM.70.4.2172-2179.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Fiber-Degrading Systems of Different Strains of the Genus Fibrobacter

Christel Béra-Maillet,* Yves Ribot, and Evelyne Forano*

Unité de Microbiologie, INRA CR de Clermont-Ferrand-Theix, 63122 Saint-Genès-Champanelle, France

Received 26 September 2003/ Accepted 27 December 2003

The S85 type strain of Fibrobacter succinogenes, a major ruminal fibrolytic species, was isolated 49 years ago from a bovine rumen and has been used since then as a model for extensive studies. To assess the validity of this model, we compared the cellulase- and xylanase-degrading activities of several other F. succinogenes strains originating from different ruminants, including recently isolated strains, and looked for the presence of 10 glycoside hydrolase genes previously identified in S85. The NR9 F. intestinalis type strain, representative of the second species of the genus, was also included in this study. DNA-DNA hybridization and 16S rRNA gene sequencing first classified the strains and provided the phylogenetic positions of isolates of both species. Cellulase and xylanase activity analyses revealed similar activity profiles for all F. succinogenes strains. However, the FE strain, phylogenetically close to S85, presented a poor xylanolytic system and weak specific activities. Furthermore, the HM2 strain, genetically distant from the other F. succinogenes isolates, displayed a larger cellulolytic profile on zymograms and higher cellulolytic specific activity. F. intestinalis NR9 presented a higher cellulolytic specific activity and a stronger extracellular xylanolytic activity. Almost all glycoside hydrolase genes studied were found in the F. succinogenes isolates by PCR, except in the HM2 strain, and few of them were detected in F. intestinalis NR9. As expected, the fibrolytic genes of strains of the genus Fibrobacter as well as the cellulase and xylanase activities are better conserved in closely related phylogenetic isolates.


* Corresponding author. Mailing address: Unité de Microbiologie, INRA CR de Clermont-Ferrand-Theix, 63122 Saint-Genès-Champanelle, France. Phone: 33-473-62-42-41. Fax: 33-473-62-45-81. E-mail for C. Béra-Maillet: cmaillet{at}clermont.inra.fr; e-mail for E. Forano: forano{at}clermont.inra.fr.


Applied and Environmental Microbiology, April 2004, p. 2172-2179, Vol. 70, No. 4
0099-2240/04/$08.00+0     DOI: 10.1128/AEM.70.4.2172-2179.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




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