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Guggenheimella bovis gen. nov., sp. nov., isolated from lesions of bovine dermatitis digitalis, by C. Wyss, F. E. Dewhirst, B. J. Paster, T. Thurnheer and A. Luginbühl

International Journal of Systematic and Evolutionary Microbiology vol. 55, part 2, pp. 667 - 671

Supplementary Table A. API ZYM activities of bovine DD isolates and reference strains.

Supplementary Table B. Cellular fatty acids of bovine isolates and Tindallia magadiensis DSM 10318^T.

[PDF file of Tables A and B] (19 KB)

Supplementary Fig. A. Transmission electron micrograph of cells of strain OMZ 913^T. Bacteria were fixed in cacodylate buffer with 2.5 % glutaraldehyde and 1 % OsO₄ and stained with 1 % uranyl acetate; Epon sections were contrasted with lead citrate. Bar, 200 nm.

Supplementary Fig. B. SDS-PAGE of cellular extracts of novel dermatitis digitalis isolates and representative phylogenetic relatives blotted onto nitrocellulose and stained for protein by the reversible copper phthalocyanine tetrasulphonic acid method (CPTS; Bickar & Reid, 1992). Lanes: 1, OMZ 915; 2, OMZ 913^T; 3, DSM 10318^T; 4, ATCC 49989^T; 5, ATCC 35585^T; 6, D6B.23; 7, ATCC 33099^T. The position of molecular mass markers is indicated on the margin in kDa.

Reference

Bickar, D. & Reid, P. D. (1992). A high-affinity protein stain for Western blots, tissue prints, and electrophoretic gels. Anal Biochem 203, 109-115.

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