Activities and Partial Purification of Extracellular Proteases of Bacteroides nodosus from Virulent and Benign Footrot

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Abstract
In an attempt to differentiate virulent and benign strains of B. nodosus, the extracellular proteolytic activity of these cultures was assayed with elastin, casein and hide powder azure, and the stability to heating at 55.degree. C was determined. Broth cultures of both strains hydrolyzed 125I-labeled elastin, indicating that this activity is not a unique marker of virulence. When cultures were grown in Trypticase-arginine-serine broth medium modified by omitting Na2CO3 and thioglycollic acid, the total proteolytic activity and its stability at 55.degree. C could be used to differentiate isolates causing virulent or benign footrot lesions. When other broth cultures were used, these parameters could no longer be used to make such a distinction. The proteases of a virulent and benign strain of B. nodosus were partially purified and characterized. Four to 5 closely related proteases were detected by polyacrylamide gel electrophoresis by pH 8.8 in both types of isolates. The proteases are serine-type enzymes requiring a divalent metal ion such as Ca for activity. The proteases of the benign strain were somewhat less stable to heat than the enzymes of the virulent strain. Differences in the relative mobilities of the proteases of virulent and benign strains of B. nodosus, on electrophoresis at pH 8.8, suggest that this property may be used to distinguish virulent and benign strains.