Purification and properties of extracellular carboxyl proteases of acid-tolerant bacteria, isolated from compost

Four strains of acid-tolerant and protein-using bacteria were isolated from compost. Two of them, Gram-negative strains MB8 and MB11, were identified as a new genus close to Stenotrophomonas species MB8 and Burkholderia speci es MB11, respectively. Both bacteria produced extracellular carboxyl protea ses (CP) in acid-casein-starch medium. The enzymes, termed CP MB8 and CP MB 11, purified through ion exchange and gel filtration chromatographies had m olecular weights of 61,000 (CP MB8) and 36,000 (CP MB11) as estimated by SD S-PAGE, and showed optimum activities with hemoglobin as a substrate at pH 3.5 (CP MB8) and pH 3.7 (CP MB11) at 55 degrees C. Both of the enzymes were not inhibited by pepstatin, DAN, or EPNP. These results suggest that both enzymes are members of the pepstatin-insensitive carboxyl proteinase family (EC 3.4.23.33), except for a larger molecular weight of the CP MB8 enzyme.