Streptomyces strain 3B constitutively secreted collagenolytic enzymes during the post-exponential growth phase. Purification is described here leading to two collagenases (I and II) with specific activity of 3350 and 3600 U/mg, respectively, the highest activity obtained as yet for any streptomycete collagenase. Analysis of the purified enzymes by the method of zymography revealed that both I and II were homogeneous, with molar mass 116 and 97 kDa, respectively. Both collagenases were identical in their pH (7.5) and temperature optimum (37 degrees C). The inhibition profile of the enzymes by EDTA and 1,10-phenanthroline confirmed these enzymes to be metalloproteinases. By testing the activity with insoluble collagen, acid soluble collagen, gelatin, casein, elastin and Pz-PLGPR it was established that I and II are very specific for insoluble collagen and gelatin, showing a high activity toward acid soluble collagen and Pz-PLGPR. However, collagenases I and II failed to hydrolyze casein and elastin; they belong to true collagenases and resemble the clostridial enzymes.

• MeSH
• Collagenases chemistry   isolation & purification   MeSH
• Hydrogen-Ion Concentration MeSH
• Streptomyces enzymology   MeSH
• Substrate Specificity MeSH
• Temperature MeSH
• Publication type
• Journal Article MeSH
• Names of Substances
• Collagenases MeSH

A total of 437 bacterial cultures was isolated from various soils and sewage water that were tested for the ability to decompose reconstituted collagen. This activity was found in 6.6% of the cultures isolated from sewage water, 15% of the cultures from organic horizons of the spruce growth soil, 30% of the cultures from the meadow soil, 29% of the cultures from the vegetable field soil and in 37% of those isolated from garden soil. The capability to produce collagenolytic enzymes does not appear to be rare among soil bacteria.

• MeSH
• Bacteria metabolism   MeSH
• Collagen metabolism   MeSH
• Cells, Cultured MeSH
• Soil Microbiology * MeSH
• Publication type
• Journal Article MeSH
• Names of Substances
• Collagen MeSH