Method of protecting an animal skin product from metalloproteinase activity
a technology of metalloproteinase activity and animal skin, applied in the field of leather processing, can solve the problems of deterioration of fresh hides and skins, economic loss, deterioration of essential components of skins and hides,
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examples 1 and 2
[0037] Collagenase activity evaluation: Inhibition of collagenase from pure cultures of bacteria by disodium EDTA, trisodium EDTA, tetrasodium EDTA, tetrasodium EGTA and trisodium EDDS.
Method
[0038] Nutrient agar amended with Azocoll (a substrate made up of insoluble particles of collagen impregnated with a bright azo dye) was used as the test medium to study collagenase activity. The nutrient agar was prepared and autoclaved and then was cooled to 55° C. Azocol was added to give a final concentration of 0.5%. The inhibitors were added to petri dishes, and the nutrient agar-azocoll medium was added and carefully mixed to give the desired concentration of the inhibitor. Using a sterile spatula or cork-borer, the middle portion of each plate of about the size of a United States quarter, was scooped out. Fresh nutrient agar-azocoll medium containing no inhibitor was added to replace the scooped out portion of the plate. Two collagenase positive bacteria, Pseudomonas fluorescens (Exam...
example 3
[0042] Inhibition of collagenase from mixed bacteria growing on fresh hides by disodium EDTA, trisodium EDTA, tetrasodium EDTA, and tetrasodium EGTA.
Method
[0043] Nutrient agar amended with 0.5% AZOCOLL was used as the test medium to study collagenase activity. The nutrient agar was prepared and autoclaved and then was cooled to 55° C. Azocol was added to give a final concentration of 0.5%. The inhibitors were added to petri dishes, and the nutrient agar-azocoll medium was added and carefully mixed to give the desired concentrations of the inhibitor. Fresh hides were obtained from a tannery and were cut into pieces of approximately 2 cm square. One 2×2 cm hide sample was placed on top of the agar containing the inhibitors. Treated samples were incubated at 30° C. and evaluated after 24 hours, 2 days, 3 or 4 days and 7 days for collagenase activity and also for the growth of the bacteria. The bacteria from the hides secreted collagenase into the medium as they grew to degrade the c...
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