Nouani, A.Belhamiche, N.Slimani, R.Fazouane, F.Belbraouet, S.Bellal, M.2015-04-142015-04-142009https://dspace.univ-boumerdes.dz/jspui/handle/123456789/357Extracellular protease from Mucor pusillus was purified 18-fold with 7.56% recovery by ion-exchange chromatography and gel filtration. The enzyme was found to be monomeric in nature, having a molecular mass of 49 kDa. The enzyme acted optimally at 50°C and was stable in the temperature range 30–50°C. It was completely inactivated by heating for 30 min at 65°C. The optimum of activity for the purified extract was observed at milk CaCl2 concentration of 0.02 m and at milk pH of 5. These properties, except for temperature, were similar to those of rennetenRennetMucor pusillusMilk-clotting activityPurificationArticle