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Isolation and screening of alkaline protease producing bacteria and physio-chemical characterization of the enzyme

机译:产生碱性蛋白酶的细菌的分离和筛选以及酶的理化特性

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Soil samples from different habitats including tanneries, soap industries, garden soil and soil compost were screened for the presence of alkalophilic?Bacillus?isolates capable of producing alkaline protease in large quantities. One hundred and eighteen?(118)?isolates were found having proteolytic activity on skim milk agar plates. Isolates forming larger zones, as a result of casein hydrolysis were further studied for quantitative production of extracellular alkaline protease activity in the shake flask studies. Isolate CEMB10370 gave maximum activity. Time course studies indicated that strain CEMB10370 had?the?highest protease activity (380 APU/mL) after 48 h of fermentation. The wild type enzyme was biochemically characterized. The enzyme exhibits optimal activity at 50°C and?pH 11.5. Theprotease?enzyme was completely inhibited by phenylmethylsulfonyl (PMSF, serine protease inhibitor) and its isoelectric point was ~9.5. The enzyme was purified by ion-exchange chromatography using CM-Sepharose column as a ~29 Kilo Dalton (kDa) protein.
机译:筛选了包括制革厂,制皂业,花园土壤和土壤堆肥在内的不同生境的土壤样品中是否存在能够大量产生碱性蛋白酶的嗜碱杆菌芽孢杆菌。发现有一百一十八个(118)?分离物在脱脂乳琼脂平板上具有蛋白水解活性。作为酪蛋白水解的结果,形成更大区域的分离物在摇瓶研究中被进一步研究以定量产生胞外碱性蛋白酶活性。分离物CEMB10370具有最大的活性。时程研究表明,CEMB10370菌株在发酵48小时后具有最高的蛋白酶活性(380 APU / mL)。对野生型酶进行了生化表征。该酶在50℃和pH 11.5下表现出最佳活性。蛋白酶被苯甲基磺酰基(PMSF,丝氨酸蛋白酶抑制剂)完全抑制,其等电点约为9.5。使用CM-琼脂糖柱作为〜29 Kilo Dalton(kDa)蛋白,通过离子交换色谱纯化该酶。

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