Protease Production by Submerged Fermentation in Shake Flasks Using Bacillus sp. Isolated from the Soil

J. Okpalla, D. A. Onyekuru, I. E. Duru, T. O. Mba
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Abstract

Proteases are one of the most industrially important enzymes, which account for about 60% of total enzyme market. Protease production by submerged fermentation in shake flasks using Bacillus sp. isolated from the soil was studied. Soil samples were collected from different locations within Chukwuemeka Odumegwu Ojukwu University, Uli, Anambra state. The soil samples were serially diluted and inoculated on sterilized skim milk agar plates. The plates were incubated at 30oC for 72 h. A clear zone around the colonies gave an indication of protease-producing bacteria isolates.   The selected protease producers were subsequently used for shake flask fermentation in 50 ml sterile medium. Optimization study was conducted to determine the effect of carbon sources, nitrogen sources, trace elements, agitation rates and pH.  Twenty one bacteria isolates were found to be active protease producers and isolates RS-5 and OS-9 had the highest zone of clearance of 13.5 and 12.1 mm respectively. The result of submerged production of protease by the  bacteria isolates  revealed that the isolates RS-5 and OS-9 accumulated maximum protease yield of 3.23 and 2.71 U/ml respectively. The isolates were Gram positive and endospore formers, and were identified as Bacillus sp. RS-5 and OS-9.The addition of Starch and maltose stimulated optimum protease production of 3.47 and 2.77 U/ml by Bacillus sp. RS-5 and OS-9 respectively. Beef extract enhanced maximum enzyme yield of 3.35 and 2.90 U/ml for Bacillus sp. RS-5 and OS-9 respectively. Maximum protease yield of 3.28 U/ml for Bacillus sp. RS-5 and 2.85 U/ml for Bacillus sp. OS-9 was obtained by the supplementation of 0.4 g/l of FeS04 respectively. The maximum protease yield was observed at agitation rate of 200 rpm for Bacillus sp. RS-5 and 170 rpm for Bacillus sp. OS-9. At pH8, protease accumulation was highest for Bacillus sp. RS-5 and OS-9. The study revealed that the soil harbours some protease-producing bacteria strains and protease production can be greatly enhanced through optimization of process parameters.
利用土壤分离芽孢杆菌在摇瓶中深层发酵生产蛋白酶
蛋白酶是工业上最重要的酶之一,约占总酶市场的60%。研究了从土壤中分离的芽孢杆菌在摇瓶中深层发酵生产蛋白酶的方法。土壤样本采集于阿南布拉州乌里的楚克乌梅卡Odumegwu Ojukwu大学的不同地点。将土壤样品依次稀释,接种于无菌脱脂牛奶琼脂板上。培养皿在30℃下孵育72小时。菌落周围有一个清晰的区域,表明有蛋白酶产生菌分离。选定的蛋白酶产生菌随后在50 ml无菌培养基中进行摇瓶发酵。对碳源、氮源、微量元素、搅拌速率和ph的影响进行了优化研究。21株分离菌为活性蛋白酶产生菌,其中分离菌RS-5和OS-9的清除区最高,分别为13.5和12.1 mm。菌株RS-5和OS-9的最大蛋白酶产率分别为3.23和2.71 U/ml。分离菌株为革兰氏阳性和内孢子形成菌,鉴定为芽孢杆菌RS-5和OS-9。淀粉和麦芽糖的添加使芽孢杆菌RS-5和OS-9的最佳蛋白酶产量分别为3.47和2.77 U/ml。牛肉提取物对芽孢杆菌RS-5和OS-9的最大产酶率分别提高了3.35和2.90 U/ml。添加0.4 g/l FeS04后,芽孢杆菌RS-5和芽孢杆菌OS-9的最大蛋白酶产量分别为3.28 U/ml和2.85 U/ml。在搅拌速率为200 rpm和170 rpm时,芽孢杆菌RS-5和OS-9的蛋白酶产量最高。ph为8时,芽孢杆菌RS-5和OS-9的蛋白酶积累量最高。研究表明,土壤中存在一些产生蛋白酶的菌株,通过优化工艺参数可以大大提高蛋白酶的产量。
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