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Identification of Suitable Condition for Mannanase Production by Bacillus sp. GA2(1)

机译:鉴定甘露聚糖酶生产的合适条件 芽孢杆菌 GA2(1)

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Aims: The effects of 1 (w/v) supplementation of additional 5 agricultural wastes, corn cob, bagasses, coffee residues, soybean meal, and copra meal for mannanase production by Bacillus sp.GA2(1) were studied. Hence, partial characterization of mannanase was determined. Methodology: The 1(v/v) overnight cultured of Bacillus sp. GA2(1) was transferred into the basal medium and shaken at 150 rpm for 18 h at 37ºC. The additional of 5 AWs, corn cob, bagasses, coffee residues, soybean meal, and copra meal for the mannanase production were investigated. The cell suspension was centrifuged, and the crude mannanases were collected and stored at – 20ºC for enzyme assay. The mannanase activities were measured by the dinitrosalicylic acid method. The optimal pH of mannanase were studied by measuring enzyme activity at pH 3-10 using 50 mM of following buffers; citrate (pH 3.0-6.0), phosphate (pH 6.0-8.0), and glycine-NaOH (pH 8.0-10.0). The optimal temperature was measured at 30-80ºC. Under standard assay conditions, locust bean gum was used as substrate to determine the optimal pH and temperature of the reaction. Thermostability was determined by preincubating the enzyme at different temperatures (30-80ºC) for 1 h. The residual mannanase activities were measured under standard condition. Results: Among bagasses, coffee residues, soybean meal, corn cob and copra meal, the coffee residues was the most effective carbon source, the maximum yield of mannanase activity was 0.26 U/ml. The optimal temperature and pH for mannanase activity was pH 6.0 and 50ºC of 0.44 and 0.35 U/ml, respectively. The stability of enzyme was determined at 30-80ºC for 60 min. The results revealed that mannanase retained more than 96 of remaining activity after incubation of 60 min at 50ºC. Conclusion: The maximum mannanase production was found when the medium was supplemented with coffee residues. Crude mannanase showed the highest activities of 0.44 U/ml at pH 6.0 and of 0.35 U/ml at 50ºC. The mannanase from Bacillus sp. GA2(1) retained more than 90 of theirs activities at 30-60ºC after preincubated for 60 min and then rapidly decreased.
机译:目的:额外 5 种农业废弃物、玉米芯、甘蔗渣、咖啡残渣、豆粕和椰干粕的 1% (w/v) 补充对芽孢杆菌生产甘露聚糖酶的影响。研究了GA2(1)。因此,确定了甘露聚糖酶的部分表征。方法:将 1%(v/v) 过夜培养的芽孢杆菌 GA2(1) 转移到基础培养基中,并在 37ºC 下以 150 rpm 振荡 18 小时。研究了用于甘露聚糖酶生产的 5 个 AW、玉米芯、甘蔗渣、咖啡残渣、豆粕和椰干粕。离心细胞悬液,收集粗甘露聚糖并储存在-20ºC进行酶测定。甘露聚糖酶活性采用二亚硝基水杨酸法测定。使用50 mM以下缓冲液测量pH值为3-10的酶活性,研究甘露聚糖酶的最佳pH值;柠檬酸盐(pH 3.0-6.0)、磷酸盐(pH 6.0-8.0)和甘氨酸-NaOH(pH 8.0-10.0)。最佳温度在30-80ºC时测量。在标准测定条件下,使用刺槐豆胶作为底物来确定反应的最佳pH值和温度。通过将酶在不同温度(30-80ºC)下预孵育1小时来测定热稳定性。在标准条件下测量残留甘露聚糖酶活性。结果:甘蔗渣、咖啡渣、豆粕、玉米芯和椰干粕中,咖啡渣是最有效的碳源,甘露聚糖酶活性最高产率为0.26 U/ml。甘露聚糖酶活性的最佳温度和pH值分别为pH 6.0和50ºC,分别为0.44和0.35 U/ml。在30-80ºC下测定酶的稳定性60分钟。结果显示,甘露聚糖酶在50ºC下孵育60 min后保留了96%以上的剩余活性。 结论:当培养基中补充咖啡残留物时,甘露聚糖酶的产量最大。粗甘露聚糖酶在pH 6.0和50ºC时分别为0.44 U/ml和0.35 U/ml。来自芽孢杆菌GA2(1)的甘露聚糖酶在预孵育60分钟后在30-60ºC下保留了90%以上的活性,然后迅速降低。

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