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Screening and Optimization of Medium Composition for Mannanase Production by Aspergillus terreus SUK-1 in Solid State Fermentation Using Statistical Experimental Methods

机译:统计实验方法筛选和优化固体发酵曲霉曲霉SUK-1生产甘露聚糖酶的培养基组成

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In this study, two statistical experimental methods including Plackett Burman design and Response Surface Methodology (RSM) were employed to optimize the medium composition for mannanase production by Aspergillus terreus SUK-1, a locally isolated fungus using Palm Kernel Cake (PKC) as the sole carbon source. A total of 19 media were screened in order to determine the optimum media for mannanase production using Plackett-Burman design. Soya bean, proteose peptone, urea and NH_4NO_3 were identified as the supplement to give positive effect on mannanase production by A. terreus SUK-1. Proteose peptone was more significant in terms of its effect on mannanase production compared to urea. The optimum of the medium composition was predicted when the concentrations of proteose peptone and urea were set at 0.5 and 1% (g g~(-1)), respectively. The optimum mannanase activity was closed to the predicted value 30.24±1.32-32.60 IU g~(-1) when the optimum medium composition was employed. Under the optimized medium (0.5% (g g~(-1)) of proteose peptone and 1% (g g~(-1)) of urea), Mannanase production was 3-fold higher than the activity obtained under original medium (9.97±1.34 IU g~(-1)).
机译:在这项研究中,采用了两种统计实验方法,包括Plackett Burman设计和响应表面方法学(RSM),以优化由曲霉曲霉SUK-1生产甘露聚糖酶的培养基组成,曲霉菌SUK-1是使用棕榈仁饼(PKC)作为唯一的本地分离真菌。碳源。总共筛选了19种培养基,以确定使用Plackett-Burman设计生产甘露聚糖酶的最佳培养基。大豆,蛋白p,尿素和NH_4NO_3被确定为对土壤曲霉SUK-1产生甘露聚糖酶产生积极作用的补充剂。与尿素相比,蛋白ept对甘露聚糖酶生产的影响更为显着。当蛋白p和尿素的浓度分别设定为0.5和1%(g g〜(-1))时,可以预测培养基的最佳组成。当使用最佳培养基组成时,最佳甘露聚糖酶活性接近于预测值30.24±1.32-32.60 IU g〜(-1)。在优化的培养基(0.5%(gg〜(-1))的蛋白p和1%(gg〜(-1))的尿素)下,甘露聚糖酶的产量是原始培养基(9.97±)的三倍。 1.34 IU g〜(-1))。

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