首页> 外文期刊>Food and bioprocess technology >Formulation of culture medium with agroindustrial waste for beta-galactosidase production from Kluyveromyces marxianus ATCC 16045.
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Formulation of culture medium with agroindustrial waste for beta-galactosidase production from Kluyveromyces marxianus ATCC 16045.

机译:用农用工业废料配制用于从马克斯克鲁维酵母ATCC 16045生产β-半乳糖苷酶的培养基。

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Seven strains of the genus Kluyveromyces were screened for beta-galactosidase activity and Kluyveromyces marxianus ATCC 16045 was selected as the best enzyme producer for culture medium optimization. The production of beta-galactosidase by submerged cultivation was evaluated using a factorial design and response surface methodology. The culture medium containing whey and parboiled rice effluent was formulated to maximize the production of beta-galactosidase. The effects of the initial pH and the concentrations of whey lactose, peptone, (NH4)2SO4, yeast extract, and parboiled rice effluent on enzyme production were studied using a 2IV6-2 fractional design. A CCRD (24 trials plus axial and central points) was used for the four variables selected from the fractional design (lactose, peptone, (NH4)2SO4 and yeast extract), with beta-galactosidase activity as the response. The optimum conditions established for production were a whey (lactose) concentration of 120 g/L, a yeast extract concentration of 5 g/L, a peptone concentration of 15 g/L, a (NH4)2SO4 concentration of 15 g/L, a parboiled rice effluent concentration of 30 g/L, and a pH value of 4.0. Under these conditions, the highest enzymatic activity of 10.4 U/mL was measured, being 9.5-9.7 as the values predicted by the proposed model, showing an enzymatic activity increase of 30% using alternative sources of lactose and nitrogen for beta-galactosidase production
机译:筛选了7种克鲁维酵母属菌株的β-半乳糖苷酶活性,并选择了马尔克斯克鲁维酵母ATCC 16045作为培养基优化的最佳酶产生剂。使用析因设计和响应面方法评估了淹没培养产生的β-半乳糖苷酶的产量。配制含有乳清和半熟大米废水的培养基,以最大程度地生产β-半乳糖苷酶。初始pH和乳清乳糖,蛋白ept,(NH 4 2 SO 4 ,酵母提取物和半熟米的浓度的影响使用2 IV 6-2 分级设计研究了废水中酶的产生。 CCRD(24个试验加上轴向和中心点)用于从分数设计中选择的四个变量(乳糖,蛋白ept,(NH 4 2 SO 4 和酵母提取物),以β-半乳糖苷酶活性为响应。建立的最佳生产条件是乳清(乳糖)浓度为120 g / L,酵母提取物浓度为5 g / L,蛋白ept浓度为15 g / L,(NH 4 2 SO 4 浓度为15 g / L,半熟米出水浓度为30 g / L,pH值为4.0。在这些条件下,测得的最高酶促活性为10.4 U / mL,为拟议模型预测的值是9.5-9.7,表明使用乳糖和氮的替代来源生产β-半乳糖苷酶的酶促活性增加了30%

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