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首页> 外文期刊>Journal of molecular catalysis, B. Enzymatic >Removal of lactose in crude galacto-oligosaccharides by beta-galactosidase from Kluyveromyces lactis
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Removal of lactose in crude galacto-oligosaccharides by beta-galactosidase from Kluyveromyces lactis

机译:β-半乳糖苷酶从乳酸克鲁维酵母中去除半乳糖低聚糖中的乳糖

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摘要

In order to remove the residual lactose in crude galacto-oligosaccharides (GOS), different commercial soluble beta-galactosidases from Kluyveromyces lactis (Lactozym Pure 6500L, Maxilact L2000, Lactase NL and Biolactasa-NL) and reaction conditions (temperature, total carbohydrate concentration and enzyme:substrate mass ratio) were evaluated. To select the best biocatalyst, the hydrolytic activity on o-NPG and thermal stability of all enzymes were evaluated in the absence and presence of three cations (Co2+, Mg2+, Mn2+) at different concentrations. The enzyme source, cation and cation concentration were selected to obtain the highest hydrolytic activity and thermal stability. Then lactose hydrolysis of raw GOS was assessed varying the temperature (30 degrees C-45 degrees C), total carbohydrate concentration (10%-50%) and enzyme:substrate mass ratio (50 ILI g(-1)-400 IU g(-1)) and considering the lactose percentage decrease as response parameter (D-L). Lactase NL was selected as the best enzyme, with a hydrolytic activity of 286 IU mg(-1) and a half-life of 9 h at 35 degrees C in the presence of 1 mM Mn2+. The best reaction conditions for lactose hydrolysis employing the selected enzyme were 35 degrees C, 50% initial carbohydrate concentration and 135 IU g(-1). At such conditions of lactose hydrolysis, 70% reduction of lactose in raw GOS was obtained, with an increase of 48% in monosaccharides and of 30% in GOS. This pre-hydrolytic step is a key aspect for the subsequent purification of GOS by nanofiltration or selected bioconversion, in which monosaccharides can be removed efficiently producing GOS of high purity. (C) 2016 Elsevier B.V. All rights reserved.
机译:为了去除半乳糖低聚糖(GOS)中的残留乳糖,从乳酸克鲁维酵母(Lactozym Pure 6500L,Maxilact L2000,Lactase NL和Biolactasa-NL)中购买了不同的商业可溶性β-半乳糖苷酶和反应条件(温度,总碳水化合物浓度和评估酶:底物质量比)。为了选择最佳的生物催化剂,在不存在和存在三种不同浓度阳离子(Co2 +,Mg2 +,Mn2 +)的情况下,对所有酶的邻-NPG水解活性和热稳定性进行了评估。选择酶源,阳离子和阳离子浓度以获得最高的水解活性和热稳定性。然后评估温度(30摄氏度至45摄氏度),总碳水化合物浓度(10%-50%)和酶与底物质量比(50 ILI g(-1)-400 IU g( -1)),并将乳糖百分比降低作为响应参数(DL)。乳糖酶NL被选为最佳酶,水解活性为286 IU mg(-1),在1 mM Mn2 +存在下于35摄氏度的半衰期为9小时。使用所选酶进行乳糖水解的最佳反应条件是35摄氏度,初始碳水化合物浓度为50%和135 IU g(-1)。在这种乳糖水解条件下,原始GOS中的乳糖减少了70%,单糖增加了48%,GOS增加了30%。该预水解步骤是随后通过纳滤或选择的生物转化法纯化GOS的关键方面,其中可以有效去除单糖,从而生产出高纯度的GOS。 (C)2016 Elsevier B.V.保留所有权利。

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