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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:通过β-半乳糖苷酶从Kluyveromyces Lactis中除去乳糖中的乳糖

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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:为了除去粗吡酰寡糖(GOS)中的残留乳糖,来自Kluyveromyces乳酸的不同商业可溶性β-半乳糖苷酶(Lactozym纯6500L,maxileact L2000,乳糖酶N1和Biolactasa-N1)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,在不同浓度下的三个阳离子(CO 2 +,Mg2 +,MN2 +)的情况下评价O-NPG的水解活性和所有酶的热稳定性。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。然后评估原料GOS的乳糖水解,改变温度(30℃-45℃),总碳水化合物浓度(10%-50%)和酶:底物质量比(50 ILI G(-1)-400 IU G( -1))并考虑乳糖百分比减少作为响应参数(DL)。将乳糖酶NL选择为最佳酶,在1mM MN2 +存在下,在35℃下,水解活性为286 IU Mg(-1)和9小时的半衰期。使用所选酶的乳糖水解的最佳反应条件为35℃,50%初始碳水化合物浓度和135 IU G(-1)。在这种乳糖水解条件下,获得了70%的原料GOS中的乳糖减少,在单糖增加48%和GOS中的30%。该预水解步骤是通过纳米过滤或选定的生物转化的随后纯化GOS的关键方面,其中可以有效地除去高纯度的单糖。 (c)2016年Elsevier B.v.保留所有权利。

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