首页> 外文期刊>Journal of Agricultural and Food Chemistry >Improvement of Chitosan Derivatization for the Immobilization of Bacillus circulons β-Galactosidase and Its Further Application in Galacto-oligosaccharide Synthesis
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Improvement of Chitosan Derivatization for the Immobilization of Bacillus circulons β-Galactosidase and Its Further Application in Galacto-oligosaccharide Synthesis

机译:壳聚糖环化酶β-半乳糖苷酶固定化壳聚糖衍生化反应的改进及其在低聚半乳糖合成中的应用

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Chitosan was derivatized by two methodologies to design a robust biocatalyst of immobilized Bacillus circuhns β-galactosidase from a low-cost support for its further application in the synthesis of galacto-oligosaccharides (GOS). In the first one, chitosan was derivatized by cross-linking with glutaraldehyde and activated with epichlorohydrin; in the second one, cross-linking and activation were done with epichlorohydrin in a two-step process, favoring first support cross-linking and then support functionalization (C-EPI-EPI). Epoxy groups were hydrolyzed and oxidized, obtaining two supports activated with different aldehyde concentrations (100—250 μmol/g). The expressed activity and stability of the immobilized biocatalysts varied according to the derivatization methodology, showing that both the cross-linking agent and the activation degree are key parameters in the final biocatalyst performance. The best compromise between expressed activity and thermal stability was obtained using C-EPI-EPI with 200μmol of aldehyde groups per gram of support. The immobilization conditions were optimized, obtaining a biocatalyst with 280 IU/g, immobilization yields in terms of activity and protein of 17.3 ± 0.4 and 61.5 ± 3.9%, respectively, and a high thermal stability, with a half-life of 449 times the value of the soluble enzyme. The biocatalyst was applied to the synthesis of GOS in repeated batch operation without affecting the product composition. Four successive batches were required for obtaining a cumulative specific productivity higher than the one obtained with the soluble enzyme.
机译:壳聚糖通过两种方法衍生化,从低成本的支持体设计出一种牢固的固定化芽孢杆菌β-半乳糖苷酶生物催化剂,以进一步应用其合成半乳糖-低聚糖(GOS)。在第一个中,壳聚糖通过与戊二醛交联而衍生化,并被表氯醇活化。在第二个步骤中,表氯醇的交联和活化过程分两步进行,首先需要支持交联然后支持功能化(C-EPI-EPI)。水解和氧化环氧基,得到两种被不同醛浓度(100-250μmol/ g)活化的载体。固定化生物催化剂的表达活性和稳定性根据衍生化方法的不同而变化,表明交联剂和活化度都是最终生物催化剂性能的关键参数。使用C-EPI-EPI,每克支持物具有200μmol醛基,可以在表达活性和热稳定性之间取得最佳折衷。对固定化条件进行了优化,获得了一种生物催化剂,其载量为280 IU / g,活性和蛋白质的固定化产率分别为17.3±0.4和61.5±3.9%,并且具有高的热稳定性,半衰期为449倍。可溶性酶的价值。在不影响产物组成的情况下,将生物催化剂以重复的间歇操作方式应用于GOS的合成。需要四个连续的批次来获得比可溶酶获得的累积比生产率更高的累积比生产率。

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