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使用同轴静电纺丝中空纳米纤维实现多酶生物催化:人工细胞的重新设计

Enabling multi-enzyme biocatalysis using coaxial-electrospun hollow nanofibers: redesign of artificial cells.

作者信息

Ji Xiaoyuan, Wang Ping, Su Zhiguo, Ma Guanghui, Zhang Songping

机构信息

National Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China.

出版信息

J Mater Chem B. 2014 Jan 14;2(2):181-190. doi: 10.1039/c3tb21232g. Epub 2013 Nov 20.

Abstract

Highly efficient immobilization of multi-enzyme systems involving cofactor regeneration represents one of the greatest challenges in bioprocessing. Particulate artificial cells with enzymes and cofactors encapsulated within microcapsules have long been the major type of multi-enzyme biocatalysts. In the present work, a novel hollow nanofiber-based artificial cell that performs multi-step reactions involving efficient coenzyme regeneration was fabricated in situ by a facile co-axial electrospinning process. To that end, a mixture of glycerol and water containing the dissolved multi-enzyme system for the bile acid assay, which included 3α-hydroxysteroid dehydrogenase (3α-HSD), diaphorase (DP) and NADH was fed as the core phase solution, and a N,N-dimethylacetylamide solution of 30 wt% polyurethane was fed as the shell phase solution during the co-axial electrospinning. The relationship between the structures of the hollow nanofibers and the activity and stability of the encapsulated enzymes was studied. At core and shell phase electrospinning solution flow rates of 0.07 and 0.5 mL h, activity recoveries as high as 76% and 82% were obtained for the encapsulated 3α-HSD and DP. The hollow nanofiber-based artificial cells were successfully used for the bile acid assay, yielding good linearity for bile acid concentrations ranging from 0-200 μM. Compared with the solution-based multi-enzyme system, the hollow nanofiber-based multi-enzyme system presented a lumped activity recovery of 75%. In addition, the hollow nanofiber provided the multi-enzyme system confined inside the nano-domain of the hollow fibers with a unique stabilizing mechanism, such that more than a 170-fold increase in half-life at 25 °C was obtained for the encapsulated 3α-HSD and DP. This study is expected to greatly promote and broaden the application of multi-enzyme systems in industry, biosensor, biomedical, and many other related research fields.

摘要

涉及辅因子再生的多酶系统的高效固定化是生物加工中最大的挑战之一。酶和辅因子封装在微胶囊内的颗粒状人工细胞长期以来一直是多酶生物催化剂的主要类型。在本工作中,通过简便的同轴静电纺丝工艺原位制备了一种新型的基于中空纳米纤维的人工细胞,该细胞能进行涉及高效辅酶再生的多步反应。为此,将含有用于胆汁酸测定的溶解多酶系统(包括3α-羟基类固醇脱氢酶(3α-HSD)、黄递酶(DP)和NADH)的甘油和水的混合物作为核相溶液进料,在同轴静电纺丝过程中,将30 wt%聚氨酯的N,N-二甲基乙酰胺溶液作为壳相溶液进料。研究了中空纳米纤维的结构与封装酶的活性和稳定性之间的关系。在核相和壳相静电纺丝溶液流速分别为0.07和0.5 mL/h时,封装的3α-HSD和DP的活性回收率分别高达76%和82%。基于中空纳米纤维的人工细胞成功用于胆汁酸测定,对于0-200 μM的胆汁酸浓度具有良好的线性关系。与基于溶液的多酶系统相比,基于中空纳米纤维的多酶系统的总活性回收率为75%。此外,中空纳米纤维为限制在中空纤维纳米域内的多酶系统提供了独特的稳定机制,使得封装的3α-HSD和DP在25°C下的半衰期增加了170多倍。预计这项研究将极大地促进和拓宽多酶系统在工业、生物传感器、生物医学及许多其他相关研究领域的应用。

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