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基于水凝胶的3D打印酶反应器的优势及其在生物催化中的局限性

Advantages of Hydrogel-Based 3D-Printed Enzyme Reactors and Their Limitations for Biocatalysis.

作者信息

Schmieg Barbara, Döbber Johannes, Kirschhöfer Frank, Pohl Martina, Franzreb Matthias

机构信息

Karlsruhe Institute of Technology, Institute of Functional Interfaces, Karlsruhe, Germany.

Forschungszentrum Jülich GmbH, IBG-1: Biotechnology, Jülich, Germany.

出版信息

Front Bioeng Biotechnol. 2019 Jan 14;6:211. doi: 10.3389/fbioe.2018.00211. eCollection 2018.

Abstract

The development of process steps catalyzed by immobilized enzymes usually encompasses the screening of enzyme variants, as well as the optimization of immobilization protocols and process parameters. Direct immobilization of biocatalysts by physical entrapment into hydrogels can be applied to reduce the effort required for immobilization, as the enzyme-specific optimization of the immobilization procedure is omitted. Physical entrapment is applicable for purified enzymes as well as crude cell extracts. Therefore, it can be used to quickly assess and compare activities of immobilized enzymes. For the application in flow reactors, we developed 3D-printed hydrogel lattices for enzyme entrapment as well as matching housings, also manufactured by 3D-printing. Testing the resulting enzyme reactors for three different enzymes, namely alcohol dehydrogenase from , benzoylformate decarboxylase from and β-galactosidase from , and four different enzymatic reactions showed the broad applicability of the approach but also its limitations. The activity of the immobilized biocatalysts was measured in batch experiments and compared to the kinetics of the respective free enzymes in solution. This comparison yields an effectiveness factor, which is a key figure to describe the extent the immobilized catalyst is effectively utilized. For the examined systems the effectiveness factor ranged between 6 and 14% and decreased with increasing absolute activity of the entrapped enzymes due to mass transfer limitations. To test the suitability of the hydrogel lattices for continuous operation, they were inserted into 3D-printed reactor housings and operated at constant flow. Stable product formation could be monitored over a period of 72 h for all four enzymatic systems, including two reactions with redox cofactor regeneration. Comparing calculated and experimental conversion in the continuous setup, higher values of the effectiveness factor in batch experiments also hint at good performance in continuous flow. This can be used to optimize complex biocatalytic reactions on a small scale.

摘要

由固定化酶催化的工艺步骤的开发通常包括酶变体的筛选,以及固定化方案和工艺参数的优化。通过物理包埋将生物催化剂直接固定在水凝胶中,可减少固定所需的工作量,因为省略了固定程序的酶特异性优化。物理包埋适用于纯化的酶以及粗细胞提取物。因此,它可用于快速评估和比较固定化酶的活性。为了应用于流动反应器,我们开发了用于酶包埋的3D打印水凝胶晶格以及同样通过3D打印制造的匹配外壳。对三种不同的酶,即来自[具体来源1]的乙醇脱氢酶、来自[具体来源2]的苯甲酰甲酸脱羧酶和来自[具体来源3]的β-半乳糖苷酶,以及四种不同的酶促反应所得到的酶反应器进行测试,结果表明该方法具有广泛的适用性,但也有其局限性。在分批实验中测量了固定化生物催化剂的活性,并与溶液中相应游离酶的动力学进行了比较。这种比较得出一个有效因子,它是描述固定化催化剂有效利用程度的关键指标。对于所研究的系统,有效因子在6%至14%之间,并且由于传质限制,随着包埋酶的绝对活性增加而降低。为了测试水凝胶晶格用于连续操作的适用性,将它们插入3D打印的反应器外壳中并在恒定流量下运行。对于所有四种酶促系统,包括两个涉及氧化还原辅因子再生的反应,都可以在72小时内监测到稳定的产物形成。在连续装置中比较计算转化率和实验转化率,分批实验中较高的有效因子值也表明在连续流动中具有良好的性能。这可用于在小规模上优化复杂的生物催化反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c632/6339869/ab68afe69574/fbioe-06-00211-g0001.jpg

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