Jussen Daniel, Soltner Helmut, Stute Birgit, Wiechert Wolfgang, von Lieres Eric, Pohl Martina
IBG-1: Biotechnology, Forschungszentrum Jülich GmbH, D-52425 Jülich, Germany.
ZEA-1: Engineering and Technology, Forschungszentrum Jülich GmbH, D-52425 Jülich, Germany.
J Biotechnol. 2016 Aug 10;231:174-182. doi: 10.1016/j.jbiotec.2016.06.006. Epub 2016 Jun 8.
Enzymatic parameter determination is an essential step in biocatalytic process development. Therefore higher throughput in miniaturized devices is urgently needed. An ideal microfluidic device should combine easy immobilization and retention of a minimal amount of biocatalyst with a well-mixed reaction volume. Together, all criteria are hardly met by current tools. Here we describe a microfluidic reactor (μMORE) which employs magnetic particles for both enzyme immobilization and efficient mixing using two permanent magnets placed in rotating cylinders next to the a glass chip reactor. The chip geometry and agitation speed was optimized by investigation of the mixing and retention characteristics using simulation and dye distribution analysis. Subsequently, the μMORE was successfully applied to determine critical biocatalytic process parameters in a parallelized manner for the carboligation of benzaldehyde and acetaldehyde to (S)-2-hydroxy-1-phenylpropan-1-one with less than 5μg of benzoylformate decarboxylase from Pseudomonas putida immobilized on magnetic beads. Here, one run of the device in six parallelized glass reactors took only 2-3h for an immobilized enzyme with very low activity (∼2U/mg). The optimized parameter set was finally tested in a 10mL enzyme membrane reactor, demonstrating that the μMORE provides a solid data base for biocatalytic process optimization.
酶参数测定是生物催化工艺开发中的关键步骤。因此,迫切需要在小型化设备中实现更高的通量。理想的微流控设备应将生物催化剂的简便固定和最少用量的保留与充分混合的反应体积相结合。然而,目前的工具很难同时满足所有这些标准。在此,我们描述了一种微流控反应器(μMORE),它利用磁性颗粒进行酶固定,并通过置于玻璃芯片反应器旁旋转圆柱体内的两块永磁体实现高效混合。通过使用模拟和染料分布分析研究混合和保留特性,对芯片几何形状和搅拌速度进行了优化。随后,μMORE成功地用于以并行方式确定关键的生物催化工艺参数,即恶臭假单胞菌的苯甲酰甲酸脱羧酶固定在磁珠上,用量少于5μg,用于将苯甲醛和乙醛碳连接生成(S)-2-羟基-1-苯基丙-1-酮。在此,该设备在六个并行玻璃反应器中运行一次,对于活性极低(约2U/mg)的固定化酶仅需2-3小时。最终在10mL酶膜反应器中对优化后的参数集进行了测试,结果表明μMORE为生物催化工艺优化提供了坚实的数据基础。