Advanced Centre for Biochemical Engineering, Department of Biochemical Engineering, University College London, Bernard Katz Building, Gordon Street, London, WC1H 0AH, UK.
Evonik Creavis GmbH, Paul-Baumann-Straße 1, 45772, Marl, Germany.
Microb Cell Fact. 2017 Oct 10;16(1):174. doi: 10.1186/s12934-017-0788-4.
Numerous challenges remain to achieve industrially competitive space-time yields for bio-oxidations. The ability to rapidly screen bioconversion reactions for characterization and optimization is of major importance in bioprocess development and biocatalyst selection; studies at conventional lab scale are time consuming and labor intensive with low experimental throughput. The direct ω-oxyfunctionalization of aliphatic alkanes in a regio- and chemoselective manner is efficiently catalyzed by monooxygenases such as the AlkBGT enzyme complex from Pseudomonas putida under mild conditions. However, the adoption of microscale tools for these highly volatile substrates has been hindered by excessive evaporation and material incompatibility.
This study developed and validated a robust high-throughput microwell platform for whole-cell two-liquid phase bio-oxidations of highly volatile n-alkanes. Using microwell plates machined from polytetrafluoroethylene and a sealing clamp, highly reproducible results were achieved with no significant variability such as edge effects determined. A design of experiment approach using a response surface methodology was adopted to systematically characterize the system and identify non-limiting conditions for a whole cell bioconversion of dodecane. Using resting E. coli cells to control cell concentration and reducing the fill volume it is possible to operate in non-limiting conditions with respect to oxygen and glucose whilst achieving relevant total product yields (combining 1-dodecanol, dodecanal and dodecanoic acid) of up to 1.5 mmol g .
Overall, the developed microwell plate greatly improves experimental throughput, accelerating the screening procedures specifically for biocatalytic processes in non-conventional media. Its simplicity, robustness and standardization ensure high reliability of results.
要实现生物氧化的具有竞争力的时空产率,仍然存在许多挑战。快速筛选生物转化反应以进行表征和优化的能力在生物过程开发和生物催化剂选择中非常重要;在常规实验室规模上进行的研究既耗时又费力,实验通量低。在温和条件下,假单胞菌中的 AlkBGT 酶复合物等单加氧酶能够有效地催化脂肪族烷烃的快速 ω-位氧官能化,具有区域和化学选择性。然而,由于挥发性过高和材料不兼容,这些高度挥发性底物采用微尺度工具受到了阻碍。
本研究开发并验证了一种用于高度挥发性正构烷烃全细胞两相生物氧化的稳健高通量微井平台。使用聚四氟乙烯加工的微井板和密封夹,实现了高度可重复的结果,没有确定的边缘效应等显著变化。采用响应面法的实验设计方法,系统地对该系统进行了表征,并确定了正十二烷全细胞生物转化的非限制条件。使用静止大肠杆菌细胞来控制细胞浓度并减少填充体积,可以在不限制氧气和葡萄糖的条件下操作,同时实现高达 1.5mmol g -1 的相关总产物产率(结合 1-十二醇、十二醛和十二酸)。
总的来说,开发的微井板大大提高了实验通量,特别是针对非传统介质中的生物催化过程加速了筛选程序。其简单性、稳健性和标准化确保了结果的高度可靠性。