Hilker Iris, Wohlgemuth Roland, Alphand Véronique, Furstoss Roland
Groupe Biocatalyse et Chimie Fine, FRE CNRS 2712, Université de la Méditerranée, Faculté des Sciences de Luminy, Case 901, 163 avenue de Luminy, 13288 Marseille Cedex 9, France.
Biotechnol Bioeng. 2005 Dec 20;92(6):702-10. doi: 10.1002/bit.20636.
This study is demonstrating the scale up of asymmetric microbial Baeyer-Villiger oxidation of racemic bicyclo[3.2.0]hept-2-en-6-one (1) to the kilogram scale using a 50 L bioreactor. The process has been optimized with respect to bottlenecks identified in downscaled experiments. A high productivity was obtained combining a resin-based in situ substrate feeding and product removal methodology (in situ SFPR), a glycerol feed control, and an improved oxygenation device (using a sintered-metal sparger). As expected both regioisomeric lactones [(-)-(1S,5R)-2 and (-)-(1R,5S)-3] were obtained in nearly enantiopure form (ee > 98%) and good yield. This represents the first example of such an asymmetric Baeyer-Villiger biooxidation reaction ever operated at that scale. This novel resin-based in situ SFPR technology therefore clearly opens the way to further (industrial) upscaling of this highly valuable (asymmetric) reaction.
本研究展示了使用50 L生物反应器将外消旋双环[3.2.0]庚-2-烯-6-酮(1)的不对称微生物拜耳-维利格氧化放大至千克规模。该工艺已针对在小规模实验中确定的瓶颈进行了优化。通过结合基于树脂的原位底物进料和产物去除方法(原位SFPR)、甘油进料控制和改进的氧化装置(使用烧结金属曝气器),获得了高生产率。正如预期的那样,两种区域异构体内酯[(-)-(1S,5R)-2和(-)-(1R,5S)-3]均以几乎对映体纯的形式(ee>98%)和良好的产率得到。这代表了此类不对称拜耳-维利格生物氧化反应在该规模下运行的首个实例。因此,这种基于树脂的新型原位SFPR技术显然为进一步(工业)扩大这种极具价值的(不对称)反应规模开辟了道路。