Davis P J, Rizzo J D
Appl Environ Microbiol. 1982 Apr;43(4):884-90. doi: 10.1128/aem.43.4.884-890.1982.
The microbiological metabolism of warfarin was examined as a model of metabolism in higher organisms, including humans, and to determine the chirality of microbial reductases for application in organic synthesis. Nineteen cultures were examined based on their reported abilities to reduce ketonic substrates, and several were shown to catalyze the desired reaction. Nocardia corallina (ATCC 19070) exhibited complete substrate and product stereoselectivity as it reduced S-warfarin to the corresponding S-alcohol. Arthrobacter species (ATCC 19140) exhibited marked substrate and complete product stereoselectivity since S-warfarin, and to a lesser extent R-warfarin, were reduced to the corresponding S-alcohols. These reductions parallel those reported to occur in mammalian species.
对华法林的微生物代谢进行了研究,以此作为包括人类在内的高等生物代谢的模型,并确定微生物还原酶的手性,以便应用于有机合成。根据已报道的还原酮底物的能力,对19种培养物进行了检测,结果表明其中几种能够催化所需的反应。珊瑚诺卡氏菌(美国典型培养物保藏中心19070)在将S-华法林还原为相应的S-醇时,表现出完全的底物和产物立体选择性。节杆菌属(美国典型培养物保藏中心19140)表现出明显的底物和完全的产物立体选择性,因为S-华法林,以及程度稍低的R-华法林,都被还原为相应的S-醇。这些还原反应与在哺乳动物物种中报道的反应相似。