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Optimizing fermentation conditions of recombinant Escherichia coli expressing cyclopentanone monooxygenase

机译:表达环戊酮单加氧酶的重组大肠杆菌的发酵条件优化

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摘要

Microbial Baeyer-Villiger oxidation of different substrates with cyclopentanone monooxygenase (CPMO) from Comamonas NCIMB 9872 was up-scaled to benchtop fermenter scale. Conditions for cell growth and biocatalyst production were optimized, and a convenient, environmentally friendly and applicable methodology for the preparation of chiral building blocks for natural product and bioactive compound synthesis was developed by applying a resin based on the concept of in situ "substrate feeding-product removal" (SFPR). Three different ketones (4-methylcyclohexanone, rac-3-methylcyclohexanone, and 8-oxabicyclo[3.2.1] oct-6-en-3-one) were converted in 5-15 g/L scale in a conventional bioreactor, with a volumetric productivity of up to 1 g L-1 h(-1) in good to excellent yield and enantiomeric purity.
机译:使用Comamonas NCIMB 9872的环戊酮单加氧酶(CPMO)对不同底物的微生物进行Baeyer-Villiger氧化,可升级至台式发酵罐规模。优化了细胞生长和生物催化剂生产的条件,并通过基于原位“底物进料-产品移除”(SFPR)。在常规生物反应器中,将三种不同的酮(4-甲基环己酮,rac-3-甲基环己酮和8-oxabicyclocyclo [3.2.1] oct-6-en-3-one)以5-15 g / L的比例进行转化,高达1 g L-1 h(-1)的体积生产率,良好且优异的收率和对映体纯度。

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