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EC Number Application Commentary Reference
Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.100synthesis expression of amidase in Escherichia coli using a T7 promoter. Amidase activity of the engineered Escherichia coli strain reaches 2963 U/l in a 5-l bioreactor, and can be further increased to 5255 U/l in a 100-l bioreactor. Using cell-free extract prepared from 1 kg (wet cell weight) of recombinant cells as catalyst, 60 kg of R,S-DMCPCA is resolved into S-DMCPCA (28.6 kg) and R-2,2-dimethylcyclopropanecarboxylic acid (31.7 kg) in 18 h, and the enantiomeric excess (ee) value of S-DMCPCA reaches 99.32%. 20.5 kg of pure S-DMCPCA is obtained after concentration and crystallization, corresponding to a total yield of 34.2% from R,S-DMCPCA 720957
Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.100synthesis R-amidase is the first enzyme useful for the enzymatic optical resolution of racemic piperazine-2-tert-butylcarboxamide carried out under mild conditions. Enantiomerically pure piperazine-2-carboxylic acid and its tert-butylcarboxamide derivative are important chiral building blocks for some pharmacologically active compounds such as N-methyl-D-aspartate antagonist for glutamate receptor, cardioprotective nucleoside transport blocker, and HIV protease inhibitor -, 664820
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