Related Experiment Video
Updated: Oct 19, 2026

A Toolkit to Enable Hydrocarbon Conversion in Aqueous Environments
Published on: October 2, 2012
Cloning and expression in Escherichia coli of a gene coding for a secondary alcohol dehydrogenase from Candida
H Yamamoto1, N Kawada, A Matsuyama
1Tsukuba Research Center, Daicel Chemical Industries, Ltd., Ibaraki, Japan. h-yamamoto@daicel.co.jp
Abstract:
A gene encoding a stereo-specific secondary alcohol dehydrogenase (CpSADH) that catalyzed the oxidation of (S)-1,3-BDO to 4-hydroxy-2-butanone was cloned from Candida parapsilosis. This CpSADH-gene consisted of 1,009 nucleotides coding for a protein with M(r) 35,964. A recombinant Escherichia coli JM109 strain harboring the expression plasmid, pKK-CPA1, produced (R)-1,3-BDO (93.5% ee., 94.7% yield) from the racemate without any additive to regenerate NAD+ from NADH.
Related Concept Videos
Exon Recombination
Exon shuffling follows “splice frame rules.” Each exon has three reading...
Bioreactor Controls-III

