Racemization of enantiopure secondary alcohols by Thermoanaerobacter ethanolicus secondary alcohol dehydrogenase
Type
ArticleAuthors
Musa, Musa M.
Phillips, Robert S.
Laivenieks, Maris
Vieille, Claire
Takahashi, Masateru
Hamdan, Samir

KAUST Department
Biological and Environmental Sciences and Engineering (BESE) DivisionBioscience Program
Date
2013Permanent link to this record
http://hdl.handle.net/10754/562489
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Show full item recordAbstract
Controlled racemization of enantiopure phenyl-ring-containing secondary alcohols is achieved in this study using W110A secondary alcohol dehydrogenase from Thermoanaerobacter ethanolicus (W110A TeSADH) and in the presence of the reduced and oxidized forms of its cofactor nicotinamide-adenine dinucleotide. Racemization of both enantiomers of alcohols accepted by W110A TeSADH, not only with low, but also with reasonably high, enantiomeric discrimination is achieved by this method. Furthermore, the high tolerance of TeSADH to organic solvents allows TeSADH-catalyzed racemization to be conducted in media containing up to 50% (v/v) of organic solvents. © 2013 The Royal Society of Chemistry.Citation
Musa, M. M., Phillips, R. S., Laivenieks, M., Vieille, C., Takahashi, M., & Hamdan, S. M. (2013). Racemization of enantiopure secondary alcohols by Thermoanaerobacter ethanolicus secondary alcohol dehydrogenase. Organic & Biomolecular Chemistry, 11(17), 2911. doi:10.1039/c3ob27415bSponsors
The authors acknowledge the support provided by King Abdulaziz City for Science and Technology (KACST) through the Science and Technology Unit at King Fahd University of Petroleum and Minerals (KFUPM) for funding this work through project no. 11-BIO1666-04 as part of the National Science, Technology and Innovation Plan.Publisher
Royal Society of Chemistry (RSC)Journal
Organic & Biomolecular ChemistryPubMed ID
23525226ae974a485f413a2113503eed53cd6c53
10.1039/c3ob27415b
Scopus Count
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