• Login
    View Item 
    •   Home
    • Research
    • Articles
    • View Item
    •   Home
    • Research
    • Articles
    • View Item
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Browse

    All of KAUSTCommunitiesIssue DateSubmit DateThis CollectionIssue DateSubmit Date

    My Account

    Login

    Quick Links

    Open Access PolicyORCID LibguideTheses and Dissertations LibguideSubmit an Item

    Statistics

    Display statistics

    Racemization of enantiopure secondary alcohols by Thermoanaerobacter ethanolicus secondary alcohol dehydrogenase

    • CSV
    • RefMan
    • EndNote
    • BibTex
    • RefWorks
    Type
    Article
    Authors
    Musa, Musa M. cc
    Phillips, Robert S.
    Laivenieks, Maris
    Vieille, Claire
    Takahashi, Masateru
    Hamdan, Samir cc
    KAUST Department
    Biological and Environmental Sciences and Engineering (BESE) Division
    Bioscience Program
    Date
    2013
    Permanent link to this record
    http://hdl.handle.net/10754/562489
    
    Metadata
    Show full item record
    Abstract
    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/c3ob27415b
    Sponsors
    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 Chemistry
    DOI
    10.1039/c3ob27415b
    PubMed ID
    23525226
    ae974a485f413a2113503eed53cd6c53
    10.1039/c3ob27415b
    Scopus Count
    Collections
    Articles; Biological and Environmental Science and Engineering (BESE) Division; Bioscience Program

    entitlement

    Related articles

    • Asymmetric reduction and oxidation of aromatic ketones and alcohols using W110A secondary alcohol dehydrogenase from Thermoanaerobacter ethanolicus.
    • Authors: Musa MM, Ziegelmann-Fjeld KI, Vieille C, Zeikus JG, Phillips RS
    • Issue date: 2007 Jan 5
    • A Thermoanaerobacter ethanolicus secondary alcohol dehydrogenase mutant derivative highly active and stereoselective on phenylacetone and benzylacetone.
    • Authors: Ziegelmann-Fjeld KI, Musa MM, Phillips RS, Zeikus JG, Vieille C
    • Issue date: 2007 Feb
    • Activity and selectivity of W110A secondary alcohol dehydrogenase from Thermoanaerobacter ethanolicus in organic solvents and ionic liquids: mono- and biphasic media.
    • Authors: Musa MM, Ziegelmann-Fjeld KI, Vieille C, Phillips RS
    • Issue date: 2008 Mar 7
    • Xerogel-encapsulated W110A secondary alcohol dehydrogenase from Thermoanaerobacter ethanolicus performs asymmetric reduction of hydrophobic ketones in organic solvents.
    • Authors: Musa MM, Ziegelmann-Fjeld KI, Vieille C, Zeikus JG, Phillips RS
    • Issue date: 2007
    • Mutation of Thermoanaerobacter ethanolicus secondary alcohol dehydrogenase at Trp-110 affects stereoselectivity of aromatic ketone reduction.
    • Authors: Patel JM, Musa MM, Rodriguez L, Sutton DA, Popik VV, Phillips RS
    • Issue date: 2014 Aug 21
    DSpace software copyright © 2002-2023  DuraSpace
    Quick Guide | Contact Us | KAUST University Library
    Open Repository is a service hosted by 
    Atmire NV
     

    Export search results

    The export option will allow you to export the current search results of the entered query to a file. Different formats are available for download. To export the items, click on the button corresponding with the preferred download format.

    By default, clicking on the export buttons will result in a download of the allowed maximum amount of items. For anonymous users the allowed maximum amount is 50 search results.

    To select a subset of the search results, click "Selective Export" button and make a selection of the items you want to export. The amount of items that can be exported at once is similarly restricted as the full export.

    After making a selection, click one of the export format buttons. The amount of items that will be exported is indicated in the bubble next to export format.