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Whole-Cell-Catalyzed Multiple Regio- and Stereoselective Functionalizations in Cascade Reactions Enabled by Directed Evolution.
Li, Aitao; Ilie, Adriana; Sun, Zhoutong; Lonsdale, Richard; Xu, Jian-He; Reetz, Manfred T.
Afiliación
  • Li A; Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470, Mülheim an der Ruhr, Germany.
  • Ilie A; Fachbereich Chemie der Philipps-Universität, Hans-Meerwein-Strasse, 35032, Marburg, Germany.
  • Sun Z; Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470, Mülheim an der Ruhr, Germany.
  • Lonsdale R; Fachbereich Chemie der Philipps-Universität, Hans-Meerwein-Strasse, 35032, Marburg, Germany.
  • Xu JH; Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470, Mülheim an der Ruhr, Germany.
  • Reetz MT; Fachbereich Chemie der Philipps-Universität, Hans-Meerwein-Strasse, 35032, Marburg, Germany.
Angew Chem Int Ed Engl ; 55(39): 12026-9, 2016 09 19.
Article en En | MEDLINE | ID: mdl-27573978
Biocatalytic cascade reactions using isolated stereoselective enzymes or whole cells in one-pot processes lead to value-added chiral products in a single workup. The concept has been restricted mainly to starting materials and intermediate products that are accepted by the respective wild-type enzymes. In the present study, we exploited directed evolution as a means to create E. coli whole cells for regio- and stereoselective cascade sequences that are not possible using man-made catalysts. The approach is illustrated using P450-BM3 in combination with appropriate alcohol dehydrogenases as catalysts in either two-, three-, or four-step cascade reactions starting from cyclohexane, cyclohexanol, or cyclohexanone, respectively, leading to either (R,R)-, (S,S)-, or meso-cyclohexane-1,2-diol. The one-pot conversion of cyclohexane into (R)- or (S)-2-hydroxycyclohexanone in the absence of ADH is also described.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2016 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2016 Tipo del documento: Article País de afiliación: Alemania