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126 related items for PubMed ID: 18404768

  • 1. Mechanistic kinetic model for symmetric carboligations using benzaldehyde lyase.
    Zavrel M, Schmidt T, Michalik C, Ansorge-Schumacher M, Marquardt W, Büchs J, Spiess AC.
    Biotechnol Bioeng; 2008 Sep 01; 101(1):27-38. PubMed ID: 18404768
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  • 2. Structure and mechanism of the ThDP-dependent benzaldehyde lyase from Pseudomonas fluorescens.
    Mosbacher TG, Mueller M, Schulz GE.
    FEBS J; 2005 Dec 01; 272(23):6067-76. PubMed ID: 16302970
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  • 3. Mechanism of benzaldehyde lyase studied via thiamin diphosphate-bound intermediates and kinetic isotope effects.
    Chakraborty S, Nemeria N, Yep A, McLeish MJ, Kenyon GL, Jordan F.
    Biochemistry; 2008 Mar 25; 47(12):3800-9. PubMed ID: 18314961
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  • 4. Simultaneous identification of reaction and inactivation kinetics of an enzyme-catalyzed carboligation.
    Ohs R, Leipnitz M, Schöpping M, Spiess AC.
    Biotechnol Prog; 2018 Sep 25; 34(5):1081-1092. PubMed ID: 29885040
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  • 5. Factors mediating activity, selectivity, and substrate specificity for the thiamin diphosphate-dependent enzymes benzaldehyde lyase and benzoylformate decarboxylase.
    Knoll M, Müller M, Pleiss J, Pohl M.
    Chembiochem; 2006 Dec 25; 7(12):1928-34. PubMed ID: 17051662
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  • 6. Benzaldehyde lyase-catalyzed enantioselective carboligation of aromatic aldehydes with mono- and dimethoxy acetaldehyde.
    Demir AS, Seşenoglu O, Dünkelmann P, Müller M.
    Org Lett; 2003 Jun 12; 5(12):2047-50. PubMed ID: 12790525
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  • 7. Biochemical peculiarities of benzaldehyde lyase from Pseudomonas fluorescens Biovar I in the dependency on pH and cosolvent concentration.
    Schmidt T, Zavrel M, Spiess A, Ansorge-Schumacher MB.
    Bioorg Chem; 2009 Jun 12; 37(3):84-9. PubMed ID: 19364619
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  • 8. The production of (R)-2-hydroxy-1-phenyl-propan-1-one derivatives by benzaldehyde lyase from Pseudomonas fluorescens in a continuously operated membrane reactor.
    Hildebrand F, Kühl S, Pohl M, Vasic-Racki D, Müller M, Wandrey C, Lütz S.
    Biotechnol Bioeng; 2007 Apr 01; 96(5):835-43. PubMed ID: 17029295
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  • 10. Characterization of benzaldehyde lyase from Pseudomonas fluorescens: A versatile enzyme for asymmetric C-C bond formation.
    Janzen E, Müller M, Kolter-Jung D, Kneen MM, McLeish MJ, Pohl M.
    Bioorg Chem; 2006 Dec 01; 34(6):345-61. PubMed ID: 17078994
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  • 12. Thiamin-diphosphate-dependent enzymes: new aspects of asymmetric C-C bond formation.
    Pohl M, Lingen B, Müller M.
    Chemistry; 2002 Dec 02; 8(23):5288-95. PubMed ID: 12432496
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  • 13. Biocatalytic strategies for the asymmetric synthesis of alpha-hydroxy ketones.
    Hoyos P, Sinisterra JV, Molinari F, Alcántara AR, Domínguez de María P.
    Acc Chem Res; 2010 Feb 16; 43(2):288-99. PubMed ID: 19908854
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  • 17. A tailor-made chimeric thiamine diphosphate dependent enzyme for the direct asymmetric synthesis of (S)-benzoins.
    Westphal R, Vogel C, Schmitz C, Pleiss J, Müller M, Pohl M, Rother D.
    Angew Chem Int Ed Engl; 2014 Aug 25; 53(35):9376-9. PubMed ID: 25044968
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  • 18. An activity, stability and selectivity comparison of propioin synthesis by thiamine diphosphate-dependent enzymes in a solid/gas bioreactor.
    Mikolajek R, Spiess AC, Pohl M, Lamare S, Büchs J.
    Chembiochem; 2007 Jun 18; 8(9):1063-70. PubMed ID: 17497614
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  • 19. Intramolecular Stereoselective Stetter Reaction Catalyzed by Benzaldehyde Lyase.
    Chen X, Wang Z, Lou Y, Peng Y, Zhu Q, Xu J, Wu Q.
    Angew Chem Int Ed Engl; 2021 Apr 19; 60(17):9326-9329. PubMed ID: 33559383
    [Abstract] [Full Text] [Related]

  • 20. Active-site engineering of benzaldehyde lyase shows that a point mutation can confer both new reactivity and susceptibility to mechanism-based inhibition.
    Brandt GS, Kneen MM, Petsko GA, Ringe D, McLeish MJ.
    J Am Chem Soc; 2010 Jan 20; 132(2):438-9. PubMed ID: 20030408
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