Synthesis with good enantiomeric excess of both enantiomers of α-ketols and acetolactates by two thiamin diphosphate-dependent decarboxylases

Bioorganic Chemistry

Volumn 34, Issue 6, 2006, Pages 380-393

  Baykal, Ahmet ^a   Chakraborty, Sumit ^a   Dodoo, Afua ^a   Jordan, Frank ^a  

^a RUTGERS UNIVERSITY   (United States)

Author keywords

Hydroxypyruvate; Acetoin; Acetolactate; Carboligase side reactions; Circular dichroism; Enantiomeric excess; Enzymatic chiral synthesis; Escherichia coli pyruvate dehydrogenase E1 subunit; Thiamin diphosphate; Yeast pyruvate decarboxylase

Indexed keywords

ACETOIN; ACETOLACTATE SYNTHASE; CARBOXYLYASE; KETOL; PYRUVATE DECARBOXYLASE; PYRUVATE DEHYDROGENASE; PYRUVIC ACID; THIAMINE DERIVATIVE;

ARTICLE; CIRCULAR DICHROISM; CONTROLLED STUDY; ENANTIOMER; ESCHERICHIA COLI; GAS CHROMATOGRAPHY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; SACCHAROMYCES CEREVISIAE; STEREOCHEMISTRY; SYNTHESIS;

ACETONE; BINDING SITES; CARBOXY-LYASES; ESCHERICHIA COLI PROTEINS; KETONE OXIDOREDUCTASES; KETONES; LACTATES; MUTATION, MISSENSE; PYRUVATE DECARBOXYLASE; PYRUVIC ACID; SACCHAROMYCES CEREVISIAE PROTEINS; STEREOISOMERISM; THIAMINE PYROPHOSPHATE;

ESCHERICHIA COLI; SACCHAROMYCES CEREVISIAE;

EID: 33750685322     PISSN: 00452068     EISSN: 10902120     Source Type: Journal    
DOI: 10.1016/j.bioorg.2006.09.006     Document Type: Article

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