New Stetter reactions catalyzed by thiamine diphosphate dependent MenD from E. coli

Journal of Biotechnology

Volumn 191, Issue , 2014, Pages 64-68

  Beigi, Maryam ^a   Waltzer, Simon ^a   Zarei, Mostafa ^a   Müller, Michael ^a  

^a UNIVERSITY OF FREIBURG   (Germany)

Author keywords

1,4 Carboligation; Biocatalysis; CC coupling; Chemoenzymatic synthesis; Umpolung

Indexed keywords

BIOCATALYSTS; CATALYSIS; ENZYMES; ESCHERICHIA COLI; KETONES; SYNTHESIS (CHEMICAL);

1,4-CARBOLIGATION; BIOCATALYSIS; C-C COUPLING; CHEMO-ENZYMATIC SYNTHESIS; UMPOLUNG;

SUBSTRATES;

CHORISMIC ACID; COCARBOXYLASE; ENZYME; KETONE DERIVATIVE; MENAQUINONE; MEND ENZYME; UNCLASSIFIED DRUG; 2-SUCCINYL-5-ENOLPYRUVYL-6-HYDROXY-3-CYCLOHEXADIENE-1-CARBOXYLATE SYNTHASE, E COLI; ESCHERICHIA COLI PROTEIN; KETONE; PYRUVATE OXIDASE; SULFIDE;

ARTICLE; BIOCATALYSIS; BIOSYNTHESIS; ENZYME ACTIVITY; ESCHERICHIA COLI; MICHAEL ADDITION; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PHYSIOLOGICAL PROCESS; PROTON NUCLEAR MAGNETIC RESONANCE; STETTER REACTION; AMINO ACID SEQUENCE; CATALYSIS; CHEMISTRY; ENZYME SPECIFICITY; ENZYMOLOGY; GENETICS; METABOLISM;

AMINO ACID SEQUENCE; BIOSYNTHETIC PATHWAYS; CATALYSIS; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; KETONES; PYRUVATE OXIDASE; SUBSTRATE SPECIFICITY; SULFIDES; THIAMINE PYROPHOSPHATE;

EID: 84912026308     PISSN: 01681656     EISSN: 18734863     Source Type: Journal    
DOI: 10.1016/j.jbiotec.2014.07.451     Document Type: Article

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