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Results 1 - 10 of 320 > >>
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.42,3-butanediol + NAD+ D(-)-2,3-butandiol Aeromonas hydrophila acetoin + NADH - r
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.4acetoin + NADH + H+ - Aeromonas hydrophila 2,3-butanediol + NAD+ - r
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.4(2R,3R)-butane-2,3-diol + NAD+ - Alkalihalobacillus clausii (3R)-acetoin + NADH + H+ - r
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.42,3-hexanedione + NADH + H+ small amounts of (2R)-2-hydroxy-3-hexanone are produced as by-product Alkalihalobacillus clausii (3R)-3-hydroxy-2-hexanone + NAD+ - r
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.42,3-pentanedione + NADH + H+ small amounts of 2,3-pentanediol are produced as by-product Alkalihalobacillus clausii 3-hydroxy-2-pentanone + NAD+ - r
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.43,4-hexanedione + 2 NADH + 2 H+ - Alkalihalobacillus clausii (3R,4R)-3,4-hexanediol + 2 NAD+ - r
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.45-methyl-2,3-hexanedione + NADH + H+ small amounts of 5-methyl-2-hydroxy-3-hexanone and traces of (3S)-5-methyl-3-hydroxy-2-hexanone are produced as by-products Alkalihalobacillus clausii (3R)-5-methyl-3-hydroxy-2-hexanone + NAD+ - r
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.4more substrate specificity analysis, overview. Enzyme BcBDH catalyzes the selective asymmetric reduction of prochiral 1,2-diketones to the corresponding HK and, in some cases, the reduction of the same to the corresponding 1,2-diols. Aliphatic diketones, like 2,3-pentanedione, 2,3-hexanedione, 5-methyl-2,3-hexanedione, 3,4-hexanedione, and 2,3-heptanedione are well transformed. In addition, surprisingly alkyl phenyl dicarbonyls, like 2-hydroxy-1-phenylpropan-1-one and phenylglyoxal are accepted, whereas their derivatives with two phenyl groups are not substrates. The biocatalytic reduction of 5-methyl-2,3-hexanedione to mainly 5-methyl-3-hydroxy-2-hexanone with only small amounts of 5-methyl-2-hydroxy-3-hexanone within an enzyme membrane reactor is demonstrated. Stereoselectivity and conversion is analyzed by carrying out the reduction reaction of selected diketones and alpha-hydroxyketones Alkalihalobacillus clausii ? - -
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.4(2R,3R)-butane-2,3-diol + NAD+ - Alkalihalobacillus clausii DSM 8716T (3R)-acetoin + NADH + H+ - r
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.42,3-hexanedione + NADH + H+ small amounts of (2R)-2-hydroxy-3-hexanone are produced as by-product Alkalihalobacillus clausii DSM 8716T (3R)-3-hydroxy-2-hexanone + NAD+ - r
Results 1 - 10 of 320 > >>