Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
6-methylhept-5-en-2-one + NADH

6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: 80% sulcatol R(-) enantiomer after 24 h reaction time
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: enantiomeric selectivity substantially affected by pregrowth period and substrate concentration
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: 80% of sulcatol R enantiomer after 48 h reaction time
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: 96% sulcatol R enantiomer after 17 h reaction time
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: only sensitive to S enantiomer, inhibited by the R enantiomer
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: mixture of 65% S(+)- and 35% S(-)-sulcatol isomers
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: R(-)-sulcatol in high enantiomeric excess formed irrespective of pregrowth period and substrate concentration
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: S enantiomer formed
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: 100% enantiomeric excess for S(+)-sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: S enantiomer formed
r
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
6-methylhept-5-en-2-one + NADH

6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: 80% sulcatol R(-) enantiomer after 24 h reaction time
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: enantiomeric selectivity substantially affected by pregrowth period and substrate concentration
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: 80% of sulcatol R enantiomer after 48 h reaction time
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: 96% sulcatol R enantiomer after 17 h reaction time
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: only sensitive to S enantiomer, inhibited by the R enantiomer
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: mixture of 65% S(+)- and 35% S(-)-sulcatol isomers
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: R(-)-sulcatol in high enantiomeric excess formed irrespective of pregrowth period and substrate concentration
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: S enantiomer formed
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: 100% enantiomeric excess for S(+)-sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: sulcatol
r
6-methylhept-5-en-2-one + NADH
6-methylhept-5-en-2-ol + NAD+
-
Substrates: sulcatone
Products: S enantiomer formed
r
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Tidswell, E.C.; Salter, G.J.; Kell, D.B.; Morris, J.G.
Enantioselectivity of sulcatone reduction by some anaerobic bacteria
Enzyme Microb. Technol.
21
143-147
1997
Clostridium tyrobutyricum, Levilactobacillus brevis
-
brenda
Tidswell, E.C.; Thompson, A.N.; Morris, J.G.
Selection in chemostat culture of a mutant strain of Clostridium tyrobutyricum improved in its reduction of ketones
Appl. Microbiol. Biotechnol.
35
317-322
1991
Clostridium tyrobutyricum, Clostridium tyrobutyricum PON5
-
brenda
Belan, A.; Bolte, J.; Fauve, A.; Gourcy, J.G.; Veschambre, H.
Use of biological systems for the preparation of chiral molecules. 3. An application in pheromone synthesis: Preparation of sulcatol enantiomers
J. Org. Chem.
52
256-260
1987
Aspergillus niger, Clostridium tyrobutyricum, Geotrichum candidum, Gnathotrichus retusus, Gnathotrichus sulcatus, Saccharomyces cerevisiae, Thermoanaerobacter brockii
-
brenda