Regulating Flavor Compound Synthesis and Cofactor Recycling in Heterogeneous Enzymatic Reactions by Mixtures of Bacterial Cell-Free Extracts
Enzymatic cofactor recycling and generation of acetic acid, 3-methylbutanal, and 3-methylbutanol were evaluated using a mixture of cell-free extracts of Gluconobacter oxydans and Streptococcus lactis var. maltigenes. Ethanol was used as a substrate by cell-free extracts of G, oxydans to produce acet...
Gespeichert in:
Veröffentlicht in: | Journal of dairy science 1986-05, Vol.69 (5), p.1209-1218 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Enzymatic cofactor recycling and generation of acetic acid, 3-methylbutanal, and 3-methylbutanol were evaluated using a mixture of cell-free extracts of Gluconobacter oxydans and Streptococcus lactis var. maltigenes. Ethanol was used as a substrate by cell-free extracts of G, oxydans to produce acetic acid and to generate reduced nicotinamide adenine dinucleotide from nicotinamide adenine dinucleotide. Leucine was converted by S. lactis var. maltigenes cell-free extracts to 3-methylbutanal and 3-methylbutanol and to regenerate nicotinamide adenine dinucleotides. Optimum pH to form 3-methylbutanal by the combined cell-free extracts was about 6.8 and that for 3-methylbutanol was 6.4. At 30°C, 3-methylbutanol reached a maximum of 73ppm after 30h but declined slightly at 48h. Concentrations of 3-methylbutanol increased gradually over 48h to a maximum of 56ppm. Rates of production of these compounds at 12.8°C were about half that at 32°C. Concentrations of 3-methylbutanol were increased to about those of 3-methylbutanal by adjusting the concentrations of substrate, nicotinamide adenine dinucleotide, cell-free extract, and pH so as to produce large amounts of acetic acid and reduced nicotinamide adenine dinucleotide. |
---|---|
ISSN: | 0022-0302 1525-3198 |
DOI: | 10.3168/jds.S0022-0302(86)80525-2 |