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Biocatalytic Synthesis of Bioactive Compounds
Biocatalytic Synthesis of Bioactive Compounds
Autore Aleu Josefina
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica 1 electronic resource (142 p.)
Soggetto topico Research & information: general
Biology, life sciences
Soggetto non controllato 8-hydroxydaidzein
stable
soluble
anti-inflammation
amylosucrase
Deinococcus geothermalis
coumarin
biotransformation
filamentous fungi
selective hydroxylation
bromination
chlorination
pharmaceuticals
active agent synthesis
biocatalysis
haloperoxidase
halogenase
glycosyltransferase
Glycine max (L.) Merr
HPLC/MS
isoflavone aglycone-rich extract
isoflavone α-glucoside
alkene cleavage
aryl alkenes
basidiomycota
carotene degradation
dye-decolorizing peroxidase (DyP)
manganese
Komagataella pfaffii
Pleurotus sapidus
monoterpenes
limonene
glycerol
mevalonate pathway
reaction engineering
bioprocess
biocatalyst
two-liquid phase fermentation
in situ product removal
lipase
unsaturated fatty acid
oxidative cleavage
oxidation
adaptation
UV/NTG mutagenesis
psychrotrophs
terpenes
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557380503321
Aleu Josefina  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Enzyme-Mediated Stereoselective Synthesis
Enzyme-Mediated Stereoselective Synthesis
Autore Serra Stefano
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2019
Descrizione fisica 1 electronic resource (116 p.)
Soggetto non controllato enantioselective synthesis
flavors
hydroxy fatty acids
chiral amines
diketones
esters
oleic acid
Burkholderia cepacia lipase
multi-enzymatic cascades
solid-state fermentation
biocatalysis
agro-industrial side stream
rapeseed cake
enzyme-mediated resolution
linolenic acid
stereoselective biotransformation
lipases
kinetic resolution
1-phenylethanol
linseed cake
bioreduction
Lactobacillus rhamnosus
alcohol-dehydrogenase
enantioselectivity
hydratase
reaction engineering
immobilization
?-transaminases
linoleic acid
cyclization
monoterpenes
1
lactones
protein engineering
asymmetric synthesis
alcohol dehydrogenases
linaloyl oxide
chiral resolution
aroma compounds
4-diols
pullulan
linalool
reduction
nitroketone
ISBN 3-03921-937-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910367738803321
Serra Stefano  
MDPI - Multidisciplinary Digital Publishing Institute, 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui