Exploring
Castellaniella defragrans
dehydratase
geraniol
hydratase
isomerase
linalool
monoterpene hydration
myrcene
tertiary alcohol
Journal
Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009
Informations de publication
Date de publication:
01 Jun 2019
01 Jun 2019
Historique:
received:
28
04
2019
revised:
30
05
2019
accepted:
31
05
2019
entrez:
5
6
2019
pubmed:
5
6
2019
medline:
26
11
2019
Statut:
epublish
Résumé
Acyclic monoterpenes constitute a large and highly abundant class of secondary plant metabolites and are, therefore, attractive low-cost raw materials for the chemical industry. To date, numerous biocatalysts for their transformation are known, giving access to highly sought-after monoterpenoids. In view of the high selectivity associated with many of these reactions, the demand for enzymes generating commercially important target molecules is unabated. Here, linalool (de)hydratase-isomerase (Ldi, EC 4.2.1.127) from
Identifiants
pubmed: 31159367
pii: molecules24112092
doi: 10.3390/molecules24112092
pmc: PMC6600392
pii:
doi:
Substances chimiques
Acyclic Monoterpenes
0
Alcohols
0
Alkenes
0
Monoterpenes
0
linalool
D81QY6I88E
Hydro-Lyases
EC 4.2.1.-
Isomerases
EC 5.-
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Austrian Science Fund
ID : J3787
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