Matthias Engleder
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View article: Exploring Castellaniella defragrans Linalool (De)hydratase-Isomerase for Enzymatic Hydration of Alkenes
Exploring Castellaniella defragrans Linalool (De)hydratase-Isomerase for Enzymatic Hydration of Alkenes Open
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 k…
View article: Weiterentwicklung der Substrattoleranz von <i>Elizabethkingia meningoseptica</i> Oleathydratase zur regio‐ und stereoselektiven Hydratisierung von Ölsäurederivaten
Weiterentwicklung der Substrattoleranz von <i>Elizabethkingia meningoseptica</i> Oleathydratase zur regio‐ und stereoselektiven Hydratisierung von Ölsäurederivaten Open
Die Addition von Wasser an nichtaktivierte Kohlenstoff‐Kohlenstoff‐Doppelbindungen von Fettsäuren wird durch Fettsäurehydratasen (FAHYs) katalysiert, und ermöglicht die hochselektive Oxyfunktionalisierung von erneuerbaren, ölhaltigen Rohst…
View article: Evolving the Promiscuity of <i>Elizabethkingia meningoseptica</i> Oleate Hydratase for the Regio‐ and Stereoselective Hydration of Oleic Acid Derivatives
Evolving the Promiscuity of <i>Elizabethkingia meningoseptica</i> Oleate Hydratase for the Regio‐ and Stereoselective Hydration of Oleic Acid Derivatives Open
The addition of water to non‐activated carbon–carbon double bonds catalyzed by fatty acid hydratases (FAHYs) allows for highly regio‐ and stereoselective oxyfunctionalization of renewable oil feedstock. So far, the applicability of FAHYs h…
View article: On the current role of hydratases in biocatalysis
On the current role of hydratases in biocatalysis Open
View article: Recombinant expression, purification and biochemical characterization of kievitone hydratase from Nectria haematococca
Recombinant expression, purification and biochemical characterization of kievitone hydratase from Nectria haematococca Open
Kievitone hydratase catalyzes the addition of water to the double bond of the prenyl moiety of plant isoflavonoid kievitone and, thereby, forms the tertiary alcohol hydroxy-kievitone. In nature, this conversion is associated with a defense…
View article: Structure‐Based Mechanism of Oleate Hydratase from <i>Elizabethkingia meningoseptica</i>
Structure‐Based Mechanism of Oleate Hydratase from <i>Elizabethkingia meningoseptica</i> Open
Hydratases provide access to secondary and tertiary alcohols by regio‐ and/or stereospecifically adding water to carbon‐carbon double bonds. Thereby, hydroxy groups are introduced without the need for costly cofactor recycling, and that ma…