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Enzymatic synthesis of glucose monodecanoate in a hydrophobic deep eutectic solvent

Hollenbach, Rebecca 1; Ochsenreither, Katrin ORCID iD icon 1; Syldatk, Christoph 1
1 Institut für Bio- und Lebensmitteltechnik (BLT), Karlsruher Institut für Technologie (KIT)

Abstract (englisch):

Environmentally friendly and biodegradable reaction media are an important part of a sustainable glycolipid production in the transition to green chemistry. Deep eutectic solvents (DESs) are an ecofriendly alternative to organic solvents. So far, only hydrophilic DESs were considered for enzymatic glycolipid synthesis. In this study, a hydrophobic DES consisting of (-)-menthol and decanoic acid is presented for the first time as an alternative to hydrophilic DES. The yields in the newly introduced hydrophobic DES are significantly higher than in hydrophilic DESs. Different reaction parameters were investigated to optimize the synthesis further. Twenty milligrams per milliliter iCalB and 0.5 M glucose resulted in the highest initial reaction velocity for the esterification reaction, while the highest initial reaction velocity was achieved with 1.5 M glucose in the transesterification reaction. The enzyme was proven to be reusable for at least five cycles without significant loss of activity.


Verlagsausgabe §
DOI: 10.5445/IR/1000120428
Veröffentlicht am 23.06.2020
Originalveröffentlichung
DOI: 10.3390/ijms21124342
Scopus
Zitationen: 41
Web of Science
Zitationen: 35
Dimensions
Zitationen: 40
Cover der Publikation
Zugehörige Institution(en) am KIT Institut für Bio- und Lebensmitteltechnik (BLT)
Publikationstyp Zeitschriftenaufsatz
Publikationsjahr 2020
Sprache Englisch
Identifikator ISSN: 1422-0067, 1661-6596
KITopen-ID: 1000120428
Erschienen in International journal of molecular sciences
Verlag MDPI
Band 21
Heft 12
Seiten Article no: 4342
Bemerkung zur Veröffentlichung Gefördert durch den KIT-Publikationsfonds
Vorab online veröffentlicht am 18.06.2020
Schlagwörter glycolipid; deep eutectic solvents; enzymatic synthesis; Candida antarctica lipase B; polarity
Nachgewiesen in Dimensions
Scopus
Web of Science
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