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Sustainable enzymatic synthesis of glycolipids in a deep eutectic solvent system

: Siebenhaller, S.; Muhle-Goll, C.; Luy, B.; Kirschhöfer, F.; Brenner-Weiss, G.; Hiller, E.; Günther, M.; Rupp, S.; Zibek, S.; Syldatk, C.


Journal of molecular catalysis. B, Enzymatic 133 (2016), Supplement 1, pp.S281-S287
ISSN: 1381-1177
ISSN: 1873-3158
Journal Article
Fraunhofer IGB ()

Environmental friendly (bio-) chemical synthesis reactions are getting ever more important for the production of ecofriendly products. In this study a reaction system based on a deep eutectic solvent consisting of choline chloride and various sugars, was used for the enzymatic synthesis of glycolipids. A wide variety of potential substrates were tested for the enzymatic glycolipid synthesis in DES, including various sugars and one anhydro-sugar in combination with up to 9 different fatty acids. It was proven that the described DES-based solvent system is suitable for the enzymatic synthesis of tailor-made glycolipids. The proposed lipase-catalyzed acylation of the different sugars, which are substrate and part of the solvent at the same time, was detected by TLC-MALDI-ToF, ESI-Q-ToF and additional MS/MS experiments. As an example of all the synthesized glycolipids, fragments and m/. z signals of the expected glycolipid arabinose-4-. O-laurate was detected, and its chemi cal structure was elucidated via NMR.