Enzymatic Synthesis of Glucose Monodecanoate in a Hydrophobic Deep Eutectic Solvent.
Candida antarctica lipase B
deep eutectic solvents
enzymatic synthesis
glycolipid
polarity
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
18 Jun 2020
18 Jun 2020
Historique:
received:
11
05
2020
revised:
13
06
2020
accepted:
16
06
2020
entrez:
24
6
2020
pubmed:
24
6
2020
medline:
16
2
2021
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 32570792
pii: ijms21124342
doi: 10.3390/ijms21124342
pmc: PMC7352255
pii:
doi:
Substances chimiques
Decanoates
0
Fungal Proteins
0
Solvents
0
Lipase
EC 3.1.1.3
lipase B, Candida antarctica
EC 3.1.1.3
Glucose
IY9XDZ35W2
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : European Regional Development Fund
ID : grant#32-7545.24-20/6/3
Références
Eur J Pharm Biopharm. 2018 Mar;124:55-62
pubmed: 29258912
Front Bioeng Biotechnol. 2020 May 05;8:382
pubmed: 32432093
Chemosphere. 2015 Aug;132:63-9
pubmed: 25800513
EFSA J. 2018 Jan 05;16(1):e05087
pubmed: 32625657
Int J Mol Sci. 2016 Mar 18;17(3):401
pubmed: 26999123
J Biotechnol. 2003 May 8;102(3):251-9
pubmed: 12730008
Ecotoxicol Environ Saf. 2015 Feb;112:46-53
pubmed: 25463852
Trends Biotechnol. 2019 Sep;37(9):943-959
pubmed: 31000203
Chem Commun (Camb). 2003 Jan 7;(1):70-1
pubmed: 12610970
Bioresour Technol. 2008 Jul;99(10):4065-72
pubmed: 17399984
Biotechnol Bioeng. 2001 Apr 20;73(2):104-10
pubmed: 11255158
Biotechnol Adv. 2012 May-Jun;30(3):550-63
pubmed: 22041165
Sci Rep. 2017 Feb 01;7:41257
pubmed: 28145498
Molecules. 2019 Aug 08;24(16):
pubmed: 31398916
Biophys J. 2004 Aug;87(2):812-21
pubmed: 15298890
ChemSusChem. 2019 Apr 23;12(8):1549-1559
pubmed: 30811105