Regioselective and Stereoselective Epoxidation of n-3 and n-6 Fatty Acids by Fungal Peroxygenases
2021
González-Benjumea, Alejandro | Linde, Dolores | Carro, Juan | Ullrich, René | Hofrichter, Martin | Martínez, Ángel T. | Gutiérrez Suárez, Ana | European Commission | Ministerio de Ciencia e Innovación (España) | Consejo Superior de Investigaciones Científicas (España) | González-Benjumea, Alejandro [0000-0003-2857-9491] | Linde, Dolores [0000-0002-0359-0566] | Carro, Juan [0000-0002-7556-9782] | Ullrich, René [0000-0002-9165-6341] | Hofrichter, Martin [0000-0001-5174-7604] | Martínez, Ángel T. [0000-0002-1584-2863] | Gutiérrez Suárez, Ana [0000-0002-8823-9029] | Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72]
17 páginas.- 7 figuras.- 2 tablas.- 53 referencias.- Supplementary Materials: The following are available online (at https://www.mdpi.com/article/10.3390/antiox10121888/s1)
Show more [+] Less [-]Epoxide metabolites from n-3 and n-6 polyunsaturated fatty acids arouse interest thanks to their physiological and pharmacological activities. Their chemical synthesis has significant drawbacks, and enzymes emerge as an alternative with potentially higher selectivity and greener nature. Conversion of eleven eicosanoid, docosanoid, and other n-3/n-6 fatty acids into mono-epoxides by fungal unspecific peroxygenases (UPOs) is investigated, with emphasis on the Agrocybe aegerita (AaeUPO) and Collariella virescens (rCviUPO) enzymes. GC-MS revealed the strict regioselectivity of the n-3 and n-6 reactions with AaeUPO and rCviUPO, respectively, yielding 91%-quantitative conversion into mono-epoxides at the last double bond. Then, six of these mono-epoxides were obtained at mg-scale, purified and further structurally characterized by 1H, 13C and HMBC NMR. Moreover, chiral HPLC showed that the n-3 epoxides were also formed (by AaeUPO) with total S/R enantioselectivity (ee > 99%) while the n-6 epoxides (from rCviUPO reactions) were formed in nearly racemic mixtures. The high regio- and enantioselectivity of several of these reactions unveils the synthetic utility of fungal peroxygenases in fatty acid epoxidation.
Show more [+] Less [-]Funding: This research was funded by BioBased Industries Joint Undertaking under the European Union’s Horizon 2020 Research and Innovation Programme, grant number 792063 (SusBind project; https://susbind.eu, accessed on 19 October 2021; to A.G., A.T.M. and M.H.), the BIO2017-86559-R and PID2020-118968RB-100 projects of the Spanish Ministry of Science & Innovation (co-financed by FEDER funds) to A.T.M. and A.G., respectively; the CSIC projects PIE-202040E185 (to A.G.) and PIE-202120E019 (to A.T.M.); and the CSIC SusPlast platform (to A.T.M.).
Show more [+] Less [-]Peer reviewed
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