Fatty acid ethanolamides (FAEAs) are bioactive lipids involved in inflammation, pain modulation, and energy homeostasis, gaining interest in the pharmaceutical, nutraceutical, and cosmetic sectors. Here, we present an intensified biocatalytic strategy for the synthesis of a mixture of FAEAs─palmitoylethanolamide (PEA), oleoylethanolamide (OLA), stearoylethanolamide (SEA), and linoleoylethanolamide (LEA)─starting from microbial lipids extracted fromCutaneotrichosporon oleaginosus, cultivated on whey permeate, a major dairy byproduct, supplemented with waste cooking oil. The two-step enzymatic cascade─transesterification of triacylglycerols into ethyl esters followed by aminolysis with ethanolamine─was catalyzed by Novozym 435 (immobilized Candida antarctica lipase B) in green solvents. Whereas ethanol has been used for the first step, eucalyptol proved particularly effective in aminolysis reaction with >99% conversion and complete selectivity. Process intensification via a SpinChem rotating bed reactor led to a 5-fold reduction in reaction time (48 to 10 h), a 5- to 7-times increase in space-time yield and quantitative yields for both steps. Biocatalyst reusability and process reproducibility was preserved. This integrated platform exemplifies a circular bioeconomy approach by valorizing agri-industrial residues into high-value compounds through clean and scalable technologies. The resulting FAEAs hold potential for synergistic therapeutic applications, while supporting cost-effective and sustainable manufacturing across diverse industries.

Spinning Green: Lipase-Catalyzed Synthesis of Bioactive Fatty Acid Amides from Renewable Lipid Feedstocks in a Rotating Bed Reactor / M. Bigliardi, S. Donzella, D. Dăescu, A. Pellis, L. Tamborini, A. Pinto, M.L. Contente. - In: ACS SUSTAINABLE CHEMISTRY & ENGINEERING. - ISSN 2168-0485. - 13:42(2025 Oct 12), pp. 18214-18222. [10.1021/acssuschemeng.5c07654]

Spinning Green: Lipase-Catalyzed Synthesis of Bioactive Fatty Acid Amides from Renewable Lipid Feedstocks in a Rotating Bed Reactor

M. Bigliardi
Primo
;
S. Donzella
Secondo
;
L. Tamborini;A. Pinto
Penultimo
;
M.L. Contente
Ultimo
2025

Abstract

Fatty acid ethanolamides (FAEAs) are bioactive lipids involved in inflammation, pain modulation, and energy homeostasis, gaining interest in the pharmaceutical, nutraceutical, and cosmetic sectors. Here, we present an intensified biocatalytic strategy for the synthesis of a mixture of FAEAs─palmitoylethanolamide (PEA), oleoylethanolamide (OLA), stearoylethanolamide (SEA), and linoleoylethanolamide (LEA)─starting from microbial lipids extracted fromCutaneotrichosporon oleaginosus, cultivated on whey permeate, a major dairy byproduct, supplemented with waste cooking oil. The two-step enzymatic cascade─transesterification of triacylglycerols into ethyl esters followed by aminolysis with ethanolamine─was catalyzed by Novozym 435 (immobilized Candida antarctica lipase B) in green solvents. Whereas ethanol has been used for the first step, eucalyptol proved particularly effective in aminolysis reaction with >99% conversion and complete selectivity. Process intensification via a SpinChem rotating bed reactor led to a 5-fold reduction in reaction time (48 to 10 h), a 5- to 7-times increase in space-time yield and quantitative yields for both steps. Biocatalyst reusability and process reproducibility was preserved. This integrated platform exemplifies a circular bioeconomy approach by valorizing agri-industrial residues into high-value compounds through clean and scalable technologies. The resulting FAEAs hold potential for synergistic therapeutic applications, while supporting cost-effective and sustainable manufacturing across diverse industries.
(bio)process intensification; biocatalysis; fatty amides; fermentation technology; green solvents; lipase; spinchem reactor;
Settore CHEM-07/B - Chimica degli alimenti
Settore CHEM-07/A - Chimica farmaceutica
Settore CHEM-07/C - Chimica e biotecnologia delle fermentazioni
   Piano di Sostegno alla Ricerca 2015-2017 - Linea 2 "Dotazione annuale per attività istituzionali" (anno 2022)
   UNIVERSITA' DEGLI STUDI DI MILANO
12-ott-2025
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1193319
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