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Lipase-catalyzed acylation of levoglucosan in continuous flow: antibacterial and biosurfactant studies

Studies involving the transformation of lignocellulosic biomass into high value-added chemical products have been intensively conducted in recent years. Its matrix is mainly composed of cellulose, hemicellulose and lignin, being, therefore, an abundant and renewable source for obtaining several plat...

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Autores principales: do Nascimento, Marcelo A., Vargas, Juan P. C., Rodrigues, José G. A., Leão, Raquel A. C., de Moura, Patricia H. B., Leal, Ivana C. R., Bassut, Jonathan, de Souza, Rodrigo O. M. A., Wojcieszak, Robert, Itabaiana, Ivaldo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8979102/
https://www.ncbi.nlm.nih.gov/pubmed/35425309
http://dx.doi.org/10.1039/d1ra08111j
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author do Nascimento, Marcelo A.
Vargas, Juan P. C.
Rodrigues, José G. A.
Leão, Raquel A. C.
de Moura, Patricia H. B.
Leal, Ivana C. R.
Bassut, Jonathan
de Souza, Rodrigo O. M. A.
Wojcieszak, Robert
Itabaiana, Ivaldo
author_facet do Nascimento, Marcelo A.
Vargas, Juan P. C.
Rodrigues, José G. A.
Leão, Raquel A. C.
de Moura, Patricia H. B.
Leal, Ivana C. R.
Bassut, Jonathan
de Souza, Rodrigo O. M. A.
Wojcieszak, Robert
Itabaiana, Ivaldo
author_sort do Nascimento, Marcelo A.
collection PubMed
description Studies involving the transformation of lignocellulosic biomass into high value-added chemical products have been intensively conducted in recent years. Its matrix is mainly composed of cellulose, hemicellulose and lignin, being, therefore, an abundant and renewable source for obtaining several platform molecules, with levoglucosan (LG) standing out. This anhydrous carbohydrate can be acylated to obtain carbohydrate fatty acid esters (CFAEs). Here, these compounds were obtained via enzymatic acylation of LG, commercially obtained (Start BioScience®), with different acyl donors in continuous flow. Through the experimental design using a model reaction, it was possible to optimize the reaction conditions, temperature and residence time, obtaining a maximum conversion at 61 °C and 77 min. In addition, there was a productivity gain of up to 100 times in all comparisons made with the batch system. Finally, CFAEs were applied in tests of interfacial tension and biological activity. For a mixture of 4- and 2-O-lauryl-1,6-anhydroglucopyranose (MONLAU), the minimum interfacial tension (IFT(min)) obtained was 96 mN m(−1) and the critical micelle concentration (CMC) was 50 mM. Similar values were obtained for a mixture of 4- and 2-O-palmitoyl-1,6-anhydroglucopyranose (MONPAL), not yet reported in the literature, of 88 mN m(−1) in 50 mM. For a mixture of 4- and 2-O-estearyl-1,6-anhydroglucopyranose (MONEST) and 4- and 2-O-oleoyl-1,6-anhydroglucopyranose (MONOLE), CMC was higher than 60 mM and IFT(min) of 141 mN m(−1) and 102 mN m(−1), respectively. Promising data were obtained for minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) of MONLAU against Staphylococcus aureus strains at 0.25 mM.
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spelling pubmed-89791022022-04-13 Lipase-catalyzed acylation of levoglucosan in continuous flow: antibacterial and biosurfactant studies do Nascimento, Marcelo A. Vargas, Juan P. C. Rodrigues, José G. A. Leão, Raquel A. C. de Moura, Patricia H. B. Leal, Ivana C. R. Bassut, Jonathan de Souza, Rodrigo O. M. A. Wojcieszak, Robert Itabaiana, Ivaldo RSC Adv Chemistry Studies involving the transformation of lignocellulosic biomass into high value-added chemical products have been intensively conducted in recent years. Its matrix is mainly composed of cellulose, hemicellulose and lignin, being, therefore, an abundant and renewable source for obtaining several platform molecules, with levoglucosan (LG) standing out. This anhydrous carbohydrate can be acylated to obtain carbohydrate fatty acid esters (CFAEs). Here, these compounds were obtained via enzymatic acylation of LG, commercially obtained (Start BioScience®), with different acyl donors in continuous flow. Through the experimental design using a model reaction, it was possible to optimize the reaction conditions, temperature and residence time, obtaining a maximum conversion at 61 °C and 77 min. In addition, there was a productivity gain of up to 100 times in all comparisons made with the batch system. Finally, CFAEs were applied in tests of interfacial tension and biological activity. For a mixture of 4- and 2-O-lauryl-1,6-anhydroglucopyranose (MONLAU), the minimum interfacial tension (IFT(min)) obtained was 96 mN m(−1) and the critical micelle concentration (CMC) was 50 mM. Similar values were obtained for a mixture of 4- and 2-O-palmitoyl-1,6-anhydroglucopyranose (MONPAL), not yet reported in the literature, of 88 mN m(−1) in 50 mM. For a mixture of 4- and 2-O-estearyl-1,6-anhydroglucopyranose (MONEST) and 4- and 2-O-oleoyl-1,6-anhydroglucopyranose (MONOLE), CMC was higher than 60 mM and IFT(min) of 141 mN m(−1) and 102 mN m(−1), respectively. Promising data were obtained for minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) of MONLAU against Staphylococcus aureus strains at 0.25 mM. The Royal Society of Chemistry 2022-01-21 /pmc/articles/PMC8979102/ /pubmed/35425309 http://dx.doi.org/10.1039/d1ra08111j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
do Nascimento, Marcelo A.
Vargas, Juan P. C.
Rodrigues, José G. A.
Leão, Raquel A. C.
de Moura, Patricia H. B.
Leal, Ivana C. R.
Bassut, Jonathan
de Souza, Rodrigo O. M. A.
Wojcieszak, Robert
Itabaiana, Ivaldo
Lipase-catalyzed acylation of levoglucosan in continuous flow: antibacterial and biosurfactant studies
title Lipase-catalyzed acylation of levoglucosan in continuous flow: antibacterial and biosurfactant studies
title_full Lipase-catalyzed acylation of levoglucosan in continuous flow: antibacterial and biosurfactant studies
title_fullStr Lipase-catalyzed acylation of levoglucosan in continuous flow: antibacterial and biosurfactant studies
title_full_unstemmed Lipase-catalyzed acylation of levoglucosan in continuous flow: antibacterial and biosurfactant studies
title_short Lipase-catalyzed acylation of levoglucosan in continuous flow: antibacterial and biosurfactant studies
title_sort lipase-catalyzed acylation of levoglucosan in continuous flow: antibacterial and biosurfactant studies
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8979102/
https://www.ncbi.nlm.nih.gov/pubmed/35425309
http://dx.doi.org/10.1039/d1ra08111j
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