Application of Stemphylium lycopersici Extracts Immobilized on MCM‐48type Mesoporous Materials as Biocatalysts for Monoacylglycerol Production

Author:

Paranhos Bruno A.1,Dallago Rogério M.2,dos S. Martins Gustavo1,Mignoni Marcelo L.2,Valduga Eunice2,Guimarães Denise O.3,Itabaiana Ivaldo4,Malafaia Camila R. A.1,Leal Ivana C. R.1

Affiliation:

1. Laboratório de Produtos Naturais e Ensaios Biológicos (LaProNEB) Departamento de Produtos Naturais e Alimentos Faculdade de Farmácia Universidade Federal do Rio de Janeiro (UFRJ) Avenida Carlos Chagas Filho, 373 21941–902 Rio de Janeiro RJ Brasil

2. Departamento de Engenharia de Alimentos Universidade Regional Integrada do Alto Uruguai e das Missões Erechim Rio Grande do Sul, Brasil.

3. Laboratório de Produtos Bioativos Instituto de Ciências Farmacêuticas Universidade Federal do Rio de Janeiro Macaé RJ, Brasil

4. Departamento de Engenharia Bioquímica Escola de Química Universidade Federal do Rio de Janeiro Rio de Janeiro, Brasil

Abstract

AbstractMonoacylglycerols are eco‐friendly and inexpensive emulsifiers with a range of applications. The traditional synthetic route is not eco‐friendly, while enzymatic catalysis offers milder reaction conditions and higher selectivity. However, its application still is limited due to the costs. In this context, endophytic fungi can be source to new biocatalysts with enhanced catalytic activity. Based on this perspective, the aim of this study was perform the synthesis of MAG‘s through transesterification reactions of solketal and different vinyl esters, using crude and immobilized lipolytic extracts from the endophytic fungi Stemphylium lycopersici, isolated from Humiria balsamifera. The reactions were conducted using 100 mg of biocatalyst, 1 mmol of substrates, 9 : 1 n‐heptane/acetone, at 40 °C, 200 rpm for 96 h. In the reactions using the ILE and stearate, laureate and decanoate vinyl esters it was possible to obtain the correspondent products with conversion rates of 52–75 %. Also, according to the structure drivers used in MCM‐48 synthesis, different morphologies and conversions rates were observed. Employing [C16MI] Cl, [C14MI] Cl and [C4MI] Cl, the 1‐lauroyl‐ glycerol conversion was 36 %, 79 % and 44 %, respectively. This is the first work involving the immobilization of an endophytic fungi and its utilization as a biocatalyst in the production of MAG's.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro

Publisher

Wiley

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