Design of a New Gemini Lipoaminoacid with Immobilized Lipases Based on an Eco-Friendly Biosynthetic Process

Lipoaminoacids (LAA) are an important group of biosurfactants, formed by a polar hydrophilic part (amino acid) and a hydrophobic tail (lipid). The gemini LAA structures allow the formation of a supramolecular complex with bioactive molecules, like DNA, which provides them with good transfection effi...

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Main Authors: Patrícia M. Carvalho, Rita C. Guedes, M. R. Bronze, Célia M. C. Faustino, Maria H. L. Ribeiro
Format: Article
Language:English
Published: MDPI AG 2021-01-01
Series:Catalysts
Subjects:
Online Access:https://www.mdpi.com/2073-4344/11/2/164
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spelling doaj-87785feff81649c59f3ebf1b4b41d5b42021-01-26T00:03:35ZengMDPI AGCatalysts2073-43442021-01-011116416410.3390/catal11020164Design of a New Gemini Lipoaminoacid with Immobilized Lipases Based on an Eco-Friendly Biosynthetic ProcessPatrícia M. Carvalho0Rita C. Guedes1M. R. Bronze2Célia M. C. Faustino3Maria H. L. Ribeiro4Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisbon, Prof. Egas Moniz, 1649-028 Lisbon, PortugalResearch Institute for Medicines (iMed.ULisboa), Faculdade de Farmácia, Universidade Lisboa, Av. Prof. Gama Pinto, 1649-003 Lisbon, PortugalDepartment of Pharmaceutical Sciences and Medicines, Faculty of Pharmacy, Universidade Lisboa, Av. Prof. Gama Pinto, 1649-003 Lisbon, PortugalResearch Institute for Medicines (iMed.ULisboa), Faculdade de Farmácia, Universidade Lisboa, Av. Prof. Gama Pinto, 1649-003 Lisbon, PortugalResearch Institute for Medicines (iMed.ULisboa), Faculdade de Farmácia, Universidade Lisboa, Av. Prof. Gama Pinto, 1649-003 Lisbon, PortugalLipoaminoacids (LAA) are an important group of biosurfactants, formed by a polar hydrophilic part (amino acid) and a hydrophobic tail (lipid). The gemini LAA structures allow the formation of a supramolecular complex with bioactive molecules, like DNA, which provides them with good transfection efficiency. Since lipases are naturally involved in lipid and protein metabolism, they are an alternative to the chemical production of LAA, offering an eco-friendly biosynthetic process option. This work aimed to design the production of novel cystine derived gemini through a bioconversion system using immobilized lipases. Three lipases were used: porcine pancreatic lipase (PPL); lipase from <i>Thermomyces lanuginosus</i> (TLL); and lipase from <i>Rizhomucor miehei</i> (RML). PPL was immobilized in sol-gel lenses. L-cystine dihydrochloride and dodecylamine were used as substrates for the bioreaction. The production of LAA was evaluated by thin layer chromatography (TLC), and colorimetric reaction with eosin. The identification and quantification was carried out by High Performance Liquid Chromatographer-Mass Spectrometry (HPLC-MS/MS). The optimization of media design included co-solvent (methanol, dimethylsulfoxide), biphasic (<i>n</i>-hexane and 2-propanol) or solvent-free media, in order to improve the biocatalytic reaction rates and yields. Moreover, a new medium was tested where dodecylamine was melted and added to the cystine and to the biocatalyst, building a system of mainly undissolved substrates, leading to 5 mg/mL of LAA. Most of the volume turned into foam, which indicated the production of the biosurfactant. For the first time, the gemini derived cystine lipoaminoacid was produced, identified, and quantified in both co-solvent and solvent-free media, with the lipases PPL, RML, and TLL.https://www.mdpi.com/2073-4344/11/2/164cystinedockinglipaselipoaminocidssol-gel
collection DOAJ
language English
format Article
sources DOAJ
author Patrícia M. Carvalho
Rita C. Guedes
M. R. Bronze
Célia M. C. Faustino
Maria H. L. Ribeiro
spellingShingle Patrícia M. Carvalho
Rita C. Guedes
M. R. Bronze
Célia M. C. Faustino
Maria H. L. Ribeiro
Design of a New Gemini Lipoaminoacid with Immobilized Lipases Based on an Eco-Friendly Biosynthetic Process
Catalysts
cystine
docking
lipase
lipoaminocids
sol-gel
author_facet Patrícia M. Carvalho
Rita C. Guedes
M. R. Bronze
Célia M. C. Faustino
Maria H. L. Ribeiro
author_sort Patrícia M. Carvalho
title Design of a New Gemini Lipoaminoacid with Immobilized Lipases Based on an Eco-Friendly Biosynthetic Process
title_short Design of a New Gemini Lipoaminoacid with Immobilized Lipases Based on an Eco-Friendly Biosynthetic Process
title_full Design of a New Gemini Lipoaminoacid with Immobilized Lipases Based on an Eco-Friendly Biosynthetic Process
title_fullStr Design of a New Gemini Lipoaminoacid with Immobilized Lipases Based on an Eco-Friendly Biosynthetic Process
title_full_unstemmed Design of a New Gemini Lipoaminoacid with Immobilized Lipases Based on an Eco-Friendly Biosynthetic Process
title_sort design of a new gemini lipoaminoacid with immobilized lipases based on an eco-friendly biosynthetic process
publisher MDPI AG
series Catalysts
issn 2073-4344
publishDate 2021-01-01
description Lipoaminoacids (LAA) are an important group of biosurfactants, formed by a polar hydrophilic part (amino acid) and a hydrophobic tail (lipid). The gemini LAA structures allow the formation of a supramolecular complex with bioactive molecules, like DNA, which provides them with good transfection efficiency. Since lipases are naturally involved in lipid and protein metabolism, they are an alternative to the chemical production of LAA, offering an eco-friendly biosynthetic process option. This work aimed to design the production of novel cystine derived gemini through a bioconversion system using immobilized lipases. Three lipases were used: porcine pancreatic lipase (PPL); lipase from <i>Thermomyces lanuginosus</i> (TLL); and lipase from <i>Rizhomucor miehei</i> (RML). PPL was immobilized in sol-gel lenses. L-cystine dihydrochloride and dodecylamine were used as substrates for the bioreaction. The production of LAA was evaluated by thin layer chromatography (TLC), and colorimetric reaction with eosin. The identification and quantification was carried out by High Performance Liquid Chromatographer-Mass Spectrometry (HPLC-MS/MS). The optimization of media design included co-solvent (methanol, dimethylsulfoxide), biphasic (<i>n</i>-hexane and 2-propanol) or solvent-free media, in order to improve the biocatalytic reaction rates and yields. Moreover, a new medium was tested where dodecylamine was melted and added to the cystine and to the biocatalyst, building a system of mainly undissolved substrates, leading to 5 mg/mL of LAA. Most of the volume turned into foam, which indicated the production of the biosurfactant. For the first time, the gemini derived cystine lipoaminoacid was produced, identified, and quantified in both co-solvent and solvent-free media, with the lipases PPL, RML, and TLL.
topic cystine
docking
lipase
lipoaminocids
sol-gel
url https://www.mdpi.com/2073-4344/11/2/164
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