Rational investigation of the potential of Aspergillus strains for lipases production: from gene prospection to application in enantioselectivity models

• Grant number: 22/04341-6
• Support Opportunities: Regular Research Grants
• Start date: September 01, 2023
• End date: November 30, 2025
• Field of knowledge: Biological Sciences - Biochemistry - Enzymology
• Principal Investigator: Patrícia de Oliveira Carvalho
• Grantee: Patrícia de Oliveira Carvalho
• Host Institution: Universidade São Francisco (USF). Campus Bragança Paulista. Bragança Paulista , SP, Brazil
• Associated researchers: Fabiano Jares Contesini ; Lucas Miguel de Carvalho ; Salvador Sánchez Vinces ; Tales Alexandre da Costa e Silva
• Associated scholarship(s): 25/01010-7 - Chromatography and mass spectrometry in the analysis of chiral compounds: development, application and data analysis., BP.TT; 23/11638-8 - Chromatography and mass spectrometry in the analysis of chiral compounds: development, application and data analysis., BP.TT

Abstract

Different rational engineering approaches based on enzyme diversity and selecting variants with improved properties have been used to improve enzyme characteristics. The use of lipases is increasingly gaining focus due to the versatility of the catalyzed reactions and their regio, chemo and enantioselectivity. Expanding the knowledge of the enantioselectivity of lipases is of great interest considering it is (1) of great industrial relevance, (2) relatively easy to investigate, and (3) closely related to the structural arrangement of the active site of the enzyme, so that it preferentially recognizes one of the enantiomers, which enables the separation and generation of the isomer of interest. In this project, we propose an unprecedented study based on the rational engineering of Aspergillus niger, a lipase-producing species previously studied by the group, which should contribute to the research of new enzymes with high enantioselectivity. The Aspergillus genome harbors many unexplored enzyme genes, potentially hiding new lipases to be used in the market. The tools used involve gene bioprospection and the production of Aspergillus recombinant lipases using the CRISPR/Cas9 (Clustered Regularly Interspaced Short Palindromic Repeats) technique, purification and immobilization of the new enzymes and the subsequent application in enantioselectivity models involving hydrolysis, esterification and aminolysis reactions of intermediates and chiral drugs. We expect that the present project will expand the knowledge and the selection of new enzymes with improved characteristics as potential biocatalysts for the fine chemical industry. (AU)

Scientific publications

(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)

SANCHEZ-LUQUEZ, KAREN; SILVEIRA, ANNE MICHELLI REIS; SANCHEZ-VINCES, SALVADOR; SILVA, ALEX AP. ROSINI; BARRETO, JOYCE; DE BRITO, RHUBIA BETHANIA SOCORRO LEMOS; GARCIA, CAROLINE DE MOURA; VIEIRA, ANA LAIS; ANTONIO, MARCIA AP.; CARVALHO, PATRICIA DE OLIVEIRA. Etodolac Single Dose Metabolic Profile Elucidation: Pharmacokinetics and Adverse Events in Healthy Volunteers. PHARMACEUTICALS, v. 18, n. 1, p. 17-pg., 2025-01-01. (22/04341-6, 23/11638-8)

SILVEIRA, ANNE MICHELLI REIS; SANCHEZ-VINCES, SALVADOR; SILVA, ALEX AP. ROSINI; SANCHEZ-LUQUEZ, KAREN; GARCIA, PEDRO HENRIQUE DIAS; DE MOURA GARCIA, CAROLINE; DE BRITO, RHUBIA BETHANIA SOCORRO LEMOS; VIEIRA, ANA LAIS; DE CARVALHO, LUCAS MIGUEL; ANTONIO, MARCIA AP.; et al. Pharmacometabolomics Approach to Explore Pharmacokinetic Variation and Clinical Characteristics of a Single Dose of Desvenlafaxine in Healthy Volunteers. PHARMACEUTICS, v. 16, n. 11, p. 15-pg., 2024-11-01. (22/04341-6, 23/11638-8)

SILVA, ALEX A. R.; COELHO, LILIA L. D.; SANCHEZ-LUQUEZ, KAREN Y.; GARCIA, PEDRO H. D.; BOLDIN, RENATA; SILVEIRA, ANNE M. R.; ANTONIO, MARCIA A.; PORCARI, ANDREIA M.; CARVALHO, PATRICIA O.. Determination of Lisdexamfetamine in Human Plasma by LC-MS/MS Method. Journal of the Brazilian Chemical Society, v. 36, n. 4, p. 8-pg., 2025-01-01. (22/04341-6, 22/15643-3)