Characterization of novel trypsin inhibitor in raw and toasted peanuts using a simple improved isolation

• Autor(a) principal: Morais, Ana Heloneida de Araújo
• Data de Publicação: 2019
• Outros Autores: Maciel, Bruna Leal Lima, Medeiros, Amanda Fernandes de, Rocha, Maria Gabriela Ferreira, Serquiz, Alexandre Coelho, Machado, Richele Janaína Araújo, Lima, Vanessa Cristina Oliveira, Carvalho, Fabiana Maria Coimbra de, Costa, Izael de Sousa, Santos, Elizeu Antunes dos
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UFRN
• Texto Completo: https://repositorio.ufrn.br/handle/123456789/58131; http://dx.doi.org/10.1556/1326.2017.00353
• topic: Arachis hypogaea L.; Protein inhibitors; Anti-trypsin activity; Chromatography thermoresistance; Bioactive protein

Trypsin inhibitors have been described in peanuts and their derived industrialized foods, demonstrating diversity and thermoresistance. Given their most varied applications, these enzymatic protease inhibitors have been isolated and characterized for their potential use as bioinsecticides, herbal medicines, or medicines, but it is not simple. There are still no reports in the literature of the isolation and characterization of trypsin inhibitors in cultivar cavalo rosa (CCR) peanut, a common variety in Brazil. However, there are biological activities related to trypsin inhibitors from peanut-derived products. In this study, we isolated and characterized a novel trypsin inhibitor in CCR peanuts (Arachis hypogaea L.) under different processing conditions using a simple improved isolation. Raw and toasted peanut inhibitor was isolated by ammonium sulfate fractionation and trypsin-cyanogen bromide-activated SepharoseW 4B (CNBr-SepharoseW 4B) chromatography. The inhibitors from raw and toasted peanut were called AhTI1 and AhTI2, respectively, with potent anti-trypsin activity. Activity at different temperatures and pH was evaluated, and both samples were similarly stable under tested conditions. Minimum concentration for inhibition to occur (IC50) was 2.78 × 10−10 M and 2.39 × 10−10 M for AhTI1 and AhTI2, and inhibition constant (Ki) was 3.26 × 10−10 M and 1.54 × 10−10 M, respectively, showing non-competitive reversible kinetics. We concluded that AhTI1 and AhTI2 presented highly specific to trypsin and stable to toasting, different temperatures, and pH ranging. These are important characteristics in the process of developing bioinsecticides or biopharmaceuticals. Thus, this may be an interesting molecule, aiming at its biotechnological application, and it was obtained using a simple and easy isolation process