Literature DB >> 34656058

A new Kunitz trypsin inhibitor from Erythrina poeppigiana exhibits antimicrobial and antibiofilm properties against bacteria.

Karina Margareti Alencar de Barros1, Janaina de Cássia Orlandi Sardi2, Simone Maria-Neto2, Alexandre José Macedo3, Suellen Rodrigues Ramalho4, Daniella Gorete Lourenço de Oliveira2, Gemilson Soares Pontes5, Simone Schneider Weber6, Caio Fernando Ramalho de Oliveira4, Maria Lígia Rodrigues Macedo7.   

Abstract

Erythrina poeppigiana belongs to Fabaceae family (subfamily Papillionoideae) and is commonly found in tropical and subtropical regions in Brazil. Herein, we described the purification and characterization of a new Kunitz-type inhibitor, obtained from E. poeppigiana seeds (EpTI). EpTI is composed by three isoforms of identical amino-terminal sequences with a molecular weight ranging from 17 to 20 kDa. The physicochemical features showed by EpTI are common to Kunitz inhibitors, including the dissociation constant (13.1 nM), stability against thermal (37-100 °C) and pH (2-10) ranging, and the presence of disulfide bonds stabilizing its reactive site. Furthermore, we investigated the antimicrobial, anti-adhesion, and anti-biofilm properties of EpTI against Gram-positive and negative bacteria. The inhibitor showed antimicrobial activity with a minimum inhibitory concentration (MIC, 5-10 µM) and minimum bactericidal concentration (MBC) of 10 µM for Enterobacter aerogenes, Enterobacter cloacae, Klebsiella pneumoniae, Staphylococcus aureus, and Staphylococcus haemolyticus. The combination of EpTI with ciprofloxacin showed a marked synergistic effect, reducing the antibiotic concentration by 150%. The increase in crystal violet uptake for S. aureus and K. pneumoniae strains was approximately 30% and 50%, respectively, suggesting that the bacteria plasma membrane is targeted by EpTI. Treatment with EpTI at 1x and 10 x MIC significantly reduced the biofilm formation and prompted the disruption of a mature biofilm. At MIC/2, EpTI decreased the bacterial adhesion to polystyrene surface within 2 h. Finally, EpTI showed low toxicity in animal model Galleria mellonella. Given its antimicrobial and anti-biofilm properties, the EpTI sequence might be used to design novel drug prototypes.
Copyright © 2021 The Authors. Published by Elsevier Masson SAS.. All rights reserved.

Entities:  

Keywords:  Adherence; Antibacterial activity; Antibiofilm activity; Erythrina poeppigiana; Peptidase inhibitor

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Year:  2021        PMID: 34656058     DOI: 10.1016/j.biopha.2021.112198

Source DB:  PubMed          Journal:  Biomed Pharmacother        ISSN: 0753-3322            Impact factor:   6.529


  2 in total

1.  Heterologous expression and physicochemical characteristics identification of Kunitz protease inhibitor in Brassica napus.

Authors:  Wei Feng; Haiying Shi; Wei Xu; Peng Song
Journal:  3 Biotech       Date:  2022-02-27       Impact factor: 2.406

Review 2.  Plant Kunitz Inhibitors and Their Interaction with Proteases: Current and Potential Pharmacological Targets.

Authors:  Camila Ramalho Bonturi; Ana Beatriz Silva Teixeira; Vitória Morais Rocha; Penélope Ferreira Valente; Juliana Rodrigues Oliveira; Clovis Macêdo Bezerra Filho; Isabel Fátima Correia Batista; Maria Luiza Vilela Oliva
Journal:  Int J Mol Sci       Date:  2022-04-25       Impact factor: 6.208

  2 in total

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