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JcTI-I: a novel trypsin inhibitor from Jatropha curcas seed cake with potential for bacterial infection treatment.
Costa, Helen P S; Oliveira, Jose T A; Sousa, Daniele O B; Morais, Janne K S; Moreno, Frederico B; Monteiro-Moreira, Ana Cristina O; Viegas, Ricardo A; Vasconcelos, Ilka M.
Afiliação
  • Costa HP; Laboratory of Plant Toxins, Department of Biochemistry and Molecular Biology, Federal University of Ceara Fortaleza, Brazil.
  • Oliveira JT; Laboratory of Plant Toxins, Department of Biochemistry and Molecular Biology, Federal University of Ceara Fortaleza, Brazil.
  • Sousa DO; Laboratory of Plant Toxins, Department of Biochemistry and Molecular Biology, Federal University of Ceara Fortaleza, Brazil.
  • Morais JK; Laboratory of Plant Toxins, Department of Biochemistry and Molecular Biology, Federal University of Ceara Fortaleza, Brazil.
  • Moreno FB; School of Pharmacy, University of Fortaleza Fortaleza, Brazil.
  • Monteiro-Moreira AC; School of Pharmacy, University of Fortaleza Fortaleza, Brazil.
  • Viegas RA; Department of Forestry Engineering, Federal University of Campina Grande Patos, Brazil.
  • Vasconcelos IM; Laboratory of Plant Toxins, Department of Biochemistry and Molecular Biology, Federal University of Ceara Fortaleza, Brazil.
Front Microbiol ; 5: 5, 2014.
Article em En | MEDLINE | ID: mdl-24523715
ABSTRACT
Jatropha curcas seed cake is a low-value by-product resulting from biodiesel production. The seed cake is highly toxic, but it has great potential for biotechnology applications as it is a repository of biomolecules that could be important in agriculture, medicine, and industry. To explore this potential, a novel trypsin inhibitor called JcTI-I was purified by fractionation of the crude extract with trichloroacetic acid (2.5%, v/v) followed by affinity chromatography (Trypsin-Sepharose 4B) and molecular exclusion (Sephacryl S-200). Non-reducing sodium dodecyl sulfate-polyacrylamide gel electrophoresis and gel filtration showed that JcTI-I has approximately 20.0~kDa. Mass spectrometry analysis revealed that the intact molecular mass of JcTI-I is 10.252~kDa. Moreover, JcTI-I is a glycoprotein with 6.4% (m/m) carbohydrates, pI of 6.6, N-terminal sequence similarity around 60% to plant albumins and high stability to heat, pH, and salinity. JcTI-I presented antibacterial activity against the human pathogenic bacteria Salmonella enterica subspecies enterica serovar choleraesuis and Staphylococcus aureus, with minimum inhibitory concentration less than 5~µg/mL. Furthermore, JcTI-I did have inhibitory activity against the serine proteases from the tested bacteria. Otherwise, no hemolytic activity of human erythrocytes and signs of acute toxicity to mice were observed for JcTI-I. The results demonstrate the benefits of J. curcas seed cake as a source of trypsin inhibitor with potential for biotechnological application as a new antimicrobial agent against human pathogenic bacteria.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2014 Tipo de documento: Article