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JcTI-I: a novel trypsin inhibitor from Jatropha curcas seed cake with potential for bacterial infection treatment

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 pote...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906595/
https://www.ncbi.nlm.nih.gov/pubmed/24523715
http://dx.doi.org/10.3389/fmicb.2014.00005
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author 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.
author_facet 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.
author_sort Costa, Helen P. S.
collection PubMed
description 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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spelling pubmed-39065952014-02-12 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. Front Microbiol Microbiology 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. Frontiers Media S.A. 2014-01-30 /pmc/articles/PMC3906595/ /pubmed/24523715 http://dx.doi.org/10.3389/fmicb.2014.00005 Text en Copyright © 2014 Costa, Oliveira, Sousa, Morais, Moreno, Monteiro-Moreira, Viegas and Vasconcelos. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
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.
JcTI-I: a novel trypsin inhibitor from Jatropha curcas seed cake with potential for bacterial infection treatment
title JcTI-I: a novel trypsin inhibitor from Jatropha curcas seed cake with potential for bacterial infection treatment
title_full JcTI-I: a novel trypsin inhibitor from Jatropha curcas seed cake with potential for bacterial infection treatment
title_fullStr JcTI-I: a novel trypsin inhibitor from Jatropha curcas seed cake with potential for bacterial infection treatment
title_full_unstemmed JcTI-I: a novel trypsin inhibitor from Jatropha curcas seed cake with potential for bacterial infection treatment
title_short JcTI-I: a novel trypsin inhibitor from Jatropha curcas seed cake with potential for bacterial infection treatment
title_sort jcti-i: a novel trypsin inhibitor from jatropha curcas seed cake with potential for bacterial infection treatment
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906595/
https://www.ncbi.nlm.nih.gov/pubmed/24523715
http://dx.doi.org/10.3389/fmicb.2014.00005
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