Evidence map›Paper›PMID 24523715›Full record

ArticleFrontiers in microbiology2014

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

Helen P S Costa, Jose T A Oliveira, Daniele O B Sousa, Janne K S Morais, Frederico B Moreno, Ana Cristina O Monteiro-Moreira, Ricardo A Viegas, Ilka M Vasconcelos

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Antibacterial action mechanisms and mode of trypsin inhibitors: a systematic review.Journal of enzyme inhibition and medicinal chemistry · 2022
    Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Protease Inhibitors from Plants as Therapeutic Agents- A Review.Plant foods for human nutrition (Dordrecht, Netherlands) · 2022
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Helen P S CostaLaboratory of Plant Toxins, Department of Biochemistry and Molecular Biology, Federal University of Ceara Fortaleza, Brazil.
Jose T A OliveiraLaboratory of Plant Toxins, Department of Biochemistry and Molecular Biology, Federal University of Ceara Fortaleza, Brazil.
Daniele O B SousaLaboratory of Plant Toxins, Department of Biochemistry and Molecular Biology, Federal University of Ceara Fortaleza, Brazil.
Janne K S MoraisLaboratory of Plant Toxins, Department of Biochemistry and Molecular Biology, Federal University of Ceara Fortaleza, Brazil.
Frederico B MorenoSchool of Pharmacy, University of Fortaleza Fortaleza, Brazil.
Ana Cristina O Monteiro-MoreiraSchool of Pharmacy, University of Fortaleza Fortaleza, Brazil.
Ricardo A ViegasDepartment of Forestry Engineering, Federal University of Campina Grande Patos, Brazil.
Ilka M VasconcelosLaboratory of Plant Toxins, Department of Biochemistry and Molecular Biology, Federal University of Ceara Fortaleza, Brazil.
Universidade Federal do Ceará · BRUniversidade de Fortaleza · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

bacterial infections, antimicrobial agentJatropha curcasseed cakeserine proteinase inhibitortrypsin inhibitor

Identifiers

PMID24523715
PMCPMC3906595
OpenAlexW2027249150

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.