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Anticariogenic and Hemolytic Activity of Selected Seed Protein Extracts In vitro conditions

OBJECTIVE: This study aimed to assess the anticariogenic and hemolytic activity of crude plant seed protein extracts against tooth decaying bacteria. MATERIALS AND METHODS: The proteins from seeds of 12 different plants were extracted and used for antimicrobial assay against six different organisms....

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Autores principales: Ishnava, Kalpesh B, Shah, Pankit P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4290778/
https://www.ncbi.nlm.nih.gov/pubmed/25628685
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author Ishnava, Kalpesh B
Shah, Pankit P.
author_facet Ishnava, Kalpesh B
Shah, Pankit P.
author_sort Ishnava, Kalpesh B
collection PubMed
description OBJECTIVE: This study aimed to assess the anticariogenic and hemolytic activity of crude plant seed protein extracts against tooth decaying bacteria. MATERIALS AND METHODS: The proteins from seeds of 12 different plants were extracted and used for antimicrobial assay against six different organisms. The extraction was carried out in 10mM of sodium phosphate buffer (pH 7.0). Protein concentrations were determined as described by Bradford method. Anticariogenic activity was studied by agar well diffusion method and Minimum Inhibitory Concentration (MIC) was evaluated by the two-fold serial broth dilution method. Hemolytic activity, treatment of proteinase K and Kinetic study in Mimusops elengi crude seed protein extract. RESULTS: The anticariogenic assay demonstrated the activity of Mimusops elengi against Staphylococcus aureus and Streptococcus pyogenes. A minor activity of Glycine wightii against Streptococcus mutans was also found. The protein content of Mimusops elengi seed protein extract was 5.84mg/ml. The MIC values for Staphylococcus aureus and Streptococcus pyogenes against Mimusops elengi seed protein extract were 364.36μg/ml and 182.19μg/ml, respectively. Kinetic study further elucidated the mode of inhibition in the presence of the Mimusops elengi plant seed protein with respect to time. The concentration of crude extract which gave 50% hemolysis compared to Triton X-100 treatment (HC(50)) value was 1.58 mg/ml; which is more than five times larger than that of the MIC. Treatment with proteinase K of the Mimusops elengi seed protein resulted in absence of the inhibition zone; which clearly indicates that the activity was only due to protein. CONCLUSION: Our results showed the prominence of Mimusops elengi plant seed protein extract as an effective herbal medication against tooth decaying bacteria.
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spelling pubmed-42907782015-01-27 Anticariogenic and Hemolytic Activity of Selected Seed Protein Extracts In vitro conditions Ishnava, Kalpesh B Shah, Pankit P. J Dent (Tehran) Original Article OBJECTIVE: This study aimed to assess the anticariogenic and hemolytic activity of crude plant seed protein extracts against tooth decaying bacteria. MATERIALS AND METHODS: The proteins from seeds of 12 different plants were extracted and used for antimicrobial assay against six different organisms. The extraction was carried out in 10mM of sodium phosphate buffer (pH 7.0). Protein concentrations were determined as described by Bradford method. Anticariogenic activity was studied by agar well diffusion method and Minimum Inhibitory Concentration (MIC) was evaluated by the two-fold serial broth dilution method. Hemolytic activity, treatment of proteinase K and Kinetic study in Mimusops elengi crude seed protein extract. RESULTS: The anticariogenic assay demonstrated the activity of Mimusops elengi against Staphylococcus aureus and Streptococcus pyogenes. A minor activity of Glycine wightii against Streptococcus mutans was also found. The protein content of Mimusops elengi seed protein extract was 5.84mg/ml. The MIC values for Staphylococcus aureus and Streptococcus pyogenes against Mimusops elengi seed protein extract were 364.36μg/ml and 182.19μg/ml, respectively. Kinetic study further elucidated the mode of inhibition in the presence of the Mimusops elengi plant seed protein with respect to time. The concentration of crude extract which gave 50% hemolysis compared to Triton X-100 treatment (HC(50)) value was 1.58 mg/ml; which is more than five times larger than that of the MIC. Treatment with proteinase K of the Mimusops elengi seed protein resulted in absence of the inhibition zone; which clearly indicates that the activity was only due to protein. CONCLUSION: Our results showed the prominence of Mimusops elengi plant seed protein extract as an effective herbal medication against tooth decaying bacteria. Tehran University of Medical Sciences 2014-09 2014-09-30 /pmc/articles/PMC4290778/ /pubmed/25628685 Text en Copyright © Dental Research Center, Tehran University of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0), which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Original Article
Ishnava, Kalpesh B
Shah, Pankit P.
Anticariogenic and Hemolytic Activity of Selected Seed Protein Extracts In vitro conditions
title Anticariogenic and Hemolytic Activity of Selected Seed Protein Extracts In vitro conditions
title_full Anticariogenic and Hemolytic Activity of Selected Seed Protein Extracts In vitro conditions
title_fullStr Anticariogenic and Hemolytic Activity of Selected Seed Protein Extracts In vitro conditions
title_full_unstemmed Anticariogenic and Hemolytic Activity of Selected Seed Protein Extracts In vitro conditions
title_short Anticariogenic and Hemolytic Activity of Selected Seed Protein Extracts In vitro conditions
title_sort anticariogenic and hemolytic activity of selected seed protein extracts in vitro conditions
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4290778/
https://www.ncbi.nlm.nih.gov/pubmed/25628685
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