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Haloalkaliphilic Streptomyces spp. AJ8 isolated from solar salt works and its’ pharmacological potential
Antagonistic Streptomyces spp. AJ8 was isolated and identified from the Kovalam solar salt works in India. The antimicrobial NRPS cluster gene was characterized by PCR, sequencing and predict the secondary structure analysis. The secondary metabolites will be extracted from different organic solvent...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4549370/ https://www.ncbi.nlm.nih.gov/pubmed/26307214 http://dx.doi.org/10.1186/s13568-015-0143-2 |
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author | Jenifer, John Selesteen Charles Adlin Donio, Mariathason Birdilla Selva Michaelbabu, Mariavincent Vincent, Samuel Gnana Prakash Citarasu, Thavasimuthu |
author_facet | Jenifer, John Selesteen Charles Adlin Donio, Mariathason Birdilla Selva Michaelbabu, Mariavincent Vincent, Samuel Gnana Prakash Citarasu, Thavasimuthu |
author_sort | Jenifer, John Selesteen Charles Adlin |
collection | PubMed |
description | Antagonistic Streptomyces spp. AJ8 was isolated and identified from the Kovalam solar salt works in India. The antimicrobial NRPS cluster gene was characterized by PCR, sequencing and predict the secondary structure analysis. The secondary metabolites will be extracted from different organic solvent extraction and studied the antibacterial, antifungal, antiviral and anticancer activities. In vitro antagonistic activity results revealed that, Streptomyces spp. AJ8 was highly antagonistic against Staphylococcus aureus, Aeromonas hydrophila WPD1 and Candida albicans. The genomic level identification revealed that, the strain was confirmed as Streptomyces spp. AJ8 and submitted the NCBI database (KC603899). The NRPS gene was generated a single gene fragment of 781 bp length (KR491940) and the database analysis revealed that, the closely related to Streptomyces spp. SAUK6068 and S. coeruleoprunus NBRC15400. The secondary metabolites extracted with ethyl acetate was effectively inhibited the bacterial and fungal growth at the ranged between 7 and 19.2 mm of zone of inhibition. The antiviral activity results revealed that, the metabolite was significantly (P < 0.001) controlled the killer shrimp virus white spot syndrome virus at the level of 85 %. The metabolite also suppressed the L929 fibroblast cancer cells at 35.7 % viability in 1000 µg treatment. |
format | Online Article Text |
id | pubmed-4549370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-45493702015-08-28 Haloalkaliphilic Streptomyces spp. AJ8 isolated from solar salt works and its’ pharmacological potential Jenifer, John Selesteen Charles Adlin Donio, Mariathason Birdilla Selva Michaelbabu, Mariavincent Vincent, Samuel Gnana Prakash Citarasu, Thavasimuthu AMB Express Original Article Antagonistic Streptomyces spp. AJ8 was isolated and identified from the Kovalam solar salt works in India. The antimicrobial NRPS cluster gene was characterized by PCR, sequencing and predict the secondary structure analysis. The secondary metabolites will be extracted from different organic solvent extraction and studied the antibacterial, antifungal, antiviral and anticancer activities. In vitro antagonistic activity results revealed that, Streptomyces spp. AJ8 was highly antagonistic against Staphylococcus aureus, Aeromonas hydrophila WPD1 and Candida albicans. The genomic level identification revealed that, the strain was confirmed as Streptomyces spp. AJ8 and submitted the NCBI database (KC603899). The NRPS gene was generated a single gene fragment of 781 bp length (KR491940) and the database analysis revealed that, the closely related to Streptomyces spp. SAUK6068 and S. coeruleoprunus NBRC15400. The secondary metabolites extracted with ethyl acetate was effectively inhibited the bacterial and fungal growth at the ranged between 7 and 19.2 mm of zone of inhibition. The antiviral activity results revealed that, the metabolite was significantly (P < 0.001) controlled the killer shrimp virus white spot syndrome virus at the level of 85 %. The metabolite also suppressed the L929 fibroblast cancer cells at 35.7 % viability in 1000 µg treatment. Springer Berlin Heidelberg 2015-08-27 /pmc/articles/PMC4549370/ /pubmed/26307214 http://dx.doi.org/10.1186/s13568-015-0143-2 Text en © Jenifer et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Jenifer, John Selesteen Charles Adlin Donio, Mariathason Birdilla Selva Michaelbabu, Mariavincent Vincent, Samuel Gnana Prakash Citarasu, Thavasimuthu Haloalkaliphilic Streptomyces spp. AJ8 isolated from solar salt works and its’ pharmacological potential |
title | Haloalkaliphilic Streptomyces spp. AJ8 isolated from solar salt works and its’ pharmacological potential |
title_full | Haloalkaliphilic Streptomyces spp. AJ8 isolated from solar salt works and its’ pharmacological potential |
title_fullStr | Haloalkaliphilic Streptomyces spp. AJ8 isolated from solar salt works and its’ pharmacological potential |
title_full_unstemmed | Haloalkaliphilic Streptomyces spp. AJ8 isolated from solar salt works and its’ pharmacological potential |
title_short | Haloalkaliphilic Streptomyces spp. AJ8 isolated from solar salt works and its’ pharmacological potential |
title_sort | haloalkaliphilic streptomyces spp. aj8 isolated from solar salt works and its’ pharmacological potential |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4549370/ https://www.ncbi.nlm.nih.gov/pubmed/26307214 http://dx.doi.org/10.1186/s13568-015-0143-2 |
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