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Identification and characterization of Streptomyces flavogriseus NJ-4 as a novel producer of actinomycin D and holomycin
This paper is the first public report that Streptomyces flavogriseus can produce both actinomycin D and holomycin. The actinomycete strain NJ-4 isolated from the soil of Nanjing Agricultural University was identified as S. flavogriseus. This S. flavogriseus strain was found for the first time to pro...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520960/ https://www.ncbi.nlm.nih.gov/pubmed/28740758 http://dx.doi.org/10.7717/peerj.3601 |
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author | Wei, Zhaohui Xu, Chao Wang, Juan Lu, Fengxia Bie, Xiaomei Lu, Zhaoxin |
author_facet | Wei, Zhaohui Xu, Chao Wang, Juan Lu, Fengxia Bie, Xiaomei Lu, Zhaoxin |
author_sort | Wei, Zhaohui |
collection | PubMed |
description | This paper is the first public report that Streptomyces flavogriseus can produce both actinomycin D and holomycin. The actinomycete strain NJ-4 isolated from the soil of Nanjing Agricultural University was identified as S. flavogriseus. This S. flavogriseus strain was found for the first time to produce two antimicrobial compounds that were identified as actinomycin D and holomycin. GS medium, CS medium and GSS medium were used for the production experiments. All three media supported the production of actinomycin D, while holomycin was detected only in GS medium and was undetectable by HPLC in the CS and GSS media. The antimicrobial activity against B. pumilus, S. aureus, Escherichia coli, F. moniliforme, F. graminearum and A. niger was tested using the agar well diffusion method. Actinomycin D exhibited strong antagonistic activities against all the indicator strains. Holomycin exhibited strong antagonistic activities against B. pumilus, S. aureus and E. coli and had antifungal activity against F. moniliforme and F. graminearum but had no antifungal activity against A. niger. The cell viability was determined using an MTT assay. Holomycin exhibited cytotoxic activity against A549 lung cancer cells, BGC823 gastric cancer cells and HepG2 hepatocellular carcinoma cells. The yield of actinomycin D from S. flavogriseus NJ-4 was 960 mg/l. S. flavogriseus NJ-4 exhibits a distinct capability and has the industrial potential to produce considerable yields of actinomycin D under unoptimized conditions. |
format | Online Article Text |
id | pubmed-5520960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55209602017-07-24 Identification and characterization of Streptomyces flavogriseus NJ-4 as a novel producer of actinomycin D and holomycin Wei, Zhaohui Xu, Chao Wang, Juan Lu, Fengxia Bie, Xiaomei Lu, Zhaoxin PeerJ Biotechnology This paper is the first public report that Streptomyces flavogriseus can produce both actinomycin D and holomycin. The actinomycete strain NJ-4 isolated from the soil of Nanjing Agricultural University was identified as S. flavogriseus. This S. flavogriseus strain was found for the first time to produce two antimicrobial compounds that were identified as actinomycin D and holomycin. GS medium, CS medium and GSS medium were used for the production experiments. All three media supported the production of actinomycin D, while holomycin was detected only in GS medium and was undetectable by HPLC in the CS and GSS media. The antimicrobial activity against B. pumilus, S. aureus, Escherichia coli, F. moniliforme, F. graminearum and A. niger was tested using the agar well diffusion method. Actinomycin D exhibited strong antagonistic activities against all the indicator strains. Holomycin exhibited strong antagonistic activities against B. pumilus, S. aureus and E. coli and had antifungal activity against F. moniliforme and F. graminearum but had no antifungal activity against A. niger. The cell viability was determined using an MTT assay. Holomycin exhibited cytotoxic activity against A549 lung cancer cells, BGC823 gastric cancer cells and HepG2 hepatocellular carcinoma cells. The yield of actinomycin D from S. flavogriseus NJ-4 was 960 mg/l. S. flavogriseus NJ-4 exhibits a distinct capability and has the industrial potential to produce considerable yields of actinomycin D under unoptimized conditions. PeerJ Inc. 2017-07-19 /pmc/articles/PMC5520960/ /pubmed/28740758 http://dx.doi.org/10.7717/peerj.3601 Text en ©2017 Wei et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Biotechnology Wei, Zhaohui Xu, Chao Wang, Juan Lu, Fengxia Bie, Xiaomei Lu, Zhaoxin Identification and characterization of Streptomyces flavogriseus NJ-4 as a novel producer of actinomycin D and holomycin |
title | Identification and characterization of Streptomyces flavogriseus NJ-4 as a novel producer of actinomycin D and holomycin |
title_full | Identification and characterization of Streptomyces flavogriseus NJ-4 as a novel producer of actinomycin D and holomycin |
title_fullStr | Identification and characterization of Streptomyces flavogriseus NJ-4 as a novel producer of actinomycin D and holomycin |
title_full_unstemmed | Identification and characterization of Streptomyces flavogriseus NJ-4 as a novel producer of actinomycin D and holomycin |
title_short | Identification and characterization of Streptomyces flavogriseus NJ-4 as a novel producer of actinomycin D and holomycin |
title_sort | identification and characterization of streptomyces flavogriseus nj-4 as a novel producer of actinomycin d and holomycin |
topic | Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520960/ https://www.ncbi.nlm.nih.gov/pubmed/28740758 http://dx.doi.org/10.7717/peerj.3601 |
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