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Paulomycin G, a New Natural Product with Cytotoxic Activity against Tumor Cell Lines Produced by Deep-Sea Sediment Derived Micromonospora matsumotoense M-412 from the Avilés Canyon in the Cantabrian Sea
The present article describes a structurally novel natural product of the paulomycin family, designated as paulomycin G (1), obtained from the marine strain Micromonospora matsumotoense M-412, isolated from Cantabrian Sea sediments collected at 2000 m depth during an oceanographic expedition to the...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618410/ https://www.ncbi.nlm.nih.gov/pubmed/28846627 http://dx.doi.org/10.3390/md15090271 |
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author | Sarmiento-Vizcaíno, Aida Braña, Alfredo F. Pérez-Victoria, Ignacio Martín, Jesús de Pedro, Nuria de la Cruz, Mercedes Díaz, Caridad Vicente, Francisca Acuña, José L. Reyes, Fernando García, Luis A. Blanco, Gloria |
author_facet | Sarmiento-Vizcaíno, Aida Braña, Alfredo F. Pérez-Victoria, Ignacio Martín, Jesús de Pedro, Nuria de la Cruz, Mercedes Díaz, Caridad Vicente, Francisca Acuña, José L. Reyes, Fernando García, Luis A. Blanco, Gloria |
author_sort | Sarmiento-Vizcaíno, Aida |
collection | PubMed |
description | The present article describes a structurally novel natural product of the paulomycin family, designated as paulomycin G (1), obtained from the marine strain Micromonospora matsumotoense M-412, isolated from Cantabrian Sea sediments collected at 2000 m depth during an oceanographic expedition to the submarine Avilés Canyon. Paulomycin G is structurally unique since—to our knowledge—it is the first member of the paulomycin family of antibiotics lacking the paulomycose moiety. It is also the smallest bioactive paulomycin reported. Its structure was determined using HRMS and 1D and 2D NMR spectroscopy. This novel natural product displays strong cytotoxic activities against different human tumour cell lines, such as pancreatic adenocarcinoma (MiaPaca_2), breast adenocarcinoma (MCF-7), and hepatocellular carcinoma (HepG2). The compound did not show any significant bioactivity when tested against a panel of bacterial and fungal pathogens. |
format | Online Article Text |
id | pubmed-5618410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-56184102017-09-30 Paulomycin G, a New Natural Product with Cytotoxic Activity against Tumor Cell Lines Produced by Deep-Sea Sediment Derived Micromonospora matsumotoense M-412 from the Avilés Canyon in the Cantabrian Sea Sarmiento-Vizcaíno, Aida Braña, Alfredo F. Pérez-Victoria, Ignacio Martín, Jesús de Pedro, Nuria de la Cruz, Mercedes Díaz, Caridad Vicente, Francisca Acuña, José L. Reyes, Fernando García, Luis A. Blanco, Gloria Mar Drugs Article The present article describes a structurally novel natural product of the paulomycin family, designated as paulomycin G (1), obtained from the marine strain Micromonospora matsumotoense M-412, isolated from Cantabrian Sea sediments collected at 2000 m depth during an oceanographic expedition to the submarine Avilés Canyon. Paulomycin G is structurally unique since—to our knowledge—it is the first member of the paulomycin family of antibiotics lacking the paulomycose moiety. It is also the smallest bioactive paulomycin reported. Its structure was determined using HRMS and 1D and 2D NMR spectroscopy. This novel natural product displays strong cytotoxic activities against different human tumour cell lines, such as pancreatic adenocarcinoma (MiaPaca_2), breast adenocarcinoma (MCF-7), and hepatocellular carcinoma (HepG2). The compound did not show any significant bioactivity when tested against a panel of bacterial and fungal pathogens. MDPI 2017-08-28 /pmc/articles/PMC5618410/ /pubmed/28846627 http://dx.doi.org/10.3390/md15090271 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sarmiento-Vizcaíno, Aida Braña, Alfredo F. Pérez-Victoria, Ignacio Martín, Jesús de Pedro, Nuria de la Cruz, Mercedes Díaz, Caridad Vicente, Francisca Acuña, José L. Reyes, Fernando García, Luis A. Blanco, Gloria Paulomycin G, a New Natural Product with Cytotoxic Activity against Tumor Cell Lines Produced by Deep-Sea Sediment Derived Micromonospora matsumotoense M-412 from the Avilés Canyon in the Cantabrian Sea |
title | Paulomycin G, a New Natural Product with Cytotoxic Activity against Tumor Cell Lines Produced by Deep-Sea Sediment Derived Micromonospora matsumotoense M-412 from the Avilés Canyon in the Cantabrian Sea |
title_full | Paulomycin G, a New Natural Product with Cytotoxic Activity against Tumor Cell Lines Produced by Deep-Sea Sediment Derived Micromonospora matsumotoense M-412 from the Avilés Canyon in the Cantabrian Sea |
title_fullStr | Paulomycin G, a New Natural Product with Cytotoxic Activity against Tumor Cell Lines Produced by Deep-Sea Sediment Derived Micromonospora matsumotoense M-412 from the Avilés Canyon in the Cantabrian Sea |
title_full_unstemmed | Paulomycin G, a New Natural Product with Cytotoxic Activity against Tumor Cell Lines Produced by Deep-Sea Sediment Derived Micromonospora matsumotoense M-412 from the Avilés Canyon in the Cantabrian Sea |
title_short | Paulomycin G, a New Natural Product with Cytotoxic Activity against Tumor Cell Lines Produced by Deep-Sea Sediment Derived Micromonospora matsumotoense M-412 from the Avilés Canyon in the Cantabrian Sea |
title_sort | paulomycin g, a new natural product with cytotoxic activity against tumor cell lines produced by deep-sea sediment derived micromonospora matsumotoense m-412 from the avilés canyon in the cantabrian sea |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618410/ https://www.ncbi.nlm.nih.gov/pubmed/28846627 http://dx.doi.org/10.3390/md15090271 |
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