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Liquid Chromatography-Mass Spectrometry-Based Rapid Secondary-Metabolite Profiling of Marine Pseudoalteromonas sp. M2

The ocean is a rich resource of flora, fauna, and food. A wild-type bacterial strain showing confluent growth on marine agar with antibacterial activity was isolated from marine water, identified using 16S rDNA sequence analysis as Pseudoalteromonas sp., and designated as strain M2. This strain was...

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Autores principales: Kim, Woo Jung, Kim, Young Ok, Kim, Jin Hee, Nam, Bo-Hye, Kim, Dong-Gyun, An, Cheul Min, Lee, Jun Sik, Kim, Pan Soo, Lee, Hye Min, Oh, Joa-Sup, Lee, Jong Suk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4728520/
https://www.ncbi.nlm.nih.gov/pubmed/26805856
http://dx.doi.org/10.3390/md14010024
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author Kim, Woo Jung
Kim, Young Ok
Kim, Jin Hee
Nam, Bo-Hye
Kim, Dong-Gyun
An, Cheul Min
Lee, Jun Sik
Kim, Pan Soo
Lee, Hye Min
Oh, Joa-Sup
Lee, Jong Suk
author_facet Kim, Woo Jung
Kim, Young Ok
Kim, Jin Hee
Nam, Bo-Hye
Kim, Dong-Gyun
An, Cheul Min
Lee, Jun Sik
Kim, Pan Soo
Lee, Hye Min
Oh, Joa-Sup
Lee, Jong Suk
author_sort Kim, Woo Jung
collection PubMed
description The ocean is a rich resource of flora, fauna, and food. A wild-type bacterial strain showing confluent growth on marine agar with antibacterial activity was isolated from marine water, identified using 16S rDNA sequence analysis as Pseudoalteromonas sp., and designated as strain M2. This strain was found to produce various secondary metabolites including quinolone alkaloids. Using high-resolution mass spectrometry (MS) and nuclear magnetic resonance (NMR) analysis, we identified nine secondary metabolites of 4-hydroxy-2-alkylquinoline (pseudane-III, IV, V, VI, VII, VIII, IX, X, and XI). Additionally, this strain produced two novel, closely related compounds, 2-isopentylqunoline-4-one and 2-(2,3-dimetylbutyl)qunoline-4-(1H)-one, which have not been previously reported from marine bacteria. From the metabolites produced by Pseudoalteromonas sp. M2, 2-(2,3-dimethylbutyl)quinolin-4-one, pseudane-VI, and pseudane-VII inhibited melanin synthesis in Melan-A cells by 23.0%, 28.2%, and 42.7%, respectively, wherein pseudane-VII showed the highest inhibition at 8 µg/mL. The results of this study suggest that liquid chromatography (LC)-MS/MS-based metabolite screening effectively improves the efficiency of novel metabolite discovery. Additionally, these compounds are promising candidates for further bioactivity development.
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spelling pubmed-47285202016-02-08 Liquid Chromatography-Mass Spectrometry-Based Rapid Secondary-Metabolite Profiling of Marine Pseudoalteromonas sp. M2 Kim, Woo Jung Kim, Young Ok Kim, Jin Hee Nam, Bo-Hye Kim, Dong-Gyun An, Cheul Min Lee, Jun Sik Kim, Pan Soo Lee, Hye Min Oh, Joa-Sup Lee, Jong Suk Mar Drugs Article The ocean is a rich resource of flora, fauna, and food. A wild-type bacterial strain showing confluent growth on marine agar with antibacterial activity was isolated from marine water, identified using 16S rDNA sequence analysis as Pseudoalteromonas sp., and designated as strain M2. This strain was found to produce various secondary metabolites including quinolone alkaloids. Using high-resolution mass spectrometry (MS) and nuclear magnetic resonance (NMR) analysis, we identified nine secondary metabolites of 4-hydroxy-2-alkylquinoline (pseudane-III, IV, V, VI, VII, VIII, IX, X, and XI). Additionally, this strain produced two novel, closely related compounds, 2-isopentylqunoline-4-one and 2-(2,3-dimetylbutyl)qunoline-4-(1H)-one, which have not been previously reported from marine bacteria. From the metabolites produced by Pseudoalteromonas sp. M2, 2-(2,3-dimethylbutyl)quinolin-4-one, pseudane-VI, and pseudane-VII inhibited melanin synthesis in Melan-A cells by 23.0%, 28.2%, and 42.7%, respectively, wherein pseudane-VII showed the highest inhibition at 8 µg/mL. The results of this study suggest that liquid chromatography (LC)-MS/MS-based metabolite screening effectively improves the efficiency of novel metabolite discovery. Additionally, these compounds are promising candidates for further bioactivity development. MDPI 2016-01-20 /pmc/articles/PMC4728520/ /pubmed/26805856 http://dx.doi.org/10.3390/md14010024 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Woo Jung
Kim, Young Ok
Kim, Jin Hee
Nam, Bo-Hye
Kim, Dong-Gyun
An, Cheul Min
Lee, Jun Sik
Kim, Pan Soo
Lee, Hye Min
Oh, Joa-Sup
Lee, Jong Suk
Liquid Chromatography-Mass Spectrometry-Based Rapid Secondary-Metabolite Profiling of Marine Pseudoalteromonas sp. M2
title Liquid Chromatography-Mass Spectrometry-Based Rapid Secondary-Metabolite Profiling of Marine Pseudoalteromonas sp. M2
title_full Liquid Chromatography-Mass Spectrometry-Based Rapid Secondary-Metabolite Profiling of Marine Pseudoalteromonas sp. M2
title_fullStr Liquid Chromatography-Mass Spectrometry-Based Rapid Secondary-Metabolite Profiling of Marine Pseudoalteromonas sp. M2
title_full_unstemmed Liquid Chromatography-Mass Spectrometry-Based Rapid Secondary-Metabolite Profiling of Marine Pseudoalteromonas sp. M2
title_short Liquid Chromatography-Mass Spectrometry-Based Rapid Secondary-Metabolite Profiling of Marine Pseudoalteromonas sp. M2
title_sort liquid chromatography-mass spectrometry-based rapid secondary-metabolite profiling of marine pseudoalteromonas sp. m2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4728520/
https://www.ncbi.nlm.nih.gov/pubmed/26805856
http://dx.doi.org/10.3390/md14010024
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