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Amycolatomycins A and B, Cyclic Hexapeptides Isolated from an Amycolatopsis sp. 195334CR

The rare actinobacterium Amycolatopsis sp. strain 195334CR was found to produce previously undescribed cyclic hexapeptides, which we named amycolatomycin A and B (1 and 2). Their planar structures were determined by high-resolution mass spectrometry as well as extensive 1D and 2D NMR spectroscopy, w...

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Autores principales: Primahana, Gian, Risdian, Chandra, Mozef, Tjandrawati, Wink, Joachim, Surup, Frank, Stadler, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8002008/
https://www.ncbi.nlm.nih.gov/pubmed/33807584
http://dx.doi.org/10.3390/antibiotics10030261
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author Primahana, Gian
Risdian, Chandra
Mozef, Tjandrawati
Wink, Joachim
Surup, Frank
Stadler, Marc
author_facet Primahana, Gian
Risdian, Chandra
Mozef, Tjandrawati
Wink, Joachim
Surup, Frank
Stadler, Marc
author_sort Primahana, Gian
collection PubMed
description The rare actinobacterium Amycolatopsis sp. strain 195334CR was found to produce previously undescribed cyclic hexapeptides, which we named amycolatomycin A and B (1 and 2). Their planar structures were determined by high-resolution mass spectrometry as well as extensive 1D and 2D NMR spectroscopy, while the absolute stereochemistry of its amino acids were determined by Marfey’s method. Moreover, 1 and 2 differ by the incorporation of l-Ile and l-allo-Ile, respectively, whose FDVA (Nα-(2,4-Dinitro-5-fluorphenyl)-L-valinamide) derivatives were separated on a C(4) column. Their hallmark in common is a unique 2,6-dichloro-tryptophan amino acid unit. Amycolatomycin A (1) exhibited weak activity against Bacillus subtilis DSM 10 (minimum inhibitory concentration (MIC) = 33.4 µg/mL).
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spelling pubmed-80020082021-03-28 Amycolatomycins A and B, Cyclic Hexapeptides Isolated from an Amycolatopsis sp. 195334CR Primahana, Gian Risdian, Chandra Mozef, Tjandrawati Wink, Joachim Surup, Frank Stadler, Marc Antibiotics (Basel) Article The rare actinobacterium Amycolatopsis sp. strain 195334CR was found to produce previously undescribed cyclic hexapeptides, which we named amycolatomycin A and B (1 and 2). Their planar structures were determined by high-resolution mass spectrometry as well as extensive 1D and 2D NMR spectroscopy, while the absolute stereochemistry of its amino acids were determined by Marfey’s method. Moreover, 1 and 2 differ by the incorporation of l-Ile and l-allo-Ile, respectively, whose FDVA (Nα-(2,4-Dinitro-5-fluorphenyl)-L-valinamide) derivatives were separated on a C(4) column. Their hallmark in common is a unique 2,6-dichloro-tryptophan amino acid unit. Amycolatomycin A (1) exhibited weak activity against Bacillus subtilis DSM 10 (minimum inhibitory concentration (MIC) = 33.4 µg/mL). MDPI 2021-03-05 /pmc/articles/PMC8002008/ /pubmed/33807584 http://dx.doi.org/10.3390/antibiotics10030261 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Primahana, Gian
Risdian, Chandra
Mozef, Tjandrawati
Wink, Joachim
Surup, Frank
Stadler, Marc
Amycolatomycins A and B, Cyclic Hexapeptides Isolated from an Amycolatopsis sp. 195334CR
title Amycolatomycins A and B, Cyclic Hexapeptides Isolated from an Amycolatopsis sp. 195334CR
title_full Amycolatomycins A and B, Cyclic Hexapeptides Isolated from an Amycolatopsis sp. 195334CR
title_fullStr Amycolatomycins A and B, Cyclic Hexapeptides Isolated from an Amycolatopsis sp. 195334CR
title_full_unstemmed Amycolatomycins A and B, Cyclic Hexapeptides Isolated from an Amycolatopsis sp. 195334CR
title_short Amycolatomycins A and B, Cyclic Hexapeptides Isolated from an Amycolatopsis sp. 195334CR
title_sort amycolatomycins a and b, cyclic hexapeptides isolated from an amycolatopsis sp. 195334cr
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8002008/
https://www.ncbi.nlm.nih.gov/pubmed/33807584
http://dx.doi.org/10.3390/antibiotics10030261
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