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The polyene antifungal candicidin is selectively packaged into membrane vesicles in Streptomyces S4

In recent years, much attention has been focused on the biogenesis, engineering and utilisation of outer membrane vesicles (OMVs) in Gram-negative bacteria in a range of environments and niches. While the precise mechanism of biogenesis is unknown, it is focused on the modification of the Gram-negat...

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Autores principales: Blackburn, Sarah A., Shepherd, Mark, Robinson, Gary K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054904/
https://www.ncbi.nlm.nih.gov/pubmed/35488016
http://dx.doi.org/10.1007/s00203-022-02906-w
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author Blackburn, Sarah A.
Shepherd, Mark
Robinson, Gary K.
author_facet Blackburn, Sarah A.
Shepherd, Mark
Robinson, Gary K.
author_sort Blackburn, Sarah A.
collection PubMed
description In recent years, much attention has been focused on the biogenesis, engineering and utilisation of outer membrane vesicles (OMVs) in Gram-negative bacteria in a range of environments and niches. While the precise mechanism of biogenesis is unknown, it is focused on the modification of the Gram-negative cell wall to facilitate blebbing at sites of weakness in and around the characteristically thin peptidoglycan layer within the periplasm. Here, we investigate the biogenesis of membrane vesicles (MVs) in the Gram-positive organism Streptomyces albus S4 (Seipke et al. J Bacteriol 193:4270–4271, 2011 and Fazal et al. Antonie Van Leeuwenhoek 113:511–520, 2020). The S. albus S4 strain is an antifungal (candicidin and antimycin) producing organism that was isolated from attine ants (Barke et al. BMC Biol 8:109, 2010). The biogenesis and characterisation of S. albus S4 MVs is demonstrated using the wild-type (WT) and mutant strains ΔantC (no antimycin production) ΔfscC (no candicidin production) and ΔantC ΔfscC (produces neither antimycin nor candicidin). Here, we have shown that the S. albus S4 strain produces MVs and that these are comprised of both specific protein profiles and secondary metabolites, with a clear demonstration of the ability to selectively package one antifungal (candicidin) but not the other (antimycin). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00203-022-02906-w.
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spelling pubmed-90549042022-05-07 The polyene antifungal candicidin is selectively packaged into membrane vesicles in Streptomyces S4 Blackburn, Sarah A. Shepherd, Mark Robinson, Gary K. Arch Microbiol Original Paper In recent years, much attention has been focused on the biogenesis, engineering and utilisation of outer membrane vesicles (OMVs) in Gram-negative bacteria in a range of environments and niches. While the precise mechanism of biogenesis is unknown, it is focused on the modification of the Gram-negative cell wall to facilitate blebbing at sites of weakness in and around the characteristically thin peptidoglycan layer within the periplasm. Here, we investigate the biogenesis of membrane vesicles (MVs) in the Gram-positive organism Streptomyces albus S4 (Seipke et al. J Bacteriol 193:4270–4271, 2011 and Fazal et al. Antonie Van Leeuwenhoek 113:511–520, 2020). The S. albus S4 strain is an antifungal (candicidin and antimycin) producing organism that was isolated from attine ants (Barke et al. BMC Biol 8:109, 2010). The biogenesis and characterisation of S. albus S4 MVs is demonstrated using the wild-type (WT) and mutant strains ΔantC (no antimycin production) ΔfscC (no candicidin production) and ΔantC ΔfscC (produces neither antimycin nor candicidin). Here, we have shown that the S. albus S4 strain produces MVs and that these are comprised of both specific protein profiles and secondary metabolites, with a clear demonstration of the ability to selectively package one antifungal (candicidin) but not the other (antimycin). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00203-022-02906-w. Springer Berlin Heidelberg 2022-04-30 2022 /pmc/articles/PMC9054904/ /pubmed/35488016 http://dx.doi.org/10.1007/s00203-022-02906-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visithttp://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Paper
Blackburn, Sarah A.
Shepherd, Mark
Robinson, Gary K.
The polyene antifungal candicidin is selectively packaged into membrane vesicles in Streptomyces S4
title The polyene antifungal candicidin is selectively packaged into membrane vesicles in Streptomyces S4
title_full The polyene antifungal candicidin is selectively packaged into membrane vesicles in Streptomyces S4
title_fullStr The polyene antifungal candicidin is selectively packaged into membrane vesicles in Streptomyces S4
title_full_unstemmed The polyene antifungal candicidin is selectively packaged into membrane vesicles in Streptomyces S4
title_short The polyene antifungal candicidin is selectively packaged into membrane vesicles in Streptomyces S4
title_sort polyene antifungal candicidin is selectively packaged into membrane vesicles in streptomyces s4
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054904/
https://www.ncbi.nlm.nih.gov/pubmed/35488016
http://dx.doi.org/10.1007/s00203-022-02906-w
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