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Polyhydroxyalkanoate (PHA) Granules Have no Phospholipids

Polyhydroxybutyrate (PHB) granules, also designated as carbonosomes, are supra-molecular complexes in prokaryotes consisting of a PHB polymer core and a surface layer of structural and functional proteins. The presence of suspected phospholipids in the surface layer is based on in vitro data of isol...

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Autores principales: Bresan, Stephanie, Sznajder, Anna, Hauf, Waldemar, Forchhammer, Karl, Pfeiffer, Daniel, Jendrossek, Dieter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4879537/
https://www.ncbi.nlm.nih.gov/pubmed/27222167
http://dx.doi.org/10.1038/srep26612
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author Bresan, Stephanie
Sznajder, Anna
Hauf, Waldemar
Forchhammer, Karl
Pfeiffer, Daniel
Jendrossek, Dieter
author_facet Bresan, Stephanie
Sznajder, Anna
Hauf, Waldemar
Forchhammer, Karl
Pfeiffer, Daniel
Jendrossek, Dieter
author_sort Bresan, Stephanie
collection PubMed
description Polyhydroxybutyrate (PHB) granules, also designated as carbonosomes, are supra-molecular complexes in prokaryotes consisting of a PHB polymer core and a surface layer of structural and functional proteins. The presence of suspected phospholipids in the surface layer is based on in vitro data of isolated PHB granules and is often shown in cartoons of the PHB granule structure in reviews on PHB metabolism. However, the in vivo presence of a phospholipid layer has never been demonstrated. We addressed this topic by the expression of fusion proteins of DsRed2EC and other fluorescent proteins with the phospholipid-binding domain (LactC2) of lactadherin in three model organisms. The fusion proteins specifically localized at the cell membrane of Ralstonia eutropha but did not co-localize with PHB granules. The same result was obtained for Pseudomonas putida, a species that accumulates another type of polyhydroxyalkanoate (PHA) granules related to PHB. Notably, DsRed2EC-LactC2 expressed in Magnetospirillum gryphiswaldense was detected at the position of membrane-enclosed magnetosome chains and at the cytoplasmic membrane but not at PHB granules. In conclusion, the carbonosomes of representatives of α-proteobacteria, β-proteobacteria and γ-proteobacteria have no phospholipids in vivo and we postulate that the PHB/PHA granule surface layers in natural producers generally are free of phospholipids and consist of proteins only.
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spelling pubmed-48795372016-06-08 Polyhydroxyalkanoate (PHA) Granules Have no Phospholipids Bresan, Stephanie Sznajder, Anna Hauf, Waldemar Forchhammer, Karl Pfeiffer, Daniel Jendrossek, Dieter Sci Rep Article Polyhydroxybutyrate (PHB) granules, also designated as carbonosomes, are supra-molecular complexes in prokaryotes consisting of a PHB polymer core and a surface layer of structural and functional proteins. The presence of suspected phospholipids in the surface layer is based on in vitro data of isolated PHB granules and is often shown in cartoons of the PHB granule structure in reviews on PHB metabolism. However, the in vivo presence of a phospholipid layer has never been demonstrated. We addressed this topic by the expression of fusion proteins of DsRed2EC and other fluorescent proteins with the phospholipid-binding domain (LactC2) of lactadherin in three model organisms. The fusion proteins specifically localized at the cell membrane of Ralstonia eutropha but did not co-localize with PHB granules. The same result was obtained for Pseudomonas putida, a species that accumulates another type of polyhydroxyalkanoate (PHA) granules related to PHB. Notably, DsRed2EC-LactC2 expressed in Magnetospirillum gryphiswaldense was detected at the position of membrane-enclosed magnetosome chains and at the cytoplasmic membrane but not at PHB granules. In conclusion, the carbonosomes of representatives of α-proteobacteria, β-proteobacteria and γ-proteobacteria have no phospholipids in vivo and we postulate that the PHB/PHA granule surface layers in natural producers generally are free of phospholipids and consist of proteins only. Nature Publishing Group 2016-05-25 /pmc/articles/PMC4879537/ /pubmed/27222167 http://dx.doi.org/10.1038/srep26612 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Bresan, Stephanie
Sznajder, Anna
Hauf, Waldemar
Forchhammer, Karl
Pfeiffer, Daniel
Jendrossek, Dieter
Polyhydroxyalkanoate (PHA) Granules Have no Phospholipids
title Polyhydroxyalkanoate (PHA) Granules Have no Phospholipids
title_full Polyhydroxyalkanoate (PHA) Granules Have no Phospholipids
title_fullStr Polyhydroxyalkanoate (PHA) Granules Have no Phospholipids
title_full_unstemmed Polyhydroxyalkanoate (PHA) Granules Have no Phospholipids
title_short Polyhydroxyalkanoate (PHA) Granules Have no Phospholipids
title_sort polyhydroxyalkanoate (pha) granules have no phospholipids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4879537/
https://www.ncbi.nlm.nih.gov/pubmed/27222167
http://dx.doi.org/10.1038/srep26612
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