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In situ visualization of glycoside hydrolase family 92 genes in marine flavobacteria

Gene clusters rich in carbohydrate-active enzymes within Flavobacteriia genera provide a competitiveness for their hosts to degrade diatom-derived polysaccharides. One such widely distributed polysaccharide is glucuronomannan, a main cell wall component of diatoms. A conserved gene cluster putativel...

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Autores principales: Zeugner, Laura E., Krüger, Karen, Barrero-Canosa, Jimena, Amann, Rudolf I., Fuchs, Bernhard M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723552/
https://www.ncbi.nlm.nih.gov/pubmed/37938716
http://dx.doi.org/10.1038/s43705-021-00082-4
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author Zeugner, Laura E.
Krüger, Karen
Barrero-Canosa, Jimena
Amann, Rudolf I.
Fuchs, Bernhard M.
author_facet Zeugner, Laura E.
Krüger, Karen
Barrero-Canosa, Jimena
Amann, Rudolf I.
Fuchs, Bernhard M.
author_sort Zeugner, Laura E.
collection PubMed
description Gene clusters rich in carbohydrate-active enzymes within Flavobacteriia genera provide a competitiveness for their hosts to degrade diatom-derived polysaccharides. One such widely distributed polysaccharide is glucuronomannan, a main cell wall component of diatoms. A conserved gene cluster putatively degrading glucuronomannan was found previously among various flavobacterial taxa in marine metagenomes. Here, we aimed to visualize two glycoside hydrolase family 92 genes coding for α-mannosidases with fluorescently-labeled polynucleotide probes using direct-geneFISH. Reliable in situ localization of single-copy genes was achieved with an efficiency up to 74% not only in the flavobacterial strains Polaribacter Hel1_33_49 and Formosa Hel1_33_131 but also in planktonic samples from the North Sea. In combination with high-resolution microscopy, direct-geneFISH gave visual evidence of the contrasting lifestyles of closely related Polaribacter species in those samples and allowed for the determination of gene distribution among attached and free-living cells. We also detected highly similar GH92 genes in yet unidentified taxa by broadening probe specificities, enabling a visualization of the functional trait in subpopulations across the borders of species and genera. Such a quantitative insight into the niche separation of flavobacterial taxa complements our understanding of the ecology of polysaccharide-degrading bacteria beyond omics-based techniques on a single-cell level.
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spelling pubmed-97235522023-01-04 In situ visualization of glycoside hydrolase family 92 genes in marine flavobacteria Zeugner, Laura E. Krüger, Karen Barrero-Canosa, Jimena Amann, Rudolf I. Fuchs, Bernhard M. ISME Commun Article Gene clusters rich in carbohydrate-active enzymes within Flavobacteriia genera provide a competitiveness for their hosts to degrade diatom-derived polysaccharides. One such widely distributed polysaccharide is glucuronomannan, a main cell wall component of diatoms. A conserved gene cluster putatively degrading glucuronomannan was found previously among various flavobacterial taxa in marine metagenomes. Here, we aimed to visualize two glycoside hydrolase family 92 genes coding for α-mannosidases with fluorescently-labeled polynucleotide probes using direct-geneFISH. Reliable in situ localization of single-copy genes was achieved with an efficiency up to 74% not only in the flavobacterial strains Polaribacter Hel1_33_49 and Formosa Hel1_33_131 but also in planktonic samples from the North Sea. In combination with high-resolution microscopy, direct-geneFISH gave visual evidence of the contrasting lifestyles of closely related Polaribacter species in those samples and allowed for the determination of gene distribution among attached and free-living cells. We also detected highly similar GH92 genes in yet unidentified taxa by broadening probe specificities, enabling a visualization of the functional trait in subpopulations across the borders of species and genera. Such a quantitative insight into the niche separation of flavobacterial taxa complements our understanding of the ecology of polysaccharide-degrading bacteria beyond omics-based techniques on a single-cell level. Nature Publishing Group UK 2021-12-18 /pmc/articles/PMC9723552/ /pubmed/37938716 http://dx.doi.org/10.1038/s43705-021-00082-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zeugner, Laura E.
Krüger, Karen
Barrero-Canosa, Jimena
Amann, Rudolf I.
Fuchs, Bernhard M.
In situ visualization of glycoside hydrolase family 92 genes in marine flavobacteria
title In situ visualization of glycoside hydrolase family 92 genes in marine flavobacteria
title_full In situ visualization of glycoside hydrolase family 92 genes in marine flavobacteria
title_fullStr In situ visualization of glycoside hydrolase family 92 genes in marine flavobacteria
title_full_unstemmed In situ visualization of glycoside hydrolase family 92 genes in marine flavobacteria
title_short In situ visualization of glycoside hydrolase family 92 genes in marine flavobacteria
title_sort in situ visualization of glycoside hydrolase family 92 genes in marine flavobacteria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723552/
https://www.ncbi.nlm.nih.gov/pubmed/37938716
http://dx.doi.org/10.1038/s43705-021-00082-4
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