Cargando…

Decomposition of plant‐sourced carbon compounds by heterotrophic betaproteobacteria isolated from a tropical Costa Rican bromeliad

Betaproteobacteria were the most common isolates from the water‐filled tank of a Costa Rican bromeliad. Isolates included eight species from the orders Neisseriales and Burkholderiales, with close relatives recovered previously from tropical soils, wetlands, freshwater, or in association with plants...

Descripción completa

Detalles Bibliográficos
Autores principales: Klann, Jane, McHenry, Alexandra, Montelongo, Carin, Goffredi, Shana K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905999/
https://www.ncbi.nlm.nih.gov/pubmed/26918550
http://dx.doi.org/10.1002/mbo3.344
_version_ 1782437337895010304
author Klann, Jane
McHenry, Alexandra
Montelongo, Carin
Goffredi, Shana K.
author_facet Klann, Jane
McHenry, Alexandra
Montelongo, Carin
Goffredi, Shana K.
author_sort Klann, Jane
collection PubMed
description Betaproteobacteria were the most common isolates from the water‐filled tank of a Costa Rican bromeliad. Isolates included eight species from the orders Neisseriales and Burkholderiales, with close relatives recovered previously from tropical soils, wetlands, freshwater, or in association with plants. Compared to close relatives, the isolates displayed high temperature and comparatively low pH optima, reflecting the tropical, acidic nature of the bromeliad tank. Bromeliad‐associated bacteria most closely related to Chromobacterium, Herbaspirillum, and Aquitalea were all isolated exclusively at pH 6, while Ralstonia, Cupriavidus, and three species of Burkholderia were isolated mostly at pH 4. Activity profiles for the isolates suggest pervasive capabilities for the breakdown of plant‐sourced organics, including d‐galacturonic acid, mannitol, d‐xylose, and l‐phenylalanine, also reflecting a niche dominated by decomposition of leaves from the overlying canopy, which become entrained in the tanks. Metabolic activity profiles were overlapping between the Burkholderiales, isolated at pH 4, and the Neisseriales, isolated at pH 6, suggesting that plant material decomposition, which is presumably the underlying process sustaining the tank community and possibly the plant itself, occurs in the tanks at both pH extremes. These results suggest that bromeliad‐associated betaproteobacteria may play an important role in the cycling of carbon in this unusual aquatic habitat.
format Online
Article
Text
id pubmed-4905999
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-49059992016-06-15 Decomposition of plant‐sourced carbon compounds by heterotrophic betaproteobacteria isolated from a tropical Costa Rican bromeliad Klann, Jane McHenry, Alexandra Montelongo, Carin Goffredi, Shana K. Microbiologyopen Original Research Betaproteobacteria were the most common isolates from the water‐filled tank of a Costa Rican bromeliad. Isolates included eight species from the orders Neisseriales and Burkholderiales, with close relatives recovered previously from tropical soils, wetlands, freshwater, or in association with plants. Compared to close relatives, the isolates displayed high temperature and comparatively low pH optima, reflecting the tropical, acidic nature of the bromeliad tank. Bromeliad‐associated bacteria most closely related to Chromobacterium, Herbaspirillum, and Aquitalea were all isolated exclusively at pH 6, while Ralstonia, Cupriavidus, and three species of Burkholderia were isolated mostly at pH 4. Activity profiles for the isolates suggest pervasive capabilities for the breakdown of plant‐sourced organics, including d‐galacturonic acid, mannitol, d‐xylose, and l‐phenylalanine, also reflecting a niche dominated by decomposition of leaves from the overlying canopy, which become entrained in the tanks. Metabolic activity profiles were overlapping between the Burkholderiales, isolated at pH 4, and the Neisseriales, isolated at pH 6, suggesting that plant material decomposition, which is presumably the underlying process sustaining the tank community and possibly the plant itself, occurs in the tanks at both pH extremes. These results suggest that bromeliad‐associated betaproteobacteria may play an important role in the cycling of carbon in this unusual aquatic habitat. John Wiley and Sons Inc. 2016-02-25 /pmc/articles/PMC4905999/ /pubmed/26918550 http://dx.doi.org/10.1002/mbo3.344 Text en © 2016 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Klann, Jane
McHenry, Alexandra
Montelongo, Carin
Goffredi, Shana K.
Decomposition of plant‐sourced carbon compounds by heterotrophic betaproteobacteria isolated from a tropical Costa Rican bromeliad
title Decomposition of plant‐sourced carbon compounds by heterotrophic betaproteobacteria isolated from a tropical Costa Rican bromeliad
title_full Decomposition of plant‐sourced carbon compounds by heterotrophic betaproteobacteria isolated from a tropical Costa Rican bromeliad
title_fullStr Decomposition of plant‐sourced carbon compounds by heterotrophic betaproteobacteria isolated from a tropical Costa Rican bromeliad
title_full_unstemmed Decomposition of plant‐sourced carbon compounds by heterotrophic betaproteobacteria isolated from a tropical Costa Rican bromeliad
title_short Decomposition of plant‐sourced carbon compounds by heterotrophic betaproteobacteria isolated from a tropical Costa Rican bromeliad
title_sort decomposition of plant‐sourced carbon compounds by heterotrophic betaproteobacteria isolated from a tropical costa rican bromeliad
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905999/
https://www.ncbi.nlm.nih.gov/pubmed/26918550
http://dx.doi.org/10.1002/mbo3.344
work_keys_str_mv AT klannjane decompositionofplantsourcedcarboncompoundsbyheterotrophicbetaproteobacteriaisolatedfromatropicalcostaricanbromeliad
AT mchenryalexandra decompositionofplantsourcedcarboncompoundsbyheterotrophicbetaproteobacteriaisolatedfromatropicalcostaricanbromeliad
AT montelongocarin decompositionofplantsourcedcarboncompoundsbyheterotrophicbetaproteobacteriaisolatedfromatropicalcostaricanbromeliad
AT goffredishanak decompositionofplantsourcedcarboncompoundsbyheterotrophicbetaproteobacteriaisolatedfromatropicalcostaricanbromeliad