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Genomic Reconstruction of Carbohydrate Utilization Capacities in Microbial-Mat Derived Consortia

Two nearly identical unicyanobacterial consortia (UCC) were previously isolated from benthic microbial mats that occur in a heliothermal saline lake in northern Washington State. Carbohydrates are a primary source of carbon and energy for most heterotrophic bacteria. Since CO(2) is the only carbon s...

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Autores principales: Leyn, Semen A., Maezato, Yukari, Romine, Margaret F., Rodionov, Dmitry A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507952/
https://www.ncbi.nlm.nih.gov/pubmed/28751880
http://dx.doi.org/10.3389/fmicb.2017.01304
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author Leyn, Semen A.
Maezato, Yukari
Romine, Margaret F.
Rodionov, Dmitry A.
author_facet Leyn, Semen A.
Maezato, Yukari
Romine, Margaret F.
Rodionov, Dmitry A.
author_sort Leyn, Semen A.
collection PubMed
description Two nearly identical unicyanobacterial consortia (UCC) were previously isolated from benthic microbial mats that occur in a heliothermal saline lake in northern Washington State. Carbohydrates are a primary source of carbon and energy for most heterotrophic bacteria. Since CO(2) is the only carbon source provided, the cyanobacterium must provide a source of carbon to the heterotrophs. Available genomic sequences for all members of the UCC provide opportunity to investigate the metabolic routes of carbon transfer between autotroph and heterotrophs. Here, we applied a subsystem-based comparative genomics approach to reconstruct carbohydrate utilization pathways and identify glycohydrolytic enzymes, carbohydrate transporters and pathway-specific transcriptional regulators in 17 heterotrophic members of the UCC. The reconstructed metabolic pathways include 800 genes, near a one-fourth of which encode enzymes, transporters and regulators with newly assigned metabolic functions resulting in discovery of novel functional variants of carbohydrate utilization pathways. The in silico analysis revealed the utilization capabilities for 40 carbohydrates and their derivatives. Two Halomonas species demonstrated the largest number of sugar catabolic pathways. Trehalose, sucrose, maltose, glucose, and beta-glucosides are the most commonly utilized saccharides in this community. Reconstructed regulons for global regulators HexR and CceR include central carbohydrate metabolism genes in the members of Gammaproteobacteria and Alphaproteobacteria, respectively. Genomics analyses were supplemented by experimental characterization of metabolic phenotypes in four isolates derived from the consortia. Measurements of isolate growth on the defined medium supplied with individual carbohydrates confirmed most of the predicted catabolic phenotypes. Not all consortia members use carbohydrates and only a few use complex polysaccharides suggesting a hierarchical carbon flow from cyanobacteria to each heterotroph. In summary, the genomics-based identification of carbohydrate utilization capabilities provides a basis for future experimental studies of carbon flow in UCC.
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spelling pubmed-55079522017-07-27 Genomic Reconstruction of Carbohydrate Utilization Capacities in Microbial-Mat Derived Consortia Leyn, Semen A. Maezato, Yukari Romine, Margaret F. Rodionov, Dmitry A. Front Microbiol Microbiology Two nearly identical unicyanobacterial consortia (UCC) were previously isolated from benthic microbial mats that occur in a heliothermal saline lake in northern Washington State. Carbohydrates are a primary source of carbon and energy for most heterotrophic bacteria. Since CO(2) is the only carbon source provided, the cyanobacterium must provide a source of carbon to the heterotrophs. Available genomic sequences for all members of the UCC provide opportunity to investigate the metabolic routes of carbon transfer between autotroph and heterotrophs. Here, we applied a subsystem-based comparative genomics approach to reconstruct carbohydrate utilization pathways and identify glycohydrolytic enzymes, carbohydrate transporters and pathway-specific transcriptional regulators in 17 heterotrophic members of the UCC. The reconstructed metabolic pathways include 800 genes, near a one-fourth of which encode enzymes, transporters and regulators with newly assigned metabolic functions resulting in discovery of novel functional variants of carbohydrate utilization pathways. The in silico analysis revealed the utilization capabilities for 40 carbohydrates and their derivatives. Two Halomonas species demonstrated the largest number of sugar catabolic pathways. Trehalose, sucrose, maltose, glucose, and beta-glucosides are the most commonly utilized saccharides in this community. Reconstructed regulons for global regulators HexR and CceR include central carbohydrate metabolism genes in the members of Gammaproteobacteria and Alphaproteobacteria, respectively. Genomics analyses were supplemented by experimental characterization of metabolic phenotypes in four isolates derived from the consortia. Measurements of isolate growth on the defined medium supplied with individual carbohydrates confirmed most of the predicted catabolic phenotypes. Not all consortia members use carbohydrates and only a few use complex polysaccharides suggesting a hierarchical carbon flow from cyanobacteria to each heterotroph. In summary, the genomics-based identification of carbohydrate utilization capabilities provides a basis for future experimental studies of carbon flow in UCC. Frontiers Media S.A. 2017-07-13 /pmc/articles/PMC5507952/ /pubmed/28751880 http://dx.doi.org/10.3389/fmicb.2017.01304 Text en Copyright © 2017 Leyn, Maezato, Romine and Rodionov. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Leyn, Semen A.
Maezato, Yukari
Romine, Margaret F.
Rodionov, Dmitry A.
Genomic Reconstruction of Carbohydrate Utilization Capacities in Microbial-Mat Derived Consortia
title Genomic Reconstruction of Carbohydrate Utilization Capacities in Microbial-Mat Derived Consortia
title_full Genomic Reconstruction of Carbohydrate Utilization Capacities in Microbial-Mat Derived Consortia
title_fullStr Genomic Reconstruction of Carbohydrate Utilization Capacities in Microbial-Mat Derived Consortia
title_full_unstemmed Genomic Reconstruction of Carbohydrate Utilization Capacities in Microbial-Mat Derived Consortia
title_short Genomic Reconstruction of Carbohydrate Utilization Capacities in Microbial-Mat Derived Consortia
title_sort genomic reconstruction of carbohydrate utilization capacities in microbial-mat derived consortia
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507952/
https://www.ncbi.nlm.nih.gov/pubmed/28751880
http://dx.doi.org/10.3389/fmicb.2017.01304
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