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Genomic analysis of Caldalkalibacillus thermarum TA2.A1 reveals aerobic alkaliphilic metabolism and evolutionary hallmarks linking alkaliphilic bacteria and plant life

The aerobic thermoalkaliphile Caldalkalibacillus thermarum strain TA2.A1 is a member of a separate order of alkaliphilic bacteria closely related to the Bacillales order. Efforts to relate the genomic information of this evolutionary ancient organism to environmental adaptation have been thwarted by...

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Autores principales: de Jong, Samuel I., van den Broek, Marcel A., Merkel, Alexander Y., de la Torre Cortes, Pilar, Kalamorz, Falk, Cook, Gregory M., van Loosdrecht, Mark C. M., McMillan, Duncan G. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Japan 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7561548/
https://www.ncbi.nlm.nih.gov/pubmed/33030592
http://dx.doi.org/10.1007/s00792-020-01205-w
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author de Jong, Samuel I.
van den Broek, Marcel A.
Merkel, Alexander Y.
de la Torre Cortes, Pilar
Kalamorz, Falk
Cook, Gregory M.
van Loosdrecht, Mark C. M.
McMillan, Duncan G. G.
author_facet de Jong, Samuel I.
van den Broek, Marcel A.
Merkel, Alexander Y.
de la Torre Cortes, Pilar
Kalamorz, Falk
Cook, Gregory M.
van Loosdrecht, Mark C. M.
McMillan, Duncan G. G.
author_sort de Jong, Samuel I.
collection PubMed
description The aerobic thermoalkaliphile Caldalkalibacillus thermarum strain TA2.A1 is a member of a separate order of alkaliphilic bacteria closely related to the Bacillales order. Efforts to relate the genomic information of this evolutionary ancient organism to environmental adaptation have been thwarted by the inability to construct a complete genome. The existing draft genome is highly fragmented due to repetitive regions, and gaps between and over repetitive regions were unbridgeable. To address this, Oxford Nanopore Technology’s MinION allowed us to span these repeats through long reads, with over 6000-fold coverage. This resulted in a single 3.34 Mb circular chromosome. The profile of transporters and central metabolism gives insight into why the organism prefers glutamate over sucrose as carbon source. We propose that the deamination of glutamate allows alkalization of the immediate environment, an excellent example of how an extremophile modulates environmental conditions to suit its own requirements. Curiously, plant-like hallmark electron transfer enzymes and transporters are found throughout the genome, such as a cytochrome b(6)c(1) complex and a CO(2)-concentrating transporter. In addition, multiple self-splicing group II intron-encoded proteins closely aligning to those of a telomerase reverse transcriptase in Arabidopsis thaliana were revealed. Collectively, these features suggest an evolutionary relationship to plant life. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00792-020-01205-w) contains supplementary material, which is available to authorized users.
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spelling pubmed-75615482020-10-19 Genomic analysis of Caldalkalibacillus thermarum TA2.A1 reveals aerobic alkaliphilic metabolism and evolutionary hallmarks linking alkaliphilic bacteria and plant life de Jong, Samuel I. van den Broek, Marcel A. Merkel, Alexander Y. de la Torre Cortes, Pilar Kalamorz, Falk Cook, Gregory M. van Loosdrecht, Mark C. M. McMillan, Duncan G. G. Extremophiles Original Paper The aerobic thermoalkaliphile Caldalkalibacillus thermarum strain TA2.A1 is a member of a separate order of alkaliphilic bacteria closely related to the Bacillales order. Efforts to relate the genomic information of this evolutionary ancient organism to environmental adaptation have been thwarted by the inability to construct a complete genome. The existing draft genome is highly fragmented due to repetitive regions, and gaps between and over repetitive regions were unbridgeable. To address this, Oxford Nanopore Technology’s MinION allowed us to span these repeats through long reads, with over 6000-fold coverage. This resulted in a single 3.34 Mb circular chromosome. The profile of transporters and central metabolism gives insight into why the organism prefers glutamate over sucrose as carbon source. We propose that the deamination of glutamate allows alkalization of the immediate environment, an excellent example of how an extremophile modulates environmental conditions to suit its own requirements. Curiously, plant-like hallmark electron transfer enzymes and transporters are found throughout the genome, such as a cytochrome b(6)c(1) complex and a CO(2)-concentrating transporter. In addition, multiple self-splicing group II intron-encoded proteins closely aligning to those of a telomerase reverse transcriptase in Arabidopsis thaliana were revealed. Collectively, these features suggest an evolutionary relationship to plant life. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00792-020-01205-w) contains supplementary material, which is available to authorized users. Springer Japan 2020-10-08 2020 /pmc/articles/PMC7561548/ /pubmed/33030592 http://dx.doi.org/10.1007/s00792-020-01205-w Text en © The Author(s) 2020 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, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Paper
de Jong, Samuel I.
van den Broek, Marcel A.
Merkel, Alexander Y.
de la Torre Cortes, Pilar
Kalamorz, Falk
Cook, Gregory M.
van Loosdrecht, Mark C. M.
McMillan, Duncan G. G.
Genomic analysis of Caldalkalibacillus thermarum TA2.A1 reveals aerobic alkaliphilic metabolism and evolutionary hallmarks linking alkaliphilic bacteria and plant life
title Genomic analysis of Caldalkalibacillus thermarum TA2.A1 reveals aerobic alkaliphilic metabolism and evolutionary hallmarks linking alkaliphilic bacteria and plant life
title_full Genomic analysis of Caldalkalibacillus thermarum TA2.A1 reveals aerobic alkaliphilic metabolism and evolutionary hallmarks linking alkaliphilic bacteria and plant life
title_fullStr Genomic analysis of Caldalkalibacillus thermarum TA2.A1 reveals aerobic alkaliphilic metabolism and evolutionary hallmarks linking alkaliphilic bacteria and plant life
title_full_unstemmed Genomic analysis of Caldalkalibacillus thermarum TA2.A1 reveals aerobic alkaliphilic metabolism and evolutionary hallmarks linking alkaliphilic bacteria and plant life
title_short Genomic analysis of Caldalkalibacillus thermarum TA2.A1 reveals aerobic alkaliphilic metabolism and evolutionary hallmarks linking alkaliphilic bacteria and plant life
title_sort genomic analysis of caldalkalibacillus thermarum ta2.a1 reveals aerobic alkaliphilic metabolism and evolutionary hallmarks linking alkaliphilic bacteria and plant life
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7561548/
https://www.ncbi.nlm.nih.gov/pubmed/33030592
http://dx.doi.org/10.1007/s00792-020-01205-w
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