Cargando…
In-Situ Metatranscriptomic Analyses Reveal the Metabolic Flexibility of the Thermophilic Anoxygenic Photosynthetic Bacterium Chloroflexus aggregans in a Hot Spring Cyanobacteria-Dominated Microbial Mat
Chloroflexus aggregans is a metabolically versatile, thermophilic, anoxygenic phototrophic member of the phylum Chloroflexota (formerly Chloroflexi), which can grow photoheterotrophically, photoautotrophically, chemoheterotrophically, and chemoautotrophically. In hot spring-associated microbial mats...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8004040/ https://www.ncbi.nlm.nih.gov/pubmed/33801086 http://dx.doi.org/10.3390/microorganisms9030652 |
_version_ | 1783671831339728896 |
---|---|
author | Kawai, Shigeru Martinez, Joval N. Lichtenberg, Mads Trampe, Erik Kühl, Michael Tank, Marcus Haruta, Shin Nishihara, Arisa Hanada, Satoshi Thiel, Vera |
author_facet | Kawai, Shigeru Martinez, Joval N. Lichtenberg, Mads Trampe, Erik Kühl, Michael Tank, Marcus Haruta, Shin Nishihara, Arisa Hanada, Satoshi Thiel, Vera |
author_sort | Kawai, Shigeru |
collection | PubMed |
description | Chloroflexus aggregans is a metabolically versatile, thermophilic, anoxygenic phototrophic member of the phylum Chloroflexota (formerly Chloroflexi), which can grow photoheterotrophically, photoautotrophically, chemoheterotrophically, and chemoautotrophically. In hot spring-associated microbial mats, C. aggregans co-exists with oxygenic cyanobacteria under dynamic micro-environmental conditions. To elucidate the predominant growth modes of C. aggregans, relative transcription levels of energy metabolism- and CO(2) fixation-related genes were studied in Nakabusa Hot Springs microbial mats over a diel cycle and correlated with microscale in situ measurements of O(2) and light. Metatranscriptomic analyses indicated two periods with different modes of energy metabolism of C. aggregans: (1) phototrophy around midday and (2) chemotrophy in the early morning hours. During midday, C. aggregans mainly employed photoheterotrophy when the microbial mats were hyperoxic (400–800 µmol L(−1) O(2)). In the early morning hours, relative transcription peaks of genes encoding uptake hydrogenase, key enzymes for carbon fixation, respiratory complexes as well as enzymes for TCA cycle and acetate uptake suggest an aerobic chemomixotrophic lifestyle. This is the first in situ study of the versatile energy metabolism of C. aggregans based on gene transcription patterns. The results provide novel insights into the metabolic flexibility of these filamentous anoxygenic phototrophs that thrive under dynamic environmental conditions. |
format | Online Article Text |
id | pubmed-8004040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80040402021-03-28 In-Situ Metatranscriptomic Analyses Reveal the Metabolic Flexibility of the Thermophilic Anoxygenic Photosynthetic Bacterium Chloroflexus aggregans in a Hot Spring Cyanobacteria-Dominated Microbial Mat Kawai, Shigeru Martinez, Joval N. Lichtenberg, Mads Trampe, Erik Kühl, Michael Tank, Marcus Haruta, Shin Nishihara, Arisa Hanada, Satoshi Thiel, Vera Microorganisms Article Chloroflexus aggregans is a metabolically versatile, thermophilic, anoxygenic phototrophic member of the phylum Chloroflexota (formerly Chloroflexi), which can grow photoheterotrophically, photoautotrophically, chemoheterotrophically, and chemoautotrophically. In hot spring-associated microbial mats, C. aggregans co-exists with oxygenic cyanobacteria under dynamic micro-environmental conditions. To elucidate the predominant growth modes of C. aggregans, relative transcription levels of energy metabolism- and CO(2) fixation-related genes were studied in Nakabusa Hot Springs microbial mats over a diel cycle and correlated with microscale in situ measurements of O(2) and light. Metatranscriptomic analyses indicated two periods with different modes of energy metabolism of C. aggregans: (1) phototrophy around midday and (2) chemotrophy in the early morning hours. During midday, C. aggregans mainly employed photoheterotrophy when the microbial mats were hyperoxic (400–800 µmol L(−1) O(2)). In the early morning hours, relative transcription peaks of genes encoding uptake hydrogenase, key enzymes for carbon fixation, respiratory complexes as well as enzymes for TCA cycle and acetate uptake suggest an aerobic chemomixotrophic lifestyle. This is the first in situ study of the versatile energy metabolism of C. aggregans based on gene transcription patterns. The results provide novel insights into the metabolic flexibility of these filamentous anoxygenic phototrophs that thrive under dynamic environmental conditions. MDPI 2021-03-21 /pmc/articles/PMC8004040/ /pubmed/33801086 http://dx.doi.org/10.3390/microorganisms9030652 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Kawai, Shigeru Martinez, Joval N. Lichtenberg, Mads Trampe, Erik Kühl, Michael Tank, Marcus Haruta, Shin Nishihara, Arisa Hanada, Satoshi Thiel, Vera In-Situ Metatranscriptomic Analyses Reveal the Metabolic Flexibility of the Thermophilic Anoxygenic Photosynthetic Bacterium Chloroflexus aggregans in a Hot Spring Cyanobacteria-Dominated Microbial Mat |
title | In-Situ Metatranscriptomic Analyses Reveal the Metabolic Flexibility of the Thermophilic Anoxygenic Photosynthetic Bacterium Chloroflexus aggregans in a Hot Spring Cyanobacteria-Dominated Microbial Mat |
title_full | In-Situ Metatranscriptomic Analyses Reveal the Metabolic Flexibility of the Thermophilic Anoxygenic Photosynthetic Bacterium Chloroflexus aggregans in a Hot Spring Cyanobacteria-Dominated Microbial Mat |
title_fullStr | In-Situ Metatranscriptomic Analyses Reveal the Metabolic Flexibility of the Thermophilic Anoxygenic Photosynthetic Bacterium Chloroflexus aggregans in a Hot Spring Cyanobacteria-Dominated Microbial Mat |
title_full_unstemmed | In-Situ Metatranscriptomic Analyses Reveal the Metabolic Flexibility of the Thermophilic Anoxygenic Photosynthetic Bacterium Chloroflexus aggregans in a Hot Spring Cyanobacteria-Dominated Microbial Mat |
title_short | In-Situ Metatranscriptomic Analyses Reveal the Metabolic Flexibility of the Thermophilic Anoxygenic Photosynthetic Bacterium Chloroflexus aggregans in a Hot Spring Cyanobacteria-Dominated Microbial Mat |
title_sort | in-situ metatranscriptomic analyses reveal the metabolic flexibility of the thermophilic anoxygenic photosynthetic bacterium chloroflexus aggregans in a hot spring cyanobacteria-dominated microbial mat |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8004040/ https://www.ncbi.nlm.nih.gov/pubmed/33801086 http://dx.doi.org/10.3390/microorganisms9030652 |
work_keys_str_mv | AT kawaishigeru insitumetatranscriptomicanalysesrevealthemetabolicflexibilityofthethermophilicanoxygenicphotosyntheticbacteriumchloroflexusaggregansinahotspringcyanobacteriadominatedmicrobialmat AT martinezjovaln insitumetatranscriptomicanalysesrevealthemetabolicflexibilityofthethermophilicanoxygenicphotosyntheticbacteriumchloroflexusaggregansinahotspringcyanobacteriadominatedmicrobialmat AT lichtenbergmads insitumetatranscriptomicanalysesrevealthemetabolicflexibilityofthethermophilicanoxygenicphotosyntheticbacteriumchloroflexusaggregansinahotspringcyanobacteriadominatedmicrobialmat AT trampeerik insitumetatranscriptomicanalysesrevealthemetabolicflexibilityofthethermophilicanoxygenicphotosyntheticbacteriumchloroflexusaggregansinahotspringcyanobacteriadominatedmicrobialmat AT kuhlmichael insitumetatranscriptomicanalysesrevealthemetabolicflexibilityofthethermophilicanoxygenicphotosyntheticbacteriumchloroflexusaggregansinahotspringcyanobacteriadominatedmicrobialmat AT tankmarcus insitumetatranscriptomicanalysesrevealthemetabolicflexibilityofthethermophilicanoxygenicphotosyntheticbacteriumchloroflexusaggregansinahotspringcyanobacteriadominatedmicrobialmat AT harutashin insitumetatranscriptomicanalysesrevealthemetabolicflexibilityofthethermophilicanoxygenicphotosyntheticbacteriumchloroflexusaggregansinahotspringcyanobacteriadominatedmicrobialmat AT nishiharaarisa insitumetatranscriptomicanalysesrevealthemetabolicflexibilityofthethermophilicanoxygenicphotosyntheticbacteriumchloroflexusaggregansinahotspringcyanobacteriadominatedmicrobialmat AT hanadasatoshi insitumetatranscriptomicanalysesrevealthemetabolicflexibilityofthethermophilicanoxygenicphotosyntheticbacteriumchloroflexusaggregansinahotspringcyanobacteriadominatedmicrobialmat AT thielvera insitumetatranscriptomicanalysesrevealthemetabolicflexibilityofthethermophilicanoxygenicphotosyntheticbacteriumchloroflexusaggregansinahotspringcyanobacteriadominatedmicrobialmat |