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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kawai, Shigeru, Martinez, Joval N., Lichtenberg, Mads, Trampe, Erik, Kühl, Michael, Tank, Marcus, Haruta, Shin, Nishihara, Arisa, Hanada, Satoshi, Thiel, Vera
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