Cargando…

Adaptation of Cyanobacteria to the Endolithic Light Spectrum in Hyper-Arid Deserts

In hyper-arid deserts, endolithic microbial communities survive in the pore spaces and cracks of rocks, an environment that enhances water retention and filters UV radiation. The rock colonization zone is enriched in far-red light (FRL) and depleted in visible light. This poses a challenge to cyanob...

Descripción completa

Detalles Bibliográficos
Autores principales: Murray, Bayleigh, Ertekin, Emine, Dailey, Micah, Soulier, Nathan T., Shen, Gaozhong, Bryant, Donald A., Perez-Fernandez, Cesar, DiRuggiero, Jocelyne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9228357/
https://www.ncbi.nlm.nih.gov/pubmed/35744716
http://dx.doi.org/10.3390/microorganisms10061198
_version_ 1784734439762296832
author Murray, Bayleigh
Ertekin, Emine
Dailey, Micah
Soulier, Nathan T.
Shen, Gaozhong
Bryant, Donald A.
Perez-Fernandez, Cesar
DiRuggiero, Jocelyne
author_facet Murray, Bayleigh
Ertekin, Emine
Dailey, Micah
Soulier, Nathan T.
Shen, Gaozhong
Bryant, Donald A.
Perez-Fernandez, Cesar
DiRuggiero, Jocelyne
author_sort Murray, Bayleigh
collection PubMed
description In hyper-arid deserts, endolithic microbial communities survive in the pore spaces and cracks of rocks, an environment that enhances water retention and filters UV radiation. The rock colonization zone is enriched in far-red light (FRL) and depleted in visible light. This poses a challenge to cyanobacteria, which are the primary producers of endolithic communities. Many species of cyanobacteria are capable of Far-Red-Light Photoacclimation (FaRLiP), a process in which FRL induces the synthesis of specialized chlorophylls and remodeling of the photosynthetic apparatus, providing the ability to grow in FRL. While FaRLiP has been reported in cyanobacteria from various low-light environments, our understanding of light adaptations for endolithic cyanobacteria remains limited. Here, we demonstrated that endolithic Chroococcidiopsis isolates from deserts around the world synthesize chlorophyll f, an FRL-specialized chlorophyll when FRL is the sole light source. The metagenome-assembled genomes of these isolates encoded chlorophyll f synthase and all the genes required to implement the FaRLiP response. We also present evidence of FRL-induced changes to the major light-harvesting complexes of a Chroococcidiopsis isolate. These findings indicate that endolithic cyanobacteria from hyper-arid deserts use FRL photoacclimation as an adaptation to the unique light transmission spectrum of their rocky habitat.
format Online
Article
Text
id pubmed-9228357
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-92283572022-06-25 Adaptation of Cyanobacteria to the Endolithic Light Spectrum in Hyper-Arid Deserts Murray, Bayleigh Ertekin, Emine Dailey, Micah Soulier, Nathan T. Shen, Gaozhong Bryant, Donald A. Perez-Fernandez, Cesar DiRuggiero, Jocelyne Microorganisms Article In hyper-arid deserts, endolithic microbial communities survive in the pore spaces and cracks of rocks, an environment that enhances water retention and filters UV radiation. The rock colonization zone is enriched in far-red light (FRL) and depleted in visible light. This poses a challenge to cyanobacteria, which are the primary producers of endolithic communities. Many species of cyanobacteria are capable of Far-Red-Light Photoacclimation (FaRLiP), a process in which FRL induces the synthesis of specialized chlorophylls and remodeling of the photosynthetic apparatus, providing the ability to grow in FRL. While FaRLiP has been reported in cyanobacteria from various low-light environments, our understanding of light adaptations for endolithic cyanobacteria remains limited. Here, we demonstrated that endolithic Chroococcidiopsis isolates from deserts around the world synthesize chlorophyll f, an FRL-specialized chlorophyll when FRL is the sole light source. The metagenome-assembled genomes of these isolates encoded chlorophyll f synthase and all the genes required to implement the FaRLiP response. We also present evidence of FRL-induced changes to the major light-harvesting complexes of a Chroococcidiopsis isolate. These findings indicate that endolithic cyanobacteria from hyper-arid deserts use FRL photoacclimation as an adaptation to the unique light transmission spectrum of their rocky habitat. MDPI 2022-06-11 /pmc/articles/PMC9228357/ /pubmed/35744716 http://dx.doi.org/10.3390/microorganisms10061198 Text en © 2022 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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Murray, Bayleigh
Ertekin, Emine
Dailey, Micah
Soulier, Nathan T.
Shen, Gaozhong
Bryant, Donald A.
Perez-Fernandez, Cesar
DiRuggiero, Jocelyne
Adaptation of Cyanobacteria to the Endolithic Light Spectrum in Hyper-Arid Deserts
title Adaptation of Cyanobacteria to the Endolithic Light Spectrum in Hyper-Arid Deserts
title_full Adaptation of Cyanobacteria to the Endolithic Light Spectrum in Hyper-Arid Deserts
title_fullStr Adaptation of Cyanobacteria to the Endolithic Light Spectrum in Hyper-Arid Deserts
title_full_unstemmed Adaptation of Cyanobacteria to the Endolithic Light Spectrum in Hyper-Arid Deserts
title_short Adaptation of Cyanobacteria to the Endolithic Light Spectrum in Hyper-Arid Deserts
title_sort adaptation of cyanobacteria to the endolithic light spectrum in hyper-arid deserts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9228357/
https://www.ncbi.nlm.nih.gov/pubmed/35744716
http://dx.doi.org/10.3390/microorganisms10061198
work_keys_str_mv AT murraybayleigh adaptationofcyanobacteriatotheendolithiclightspectruminhyperariddeserts
AT ertekinemine adaptationofcyanobacteriatotheendolithiclightspectruminhyperariddeserts
AT daileymicah adaptationofcyanobacteriatotheendolithiclightspectruminhyperariddeserts
AT souliernathant adaptationofcyanobacteriatotheendolithiclightspectruminhyperariddeserts
AT shengaozhong adaptationofcyanobacteriatotheendolithiclightspectruminhyperariddeserts
AT bryantdonalda adaptationofcyanobacteriatotheendolithiclightspectruminhyperariddeserts
AT perezfernandezcesar adaptationofcyanobacteriatotheendolithiclightspectruminhyperariddeserts
AT diruggierojocelyne adaptationofcyanobacteriatotheendolithiclightspectruminhyperariddeserts