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Comparative Genomic Analysis Revealed Distinct Molecular Components and Organization of CO(2)-Concentrating Mechanism in Thermophilic Cyanobacteria

Cyanobacteria evolved an inorganic carbon-concentrating mechanism (CCM) to perform effective oxygenic photosynthesis and prevent photorespiratory carbon losses. This process facilitates the acclimation of cyanobacteria to various habitats, particularly in CO(2)-limited environments. To date, there i...

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Autores principales: Tang, Jie, Zhou, Huizhen, Yao, Dan, Riaz, Sadaf, You, Dawei, Klepacz-Smółka, Anna, Daroch, Maurycy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120777/
https://www.ncbi.nlm.nih.gov/pubmed/35602029
http://dx.doi.org/10.3389/fmicb.2022.876272
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author Tang, Jie
Zhou, Huizhen
Yao, Dan
Riaz, Sadaf
You, Dawei
Klepacz-Smółka, Anna
Daroch, Maurycy
author_facet Tang, Jie
Zhou, Huizhen
Yao, Dan
Riaz, Sadaf
You, Dawei
Klepacz-Smółka, Anna
Daroch, Maurycy
author_sort Tang, Jie
collection PubMed
description Cyanobacteria evolved an inorganic carbon-concentrating mechanism (CCM) to perform effective oxygenic photosynthesis and prevent photorespiratory carbon losses. This process facilitates the acclimation of cyanobacteria to various habitats, particularly in CO(2)-limited environments. To date, there is limited information on the CCM of thermophilic cyanobacteria whose habitats limit the solubility of inorganic carbon. Here, genome-based approaches were used to identify the molecular components of CCM in 17 well-described thermophilic cyanobacteria. These cyanobacteria were from the genus Leptodesmis, Leptolyngbya, Leptothermofonsia, Thermoleptolyngbya, Thermostichus, and Thermosynechococcus. All the strains belong to β-cyanobacteria based on their β-carboxysome shell proteins with 1B form of Rubisco. The diversity in the C(i) uptake systems and carboxysome composition of these thermophiles were analyzed based on their genomic information. For C(i) uptake systems, two CO(2) uptake systems (NDH-1(3) and NDH-1(4)) and BicA for HCO(3)(–) transport were present in all the thermophilic cyanobacteria, while most strains did not have the Na(+)/HCO(3)(–) Sbt symporter and HCO(3)(–) transporter BCT1 were absent in four strains. As for carboxysome, the β-carboxysomal shell protein, ccmK2, was absent only in Thermoleptolyngbya strains, whereas ccmK3/K4 were absent in all Thermostichus and Thermosynechococcus strains. Besides, all Thermostichus and Thermosynechococcus strains lacked carboxysomal β-CA, ccaA, the carbonic anhydrase activity of which may be replaced by ccmM proteins as indicated by comparative domain analysis. The genomic distribution of CCM-related genes was different among the thermophiles, suggesting probably distinct expression regulation. Overall, the comparative genomic analysis revealed distinct molecular components and organization of CCM in thermophilic cyanobacteria. These findings provided insights into the CCM components of thermophilic cyanobacteria and fundamental knowledge for further research regarding photosynthetic improvement and biomass yield of thermophilic cyanobacteria with biotechnological potentials.
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spelling pubmed-91207772022-05-21 Comparative Genomic Analysis Revealed Distinct Molecular Components and Organization of CO(2)-Concentrating Mechanism in Thermophilic Cyanobacteria Tang, Jie Zhou, Huizhen Yao, Dan Riaz, Sadaf You, Dawei Klepacz-Smółka, Anna Daroch, Maurycy Front Microbiol Microbiology Cyanobacteria evolved an inorganic carbon-concentrating mechanism (CCM) to perform effective oxygenic photosynthesis and prevent photorespiratory carbon losses. This process facilitates the acclimation of cyanobacteria to various habitats, particularly in CO(2)-limited environments. To date, there is limited information on the CCM of thermophilic cyanobacteria whose habitats limit the solubility of inorganic carbon. Here, genome-based approaches were used to identify the molecular components of CCM in 17 well-described thermophilic cyanobacteria. These cyanobacteria were from the genus Leptodesmis, Leptolyngbya, Leptothermofonsia, Thermoleptolyngbya, Thermostichus, and Thermosynechococcus. All the strains belong to β-cyanobacteria based on their β-carboxysome shell proteins with 1B form of Rubisco. The diversity in the C(i) uptake systems and carboxysome composition of these thermophiles were analyzed based on their genomic information. For C(i) uptake systems, two CO(2) uptake systems (NDH-1(3) and NDH-1(4)) and BicA for HCO(3)(–) transport were present in all the thermophilic cyanobacteria, while most strains did not have the Na(+)/HCO(3)(–) Sbt symporter and HCO(3)(–) transporter BCT1 were absent in four strains. As for carboxysome, the β-carboxysomal shell protein, ccmK2, was absent only in Thermoleptolyngbya strains, whereas ccmK3/K4 were absent in all Thermostichus and Thermosynechococcus strains. Besides, all Thermostichus and Thermosynechococcus strains lacked carboxysomal β-CA, ccaA, the carbonic anhydrase activity of which may be replaced by ccmM proteins as indicated by comparative domain analysis. The genomic distribution of CCM-related genes was different among the thermophiles, suggesting probably distinct expression regulation. Overall, the comparative genomic analysis revealed distinct molecular components and organization of CCM in thermophilic cyanobacteria. These findings provided insights into the CCM components of thermophilic cyanobacteria and fundamental knowledge for further research regarding photosynthetic improvement and biomass yield of thermophilic cyanobacteria with biotechnological potentials. Frontiers Media S.A. 2022-05-06 /pmc/articles/PMC9120777/ /pubmed/35602029 http://dx.doi.org/10.3389/fmicb.2022.876272 Text en Copyright © 2022 Tang, Zhou, Yao, Riaz, You, Klepacz-Smółka and Daroch. https://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) and the copyright owner(s) 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
Tang, Jie
Zhou, Huizhen
Yao, Dan
Riaz, Sadaf
You, Dawei
Klepacz-Smółka, Anna
Daroch, Maurycy
Comparative Genomic Analysis Revealed Distinct Molecular Components and Organization of CO(2)-Concentrating Mechanism in Thermophilic Cyanobacteria
title Comparative Genomic Analysis Revealed Distinct Molecular Components and Organization of CO(2)-Concentrating Mechanism in Thermophilic Cyanobacteria
title_full Comparative Genomic Analysis Revealed Distinct Molecular Components and Organization of CO(2)-Concentrating Mechanism in Thermophilic Cyanobacteria
title_fullStr Comparative Genomic Analysis Revealed Distinct Molecular Components and Organization of CO(2)-Concentrating Mechanism in Thermophilic Cyanobacteria
title_full_unstemmed Comparative Genomic Analysis Revealed Distinct Molecular Components and Organization of CO(2)-Concentrating Mechanism in Thermophilic Cyanobacteria
title_short Comparative Genomic Analysis Revealed Distinct Molecular Components and Organization of CO(2)-Concentrating Mechanism in Thermophilic Cyanobacteria
title_sort comparative genomic analysis revealed distinct molecular components and organization of co(2)-concentrating mechanism in thermophilic cyanobacteria
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120777/
https://www.ncbi.nlm.nih.gov/pubmed/35602029
http://dx.doi.org/10.3389/fmicb.2022.876272
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