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Characterization of a novel type of carbonic anhydrase that acts without metal cofactors
BACKGROUND: Carbonic anhydrases (CAs) are universal metalloenzymes that catalyze the reversible conversion of carbon dioxide (CO(2)) and bicarbonate (HCO(3)(-)). They are involved in various biological processes, including pH control, respiration, and photosynthesis. To date, eight evolutionarily un...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8132391/ https://www.ncbi.nlm.nih.gov/pubmed/34006275 http://dx.doi.org/10.1186/s12915-021-01039-8 |
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author | Hirakawa, Yoshihisa Senda, Miki Fukuda, Kodai Yu, Hong Yang Ishida, Masaki Taira, Masafumi Kinbara, Kazushi Senda, Toshiya |
author_facet | Hirakawa, Yoshihisa Senda, Miki Fukuda, Kodai Yu, Hong Yang Ishida, Masaki Taira, Masafumi Kinbara, Kazushi Senda, Toshiya |
author_sort | Hirakawa, Yoshihisa |
collection | PubMed |
description | BACKGROUND: Carbonic anhydrases (CAs) are universal metalloenzymes that catalyze the reversible conversion of carbon dioxide (CO(2)) and bicarbonate (HCO(3)(-)). They are involved in various biological processes, including pH control, respiration, and photosynthesis. To date, eight evolutionarily unrelated classes of CA families (α, β, γ, δ, ζ, η, θ, and ι) have been identified. All are characterized by an active site accommodating the binding of a metal cofactor, which is assumed to play a central role in catalysis. This feature is thought to be the result of convergent evolution. RESULTS: Here, we report that a previously uncharacterized protein group, named “COG4337,” constitutes metal-independent CAs from the newly discovered ι-class. Genes coding for COG4337 proteins are found in various bacteria and photosynthetic eukaryotic algae. Biochemical assays demonstrated that recombinant COG4337 proteins from a cyanobacterium (Anabaena sp. PCC7120) and a chlorarachniophyte alga (Bigelowiella natans) accelerated CO(2) hydration. Unexpectedly, these proteins exhibited their activity under metal-free conditions. Based on X-ray crystallography and point mutation analysis, we identified a metal-free active site within the cone-shaped α+β barrel structure. Furthermore, subcellular localization experiments revealed that COG4337 proteins are targeted into plastids and mitochondria of B. natans, implicating their involvement in CO(2) metabolism in these organelles. CONCLUSIONS: COG4337 proteins shared a short sequence motif and overall structure with ι-class CAs, whereas they were characterized by metal independence, unlike any known CAs. Therefore, COG4337 proteins could be treated as a variant type of ι-class CAs. Our findings suggested that this novel type of ι-CAs can function even in metal-poor environments (e.g., the open ocean) without competition with other metalloproteins for trace metals. Considering the widespread prevalence of ι-CAs across microalgae, this class of CAs may play a role in the global carbon cycle. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01039-8. |
format | Online Article Text |
id | pubmed-8132391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81323912021-05-19 Characterization of a novel type of carbonic anhydrase that acts without metal cofactors Hirakawa, Yoshihisa Senda, Miki Fukuda, Kodai Yu, Hong Yang Ishida, Masaki Taira, Masafumi Kinbara, Kazushi Senda, Toshiya BMC Biol Research Article BACKGROUND: Carbonic anhydrases (CAs) are universal metalloenzymes that catalyze the reversible conversion of carbon dioxide (CO(2)) and bicarbonate (HCO(3)(-)). They are involved in various biological processes, including pH control, respiration, and photosynthesis. To date, eight evolutionarily unrelated classes of CA families (α, β, γ, δ, ζ, η, θ, and ι) have been identified. All are characterized by an active site accommodating the binding of a metal cofactor, which is assumed to play a central role in catalysis. This feature is thought to be the result of convergent evolution. RESULTS: Here, we report that a previously uncharacterized protein group, named “COG4337,” constitutes metal-independent CAs from the newly discovered ι-class. Genes coding for COG4337 proteins are found in various bacteria and photosynthetic eukaryotic algae. Biochemical assays demonstrated that recombinant COG4337 proteins from a cyanobacterium (Anabaena sp. PCC7120) and a chlorarachniophyte alga (Bigelowiella natans) accelerated CO(2) hydration. Unexpectedly, these proteins exhibited their activity under metal-free conditions. Based on X-ray crystallography and point mutation analysis, we identified a metal-free active site within the cone-shaped α+β barrel structure. Furthermore, subcellular localization experiments revealed that COG4337 proteins are targeted into plastids and mitochondria of B. natans, implicating their involvement in CO(2) metabolism in these organelles. CONCLUSIONS: COG4337 proteins shared a short sequence motif and overall structure with ι-class CAs, whereas they were characterized by metal independence, unlike any known CAs. Therefore, COG4337 proteins could be treated as a variant type of ι-class CAs. Our findings suggested that this novel type of ι-CAs can function even in metal-poor environments (e.g., the open ocean) without competition with other metalloproteins for trace metals. Considering the widespread prevalence of ι-CAs across microalgae, this class of CAs may play a role in the global carbon cycle. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01039-8. BioMed Central 2021-05-18 /pmc/articles/PMC8132391/ /pubmed/34006275 http://dx.doi.org/10.1186/s12915-021-01039-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Hirakawa, Yoshihisa Senda, Miki Fukuda, Kodai Yu, Hong Yang Ishida, Masaki Taira, Masafumi Kinbara, Kazushi Senda, Toshiya Characterization of a novel type of carbonic anhydrase that acts without metal cofactors |
title | Characterization of a novel type of carbonic anhydrase that acts without metal cofactors |
title_full | Characterization of a novel type of carbonic anhydrase that acts without metal cofactors |
title_fullStr | Characterization of a novel type of carbonic anhydrase that acts without metal cofactors |
title_full_unstemmed | Characterization of a novel type of carbonic anhydrase that acts without metal cofactors |
title_short | Characterization of a novel type of carbonic anhydrase that acts without metal cofactors |
title_sort | characterization of a novel type of carbonic anhydrase that acts without metal cofactors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8132391/ https://www.ncbi.nlm.nih.gov/pubmed/34006275 http://dx.doi.org/10.1186/s12915-021-01039-8 |
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