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Endogenous clock-mediated regulation of intracellular oxygen dynamics is essential for diazotrophic growth of unicellular cyanobacteria
The discovery of nitrogen fixation in unicellular cyanobacteria provided the first clues for the existence of a circadian clock in prokaryotes. However, recalcitrance to genetic manipulation barred their use as model systems for deciphering the clock function. Here, we explore the circadian clock in...
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Published in: | Nature communications 2024-05, Vol.15 (1), p.3712-3712, Article 3712 |
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description | The discovery of nitrogen fixation in unicellular cyanobacteria provided the first clues for the existence of a circadian clock in prokaryotes. However, recalcitrance to genetic manipulation barred their use as model systems for deciphering the clock function. Here, we explore the circadian clock in the now genetically amenable
Cyanothece
51142, a unicellular, nitrogen-fixing cyanobacterium. Unlike non-diazotrophic clock models,
Cyanothece
51142 exhibits conspicuous self-sustained rhythms in various discernable phenotypes, offering a platform to directly study the effects of the clock on the physiology of an organism. Deletion of
kaiA
, an essential clock component in the cyanobacterial system, impacted the regulation of oxygen cycling and hindered nitrogenase activity. Our findings imply a role for the KaiA component of the clock in regulating the intracellular oxygen dynamics in unicellular diazotrophic cyanobacteria and suggest that its addition to the KaiBC clock was likely an adaptive strategy that ensured optimal nitrogen fixation as microbes evolved from an anaerobic to an aerobic atmosphere under nitrogen constraints.
The authors investigate the circadian clock in a unicellular diazotrophic cyanobacterium. They demonstrate the role of the clock in regulating intracellular oxygen dynamics, a necessity to accommodate nitrogen fixation in an oxygen-producing cell. |
doi_str_mv | 10.1038/s41467-024-48039-0 |
format | article |
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Cyanothece
51142, a unicellular, nitrogen-fixing cyanobacterium. Unlike non-diazotrophic clock models,
Cyanothece
51142 exhibits conspicuous self-sustained rhythms in various discernable phenotypes, offering a platform to directly study the effects of the clock on the physiology of an organism. Deletion of
kaiA
, an essential clock component in the cyanobacterial system, impacted the regulation of oxygen cycling and hindered nitrogenase activity. Our findings imply a role for the KaiA component of the clock in regulating the intracellular oxygen dynamics in unicellular diazotrophic cyanobacteria and suggest that its addition to the KaiBC clock was likely an adaptive strategy that ensured optimal nitrogen fixation as microbes evolved from an anaerobic to an aerobic atmosphere under nitrogen constraints.
The authors investigate the circadian clock in a unicellular diazotrophic cyanobacterium. They demonstrate the role of the clock in regulating intracellular oxygen dynamics, a necessity to accommodate nitrogen fixation in an oxygen-producing cell.</description><identifier>ISSN: 2041-1723</identifier><identifier>EISSN: 2041-1723</identifier><identifier>DOI: 10.1038/s41467-024-48039-0</identifier><identifier>PMID: 38697963</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>38/77 ; 42/41 ; 42/44 ; 631/326/41 ; 631/326/88 ; 631/80/105 ; 82/1 ; 82/29 ; Atmospheric models ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Biological clocks ; Circadian Clocks - genetics ; Circadian Clocks - physiology ; Circadian rhythm ; Circadian Rhythm Signaling Peptides and Proteins - genetics ; Circadian Rhythm Signaling Peptides and Proteins - metabolism ; Circadian rhythms ; Cyanobacteria ; Cyanobacteria - genetics ; Cyanobacteria - metabolism ; Cyanothece ; Cyanothece - genetics ; Cyanothece - metabolism ; Gene Expression Regulation, Bacterial ; Humanities and Social Sciences ; Intracellular ; multidisciplinary ; Nitrogen ; Nitrogen Fixation ; Nitrogenase ; Nitrogenase - genetics ; Nitrogenase - metabolism ; Nitrogenation ; Oxygen ; Oxygen - metabolism ; Phenotypes ; Prokaryotes ; Science ; Science (multidisciplinary)</subject><ispartof>Nature communications, 2024-05, Vol.15 (1), p.3712-3712, Article 3712</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c436t-7b65df8b02d92da6b052fca744b9599e1025e4f484610b66a804ab628bc30ed3</cites><orcidid>0009-0008-7390-8921 ; 0000-0001-8240-2123 ; 0000-0002-9137-4379 ; 0000-0002-5713-6019</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3049932301/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3049932301?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,25731,27901,27902,36989,36990,44566,75096</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38697963$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bandyopadhyay, Anindita</creatorcontrib><creatorcontrib>Sengupta, Annesha</creatorcontrib><creatorcontrib>Elvitigala, Thanura</creatorcontrib><creatorcontrib>Pakrasi, Himadri B.</creatorcontrib><title>Endogenous clock-mediated regulation of intracellular oxygen dynamics is essential for diazotrophic growth of unicellular cyanobacteria</title><title>Nature communications</title><addtitle>Nat Commun</addtitle><addtitle>Nat Commun</addtitle><description>The discovery of nitrogen fixation in unicellular cyanobacteria provided the first clues for the existence of a circadian clock in prokaryotes. However, recalcitrance to genetic manipulation barred their use as model systems for deciphering the clock function. Here, we explore the circadian clock in the now genetically amenable
Cyanothece
51142, a unicellular, nitrogen-fixing cyanobacterium. Unlike non-diazotrophic clock models,
Cyanothece
51142 exhibits conspicuous self-sustained rhythms in various discernable phenotypes, offering a platform to directly study the effects of the clock on the physiology of an organism. Deletion of
kaiA
, an essential clock component in the cyanobacterial system, impacted the regulation of oxygen cycling and hindered nitrogenase activity. Our findings imply a role for the KaiA component of the clock in regulating the intracellular oxygen dynamics in unicellular diazotrophic cyanobacteria and suggest that its addition to the KaiBC clock was likely an adaptive strategy that ensured optimal nitrogen fixation as microbes evolved from an anaerobic to an aerobic atmosphere under nitrogen constraints.
The authors investigate the circadian clock in a unicellular diazotrophic cyanobacterium. 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Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Nature communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bandyopadhyay, Anindita</au><au>Sengupta, Annesha</au><au>Elvitigala, Thanura</au><au>Pakrasi, Himadri B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Endogenous clock-mediated regulation of intracellular oxygen dynamics is essential for diazotrophic growth of unicellular cyanobacteria</atitle><jtitle>Nature communications</jtitle><stitle>Nat Commun</stitle><addtitle>Nat Commun</addtitle><date>2024-05-02</date><risdate>2024</risdate><volume>15</volume><issue>1</issue><spage>3712</spage><epage>3712</epage><pages>3712-3712</pages><artnum>3712</artnum><issn>2041-1723</issn><eissn>2041-1723</eissn><abstract>The discovery of nitrogen fixation in unicellular cyanobacteria provided the first clues for the existence of a circadian clock in prokaryotes. However, recalcitrance to genetic manipulation barred their use as model systems for deciphering the clock function. Here, we explore the circadian clock in the now genetically amenable
Cyanothece
51142, a unicellular, nitrogen-fixing cyanobacterium. Unlike non-diazotrophic clock models,
Cyanothece
51142 exhibits conspicuous self-sustained rhythms in various discernable phenotypes, offering a platform to directly study the effects of the clock on the physiology of an organism. Deletion of
kaiA
, an essential clock component in the cyanobacterial system, impacted the regulation of oxygen cycling and hindered nitrogenase activity. Our findings imply a role for the KaiA component of the clock in regulating the intracellular oxygen dynamics in unicellular diazotrophic cyanobacteria and suggest that its addition to the KaiBC clock was likely an adaptive strategy that ensured optimal nitrogen fixation as microbes evolved from an anaerobic to an aerobic atmosphere under nitrogen constraints.
The authors investigate the circadian clock in a unicellular diazotrophic cyanobacterium. They demonstrate the role of the clock in regulating intracellular oxygen dynamics, a necessity to accommodate nitrogen fixation in an oxygen-producing cell.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>38697963</pmid><doi>10.1038/s41467-024-48039-0</doi><tpages>1</tpages><orcidid>https://orcid.org/0009-0008-7390-8921</orcidid><orcidid>https://orcid.org/0000-0001-8240-2123</orcidid><orcidid>https://orcid.org/0000-0002-9137-4379</orcidid><orcidid>https://orcid.org/0000-0002-5713-6019</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 38/77 42/41 42/44 631/326/41 631/326/88 631/80/105 82/1 82/29 Atmospheric models Bacterial Proteins - genetics Bacterial Proteins - metabolism Biological clocks Circadian Clocks - genetics Circadian Clocks - physiology Circadian rhythm Circadian Rhythm Signaling Peptides and Proteins - genetics Circadian Rhythm Signaling Peptides and Proteins - metabolism Circadian rhythms Cyanobacteria Cyanobacteria - genetics Cyanobacteria - metabolism Cyanothece Cyanothece - genetics Cyanothece - metabolism Gene Expression Regulation, Bacterial Humanities and Social Sciences Intracellular multidisciplinary Nitrogen Nitrogen Fixation Nitrogenase Nitrogenase - genetics Nitrogenase - metabolism Nitrogenation Oxygen Oxygen - metabolism Phenotypes Prokaryotes Science Science (multidisciplinary) |
title | Endogenous clock-mediated regulation of intracellular oxygen dynamics is essential for diazotrophic growth of unicellular cyanobacteria |
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