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Polyphosphate-kinase-1 dependent polyphosphate hyperaccumulation for acclimation to nutrient loss in the cyanobacterium, Synechocystis sp. PCC 6803
Polyphosphate is prevalent in living organisms. To obtain insights into polyphosphate synthesis and its physiological significance in cyanobacteria, we characterize , a homolog of the polyphosphate-kinase-1 gene, in the freshwater cyanobacterium sp. PCC 6803. The Sll0290 protein structure reveals ch...
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Published in: | Frontiers in plant science 2024-07, Vol.15, p.1441626 |
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description | Polyphosphate is prevalent in living organisms. To obtain insights into polyphosphate synthesis and its physiological significance in cyanobacteria, we characterize
, a homolog of the polyphosphate-kinase-1 gene, in the freshwater cyanobacterium
sp. PCC 6803. The Sll0290 protein structure reveals characteristics of Ppk1. A
disruptant and
-overexpressing
transformant demonstrated loss and gain of polyphosphate synthesis ability, respectively. Accordingly,
is identified as
. The disruptant (Δ
) grows normally with aeration of ordinary air (0.04% CO
), consistent with its photosynthesis comparable to the wild type level, which contrasts with a previously reported high-CO
(5%) requirement for Δ
in an alkaline hot spring cyanobacterium,
OS-B'.
Δ
is defective in polyphosphate hyperaccumulation and survival competence at the stationary phase, and also under sulfur-starvation conditions, implying that sulfur limitation is one of the triggers to induce polyphosphate hyperaccumulation in stationary cells. Furthermore, Δ
is defective in the enhancement of total phosphorus contents under sulfur-starvation conditions, a phenomenon that is only partially explained by polyphosphate hyperaccumulation. This study therefore demonstrates that in
,
is not essential for low-CO
acclimation but plays a crucial role in dynamic P-metabolic regulation, including polyP hyperaccumulation, to maintain physiological fitness under sulfur-starvation conditions. |
doi_str_mv | 10.3389/fpls.2024.1441626 |
format | article |
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, a homolog of the polyphosphate-kinase-1 gene, in the freshwater cyanobacterium
sp. PCC 6803. The Sll0290 protein structure reveals characteristics of Ppk1. A
disruptant and
-overexpressing
transformant demonstrated loss and gain of polyphosphate synthesis ability, respectively. Accordingly,
is identified as
. The disruptant (Δ
) grows normally with aeration of ordinary air (0.04% CO
), consistent with its photosynthesis comparable to the wild type level, which contrasts with a previously reported high-CO
(5%) requirement for Δ
in an alkaline hot spring cyanobacterium,
OS-B'.
Δ
is defective in polyphosphate hyperaccumulation and survival competence at the stationary phase, and also under sulfur-starvation conditions, implying that sulfur limitation is one of the triggers to induce polyphosphate hyperaccumulation in stationary cells. Furthermore, Δ
is defective in the enhancement of total phosphorus contents under sulfur-starvation conditions, a phenomenon that is only partially explained by polyphosphate hyperaccumulation. This study therefore demonstrates that in
,
is not essential for low-CO
acclimation but plays a crucial role in dynamic P-metabolic regulation, including polyP hyperaccumulation, to maintain physiological fitness under sulfur-starvation conditions.</description><identifier>ISSN: 1664-462X</identifier><identifier>EISSN: 1664-462X</identifier><identifier>DOI: 10.3389/fpls.2024.1441626</identifier><identifier>PMID: 39145186</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>cyanobacteria ; Plant Science ; polyphosphate ; polyphosphate kinase1 ; PPK1 ; sulfur starvation ; Synechocystis</subject><ispartof>Frontiers in plant science, 2024-07, Vol.15, p.1441626</ispartof><rights>Copyright © 2024 Sato, Endo, Nishi, Fujiwara and Tsuzuki.</rights><rights>Copyright © 2024 Sato, Endo, Nishi, Fujiwara and Tsuzuki 2024 Sato, Endo, Nishi, Fujiwara and Tsuzuki</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c348t-cf1cfc925caa3a9a75b8664d8a3822a0a771c8bd15259d5d57f1a9620608f6de3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11322815/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11322815/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39145186$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sato, Norihiro</creatorcontrib><creatorcontrib>Endo, Mizuki</creatorcontrib><creatorcontrib>Nishi, Hiroki</creatorcontrib><creatorcontrib>Fujiwara, Shoko</creatorcontrib><creatorcontrib>Tsuzuki, Mikio</creatorcontrib><title>Polyphosphate-kinase-1 dependent polyphosphate hyperaccumulation for acclimation to nutrient loss in the cyanobacterium, Synechocystis sp. PCC 6803</title><title>Frontiers in plant science</title><addtitle>Front Plant Sci</addtitle><description>Polyphosphate is prevalent in living organisms. To obtain insights into polyphosphate synthesis and its physiological significance in cyanobacteria, we characterize
, a homolog of the polyphosphate-kinase-1 gene, in the freshwater cyanobacterium
sp. PCC 6803. The Sll0290 protein structure reveals characteristics of Ppk1. A
disruptant and
-overexpressing
transformant demonstrated loss and gain of polyphosphate synthesis ability, respectively. Accordingly,
is identified as
. The disruptant (Δ
) grows normally with aeration of ordinary air (0.04% CO
), consistent with its photosynthesis comparable to the wild type level, which contrasts with a previously reported high-CO
(5%) requirement for Δ
in an alkaline hot spring cyanobacterium,
OS-B'.
Δ
is defective in polyphosphate hyperaccumulation and survival competence at the stationary phase, and also under sulfur-starvation conditions, implying that sulfur limitation is one of the triggers to induce polyphosphate hyperaccumulation in stationary cells. Furthermore, Δ
is defective in the enhancement of total phosphorus contents under sulfur-starvation conditions, a phenomenon that is only partially explained by polyphosphate hyperaccumulation. This study therefore demonstrates that in
,
is not essential for low-CO
acclimation but plays a crucial role in dynamic P-metabolic regulation, including polyP hyperaccumulation, to maintain physiological fitness under sulfur-starvation conditions.</description><subject>cyanobacteria</subject><subject>Plant Science</subject><subject>polyphosphate</subject><subject>polyphosphate kinase1</subject><subject>PPK1</subject><subject>sulfur starvation</subject><subject>Synechocystis</subject><issn>1664-462X</issn><issn>1664-462X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVUsFu1DAUjBCIVqUfwAX5yIEsfnbi2CeEVkArVaISIHGzXhynccnGwXaQ8h38MN7uUm19sT1-M89jT1G8BrrhXKr3_TzGDaOs2kBVgWDiWXEOQlRlJdjP5yfrs-IyxnuaR02pUs3L4owrqGqQ4rz4e-vHdR58nAdMtvzlJoy2BNLZ2U6dnRKZTwvIsM42oDHLbhkxOT-R3geSgdHtDvvkybSk4Pbc0cdIXMYGS8yKk2_RJBvcsntHvq2TNYM3a0wukjhvyO12S4Sk_FXxoscx2svjfFH8-Pzp-_aqvPn65Xr78aY0vJKpND2Y3ihWG0SOCpu6ldlzJ5FLxpBi04CRbQc1q1VXd3XTAyrBqKCyF53lF8X1QbfzeK_nkB2EVXt0-gHw4U5jSM6MVgsKjHPFe8tkxaFpW8NBKSOAC8lFk7U-HLTmpd3ZzmT3Accnok9PJjfoO_9HA3DGJNRZ4e1RIfjfi41J71w0dhxxsn6JmlOVG1f5x3MpHEpNyA8cbP_YB6jeh0Pvw6H34dDHcGTOm9MLPjL-R4H_A9_iuO4</recordid><startdate>20240731</startdate><enddate>20240731</enddate><creator>Sato, Norihiro</creator><creator>Endo, Mizuki</creator><creator>Nishi, Hiroki</creator><creator>Fujiwara, Shoko</creator><creator>Tsuzuki, Mikio</creator><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20240731</creationdate><title>Polyphosphate-kinase-1 dependent polyphosphate hyperaccumulation for acclimation to nutrient loss in the cyanobacterium, Synechocystis sp. PCC 6803</title><author>Sato, Norihiro ; Endo, Mizuki ; Nishi, Hiroki ; Fujiwara, Shoko ; Tsuzuki, Mikio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c348t-cf1cfc925caa3a9a75b8664d8a3822a0a771c8bd15259d5d57f1a9620608f6de3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>cyanobacteria</topic><topic>Plant Science</topic><topic>polyphosphate</topic><topic>polyphosphate kinase1</topic><topic>PPK1</topic><topic>sulfur starvation</topic><topic>Synechocystis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sato, Norihiro</creatorcontrib><creatorcontrib>Endo, Mizuki</creatorcontrib><creatorcontrib>Nishi, Hiroki</creatorcontrib><creatorcontrib>Fujiwara, Shoko</creatorcontrib><creatorcontrib>Tsuzuki, Mikio</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in plant science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sato, Norihiro</au><au>Endo, Mizuki</au><au>Nishi, Hiroki</au><au>Fujiwara, Shoko</au><au>Tsuzuki, Mikio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polyphosphate-kinase-1 dependent polyphosphate hyperaccumulation for acclimation to nutrient loss in the cyanobacterium, Synechocystis sp. PCC 6803</atitle><jtitle>Frontiers in plant science</jtitle><addtitle>Front Plant Sci</addtitle><date>2024-07-31</date><risdate>2024</risdate><volume>15</volume><spage>1441626</spage><pages>1441626-</pages><issn>1664-462X</issn><eissn>1664-462X</eissn><abstract>Polyphosphate is prevalent in living organisms. To obtain insights into polyphosphate synthesis and its physiological significance in cyanobacteria, we characterize
, a homolog of the polyphosphate-kinase-1 gene, in the freshwater cyanobacterium
sp. PCC 6803. The Sll0290 protein structure reveals characteristics of Ppk1. A
disruptant and
-overexpressing
transformant demonstrated loss and gain of polyphosphate synthesis ability, respectively. Accordingly,
is identified as
. The disruptant (Δ
) grows normally with aeration of ordinary air (0.04% CO
), consistent with its photosynthesis comparable to the wild type level, which contrasts with a previously reported high-CO
(5%) requirement for Δ
in an alkaline hot spring cyanobacterium,
OS-B'.
Δ
is defective in polyphosphate hyperaccumulation and survival competence at the stationary phase, and also under sulfur-starvation conditions, implying that sulfur limitation is one of the triggers to induce polyphosphate hyperaccumulation in stationary cells. Furthermore, Δ
is defective in the enhancement of total phosphorus contents under sulfur-starvation conditions, a phenomenon that is only partially explained by polyphosphate hyperaccumulation. This study therefore demonstrates that in
,
is not essential for low-CO
acclimation but plays a crucial role in dynamic P-metabolic regulation, including polyP hyperaccumulation, to maintain physiological fitness under sulfur-starvation conditions.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>39145186</pmid><doi>10.3389/fpls.2024.1441626</doi><oa>free_for_read</oa></addata></record> |
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subjects | cyanobacteria Plant Science polyphosphate polyphosphate kinase1 PPK1 sulfur starvation Synechocystis |
title | Polyphosphate-kinase-1 dependent polyphosphate hyperaccumulation for acclimation to nutrient loss in the cyanobacterium, Synechocystis sp. PCC 6803 |
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