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Lack of Phosphatidylglycerol Inhibits Chlorophyll Biosynthesis at Multiple Sites and Limits Chlorophyllide Reutilization in Synechocystis sp Strain PCC 6803
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SYSNO ASEP 0454042 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Lack of Phosphatidylglycerol Inhibits Chlorophyll Biosynthesis at Multiple Sites and Limits Chlorophyllide Reutilization in Synechocystis sp Strain PCC 6803 Author(s) Kopečná, Jana (MBU-M) RID
Pilný, Jan (MBU-M) ORCID
Krynická, Vendula (MBU-M) RID
Tomčala, Aleš (BC-A) RID
Kis, M. (HU)
Gombos, Z. (HU)
Komenda, Josef (MBU-M) RID, ORCID
Sobotka, Roman (MBU-M) RID, ORCIDSource Title Plant Physiology. - : Oxford University Press - ISSN 0032-0889
Roč. 169, č. 2 (2015), s. 1307-1317Number of pages 11 s. Language eng - English Country US - United States Keywords II REACTION-CENTER ; PHOTOSYSTEM-II ; SP PCC-6803 Subject RIV CE - Biochemistry R&D Projects LO1416 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) EE2.3.30.0059 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) GBP501/12/G055 GA ČR - Czech Science Foundation (CSF) Institutional support MBU-M - RVO:61388971 ; BC-A - RVO:60077344 UT WOS 000365401000036 DOI 10.1104/pp.15.01150 Annotation The negatively charged lipid phosphatidylglycerol (PG) constitutes up to 10% of total lipids in photosynthetic membranes, and its deprivation in cyanobacteria is accompanied by chlorophyll (Chl) depletion. Indeed, radioactive labeling of the PG-depleted Delta pgsA mutant of Synechocystis sp. strain PCC 6803, which is not able to synthesize PG, proved the inhibition of Chl biosynthesis caused by restriction on the formation of 5-aminolevulinic acid and protochlorophyllide. Although the mutant accumulated chlorophyllide, the last Chl precursor, we showed that it originated from dephytylation of existing Chl and not from the block in the Chl biosynthesis. The lack of de novo-produced Chl under PG depletion was accompanied by a significantly weakened biosynthesis of both monomeric and trimeric photosystem I (PSI) complexes, although the decrease in cellular content was manifested only for the trimeric form. However, our analysis of DpgsA mutant, which lacked trimeric PSI because of the absence of the PsaL subunit, suggested that the virtual stability of monomeric PSI is a result of disintegration of PSI trimers. Interestingly, the loss of trimeric PSI was accompanied by accumulation of monomeric PSI associated with the newly synthesized CP43 subunit of photosystem II. We conclude that the absence of PG results in the inhibition of Chl biosynthetic pathway, which impairs synthesis of PSI, despite the accumulation of chlorophyllide released from the degraded Chl proteins. Based on the knowledge about the role of PG in prokaryotes, we hypothesize that the synthesis of Chl and PSI complexes are colocated in a membrane microdomain requiring PG for integrity. Workplace Institute of Microbiology Contact Eliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231 Year of Publishing 2016
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