Lack of Phosphatidylglycerol Inhibits Chlorophyll Biosynthesis at Multiple Sites and Limits Chlorophyllide Reutilization in Synechocystis sp. Strain PCC 6803
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
26269547
PubMed Central
PMC4587476
DOI
10.1104/pp.15.01150
PII: pp.15.01150
Knihovny.cz E-zdroje
- MeSH
- bakteriální proteiny genetika metabolismus MeSH
- chlorofyl biosyntéza metabolismus MeSH
- chlorofylidy metabolismus MeSH
- fosfatidylglyceroly genetika metabolismus MeSH
- fotosystém I - proteinový komplex metabolismus MeSH
- ligasy tvořící vazby C-O metabolismus MeSH
- protochlorofylid metabolismus MeSH
- světlosběrné proteinové komplexy metabolismus MeSH
- Synechocystis genetika metabolismus MeSH
- transferasy pro jiné substituované fosfátové skupiny genetika metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- bakteriální proteiny MeSH
- CDP-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase MeSH Prohlížeč
- chlorofyl MeSH
- chlorofylidy MeSH
- chlorophyll A binding protein CP43, Cyanobacteria MeSH Prohlížeč
- chlorophyll synthetase MeSH Prohlížeč
- fosfatidylglyceroly MeSH
- fotosystém I - proteinový komplex MeSH
- ligasy tvořící vazby C-O MeSH
- protochlorofylid MeSH
- světlosběrné proteinové komplexy MeSH
- transferasy pro jiné substituované fosfátové skupiny MeSH
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 ΔpgsA 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 ΔpgsA 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.
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