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The Arabidopsis thylakoid transporter PHT 4;1 influences phosphate availability for ATP synthesis and plant growth
Author(s) -
Karlsson Patrik M.,
Herdean Andrei,
Adolfsson Lisa,
Beebo Azeez,
Nziengui Hugues,
Irigoyen Sonia,
Ünnep Renáta,
Zsiros Ottó,
Nagy Gergely,
Garab Győző,
Aronsson Henrik,
Versaw Wayne K.,
Spetea Cornelia
Publication year - 2015
Publication title -
the plant journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.058
H-Index - 269
eISSN - 1365-313X
pISSN - 0960-7412
DOI - 10.1111/tpj.12962
Subject(s) - thylakoid , chloroplast , photosystem ii , arabidopsis , biochemistry , mutant , biology , atp synthase , photosynthesis , wild type , phosphate , biophysics , microbiology and biotechnology , chemistry , gene
Summary The Arabidopsis phosphate transporter PHT 4;1 was previously localized to the chloroplast thylakoid membrane. Here we investigated the physiological consequences of the absence of PHT 4;1 for photosynthesis and plant growth. In standard growth conditions, two independent Arabidopsis knockout mutant lines displayed significantly reduced leaf size and biomass but normal phosphorus content. When mutants were grown in high‐phosphate conditions, the leaf phosphorus levels increased and the growth phenotype was suppressed. Photosynthetic measurements indicated that in the absence of PHT 4;1 stromal phosphate was reduced to levels that limited ATP synthase activity. This resulted in reduced CO 2 fixation and accumulation of soluble sugars, limiting plant growth. The mutants also displayed faster induction of non‐photochemical quenching than the wild type, in line with the increased contribution of ΔpH to the proton‐motive force across thylakoids. Small‐angle neutron scattering showed a smaller lamellar repeat distance, whereas circular dichroism spectroscopy indicated a perturbed long‐range order of photosystem II ( PSII ) complexes in the mutant thylakoids. The absence of PHT 4;1 did not alter the PSII repair cycle, as indicated by wild‐type levels of phosphorylation of PSII proteins, inactivation and D1 protein degradation. Interestingly, the expression of genes for several thylakoid proteins was downregulated in the mutants, but the relative levels of the corresponding proteins were either not affected or could not be discerned. Based on these data, we propose that PHT 4;1 plays an important role in chloroplast phosphate compartmentation and ATP synthesis, which affect plant growth. It also maintains the ionic environment of thylakoids, which affects the macro‐organization of complexes and induction of photoprotective mechanisms.