4.4 Article

Chlorophyll Degradation and Light-harvesting Complex II Aggregate Formation During Dark-induced Leaf Senescence in Arabidopsis Pheophytinase Mutants

Journal

JOURNAL OF PLANT BIOLOGY
Volume 62, Issue 1, Pages 27-38

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s12374-018-0242-0

Keywords

Aggregate; Chlorophyll degradation; Chlorophyllprotein complexes; Dark-induced senescence; Light-harvesting

Categories

Funding

  1. Next-Generation Biogreen 21 Program (SSAC), Rural Development Administration, Republic of Korea [PJ013155012019]
  2. Basic Science Research Program of the National Foundation of Korea (NRF) - Ministry of Science, ICT and Future Planning [NRF-2017R1A2A2A05001287]
  3. National Research Foundation of Korea (NRF) [NRF-2011-616-C00028]
  4. Rural Development Administration (RDA), Republic of Korea [PJ013155012019] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The stay-green mutant of Arabidopsis thaliana, ore10 forms stable light-harvesting complex II (LHCII) aggregates during dark-induced senescence, which showed a single base deletion (G1351) in the coding region of the pheophytinase (PPH) gene. PPH specifically dephytylates the Mg-free chlorophyll (Chl) pigment pheophytin, yielding pheophorbide. In both ore10 and pph-1 mutants, pheophytin a accumulated due to the deficiency of PPH gene, but the amount was relatively smaller than that of degraded Chl, and most of the pheophytin a was bound to the stable LHCII forming aggregates with some other Chl-protein (CP) complexes. Comparison of Chl a/b ratios in thylakoids, aggregates, and LHCII indicated that the suppression of Chl b to Chl a conversion was stronger when Chl b reductase was missing and weak when PPH is missing in the large Chl catabolic complex, which allowed the partial degradation of Chl b. These results suggest that the PPH-dependent pathway is not specific for LHCII, but common for all CP complexes, including LHCII. In PPH-deficient mutants, the degradation of LHCII was suppressed by the formation of aggregates, and some of the remaining CP complexes and pheophytin a were included in the aggregates. Non-included CP complexes were degraded via an unknown mechanism.

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