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

被引:10
|
作者
Yang, Young Nam [1 ,2 ]
Safarova, Rana B. [1 ,2 ]
Park, So-Yon [3 ]
Sakuraba, Yasuhito [3 ]
Oh, Min-Hyuk [1 ,2 ,7 ]
Zulfugarov, Ismayil S. [1 ,2 ]
Lee, Chin Bum [4 ]
Tanaka, Ayumi [5 ]
Paek, Nam-Chon [3 ,6 ]
Lee, Choon-Hwan [1 ,2 ]
机构
[1] Pusan Natl Univ, Dept Integrated Biol Sci, Busan 46241, South Korea
[2] Pusan Natl Univ, Dept Mol Biol, Busan 46241, South Korea
[3] Seoul Natl Univ, Res Inst Agr & Life Sci, Dept Plant Sci, Plant Genom & Breeding Inst, Seoul 08826, South Korea
[4] Dong Eui Univ, Dept Mol Biol, Busan 47340, South Korea
[5] Hokkaido Univ, Inst Low Temp Sci, Sapporo, Hokkaido 0600819, Japan
[6] Seoul Natl Univ, Inst Green Bio Sci & Technol, Crop Biotechnol Inst, Pyeongchang 25354, South Korea
[7] Anim & Plant Quarantine Agcy, Yeongnam Reg Off, Busan 48943, South Korea
基金
新加坡国家研究基金会;
关键词
Aggregate; Chlorophyll degradation; Chlorophyllprotein complexes; Dark-induced senescence; Light-harvesting; STAY-GREEN PHENOTYPE; PROTEIN COMPLEXES; A REDUCTASE; B REDUCTASE; BREAKDOWN; GENE; PHEOPHORBIDE; CATABOLITES; CLONING; IDENTIFICATION;
D O I
10.1007/s12374-018-0242-0
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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.
引用
收藏
页码:27 / 38
页数:12
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