Proteomic analysis of chloroplasts from chlorophyll-deficient melon mutant

被引:0
|
作者
Zhao, C. M. [1 ,2 ]
Cui, J. Z. [3 ]
Li, X. G. [1 ]
Chen, B. J. [2 ]
Jin, R. R. [2 ]
Yu, Z. Y. [1 ]
机构
[1] Northeast Agr Univ, Hort Coll, 59 Mucai St, Harbin 150030, Heilongjiang, Peoples R China
[2] Harbin Acad Agr Sci, Harbin, Heilongjiang, Peoples R China
[3] Harbin Normal Univ, Life Sci & Technol Inst, Harbin, Heilongjiang, Peoples R China
关键词
label-free protein quantification; photosynthetic pathways; proteome analysis; qRT-PCR; ARABIDOPSIS-THALIANA; LIPID-PEROXIDATION; PHOTOSYSTEM-II; GREEN MUTANTS; MG-CHELATASE; PROTEINS; GENE; STROMULES; REVEALS; BIOSYNTHESIS;
D O I
10.32615/ps.2019.078
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
We aimed to understand the molecular-level changes occurring in the photosynthetic metabolic network in mutant chloroplasts. We performed comparative liquid chromatography-mass spectrometry protein profiling of wild-type (WT) and chlorophyll-deficient melon (Cucumis melo L.) mutants. We identified 390 differentially expressed proteins and 81 shared proteins varied significantly in abundance, of which 76 were upregulated and 5 were downregulated. Differentially expressed proteins were involved in the following biological processes: binding, catalytic, structural, transporter, and antioxidant activities. The mutant had 6.08-fold higher expression of glutamate-1-semialdehyde 2,1-aminomutase (GSAM), an enzyme that synthesizes the chlorophyll precursor, 5-aminolevulinic acid, and a 5.02-fold higher expression of pyridoxal biosynthesis protein, a GSAM coenzyme. An RNA recognition motif-containing protein (RRM) decreased in expression by 5.22-fold. This suggests that GSAM and RRM are particularly relevant to chlorophyll deficiency.
引用
收藏
页码:866 / 874
页数:9
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