Identification of Arabidopsis salt and osmotic stress responsive proteins using two-dimensional difference gel electrophoresis and mass spectrometry

被引:244
作者
Ndimba, BK
Chivasa, S
Simon, WJ
Slabas, AR [1 ]
机构
[1] Univ Durham, Sch Biol & Biomed sci, Durham DH1 3LE, England
[2] Univ Western Cape, Dept Biotechnol, Cape Town, South Africa
[3] Univ Durham, Creat Gene Technol Lab, Durham DH1 3LE, England
[4] Univ Durham, Integrat Cell Biol Lab, Durham DH1 3LE, England
关键词
2-D DIGE; Arabidopsis; drought; proteome; salinity;
D O I
10.1002/pmic.200401282
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Arabidopsis thaliana cell suspension cultures have been used to investigate the effects of salinity and hyperosmotic stress on plant cellular proteins. We show that 200 mm NaCl and 400 mm sorbitol treatments induce extracellular medium acidification in Arabidopsis cell cultures, a typical response of plant cells to salt and hyperosmotic stress. Using 15 S-labelled amino acids, we demonstrated that NaCl causes a transient suppression of de novo protein synthesis, from which the cells recover within 4 h. Changes in the abundance of cellular proteins 6 h post NaCl and sorbitol treatments were analysed by 2-DE. Of a total of 2,949 protein spots detected on the gels, 266 showed significant changes in abundance across five independent experiments. Using MALDI-TOF MS, we identified 75 salt and sorbitol responsive spots. These fall into 10 functional categories that include H+ transporting ATPases, signal transduction related. proteins, transcription/translation related proteins, detoxifying enzymes, amino acid and purine biosynthesis related proteins, proteolytic enzymes, heat-shock proteins, carbohydrate metabolism-associated proteins and proteins with no known biological functions.
引用
收藏
页码:4185 / 4196
页数:12
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