Proteomic approach to blossom-end rot in tomato fruits (Lycopersicon esculentum M.):: Antioxidant enzymes and the pentose phosphate pathway

被引:35
作者
Casado-Vela, J [1 ]
Sellés, S [1 ]
Martínez, RB [1 ]
机构
[1] Univ Alicante, Fac Ciencias, Dept Agroquim & Bioquim, E-03080 Alicante, Spain
关键词
antioxidant; blossom-end rot; tomato; Triton X-114;
D O I
10.1002/pmic.200401146
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Blossom-end rot (BER) is a physiopathy that affects tomato fruits causing disorganisation, cell breakage and darkening of the tissues. In this study we describe a tomato fruit protein extraction protocol that includes polyvinyl polypyrrolidone, ascorbic acid and protease inhibitors to promote depletion of phenolics and to avoid protein degradation. The temperature-induced phase separation of plant extracts with nonionic detergent Triton X-114 favours the solubilisation of partially-hydrophobic species in the low-detergent upper phase, making them suitable for further analysis using two-dimensional gel electrophoresis. The analysis of two-dimensional images revealed differences in number and expression levels of several proteins from the control and BER-affected tomato fruits. Although the appearance of BER in tomato is primarily attributed to a lack of calcium supply to fruits, very little is known about the molecular and biochemical mechanisms involved. The identification of differential proteins from affected fruits with matrix-assisted laser desorption/ionisation-time of flight and peptide mass fingerprinting analysis revealed the induction of proteins participating in antioxidant processes (ascorbate-glutathione cycle) and the pentose phosphate pathway. We suggest that these two biochemical pathways, acting as reactive oxygen species scavengers in BER-affected fruits, restrain the spread of the blackening to the whole fruit.
引用
收藏
页码:2488 / 2496
页数:9
相关论文
共 66 条
[1]   Two-dimensional gel electrophoresis pattern (pH 6-11) and identification of water-soluble barley seed and malt proteins by mass spectrometry [J].
Bak-Jensen, KS ;
Laugesen, S ;
Roepstorff, P ;
Svensson, B .
PROTEOMICS, 2004, 4 (03) :728-742
[2]  
BORDIER C, 1981, J BIOL CHEM, V256, P1604
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]  
CASADOVELA J, 2005, IN PRESS J FOOD BIOC
[5]   Role of accurate mass measurement (±10 ppm) in protein identification strategies employing MS or MS MS and database searching [J].
Clauser, KR ;
Baker, P ;
Burlingame, AL .
ANALYTICAL CHEMISTRY, 1999, 71 (14) :2871-2882
[6]   Interactive effects of air humidity, calcium and phosphate on blossom-end rot, leaf deformation, production and nutrient contents of tomato [J].
deKreij, C .
JOURNAL OF PLANT NUTRITION, 1996, 19 (02) :361-377
[7]   Feasibility study of a tissue-specific approach to barley proteome analysis: aleurone layer, endosperm, embryo and single seeds [J].
Finnie, C ;
Svensson, B .
JOURNAL OF CEREAL SCIENCE, 2003, 38 (02) :217-227
[8]   Proteome analysis of grain filling and seed maturation in barley [J].
Finnie, C ;
Melchior, S ;
Roepstorff, P ;
Svensson, B .
PLANT PHYSIOLOGY, 2002, 129 (03) :1308-1319
[9]   The plant glutathione transferase gene family: genomic structure, functions, expression and evolution [J].
Frova, C .
PHYSIOLOGIA PLANTARUM, 2003, 119 (04) :469-479
[10]   Proteomics of Arabidopsis seed germination. A comparative study of wild-type and gibberellin-deficient seeds [J].
Gallardo, K ;
Job, C ;
Groot, SPC ;
Puype, M ;
Demol, H ;
Vandekerckhove, J ;
Job, D .
PLANT PHYSIOLOGY, 2002, 129 (02) :823-837