Effect of Manganese toxicity on the proteome of the leaf apoplast in cowpea

被引:149
作者
Fecht-Christoffers, MM
Braun, HP
Lemaitre-Guillier, C
VanDorsselaer, A
Horst, WJ
机构
[1] Univ Hannover, Inst Plant Nutr, D-30419 Hannover, Germany
[2] Univ Hannover, Dept Appl Genet, D-30419 Hannover, Germany
[3] Lab Spectrometrie Masse Bioorgan, UMR 7509, F-67087 Strasbourg, France
关键词
D O I
10.1104/pp.103.029215
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Excess manganese (Mn) supply causes formation of visible brown depositions in the cell walls of leaves of cowpea (Vigna unguiculata), which consist of oxidized Mn and oxidized phenols. Because oxidation of Mn and phenolic compounds in the leaf apoplast was proposed to be catalyzed by apoplastic peroxidases (PODs), induction of these enzymes by Mn excess was investigated. POD activity increased upon prolonged Mn treatment in the leaf tissue. Simultaneously, a significant increase in the concentration of soluble apoplastic proteins in "apoplastic washing fluid" was observed. The identity of the released proteins was systematically characterized by analysis of the apoplast proteome using two-dimensional gel electrophoresis and liquid chromatography-tandem mass spectrometry. Some of the identified proteins exhibit sequence identity to acidic PODs from other plants. Several other proteins show homologies to pathogenesis-related proteins, e.g. glucanase, chitinase, and thaumatin-like proteins. Because pathogenesis-related-like proteins are known to be induced by various other abiotic and biotic stresses, a specific physiological role of these proteins in response to excess Mn supply remains to be established. The specific role of apoplastic PODs in the response of plants to Mn stress is discussed.
引用
收藏
页码:1935 / 1946
页数:12
相关论文
共 88 条
[1]   Molecular cloning, characterization and in vitro expression of a novel endo-1,3-β-glucanase up-regulated by ABA and drought stress in rice (Oryza sativa L.) [J].
Akiyama, T ;
Pillai, MA .
PLANT SCIENCE, 2001, 161 (06) :1089-1098
[2]   Immunolocalization of antifreeze proteins in winter rye leaves, crowns, and roots by tissue printing [J].
Antikainen, M ;
Griffith, M ;
Zhang, J ;
Hon, WC ;
Yang, DSC ;
PihakaskiMaunsbach, K .
PLANT PHYSIOLOGY, 1996, 110 (03) :845-857
[3]   LUPIN PEROXIDASES .1. ISOLATION AND CHARACTERIZATION OF CELL WALL-BOUND ISOPEROXIDASE ACTIVITY [J].
BARCELO, AR ;
MUNOZ, R ;
SABATER, F .
PHYSIOLOGIA PLANTARUM, 1987, 71 (04) :448-454
[4]   ROLE OF TRICHOMES IN SUNFLOWER TOLERANCE TO MANGANESE TOXICITY [J].
BLAMEY, FPC ;
JOYCE, DC ;
EDWARDS, DG ;
ASHER, CJ .
PLANT AND SOIL, 1986, 91 (02) :171-180
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]  
BRYNGELSSON T, 1994, MOL PLANT MICROBE IN, V7, P268
[7]   Differential expression of chitinases in Vitis vinifera L. responding to systemic acquired resistance activators or fungal challenge [J].
Busam, G ;
Kassemeyer, HH ;
Matern, U .
PLANT PHYSIOLOGY, 1997, 115 (03) :1029-1038
[8]  
CAMPA A, 1991, PEROXIDASE CHEM BIOL, V2, P26
[9]  
Castillo F. J., 1986, MOL PHYSL ASPECTS PL, P419
[10]   PEROXIDASE RELEASE INDUCED BY OZONE IN SEDUM-ALBUM LEAVES INVOLVEMENT OF CA-2+ [J].
CASTILLO, FJ ;
PENEL, C ;
GREPPIN, H .
PLANT PHYSIOLOGY, 1984, 74 (04) :846-851