Cypress canker induced inhibition of photosynthesis in field grown cypress (Cupressus sempervirens L.) needles

被引:11
作者
Muthuchelian, K [1 ]
La Porta, N
Bertamini, M
Nedunchezhian, N
机构
[1] Madurai Kamaraj Univ, Sch Energy Environm & Nat Resources, Ctr Biodivers & Forest Studies, Madurai 625021, Tamil Nadu, India
[2] Ist Agrario San Michele All Adige, I-38010 San Michele All Adige, Italy
关键词
donor side; electron transport; fluorescence; nitrate reductase;
D O I
10.1016/j.pmpp.2005.08.007
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Investigations were carried out to envisage the effect of the cypress canker infection on some features of the thylakoids from field grown cypress (Cupressus sempervirens) needles. Changes in photosynthetic pigments, soluble proteins, soluble starch, starch, ribulose-1,5-bisphosphate carboxylase, nitrate reductase, photosynthetic activities and thylakoid membrane proteins were investigated. The level of total chlorophyll and carotenoids were markedly reduced in cypress canker-infected needles. Similar results were also observed for soluble proteins, nitrate reductase and ribulose-1,5-bisphosphate carboxylase activity. In contrast, the content of soluble starch and sugar were increased in infected needles. In isolated thylakoids, cypress canker infection caused marked inhibition of whole chain and photosystem II activity while the inhibition of photosystem I activity was only marginal. The artificial exogenous electron donors, diphenyl carbazide and hydroxylamine significantly restored the loss of photosystem II activity in infected needles. The same results were obtained when Fv/Fm was evaluated by chlorophyll fluorescence measurements. The marked loss of photosystem II activity in infected needles could be due to the loss of 47, 43, 33, 28, 25, 23, 17 and 15 kDa polypeptides. It is concluded that cypress canker infection inactivates the donor side of photosystem II. This conclusion was confirmed by immunological studies showing that the content of the 33 kDa protein of the water-splitting complex was diminished significantly in infected needles. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:33 / 39
页数:7
相关论文
共 39 条
[21]  
LICHTENTHALER HK, 1987, METHOD ENZYMOL, V148, P350
[22]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265
[23]  
MAE T, 1993, PLANT CELL PHYSIOL, V34, P391
[24]   EFFECT OF A SYSTEMIC VIRUS-INFECTION ON CHLOROPLAST FUNCTION AND STRUCTURE [J].
MAGYAROSY, AC ;
BUCHANAN, BB ;
SCHURMANN, P .
VIROLOGY, 1973, 55 (02) :426-438
[25]   DETERMINATION OF STARCH AND AMYLOSE IN VEGETABLES - APPLICATION TO PEAS [J].
MCCREADY, RM ;
GUGGOLZ, J ;
SILVIERA, V ;
OWENS, HS .
ANALYTICAL CHEMISTRY, 1950, 22 (09) :1156-1158
[26]   INVESTIGATION OF THE SPATIAL RELATIONSHIPS BETWEEN PHOTOSYSTEM-2 POLYPEPTIDES BY REVERSIBLE CROSS-LINKING AND DIAGONAL ELECTROPHORESIS [J].
MILLNER, PA ;
GOGEL, G ;
BARBER, J .
PHOTOSYNTHESIS RESEARCH, 1987, 13 (02) :185-198
[27]   STOICHIOMETRY OF COMPONENTS IN THE PHOTOSYNTHETIC OXYGEN EVOLUTION SYSTEM OF PHOTOSYSTEM-II PARTICLES PREPARED WITH TRITON X-100 FROM SPINACH-CHLOROPLASTS [J].
MURATA, N ;
MIYAO, M ;
OMATA, T ;
MATSUNAMI, H ;
KUWABARA, T .
BIOCHIMICA ET BIOPHYSICA ACTA, 1984, 765 (03) :363-369
[28]   Decline in photosynthetic electron transport activity and changes in thylakoid protein pattern in field grown iron deficient Peach (Prunus persica L.) [J].
Nedunchezhian, N ;
Morales, F ;
Abadia, A ;
Abadia, J .
PLANT SCIENCE, 1997, 129 (01) :29-38
[29]  
NEDUNCHEZHIAN N, 1991, PHOTOSYNTHETICA, V25, P431
[30]  
PONCHET J, 1989, EUR J FOREST PATHOL, V19, P212