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
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页码:33 / 39
页数:7
相关论文
共 39 条
[11]  
Del Sorbo Giovanni, 1994, Natural Toxins, V2, P136, DOI 10.1002/nt.2620020309
[12]   COLORIMETRIC METHOD FOR DETERMINATION OF SUGARS AND RELATED SUBSTANCES [J].
DUBOIS, M ;
GILLES, KA ;
HAMILTON, JK ;
REBERS, PA ;
SMITH, F .
ANALYTICAL CHEMISTRY, 1956, 28 (03) :350-356
[13]   IS THE PRIMARY CAUSE OF THERMAL INACTIVATION OF OXYGEN EVOLUTION IN SPINACH PS-II MEMBRANES RELEASE OF THE EXTRINSIC 33 KDA PROTEIN OR OF MN [J].
ENAMI, I ;
KITAMURA, M ;
TOMO, T ;
ISOKAWA, Y ;
OHTA, H ;
KATOH, S .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1994, 1186 (1-2) :52-58
[14]   Cacopsylla costalis (Flor 1861), as a vector of apple proliferation in Trentino [J].
Frisinghelli, C ;
Delaiti, L ;
Grando, MS ;
Forti, D ;
Vindimian, ME .
JOURNAL OF PHYTOPATHOLOGY-PHYTOPATHOLOGISCHE ZEITSCHRIFT, 2000, 148 (7-8) :425-431
[15]  
GRANITI A, 1992, PLANT PATHOL, V41, P563, DOI 10.1111/j.1365-3059.1992.tb02454.x
[16]  
HUNTER CS, 1973, PHYSL PLANT PATHOLOG, V3, P95
[17]   Genetic variability of apple proliferation phytoplasmas as determined by PCR-RFLP and sequencing of a non-ribosomal fragment [J].
Jarausch, W ;
Saillard, C ;
Helliot, B ;
Garnier, M ;
Dosba, F .
MOLECULAR AND CELLULAR PROBES, 2000, 14 (01) :17-24
[18]   NITRATE REDUCTASE ASSAY IN INTACT PLANT TISSUES [J].
JAWORSKI, EG .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1971, 43 (06) :1274-&
[19]  
KYLE DJ, 1987, TOPICS PHOTOSYNTHESI, V9, P197
[20]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+