Isolation and characterisation of a protein elicitor from Sclerospora graminicola and elicitor-mediated induction of defence responses in cultured cells of Pennisetum glaucum
R. G. Sharathchandra A , N. P. Geetha A , K. N. Amruthesh A , K. Ramachandra Kini A , B. R. Sarosh A , N. P. Shetty B and H. S. Shetty A CA Downy Mildew Research Laboratory, Department of Studies in Applied Botany and Biotechnology, University of Mysore, Manasagangotri Mysore-570 006, India.
B Section for Plant Pathology, The Royal Veterinary and Agricultural University, Thorvaldsensvej 40, DK-1871 Frederiksberg C, Copenhagen, Denmark.
C Corresponding author. Email: hss@appbot.uni-mysore.ac.in
Functional Plant Biology 33(3) 267-278 https://doi.org/10.1071/FP05197
Submitted: 8 August 2005 Accepted: 10 October 2005 Published: 2 March 2006
Abstract
Sclerospora graminicola (Sacc.) Schroet., an oomycete pathogen of Pennisetum glaucum (L.) R.Br. infects the meristematic tissues of young seedlings. The motile zoospores from the sporangia encyst, germinate and penetrate the plant tissue. Resistance to the invading pathogen is governed by the specific recognition of conserved pathogen-associated proteins or elicitors. In the present study, a zoospore protein was isolated and purified to homogeneity by a combination of size exclusion and high-performance liquid chromatography (HPLC). The crude fractionated protein was able to elicit an array of defence responses in resistant and susceptible cells of pearl millet. Treatment of cultured cells of pearl millet with partially purified elicitor protein resulted in a rapid loss of cell viability in the resistant cells and the percentage of cell death was higher in the resistant than in the susceptible cells. Cultures of resistant cells showed a sharp increase in the extra cellular pH compared with susceptible cells when treated with the crude elicitor. Increased oxidative burst was also recorded in the cells treated with the crude elicitor. The purified elicitor showed unique properties. The purified protein was acidic with a pI of 5.6 as revealed by isoelectric focusing (IEF) and matrix-assisted laser desorption ionisation (MALDI) analysis showed that the elicitor had a molecular mass of 7040 daltons. The primary structure determined by N-terminal Edman degradation and searches with BLAST did not reveal similarities to any known plant pathogenic or oomycete elicitor. Higher activities of the important defence-related enzymes phenylalanine ammonia lyase (PAL) and peroxidase in the resistant cell cultures than in the susceptible cell cultures treated with the purified elicitor were clearly evident. Studies of gene expression by northern blotting with heterologus peroxidase, PAL and oxalate oxidase probes showed that the mRNA transcripts were strongly up-regulated in resistant cell cultures within 30 min of elicitor treatment. The purified elicitor also demonstrated a very strong concentration-dependent sterol binding. The purified elicitor protein belongs to a class of low molecular weight oomycete elicitors with sterol carrier properties. The identified low molecular weight protein elicitor displays unique properties that can be exploited for synthesis of novel molecules for eco-friendly crop protection.
Keywords: biological activity, cell suspension culture, protein elicitor, Sclerospora graminicola, sterol binding, transcripts.
Acknowledgments
This work was conducted under the Project on Systemic Acquired Resistance funded by the Danish International Development Agency under the Enhancement of Research Capacity Program (DANIDA ENRECA). We are grateful to Dr Eigil de Neergard, the Principal Responsible Leader of the DANIDA ENRECA Project for his co-operation during this study. We also thank Dr Hans J. Lyngs Jørgensen, Section for Plant Pathology, The Royal Veterinary and Agricultural University, Denmark for critical review of the manuscript. The facilities provided by Indian Council of Agricultural Research, Government of India through All India Coordinated Pearl Millet Improvement Project are also gratefully acknowledged. The authors also thank Department of Science and Technology, New Delhi, India for providing facilities for cell line maintenance.
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