Construction of Cryptogein Mutants, a Proteinaceous Elicitor from Phytophthora, with Altered Abilities To Induce a Defense Reaction in Tobacco Cells

Jan Lochman, Tomas Kasparovsky, Jiri Damborsky,§ Hanan Osman, Antoine Marais, Radka Chaloupkova,§ Michel Ponchet, Jean-Pierre Blein, and Vladimir Mikes*
Department of Biochemistry, Faculty of Science, and National Center for Biomolecular Research, Faculty of Science, Masaryk University, Kotlsk 2, 61137 Brno, Czech Republic, UMR IPMSV, Sophia Antipolis, 400 Route des Chappes, France, and Unit Mixte de Recherche 692, INRA, 21065 Dijon-Cedex, France
Biochemistry, 2005, 44 (17), pp 6565–6572
DOI: 10.1021/bi0502285
Publication Date (Web): April 9, 2005
Copyright © 2005 American Chemical Society

 Financial support by the Czech Grant Agency (522/02/0925), by the Ministry of Education, Youth and Sports (MSM0021622413), and by the French Embassy in Prague is gratefully acknowledged.

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 Department of Biochemistry, Masaryk University.

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 National Center for Biomolecular Researche, Masaryk University.

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 UMR IPMSV.

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 Unité Mixte de Recherche 692.

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*

 To whom correspondence should be addressed. Phone: (+420)549495852. Fax:  (+420)549492690. E-mail:  mikes@chemi.muni.cz.

Abstract

Abstract Image

We prepared a series of cryptogein mutants, an elicitor from Phytophthora cryptogea, with altered abilities to bind sterols and fatty acids. The induction of the early events, i.e., synthesis of active oxygen species and pH changes, in suspension tobacco cells by these mutated proteins was proportional to their ability to bind sterols but not fatty acids. Although the cryptogein−sterol complex was suggested to be a form triggering a defense reaction in tobacco, some proteins unable to bind sterols induced the synthesis of active oxygen species and pH changes. The modeling experiments showed that conformational changes after the introduction of bulky residues into the ω loop of cryptogein resemble those induced by sterol binding. These changes may be necessary for the ability to trigger the early events by elicitins. However, the ability to stimulate necrosis in suspension tobacco cells and the expression of defense proteins in tobacco plants were linked neither to the lipid binding capacity nor to the capacity to provoke the early events. On the basis of these experiments and previous results, we propose that elicitins could stimulate two signal pathways. The first one induces necroses and the expression of pathogen-related proteins, includes tyrosine protein kinases and mitogen-activated protein kinases, and depends on the overall structure and charge distribution. The second type of interaction is mediated by phospholipase C and protein kinase C. It triggers the synthesis of active oxygen species and pH changes. This interaction depends on the ability of elicitins to bind sterols.

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History

  • Published In Issue May 03, 2005
  • Received February 8, 2005
    Revised Manuscript Received March 14, 2005

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