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First published online January 11, 2008; 10.1104/pp.108.115741

Plant Physiology 146:1010-1019 (2008)
© 2008 American Society of Plant Biologists

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Tailoring the Specificity of a Plant Cystatin toward Herbivorous Insect Digestive Cysteine Proteases by Single Mutations at Positively Selected Amino Acid Sites1,[OA]

Marie-Claire Goulet, Cindy Dallaire, Louis-Philippe Vaillancourt, Moustafa Khalf, Amine M. Badri, Andreja Preradov, Marc-Olivier Duceppe, Charles Goulet, Conrad Cloutier and Dominique Michaud*

Département de Phytologie, Pavillon des Services (M.-C.G., C.D., L.-P.V., M.K., A.M.B., A.P., M.-O.D., C.G., D.M.), and Département de Biologie (C.C.), Centre de Recherche en Horticulture, Université Laval, Quebec, Canada G1K 7P4

Plant cystatins, similar to other defense proteins, include hypervariable, positively selected amino acid sites presumably impacting their biological activity. Using 29 single mutants of the eighth domain of tomato (Solanum lycopersicum) multicystatin, SlCYS8, we assessed here the potential of site-directed mutagenesis at positively selected amino acid sites to generate cystatin variants with improved inhibitory potency and specificity toward herbivorous insect digestive cysteine (Cys) proteases. Compared to SlCYS8, several mutants (22 out of 29) exhibited either improved or lowered potency against different model Cys proteases, strongly suggesting the potential of positively selected amino acids as target sites to modulate the inhibitory specificity of the cystatin toward Cys proteases of agronomic significance. Accordingly, mutations at positively selected sites strongly influenced the inhibitory potency of SlCYS8 against digestive Cys proteases of the insect herbivore Colorado potato beetle (Leptinotarsa decemlineata). In particular, several variants exhibited improved potency against both cystatin-sensitive and cystatin-insensitive digestive Cys proteases of this insect. Of these, some variants also showed weaker activity against leaf Cys proteases of the host plant (potato [Solanum tuberosum]) and against a major digestive Cys protease of the two-spotted stinkbug Perillus bioculatus, an insect predator of Colorado potato beetle showing potential for biological control. Overall, these observations suggest the usefulness of site-directed mutagenesis at positively selected amino acid sites for the engineering of recombinant cystatins with both improved inhibitory potency toward the digestive proteases of target herbivores and weaker potency against nontarget Cys proteases in the host plant or the environment.


1 This work was supported by the Natural Science and Engineering Research Council of Canada (Discovery grant to D.M., and graduate scholarships to M.-C.G., C.G., and M.-O.D.), by the Government of Egypt (Ph.D. fellowship to M.K.), and by the Government of Tunisia (Ph.D. fellowship to A.M.B.).

The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Dominique Michaud (dominique.michaud{at}plg.ulaval.ca).

[OA] Open Access articles can be viewed online without a subscription.

www.plantphysiol.org/cgi/doi/10.1104/pp.108.115741

* Corresponding author; e-mail dominique.michaud{at}plg.ulaval.ca.

Received January 1, 2008; accepted January 8, 2008; published January 11, 2008.







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