Expression and biological activity of the cystine knot bioinsecticide PA1b (Pea Albumin 1 Subunit b)
2013
EYRAUD , Vanessa (INRA , Villeurbanne (France). UMR 0203 Biologie Fonctionnelle, Insectes et Interactions) | Karaki , Lamis (INRA , Villeurbanne (France). UMR 0203 Biologie Fonctionnelle, Insectes et Interactions) | Rahioui-Chabaux , Isabelle (INRA , Villeurbanne (France). UMR 0203 Biologie Fonctionnelle, Insectes et Interactions) | Sivignon , Catherine (INRA , Villeurbanne (France). UMR 0203 Biologie Fonctionnelle, Insectes et Interactions) | Da Silva , Pedro (INRA , Villeurbanne (France). UMR 0203 Biologie Fonctionnelle, Insectes et Interactions) | Rahbé , Yves (INRA , Villeurbanne (France). UMR 0203 Biologie Fonctionnelle, Insectes et Interactions) | Royer , Corinne (INRA , Villeurbanne (France). UMR 0203 Biologie Fonctionnelle, Insectes et Interactions) | Gressent , Frederic (INRA , Villeurbanne (France). UMR 0203 Biologie Fonctionnelle, Insectes et Interactions)
The PA1b (Pea Albumin 1, subunit b) peptide is an entomotoxin extract from Legume seeds with lethal activity on several insect pests, such as mosquitoes, some aphids and cereal weevils. This 37 amino-acid cysteine-rich peptide has been, until now, obtained by biochemical purification or chemical synthesis. In this paper, we present our results for the transient production of the peptide in Nicotiana benthamiana by agro-infiltration, with a yield of about 35 µg/g of fresh leaves and maximum production 8 days after infiltration. PA1b is part of the PA1 gene which, after post-translational modifications, encodes two peptides (PA1b and PA1a). We show that transforming tobacco with the PA1b cDNA alone does not result in production of the toxin and, in fact, the entire cDNA is necessary, raising the question of the role of PA1a. We constructed a PA1-cassette, allowing for the quick "cut/paste" of different PA1b mutants within a conserved PA1 cDNA. This cassette enabled us to produce the six isoforms of PA1b which exist in pea seeds. Biological tests revealed that all the isoforms display similar activity, with the exception of one which is inactive. The lack of activity in this isoform led us to conclude that the amphiphilic nature of the peptide is necessary for activity. The possible applications of this expression system for other cysteine-rich biomolecules are discussed.
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