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1.
An Acad Bras Cienc ; 84(1): 185-90, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22441608

ABSTRACT

Chagasin may be considered a potential plant-incorporated protectant (PIP) protein due to its deleterious effects on insect pests. However, extensive safety studies with PIP's are necessary before introducing them into the target plant. Thus, a short-term feeding trial in rats with high doses of r-chagasin was conducted to provide evidences about its safety. Three test diets containing casein + r-chagasin (0.25, 0.5 and 1% of total protein) were offered to rats (10 days). The test diets did not show adverse effects upon the development, organ weight, hematological parameters and serum protein profiles of rats, providing preliminary information on the safety of r-chagasin.


Subject(s)
Animal Feed/toxicity , Insect Proteins/toxicity , Organ Size/drug effects , Animals , Insect Proteins/administration & dosage , Male , Models, Animal , Pest Control, Biological , Rats , Recombinant Proteins/administration & dosage , Recombinant Proteins/toxicity , Toxicity Tests/methods , Weight Gain
2.
Proteins ; 63(3): 662-70, 2006 May 15.
Article in English | MEDLINE | ID: mdl-16470583

ABSTRACT

Plant cystatins show great potential as tools to genetically engineer resistance of crop plants against pests. Two important potential targets are the bean weevils Acanthoscelides obtectus and Zabrotes subfasciatus, which display major activities of digestive cysteine proteinases in midguts. In this study a cowpea cystatin, a cysteine proteinase inhibitor found in cowpea (Vigna unguiculata) seeds, was expressed in Escherichia coli and purified with a Ni-NTA agarose column. It strongly inhibited papain and proteinases from midguts of both A. obtectus and Z. subfasciatus bruchids, as seen by in vitro assays. When the protein was incorporated into artificial seeds at concentrations as low as 0.025%, and seeds were consumed by the bruchids larva, dramatic reductions in larval weight, and increases in insect mortality were observed. Molecular modeling studies of cowpea cystatin in complex with papain revealed that five N-terminal residues responsible for a large proportion of the hydrophobic interactions involved in the stabilization of the enzyme-inhibitor complex are absent in the partial N-terminal amino acid sequencing of soybean cystatin. We suggest that this structural difference could be the reason for the much higher effectiveness of cowpea cystatin when compared to that previously tested phytocystatin. The application of this knowledge in plant protein mutation programs aiming at enhancement of plant defenses to pests is discussed.


Subject(s)
Cystatins/chemistry , Fabaceae/chemistry , Models, Molecular , Plant Proteins/chemistry , Weevils , Agriculture/methods , Amino Acid Sequence , Animals , Cystatins/genetics , Cystatins/metabolism , Cysteine Proteinase Inhibitors/chemistry , Cysteine Proteinase Inhibitors/genetics , Cysteine Proteinase Inhibitors/metabolism , Fabaceae/genetics , Fabaceae/metabolism , Molecular Sequence Data , Pest Control, Biological/methods , Plant Proteins/genetics , Plant Proteins/metabolism , Protein Engineering/methods , Protein Structure, Secondary
3.
Phytochemistry ; 65(1): 81-9, 2004 Jan.
Article in English | MEDLINE | ID: mdl-14697273

ABSTRACT

The cotton boll weevil, Anthonomus grandis, is an economically important pest of cotton in tropical and subtropical areas of several countries in the Americas, causing severe losses due to their damage in cotton floral buds. Enzymatic assays using gut extracts from larval and adult boll weevil have demonstrated the presence of digestive serine proteinase-like activities. Furthermore, in vitro assays showed that soybean Kunitz trypsin inhibitor (SKTI) was able to inhibit these enzymes. Previously, in vivo effects of black-eyed pea trypsin chymotrypsin inhibitor (BTCI) have been demonstrated towards the boll weevil pest. Here, when neonate larvae were reared on an artificial diet containing SKTI at three different concentrations, a reduction of larval weight of up to 64% was observed for highest SKTI concentration 500 microM. The presence of SKTI caused an increase in mortality and severe deformities of larvae, pupae and adult insects. This work therefore represents the first observation of a Kunitz trypsin inhibitor active in vivo and in vitro against A. grandis. Bioassays suggested that SKTI could be used as a tool in engineering crop plants, which might exhibit increased resistance against cotton boll weevil.


Subject(s)
Coleoptera/drug effects , Coleoptera/enzymology , Trypsin Inhibitor, Kunitz Soybean/pharmacology , Animal Feed , Animals , Cattle , Digestive System/enzymology , Dose-Response Relationship, Drug , Larva/drug effects , Larva/growth & development , Pupa/drug effects , Pupa/growth & development , Serine Endopeptidases/metabolism , Survival Analysis , Trypsin/metabolism , Trypsin Inhibitors/pharmacology
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