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J Insect Sci ; 142014.
Article in English | MEDLINE | ID: mdl-25528751

ABSTRACT

Amylases are an important family of enzymes involved in insect carbohydrate metabolism that are required for the survival of insect larvae. For this reason, enzymes from starch-dependent insects are targets for insecticidal control. PF2 (Olneya tesota) is a lectin that is toxic to Zabrotes subfasciatus (Coleoptera: Bruchidae) larvae. In this study, we evaluated recognition of the PF2 lectin to α-amylases from Z. subfasciatus midgut and the effect of PF2 on α-amylase activity. PF2 caused a decrease of total amylase activity in vitro. Subsequently, several α-amylase isoforms were isolated from insect midgut tissues using ion exchange chromatography. Three enzyme isoforms were verified by an in-gel assay for amylase activity; however, only one isoform was recognized by antiamylase serum and PF2. The identity of this Z. subfasciatus α-amylase was confirmed by liquid chromatography-tandem mass spectrometry. The findings strongly suggest that a glycosylated α-amylase isoform from larval Z. subfasciatus midgut interacts with PF2, which interferes with starch digestion.


Subject(s)
Coleoptera/physiology , Digestive System/drug effects , Fabaceae/chemistry , Lectins/metabolism , Plant Proteins/metabolism , alpha-Amylases/biosynthesis , Animals , Digestive System/metabolism , Fabaceae/metabolism , Larva/drug effects , Larva/physiology , Plant Lectins , alpha-Amylases/antagonists & inhibitors
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