A bifunctional α-amylase/trypsin inhibitor from pigeonpea seeds: Purification, biochemical characterization and its bio-efficacy against Helicoverpa armigera

• This paper evaluates amylase inhibitor mediated defense of pigeonpea against H. armigera.
• Bifunctional amylase/trypsin inhibitor is purified from pigeonpea cultivar BSMR-736.
• It was found to be multi-isomeric glycoprotein shared homology with cereal type AIs.
• Upon ingestion it negatively affected growth rate of H. armigera.
• In-vivo studies indicated increase in midgut amylase activity of H. armigera.

This paper evaluates α-amylase inhibitor (α-AI) mediated defense of pigeonpea against Helicoverpa armigera. A bifunctional α-amylase/trypsin inhibitor was purified from the seeds of pigeonpea by native liquid phase isoelectric focusing (N-LP-IEF), affinity chromatography and preparative electrophoresis. Its in-vivo and in-vitro interaction with midgut amylases of H. armigera was studied along with growth inhibitory activity. One and two dimensional (2D) zymographic analyses revealed that the purified inhibitor is dimeric glycoprotein (60.2 kDa and 56 kDa) exist in a multi-isomeric form with five pI variants (pI 5.5 to 6.3). It was found to be heat labile with complete inactivation up to 80 °C and stable over a wide range of pH (4–11). The slow binding and competitive type of α-amylase inhibition was observed with 0.08 μM of dissociation constant (Ki) for the enzyme–inhibitor complex (EI). The internal protein sequence of two subunits obtained by mass spectrometry matched with cereal-type α-AI, a conserved domain from AAI_LTSS superfamily and sialyltransferase-like protein respectively. In-vivo studies indicated up-regulation of total midgut α-amylase activity with negative effect on growth rate of H. armigera suggesting its suitability for pest control.

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