Bowman-birk proteinase inhibitor from Cajanus cajan seeds: Purification, characterization, and insecticidal properties

Abstract

A red gram proteinase inhibitor (RgPI) was purified from red gram (Cajanus cajan) seeds by using ammonium sulfate precipitation and ion-exchange, affinity, and gel filtration chromatography. SDSPAGE under nonreducing condition revealed two protein bands with molecular masses of ∼8.5 and ∼16.5 kDa corresponding to monomeric and dimeric forms of RgPI, respectively. Similarly, matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry also confirmed the presence of dimer as well as other oligomeric forms: trimer, tetramer, and pentamer. Reduction of RgPI with dithiothreitol (DTT) led to the dissociation of the dimeric and oligomeric forms. Native-PAGE and two-dimensional gel electrophoresis indicated the existence of isoinhibitors with p/values of 5.95, 6.25, 6.50, 6.90, and 7.15, respectively. The MALDI-TOF-TOF mass spectrum and N-terminal sequence 'DQHHSSKACC' suggested that the isolated RgPI is a member of the Bowman-Birk inhibitor family. RgPI exhibited noncompetitive type inhibitory activity against bovine pancreatic trypsin and chymotrypsin, with inhibition constants of 292 and 2265 nM, respectively. It was stable up to a temperature of 80 °C and was active over a wide pH range between 2 and 12. However, reduction with DTT or 2-mercaptoethanol resulted in loss of inhibitory activity against trypsin and chymotrypsin. It also decreased the activity of larval midgut trypsin-like proteinases in Manduca sexta. Its insecticidal property was further confirmed by reduction in the growth and development of these larvae, when supplemented in the diet. © 2010 American Chemical Society.