purification and quantification of kunitz trypsin inhibitor in soybean using two-dimensional liquid chromatography

Kunitz trypsin inhibitor (kti) is one of the major antinutritional factors in soybean and results in inhibition of digestion of dietary protein. in this study, we developed a novel strategy to purify and quantify kti from soybean using two-dimensional liquid chromatography. lipids from ground soybean were removed using hexane after which the ground soybean was extracted with protein extraction buffer. the crude extract was first purified by weak anion exchange chromatography, and then the fraction containing kti was further separated by size exclusion chromatography. the fraction containing kti was collected and analyzed by sds-page and electrospray ionization mass spectrometry. results indicated that purified kti has a molecular mass of 20 kda and a purity of ~98% with inhibitory activity of 2425 tiu/mg protein. this assay was used for the quantification of kti in soybean samples. the assay showed concentrations with a range between 7.81 and 500.00 μg/ml and a limit of detection of 0.12 mg/g. the recoveries of kti in spiked soybean samples were between 82.19% and 86.65%, and intra- and interday precisions (% cv) were less than 7.35% and 8.42%. the developed method was used to analyze soybean samples from different sources and soybean products derived from different processing techniques, which demonstrated that the developed procedure provided an accurate and sensitive tool for separation and quantification of intact kti in soybean.