Author/Authors :
Maghsoudi, Shabnam Medical Biology Research Center - Kermanshah University of Medical Sciences, Kermanshah , Ghorbani, Fatemeh Medical Biology Research Center - Kermanshah University of Medical Sciences, Kermanshah , Ashrafi-Kooshk, Mohammad Reza Medical Biology Research Center - Kermanshah University of Medical Sciences, Kermanshah , Fattahi, Ali Medical Biology Research Center - Kermanshah University of Medical Sciences, Kermanshah , Khodarahmi, Reza Medical Biology Research Center - Kermanshah University of Medical Sciences, Kermanshah
Abstract :
Plant α-amylase inhibitors (αAIs) show great potential as tools to manipulate
resistance of crop plants against pests. They can be also considered as drugdesign
target for treatment of diabetes and digestion disorder. In this study, an
amylase inhibitor-rich fraction was purified by ethanol precipitation and
affinity chromatography on chitosan beads column from white common bean
(Phaseolus vulgaris) extract, and then its in vitro interaction with porcine
pancreatic α-amylase (PPA) was studied. A commercially available amylase
inhibitor, Phase 2, was also used to serve as a comparative reference. The
results showed that inhibitory activity of the αAI extracted from white kidney
bean was much higher than that of Phase 2. The purified inhibitor displayed
significant heat stability, so that remaining inhibitory activity was ~80%, even
at 60 °C for 30 min incubation. Fraction 3 retained ~84% of its initial activity
after long term (45 days) dry storage at room temperature. Due to potency
and appropriate heat/storage stability, this αAI preparation may be
reconsidered as raw material for preparation of commercial αAI to control
appetite and energy intake.