A heat-stable trypsin inhibitor in adzuki bean (Vigna angularis): effect of extraction media, purification and biochemical characteristics

被引:34
作者
Klomklao, Sappasith [1 ]
Benjakul, Soottawat [2 ]
Kishimura, Hideki [3 ]
Osako, Kazufumi [4 ]
Tanaka, Munehiko [4 ]
机构
[1] Thaksin Univ, Fac Technol & Community Dev, Dept Food Sci & Technol, Phattalung 93110, Thailand
[2] Prince Songkla Univ, Fac Agroind, Dept Food Technol, Hat Yai 90112, Songkhla, Thailand
[3] Hokkaido Univ, Res Fac Fisheries Sci, Hakodate, Hokkaido 0418611, Japan
[4] Tokyo Univ Marine Sci & Technol, Dept Food Sci & Technol, Minato Ku, Tokyo 1088477, Japan
关键词
Inhibitor; isolation; legume; proteinase; trypsin; PROTEINASE-INHIBITORS; SEEDS;
D O I
10.1111/j.1365-2621.2009.02117.x
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
P>Trypsin inhibitor from adzuki bean (Vigna angularis) seed was isolated and characterised. Extraction of seed with NaCl at the concentration of 0.15 m showed a higher recovery of trypsin inhibitor than other solvents tested (P < 0.05). Optimal extraction time for the recovery trypsin inhibitor from adzuki bean seed was 30 min (P < 0.05). Purification of inhibitor was achieved by heat-treatment at 90 degrees C for 10 min, followed by ammonium sulphate precipitation with 30-65% saturation and size exclusion chromatography on Sephacryl S-200, presenting a yield and purification of 53.9% and 10.91-fold, respectively. The apparent molecular weight of trypsin inhibitor was estimated to be 14 kDa based on SDS-PAGE and inhibitor activity of zones separated by electrophoresis. The purified inhibitor was stable over a broad pH range and retained high inhibitory activity toward trypsin after incubation at 90 degrees C for 60 min. NaCl, at 0-3% concentration, did not affect the inhibitory activity of purified trypsin inhibitor, however, the activity was lost when sample was treated with beta-mercaptoethanol prior to electrophoresis.
引用
收藏
页码:163 / 169
页数:7
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