A stable trypsin inhibitor from Chinese dull black soybeans with potentially exploitable activities

被引:23
作者
Lin, Peng [1 ]
Ng, Tzi Bun [1 ]
机构
[1] Chinese Univ Hong Kong, Fac Med, Dept Biochem, Shatin, Hong Kong, Peoples R China
关键词
Kunitz-type trypsin inhibitor; black soybean; anti-proliferative; isolation; characterization; seeds;
D O I
10.1016/j.procbio.2008.05.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A dimeric 40-kDa Kunitz-type trypsin inhibitor was isolated from seeds of the Chinese black soybean Glycine max cv. 'Dull Black'. The purification protocol comprised ion exchange chromatography on Q-Sepharose, SP-Sepharose, and Mono Q, and gel filtration on Superdex 75. The trypsin inhibitor inhibited chymotrypsin, albeit to a lesser extent than it inhibited trypsin. Its trypsin-inhibitory activity was unaffected after exposure to pH 1-14, or to temperatures up to 80 degrees C. The trypsin inhibitor was inhibited by dithiothreitol in a dose-dependent (from 2.5 to 50 mM) and a time-dependent (from 5 to 120 min) manner. Besides inhibiting serine proteases, the trypsin inhibitor demonstrated additional biological activities including stimulation of nitric oxide production by macrophages. It inhibited HIV-1 reverse transcriptase, cell-free translation and proliferation of liver cancer cells and breast cancer cells, with an IC50 value 9.4, 14, 39 and 70 mu M. respectively. However, it did not exhibit antifungal, antibacterial or mitogenic activity. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:992 / 998
页数:7
相关论文
共 56 条
[1]   The plant ribosome inactivating proteins luffin and saporin are potent inhibitors of HIV-1 integrase [J].
Au, TK ;
Collins, RA ;
Lam, TL ;
Ng, TB ;
Fong, WP ;
Wan, DCC .
FEBS LETTERS, 2000, 471 (2-3) :169-172
[2]   The papaya Kunitz-type trypsin inhibitor is a highly stable β-sheet glycoprotein [J].
Azarkan, Mohamed ;
Dibiani, Rachid ;
Goormaghtigh, Erik ;
Raussens, Vincent ;
Baeyens-Volant, Danielle .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 2006, 1764 (06) :1063-1072
[3]   Treatment with field bean protease inhibitor can effectively repress ethylnitrosourea (ENU)-induced neoplasms of the nervous system in Sprague-Dawley rats [J].
Banerji, A ;
Fernandes, A ;
Bane, S .
CANCER LETTERS, 1998, 130 (1-2) :161-167
[4]   The field bean protease inhibitor has the potential to suppress B16F10 melanoma cell lung metastasis in mice [J].
Banerji, A ;
Fernandes, A ;
Bane, S ;
Ahire, S .
CANCER LETTERS, 1998, 129 (01) :15-20
[5]   FIELD BEAN PROTEASE INHIBITOR PREPARATION, UNLIKE METHOTREXATE, CAN COMPLETELY SUPPRESS YOSHIDA SARCOMA TUMOR IN RATS [J].
BANERJI, AP ;
FERNANDES, AO .
CELL BIOLOGY INTERNATIONAL, 1994, 18 (11) :1025-1034
[6]   Primary structure of a Kunitz-type trypsin inhibitor from Enterolobium contortisiliquum seeds [J].
Batista, IFC ;
Oliva, MLV ;
Araujo, MS ;
Sampaio, MU ;
Richardson, M ;
Fritz, H ;
Sampaio, CAM .
PHYTOCHEMISTRY, 1996, 41 (04) :1017-1022
[7]  
Birk Y., 2003, Plant protease inhibitors, V1st
[8]   Characterization of a Kunitz trypsin inhibitor with one disulfide bridge purified from Swartzia pickellii [J].
Cavalcanti, MDM ;
Oliva, MLV ;
Fritz, H ;
Jochum, M ;
Mentele, R ;
Sampaio, M ;
Coelho, LCBB ;
Batista, IFC ;
Sampaio, CAM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 291 (03) :635-639
[9]   Isolation and characterization of a trypsin-chymotrypsin inhibitor from the seeds of green lentil (Lens culinaris) [J].
Cheung, Allen H. K. ;
Ng, Tzi Bun .
PROTEIN AND PEPTIDE LETTERS, 2007, 14 (09) :859-864
[10]   Ancordin, the major rhizome protein of madeira-vine, with trypsin inhibitory and stimulatory activities in nitric oxide productions [J].
Chuang, Mao-Te ;
Lin, Yin-Shiou ;
Hou, Wen-Chi .
PEPTIDES, 2007, 28 (06) :1311-1316