Abstract | BACKGROUND: A haemagglutinin was purified from Japanese Hokkaido red beans (Phaseolus vulgaris cv. Hokkaido red bean) with a procedure that included three chromatographic media. RESULTS: Haemagglutinating activity was adsorbed on DEAE cellulose, Affi-gel blue gel and Mono S. The pure haemagglutinin was a homodimer and each subunit was around 30 kDa in molecular mass. The haemagglutinating activity of this agglutinin could not be inhibited by a variety of simple sugars at 200 mmol L(-1) concentration including alpha-L- fucose, D(+)-galactose, D(+)-glucose, D(+)- glucosamine, D(-) galactosamine, galacturonic acid, (+)- lactose, D(+)-melibose, L(-)- mannose, D(+)-mannose, D-mannosamine, D(+)- raffinose, L- rhamnose, (+)- xylose and galacturonic acid. The haemagglutinating activity was fully retained at pH 4-11 and at 0-80 degrees C, but was completely lost at extreme pH values (0-2 and 13-14) and at very high temperatures (90 degrees C and 100 degrees C). The haemagglutinin exhibited a weak mitogenic activity toward mouse splenocytes, a stronger anti-proliferative activity than Con A toward HepG2 (human hepatoma) cells and inhibited >80% of HIV-1 reverse transcriptase inhibitory activity at 3.3 micromol L(-1). It was devoid of anti-fungal activity. CONCLUSION: Hokkaido red bean haemagglutinin possesses a potent anti-proliferative effect on HepG2 cells.
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Authors | Jack H Wong, Chung T Wan, Tzi B Ng |
Journal | Journal of the science of food and agriculture
(J Sci Food Agric)
Vol. 90
Issue 1
Pg. 70-7
(Jan 15 2010)
ISSN: 1097-0010 [Electronic] England |
PMID | 20355014
(Publication Type: Journal Article)
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Copyright | Copyright (c) 2009 Society of Chemical Industry. |
Chemical References |
- Antineoplastic Agents, Phytogenic
- Carbohydrates
- Mitogens
- Phytohemagglutinins
- Reverse Transcriptase Inhibitors
- Concanavalin A
- DEAE-Cellulose
- reverse transcriptase, Human immunodeficiency virus 1
- HIV Reverse Transcriptase
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Topics |
- Adsorption
- Antineoplastic Agents, Phytogenic
(chemistry, isolation & purification, pharmacology)
- Carbohydrates
- Carcinoma, Hepatocellular
(drug therapy)
- Cell Proliferation
(drug effects)
- Chromatography
(methods)
- Concanavalin A
- DEAE-Cellulose
- HIV Reverse Transcriptase
(antagonists & inhibitors)
- Hep G2 Cells
- Hot Temperature
- Humans
- Hydrogen-Ion Concentration
- Mitogens
(chemistry, isolation & purification, pharmacology)
- Molecular Structure
- Phaseolus
(chemistry)
- Phytohemagglutinins
(chemistry, isolation & purification, pharmacology)
- Reverse Transcriptase Inhibitors
(chemistry, isolation & purification, pharmacology)
- Spleen
(cytology, drug effects)
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