Planta Med 2001; 67(7): 669-672
DOI: 10.1055/s-2001-17359
Letter

© Georg Thieme Verlag Stuttgart · New York

Examination of Lectins, Polysaccharopeptide, Polysaccharide, Alkaloid, Coumarin and Trypsin Inhibitors for Inhibitory Activity Against Human Immunodeficiency Virus Reverse Transcriptase and Glycohydrolases

H. X. Wang1 , T. B. Ng2,*
  • 1 Department of Microbiology, China Agricultural University, Beijing, China
  • 2 Department of Biochemistry, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, Hong Kong, China
Further Information

Publication History

Oktober 25, 2000

December 19, 2000

Publication Date:
24 September 2001 (online)

Abstract

A variety of lectins were tested in vitro for inhibitory action against the activities of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase and the N-glycohydrolases (α-glucosidase, β-glucosidase and β-glucuronidase). Lectins from Phaseolus vulgaris, Momordica charantia, Ricinus communis and its constituent chains, and Agaricus bisporus were able to inhibit HIV-1 reverse transcriptase. P. vulgaris lectin and A. bisporus lectin were the most potent. The aforementioned lectins had only weak or no inhibitory effects on the glycohydrolases. The inhibitory effect of polysaccharopeptide from the mushroom Coriolus versicolor on HIV-1 reverse transcriptase and α-glucosidase was enhanced after chemical modification with chlorosulfonic acid. However, the inhibitory effect of the algal polysaccharide fucoidan on HIV-1 reverse transcriptase and α-glucosidase was not augmented by sulfation. Trypsin inhibitors from Phaseolus lunatus and Glycine max, gossypol and alkaloids from Corydalis yanhusuo were able to inhibit HIV-1 reverse transcriptase. Dicoumarol was capable of inhibiting HIV-1 reverse transcriptase, α-glucosidase, β-glucosidase and β-glucuronidase.

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T. B. Ng

Department of Biochemistry

Chinese University of Hong Kong

Shatin

Hong Kong

China

Email: biochemistry@cuhk.edu.hk

Fax: +852-2609-5123

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