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酶促合成的酚类和维生素糖苷的血管紧张素转换酶抑制及抗氧化活性

Angiotensin-converting enzyme inhibitory and antioxidant activities of enzymatically synthesized phenolic and vitamin glycosides.

作者信息

Charles Rajachristu Einstein, Ponrasu Thangavel, Sivakumar Ramaiah, Divakar Soundar

机构信息

Fermentation Technology and Bioengineering, Central Food Technological Research Institute, Council of Scientific and Industrial Research, Mysore 570 020, India.

出版信息

Biotechnol Appl Biochem. 2009 Mar;52(Pt 3):177-84. doi: 10.1042/BA20080041.

Abstract

Amyloglucosidase from Rhizopus mould and beta-glucosidase from sweet almond were employed for the preparation of phenolic and vitamin glycosides of vanillin, N-vanillylnonanamide, DL-dopa, dopamine, curcumin, alpha-tocopherol (vitamin E), pyridoxine (vitamin B(6)), ergocalciferol (vitamin D(2)), thiamin (vitamin B(1)) and riboflavin (vitamin B(2)). Approx. 20 enzymatically prepared phenolic and vitamin glycosides were subjected to ACE (angiotensin-converting enzyme) inhibition activity measurements, and 14 glycosides were tested for antioxidant activities. Both phenolic and vitamin glycosides exhibited IC(50) values for ACE inhibition in the 0.52+/-0.03-3.33+/-0.17 mM range and antioxidant activities ranging from 0.8+/-0.04 to 1.18+/-0.06 mM. Comparable ACE inhibition values were observed between free phenols and vitamin glycosides. However, antioxidant activities of glycosides were, in general, lesser than those of free phenols. Best IC(50) value for ACE inhibition were observed for 11-O-(D-fructofuranosyl)thiamin (0.52+/-0.03 mM), 3-hydroxy-4-O-(6-D-sorbitol)phenylalanine (0.56+/-0.03 mM), 4-O-(beta-D-glucopyranosyl)vanillin (0.61+/-0.03 mM), 4-O-(D-galactopyranosyl)vanillin (0.61+/-0.03 mM) and pyridoxine-D-glucoside (0.84+/-0.04 mM). Similarly, best IC(50) values for antioxidant activity were observed for 1,7-O-(bis-beta-D-glucopyranosyl)curcumin (0.8+/-0.04 mM), 4-O-(beta-D-glucopyranosyl)vanillin (0.9+/-0.05 mM), 3-hydroxy-4-O-(beta-D-galactopyranosyl-(1'-->4)beta-D-glucopyranosyl)phenylalanine (0.9+/-0.05 mM), 20-O-(D-glucopyranosyl)ergocalciferol (0.9+/-0.05 mM) and dopamine-D-galactoside (0.93+/-0.05 mM).

摘要

来自根霉的淀粉葡萄糖苷酶和甜杏仁中的β-葡萄糖苷酶被用于制备香草醛、N-香草基壬酰胺、DL-多巴、多巴胺、姜黄素、α-生育酚(维生素E)、吡哆醇(维生素B6)、麦角钙化醇(维生素D2)、硫胺素(维生素B1)和核黄素(维生素B2)的酚类和维生素糖苷。大约20种酶法制备的酚类和维生素糖苷进行了血管紧张素转换酶(ACE)抑制活性测定,14种糖苷进行了抗氧化活性测试。酚类和维生素糖苷的ACE抑制IC50值在0.52±0.03 - 3.33±0.17 mM范围内,抗氧化活性在0.8±0.04至1.18±0.06 mM之间。游离酚和维生素糖苷之间观察到相当的ACE抑制值。然而,糖苷的抗氧化活性总体上低于游离酚。ACE抑制的最佳IC50值观察到的有11-O-(D-呋喃果糖基)硫胺素(0.52±0.03 mM)、3-羟基-4-O-(6-D-山梨醇)苯丙氨酸(0.56±0.

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