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NEW APPLICATION OF TRANSGLUCOSIDASE WITH α-GLUCOSIDASE INHIBITOR IN THE DIGESTIVE TRACT

机译:转葡糖苷酶与α-葡糖苷酶抑制剂在消化道中的新应用

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We have studied transglucosidase derived from Aspergillus niger for self-mediation in the gastrointestinal tract as a dietary supplement. This enzyme is very popular to produce oligosaccharides in industry. Prof. Sasaki already reported this enzyme showed oligosaccharides production in the digestive tract which improved microflora level in large intestine and decreased the blood glucose level and the excretion of insulin. The clinical study of this enzyme was performed in 21 healthy volunteers and patients with type 2 diabetes mellitus to check the glucose level in blood and secretion of insulin after meal. This enzyme showed good improvement in biological parameters. But, the result was very similar and did not show good dose dependent to prevent the increase of blood glucose after meal, when the dose of this enzyme was 150mg and 300mg at the preliminary test. The key point is to decrease the absorption of glucose by forming indigestive oligosaccharides in stomach. But this enzyme shows a-glucosidase activity as well as transglucosidase activity and both activities are competitive. Transglucosidase produced some oligosaccharides at first, however gradually decreased with time and finally produced only glucose. In result, transglucosidase hydrolyzed starch to glucose, through oligosaccharides. We have investigated the control of this reaction using maltose as a substrate with α-glucosidase inhibitor (α-GI) in vitro. We found that α-GI inhibited directly the hydrolyze activity of transglucosidase and not inhibited the transglucosidase activity, but delayed. We will try the clinical test of combination of trasglucosidase and α-GI with healthy volunteers.
机译:我们已经研究了源自黑曲霉的转葡糖苷酶作为饮食补充剂在胃肠道中的自我调节作用。该酶在工业中非常流行用于生产寡糖。 Sasaki教授已经报道了这种酶在消化道中显示寡糖生成,从而改善了大肠中的菌群水平,并降低了血糖水平和胰岛素排泄。在21名健康志愿者和2型糖尿病患者中进行了该酶的临床研究,以检查餐后血液中的葡萄糖水平和胰岛素分泌。该酶在生物学参数上显示出良好的改善。但是,当初步试验中该酶的剂量为150mg和300mg时,结果非常相似,并且没有显示出良好的剂量依赖性以防止餐后血糖升高。关键是通过在胃中形成消化性低聚糖来减少葡萄糖的吸收。但是这种酶显示出α-葡糖苷酶活性和转葡糖苷酶活性,并且两种活性都是竞争性的。转葡糖苷酶起初产生一些寡糖,但是随着时间逐渐减少,最后仅产生葡萄糖。结果,转葡糖苷酶通过寡糖将淀粉水解为葡萄糖。我们已经研究了使用麦芽糖作为底物与α-葡萄糖苷酶抑制剂(α-GI)的体外控制。我们发现α-GI直接抑制转葡糖苷酶的水解活性,而不抑制转葡糖苷酶的活性,但是延迟。我们将尝试将葡萄糖苷酶和α-GI与健康志愿者联合使用的临床测试。

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