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作 者:齐西珍[1] 任丽梅[1] 郑芳[1] 张奇[1] 白芳[1] 白钢[1,2]
机构地区:[1]南开大学药学院 [2]生命科学学院,天津300071
出 处:《微生物学报》2011年第8期1106-1112,共7页Acta Microbiologica Sinica
基 金:国家自然科学基金项目(21002052);天津市应用基础及前沿技术研究计划项目(10JCYBJC14300);中央高校基本科研业务费专项资金(65011161)~~
摘 要:【目的】针对人胰腺α-淀粉酶这个糖代谢途径中重要的靶蛋白,建立α-淀粉酶抑制剂高通量筛选模型。【方法】采用毕赤酵母表达系统克隆和表达人胰腺α-淀粉酶;利用酶的催化特性建立α-淀粉酶抑制剂筛选模型;应用该模型对放线菌发酵液冻干物进行高通量筛选;通过构建16S rRNA系统发育树分析阳性菌株的分类地位。【结果】成功克隆、表达了具催化活性的人胰腺α-淀粉酶;建立了α-淀粉酶抑制剂的筛选模型;对近2000株放线菌的发酵液冻干物进行高通量筛选,最终得到14株α-淀粉酶抑制剂产生菌株,且在分类学上具有丰富的菌种多样性。【结论】本研究建立的α-淀粉酶抑制剂高通量筛选模型具有很强的实用价值,可用于新型淀粉酶抑制剂类降糖药物的开发。[Objective] Targeting the important enzyme in human glucose metabolic pathway,we established a high throughput screening model for human pancreatic α-amylase inhibitors.[Methods] Pichia pastoris expression system was used to clone and express the human pancreatic α-amylase;we established the α-amylase inhibitor screening model using the catalytic properties of enzyme;this model was applied in screening of actinomycete' metabolites;the taxonomic status of positive strains were analyzed by constructing 16S rRNA phylogenetic tree.[Results] We cloned and expressed the intact gene of human pancreatic α-amylase successfully;the high-throughput screening model of α-amylase inhibitors was established;nearly 2000 actinomycete' metabolites were screened,14 α-amylase inhibitor producing strains were obtained finally,and showed taxonomically rich diversity.[Conclusion] The α-amylase inhibitor high-throughput screening model had high practical value for developing new hypoglycemic drugs.
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