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不同载体固定化GOD-GAL双酶乳糖生物传感器核微孔膜的研究 被引量:2

Bi-enzyme Biosensor for Lactose Detection Based on Immobilized Glucose Oxidase and β-galactosidase onto Different Carriers
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摘要 分别以酵母细胞壁微粒、醛基化环糊精微粒(β-CDP)和醛基化淀粉胶材料为载体固定葡萄糖氧化酶(GOD)和β-半乳糖苷酶(β-GAL)双酶,制作三种乳糖酶膜,并用生物传感分析仪测试它们的性能。实验结果表明,用这三种材料制成的酶膜均表现出优良的性能,在乳糖溶液浓度为0.02%~2%的范围内具有良好的线性关系,R2都在0.995以上,乳糖最低检出浓度可达0.001g/L,具有良好的响应性能,响应时间为20~40s。在这三种酶膜中,酵母壁微粒酶膜的线性范围最宽,达0%~10%,这种传感器可广泛应用于原料乳和乳制品中乳糖的检测;β-CDP酶膜具有较强的吸附酶分子的能力,响应值高达2500;醛基化淀粉胶制成的酶膜材质具有良好的均一性,且制作工艺简单。 Glucose oxidase (GOD), together withβ-galactosidase (β-GAL), was immobilized onto yeast cell wall particulates, [^-cyclodextrin glutaraldehyde particulates (β-CDP) and starch glutaraldehyde adhesive respectively to construct bi-enzyme membranes, whose lactose detection performances were tested using an SBA-40C biosensor. All hi-enzyme membranes performed a good detection capability, with a linear calibration range of 0.02%--2% lactose (R2 above 0.995) and a detection limit of 0.001 g/L and had a fast response, with response lime within 20--40s. Among them, bi-enzyme membranes made with yeast cell wall particulates as a carrier had the widest linear calibration range of 0 -- 10% and therefore could be widely used for the detection of lactose in raw milk and dairy products; β-CDP bi-enzyme membranes had a strong adsorption capacity to enzyme molecules and the response values were as high as 2500; hi-enzyme membranes made with starch glntaraldehyde adhesive as a carrier had a good homogeneity and were easy to prepare and could be used to detect lactose in milk.
出处 《食品科学》 EI CAS CSCD 北大核心 2009年第17期239-243,共5页 Food Science
基金 国家科技攻关计划课题(2006BAD04A00)
关键词 固定化酶 酵母细胞壁微粒 醛基化环糊精微粒 醛基化淀粉胶 乳糖酶膜 immobilization carrier yeast cell wall particulates: β-cyclodextrin glutaraldehyde particulates (β--CDP) starch glutaraldehyde adhesive lactose membrane
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参考文献13

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