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使用基于荧光共振能量转移的生物传感器对混合物中的单糖进行定量分析。

Quantitative analyses of individual sugars in mixture using FRET-based biosensors.

机构信息

Systems & Synthetic Biology Research Center, KRIBB, Daejeon 305-806, Korea.

出版信息

Biotechnol Prog. 2012 Sep-Oct;28(5):1376-83. doi: 10.1002/btpr.1592. Epub 2012 Jul 31.

Abstract

Molecular biosensors were developed and applied to measure individual sugars in biological mixtures such as bacterial culture broths. As the sensing units, four sugar-binding proteins (SBPs for allose, arabinose, ribose, and glucose) were selected from the Escherichia coli genome and connected to a cyan fluorescent protein and yellow fluorescent protein via dipeptide linkers (CFP-L-SBP-YFP). The putative sensors were randomized in the linker region (L) and then investigated with regard to the intensity of fluorescence resonance energy transfer on the binding of the respective sugars. As a result, four representatives were selected from each library and examined for their specificity using 16 available sugars. The apparent dissociation constants of the allose, arabinose, ribose, and glucose sensors were estimated to be 0.35, 0.36, 0.17, and 0.18 μM. Finally, the sugar sensors were applied to monitor the consumption rate of individual sugars in an E. coli culture broth. The individual sugar profiles exhibited a good correlation with those obtained using an HPLC method, confirming that the biosensors offer a rapid and easy-to-use method for monitoring individual sugars in mixed compositions.

摘要

分子生物传感器被开发并应用于测量生物混合物(如细菌培养物)中的单个糖。作为传感单元,从大肠杆菌基因组中选择了四种糖结合蛋白(用于所有糖、阿拉伯糖、核糖和葡萄糖的 SBP),并通过二肽接头(CFP-L-SBP-YFP)连接到一个青色荧光蛋白和一个黄色荧光蛋白上。假定的传感器在接头区域(L)随机化,然后研究各自糖结合时荧光共振能量转移的强度。结果,从每个文库中选择了四个代表,并使用 16 种可用糖检查它们的特异性。估计所有糖、阿拉伯糖、核糖和葡萄糖传感器的表观解离常数分别为 0.35、0.36、0.17 和 0.18 μM。最后,将糖传感器应用于监测大肠杆菌培养液中各糖的消耗速率。个体糖谱与使用 HPLC 方法获得的谱具有很好的相关性,证实该生物传感器为监测混合成分中的个体糖提供了一种快速简便的方法。

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