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微流控高通量筛选浮游生物碱性磷酸酶活性

High-Content Screening of Plankton Alkaline Phosphatase Activity in Microfluidics.

机构信息

Centre de Recherche Paul Pascal, Unité Mixte de Recherche 5031 , Université de Bordeaux, Centre National de la Recherche Scientifique , 33600 Pessac , France.

Laboratoire d'Environnements et Paléoenvironnements Océaniques et Continentaux, Unité Mixte de Recherche 5805 , Centre National de la Recherche Scientifique , 33615 Pessac , France.

出版信息

Anal Chem. 2018 Mar 20;90(6):4174-4181. doi: 10.1021/acs.analchem.8b00234. Epub 2018 Feb 28.

Abstract

One way for phytoplankton to survive orthophosphate depletion is to utilize dissolved organic phosphorus by expressing alkaline phosphatase. The actual methods to assay alkaline phosphate activity-either in bulk or as a presence/absence of enzyme activity-fail to provide information on individual living cells. In this context, we develop a new microfluidic method to compartmentalize cells in 0.5 nL water-in-oil droplets and measure alkaline phosphatase activity at the single-cell level. We use enzyme-labeled fluorescence (ELF), which is based on the hydrolysis of ELF-P substrate, to monitor in real time and at the single-cell level both qualitative and quantitative information on cell physiology (i.e., localization and number of active enzyme sites and alkaline phosphatase kinetics). We assay the alkaline phosphatase activity of Tetraselmis sp. as a function of the dissolved inorganic phosphorus concentration and show that the time scale of the kinetics spans 1 order of magnitude. The advantages of subnanoliter-scale compartmentalization in droplet-based microfluidics provide a precise characterization of a population with single-cell resolution. Our results highlight the key role of cell physiology to efficiently access dissolved organic phosphorus.

摘要

浮游植物在正磷酸盐耗尽时可以通过表达碱性磷酸酶来利用溶解有机磷。用于测定碱性磷酸酶活性的实际方法——无论是批量测定还是存在/不存在酶活性——都无法提供关于单个活细胞的信息。在这种情况下,我们开发了一种新的微流控方法,将细胞分隔在 0.5nL 的油包水液滴中,并在单细胞水平上测量碱性磷酸酶活性。我们使用基于 ELF-P 底物水解的酶标记荧光 (ELF),实时监测单细胞水平上细胞生理学的定性和定量信息(即,活性酶位点数和碱性磷酸酶动力学的定位和数量)。我们测定了 Tetraselmis sp. 的碱性磷酸酶活性作为溶解无机磷浓度的函数,并表明动力学的时间尺度跨越了 1 个数量级。基于液滴的微流控中纳升级分隔的优势提供了对具有单细胞分辨率的群体的精确表征。我们的结果强调了细胞生理学在有效获取溶解有机磷方面的关键作用。

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