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基于群体感应淬灭的酶固定化纳滤膜减轻生物污染。

Enzyme-immobilized nanofiltration membrane to mitigate biofouling based on quorum quenching.

机构信息

School of Chemical and Biological Engineering, Seoul National University, Seoul 151-744, Korea.

出版信息

Environ Sci Technol. 2011 Feb 15;45(4):1601-7. doi: 10.1021/es103483j. Epub 2011 Jan 4.

Abstract

Recently, enzymatic quorum quenching (in the form of a free enzyme or an immobilized form on a bead) was successfully applied to a submerged membrane bioreactor with a microfiltration membrane for wastewater treatment as a novel approach to control membrane biofouling. In this study, a quorum quenching enzyme (acylase) was directly immobilized onto a nanofiltration membrane to mitigate biofouling in a nanofiltration process. In a flow cell experiment, the acylase-immobilized membrane with quorum quenching activity prohibited the formation of mushroom-shaped mature biofilm due to the reduced secretion of extracellular polymeric substances (EPS). The acylase-immobilized membrane maintained more than 90% of its initial enzyme activity for more than 20 iterative cycles of reaction and washing procedure. In the lab-scale continuous crossflow nanofiltration system operated at a constant pressure of 2 bar, the flux with the acylase-immobilized nanofiltration (NF) membrane was maintained at more than 90% of its initial flux after a 38-h operation, whereas that with the raw NF membrane decreased to 60% accompanied with severe biofouling. The quorum quenching activity of the acylase-immobilized membrane was also confirmed by visualizing the spatial distribution of cells and polysaccharides on the surface of each membrane using confocal laser scanning microscopy (CLSM) image analysis technique.

摘要

最近,酶学群体感应淬灭(以游离酶或固定在珠上的形式)成功地应用于浸没式膜生物反应器中的微滤膜,作为控制膜生物污染的一种新方法。在这项研究中,将一种群体感应淬灭酶(酰基酶)直接固定在纳滤膜上,以减轻纳滤过程中的生物污染。在流动池实验中,具有群体感应淬灭活性的酰基酶固定膜由于胞外聚合物(EPS)分泌减少而阻止了蘑菇状成熟生物膜的形成。酰基酶固定膜在反应和清洗过程的 20 多次迭代中保持了超过 90%的初始酶活性。在实验室规模的连续错流纳滤系统中,在 2 巴的恒定压力下运行,用酰基酶固定纳滤(NF)膜的通量在 38 小时的运行后保持在初始通量的 90%以上,而原始 NF 膜的通量则下降到 60%,同时伴有严重的生物污染。通过使用共聚焦激光扫描显微镜(CLSM)图像分析技术可视化每个膜表面上细胞和多糖的空间分布,也证实了酰基酶固定膜的群体感应淬灭活性。

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