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用流式细胞术检测细胞的 DNA 分化或细胞膜损伤情况来进行消毒。

Differentiation of DNA or membrane damage of the cells in disinfection by flow cytometry.

机构信息

Key Laboratory of Northwest Water Resource, Environment and Ecology, MOE, Xi'an University of Architecture and Technology, Xi'an 710055, PR China; Shaanxi Key Laboratory of Environmental Engineering, Xi'an University of Architecture and Technology, Xi'an 710055, PR China.

Key Laboratory of Northwest Water Resource, Environment and Ecology, MOE, Xi'an University of Architecture and Technology, Xi'an 710055, PR China; Shaanxi Key Laboratory of Environmental Engineering, Xi'an University of Architecture and Technology, Xi'an 710055, PR China.

出版信息

J Hazard Mater. 2022 Aug 5;435:128924. doi: 10.1016/j.jhazmat.2022.128924. Epub 2022 Apr 15.

Abstract

Recently, the viabilities changes of fungal spores in the water supply system during different disinfection processes have been revealed. SYBR Green I (SG), a nucleic acid stain, its fluorescence intensity is correlated with the amount of double-stranded DNA. This study established a new method through successive SG-SG-PI staining (PI: Propidium Iodide) with flow cytometry (FCM). It could successfully distinguish DNA damage and membrane damage of fungal spores, clearly elucidating the intrinsic disinfection mechanism during the chemical disinfection. This method was briefly described as follows: firstly, (1) the fungal spores were stained with SG and washed by centrifugation; and then, (2) the washed spores were treated with disinfectants and terminated; after that, (3) the disinfected spores were re-stained with SG and analyzed by FCM; finally, (4) the SG re-stained spores were stained with PI and analyzed by FCM. The percentages of spores with DNA damage and membrane damage were determined by the fluorescence intensity obtained from steps (3) and (4), respectively. The repeatability and applicability of this developed method were confirmed. It was further applied to explore the inactivation mechanism during chlorine-based disinfection, and results demonstrated that chloramine attacked the DNA more seriously than the membrane, while chlorine and chlorine dioxide worked in a reverse way.

摘要

最近,已经揭示了在不同消毒过程中供水系统中真菌孢子活力的变化。SYBR Green I(SG)是一种核酸染料,其荧光强度与双链 DNA 的量相关。本研究通过流式细胞术(FCM)用连续的 SG-SG-PI 染色(PI:碘化丙啶)建立了一种新方法。它可以成功区分真菌孢子的 DNA 损伤和膜损伤,清楚阐明了化学消毒过程中的内在消毒机制。该方法简要描述如下:首先,(1)用 SG 对真菌孢子进行染色并用离心法洗涤;然后,(2)用消毒剂处理并终止洗涤后的孢子;之后,(3)用 SG 对消毒后的孢子进行再染色并用 FCM 分析;最后,(4)用 SG 对再染色的孢子进行 PI 染色并用 FCM 分析。步骤(3)和(4)中获得的荧光强度分别确定具有 DNA 损伤和膜损伤的孢子的百分比。该方法的重复性和适用性已得到确认。它进一步被应用于探索基于氯的消毒过程中的失活动力学,结果表明,一氯胺比膜更严重地攻击 DNA,而氯和二氧化氯的作用方式相反。

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