National Institute for Plant Genome Research, New Delhi, India.
Amity Institute of Biotechnology, Amity University, Uttar Pradesh, India.
Curr Protoc. 2022 Apr;2(4):e420. doi: 10.1002/cpz1.420.
The free radical nitric oxide (NO) has emerged as an important signal molecule in plants, due to its involvement in various plant growth, development, and stress responses. For elucidating the role of NO, it is very important to precisely determine, localize, and quantify NO levels. Due to a relatively short half-life and its rapid, complex reactivity with other radicals, together with its capacity to diffuse from the source of production, the quantification of NO in whole plants, tissues, organelles, and extracts is notoriously difficult. Hence, it is essential to employ sensitive procedures for precise detection of NO. Currently available methods can fulfill many requirements to precisely determine NO, but each method has several advantages and pitfalls. In this article, we describe a detailed procedure for the measurement of NO by diaminofluorescein (DAF) in cell-permeable forms (DAF-FM-DA). In this method, the tissues are immersed in DAF-FM DA, leading to their diffusion from the plasma membrane to the inside of the cell, where intracellular esterases cleave the ester bonds, leading to DAF-FM release. The resulting DAF-FM reacts with intracellularly generated NO and forms highly fluorescent triazolofluorescein (DAF-FMT), which can be localized and monitored by fluorescence or confocal microscopy, and can also be detected via fluorimetry and flow cytometry. DAF dyes are very popular as they are non-invasive, relatively easy to handle, and commercially available. Another precise and very sensitive method is chemiluminescence detection of NO, where NO reacts with ozone (O ), leading to emission of a quantum of light from which NO can be calculated. Using chickpea seedlings, we describe in detail the measurement of NO using DAF-FM-DA and chemiluminescence methods. © 2022 Wiley Periodicals LLC. Basic Protocol 1: Measurement of nitric oxide from chickpea seedlings using DAF-FM DA fluorescence with fluorescence and confocal microscopy Basic Protocol 2: Chemiluminescence detection of nitric oxide from chickpea seedlings.
自由基一氧化氮 (NO) 已成为植物中一种重要的信号分子,因为它参与了各种植物生长、发育和应激反应。为了阐明 NO 的作用,精确地确定、定位和定量 NO 水平非常重要。由于其半衰期相对较短,并且与其他自由基迅速、复杂地反应,加上其从产生源扩散的能力,因此,在整个植物、组织、细胞器和提取物中定量 NO 非常困难。因此,必须采用敏感的程序来精确检测 NO。目前可用的方法可以满足精确测定 NO 的许多要求,但每种方法都有几个优点和缺点。在本文中,我们描述了一种使用可穿透细胞膜的二氨基荧光素 (DAF) 形式 (DAF-FM-DA) 测量 NO 的详细程序。在该方法中,将组织浸入 DAF-FM DA 中,导致其从质膜扩散到细胞内部,细胞内的酯酶在此处切开酯键,导致 DAF-FM 释放。生成的 DAF-FM 与细胞内生成的 NO 反应,形成高度荧光的三唑荧光素 (DAF-FMT),可以通过荧光或共聚焦显微镜进行定位和监测,也可以通过荧光光度法和流式细胞术进行检测。DAF 染料非常受欢迎,因为它们是非侵入性的、相对容易处理的,并且可以从商业途径获得。另一种精确且非常灵敏的方法是通过化学发光检测 NO,其中 NO 与臭氧 (O ) 反应,导致发出光量子,从中可以计算出 NO。我们使用鹰嘴豆幼苗详细描述了使用 DAF-FM-DA 和化学发光法测量 NO 的方法。