发布: 2016年07月20日第6卷第14期 DOI: 10.21769/BioProtoc.1878 浏览次数: 8813
评审: Valentine V TrotterLionel SchiavolinAnonymous reviewer(s)
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Abstract
Nitric Oxide (NO) is a highly-reactive radical gas that can modify a variety of cellular targets in both eukaryotes and bacteria. NO is produced endogenously by a wide variety of organisms: For example, as a cell-signaling molecule in mammals and bacteria via nitric oxide synthase (NOS) enzymes, and as a product of denitrification. As such, it is of great benefit to NO researchers to be able to sensitively detect intracellular NO and stable reactive nitrogen species (RNS) derived from NO. To this end, a protocol for fluorescent detection of intracellular NO/RNS in biofilm cultures of the Gram-positive pathogen Staphylococcus aureus has been optimized using the commercially-available cell-permeable fluorescent stain 4-Amino-5-Methylamino-2’,7’-Difluorofluorescein Diacetate (DAF-FM diacetate). This compound diffuses into cells and intracellular cleavage by esterase enzymes liberates weakly-fluorescent DAF-FM, which reacts with NO or other specific RNS to become highly fluorescent (Kojima et al., 1999). Although quantification of fluorescence is performed using a fluorescent plate reader, it is envisioned that this protocol could be adapted for intracellular NO/RNS imaging of S. aureus biofilms by confocal microscopy. Likewise, this technique could be optimized for the detection of intracellular NO/RNS in other growth conditions (i.e., planktonic cultures) and/or in other bacteria/archaea.
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文章信息
版权信息
© 2016 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Lewis, A. M., Matzdorf, S. S. and Rice, K. C. (2016). Fluorescent Detection of Intracellular Nitric Oxide in Staphylococcus aureus. Bio-protocol 6(14): e1878. DOI: 10.21769/BioProtoc.1878.
分类
微生物学 > 微生物新陈代谢 > 其它化合物
微生物学 > 微生物信号传导 > 第二信使
生物化学 > 其它化合物
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