发布: 2015年07月05日第5卷第13期 DOI: 10.21769/BioProtoc.1523 浏览次数: 7828
评审: Ru ZhangHarrie van ErpAnonymous reviewer(s)
Abstract
We developed this protocol to assay and quantify the content of uric acid or xanthine in various tissues of Arabidopsis thaliana mutant lines with defective urate oxidase or xanthine dehydrogenase1 and in their complementation and suppressor lines (Hauck et al., 2014).
The protocol is based on a method developed by Invitrogen Life Technologies for measuring uric acid or xanthine in human serum (see References 2 and 3). That protocol though required two adaptions for its use in plant science. Firstly by heating the plant samples, the activity of urate oxidase and xanthine dehydrogenase in the wild type samples is eliminated. Wild type extracts always serve as the proper pigmentation background when calculating the standard curves of uric acid and xanthine. Secondly, all samples are measured with and without the addition of urate oxidase or xanthine dehydrogenase to correct for any H2O2 in the samples induced by previous stress.
The assay is based on the following pair of coupled reactions:
1) Uric acid + O2 → Hydroxyisourate + H2O2 (urate oxidase reaction)
2) AR + H2O2 → Resorufin + O2 (horse radish peroxidase reaction)
Accordingly for Xanthine:
1) Xanthine + H2O + O2 → Uric acid + H2O2 (xanthine oxidase reaction)
2) AR + H2O2 → Resorufin + O2 (horse radish peroxidase reaction)
Materials and Reagents
Equipment
Procedure
文章信息
版权信息
© 2015 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Hauck, O. K. and Witte, C. (2015). Quantification of Uric Acid or Xanthine in Plant Samples. Bio-protocol 5(13): e1523. DOI: 10.21769/BioProtoc.1523.
分类
植物科学 > 植物生物化学 > 其它化合物
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