The determination of 22 natural brassinosteroids in a minute sample of plant tissue by UHPLC-ESI-MS/MS
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články, validační studie
PubMed
27531032
DOI
10.1007/s00216-016-9807-2
PII: 10.1007/s00216-016-9807-2
Knihovny.cz E-zdroje
- Klíčová slova
- Arabidopsis thaliana, Brassica napus, Brassinosteroids, Solid-phase extraction, Tandem mass spectrometry, Ultra-high performance liquid chromatography,
- MeSH
- Arabidopsis chemie MeSH
- Brassica napus chemie MeSH
- brassinosteroidy analýza MeSH
- extrakce na pevné fázi metody MeSH
- hmotnostní spektrometrie s elektrosprejovou ionizací metody MeSH
- limita detekce MeSH
- reprodukovatelnost výsledků MeSH
- rostlinné extrakty chemie MeSH
- tandemová hmotnostní spektrometrie metody MeSH
- vysokoúčinná kapalinová chromatografie metody MeSH
- Publikační typ
- časopisecké články MeSH
- validační studie MeSH
- Názvy látek
- brassinosteroidy MeSH
- rostlinné extrakty MeSH
The triterpenoid plant hormones brassinosteroids (BRs) are believed to influence almost every aspect of plant growth and development. We have developed a sensitive mass spectrometry-based method for the simultaneous profiling of twenty-two naturally occurring brassinosteroids including biosynthetic precursors and the majority of biologically active metabolites. Using ultra-high performance liquid chromatographic (UHPLC) analysis, the run time was reduced up to three times (to 9 min) in comparison to standard HPLC BRs analyses, the retention time stability was improved to 0.1-0.2 % RSD and the injection accuracy was increased to 1.1-4.9 % RSD. The procedures for extraction and for two-step purification based on solid-phase extraction (SPE) were optimised in combination with subsequent UHPLC analysis coupled to electrospray ionisation tandem mass spectrometry (ESI-MS/MS) using Brassica flowers and Arabidopsis plant tissue extracts. In multiple reaction monitoring (MRM) mode, the average detection limit for BRs analysed was close to 7 pg, and the linear range covered up to 3 orders of magnitude. The low detection limits for this broad range of BR metabolites enabled as little as 50 mg of plant tissue to be used for quantitative analyses. The results of determinations exploiting internal standards showed that this approach provides a high level of practicality, reproducibility and recovery. The method we have established will enable researchers to gain a better understanding of the dynamics of the biosynthesis and metabolism of brassinosteroids and their modes of action in plant growth and development.
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