Abstract

BackgroundThe plant hormone auxin plays a central role in regulation of plant growth and response to environmental stimuli. Multiple pathways have been proposed for biosynthesis of indole-3-acetic acid (IAA), the primary auxin in a number of plant species. However, utilization of these different pathways under various environmental conditions and developmental time points remains largely unknown.ResultsMonitoring incorporation of stable isotopes from labeled precursors into proposed intermediates provides a method to trace pathway utilization and characterize new biosynthetic routes to auxin. These techniques can be aided by addition of chemical inhibitors to target specific steps or entire pathways of auxin synthesis.ConclusionsHere we describe techniques for pathway analysis in Arabidopsis thaliana seedlings using multiple stable isotope-labeled precursors and chemical inhibitors coupled with highly sensitive liquid chromatography-mass spectrometry (LC–MS) methods. These methods should prove to be useful to researchers studying routes of IAA biosynthesis in vivo in a variety of plant tissues.

Highlights

  • The plant hormone auxin plays a central role in regulation of plant growth and response to environmental stimuli

  • In this paper, we describe methods utilizing metabolic inhibitors coupled with a modified approach of isotope dilution/tracing and using liquid chromatography–high resolution-mass spectrometry (LC-HR-Mass spectrometry (MS)) for qualitative and quantitative analysis of a comprehensive set of indole-3-acetic acid (IAA) precursors and IAA itself to characterize auxin biosynthesis in Arabidopsis

  • Readers may consult a complementary paper that was published while this manuscript was in preparation [34]

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Summary

Results

Monitoring incorporation of stable isotopes from labeled precursors into proposed intermediates provides a method to trace pathway utilization and characterize new biosynthetic routes to auxin. These techniques can be aided by addition of chemical inhibitors to target specific steps or entire pathways of auxin synthesis

Conclusions
Background
Results and discussion
Materials and methods
Methods
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