Application of GC-MS for the detection of lipophilic compounds in diverse plant tissues

被引:54
作者
Lytovchenko, Anna [1 ]
Beleggia, Romina [2 ]
Schauer, Nicolas [1 ]
Isaacson, Tal [3 ]
Leuendorf, Jan E. [4 ]
Hellmann, Hanjo [5 ]
Rose, Jocelyn K. C. [3 ]
Fernie, Alisdair R. [1 ]
机构
[1] Max Planck Inst Mol Plant Physiol, D-14476 Potsdam, Germany
[2] CRA Cereal Res Ctr, I-71100 Foggia, Italy
[3] Cornell Univ, Dept Plant Biol, Ithaca, NY 14853 USA
[4] Free Univ Berlin, Inst Biol Appl Genet, D-14195 Berlin, Germany
[5] Washington State Univ, Sch Biol Sci, Pullman, WA 99164 USA
关键词
CHROMATOGRAPHY-MASS SPECTROMETRY; SYSTEMS BIOLOGY; ARABIDOPSIS-THALIANA; FUNCTIONAL GENOMICS; FRUIT-DEVELOPMENT; INTEGRATED ANALYSIS; LIPID-PEROXIDATION; SURFACE WAX; FATTY-ACIDS; METABOLISM;
D O I
10.1186/1746-4811-5-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: The concept of metabolite profiling has been around for decades and technical innovations are now enabling it to be carried out on a large scale with respect to the number of both metabolites measured and experiments carried out. However, studies are generally confined to polar compounds alone. Here we describe a simple method for lipophilic compounds analysis in various plant tissues. Results: We choose the same preparative and instrumental platform for lipophilic profiling as that we routinely use for polar metabolites measurements. The method was validated in terms of linearity, carryover, reproducibility and recovery rates, as well as using various plant tissues. As a first case study we present metabolic profiling of Arabidopsis root and shoot tissue of wild type (C24) and mutant (rsr4-1) plants deficient on vitamin B6. We found significant alterations in lipid constituent contents, especially in the roots, which were characterised by dramatic increases in several fatty acids, thus providing further hint for the role of pyridoxine in oxidative stress and lipid peroxidation. The second example is the lipophilic profiling of red and green tomato fruit cuticles of wild type (Alisa Craig) and the DFD (delayed fruit deterioration) mutant, which we compared and contrasted with the more focused wax analysis of these plants reported before. Conclusion: We can rapidly and reliably detect and quantify over 40 lipophilic metabolites including fatty acids, fatty alcohols, alkanes, sterols and tocopherols. The method presented here affords a simple and rapid, yet robust complement to previously validated methods of polar metabolite profiling by gas-chromatography mass-spectrometry.
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页数:11
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