Metabolite analysis for the comparison of irrigated and non-irrigated field grown tomato of varying genotype
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Every year the consequences of water deficit on crop yield and quality are profound. The observation that many wild species relatives of cultivated crops display a greater stress tolerance and the fact that the cultivated species generally display only a fraction of the allelic diversity available within the tomato clade suggest that crossing of wild species with elite cultivars could improve the stress physiology of modern crops. To assess this from the basis of chemical composition we applied an established GC-MS based metabolite profiling method to fruits from irrigated and non-irrigated tomato plants either of the cultivated tomato (Solanum lycopersicum) or of its hybrid with its wild species relative (Solanum pennellii). Results are discussed in terms of both the metabolic response to drought stress and the potential of utilizing exotic germplasm as a means to improve agronomically important characteristics of crop species.
KeywordsS. lycopersicum S. pennelli water stress transgenesis plant breeding GC-MS metabolite profiling
Plant evolution under domestication has lead to increased productivity, but at the same time it narrowed the genetic basis of crop species (Zamir, 2001). Natural biodiversity is an under-exploited sustainable resource that can enrich the genetic basis of cultivated plants with novel alleles that improve productivity and adaptation. A major challenge in modern breeding is to return to the wild ancestors of crop plants and employ some of the diversity that was lost during domestication for the improvement of agricultural yields under optimal as well as stress conditions such as those found in the field. Metabolite profiling is being extensively utilized to gain both diagnostic and mechanistic insight into plant responses and adaptations to a wide range of stresses including, but not limited to nutrient deficiency (Urbanczyk-Wochniak et al., 2005), mineral toxicity (Roessner et al., 2006), temperature and oxidative stresses (Kaplan et al., 2004) and osmotic stress (Gong et al., 2005). As a first study aimed at understanding the chemico-genetic basis of the different stress tolerances exhibited by wild species tomato we recently performed a broad range GC-MS metabolite profiling of species of the tomato clade (Schauer et al., 2005). Some of the metabolic variance observed in these species indicates that they could be useful breeding stock for engineering stress tolerance. In order to enhance the rate of progress of exotic introgression breeding a population of tomato segmental introgression lines (ILs) comprised of marker-defined genomic regions taken from the drought tolerant wild species S. pennellii and introduced into the genetic background of an elite inbred variety was created some years ago (M82; Eshed and Zamir, 1994; 1995). In the mean time these lines have been extensively analysed at the level of various important quality parameters including yield associated traits such as fruit weight, harvest index, seed per fruit etc. (Gur et al., 2004a; Semel et al., 2006), plant architecture (Fridman et al., 2002), leaf morphology (Holtan and Hake, 2003), fruit morphology (Gur et al., 2004b; Semel et al., 2006), fruit pigmentation (Liu et al., 2003) and fruit metabolite content (Schauer et al., 2006).
Much research over the past few years has been focussed on the development of drought tolerant plant genotypes (Hsieh et al., 2002; Kalifa et al., 2004; Bartels and Sunkar, 2005). There is considerable interest in enhancing drought tolerance in crops and in understanding the mechanisms by which plants naturally respond to osmotic stress (Grainer et al., 2005; Bohnert et al., 2006; Mittler 2006; Yamaguchi-Shinozaki and Shinozaki, 2006). Although yield of lines carrying the S. pennellii introgressions increased dramatically in non-irrigated trials compared to the control genotype, the final yield was considerably lower than that obtained in the irrigated treatment (Gur and Zamir 2004). Here we evaluate the metabolite content of pericarp of tomato fruit from M82 and its interspecific hybrid with S. pennellii under irrigated and non-irrigated conditions. We evaluate the degree of metabolic variance due to genotypic and environmental influences and additionally compare the magnitude of changes observed in this study with that we have previously characterized in greenhouse grown transgenic tomato lines. Finally, data are discussed in the context of current models of drought stress tolerance.
Materials and methods
All chemicals and pure standard substances were purchased from either Sigma-Aldrich Chemie GmbH (Deisenhofen, Germany) or Merck KGaA (Damstadt, Germany).
Plant growth and harvesting
Plants were grown in Akko, Israel and were handled largely as described in the literature (Schauer et al., 2006). In detail seedlings (35 days old) were transplanted in the field with 50 cm between plants and 2 m between rows (1 plant per m2). All the plants were sprinkler irrigated immediately after transplanting with 30 m3 of water for every 1000 m2 of field area. For the rest of the growing period the wet treatment was drip-irrigated with 320 m3 of water per 1000 m2 throughout the growing season according to the irrigation protocols in the area, while no water was applied to the dry treatment. For each set of samples biological replication of six fruits was used.
Metabolite extraction and derivatization
Tomato pericarp tissue was extracted in 4500 μl of water/methanol (1:2) as described in Roessner-Tunali et al. (2003); 50 μl of internal standard (2 mg of ribitol per ml) was added for quantification. All other details were exactly the same as in Roessner et al., (2001).
GC-MS analysis and chromatogram evaluation
The gas chromatography mass spectrometry (GC-MS) system was composed of an AS 2000 autosampler, a GC 8000 gas chromatograph and a Voyager quadrupole mass spectrometer (ThermoFinnigan, Manchester, UK). The mass spectrometer was tuned according to the manufacturer´s recommendations, using tris-(perflurobutyl)-amine (CF43). GC was performed on a 5MS column (Varian Deutschland GmbH, Darmstadt, Germany), using the exact same conditions defined in Roessner et al. (2001). Substances were identified by comparison to mass spectral tags represented in our in-house database (Kopka et al., 2005; Schauer et al., 2005b). They were quantified following the same procedure as described in Roessner et al. (2001), the recovery of small representative amounts of each metabolite through the extraction, derivatization, storage and quantification process has been documented previously (Roessner et al., 2000), as has the validity of this method for use with tomato derived extracts (Roessner-Tunali et al., 2003).
Principal component analysis (PCA) on the log10-normalized dataset was performed with the TIGR MultiExperiment Viewer 4.0 (Saeed et al., 2003). Missing values were imputed using the inbuilt KNN algorithm of TMev 4.0 with default settings (Theilhaber et al., 2002). If two observations are described in the text as different, this means that their difference was determined to be statistically different (p ≤ 0.05) by the performance of the students t-test using the algorithm embedded into Microsoft Excel, differences at the p ≤ 0.01 level are additionally demarcated within the Supplementary data set (Microsoft, Seattle, WA). The less stringent level was used predominantly since this is more or less standard with respect to plant physiology, however, in light of recent reports on metabolite data sets (see for example Broadhurst and Kell, 2006), we additionally chose to display the results at a more stringent cut off for reference at the readers discretion.
Results and discussion
Morphology of tomato plants of M82 and its interspecific hybrid with S. pennellii under irrigated and non-irrigated conditions
Metabolite profiles of tomato plants of M82 and its interspecific hybrid with S. pennellii under irrigated and non-irrigated conditions
Comparison of the two genotypes under water replete conditions gave results that could perhaps have been anticipated from previous studies in which the metabolite levels of fruit pericarp of either S. lycopersicum and S. pennellii (Schauer et al., 2005) or the introgression line population resulting from the crossing of these species (Schauer et al., 2006) were investigated. Amino acid levels showed considerable variance between the genotypes with alanine, asparagine, methionine, phenylalanine, serine, threonine and valine all decreasing to levels between 8 and 49 % of those observed in the elite cultivar. In contrast, the majority of fatty and organic acids increased in the F1 hybrid relative to the S. lycopersicum control. The increase in fatty acids being 1.65 to 1.8-fold, whilst that in organic acids was much greater, reaching as much as 11-fold in the case of malate. These large changes are surprising in light of our previous study which encompassed analysis of fruit pericarp of S. lycopersicum and S. pennellii since the acid content in both parents was remarkably similar (Schauer et al., 2005). That said the range in the content observed in organic acids in the S. pennellii introgression population was similar to that seen for the other metabolites and clear examples of transgressive behaviour were also observed in this population (Schauer et al., 2006). Analysis of the levels of sugars, sugar phosphates, sugar alcohols and miscellaneous metabolites revealed that the genotypes were quite distinct from one another with respect to their contents of these metabolites also. In general there was a tendency for these metabolites to be elevated in level in the F1 hybrid. Fructose, gentiobiose, glucose, maltose, melizitose, ribose, sucrose, trehalose, xylose and myo-inositol were all present at considerably higher levels in the hybrid with putrescine and fructose 6-phosphate being present at significantly lower levels than in M82.
Comparison of S. lycopersicum under irrigated and non-irrigated plots in the same field also revealed large changes in metabolite contents. In this case, however, more dramatic changes in amino acid content were observed with large increases in alanine, aspartate, β-alanine, GABA, glutamate, glycine, homoserine, isoleucine, proline, serine and valine, with decreased observed for cysteine, glutamine and glycine. Of these amino acids there is an abundant literature suggesting a role of proline in response to water stress (reviewed in Bartels and Sunkar, 2005; Zhu, 2000), however, whilst this also explains the increase in glutamate which is a precursor in the predominant pathway of proline synthesis (Yoshiba et al., 1997) and the documented increase in glycine could reflect accumulation of another commonly mentioned compatible solute – glycine betaine (Rhoades and Hanson, 1993), the majority of these changes have not been described before. The increase in the branched chain amino acids is intriguing, however, our understanding of the exact role and regulation of these metabolites in plants is currently somewhat lacking (Ishizaki et al., 2005). In addition to these changes the levels of fatty and organic acids generally increased with particularly large increases in intermediates of the TCA cycle but a decrease in the level of citramalate (however the function of this metabolite in plants is very poorly understood). An increased activity of the TCA cycle under conditions of osmotic stress has not been reported per se, however, it is known that this stress often also produces oxidative stress which is intimately associated with mitochondrial metabolism as well as being necessary for the assimilation of nitrate that is essential for the production of glutamate (Fernie et al., 2004). There are also large changes in many sugars and sugar derivatives including erythritol, fructose, glucose, isomaltose, sucrose, ribose and trehalose and the oligosaccharide gentiobiose (Dumville and Fry, 2002). With the exception of that in gentiobiose the changes in these solutes have largely been documented previously (see for example Dancer et al., 1990; Büssis and Heineke, 1998; Avelange-Macheral et al., 2006), and the role of sugar accumulation under conditions of water stress is now firmly established (Bartels and Sunkar, 2005). The change in gentiobiose is intriguing, particularly given its proposed signalling role during tomato fruit development (Dumville and Fry, 2002), however, further experimentation is clearly required before a functional role for the change in the level of this metabolite can be defined.
In contrast comparison of the F1 hybrid under irrigated and non-irrigated plots in the same field revealed very few changes in metabolite contents. These were restricted to the large decrease in Pro, isocitrate, maltose, fructose, and nictonate content and increases in mannitol content in the non-irrigated plants. This suggests that if the metabolite levels are contrasted to those of the S. lycopersicum under irrigated conditions the changes observed would be broadly similar. For this reason we also analysed this meta-comparison statistically. With the exception of citramalate, glycolate and quinate (for which only the irrigated F1 hybrid was significantly different from the wild type) and uracil, maltose, and rhamnose (for which only the non-irrigated F1 hybrid was significantly different from the wild type), the changes in metabolite level in the F1 hybrid were broadly similar irrespective of water supply (see figure 3 and Supplementary data).
The authors would like to thank the BMBF for funding in the frame of a DIP grant (Deutsch-Israeli Project).
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