The emerging field of rhizosphere metabolomics involves analysis of entire metabolite complement (metabolome), in an unbiased way to understand complex physiological, pathological, symbiotic and other relationships among the inhabitants of the rhizosphere. Metabolomic studies of the rhizosphere are quite challenging since the rhizosphere is a complex as well as a dynamic microenvironment. Metabolite composition in the rhizosphere is primarily governed by the nature of root exudates, secretions from rhizobacteria, fungi and other soil organisms. Conversely, the nature of these root exudates also directly or indirectly affects microbial growth in the rhizosphere. While some compounds enhance growth, others have antimicrobial activities. Apart from the diverse roles of compounds present, the complexity of the rhizosphere also stems from competition among rhizosphere microbes. Some of them are growth-promoting, while others are pathogenic. These effects are not only confined to the microbes but also extend to the plants growing in the rhizosphere. Hence, gaining knowledge of these rhizosphere metabolites as well as the effect of the biota will help us better understand this ecological niche.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Bajic VB, Veronika M, Veladandi PS, Meka A, Heng M-W, Rajaraman K, Pan H, Swarup S (2005) Dragon Plant Biology Explorer. A text-mining tool for integrating associations between genetic and biochemical entities with genome annotation and biochemical terms lists. Plant Physiol 138:1914–1925
Bais HP, Weir TL, Perry LG, Gilroy S, Vivanco JM (2006) The role of root exudates in rhizosphere interactions with plants and other organisms. Annu Rev Plant Biol 57:233–266
Bending GD, Poole EJ, Whipps JM, Read DJ (2002) Characterisation of bacteria from Pinus sylvestris-Suillus luteus mycorrhizas and their effects on root-fungus interactions and plant growth. FEMS Microbiol Ecol 39:219–227
Bhalla R, Narasimhan K, Swarup S (2005) Metabolomics and its role in understanding cellular responses in plants. Plant Cell Rep 24:562–571
Bode HB, Zeeck A, Plückhahn K, Jendrossek D (2000). Physiological and chemical investigtions into microbial degradation of synthetic poly (cis-1, 4-isoprene). Appl Environ Microbiol 66:3680–3685
Boersma MG, Solyanikova IP, Van Berkel WJ, Vervoort J, Golovleva LA, Rietjens IM (2001) 19F NMR metabolomics for the elucidation of microbial degradation pathways of fluorophenols. J Ind Microbiol Biotechnol 26:22–34
Bonnington L, Eljarrat E, Guillamón M, Eichhorn P, Taberner A, Barceló D (2003) Development of a liquid chromatography-electrospray-tandem mass spectrometry method for the quantitative determination of benzoxazinone derivatives in plants. Anal Chem 75:3128–3136
Cataldi TRI, Margiotta G, Iasi L, Di Chio B, Xiloyannis C, Bufo SA (2000) Determination of Sugar Compounds in olive plant extracts by anion-exchange chromatography with pulsed amperometric detection. Anal Chem 72:3902–3907
Chang H-K, Zylstra GJ (1998) Novel organization of the genes for phthalate degradation from Burkholderia cepacia DBO1. J Bacteriol 180:6529–6537
Chin-A-Woeng TFC, van den Broek D, Lugtenberg BJJ, Bloemberg GV (2005) The Pseudomonas chlororaphis PCL1391 sigma regulator psrA represses the production of the antifungal metabolite phenazine-1-carboxamide. Mol Plant Microbe Interact 18:244–253
Czarnota MA, Rimando AM, Weston LA (2003). Evaluation of root exudates of seven sorghum accessions. J Chem Ecol 29(9):2073–2083
Dagley S (1981) New perspectives in aromatic catabolism. In: Leisinger T, Cook AM, Hütter R, Nüesch J (eds) Microbial degradation of xenobiotics and recalcitrant compounds. Academic, New York, pp 181–186
Davies JI, Evans WC (1964) Oxidative metabolism of naphthalene by soil pseudomonads. Biochem J 91:251–261
Derrien D, Balesdent J, Marol, Santaella C (2003) Measurement of the 13C/12C ratio of soil-plant individual sugars by gas chromatography/combustion/isotope-ratio mass spectrometry of silylated derivatives. Rapid Commun Mass Spectrom 17:2626–2631
Desbrosses GG, Kopka J, Udvardi MK (2005) Lotus japonicus metabolic profiling. Development of gas chromatography-mass spectrometry resources for the study of plant-microbe interactions. Plant Physiol 137:1302–1318
Dunn WB, Ellis DI (2005) Metabolomics: current analytical platforms and methodologies. Trends Anal Chem 24:285–294
Dunn WB, Bailey NJ, Johnson HE (2005) Measuring the metabolome: current analytical technologies. Analyst 130:606–625
Duran AL, Yang J, Wang L, Sumner LW (2003) Metabolomics spectral formatting, alignment and conversion tools (MSFACTs). Bioinformatics 19:2283–2293
Dutton PL, Evans WC (1967). Dissimilation of aromatic substrates by Rhodopseudomonas palustris. Biochem J 104:30–31
Dutton PL, Evans WC (1969) The metabolism of aromatic compounds by Rhodopseudomonas palustris: a new reductive method of aromatic ring metabolism. Biochem J 113:525–536
Eljarrat E, Barcelo D (2001) Sample handling and analysis of allelochemical compounds in plants. Trends Anal Chem 20:584–590
Evans CJ, Evershed RP (2003) Compound-specific stable isotope analysis of soil mesofauna using thermally assisted hydrolysis and methylation for ecological investigations Anal Chem 75:6056–6062
Evans WC, Fuchs G (1988) Anaerobic degradation of aromatic compounds. Annu Rev Microbiol 42:289–317
Fan TWM, Lane AN, Shenker M, Bartley JP, Crowley D, Higashi RM (2001) Comprehensive chemical profiling of gramineous plant root exudates using high resolution NMR and MS. Phytochemistry 57:209–221
Formanek P, Ambus P (2004) Assessing the use of delta C-13 natural abundance in separation of root and microbial respiration in a Danish beech (Fagus sylvatica L.) forest. Rapid Commun Mass Spectrom 18:897–902
Gibson DT, Subramanian V (1984) Microbial degradation of aromatic hydrocarbons. In Gibson DT (ed) Microbial degradation of organic compounds. Dekker, New York, pp 181–252
Gibson J, Harwood CS (2002) Metabolic diversity in aromatic compound utilization by anerobic microbes. Annu Rev Microbiol 56:345–369
Gleye C, Laurens A, Hocquemiller R, Cave A, Laprevote O, Serani L (1997) Isolation of montecristin, a key metabolite in biogenesis of acetogenins from Annona muricata and its structure elucidation by using tandem mass spectrometry. J Org Chem 62:510–513
Goodacre R (2005) Making sense of the metabolome using evolutionary computation: seeing the wood with the trees. J Exp Bot 56:245–254
Goodacre R, Shann B, Gilbert RJ, Timmins EM, McGovern AC, Alsberg BK, Kell DB, Logan NA (2000) Detection of the dipicolinic acid biomarker in Bacillus spores using Curie-point pyrolysis mass spectrometry and Fourier transform infrared spectroscopy. Anal Chem 72:119–127
Goto S, Okuno Y, Hattori M, Nishioka T, Kanehisa M (2002) LIGAND: database of chemivcal compounds and reactions in biological pathways. Nucleic Acids Res 30:402–404
Griffin JL (2004) Metabolic profiles to define the genome: can we hear the phenotypes? Philos Trans R Soc Lond B Biol Sci 359:857–871
Harayama S, Timmis KN (1992) Aerobic biodegradation of aromatic hydrocarbons by bacteria. In: Sigel H, Sigel A (eds) Metal ions in biological systems, vol 28. Dekker, New York, pp 99–156
Harwood CS, Parales RE (1996) The B-ketoadipate pathway and the biology of self-identity. Annu Rev Microbiol 50:553–590
Hollman PCH, van Trijp JMP, Buysman MNCP, Gaga MSVD, Mengelers MJB, Vries JHM, Katan MB (1997) Relative bioavailability of the antioxidant flavonoid quercetin from various foods in man. FEBS Lett 418:152–156
Hopper W, Mahadevan A (1991) Utilization of catechin and its metabolites by Bradyrhizobium japonicum. Appl Microbiol Biotechnol 35:411–415
Huang WE, Griffiths RI, Thompson IP, Bailey MJ, Whiteley AS (2004) Raman microscopic analysis of single microbial cells. Anal Chem 76:4452–4458
Inderjit (1996) Plant phenolics in allelopathy. Bot Rev 62:186–202
Inderjit, Duke SO (2003) Ecophysiological aspects of allelopathy. Planta 217:529–539
Jansen JJ, Hoefsloot HCJ, Boelens HFM, van der Greef J, Smilde AK (2004) Analysis of longitudinal metabolomics data. Bioinformatics 20:2438–2446
Jeffrey AM, Knight M, Evans WC (1972a) The bacterial degradation of flavonoids: hydroxylation of the A-ring of taxifolin by a soil pseudomonad. Biochem J 130:373–380
Jeffrey AM, Jerina DM, Self R, Evans WC (1972b) The bacterial degradation of flavonoids: oxidative fission of the A-ring of dihydrogossypetin by a Pseudomonas sp. Biochem J 130:383–390
Jenkins H, Hardy N, Beckmann M, Draper J, Smith A, Taylor J et al. (2004) A proposed framework for the description of plant metyabolomics experiments and their results. Nat Biotechnol 22:1601–1607
Jonsson P, Gullberg J, Nordstrom A, Kusano M, Kowalczyk M, Sjostrom M, Moritz T (2004) A strategy for identifying differences in large series of metabolomic samples analyzed by GC/MS. Anal Chem 76:1738–1745
Jonsson P, Bruce SJ, Moritz T, Trygg J, Sjöström M, Plumb R, Granger J, Maibaum J, Nicholson JK, Holmes E, Antti H (2005) Extraction, interpretation and validation of information for comparing samples in metabolic LC/MS data sets. Analyst 130:701–707
Kachlicki P, Marczak L, Kerhoas L, Einhorn J, Stobiecki M (2005) Profiling isoflavone conjugates in root extracts of lupine species with LC/ESI/MSn systems. J Mass Spectrom 40:1088–1103
Kanaly RA, Harayama S (2000) Biodegradation of high-molecular-weight polycyclic aromatic hydrocarbons by bacteria. J Bacteriol 182:2059–2067
Kanehisa M, Goto S, Kawashima S, Okuno Y, Hattori M (2004) The KEGG resource for deciphering the genome Nucleic Acids Rese 32:D277–D280
Kanehisa M, Goto S, Hattori M, Aoki-Kinoshita KF, Itoh M, Kawashima S, Katayama T, Araki M, Hirakawa M (2006) From genomics to chemical genomics: new developments in KEGG. Nucleic Acids Res 34:D354–D357
Katajamaa M, Oresic M (2005) Processing methods for differential analysis of LC/MS profile data. BMC Bioinformatics 6:179
Kerry BR (2000) Rhizosphere interactions and the exploitation of microbial agents for the biological control of plant parasitic nematodes. Annu Rev Phytopathol 38:423–441
Krishnan P, Kruger NJ, Ratcliffe RG (2005) Metabolite fingerprinting and profiling in plants using NMR. J Exp Bot 56:255–265
Kuiper I, Lagendijk EL, Bloemberg GV, Lugtenberg BJJ (2004) Rhizoremediation: a beneficial plant-microbe interaction. Mol Plant Microbe Interact 17 6–15
Lange BM, Ghassemian M (2005) Comprehensive post-genomic data analysis approaches integrating biochemical pathway maps. Phytochemistry 66:413–451
López-DÃez EC, Goodacre R (2004) Characterization of microorganisms using UV resonance raman spectroscopy and chemometrics. Anal Chem 76:585–591
Martens H, Naes T (1989) Multivariate calibration. Wiley, New York
Mendes P (2002) Emerging bioinformatics for the metabolome. Brief Bioinformatics 3:134–145
Menotta M, Gioacchini AM, Amicucci A, Buffalini M, Sisti D, Stocchi V (2004) Headspace solid-phase microextraction with gas chromatography and mass spectrometry in the investigation of volatile organic compounds in an ectomycorrhizae synthesis system. Rapid Commun Mass Spectrom 18:206–210
Mesnard F, Ratcliffe RG (2005) NMR analysis of plant nitrogen metabolism. Photosynth Res 83:163–180
Mueller LA, Zhang P, Rhee SY (2003) AraCyc: a biochemical pathway database for Arabidopsis. Plant Physiol 132:453–460
Mukerji KG, Manoharachary C, Singh J (eds) (2006) Microbial activity in the rhizosphere. Soil biology, vol 7, Springer, Heidelberg
Narasimhan K, Basheer C, Bajic VB, Swarup S (2003) Enhancement of plant-microbe interactions using a rhizosphere metabolomics-driven approach and its application in the removal of polychlorinated biphenyls. Plant Physiol 132:146–153
O’Connell KP, Goodman RM, Handelsman J (1996) Engineering the rhizosphere: expressing a bias. Trends Biotechnol 14:83–88
Oger P, Petit A, Dessaux Y (1997) Genetically engineered plants producing opines alter their biological environment. Nature biotechnology 15:369–372
Pasteur L (1857) Mémoire sur la fermentation appelée lactique. Mém Soc Sci Agric Arts 5:13–37
Perera MR, Vanstone VA, Jones MGK (2005) A novel approach to identify plant parasitic nematodes using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Rapid Commun Mass Spectrom 19:1454–1460
Pfeffer PE, Rolin DB, Schimdt JH, Tu SI, Kumosinski TF, Douds DD (1992) Ion transport and subcellular compartmentation in maize root tissue as examined by in vivo CS-133 NMR spectroscopy. J Plant Nutr 15:913–927
Pillai BVS, Swarup S (2002) Elucidation of the flavonoid catabolism pathway in Pseudomonas putida PML2 strain by comparative metabolic profiling. Appl Environ Microbiol 68:143–151
Pinton R, Varanni Z, Nannipier Pi, Willig W (eds) (2000) The rhizosphere: biochemistry and organic dubstance at the soil-plant interface. Dekker, New York
Rao RJ, Cooper JE (1994) Rhizobia catabolize nod gene-inducing flavonoids via C-ring fission mechanisms. J Bacteriol 176:5409–5413
Rao RJ, Sharma ND, Hamilton JTG, Boyd DR, Cooper JE (1991) Biotransformation of the pentahydroxy flavone quercetin by Rhizobium loti and Bradyrhizobium strains (Lotus). Appl Environ Microbiol 57:1563–1565
Ratcliffe RG, Shachar-Hill Y (2005) Revealing metabolic phenotypes in plants: inputs from NMR analysis. Biol Rev Camb Philos Soc 80:27–43
Reo NV (2002) NMR-based metabolomics. Drug Chem Toxicol 25:375–382
Rice EL (1984) Allelopathy 2nd edn. Academic, Orlando
Rugh CL, Susilawati E, Kravchenko AN, Thomas JC (2005) Biodegrader metabolic expansion during polyaromatic hydrocarbons rhizoremediation. Z Naturforsch C 60:331–339
Ryals J (2004) Drug discovery metabolomics. Metabolomics–an important emerging science. Business briefing: Pharmatech 51–54
Shultz E, Engle FE, Wood JM (1974) New oxygenases in the degradation of flavones and flavonones by Pseudomonas putida. Biochemistry 13:1768–1776
Siciliano SD, Fortin N, Mihoc A, Wisse G, Labelle S, Beaumier D, Ouellette D, Roy R, Whyte LG, Banks MK, Schwab P, Lee K, Greer CW (2001) Selection of specific endophytic bacterial genotypes by plants in response to soil contamination. Appl Environ Microbiol 67:2469–2475
Smilde AK, Jansen JJ, Hoefsloot HCJ, Lamers R-J AN, van der Greef J, Timmerman ME (2005) ANOVA-Simultaneous component analysis (ASCA): a new tool for analyzing designed metabolomics data. Bioinformatics 21:3043–3048
Spaink HP, Wijfjes AHM, Vanvliet TB, Kijne JW, Lugtenberg BJJ (1993) Rhizobial lipo-oligosaccharide signals and their role in plant morphogenesis are analogous lipophilic chitin derivatives produced by the plant. Aust J Plant Physiol 20:381–392
Steeghs M, Bais HP, de Gouw J et al. (2004) Proton-transfer-reaction mass spectrometry as a new tool for real time analysis of root-secreted volatile organic compounds in Arabidopsis. Plant Physiol 135:47–58
Sumner LW, Mendes P, Dixon RA (2003) Plant metabolomics: large-scale phytochemistry in the functional genomics era Phytochemistry 62:817–836
Tarvin D, Buswell AM (1934) The methane fermentation of organic acids and carbohydrates. J Am Chem Soc 56:1751–1755
The Standard Metabolic Reporting Structures Working Group (2005) Summary Recommendations for standardization and reporting of metabolic analyses. Nat Biotechnol 23:833–839
van der Meer JR, de Vos WM, Harayama S, Zehnder AJB (1992) Molecular mechanisms of genetic adaptation to xenobiotic compounds. Microbiol Rev 56:677–694
van der Werf MJ, Jellema RH, Hankemeier T (2005) Microbial metabolomics: replacing trial-and-error by the unbiased selection and ranking of targets. J Ind Microbiol Biotechnol 32:234–252
Villas-Boas SG, Rasmussen S, Lane GA (2005) Metabolomics or metabolite profiles? Trends Biotechnol 23:385–386
Walker TS, Bais HP, Halligan KM, Stermitz FR, Vivanco JM (2003) Metabolic profiling of root exudates of Arabidopsis thaliana. J Agric Food Chem 51:2548–2554
Warhurst AM, Clarke KF, Hill RA, Holt RA, Fewson CA (1994) Metabolism of styrene by Rhodococcus rhodochrous NCIMB 13259. Appl Environ Microbiol 60:1137–1145
Weir TL, Park SW, Vivanco JM (2004) Biochemical and physiological mechanisms mediated by allelochemicals. Curr Opin Plant Biol 7:472–479
Weidenhamer JD (2005). Biomimetic measurement of allelochemical dynamics in the rhizosphere. J Chem Ecol 31(2):221–236
Sun W, Liu S, Liu Z, Song F, Fang S (1998) A study of Aconitum alkaloids from aconite roots in Aconitum carmichaeli Debx using matrix-assisted laser desorption/ionization mass spectrometry. Rapid Commun Mass Spectrom 12:821–824
Wittig U, De Beuckelaer A (2001) Analysis and comparison of metabolic pathway databases. Brief Bioinformatics 2:126–142
Young LY, Frazer AC (1987) The fate of lignin and lignin-derived compounds in anaerobic ecosystems. Geomicrobiol J 5:261–293
Zhang P, Foerster H, Tissier CP, Mueller L, Paley S, Karp PD, Rhee SY (2005) MetaCyc and AraCyc. Metabolic pathway databases for plant research. Plant Physiol 138:27–37
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2008 Springer-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Reuben, S., Bhinu, V.S., Swarup, S. (2008). Rhizosphere Metabolomics: Methods and Applications. In: Karlovsky, P. (eds) Secondary Metabolites in Soil Ecology. Soil Biology, vol 14. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-74543-3_3
Download citation
DOI: https://doi.org/10.1007/978-3-540-74543-3_3
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-540-74542-6
Online ISBN: 978-3-540-74543-3
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)