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Prof. R.C. (Rob) Schuurink

Faculty of Science
Swammerdam Institute for Life Sciences
Photographer: onbekend

Visiting address
  • Science Park 904
  • Room number: C2.211
Postal address
  • Postbus 1210
    1000 BE Amsterdam
  • Profile

    Research Interests

    The topics in my group concern the biosynthesis, regulation and biological role of volatiles for plants in their environment. In the last decade Petunia hybrida has emerged as the model of choice to study volatile benzenoid and phenylpropanoid synthesis, emission and regulation. These volatiles are synthesized predominantly in the corolla limb and emission is highly regulated, with a circadian rhythm, during corolla development, pollination and senescence. With all the biochemical and molecular tools available much of our understanding of volatile benzenoid/phenylpropanoid has been obtained with Petunia. The knowledge obtained with this system is being applied to tomato fruit and strawberry volatile production and thereby taste. In addition, we use tomato as a model system to study the role of terpenoids in its interaction with insects. We focus on terpene synthases expressed in trichomes and have identified several terpenoids that repel or attract whiteflies. Our aim is to engineer the production of these terpenoids for which we have identified trichome specific promoters. We use Arabidopsis for forward genetic screens to identify genes important in the response to the wound-induced C6-volatile E -2-hexenal. We also aim to identify genes that are specifically regulated by E -2-hexenal using a transcriptomics approach. Finally, a relative new topic in my group concerns effectors produced by herbivores that manipulate plant defenses. Together with the IBED at UvA we have discovered the first effectors from spider mites that manipulate the SA defense response. We are now focusing on their interactors in the plant and on effectors from whiteflies and thrips.

    Floral scent production by Petunia

    We study the biosynthesis of volatile benzenoids in Petunia and the regulation thereof. We have discovered, through a targeted metabolomics and transcriptomics approach, ODORANT1, the first transcription factor that regulates volatile benzenoid synthesis and provided insight in how Petunia flowers developmentally separate color and scent biosynthesis; we have recently discovered that the transcription factor EOBII (Emission of benzenoids II) acts upstream of ODO1. We are currently using Chip-Seq to identify all targets of ODO1 and EOBII. Moreover, we identified a 3-keto-acylthiolase that catalyzes an important step in benzoic acid biosynthesis, a crucial precursor for several benzenoids. Together with the lab of Natalia Dudareva (Purdue) we discovered that an ABC transporter is involved in active transport of some volatile benzenoids/phenylpropanoids.

    The role of volatile terpenoids in tomato-insect interactions.

    We are particularly interested in the role of volatile terpenoids in tomato-insect interactions. We have established a role for jasmonate (JA) in the production of volatile terpenoids in tomato upon herbivory and discovered that JA induces the expression of salicylic acid (SA) methyl transferase that converts SA to the volatile methyl salicylate, an volatile crucial in attracting predatory mites as shown by silencing SAMT in tomato. We have also identified and characterized the first monoterpene synthases from tomato that are specifically expressed and induced by JA in trichomes. This was recently followed up by the identification and characterization of all terpene synthases in tomato. Recently we identified the terpenoids that are directly involved in repelling or attracting whiteflies. Through 454 and GS-flex sequencing of trichome cDNAs of wild tomatoes we identified the corresponding terpenoid synthases. We modified cultivated tomato plants to produce the relevant terpenoids using trichome specific promoters that were discovered in my lab and made them more resistant to herbivorous insects. With yeast-1-hybrid we have identified a transcription factor that specifically can upregulate certain terpene synthases in the glandular trichomes of tomato. Furthermore, we have shown that the bHLH MYC1 transcription factor is involved in both the development of type VI glandular trichomes as in regulating terpene synthases in the glandular heads.

    Identification of effectors of whiteflies and thrips that manipulate plant responses.

    Whitefly saliva contains many proteins and since whiteflies suppress certain defenses in plants it is thought that this occurs via effectors, similar to the situation in plant pathogenic bacteria and fungi. Together with the IBED at UvA we have discovered the first effectors from spider mites that manipulate the SA defense response and we have just submitted a manuscript describing these effectors. We are now focusing on on effectors from whiteflies and thrips and their interactors in the plant. We have discovered several plant proteins with which these effectors interact and are perturbing these interactors in planta to determine effect on insect performance.

    Green leaf volatiles

    As a fourth topic we study the role of C6 volatiles as signaling and priming molecules. These C6 volatiles are produced in most, if not all, plants upon wounding, pathogen infection and insect herbivory and can prime the defense of neighboring plants. We have identified the first Arabidopsis mutants that are resistant to E-2-hexenal (her mutants) and have mapped the her1 mutation to discover a role for GABA in this process as well as in the defense against Pseudomonas. We also mapped and cloned the her2 mutant and determined that several WRKY transcription factors may regulate the E-2-hexenal response in Arabidopsis. Moreover, in the Arabidopsis-Pseudomonas interaction, the microbe seems to hijack the C6 volatiles to enhance jasmonate biosynthesis and susceptibility. This work is continued by Silke Allmann.

    Section of Plant Physiology

    I work within the Plant Physiology group headed by Prof. dr. Michel Haring. Dr. Petra Bleeker (natural variation of metabolic defense pathways) and Dr. Silke Allmann are the other staff members.


    Teaching interests

    I coordinate the first year course 'Plant Biology' and the MSc course 'Biotic Interactions'. I also give lectures in various other courses. I am chair of the program committee BSc biology and are preparing the specialization Molecular Life Sciences in the third year BSc Biology. 

  • Lab members

    Current members of the lab

    Paula van Kleeff Postdoc

    Diana Naalden Postdoc

    Sarmina Dangol Postdoc

    Pulu Sun Lab manager

    Marieke Mastop technician

    Milan Plasmeier PhD student

    Pietro Zocca PhD student

    Andreia Rodrigues technician

    Jurre Bleeker, technician


    Previous members of the lab

    Fariza Shaipulah (Malaysia) 
    Maaike Boersma (In Holland)

    Ahmed Abd-el-Haliem (RijkZwaan)

    Suzanne Alves Aflitos-Hoogstrate (UvA)

    Sonia Jillings (In Holland)

    Silke Allmann (UvA)
    Michel de Vries (UvA)

    Jiesen Xu (China)

    Aldana Ramirez (Gent)

    Chun Sui (China)

    Carlos Alberto Villarroel (Chile)

    Eleni Spyropoulou (UvA)

    Alessandra Scala, Frontiers

    Arjen van Doorn (Munich)) 

    Petra Bleeker (UvA) 

    Julian Verdonk (WUR)
    Merijn Kant (UvA, IBED)
    Chris van Schie (ENZA Seeds)
    Doerte Klaus (Toulouse)
    Chunlin Liu (China)
    Kai Ament (Bejo Seeds) 
    Alex Van Moerkercke (Sweden)  
    Rossana Mirabella, Fontiers
    Vangelis Panagiotou



  • Student projects

    Unravelling plant defence signals

      Plants are organisms that cannot move so they have evolved several mechanisms to face environmental stress. When a leaf is wounded or is infected by pathogenic bacteria many signals are triggered into the whole plant and the combination of these informations are fundamental for life and death struggle. In our lab we are interested in shedding light in this complex field, plant signal transduction, to reach a basal knowledge on which applied research is established ( develop resistance to stress ). In particular we pointed our attention on E-2-hexenal, a volatile compound, emitted under mechanical or biotic stress, that we have found   is related with GABA, another molecule that is induced during several kinds of stress. Our aim is to discover the connection between these two signals and also with the others plant signals that trigger defences, such as jasmonic acid and salicylicacid.

    Pseudomonas syringae and Arabidopsis thaliana

    are the two components of our biological system. We have several lines of Arabidopsis, for example one which overproduce GABA, another one that has a lower synthesis of E-2-hexenal, and different strains of Pseudomonas that we would like to use to trigger a response in these plants.

    To analyse the plant-pathogen system we use a wide range of experimental approaches like molecular biology techniques (DNA/RNA isolation, cDNA synthesis, PCR, quantitative PCR, plant transformation), biochemistry techniques (quantification of plant hormones an signalling molecules with LC/MS and GC/MS), biological assays (Pseudomonas infection of plants and score symptoms on leaves) and microbiology techniques (collect leaves infiltrated with bacteria and check their growth after it).

    Controlling insect pest by improving the plants defence

    On commercial tomato three arthropod pests constitute enormous problems for agriculture; aphids, whiteflies and spider mites. In our lab we have been working on tomato-whitefly and tomato-spider mite interactions for many years. The long-term aim of this research is to develop resistance to infestation.

    Whitefly ( Bemisia tabaci ) is the vector of viruses in tomato and control of virus infection will be based on prevention of infection. It appears that the host plant is an important factor in selection for resistance; some tomato cultivars appear to exhibit resistance to whitefly infestation and repel whitefly through the production of specific compounds (terpenoids). Previously we established which compounds can decrease whitefly visitation. Forthis internship we will try to elucidate partof thepathway ofterpenoid production and its regulation at the level of terpene biosynthesis which finally will result in application in breeding programmes.

    We have cloned several key enzymes in the terpenoid biosynthesis pathway and have created transgenic tomato lines. These lines will be characterised at gene-expression level (Q-PCR) and production of volatile terpenes (Gas Chromatography-Mass Spectrometry). The effect of altered terpene biosynthesis on whitefly (or spider mite) visitation can then be assessed in bioassays.

    New terpene synthases will be cloned in expression vectors for in-vivo production of terpenes (by expression in E. coli ), in order to find out which products they actually make. This can also be done by transient expression in a tobacco plant via A grobacterium infiltration. We check whether the gene is expressed and if so, which volatiles are produced.

     Experimental techniques include molecular, biochemical and ecological assays (cloning, E. coli expression, GG-MS, DNA/RNA isolation, cDNA synthesis, PCR and quantitative PCR, bioassays)


    Characterizing a candidate gene required for scent biosynthesis in Petunia flowers


    The reproductive success of many plants is dependent on pollination by animals like hummingbirds and bees. Attractive floral traits like color and scent can enhance the reproductive success of a plant.  Petunia is a wonderful plant to study the biosynthesis of these scent molecules, so called floral volatiles.  A mix of floral volatiles is synthesized and emitted by Petunia flowers in a highly regulated manner. These volatiles are synthesized when the pollinators are active and the flower ready to be pollinated. The biosynthesis pathway of floral volatiles is described, but still some enzymes in this pathway are missing. Moreover, the regulation of this pathway is poorly understood. Four transcription factors are known to regulate this pathway, but how they regulate volatile biosynthesis remains largely unknown. Recently we have done Next Generation Sequencing on RNA of several transgenic petunia’s. From this sequencing data we can pick candidate genes that either regulate biosynthesis (transcription factors) or synthesize specific volatiles (biosynthetic genes).


    Hypothesis and objectives

    The project aims to characterize a new biosynthetic gene or transcription factor and determine its role in floral volatile biosynthesis. For this purpose three objectives will be addressed:


    1. Determine the expression pattern of the candidate gene

    Floral volatile genes are expressed mainly in the flower and expression cycles in time.  To determine if the candidate displays the same tissue specific and rhythmic expression as other floral volatile genes expression analysis will be performed. For this purpose RNA will be isolated, cDNA synthesized and the expression level will be determined with quantitative RT-PCR.

     2. To elucidate the subcellular localization of the candidate

    To determine if the candidate localizes to the same subcellular compartments as related floral volatile enzymes Agrobacterium Transient Transformatiom Assays (ATTA) will be performed. The candidate will be labeled with a fluorescent tag to visualize its subcellular localization in Nicotiana benthamiana leaves and Petunia flowers.

     3a. To determine the function of the biosynthetic gene

    To test if the candidate has the predicted enzymatic activity it will be expressed in vitro in E.coli. The produced protein will be analyzed by Western blotting and enzymatic assays.

     3b. To determine the function of the transcription factor

    To elucidate the role of the transcription factor in floral volatile biosynthesis the gene will be silenced in petunia plants. For this purpose a RNAi construct will be cloned and Petunia petals will be transient silenced. Volatile emission will be measured by GC-MS.


     Cloning, RNA isolation, cDNA synthesis, qPCR, ATTA, microscopy,

    In vitro E. coli expression, Western blotting and enzymatic assays or GC-MS



  • Publications





    • Kawa, D., Meyer, A. J., Dekker, H. L., Abd-El-Haliem, A. M., Gevaert, K., Van De Slijke, E., Maszkowska, J., Bucholc, M., Dobrowolska, G., De Jaeger, G., Schuurink, R. C., Haring, M. A., & Testerink, C. (2020). SnRK2 Protein Kinases and mRNA Decapping Machinery Control Root Development and Response to Salt. Plant Physiology, 182(1), 361-377. [details]
    • Schuurink, R., & Tissier, A. (2020). Glandular trichomes: micro-organs with model status? New Phytologist, 225(6), 2251-2266. [details]
    • Sun, P., Dégut, C., Réty, S., Caissard, J-C., Hibrand-Saint Oyant, L., Bony, A., Paramita, S. N., Conart, C., Magnard, J-L., Jeauffre, J., Abd-El-Haliem, A. M., Marie-Magdelaine, J., Thouroude, T., Baltenweck, R., Tisné, C., Foucher, F., Haring, M., Hugueney, P., Schuurink, R. C., & Baudino, S. (2020). Functional diversification in the Nudix hydrolase gene family drives sesquiterpene biosynthesis in Rosa × wichurana. Plant Journal, 104(1), 185-199. [details]








    • Scala, A., Allmann, S., Mirabella, R., Haring, M. A., & Schuurink, R. C. (2013). Green leaf volatiles: a plant's multifunctional weapon against herbivores and pathogens. International Journal of Molecular Sciences, 14(9), 17781-177811. [details]
    • Scala, A., Mirabella, R., Mugo, C., Matsui, K., Haring, M. A., & Schuurink, R. C. (2013). E-2-hexenal promotes susceptibility to Pseudomonas syringae by activating jasmonic acid pathways in Arabidopsis. Frontiers in Plant Science, 4, 74. [details]
    • Vos, I. A., Verhage, A., Schuurink, R. C., Watt, L. G., Pieterse, C. M. J., & van Wees, S. C. M. (2013). Onset of herbivore-induced resistance in systemic tissue primed for jasmonate-dependent defenses is activated by abscisic acid. Frontiers in Plant Science, 4, Article 539. [details]
    • van Schie, C. C. N., Haring, M. A., & Schuurink, R. C. (2013). Prenyldiphosphate synthases and gibberellin biosynthesis. In T. J. Bach, & M. Rohmer (Eds.), Isoprenoid synthesis in plants and microorganisms: new concepts and experimental approaches (pp. 213-232). Springer. [details]


    • Alba, J. M., Bleeker, P. M., Glas, J. J., Schimmel, B. C. J., van Wijk, M., Sabelis, M. W., Schuurink, R. C., & Kant, M. R. (2012). The impact of induced plant volatiles on lant-arthropod interactions. In G. Smagghe, & I. Diaz (Eds.), Arthropod-plant interactions: novel insights and approaches for IPM (pp. 15-73). (Progress in biological control; No. 14). Springer. [details]
    • Bleeker, P. M., Mirabella, R., Diergaarde, P. J., Vandoorn, A., Tissier, A., Kant, M. R., Prins, M., de Vos, M., Haring, M. A., & Schuurink, R. C. (2012). Improved herbivore resistance in cultivated tomato with the sesquiterpene biosynthetic pathway from a wild relative. Proceedings of the National Academy of Sciences of the United States of America, 109(49), 20124-20129. [details]
    • Colquhoun, T. A., Marciniak, D. M., Wedde, A. E., Kim, J. Y., Schwieterman, M. L., Levin, L. A., Van Moerkercke, A., Schuurink, R. C., & Clark, D. G. (2012). A peroxisomally localized acyl-activating enzyme is required for volatile benzenoid formation in a Petuniaxhybrida cv. 'Mitchell Diploid' flower. Journal of Experimental Botany, 63(13), 4821-4833. Advance online publication. [details]
    • Ducluzeau, A-L., Wamboldt, Y., Elowsky, C. G., Mackenzie, S. A., Schuurink, R. C., & Basset, G. J. (2012). Gene network reconstruction identifies the authentic trans-prenyl diphosphate synthase that makes the solanesyl moiety of ubiquinone-9 in Arabidopsis. Plant Journal, 69(2), 366-375. Advance online publication. [details]
    • Glas, J. J., Schimmel, B. C. J., Alba, J. M., Escobar-Bravo, R., Schuurink, R. C., & Kant, M. R. (2012). Plant glandular trichomes as targets for breeding or engineering of resistance to herbivores. International Journal of Molecular Sciences, 13(12), 17077-17103. [details]
    • Van Moerkercke, A., Galván-Ampudia, C. S., Verdonk, J. C., Haring, M. A., & Schuurink, R. C. (2012). Regulators of floral fragrance production and their target genes in petunia are not exclusively active in the epidermal cells of petals. Journal of Experimental Botany, 63(8), 3157-3171. Advance online publication. [details]
    • Van Moerkercke, A., Haring, M. A., & Schuurink, R. C. (2012). A model for combinatorial regulation of the petunia R2R3-MYB transcription factor ODORANT1. Plant Signaling & Behavior, 7(4), 518-520. [details]


    • Almeida Sarmento, R., Lemos, F., Bleeker, P. M., Schuurink, R. C., Pallini, A., Oliveira, M. G. A., Lima, E. R., Kant, M., Sabelis, M. W., & Janssen, A. (2011). A herbivore that manipulates plant defence. Ecology Letters, 14(3), 229-236. [details]
    • Bleeker, P. M., Diergaarde, P. J., Ament, K., Schütz, S., Johne, B., Dijkink, J., Hiemstra, H., de Gelder, R., de Both, M. T. J., Sabelis, M. W., Haring, M. A., & Schuurink, R. C. (2011). Tomato-produced 7-epizingiberene and R-curcumene act as repellents to whiteflies. Phytochemistry, 72(1), 68-73. [details]
    • Bleeker, P. M., Spyropoulou, E. A., Diergaarde, P. J., Volpin, P., de Both, M. T. J., Zerbe, P., Bohlmann, J., Falara, V., Matsuba, Y., Pichersky, E., Haring, M. A., & Schuurink, R. C. (2011). RNA-seq discovery, functional characterization, and comparison of sesquiterpene synthases from Solanum lycopersicum and Solanum habrochaites trichomes. Plant Molecular Biology, 77(4-5), 323-336. [details]
    • Colquhoun, T. A., Kim, J. Y., Wedde, A. E., Levin, L. A., Schmitt, K. C., Schuurink, R. C., & Clark, D. G. (2011). PhMYB4 fine-tunes the floral volatile signature of Petunia×hybrida through PhC4H. Journal of Experimental Botany, 62(3), 1133-1143. [details]
    • Dal Cin, V., Tieman, D. M., Tohge, T., McQuinn, R., de Vos, R. C. H., Osorio, S., Schmelz, E. A., Taylor, M. G., Smits-Kroon, M. T., Schuurink, R. C., Haring, M. A., Giovannoni, J., Fernie, A. R., & Klee, H. J. (2011). Identification of genes in the phenylalanine metabolic pathway by ectopic expression of a MYB transcription factor in tomato fruit. The Plant Cell, 23(7), 2738-2753. [details]
    • Falara, V., Akhtar, T. A., Nguyen, T. T. H., Spyropoulou, E. A., Bleeker, P. M., Schauvinhold, I., Matsuba, Y., Bonini, M. E., Schilmiller, A. L., Last, R. L., Schuurink, R. C., & Pichersky, E. (2011). The tomato terpene synthase gene family. Plant Physiology, 157(2), 770-789. [details]
    • Van Moerkercke, A., Haring, M. A., & Schuurink, R. C. (2011). The transcription factor EMISSION OF BENZENOIDS II activates the MYB ODORANT1 promoter at a MYB binding site specific for fragrant petunias. Plant Journal, 67(5), 917-928. [details]


    • Allmann, S., Halitschke, R., Schuurink, R. C., & Baldwin, I. T. (2010). Oxylipin channelling in Nicotiana attenuata: lipoxygenase 2 supplies substrates for green leaf volatile production. Plant, cell and environment, 33(12), 2028-2040. Advance online publication. [details]
    • Ament, K., Krasikov, V., Allmann, S., Rep, M., Takken, F. L. W., & Schuurink, R. C. (2010). Methyl salicylate production in tomato affects biotic interactions. Plant Journal, 62(1), 124-134. [details]
    • Park, D. H., Mirabella, R., Bronstein, P. A., Preston, G. M., Haring, M. A., Lim, C. K., Collmer, A., & Schuurink, R. C. (2010). Mutations in γ-aminobutyric acid (GABA) transaminase genes in plants or Pseudomonas syringae reduce bacterial virulence. Plant Journal, 64(2), 318-330. [details]
    • van den Burg, H. A., Kini, R. K., Schuurink, R. C., & Takken, F. L. W. (2010). Arabidopsis small ubiquitin-like modifier paralogs have distinct functions in development and defense. The Plant Cell, 22(6), 1998-2016. [details]


    • Bleeker, P. M., Diergaarde, P. J., Ament, K., Guerra, J., Weidner, M., Schütz, S., de Both, M. T. J., Haring, M. A., & Schuurink, R. C. (2009). The role of specific tomato volatiles in tomato-whitefly interaction. Plant Physiology, 151(2), 925-935. [details]
    • Kant, M. R., Bleeker, P. M., van Wijk, M., Schuurink, R. C., & Haring, M. A. (2009). Plant Volatiles in Defence. In L. C. van Loon (Ed.), Plant innate immunity (pp. 613-666). (ADVANCES IN BOTANICAL RESEARCH; No. 51). Academic Press. [details]
    • Van Moerkercke, A., Schauvinhold, I., Pichersky, E., Haring, M. A., & Schuurink, R. C. (2009). A plant thiolase involved in benzoic acid biosynthesis and volatile benzenoid production. Plant Journal, 60(2), 292-302. [details]


    • Kant, M. R., Sabelis, M. W., Haring, M. A., & Schuurink, R. C. (2008). Intraspecific variation in a generalist herbivore accounts for differential induction and impact of host plant defences. Proceedings of the Royal Society B-Biological Sciences, 275(1633), 443-452. [details]
    • Mirabella, R., Rauwerda, H., Struys, E. A., Jakobs, C., Triantaphylidès, C., Haring, M. A., & Schuurink, R. C. (2008). The Arabidopsis her1 mutant implicates GABA in E-2-hexenal responsiveness. Plant Journal, 53(2), 197-213. [details]


    • Lee, H. R., Lee, S., Kleeff, P. J. M. V., Schuurink, R. C., & Ryu, C. M. (2019). Transient Expression of Whitefly Effectors in Nicotiana benthamiana Leaves Activates Systemic Immunity Against the Leaf Pathogen Pseudomonas syringae and Soil-Borne Pathogen Ralstonia solanacearum. Molecular Plant-Microbe Interactions, 32(10), 150-151.


    • Zhang, N. X., Messelink, G. J., Alba, J. M., Schuurink, R. C., Kant, M. R., & Janssen, A. (2018). Correction to: Phytophagy of omnivorous predator Macrolophus pygmaeus affects performance of herbivores through induced plant defences. Oecologia, 186(1), 115.


    • Clark, D. G., Pichersky, E., Verdonk, J., Dudareva, N., Haring, M., Klahre, U., & Schuurink, R. (2009). Benzenoids dominate the fragrance of Petunia flowers. In T. Gerats, & J. Strommer (Eds.), Petunia: evolutionary, developmental and physiological genetics. - 2nd ed. (pp. 51-69). Springer. [details]



    • Villarroel Figueroa, C. A., Jonckheere, W., Alba Cano, J. M., Glas, J. J., Dermauw, W., Haring, M. A., Van Leeuwen, T. B. S., Schuurink, R. C., & Kant, M. (2016). Effector proteins of spider mites improve their performance by plant defense manipulation. Abstract from EURAAC 2016 Valencia, Valencia, Spain.

    Talk / presentation

    • Schuurink, R. C. (invited speaker) (8-12-2016). Regulation of terpene biosynthesis in tomato trichomes., John Innes Center, Norwich.
    • Schuurink, R. C. (invited speaker) (10-9-2016). Circadian rhythm of volatile production., 15th World Petunia Days, Wittenberg.
    • Schuurink, R. C. (invited speaker) (11-5-2016). Plants and insects, a volatile interaction., International Centre of Insect Physiology and Ecology (icipe).
    • Schuurink, R. C. (invited speaker) (4-2-2016). Signal Transduction by Green Leaf Volatiles, Plant Volatiles Gordon Research Conference 2016, Ventura.


    • Zhang, X., Wang, D., Elberse, J., Qi, L., Shi, W., Peng, Y.-L., Schuurink, R. C., Van den Ackerveken, G. & Liu, J. (10-2-2021). Crystal structure of JOX2 in complex with 2OG, Fe, and JA. Protein Data Bank (PDB).
    • Kortbeek, R. W. J., Galland, M., Muras, A., van der Kloet, F., André, B., Heilijgers, M., van Hijum, S. A. F. T., Haring, M. A., Schuurink, R. C. & Bleeker, P. (2021). Additional file 9 of Natural variation in wild tomato trichomes; selecting metabolites that contribute to insect resistance using a random forest approach. Figshare.
    • Kortbeek, R. W. J., Galland, M., Muras, A., van der Kloet, F., André, B., Heilijgers, M., van Hijum, S. A. F. T., Haring, M. A., Schuurink, R. C. & Bleeker, P. (2021). Additional file 10 of Natural variation in wild tomato trichomes; selecting metabolites that contribute to insect resistance using a random forest approach. Figshare.
    • Kortbeek, R. W. J., Galland, M., Muras, A., van der Kloet, F., André, B., Heilijgers, M., van Hijum, S. A. F. T., Haring, M. A., Schuurink, R. C. & Bleeker, P. (2021). Additional file 11 of Natural variation in wild tomato trichomes; selecting metabolites that contribute to insect resistance using a random forest approach. Figshare.


    • Sun, P., Dégut, C., Réty, S., Caissard, J.-C., Hibrand-Saint Oyant, L., Bony, A., Paramita, S. N., Conart, C., Magnard, J.-L., Jeauffre, J., Abd-El-Haliem, A. M., Marie-Magdelaine, J., Thouroude, T., Baltenweck, R., Tisné, C., Foucher, F., Haring, M., Hugueney, P., Schuurink, R. C. & Baudino, S. (22-7-2020). NUDIX1 hydrolase from Rosa x hybrida in complex with geranyl pyrophosphate. Protein Data Bank (PDB).
    • Sun, P., Dégut, C., Réty, S., Caissard, J.-C., Hibrand-Saint Oyant, L., Bony, A., Paramita, S. N., Conart, C., Magnard, J.-L., Jeauffre, J., Abd-El-Haliem, A. M., Marie-Magdelaine, J., Thouroude, T., Baltenweck, R., Tisné, C., Foucher, F., Haring, M., Hugueney, P., Schuurink, R. C. & Baudino, S. (22-7-2020). NUDIX1 hydrolase from Rosa x hybrida. Protein Data Bank (PDB).


    • Schimmel, B. C. J., Ataide, L. M. S., Chafi, R., Villarroel Figueroa, C., Alba, J. M., Schuurink, R. C. & Kant, M. R. (2017). Schimmel et al. 2017 New Phytologist raw data. Figshare.
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  • Ancillary activities
    • SILS
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