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Burger, I., Schmal, M., Peikert, K., Fourtis, L., Suster, C., Stanetty, C., Schnalzer, D., Hufnagel, B., Böttcher, T., Birner-Gruenberger, R., Mach, R. L., Mach-Aigner, A. R., Schittmayer, M., & Zimmermann, C. (2025). Discovery of the antifungal compound ilicicolin K through genetic activation of the ilicicolin biosynthetic pathway in Trichoderma reesei. Biotechnology for biofuels and bioproducts, 18(1), 32. https://doi.org/10.1186/s13068-025-02628-3

Savchenko, V., Yu, X. A., Polz, M. F., & Böttcher, T. (2025). Chitinivorax: The New Kid on the Block of Bacterial 2-Alkyl-4(1H)-quinolone Producers. ACS Chemical Biology. Vorzeitige Online-Publikation. https://doi.org/10.1021/acschembio.5c00046

Pereira, F. C., Ge, X., Kristensen, J. M., Kirkegaard, R. H., Maritsch, K., Szamosvári, D., Imminger, S., Seki, D., Shazzad, J. B., Zhu, Y., Decorte, M., Hausmann, B., Berry, D., Wasmund, K., Schintlmeister, A., Böttcher, T., Cheng, J.-X., & Wagner, M. (2024). The Parkinson's disease drug entacapone disrupts gut microbiome homoeostasis via iron sequestration. Nature Microbiology, 9(12), 3165–3183. https://doi.org/10.1038/s41564-024-01853-0

Steuer, J., Sinn, M., Eble, F., Rütschlin, S., Böttcher, T., Hartig, J. S., & Peter, C. (2024). Cooperative binding of bivalent ligands yields new insights into the guanidine-II riboswitch. NAR Genomics and Bioinformatics, 6(3), Artikel lqae132. https://doi.org/10.1093/nargab/lqae132

Savchenko, V., Jaegers, M., Rasche, R., Herrmann, E., König, S., Kümmel, D., Böttcher, T., Fetzner, S., & Ernst, S. (2024). Unraveling key steps in the biosynthesis of antimicrobial methylated unsaturated 2-alkyl-4-quinolones of Burkholderia thailandensis. Cell Reports Physical Science, 5(8), Artikel 102100. https://doi.org/10.1016/j.xcrp.2024.102100

Mou, S., Savchenko, V., Filz, V., Böttcher, T., & DeShazer, D. (2024). Burkholderia pseudomallei produces 2-alkylquinolone derivatives important for host virulence and competition with bacteria that employ naphthoquinones for aerobic respiration. Frontiers in Microbiology, 15, Artikel 1474033. https://doi.org/10.3389/fmicb.2024.1474033

Savchenko, V., Szamosvári, D., Bao, Y., Pignitter, M., & Böttcher, T. (2023). Biosynthetic flexibility of Pseudomonas aeruginosa leads to hydroxylated 2-alkylquinolones with proinflammatory host response. Communications Chemistry, 6(1), Artikel 138. https://doi.org/10.1038/s42004-023-00937-y

Ückert, A. K., Rütschlin, S., Gutbier, S., Wörz, N. C., Miah, M. R., Martins, A. C., Hauer, I., Holzer, A. K., Meyburg, B., Mix, A. K., Hauck, C., Aschner, M., Böttcher, T., & Leist, M. (2023). Identification of the bacterial metabolite aerugine as potential trigger of human dopaminergic neurodegeneration. Environment International, 180, Artikel 108229. https://doi.org/10.1016/j.envint.2023.108229

Szamosvari, D., Savchenko, V., Badouin, N., & Böttcher, T. (2023). Beyond iron: metal-binding activity of the Pseudomonas quinolone signal-motif. Organic & Biomolecular Chemistry, 21(25), 5158-5163. https://doi.org/10.1039/d3ob00710c

Klein, K., Garkov, D., Rütschlin , S., Böttcher, T., & Schreiber, F. (2021). QSDB—a graphical Quorum Sensing Database. Database: The Journal of Biological Databases and Curation, 2021, Artikel baab058. https://doi.org/10.1093/database/baab058

Klein, K., Garkov, D., Ruetschlin, S., Boettcher, T., & Schreiber, F. (2021). QSDB-a graphical Quorum Sensing Database (vol 2021, baab058, 2021). Database: The Journal of Biological Databases and Curation, 2021, Artikel baab071. https://doi.org/10.1093/database/baab071

Böttcher, T., Nguyen , T. H. N., & Szamosvari, D. (2021). Synthesis of bacterial 2-alkyl-4(1H)-quinolone derivatives. ARKIVOC, 2021(9), 218-239. https://doi.org/10.24820/ark.5550190.p011.547

Jancheva, M., & Boettcher, T. (2021). A Metabolite of Pseudomonas Triggers Prophage-Selective Lysogenic to Lytic Conversion in Staphylococcus aureus. Journal of the American Chemical Society, 143(22), 8344-8351. https://doi.org/10.1021/jacs.1c01275

Prothiwa, M., Filz, V., Oehler, S., & Boettcher, T. (2021). Inhibiting quinolone biosynthesis of Burkholderia. Chemical Science, 12(20), 6908-6912. https://doi.org/10.1039/d0sc06167k

Penalver, L., Schmid, P., Szamosvari, D., Schildknecht, S., Globisch, C., Sawade, K., Peter, C., & Boettcher, T. (2021). A Ligand Selection Strategy Identifies Chemical Probes Targeting the Proteases of SARS-CoV-2. Angewandte Chemie (International Edition), 60(12), 6799-6806. https://doi.org/10.1002/anie.202016113

Boettcher, T. (2020). Unveiling the Hidden Theatre of Microbes. ChemBioChem: a european journal of chemical biology, 21(20), 2869-2869. https://doi.org/10.1002/cbic.202000554

Szamosvari, D., Prothiwa, M., Dieterich, C. L., & Boettcher, T. (2020). Profiling structural diversity and activity of 2-alkyl-4(1H)-quinolone N-oxides of Pseudomonas and Burkholderia. Chemical Communications, 56(47), 6328-6331. https://doi.org/10.1039/d0cc02498h