Publikationen der Arbeitsgruppe Synthetische Biologie

2021


Essoung, F. R. E., Mba'ning, B. M., Tcho, A. T., Chhabra, S. C., Mohamed, S. A., Lenta, B. N., Ngouela, S. A., Tsamo, E., Hassanali, A., & Cox, R. J. (2021). Antifeedant and ovicidal activities of a new cassane and other compounds from Caesalpinia welwitschiana Oliv. and Caesalpinia bonducL. against Tuta absoluta (Lepidoptera: Gelechiidae). Natural product research, 35(24), 5681-5691. https://doi.org/10.1080/14786419.2020.1825424

2020


Schotte, C., Li, L., Wibberg, D., Kalinowski, J., & Cox, R. J. (2020). Synthetic Biology Driven Biosynthesis of Unnatural Tropolone Sesquiterpenoids. Angewandte Chemie - International Edition, 59(52), 23870-23878. https://doi.org/10.1002/anie.202009914, https://doi.org/10.1002/ange.202009914
de Mattos-Shipley, K. M. J., Spencer, C. E., Greco, C., Heard, D. M., O'Flynn, D. E., Dao, T. T., Song, Z., Mulholland, N. P., Vincent, J. L., Simpson, T. J., Cox, R. J., Bailey, A. M., & Willis, C. L. (2020). Uncovering biosynthetic relationships between antifungal nonadrides and octadrides. Chemical science, 11(42), 11570-11578. https://doi.org/10.1039/d0sc04309e
Wang, C., Lambert, C., Hauser, M., Deuschmann, A., Zeilinger, C., Rottner, K., Stradal, T. E. B., Stadler, M., Skellam, E. J., & Cox, R. J. (2020). Cover Feature: Diversely Functionalised Cytochalasins through Mutasynthesis and Semi‐Synthesis (Chem. Eur. J. 60/2020). Chemistry – A European Journal, 26(60), 13535-13535. https://doi.org/10.1002/chem.202003294
Wang, C., Lambert, C., Hauser, M., Deuschmann, A., Zeilinger, C., Rottner, K., Stradal, T. E. B., Stadler, M., Skellam, E. J., & Cox, R. J. (2020). Diversely Functionalised Cytochalasins through Mutasynthesis and Semi-Synthesis. Chemistry - A European Journal, 26(60), 13578-13583. https://doi.org/10.1002/chem.202002241
Feng, J., Surup, F., Hauser, M., Miller, A., Wennrich, J.-P., Stadler, M., Cox, R. J., & Kuhnert, E. (2020). Biosynthesis of oxygenated brasilane terpene glycosides involves a promiscuousN-acetylglucosamine transferase. Chemical communications, 56(82), 12419-12422. https://doi.org/10.1039/d0cc03950k
Tian, D.-S., Kuhnert, E., Ouazzani, J., Wibberg, D., Kalinowski, J., & Cox, R. J. (2020). The sporothriolides: A new biosynthetic family of fungal secondary metabolites. Chemical science, 11(46), 12477-12484. https://doi.org/10.1039/d0sc04886k
Kahlert, L., Cox, R. J., & Skellam, E. (2020). The same but different: multiple functions of the fungal flavin dependent monooxygenase SorD fromPenicillium chrysogenum. Chemical communications, 56(74), 10934-10937. https://doi.org/10.1039/d0cc03203d
Zulqarnain, Iqbal, Z., Cox, R., Anwar, J., Ahmad, N., Khan, K., Iqbal, M., Manzoor, N., & Khattak, S. U. (2020). Antifungal activity of compounds isolated from Aspergillus niger and their molecular docking studies with tomatinase. Natural product research, 34(18), 2642-2646. https://doi.org/10.1080/14786419.2018.1548447
Trenti, F., Lebe, K. E., Adelin, E., Ouazzani, J., Schotte, C., & Cox, R. J. (2020). Investigating the biosynthesis of Sch-642305 in the fungus Phomopsis sp. CMU-LMA. RSC Advances, 10(46), 27369-27376. https://doi.org/10.1039/d0ra05311b