Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Thomas Tørring"'
Autor:
Malene Wollesen, Kasper Mikkelsen, Marie Selch Tvilum, Martin Vestergaard, Mikala Wang, Rikke L. Meyer, Hanne Ingmer, Thomas B. Poulsen, Thomas Tørring
Publikováno v:
Microbiology Spectrum, Vol 11, Iss 4 (2023)
ABSTRACT Polyether ionophores are complex natural products known to transport various cations across biological membranes. While several members of this family are used in agriculture (e.g., as anti-coccidiostats) and have potent antibacterial activi
Externí odkaz:
https://doaj.org/article/bcbdb837da96405c82180f4578ebe063
Autor:
Morten Busk, Peter P Eggertsen, Jens Overgaard, Michael R Horsman, Thomas Tørring, Kristian M Jacobsen, Thomas B Poulsen
Hypoxia-activated pro-drugs like TH-302 have failed clinically, possible due to variable activity of drug-activating reductases. Here we compared TH-302 and the natural product BE-43547, that targets hypoxic cells independently of reductases. Tumor c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65a49c47bc6cd225d3638ec610a4ca20
https://doi.org/10.21203/rs.3.rs-2755525/v1
https://doi.org/10.21203/rs.3.rs-2755525/v1
Autor:
Camilla Kjeldgaard Larsen, Peter Lindquist, Mette Rosenkilde, Alice Ravn Madsen, Kim Haselmann, Tine Glendorf, Kjeld Olesen, Anne Louise Bank Kodal, Thomas Tørring
Selective modification of peptides is often exploited to improve pharmaceutically relevant properties of bioactive peptides like stability, circulation time, and potency. In Nature, natural products belonging to the class of ribosomally synthesized a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff5875e643365b69c45874bfbefbef2f
https://doi.org/10.1101/2023.03.20.532734
https://doi.org/10.1101/2023.03.20.532734
Autor:
Esben B. Svenningsen, Rasmus N. Ottosen, Katrine H. Jørgensen, Marija Nisavic, Camilla K. Larsen, Bente K. Hansen, Yong Wang, Kresten Lindorff-Larsen, Thomas Tørring, Stephan M. Hacker, Johan Palmfeldt, Thomas B. Poulsen
Publikováno v:
Svenningsen, E B, Ottosen, R N, Jørgensen, K H, Nisavic, M, Larsen, C K, Hansen, B K, Wang, Y, Lindorff-Larsen, K, Tørring, T, Hacker, S M, Palmfeldt, J & Poulsen, T B 2022, ' The covalent reactivity of functionalized 5-hydroxy-butyrolactams is the basis for targeting of fatty acid binding protein 5 (FABP5) by the neurotrophic agent MT-21 ', RSC Chemical Biology, vol. 3, no. 10, pp. 1216-1229 . https://doi.org/10.1039/d2cb00161f
RSC Chemical Biology, 3(10), 1216-1229. ROYAL SOC CHEMISTRY
RSC Chemical Biology, 3(10), 1216-1229. ROYAL SOC CHEMISTRY
Covalently acting compounds experience a strong interest within chemical biology both as molecular probes in studies of fundamental biological mechanisms and/or as novel drug candidates. In this context, the identification of new classes of reactive
Autor:
Barbara R Terlouw, Kai Blin, Jorge C Navarro-Muñoz, Nicole E Avalon, Marc G Chevrette, Susan Egbert, Sanghoon Lee, David Meijer, Michael J J Recchia, Zachary L Reitz, Jeffrey A van Santen, Nelly Selem-Mojica, Thomas Tørring, Liana Zaroubi, Mohammad Alanjary, Gajender Aleti, César Aguilar, Suhad A A Al-Salihi, Hannah E Augustijn, J Abraham Avelar-Rivas, Luis A Avitia-Domínguez, Francisco Barona-Gómez, Jordan Bernaldo-Agüero, Vincent A Bielinski, Friederike Biermann, Thomas J Booth, Victor J Carrion Bravo, Raquel Castelo-Branco, Fernanda O Chagas, Pablo Cruz-Morales, Chao Du, Katherine R Duncan, Athina Gavriilidou, Damien Gayrard, Karina Gutiérrez-García, Kristina Haslinger, Eric J N Helfrich, Justin J J van der Hooft, Afif P Jati, Edward Kalkreuter, Nikolaos Kalyvas, Kyo Bin Kang, Satria Kautsar, Wonyong Kim, Aditya M Kunjapur, Yong-Xin Li, Geng-Min Lin, Catarina Loureiro, Joris J R Louwen, Nico L L Louwen, George Lund, Jonathan Parra, Benjamin Philmus, Bita Pourmohsenin, Lotte J U Pronk, Adriana Rego, Devasahayam Arokia Balaya Rex, Serina Robinson, L Rodrigo Rosas-Becerra, Eve T Roxborough, Michelle A Schorn, Darren J Scobie, Kumar Saurabh Singh, Nika Sokolova, Xiaoyu Tang, Daniel Udwary, Aruna Vigneshwari, Kristiina Vind, Sophie P J M Vromans, Valentin Waschulin, Sam E Williams, Jaclyn M Winter, Thomas E Witte, Huali Xie, Dong Yang, Jingwei Yu, Mitja Zdouc, Zheng Zhong, Jérôme Collemare, Roger G Linington, Tilmann Weber, Marnix H Medema
Publikováno v:
Nucleic Acids Research, 51(D1), D603-D610. Oxford University Press
Terlouw, B R, Blin, K, Navarro-Muñoz, J C, Avalon, N E, Chevrette, M G, Egbert, S, Lee, S, Meijer, D, Recchia, M J J, Reitz, ZL, van Santen, JA, Selem-Mojica, N, Tørring, T, Zaroubi, L, Alanjary, M, Aleti, G, Aguilar, C, Al-Salihi, S A A, Augustijn, HE, Avelar-Rivas, JA, Avitia-Domínguez, LA, Barona-Gómez, F, Bernaldo-Agüero, J, Bielinski, V A, Biermann, F, Booth, TJ, Carrion Bravo, VJ, Castelo-Branco, R, Chagas, FO, Cruz-Morales, P, Du, C, Duncan, KR, Gavriilidou, A, Gayrard, D, Gutiérrez-García, K, Haslinger, K, Helfrich, E J N, van der Hooft, J J J, Jati, AP, Kalkreuter, E, Kalyvas, N, Kang, KB, Kautsar, S, Kim, W, Kunjapur, AM, Li, Y-X, Lin, G-M, Loureiro, C, Louwen, J J R, Louwen, N L L, Lund, G, Parra, J, Philmus, B, Pourmohsenin, B, Pronk, L J U, Rego, A, Rex, DAB, Robinson, S, Rosas-Becerra, LR, Roxborough, ET, Schorn, MA, Scobie, DJ, Singh, KS, Sokolova, N, Tang, X, Udwary, D, Vigneshwari, A, Vind, K, Vromans, S P J M, Waschulin, V, Williams, SE, Winter, JM, Witte, TE, Xie, H, Yang, D, Yu, J, Zdouc, M, Zhong, Z, Collemare, J, Linington, RG, Weber, T & Medema, MH 2023, ' MIBiG 3.0: a community-driven effort to annotate experimentally validated biosynthetic gene clusters ', Nucleic Acids Research, vol. 51, no. D1, gkac1049, pp. D603-D610 . https://doi.org/10.1093/nar/gkac1049
Terlouw, B R, Blin, K, Navarro-Muñoz, J C, Avalon, N E, Chevrette, M G, Egbert, S, Lee, S, Meijer, D, Recchia, M J J, Reitz, Z L, van Santen, J A, Selem-Mojica, N, Tørring, T, Zaroubi, L, Alanjary, M, Aleti, G, Aguilar, C, Al-Salihi, S A A, Augustijn, H E, Avelar-Rivas, J A, Avitia-Domínguez, L A, Barona-Gómez, F, Bernaldo-Agüero, J, Bielinski, V A, Biermann, F, Booth, T J, Carrion Bravo, V J, Castelo-Branco, R, Chagas, F O, Cruz-Morales, P, Du, C, Duncan, K R, Gavriilidou, A, Gayrard, D, Gutiérrez-García, K, Haslinger, K, Helfrich, E J N, van der Hooft, J J J, Jati, A P, Kalkreuter, E, Kalyvas, N, Kang, K B, Kautsar, S, Kim, W, Kunjapur, A M, Li, Y-X, Lin, G-M, Loureiro, C, Louwen, J J R, Louwen, N L L, Lund, G, Parra, J, Philmus, B, Pourmohsenin, B, Pronk, L J U, Rego, A, Rex, D A B, Robinson, S, Rosas-Becerra, L R, Roxborough, E T, Schorn, M A, Scobie, D J, Singh, K S, Sokolova, N, Tang, X, Udwary, D, Vigneshwari, A, Vind, K, Vromans, S P J M, Waschulin, V, Williams, S E, Winter, J M, Witte, T E, Xie, H, Yang, D, Yu, J, Zdouc, M, Zhong, Z, Collemare, J, Linington, R G, Weber, T & Medema, M H 2023, ' MIBiG 3.0: a community-driven effort to annotate experimentally validated biosynthetic gene clusters ', Nucleic Acids Research, vol. 51, no. D1, pp. D603–D610 . https://doi.org/10.1093/nar/gkac1049
Terlouw, B R, Blin, K, Navarro-Muñoz, J C, Avalon, N E, Chevrette, M G, Egbert, S, Lee, S, Meijer, D, Recchia, M J J, Reitz, Z L, van Santen, J A, Selem-Mojica, N, Tørring, T, Zaroubi, L, Alanjary, M, Aleti, G, Aguilar, C, Al-Salihi, S A A, Augustijn, H E, Avelar-Rivas, J A, Avitia-Domínguez, L A, Barona-Gómez, F, Bernaldo-Agüero, J, Bielinski, V A, Biermann, F, Booth, T J, Carrion Bravo, V J, Castelo-Branco, R, Chagas, F O, Cruz-Morales, P, Du, C, Duncan, K R, Gavriilidou, A, Gayrard, D, Gutiérrez-García, K, Haslinger, K, Helfrich, E J N, van der Hooft, J J J, Jati, A P, Kalkreuter, E, Kalyvas, N, Kang, K B, Kautsar, S, Kim, W, Kunjapur, A M, Li, Y-X, Lin, G-M, Loureiro, C, Louwen, J J R, Louwen, N L L, Lund, G, Parra, J, Philmus, B, Pourmohsenin, B, Pronk, L J U, Rego, A, Rex, D A B, Robinson, S, Rosas-Becerra, L R, Roxborough, E T, Schorn, M A, Scobie, D J, Singh, K S, Sokolova, N, Tang, X, Udwary, D, Vigneshwari, A, Vind, K, Vromans, S P J M, Waschulin, V, Williams, S E, Winter, J M, Witte, T E, Xie, H, Yang, D, Yu, J, Zdouc, M, Zhong, Z, Collemare, J, Linington, R G, Weber, T & Medema, M H 2023, ' MIBiG 3.0 : a community-driven effort to annotate experimentally validated biosynthetic gene clusters ', Nucleic Acids Research, vol. 51, no. D1, pp. D603–D610 . https://doi.org/10.1093/nar/gkac1049
Nucleic acids research, 51(D1), D603-D610
Nucleic acids research 51 (2023) D1
Terlouw, B R, Blin, K, Navarro-Muñoz, J C, Avalon, N E, Chevrette, M G, Egbert, S, Lee, S, Meijer, D, Recchia, M J J, Reitz, ZL, van Santen, JA, Selem-Mojica, N, Tørring, T, Zaroubi, L, Alanjary, M, Aleti, G, Aguilar, C, Al-Salihi, S A A, Augustijn, HE, Avelar-Rivas, JA, Avitia-Domínguez, LA, Barona-Gómez, F, Bernaldo-Agüero, J, Bielinski, V A, Biermann, F, Booth, TJ, Carrion Bravo, VJ, Castelo-Branco, R, Chagas, FO, Cruz-Morales, P, Du, C, Duncan, KR, Gavriilidou, A, Gayrard, D, Gutiérrez-García, K, Haslinger, K, Helfrich, E J N, van der Hooft, J J J, Jati, AP, Kalkreuter, E, Kalyvas, N, Kang, KB, Kautsar, S, Kim, W, Kunjapur, AM, Li, Y-X, Lin, G-M, Loureiro, C, Louwen, J J R, Louwen, N L L, Lund, G, Parra, J, Philmus, B, Pourmohsenin, B, Pronk, L J U, Rego, A, Rex, DAB, Robinson, S, Rosas-Becerra, LR, Roxborough, ET, Schorn, MA, Scobie, DJ, Singh, KS, Sokolova, N, Tang, X, Udwary, D, Vigneshwari, A, Vind, K, Vromans, S P J M, Waschulin, V, Williams, SE, Winter, JM, Witte, TE, Xie, H, Yang, D, Yu, J, Zdouc, M, Zhong, Z, Collemare, J, Linington, RG, Weber, T & Medema, MH 2023, ' MIBiG 3.0: a community-driven effort to annotate experimentally validated biosynthetic gene clusters ', Nucleic Acids Research, vol. 51, no. D1, gkac1049, pp. D603-D610 . https://doi.org/10.1093/nar/gkac1049
Terlouw, B R, Blin, K, Navarro-Muñoz, J C, Avalon, N E, Chevrette, M G, Egbert, S, Lee, S, Meijer, D, Recchia, M J J, Reitz, Z L, van Santen, J A, Selem-Mojica, N, Tørring, T, Zaroubi, L, Alanjary, M, Aleti, G, Aguilar, C, Al-Salihi, S A A, Augustijn, H E, Avelar-Rivas, J A, Avitia-Domínguez, L A, Barona-Gómez, F, Bernaldo-Agüero, J, Bielinski, V A, Biermann, F, Booth, T J, Carrion Bravo, V J, Castelo-Branco, R, Chagas, F O, Cruz-Morales, P, Du, C, Duncan, K R, Gavriilidou, A, Gayrard, D, Gutiérrez-García, K, Haslinger, K, Helfrich, E J N, van der Hooft, J J J, Jati, A P, Kalkreuter, E, Kalyvas, N, Kang, K B, Kautsar, S, Kim, W, Kunjapur, A M, Li, Y-X, Lin, G-M, Loureiro, C, Louwen, J J R, Louwen, N L L, Lund, G, Parra, J, Philmus, B, Pourmohsenin, B, Pronk, L J U, Rego, A, Rex, D A B, Robinson, S, Rosas-Becerra, L R, Roxborough, E T, Schorn, M A, Scobie, D J, Singh, K S, Sokolova, N, Tang, X, Udwary, D, Vigneshwari, A, Vind, K, Vromans, S P J M, Waschulin, V, Williams, S E, Winter, J M, Witte, T E, Xie, H, Yang, D, Yu, J, Zdouc, M, Zhong, Z, Collemare, J, Linington, R G, Weber, T & Medema, M H 2023, ' MIBiG 3.0: a community-driven effort to annotate experimentally validated biosynthetic gene clusters ', Nucleic Acids Research, vol. 51, no. D1, pp. D603–D610 . https://doi.org/10.1093/nar/gkac1049
Terlouw, B R, Blin, K, Navarro-Muñoz, J C, Avalon, N E, Chevrette, M G, Egbert, S, Lee, S, Meijer, D, Recchia, M J J, Reitz, Z L, van Santen, J A, Selem-Mojica, N, Tørring, T, Zaroubi, L, Alanjary, M, Aleti, G, Aguilar, C, Al-Salihi, S A A, Augustijn, H E, Avelar-Rivas, J A, Avitia-Domínguez, L A, Barona-Gómez, F, Bernaldo-Agüero, J, Bielinski, V A, Biermann, F, Booth, T J, Carrion Bravo, V J, Castelo-Branco, R, Chagas, F O, Cruz-Morales, P, Du, C, Duncan, K R, Gavriilidou, A, Gayrard, D, Gutiérrez-García, K, Haslinger, K, Helfrich, E J N, van der Hooft, J J J, Jati, A P, Kalkreuter, E, Kalyvas, N, Kang, K B, Kautsar, S, Kim, W, Kunjapur, A M, Li, Y-X, Lin, G-M, Loureiro, C, Louwen, J J R, Louwen, N L L, Lund, G, Parra, J, Philmus, B, Pourmohsenin, B, Pronk, L J U, Rego, A, Rex, D A B, Robinson, S, Rosas-Becerra, L R, Roxborough, E T, Schorn, M A, Scobie, D J, Singh, K S, Sokolova, N, Tang, X, Udwary, D, Vigneshwari, A, Vind, K, Vromans, S P J M, Waschulin, V, Williams, S E, Winter, J M, Witte, T E, Xie, H, Yang, D, Yu, J, Zdouc, M, Zhong, Z, Collemare, J, Linington, R G, Weber, T & Medema, M H 2023, ' MIBiG 3.0 : a community-driven effort to annotate experimentally validated biosynthetic gene clusters ', Nucleic Acids Research, vol. 51, no. D1, pp. D603–D610 . https://doi.org/10.1093/nar/gkac1049
Nucleic acids research, 51(D1), D603-D610
Nucleic acids research 51 (2023) D1
With an ever-increasing amount of (meta)genomic data being deposited in sequence databases, (meta)genome mining for natural product biosynthetic pathways occupies a critical role in the discovery of novel pharmaceutical drugs, crop protection agents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e557bd5c3d2ddd7d6574fc9d08027c2
https://pure.knaw.nl/portal/en/publications/4e99309a-6840-4150-801f-070cfa20d40c
https://pure.knaw.nl/portal/en/publications/4e99309a-6840-4150-801f-070cfa20d40c
Autor:
Esben Svenningsen, Rasmus Ottosen, Katrine Jørgensen, Marija Nisavic, Camilla Larsen, Bente Hansen, Yong Wang, Kresten Lindorff-Larsen, Thomas Tørring, Stephan Hacker, Johan Palmfeldt, Thomas Poulsen
Covalently acting compounds experience a strong interest within chemical biology both as molecular probes in studies of fundamental biological mechanisms and/or as novel drug candidates. In this context, the identification of new classes of reactive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c57c62c18dec174fb011f99e98b4614
https://doi.org/10.26434/chemrxiv-2022-knt5m
https://doi.org/10.26434/chemrxiv-2022-knt5m
Autor:
Thomas Tørring, Jaime Moyano-Villameriel, Malene Wollesen, Thomas B. Poulsen, Christine N. Pedersen, Frederikke D. Andersen, Han Liu, Kristian M. Jacobsen, Peter Nørby, Shaoquan Lin, Esben B. Svenningsen
Publikováno v:
Nature Chemistry
Nature chemistry
Lin, S, Liu, H, Svenningsen, E B, Wollesen, M, Jacobsen, K M, Andersen, F D, Moyano-Villameriel, J, Pedersen, C N, Nørby, P, Tørring, T & Poulsen, T B 2021, ' Expanding the antibacterial selectivity of polyether ionophore antibiotics through diversity-focused semisynthesis ', Nature Chemistry, vol. 13, no. 1, pp. 47-55 . https://doi.org/10.1038/s41557-020-00601-1
Nature chemistry
Lin, S, Liu, H, Svenningsen, E B, Wollesen, M, Jacobsen, K M, Andersen, F D, Moyano-Villameriel, J, Pedersen, C N, Nørby, P, Tørring, T & Poulsen, T B 2021, ' Expanding the antibacterial selectivity of polyether ionophore antibiotics through diversity-focused semisynthesis ', Nature Chemistry, vol. 13, no. 1, pp. 47-55 . https://doi.org/10.1038/s41557-020-00601-1
Polyether ionophores are complex natural products capable of transporting cations across biological membranes. Many polyether ionophores possess potent antimicrobial activity and a few selected compounds have the ability to target aggressive cancer c
Autor:
Thomas Tørring, Ditte Hededam Welner, Cristina Fortuna, Selin Kara, Gonzalo N. Bidart, Kathrine M. Hübschmann, David Teze, Philipp Petermeier
Publikováno v:
Petermeier, P, Fortuna, C, M. Hübschmann, K, Nahuel Bidart Costoya, G, Tørring, T, Teze, D, Welner, D H & Kara, S 2021, ' Exploring the in Vitro Operating Window of Glycosyltransferase PtUGT1 from Polygonum tinctorium for a Biocatalytic Route to Indigo Dye ', ACS Sustainable Chemistry & Engineering, vol. 9, no. 25, pp. 8497-8506 . https://doi.org/10.1021/acssuschemeng.1c01536
ACS Sustainable Chemistry & Engineering
Petermeier, P, Fortuna, C, Hübschmann, K M, Bidart, G N, Tørring, T, Teze, D, Welner, D H & Kara, S 2021, ' Exploring the in Vitro Operating Window of Glycosyltransferase PtUGT1 from Polygonum tinctorium for a Biocatalytic Route to Indigo Dye ', ACS Sustainable Chemistry and Engineering, vol. 9, no. 25, pp. 8497-8506 . https://doi.org/10.1021/acssuschemeng.1c01536
ACS Sustainable Chemistry & Engineering
Petermeier, P, Fortuna, C, Hübschmann, K M, Bidart, G N, Tørring, T, Teze, D, Welner, D H & Kara, S 2021, ' Exploring the in Vitro Operating Window of Glycosyltransferase PtUGT1 from Polygonum tinctorium for a Biocatalytic Route to Indigo Dye ', ACS Sustainable Chemistry and Engineering, vol. 9, no. 25, pp. 8497-8506 . https://doi.org/10.1021/acssuschemeng.1c01536
The eobiotic compound indican lends itself to a compelling biocatalytic dyeing strategy for denim, in which the formation of corrosive by-products is avoided. However, the efficient and scalable production of indican remains a key bottleneck. This wo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::824003fe8f17726a75797b7ba2a3ee39
https://doi.org/10.26434/chemrxiv.14171342
https://doi.org/10.26434/chemrxiv.14171342
Autor:
Kasper R. Andersen, Thomas Tørring, Veronica Liv Andersen, Mikkel B. Skovsgaard, Thorbjørn B. Nielsen, Nick S. Laursen, Johan Palmfeldt, Kurt V. Gothelf, Michael Rosholm Mortensen, Anders Märcher, Jørgen Kjems
Publikováno v:
Mortensen, M R, Skovsgaard, M B, Märcher, A, Andersen, V L, Palmfeldt, J, Nielsen, T B, Tørring, T, Laursen, N S, Andersen, K R, Kjems, J & Gothelf, K V 2020, ' Introduction of an Aldehyde Handle on Nanobodies by Affinity-Guided Labeling ', Bioconjugate Chemistry, vol. 31, no. 5, pp. 1295-1300 . https://doi.org/10.1021/acs.bioconjchem.0c00151
Chemically modified antigen-binding proteins are widely applied for their targeting abilities in the fields of biotechnology, medicine, and diagnostics. However, the production of site-selectively modified proteins remains a challenge. Here, we have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::626942fa10869db6f873003ab26174bc
https://pure.au.dk/portal/da/publications/introduction-of-an-aldehyde-handle-on-nanobodies-by-affinityguided-labeling(9a75013f-632d-45ff-b3f3-cf6128afef82).html
https://pure.au.dk/portal/da/publications/introduction-of-an-aldehyde-handle-on-nanobodies-by-affinityguided-labeling(9a75013f-632d-45ff-b3f3-cf6128afef82).html
Publikováno v:
Hjerrild, P, Tørring, T & Poulsen, T B 2020, ' Dehydration reactions in polyfunctional natural products ', Natural Product Reports, vol. 37, no. 8, pp. 1043-1064 . https://doi.org/10.1039/d0np00009d
Covering: up to 2020In this review, we present state of the art methods for performing dehydration reactions in alcohol substrates to deliver alkene products. The dehydration of alcohols typically proceeds through activation of the alcoholic moiety t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1dfff55cf855edbad19ebd41007b3da
https://pure.au.dk/portal/da/publications/dehydration-reactions-in-polyfunctional-natural-products(c76b9bc6-1023-4381-aa64-de09480290ba).html
https://pure.au.dk/portal/da/publications/dehydration-reactions-in-polyfunctional-natural-products(c76b9bc6-1023-4381-aa64-de09480290ba).html