Kirschnings grupp

Naturprodukter, antiinfektiva medel, kemobiosyntes och livets uppkomst
Naturprodukter är fortfarande en viktig drivkraft bakom utvecklingen av nya antibiotika och antivirala medel. Som en del av flera tvärvetenskapliga nätverk är vi involverade i sökandet efter nya naturprodukter och den medicinsk-kemiska vidareutvecklingen av dem till läkemedel. En andra forskningslinje handlar om kemisk användning av terpencyklaser för att utveckla nya terpenoider. I detta sammanhang adresserar vi också frågor om kemisk evolution och livets uppkomst.
Gruppmedlemmar
Publikationer
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Ingår i Journal of the American Chemical Society, s. 525-536, 2026
- DOI för Chemoenzymatic Synthesis of Structurally Diverse Terpenoids from Farnesyl Pyrophosphates Modified at the Central Alkene Unit
- Ladda ner fulltext (pdf) av Chemoenzymatic Synthesis of Structurally Diverse Terpenoids from Farnesyl Pyrophosphates Modified at the Central Alkene Unit
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Time- and spatially resolved LNA delivery via thermally controlled SPION technology
Ingår i Molecular Therapy Nucleic Acids, 2026
- DOI för Time- and spatially resolved LNA delivery via thermally controlled SPION technology
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Nickel: Geochemistry, biochemistry and its role in chemical and biological evolutions
Ingår i Earth-Science Reviews, 2026
- DOI för Nickel: Geochemistry, biochemistry and its role in chemical and biological evolutions
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Ingår i Organic and biomolecular chemistry, s. 2893-2898, 2026
- DOI för Cyclisations and hydrolysis of geranyl and farnesyl halides in water facilitated by ultrasound-induced emulsification
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Gravity as a Physical Selector of Chemical Evolution and the Origin of Life
Ingår i Physics of Life Reviews, s. 166-195, 2026
- DOI för Gravity as a Physical Selector of Chemical Evolution and the Origin of Life
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Terpene synthases are highly substrate tolerant – among them BcBOT2 is a “jack of all trades”
Ingår i Natural Product Reports, s. 10-1039, 2026
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Ingår i Journal of the American Chemical Society, s. 5496-5507, 2026
- DOI för Introducing Small Rings into Farnesyl Pyrophosphates Paves the Way for the Enzymatic Generation of Unnatural Sesquiterpene Scaffolds
- Ladda ner fulltext (pdf) av Introducing Small Rings into Farnesyl Pyrophosphates Paves the Way for the Enzymatic Generation of Unnatural Sesquiterpene Scaffolds
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Structure and function of the geldanamycin amide synthase from Streptomyces hygroscopicus
Ingår i Nature Communications, 2025
- DOI för Structure and function of the geldanamycin amide synthase from Streptomyces hygroscopicus
- Ladda ner fulltext (pdf) av Structure and function of the geldanamycin amide synthase from Streptomyces hygroscopicus
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Ingår i ChemCatChem, 2025
- DOI för Expanding the "Terpenome": Applications of Unspecific Peroxygenases (UPOs) in Oxidations of Unnatural Terpenoids
- Ladda ner fulltext (pdf) av Expanding the "Terpenome": Applications of Unspecific Peroxygenases (UPOs) in Oxidations of Unnatural Terpenoids
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Expanding the "Terpenome": Diterpene Synthases Accept GGPP-Ether Substrates
Ingår i ACS Catalysis, s. 6796-6811, 2025
- DOI för Expanding the "Terpenome": Diterpene Synthases Accept GGPP-Ether Substrates
- Ladda ner fulltext (pdf) av Expanding the "Terpenome": Diterpene Synthases Accept GGPP-Ether Substrates
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Ingår i Reaction Chemistry & Engineering, s. 1048-1053, 2025
- DOI för The "factory in a lab": telescoping the Matteson and Matteson-Hoppe-Aggarwal boronate chemistry under flow conditions
- Ladda ner fulltext (pdf) av The "factory in a lab": telescoping the Matteson and Matteson-Hoppe-Aggarwal boronate chemistry under flow conditions
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Ingår i ACS Catalysis, s. 8125-8139, 2025
- DOI för Reprogramming the Cyclization of the Sesquiterpene Synthase BcBOT2 Using 2,3-Z-Configured FPP Derivatives and by Means of "Methyl Mapping"
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Ingår i Journal of Natural Products, s. 1653-1662, 2025
- DOI för Chemoenzymatic Generation of Thio-analogues of ÎŽ-Cadinene, ÎŽ-Cadinol, and a Thio-diquinane Using 8-Thio-farnesylpyrophosphate
- Ladda ner fulltext (pdf) av Chemoenzymatic Generation of Thio-analogues of ÎŽ-Cadinene, ÎŽ-Cadinol, and a Thio-diquinane Using 8-Thio-farnesylpyrophosphate
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Ingår i Chemistry - A European Journal, 2025
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Ingår i Organic Letters, s. 5888-5892, 2024
- DOI för Telescoping a Prenyltransferase and a Diterpene Synthase to Transform Unnatural FPP Derivatives to Diterpenoids
- Ladda ner fulltext (pdf) av Telescoping a Prenyltransferase and a Diterpene Synthase to Transform Unnatural FPP Derivatives to Diterpenoids
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Ingår i Communications Chemistry, 2024
- DOI för Synthetic studies on the tetrasubstituted D-ring of cystobactamids lead to potent terephthalic acid antibiotics
- Ladda ner fulltext (pdf) av Synthetic studies on the tetrasubstituted D-ring of cystobactamids lead to potent terephthalic acid antibiotics
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Ingår i Journal of Medicinal Chemistry, s. 17162-17190, 2024
- DOI för Optimization of the Central α-Amino Acid in Cystobactamids to the Broad-Spectrum, Resistance-Breaking Antibiotic CN-CC-861
- Ladda ner fulltext (pdf) av Optimization of the Central α-Amino Acid in Cystobactamids to the Broad-Spectrum, Resistance-Breaking Antibiotic CN-CC-861
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Ingår i Biochemistry, s. 498-508, 2024
- DOI för Chemoenzymatic Formation of Oxa-Terpenoids by Sesqui- and Diterpene Synthase-Mediated Biotransformations with 9-Oxy-FPP Ether Derivatives
- Ladda ner fulltext (pdf) av Chemoenzymatic Formation of Oxa-Terpenoids by Sesqui- and Diterpene Synthase-Mediated Biotransformations with 9-Oxy-FPP Ether Derivatives
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Ingår i Journal of the American Chemical Society, s. 17838-17846, 2024
- DOI för Sesquiterpene Cyclase BcBOT2 Promotes the Unprecedented Wagner-Meerwein Rearrangement of the Methoxy Group
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Ingår i RSC Chemical Biology, s. 508-517, 2024
- DOI för Why pyridoxal phosphate could be a functional predecessor of thiamine pyrophosphate and speculations on a primordial metabolism
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Ingår i npj Antimicrobials and Resistance, 2024
- DOI för YgiV promoter mutations cause resistance to cystobactamids and reduced virulence factor expression in Escherichia coli
- Ladda ner fulltext (pdf) av YgiV promoter mutations cause resistance to cystobactamids and reduced virulence factor expression in Escherichia coli