Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Laurence Hecquet"'
Cleavage of Aliphatic α-Hydroxy Ketones by Evolved Transketolase from Geobacillus stearothermophilus
Autor:
Hubert Casajus, Aurélie Lagarde, Lionel Nauton, Nazim Ocal, Martin Leremboure, Wolf-Dieter Fessner, Nicolas Duguet, Franck Charmantray, Laurence Hecquet
Publikováno v:
ACS Catalysis
ACS Catalysis, 2022, 12, pp.3566-3576. ⟨10.1021/acscatal.1c05140⟩
ACS Catalysis, 2022, 12, pp.3566-3576. ⟨10.1021/acscatal.1c05140⟩
International audience; The reaction catalyzed by ubiquitous thiamine pyrophosphate-dependent transketolase engaged in cells in the pentose phosphate pathway can be applied in vitro to the cleavage of aliphatic α-hydroxy ketones with thermostable tr
Autor:
Daria Świętochowska, Aleksandra Łochowicz, Nazim Ocal, Loredano Pollegioni, Franck Charmantray, Laurence Hecquet, Katarzyna Szymańska
Publikováno v:
Catalysts
Catalysts, 2023, 13 (1), pp.95. ⟨10.3390/catal13010095⟩
Catalysts; Volume 13; Issue 1; Pages: 95
Catalysts, 2023, 13 (1), pp.95. ⟨10.3390/catal13010095⟩
Catalysts; Volume 13; Issue 1; Pages: 95
International audience; Here, we present an immobilized enzyme cascade in a basket-type reactor allowing a one-pot, two-step enzymatic synthesis of L-erythrulose from D-serine and glycolaldehyde. Three enzymes, D-amino acid oxidase from Rhodotorula g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e2894d2429a6959839b628ca1cf711c
https://hal.science/hal-03922760
https://hal.science/hal-03922760
Publikováno v:
Advanced Synthesis and Catalysis
Advanced Synthesis and Catalysis, 2022, 364 (3), pp.612-621. ⟨10.1002/adsc.202101100⟩
Advanced Synthesis and Catalysis, 2022, 364 (3), pp.612-621. ⟨10.1002/adsc.202101100⟩
International audience; Hydroxamic acids are metal-chelating compounds that show important biological activity including anti-tumor effects. We have recently engineered the transketolase from Geobacillus stearothermopilus (TKgst) to convert benzaldeh
Autor:
Nazim Ocal, Giuseppe Arbia, Aurélie Lagarde, Muriel Joly, Samantha Gittings, Kirsty M. Graham, Franck Charmantray, Laurence Hecquet
Publikováno v:
Advanced Synthesis and Catalysis
Advanced Synthesis and Catalysis, 2022, ⟨10.1002/adsc.202201190⟩
Advanced Synthesis and Catalysis, 2022, ⟨10.1002/adsc.202201190⟩
International audience; We described a strategy for the enzymatic synthesis of 1-deoxy and 1,2-deoxyketoses from the aliphatic α-ketoacids, pyruvate and 2-oxobutyrate, as donors and natural aldoses of variable chain length as acceptors, catalyzed by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de317af02878265368c30ea339ff185a
https://hal.science/hal-03918083/document
https://hal.science/hal-03918083/document
Publikováno v:
Journal of Chemical Information and Modeling
Journal of Chemical Information and Modeling, American Chemical Society, 2021, ⟨10.1021/acs.jcim.1c00190⟩
Journal of Chemical Information and Modeling, 2021, ⟨10.1021/acs.jcim.1c00190⟩
Journal of Chemical Information and Modeling, American Chemical Society, 2021, ⟨10.1021/acs.jcim.1c00190⟩
Journal of Chemical Information and Modeling, 2021, ⟨10.1021/acs.jcim.1c00190⟩
International audience; A computational model for human transketolase was proposed, showing that thiamine diphosphate activation was based on His110 in place of His481 reported in yeast transketolase. In addition, a complete catalytic reaction pathwa
Autor:
Mélanie L’enfant, Romain Dumoulin, Wolf-Dieter Fessner, Franck Charmantray, Agnès Rambourdin, Lionel Nauton, Laurence Hecquet, Marion Lorillière, Vincent Théry
Publikováno v:
ACS Catalysis
ACS Catalysis, American Chemical Society, 2019, 9 (6), pp.4754-4763. ⟨10.1021/acscatal.9b01339⟩
ACS Catalysis, 2019, 9 (6), pp.4754-4763. ⟨10.1021/acscatal.9b01339⟩
ACS Catalysis, American Chemical Society, 2019, 9 (6), pp.4754-4763. ⟨10.1021/acscatal.9b01339⟩
ACS Catalysis, 2019, 9 (6), pp.4754-4763. ⟨10.1021/acscatal.9b01339⟩
International audience; We propose an ecofriendly, efficient, stereoselective procedure for the two-carbon elongation of nonphosphorylated aldoses (C4–C6) to the corresponding Cn+2 ketoses (C6–C8) in one step, using hydroxypyruvate (HPA) as a ket
Publikováno v:
ChemBioChem
ChemBioChem, Wiley-VCH Verlag, In press, ⟨10.1002/cbic.202100356⟩
ChemBioChem, In press, ⟨10.1002/cbic.202100356⟩
ChemBioChem, Wiley-VCH Verlag, In press, ⟨10.1002/cbic.202100356⟩
ChemBioChem, In press, ⟨10.1002/cbic.202100356⟩
International audience; Thiamine diphosphate-dependent enzymes, and specifically transketolases, form one of the most important families of biocatalytic tools for enantioselective carbon-carbon bond formation yielding various hydroxyketones of biolog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8d6ad3900d61a8def8fca0beebfdd63
https://hal.archives-ouvertes.fr/hal-03329188
https://hal.archives-ouvertes.fr/hal-03329188
Autor:
Franck Charmantray, Nazim Ocal, Laurence Hecquet, Loredano Pollegioni, Jérôme Collin, Pascal Auffray, Juliette Martin, Mélanie L’enfant
Publikováno v:
Organic Process Research and Development
Organic Process Research and Development, American Chemical Society, 2020, 24 (5), pp.769-775. ⟨10.1021/acs.oprd.0c00024⟩
Organic Process Research and Development, 2020, 24 (5), pp.769-775. ⟨10.1021/acs.oprd.0c00024⟩
Organic Process Research and Development, American Chemical Society, 2020, 24 (5), pp.769-775. ⟨10.1021/acs.oprd.0c00024⟩
Organic Process Research and Development, 2020, 24 (5), pp.769-775. ⟨10.1021/acs.oprd.0c00024⟩
International audience; An efficient enzymatic method catalyzed by an enzyme from the d-threonine aldolase (DTA) family was developed for d-serine production at industrial scale. This process was used for the synthesis of two valuable ketoses, l-eryt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1a007f821f0e46cb08c437756212e8a
https://hal.archives-ouvertes.fr/hal-02907525
https://hal.archives-ouvertes.fr/hal-02907525
Autor:
Marion Lorillière, Laurence Hecquet, Wolf-Dieter Fessner, Pere Clapés, Christine Guérard-Hélaine, Franck Charmantray, Thierry Gefflaut
Publikováno v:
ChemCatChem
ChemCatChem, Wiley, 2020, 12 (3), pp.812-817. ⟨10.1002/cctc.201901756⟩
ChemCatChem, 2020, 12 (3), pp.812-817. ⟨10.1002/cctc.201901756⟩
Digital.CSIC. Repositorio Institucional del CSIC
instname
ChemCatChem, Wiley, 2020, 12 (3), pp.812-817. ⟨10.1002/cctc.201901756⟩
ChemCatChem, 2020, 12 (3), pp.812-817. ⟨10.1002/cctc.201901756⟩
Digital.CSIC. Repositorio Institucional del CSIC
instname
International audience; We describe an efficient three‐enzyme, sequential one‐pot cascade reaction where both transketolase substrates are generated in situ in a convergent fashion. The nucleophilic donor substrate hydroxypyruvate was obtained fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::937909a3b48328dbabf3143197c8921e
https://hal.archives-ouvertes.fr/hal-02991624
https://hal.archives-ouvertes.fr/hal-02991624
Autor:
Hubert Casajus, Martin Leremboure, Wolf-Dieter Fessner, Nicolas Duguet, Aurélie Lagarde, Vincent Théry, Laurence Hecquet, Lionel Nauton, Franck Charmantray, Thomas De Dios Miguel
Publikováno v:
ChemCatChem
ChemCatChem, Wiley, 2020, ⟨10.1002/cctc.202001160⟩
ChemCatChem, Wiley, 2020, ⟨10.1002/cctc.202001160⟩
International audience; The thermostable transketolase from Geobacillus stearothermophilus (TKgst) was successfully engineered for the synthesis of aliphatic acyloins with varying carbon backbone lengths (C5−C10) based on protein structure‐guided
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bec689b8cffbb4a37fc0b6f14430fce
https://hal.archives-ouvertes.fr/hal-02989932
https://hal.archives-ouvertes.fr/hal-02989932