Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Alhosna Benjdia"'
Autor:
Alhosna Benjdia, Olivier Berteau
Publikováno v:
Frontiers in Chemistry, Vol 9 (2021)
To face the current antibiotic resistance crisis, novel strategies are urgently required. Indeed, in the last 30 years, despite considerable efforts involving notably high-throughput screening and combinatorial libraries, only few antibiotics have be
Externí odkaz:
https://doaj.org/article/28bb5dba4fda42c3a669216be295042e
Publikováno v:
Frontiers in Microbiology, Vol 11 (2020)
The Gram-positive model organism and soil bacterium Bacillus subtilis naturally produces a variety of antimicrobial peptides (AMPs), including the ribosomally synthesized and post-translationally modified AMP YydF, which is encoded in the yydFGHIJ lo
Externí odkaz:
https://doaj.org/article/d5df81bf32fc468d8c3f3abb0ae43cce
Publikováno v:
Frontiers in Chemistry, Vol 5 (2017)
Ribosomally-synthesized and post-translationally modified peptides (RiPPs) are a large and diverse family of natural products. They possess interesting biological properties such as antibiotic or anticancer activities, making them attractive for ther
Externí odkaz:
https://doaj.org/article/7358b6ba73954a849901ffcfe48c86a5
Autor:
Feryel Soualmia, Alain Guillot, Nazarii Sabat, Clémence Brewee, Xavier Kubiak, Michael Haumann, Xavier Guinchard, Alhosna Benjdia, Olivier Berteau
Publikováno v:
Chemistry – A European Journal. 28
Autor:
Olivier Berteau, Lena Friebel, Thorsten Mascher, Alain Guillot, Philipp F. Popp, Alhosna Benjdia
Publikováno v:
Microbial Physiology. 31:306-318
The epeXEPAB (formerly yydFGHIJ) locus of Bacillus subtilis encodes a minimalistic biosynthetic pathway for a linear antimicrobial epipeptide, EpeX, which is ribosomally produced and post-translationally processed by the action of the radical-SAM epi
Autor:
Cameron D. Fyfe, Noelia Bernardo-García, Laura Fradale, Stéphane Grimaldi, Alain Guillot, Clémence Brewee, Leonard M. G. Chavas, Pierre Legrand, Alhosna Benjdia, Olivier Berteau
Publikováno v:
Nature
Nature, 2022, 602 (7896), pp.336-342. ⟨10.1038/s41586-021-04355-9⟩
Nature, 2022, 602 (7896), pp.336-342. ⟨10.1038/s41586-021-04355-9⟩
By catalysing the microbial formation of methane, methyl-coenzyme M reductase has a central role in the global levels of this greenhouse gas1,2. The activity of methyl-coenzyme M reductase is profoundly affected by several unique post-translational m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::467c06b7db558a47cca088e15883638a
https://hal.inrae.fr/hal-03808863/file/2022-Fyfe-Nature.pdf
https://hal.inrae.fr/hal-03808863/file/2022-Fyfe-Nature.pdf
Autor:
Cameron D, Fyfe, Noelia, Bernardo-García, Laura, Fradale, Stéphane, Grimaldi, Alain, Guillot, Clémence, Brewee, Leonard M G, Chavas, Pierre, Legrand, Alhosna, Benjdia, Olivier, Berteau
Publikováno v:
Nature. 602(7896)
By catalysing the microbial formation of methane, methyl-coenzyme M reductase has a central role in the global levels of this greenhouse gas
Autor:
Philipp F, Popp, Lena, Friebel, Alhosna, Benjdia, Alain, Guillot, Olivier, Berteau, Thorsten, Mascher
Publikováno v:
Microbial physiology. 31(3)
The epeXEPAB (formerly yydFGHIJ) locus of Bacillus subtilis encodes a minimalistic biosynthetic pathway for a linear antimicrobial epipeptide, EpeX, which is ribosomally produced and post-translationally processed by the action of the radical-SAM epi
Autor:
Nazarii Sabat, Xavier Guinchard, Olivier Berteau, Feryel Soualmia, Alhosna Benjdia, Pascal Retailleau
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2020, 22 (11), pp.4344-4349. ⟨10.1021/acs.orglett.0c01370⟩
Organic Letters, 2020, 22 (11), pp.4344-4349. ⟨10.1021/acs.orglett.0c01370⟩
Organic Letters, American Chemical Society, 2020, 22 (11), pp.4344-4349. ⟨10.1021/acs.orglett.0c01370⟩
Organic Letters, 2020, 22 (11), pp.4344-4349. ⟨10.1021/acs.orglett.0c01370⟩
N-Propargyl tryptamine and tryptophan derivatives that are readily available from both synthetic and biocatalytic approaches, undergo gold-catalyzed dearomative cyclizations in aqueous media to the corresponding spirocyclic derivatives. In addition t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a15b0661eea9047e0320857cfddb0ac7
https://hal.inrae.fr/hal-02933778
https://hal.inrae.fr/hal-02933778
Autor:
Nazarii Sabat, Xavier Guinchard, Olivier Berteau, Alhosna Benjdia, Feryel Soualmia, Pascal Retailleau
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2020, 22 (14), pp.5714. ⟨10.1021/acs.orglett.0c02206⟩
Organic Letters, American Chemical Society, 2020, 22 (14), pp.5714. ⟨10.1021/acs.orglett.0c02206⟩
International audience; Reactions were performed using oven-dried glassware under the argon atmosphere. All separations were carried out under flash-chromatographic conditions on silica gel (prepacked column, 230–400 mesh) at medium pressure (20 ps
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e8bfe2ae5ad4e6c212954d7fdce7e02
https://hal.inrae.fr/hal-02933787
https://hal.inrae.fr/hal-02933787