Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Tamimount, Mohammadi"'
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-8 (2020)
Abstract Lipid II precursor and its processing by a flippase and peptidoglycan polymerases are considered key hot spot targets for antibiotics. We have developed a fluorescent anisotropy (FA) assay using a unique and versatile probe (fluorescent lipi
Externí odkaz:
https://doaj.org/article/01e5e5b8ff56424899107e86065805e5
Autor:
Yao Liu, Elisabete C C M Moura, Jonas M Dörr, Stefan Scheidelaar, Michal Heger, Maarten R Egmond, J Antoinette Killian, Tamimount Mohammadi, Eefjan Breukink
Publikováno v:
PLoS ONE, Vol 13, Iss 12, p e0210135 (2018)
[This corrects the article DOI: 10.1371/journal.pone.0206692.].
Externí odkaz:
https://doaj.org/article/01eb26ab82a0481484a2759e72383e10
Autor:
Yao Liu, Elisabete C C M Moura, Jonas M Dörr, Stefan Scheidelaar, Michal Heger, Maarten R Egmond, J Antoinette Killian, Tamimount Mohammadi, Eefjan Breukink
Publikováno v:
PLoS ONE, Vol 13, Iss 11, p e0206692 (2018)
As an integral membrane protein, purification and characterization of phospho-N- acetylmuramyl- pentapeptide translocase MraY have proven difficult. Low yield and concerns of retaining stability and activity after detergent solubilization have hamper
Externí odkaz:
https://doaj.org/article/8c3f1fcc5d7a4a379f1551a30d646bc7
Autor:
Ahmed Bouhss, Ben de Kruijff, Thierry Vernet, Marlies Diepeveen-de Bruin, Martine Nguyen-Distèche, Robert Sijbrandi, Vincent van Dam, André Zapun, Tamimount Mohammadi, Eefjan Breukink
Publikováno v:
The EMBO Journal. 30:1425-1432
Bacterial cell growth necessitates synthesis of peptidoglycan. Assembly of this major constituent of the bacterial cell wall is a multistep process starting in the cytoplasm and ending in the exterior cell surface. The intracellular part of the pathw
Autor:
Muriel Crouvoisier, Dominique Mengin-Lecreulx, Aneta Karczmarek, Ahmed Bouhss, Tamimount Mohammadi, Tanneke den Blaauwen
Publikováno v:
Molecular Microbiology
Molecular Microbiology, 65(4), 1106-1121. Wiley-Blackwell
Molecular Microbiology, 65(4), 1106-1121. Wiley-Blackwell
In Escherichia coli many enzymes including MurG are directly involved in the synthesis and assembly of peptidoglycan. MurG is an essential glycosyltransferase catalysing the last intracellular step of peptidoglycan synthesis. To elucidate its role du
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bb01b9cf6aaf7a2ed5e65554ee1bcca
https://dare.uva.nl/personal/pure/en/publications/the-essential-peptidoglycan-glycosyltransferase-murg-forms-a-complex-with-proteins-involved-in-lateral-envelope-growth-as-well-as-with-proteins-involved-in-cell-division-in-escherichia-coli(70a32b51-c964-418f-890a-338c6d90b76f).html
https://dare.uva.nl/personal/pure/en/publications/the-essential-peptidoglycan-glycosyltransferase-murg-forms-a-complex-with-proteins-involved-in-lateral-envelope-growth-as-well-as-with-proteins-involved-in-cell-division-in-escherichia-coli(70a32b51-c964-418f-890a-338c6d90b76f).html
Publikováno v:
LaboratoriumsMedizin. 30:402-411
Autor:
Christina M. J. E. Vandenbroucke-Grauls, Tamimount Mohammadi, Paul H. M. Savelkoul, Henk W. Reesink
Publikováno v:
Journal of microbiological methods, 61(2), 285-288. Elsevier
Mohammadi, T, Reesink, H W, Vandenbroucke-Grauls, C M J E & Savelkoul, P H M 2005, ' Removal of contaminating DNA from commercial nucleic acid extraction kit reagents ', Journal of Microbiological Methods, vol. 61, no. 2, pp. 285-288 . https://doi.org/10.1016/j.mimet.2004.11.018
Journal of Microbiological Methods, 61(2), 285-288. Elsevier
Mohammadi, T, Reesink, H W, Vandenbroucke-Grauls, C M J E & Savelkoul, P H M 2005, ' Removal of contaminating DNA from commercial nucleic acid extraction kit reagents ', Journal of Microbiological Methods, vol. 61, no. 2, pp. 285-288 . https://doi.org/10.1016/j.mimet.2004.11.018
Journal of Microbiological Methods, 61(2), 285-288. Elsevier
Due to contamination of DNA extraction reagents, false-positive results can occur when applying broad-range real-time PCR based on bacterial 16S rDNA. Filtration of the nucleic acid extraction kit reagents with GenElute Maxiprep binding columns was e
Autor:
Christina M. J. E. Vandenbroucke-Grauls, Paul H. M. Savelkoul, Henk W. Reesink, Tamimount Mohammadi
Publikováno v:
Transfusion. 44:1314-1318
UNLABELLED BACKGROUND A real-time polymerase chain reaction (PCR) assay based on amplification of a conserved region of the HLA-DQA1 locus was developed and validated to assess its suitability in quantitating low levels of white blood cells (WBCs) in
Autor:
Tamimount, Mohammadi, Vincent, van Dam, Robert, Sijbrandi, Thierry, Vernet, André, Zapun, Ahmed, Bouhss, Marlies, Diepeveen-de Bruin, Martine, Nguyen-Distèche, Ben, de Kruijff, Eefjan, Breukink
Publikováno v:
The EMBO journal. 30(8)
Bacterial cell growth necessitates synthesis of peptidoglycan. Assembly of this major constituent of the bacterial cell wall is a multistep process starting in the cytoplasm and ending in the exterior cell surface. The intracellular part of the pathw
Autor:
Germán Rivas, Jan van Marle, Tanneke den Blaauwen, Jolanda Verheul, Anouskha D. Comvalius, Ginette E. J. Ploeger, Ariadna Martos, Tamimount Mohammadi, Carlos Alfonso
Publikováno v:
Biochemistry, 48(46), 11056-11066. American Chemical Society
Digital.CSIC. Repositorio Institucional del CSIC
instname
Biochemistry
Digital.CSIC. Repositorio Institucional del CSIC
instname
Biochemistry
11 páginas, 10 figuras -- PAGS nros. 11056-11066
FtsZ polymerizes in a ring-like structure at mid cell to initiate cell division in Escherichia coli. The ring is stabilized by a number of proteins among which the widely conserved ZapA protein.
FtsZ polymerizes in a ring-like structure at mid cell to initiate cell division in Escherichia coli. The ring is stabilized by a number of proteins among which the widely conserved ZapA protein.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a97f433fd856af9069dd5b1022c863a
https://dare.uva.nl/personal/pure/en/publications/the-gtpase-activity-of-escherichia-coli-ftsz-determines-the-magnitude-of-the-ftsz-polymer-bundling-by-zapa-in-vitro(0773b0f1-1764-4eba-99e3-95d3b6a6a8ae).html
https://dare.uva.nl/personal/pure/en/publications/the-gtpase-activity-of-escherichia-coli-ftsz-determines-the-magnitude-of-the-ftsz-polymer-bundling-by-zapa-in-vitro(0773b0f1-1764-4eba-99e3-95d3b6a6a8ae).html