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9篇 您的检索式:作者名="Mugat"
    题名 作者 年代 出处 被引量
1Cucurbitacins are insect steroid hormone antagonists acting on the ecdysteroid receptor显示文摘Dinan L Whiting P Girault J P Lafont R Dhadialla T S Cress D E Mugat B Antoniewski C and Lepesant J A 0,,:1
2Engrailed homeoprotein acts as a signaling molecule in the developing fly显示文摘Layalle S Volovitch M Mugat B 2011Development2011,138,11:1
3Direct repeats bind the EcR/USP receptor and mediate ecdysteroid responses in Drosophila rnelanogaster显示文摘Antoniewski C Mugat B Delbac F et ol 1996Mol Cell Biol1996,16,:1
4Genome-wide identification ofin vivo drosophila engrailed-binding DNA fragments and related target genes显示文摘SOLANO P J MUGAT B MARTIN D 2003Development2003,130,7:1
5Absence of transitive and systemic pathways allows cell-specific and isoform-specific RNAi in Drosophila 显示文摘Roignant JY Carre C Mugat B 2003RNA2003,9,3:1
6Absence of transitive and sys- temic pathways allows cell - specific and isoform - specific RNAi in Drosophila 显示文摘Roignant J Y Carre C Mugat R 2003RNA2003,9,3:1
7Dual requirement for the EeR/USP nuclear receptor and the dGATAb factor in an ecdys- one response in Drosophila melanogaster 显示文摘Voronique B Mugat B Roignant J-Y 1999Mol Cellu Biol1999,19,8:1
8Genomic scanning enabling discovery of a new antibacterial bicyclic carbamate-containing alkaloid显示文摘Non-ribosomal peptides are a group of structurally diverse natural products with various important therapeutic and agrochemical applications.Bacterial pyrrolizidine alkaloids(PAs),containing a scaffold of two fused five-membered ring system with a nitrogen atom at the bridgehead,have been found to originate from a multidomain non-ribosomal peptide synthetase to generate indolizidine intermediates,followed by multistep oxidation,catalysed by single Bayer-Villiger(BV)enzymes,to yield PA scaffolds.Although bacterial PAs are rare in natural product inventory,bioinformatics analysis suggested that the biosynthetic gene clusters(BGCs)that are likely to be responsible for the production of PA-like metabolites are widely distributed in bacterial genomes.However,most of the strains containing PA-like BGCs are not deposited in the public domain,therefore preventing further assessment of the chemical spaces of this group of bioactive metabolites.Here,we report a genomic scanning strategy to assess the potential of PA metabolites production in our culture collection without prior knowledge of genome information.Among the strains tested,we found fifteen contain the key BV enzymes that are likely to be involved in the last step of PA ring formation.Subsequently one-strain-many-compound(OSMAC)method,supported by a combination of HR-MS,NMR,SMART 2.0 technology,and GNPS analysis,allowed identification and characterization of a new[5+7]heterobicyclic carbamate,legoncarbamate,together with five known PAs,bohemamine derivatives,from Streptomyces sp.CT37,a Ghanaian soil isolate.The absolute stereochemistry of legoncarbamate was determined by comparison of measured and calculated ECD spectra.Legoncarbamate displays antibacterial activity against E.coli ATCC 25922 with an MIC value of 3.1μg/mL.Finally,a biosynthetic model of legoncarbamate and other bohemamines was proposed based on the knowledge we have gained so far.Qing Fang Linrui Wu Caroline Urwald Morgane Mugat Shan Wang Kwaku Kyeremeh Carol Philips Samantha Law d Yongjun Zhou Hai Deng 2021Synthetic and Systems Biotechnology2021,6,1:1
9Dynamic expres- sion of broad-complex isoforms mediates temporal control of an ecdysteroid target gene at the onset of Drosophila metamorphosis 显示文摘Mugat B Brodu V Kejzlarova-Lepesant J 2000Dev Biol2000,227,1:1
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