Forming cross-linked peptidoglycan from synthetic gram-negative Lipid II
about
Peptidoglycan remodeling by the coordinated action of multispecific enzymesAntimicrobial lipopeptide tridecaptin A1 selectively binds to Gram-negative lipid IID-amino acids indirectly inhibit biofilm formation in Bacillus subtilis by interfering with protein synthesis.One-pot protection-glycosylation reactions for synthesis of lipid II analoguesBacterial cell wall. MurJ is the flippase of lipid-linked precursors for peptidoglycan biogenesis.A mutant Escherichia coli that attaches peptidoglycan to lipopolysaccharide and displays cell wall on its surface.Reconstitution of membrane protein complexes involved in pneumococcal septal cell wall assemblyProfiling of β-lactam selectivity for penicillin-binding proteins in Escherichia coli strain DC2.Chemoenzymatic syntheses of water-soluble lipid I fluorescent probes.Lipoprotein activators stimulate Escherichia coli penicillin-binding proteins by different mechanisms.Peptidoglycan Cross-Linking Preferences of Staphylococcus aureus Penicillin-Binding Proteins Have Implications for Treating MRSA Infections.Isoprenoid phosphonophosphates as glycosyltransferase acceptor substrates.D-amino carboxamide-based recruitment of dinitrophenol antibodies to bacterial surfaces via peptidoglycan remodeling.In vitro reconstitution demonstrates the cell wall ligase activity of LCP proteins.Reconstitution of peptidoglycan cross-linking leads to improved fluorescent probes of cell wall synthesis.Detection of lipid-linked peptidoglycan precursors by exploiting an unexpected transpeptidase reaction.Lipid II overproduction allows direct assay of transpeptidase inhibition by β-lactams.Identification of a Functionally Unique Family of Penicillin-Binding Proteins.Substrate Preferences Establish the Order of Cell Wall Assembly in Staphylococcus aureus.Chemoenzymatic synthesis of the bacterial polysaccharide repeating unit undecaprenyl pyrophosphate and its analogs.Membrane Potential Is Required for MurJ Function.Continuous-flow thermolysis for the preparation of vinylglycine derivatives.Enantioselective synthesis of α-alkenyl α-amino acids via N-H insertion reactions.
P2860
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P2860
Forming cross-linked peptidoglycan from synthetic gram-negative Lipid II
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Forming cross-linked peptidoglycan from synthetic gram-negative Lipid II
@en
type
label
Forming cross-linked peptidoglycan from synthetic gram-negative Lipid II
@en
prefLabel
Forming cross-linked peptidoglycan from synthetic gram-negative Lipid II
@en
P2093
P2860
P356
P1476
Forming cross-linked peptidoglycan from synthetic gram-negative Lipid II
@en
P2093
Daniel Kahne
Hirokazu Tsukamoto
Janine M May
Suzanne Walker
Tania J Lupoli
P2860
P304
P356
10.1021/JA312510M
P407
P577
2013-03-13T00:00:00Z