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Insights into the Roles of Lipoteichoic Acids and MprF in Bacillus subtilis

https://doi.org/10.1128/mbio.02667-22
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/82_2015_5021openalex-snapshot
Envelope Structures of Gram-Positive Bacteria
inferredcites →https://doi.org/10.1007/978-3-319-50430-8_17openalex-snapshot
Lipoteichoic Acid Synthesis and Function in Gram-Positive Bacteria
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Characterization of N-Succinylation of L-Lysylphosphatidylglycerol in Bacillus subtilis Using Tandem Mass Spectrometry
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Plasmids designed to alter the antibiotic resistance expressed by insertion mutations in Bacillus subtilis, through in vivo recombination
inferredcites →https://doi.org/10.1016/j.bbalip.2016.11.013openalex-snapshot
Bacterial aminoacyl phospholipids – Biosynthesis and role in basic cellular processes and pathogenicity
inferredcites →https://doi.org/10.1016/j.cels.2016.12.013openalex-snapshot
Construction and Analysis of Two Genome-Scale Deletion Libraries for Bacillus subtilis
inferredcites →https://doi.org/10.1016/j.ijmm.2019.05.010openalex-snapshot
MprF-mediated daptomycin resistance
inferredcites →https://doi.org/10.1016/j.mib.2011.12.011openalex-snapshot
Coordinate regulation of Gram-positive cell surface components
inferredcites →https://doi.org/10.1016/j.mib.2021.01.008openalex-snapshot
Regulation and function of class A Penicillin-binding proteins
inferredcites →https://doi.org/10.1021/acs.jcim.2c00300openalex-snapshot
Structure-Based Discovery of Lipoteichoic Acid Synthase Inhibitors
inferredcites →https://doi.org/10.1021/jacs.1c12697openalex-snapshot
Rapid Inhibitor Discovery by Exploiting Synthetic Lethality
inferredcites →https://doi.org/10.1038/emboj.2009.25openalex-snapshot
Distinct and essential morphogenic functions for wall‐ and lipo‐teichoic acids in Bacillus subtilis
inferredcites →https://doi.org/10.1038/nature19331openalex-snapshot
SEDS proteins are a widespread family of bacterial cell wall polymerases
inferredcites →https://doi.org/10.1038/nmicrobiol.2016.253openalex-snapshot
RodA as the missing glycosyltransferase in Bacillus subtilis and antibiotic discovery for the peptidoglycan polymerase pathway
inferredcites →https://doi.org/10.1038/s41467-020-15257-1openalex-snapshot
Ca2+-Daptomycin targets cell wall biosynthesis by forming a tripartite complex with undecaprenyl-coupled intermediates and membrane lipids
inferredcites →https://doi.org/10.1038/s41467-021-23248-zopenalex-snapshot
Phospholipid translocation captured in a bifunctional membrane protein MprF
inferredcites →https://doi.org/10.1038/s41598-020-73108-xopenalex-snapshot
Association of mprF mutations with cross-resistance to daptomycin and vancomycin in methicillin-resistant Staphylococcus aureus (MRSA)
inferredcites →https://doi.org/10.1038/s41598-021-04294-5openalex-snapshot
Magnesium rescues the morphology of Bacillus subtilis mreB mutants through its inhibitory effect on peptidoglycan hydrolases
inferredcites →https://doi.org/10.1046/j.1365-2958.1998.00930.xopenalex-snapshot
A UDP glucosyltransferase from Bacillus subtilis successively transfers up to four glucose residues to 1,2‐diacylglycerol: expression of ypfP in Escherichia coli and structural analysis of its reaction products
inferredcites →https://doi.org/10.1073/pnas.0701821104openalex-snapshot
Synthesis of glycerol phosphate lipoteichoic acid in Staphylococcus aureus
inferredcites →https://doi.org/10.1073/pnas.1611173113openalex-snapshot
Daptomycin inhibits cell envelope synthesis by interfering with fluid membrane microdomains
inferredcites →https://doi.org/10.1073/pnas.2008929117openalex-snapshot
Lipoteichoic acid polymer length is determined by competition between free starter units
inferredcites →https://doi.org/10.1074/jbc.270.26.15598openalex-snapshot
Incorporation of D-Alanine into Lipoteichoic Acid and Wall Teichoic Acid in Bacillus subtilis
inferredcites →https://doi.org/10.1074/jbc.ra118.004561openalex-snapshot
A partial reconstitution implicates DltD in catalyzing lipoteichoic acid d-alanylation
inferredcites →https://doi.org/10.1074/jbc.rev119.010155openalex-snapshot
Uncovering the activities, biological roles, and regulation of bacterial cell wall hydrolases and tailoring enzymes
inferredcites →https://doi.org/10.1084/jem.193.9.1067openalex-snapshot
Staphylococcus aureus Resistance to Human Defensins and Evasion of Neutrophil Killing via the Novel Virulence Factor Mprf Is Based on Modification of Membrane Lipids with l -Lysine
inferredcites →https://doi.org/10.1093/nar/gkab943openalex-snapshot
The current state of Subti Wiki, the database for the model organism Bacillus subtilis
inferredcites →https://doi.org/10.1093/nar/gkf698openalex-snapshot
Improving the predictive value of the competence transcription factor (ComK) binding site in Bacillus subtilis using a genomic approach
inferredcites →https://doi.org/10.1099/00221287-148-11-3331openalex-snapshot
MprF-mediated lysinylation of phospholipids in Bacillus subtilis – protection against bacteriocins in terrestrial habitats?
inferredcites →https://doi.org/10.1099/00221287-148-7-2079openalex-snapshot
tagO is involved in the synthesis of all anionic cell-wall polymers in Bacillus subtilis 168 a aThe EMBL accession number for the nucleotide sequence reported in this paper is AJ004803.
inferredcites →https://doi.org/10.1099/mic.0.063420-0openalex-snapshot
Induction of extracytoplasmic function sigma factors in Bacillus subtilis cells with defects in lipoteichoic acid synthesis
inferredcites →https://doi.org/10.1111/j.1365-2958.2005.04506.xopenalex-snapshot
A magnesium‐dependent mreB null mutant: implications for the role of mreB in Bacillus subtilis
inferredcites →https://doi.org/10.1111/j.1365-2958.2006.05184.xopenalex-snapshot
A new FtsZ‐interacting protein, YlmF, complements the activity of FtsA during progression of cell division in Bacillus subtilis
inferredcites →https://doi.org/10.1111/j.1365-2958.2008.06210.xopenalex-snapshot
Control of the cell elongation–division cycle by shuttling of PBP1 protein in Bacillus subtilis
inferredcites →https://doi.org/10.1111/j.1365-2958.2009.06601.xopenalex-snapshot
Regulation of cell wall morphogenesis in Bacillus subtilis by recruitment of PBP1 to the MreB helix
inferredcites →https://doi.org/10.1111/j.1365-2958.2009.06805.xopenalex-snapshot
Partial functional redundancy of MreB isoforms, MreB, Mbl and MreBH, in cell morphogenesis of Bacillus subtilis
inferredcites →https://doi.org/10.1111/j.1365-2958.2010.07472.xopenalex-snapshot
Enzymatic activities and functional interdependencies of Bacillus subtilis lipoteichoic acid synthesis enzymes
inferredcites →https://doi.org/10.1111/jam.14790openalex-snapshot
Inactivation of the gene encoding the cationic antimicrobial peptide resistance factor MprF increases biofilm formation but reduces invasiveness of Listeria monocytogenes
inferredcites →https://doi.org/10.1111/mmi.12092openalex-snapshot
The WalRK ( YycFG ) and σ I RsgI regulators cooperate to control CwlO and LytE expression in exponentially growing and stressed B acillus subtilis cells
inferredcites →https://doi.org/10.1111/mmi.12335openalex-snapshot
Differentiated roles for MreB ‐actin isologues and autolytic enzymes in B acillus subtilis morphogenesis
inferredcites →https://doi.org/10.1111/mmi.12380openalex-snapshot
Contributions of the σ W , σ M and σ X regulons to the lantibiotic resistome of B acillus subtilis
inferredcites →https://doi.org/10.1111/mmi.14714openalex-snapshot
Class A PBPs: It is time to rethink traditional paradigms
inferredcites →https://doi.org/10.1126/science.1206848openalex-snapshot
Condition-Dependent Transcriptome Reveals High-Level Regulatory Architecture in Bacillus subtilis
inferredcites →https://doi.org/10.1128/aac.00039-06openalex-snapshot
Genetic Changes That Correlate with Reduced Susceptibility to Daptomycin in Staphylococcus aureus
inferredcites →https://doi.org/10.1128/aac.00122-10openalex-snapshot
Cell Wall Thickening Is Not a Universal Accompaniment of the Daptomycin Nonsusceptibility Phenotype in Staphylococcus aureus : Evidence for Multiple Resistance Mechanisms
inferredcites →https://doi.org/10.1128/aac.01329-08openalex-snapshot
Genetic Analysis of Factors Affecting Susceptibility ofBacillus subtilisto Daptomycin
inferredcites →https://doi.org/10.1128/aac.01819-10openalex-snapshot
Reduction in Membrane Phosphatidylglycerol Content Leads to Daptomycin Resistance in Bacillus subtilis
inferredcites →https://doi.org/10.1128/aem.71.1.39-45.2005openalex-snapshot
Bacillus subtilis α-Phosphoglucomutase Is Required for Normal Cell Morphology and Biofilm Formation
inferredcites →https://doi.org/10.1128/aem.72.1.327-333.2006openalex-snapshot
In Vivo Random Mutagenesis of Bacillus subtilis by Use of TnYLB-1, a mariner -Based Transposon
inferredcites →https://doi.org/10.1128/jb.00003-16openalex-snapshot
Teichoic Acid Polymers Affect Expression and Localization of dl -Endopeptidase LytE Required for Lateral Cell Wall Hydrolysis in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.00149-20openalex-snapshot
The Length of Lipoteichoic Acid Polymers Controls Staphylococcus aureus Cell Size and Envelope Integrity
inferredcites →https://doi.org/10.1128/jb.00507-13openalex-snapshot
The Conserved DNA-Binding Protein WhiA Is Involved in Cell Division in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.00720-08openalex-snapshot
Phenotypic and Transcriptomic Characterization of Bacillus subtilis Mutants with Grossly Altered Membrane Composition
inferredcites →https://doi.org/10.1128/jb.01044-15openalex-snapshot
The Composition of the Cell Envelope Affects Conjugation in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.01155-13openalex-snapshot
Lipoteichoic Acids, Phosphate-Containing Polymers in the Envelope of Gram-Positive Bacteria
inferredcites →https://doi.org/10.1128/jb.01221-08openalex-snapshot
Pleiotropic Roles of Polyglycerolphosphate Synthase of Lipoteichoic Acid in Growth of Staphylococcus aureus Cells
inferredcites →https://doi.org/10.1128/jb.01497-08openalex-snapshot
The Cell Wall Regulator σISpecifically Suppresses the Lethal Phenotype ofmblMutants inBacillus subtilis
inferredcites →https://doi.org/10.1128/jb.01683-06openalex-snapshot
Genes Required for Glycolipid Synthesis and Lipoteichoic Acid Anchoring in Staphylococcus aureus
inferredcites →https://doi.org/10.1128/jb.05569-11openalex-snapshot
Synthetic Lethality of the lytE cwlO Genotype in Bacillus subtilis Is Caused by Lack of d , l -Endopeptidase Activity at the Lateral Cell Wall
inferredcites →https://doi.org/10.1128/jb.180.17.4555-4563.1998openalex-snapshot
Bacillus subtilis Cells Lacking Penicillin-Binding Protein 1 Require Increased Levels of Divalent Cations for Growth
inferredcites →https://doi.org/10.1128/jb.183.20.6046-6053.2001openalex-snapshot
Two Class A High-Molecular-Weight Penicillin-Binding Proteins of Bacillus subtilis Play Redundant Roles in Sporulation
inferredcites →https://doi.org/10.1128/jb.185.4.1423-1431.2003openalex-snapshot
Peptidoglycan Synthesis in the Absence of Class A Penicillin-Binding Proteins in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.186.12.3970-3979.2004openalex-snapshot
Genes Involved in Formation of Structured Multicellular Communities by Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.188.8.3099-3109.2006openalex-snapshot
Effects of Phosphorelay Perturbations on Architecture, Sporulation, and Spore Resistance in Biofilms of Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.81.5.741-746.1961openalex-snapshot
REQUIREMENTS FOR TRANSFORMATION IN BACILLUS SUBTILIS
inferredcites →https://doi.org/10.1128/mbio.00092-22openalex-snapshot
A Central Role for Magnesium Homeostasis during Adaptation to Osmotic Stress
inferredcites →https://doi.org/10.1128/mbio.01659-18openalex-snapshot
Gain-of-Function Mutations in the Phospholipid Flippase MprF Confer Specific Daptomycin Resistance
inferredcites →https://doi.org/10.1128/mbio.01760-23openalex-snapshot
An exhaustive multiple knockout approach to understanding cell wall hydrolase function in Bacillus subtilis
inferredcites →https://doi.org/10.1128/mmbr.67.4.686-723.2003openalex-snapshot
A Continuum of Anionic Charge: Structures and Functions of d -Alanyl-Teichoic Acids in Gram-Positive Bacteria
inferredcites →https://doi.org/10.1146/annurev-micro-091213-112949openalex-snapshot
Lipoteichoic Acid Synthesis and Function in Gram-Positive Bacteria
inferredcites →https://doi.org/10.1266/ggs.86.365openalex-snapshot
The Bacillus subtilis essential gene dgkB is dispensable in mutants with defective lipoteichoic acid synthesis
inferredcites →https://doi.org/10.1371/journal.pbio.3001555openalex-snapshot
Identification of a novel cationic glycolipid in Streptococcus agalactiae that contributes to brain entry and meningitis
inferredcites →https://doi.org/10.1371/journal.pgen.1008296openalex-snapshot
SweC and SweD are essential co-factors of the FtsEX-CwlO cell wall hydrolase complex in Bacillus subtilis
inferredcites →https://doi.org/10.1371/journal.pone.0067398openalex-snapshot
Increased Cell Wall Teichoic Acid Production and D-alanylation Are Common Phenotypes among Daptomycin-Resistant Methicillin-Resistant Staphylococcus aureus (MRSA) Clinical Isolates
inferredcites →https://doi.org/10.1371/journal.pone.0107426openalex-snapshot
Phenotypic and Genotypic Characterization of Daptomycin-Resistant Methicillin-Resistant Staphylococcus aureus Strains: Relative Roles of mprF and dlt Operons
inferredcites →https://doi.org/10.1371/journal.ppat.1007862openalex-snapshot
Multi-strain Tn-Seq reveals common daptomycin resistance determinants in Staphylococcus aureus
inferredcites →https://doi.org/10.3389/fmicb.2017.01991openalex-snapshot
Deficiency in Lipoteichoic Acid Synthesis Causes a Failure in Executing the Colony Developmental Program in Bacillus subtilis
inferredcites →https://doi.org/10.3389/fmicb.2021.664704openalex-snapshot
How Teichoic Acids Could Support a Periplasm in Gram-Positive Bacteria, and Let Cell Division Cheat Turgor Pressure
inferredcites →https://doi.org/10.3390/antibiotics9010017openalex-snapshot
More Than a Pore: A Current Perspective on the In Vivo Mode of Action of the Lipopeptide Antibiotic Daptomycin
inferredcites →https://doi.org/10.7554/elife.44912openalex-snapshot
A switch in surface polymer biogenesis triggers growth-phase-dependent and antibiotic-induced bacteriolysis
inferredcites →https://doi.org/10.7554/elife.52088openalex-snapshot
Homeostatic control of cell wall hydrolysis by the WalRK two-component signaling pathway in Bacillus subtilis
inferredcites →https://doi.org/10.7554/elife.57902openalex-snapshot
A regulatory pathway that selectively up-regulates elongasome function in the absence of class A PBPs
inferredcites →https://doi.org/10.7554/elife.66376openalex-snapshot
Sensitizing Staphylococcus aureus to antibacterial agents by decoding and blocking the lipid flippase MprF

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inferred← citeshttps://doi.org/10.1101/2024.01.09.574795openalex-snapshot
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