| scholarly article | Q13442814 |
| P2093 | author name string | H Labischinski | |
| M L Hochberg | |||
| E W Goodell | |||
| A Goodell | |||
| P2860 | cites work | The structure of the cell wall of Staphylococcus aureus studied with neutron scattering and magnetic birefringence | Q70599573 |
| THE LOCATION OF THE MUCOPEPTIDE IN SECTIONS OF THE CELL WALL OF ESCHERICHIA COLI AND OTHER GRAM-NEGATIVE BACTERIA | Q78556628 | ||
| Conformational and topological aspects of the three-dimensional architecture of bacterial peptidoglycan | Q93566571 | ||
| Cellular responses of Bacillus subtilis and Escherichia coli to the Gram stain | Q24685116 | ||
| On the Secondary and Tertiary Structure of Murein. Low and Medium-Angle X-Ray Evidence against Chitin-Based Conformations of Bacterial Peptidoglycan | Q30111106 | ||
| Distinct penicillin binding proteins involved in the division, elongation, and shape of Escherichia coli K12 | Q35085145 | ||
| Uptake of cell wall peptides by Salmonella typhimurium and Escherichia coli | Q36241302 | ||
| Molecular model for elongation of the murein sacculus of Escherichia coli | Q36256169 | ||
| Periplasmic gel: new concept resulting from the reinvestigation of bacterial cell envelope ultrastructure by new methods | Q36285770 | ||
| Evidence for involvement of penicillin-binding protein 3 in murein synthesis during septation but not during cell elongation | Q36323172 | ||
| Peptidoglycan synthesis during the cell cycle of Escherichia coli: composition and mode of insertion | Q39950701 | ||
| Recycling of murein by Escherichia coli | Q39980805 | ||
| Cell shape and division in Escherichia coli: experiments with shape and division mutants | Q39981015 | ||
| Model for the Structure of the Shape-Maintaining Layer of the Escherichia coli Cell Envelope | Q40290097 | ||
| Structure of the peptidoglycan of bacterial cell walls. I | Q44077493 | ||
| Multilayered distribution of peptidoglycan in the periplasmic space of Escherichia coli. | Q54731013 | ||
| The composition of the murein of Escherichia coli. | Q54745091 | ||
| DNA synthesis during the division cycle of rapidly growing Escherichia coli B/r | Q69834498 | ||
| Autolytic enzymes and cell division of Escherichia coli | Q69884368 | ||
| Ultrastructure of the cell wall of Escherichia coli and chemical nature of its constituent layers | Q69993894 | ||
| The variable T model for gram-negative morphology | Q70396672 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Escherichia coli | Q25419 |
| P1104 | number of pages | 6 | |
| P304 | page(s) | 751-756 | |
| P577 | publication date | 1991-01-01 | |
| P1433 | published in | Journal of Bacteriology | Q478419 |
| P1476 | title | Direct proof of a "more-than-single-layered" peptidoglycan architecture of Escherichia coli W7: a neutron small-angle scattering study | |
| P478 | volume | 173 |
| Q39958154 | Amount of peptidoglycan in cell walls of gram-negative bacteria |
| Q50106278 | Analysis of Salmonella invasion protein-peptidoglycan interactions |
| Q28261252 | Bacterial cell shape |
| Q34474627 | Bacterial cell wall synthesis: new insights from localization studies |
| Q41466090 | Bacterial cytoplasmic display platform Retained Display (ReD) identifies stable human germline antibody frameworks |
| Q34149620 | Bacteriophage Tuc2009 encodes a tail-associated cell wall-degrading activity |
| Q36993740 | Cell shape and cell-wall organization in Gram-negative bacteria |
| Q35695118 | Cell surface characteristics of environmental and clinical isolates of Vibrio cholerae non-O1 |
| Q88918474 | Cell-Wall Recycling of the Gram-Negative Bacteria and the Nexus to Antibiotic Resistance |
| Q35642011 | Consequences of the interaction of beta-lactam antibiotics with penicillin binding proteins from sensitive and resistant Staphylococcus aureus strains |
| Q39997774 | Cryo-Transmission Electron Microscopy of Frozen-Hydrated Sections ofEscherichia coliandPseudomonas aeruginosa |
| Q27651052 | Crystal and cryoEM structural studies of a cell wall degrading enzyme in the bacteriophage 29 tail |
| Q42146913 | Deformations in the cytoplasmic membrane of Escherichia coli direct the synthesis of peptidoglycan. The hernia model |
| Q38176980 | Different walls for rods and balls: the diversity of peptidoglycan |
| Q34676672 | DipM, a new factor required for peptidoglycan remodelling during cell division in Caulobacter crescentus |
| Q31032922 | Direct quantitation of the numbers of individual penicillin-binding proteins per cell in Staphylococcus aureus |
| Q39935416 | Elasticity of the sacculus of Escherichia coli |
| Q27323050 | Escherichia coli peptidoglycan structure and mechanics as predicted by atomic-scale simulations |
| Q36735836 | Freeze-substitution studies of bacteria |
| Q40374892 | From growth to autolysis: the murein hydrolases in Escherichia coli |
| Q36672951 | Growth of Escherichia coli: significance of peptidoglycan degradation during elongation and septation |
| Q39523292 | Growth of the stress-bearing and shape-maintaining murein sacculus of Escherichia coli. |
| Q36661981 | High-pressure homogenization as a non-thermal technique for the inactivation of microorganisms |
| Q34068295 | How did bacteria come to be? |
| Q38019036 | Mechanisms of iron and haem transport by Listeria monocytogenes |
| Q64992611 | Minimal exposure of lipid II cycle intermediates triggers cell wall antibiotic resistance. |
| Q51730945 | Molecular imaging of glycan chains couples cell-wall polysaccharide architecture to bacterial cell morphology. |
| Q28756346 | Molecular organization of Gram-negative peptidoglycan |
| Q34009977 | Morphogenesis of Escherichia coli |
| Q41613859 | Native cell wall organization shown by cryo-electron microscopy confirms the existence of a periplasmic space in Staphylococcus aureus |
| Q39501003 | On the architecture of the gram-negative bacterial murein sacculus |
| Q77915163 | Orientation of the peptidoglycan chains in the sacculus of Escherichia coli |
| Q39842837 | Peptidoglycan as a barrier to transenvelope transport |
| Q28730466 | Possible import routes of proteins into the cyanobacterial endosymbionts/plastids of Paulinella chromatophora |
| Q35581769 | Staphylococcus aureus Survives with a Minimal Peptidoglycan Synthesis Machine but Sacrifices Virulence and Antibiotic Resistance. |
| Q38501132 | Structural constraints and dynamics of bacterial cell wall architecture |
| Q28647950 | Structure-activity exploration of a small-molecule Lipid II inhibitor |
| Q39943125 | Subcellular distribution of the soluble lytic transglycosylase in Escherichia coli |
| Q36712029 | Surface layers of bacteria |
| Q36930465 | Synthesis of the cell surface during the division cycle of rod-shaped, gram-negative bacteria |
| Q35876950 | The architecture of the murein (peptidoglycan) in gram-negative bacteria: vertical scaffold or horizontal layer(s)? |
| Q34019335 | The bacterium's way for safe enlargement and division |
| Q41750914 | The biophysics of the gram-negative periplasmic space |
| Q68032510 | The macrophage response to bacteria. Modulation of macrophage functional activity by peptidoglycan from Moraxella (Branhamella) catarrhalis |
| Q28300374 | The peptidoglycan sacculus of Myxococcus xanthus has unusual structural features and is degraded during glycerol-induced myxospore development |
| Q30811687 | Thickness and elasticity of gram-negative murein sacculi measured by atomic force microscopy. |
| Q28534946 | Turning defense into offense: defensin mimetics as novel antibiotics targeting lipid II |
| Q35965731 | Turnover and recycling of the murein sacculus in oligopeptide permease-negative strains of Escherichia coli: indirect evidence for an alternative permease system and for a monolayered sacculus |
| Q30881142 | Use of RNA arbitrarily primed-PCR fingerprinting to identify Vibrio cholerae genes differentially expressed in the host following infection |
| Q37768120 | Viability states of bacteria--specific mechanisms of selected probes |
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