| scholarly article | Q13442814 |
| P356 | DOI | 10.1128/JB.171.6.3412-3419.1989 |
| P8608 | Fatcat ID | release_w2v3or5qbvb7dmxsg5ax467lm4 |
| P932 | PMC publication ID | 210065 |
| P698 | PubMed publication ID | 2656655 |
| P2093 | author name string | Wientjes FB | |
| Nanninga N | |||
| P2860 | cites work | Distinct penicillin binding proteins involved in the division, elongation, and shape of Escherichia coli K12 | Q35085145 |
| Rate and topography of cell wall synthesis during the division cycle of Salmonella typhimurium | Q36186588 | ||
| Variation in precursor pool size during the division cycle of Escherichia coli: further evidence for linear cell growth | Q36186617 | ||
| Membrane-murein attachment at the leading edge of the division septum: a second membrane-murein structure associated with morphogenesis of the gram-negative bacterial division septum | Q36264040 | ||
| Evidence for involvement of penicillin-binding protein 3 in murein synthesis during septation but not during cell elongation | Q36323172 | ||
| Evidence for diffuse growth of the cylindrical portion of the Escherichia coli murein sacculus | Q36332162 | ||
| Regulation of bacterial cell division: temperature-sensitive mutants of Escherichia coli that are defective in septum formation | Q36605649 | ||
| Growth and form in microorganisms: morphogenesis of Escherichia coli | Q39533176 | ||
| Division behavior and shape changes in isogenic ftsZ, ftsQ, ftsA, pbpB, and ftsE cell division mutants of Escherichia coli during temperature shift experiments | Q39952713 | ||
| Genetic and morphological characterization of ftsB and nrdB mutants of Escherichia coli | Q39955373 | ||
| Effect of growth rate and cell shape on the peptidoglycan composition in Escherichia coli | Q39955409 | ||
| Kinetics of uptake and incorporation of meso-diaminopimelic acid in different Escherichia coli strains | Q39964056 | ||
| Cell cycle parameters of Proteus mirabilis: interdependence of the biosynthetic cell cycle and the interdivision cycle | Q39964291 | ||
| Interaction of FtsA and PBP3 proteins in the Escherichia coli septum | Q39967556 | ||
| Cell shape and division in Escherichia coli: experiments with shape and division mutants | Q39981015 | ||
| Volume growth, murein synthesis, and murein cross-linkage during the division cycle of Escherichia coli PA3092. | Q39988210 | ||
| Labeling pattern of major penicillin-binding proteins of Escherichia coli during the division cycle | Q39988707 | ||
| Morphological analysis of the division cycle of two Escherichia coli substrains during slow growth | Q40034444 | ||
| Pattern of meso-dl-2,6-diaminopimelic acid incorporation during the division cycle of Escherichia coli | Q40337970 | ||
| Regulation of polar cap formation in the life cycle ofEscherichia coli | Q69233353 | ||
| Autolytic enzymes and cell division of Escherichia coli | Q69884368 | ||
| The variable T model for gram-negative morphology | Q70396672 | ||
| Patterns of protein synthesis during the cell cycle of the fission yeast Schizosaccharomyces pombe | Q70631334 | ||
| Index for measurement of synchronization of cell populations | Q79352917 | ||
| Process of cellular division in Escherichia coli growth pattern of E. coli murein | Q93744990 | ||
| P433 | issue | 6 | |
| P921 | main subject | Escherichia coli | Q25419 |
| P304 | page(s) | 3412-3419 | |
| P577 | publication date | 1989-06-01 | |
| P1433 | published in | Journal of Bacteriology | Q478419 |
| P1476 | title | Rate and topography of peptidoglycan synthesis during cell division in Escherichia coli: concept of a leading edge | |
| P478 | volume | 171 |
| Q35192443 | A fail-safe mechanism in the septal ring assembly pathway generated by the sequential recruitment of cell separation amidases and their activators |
| Q36253997 | A locus affecting nucleoid segregation in Salmonella typhimurium |
| Q39958154 | Amount of peptidoglycan in cell walls of gram-negative bacteria |
| Q51146982 | Asymmetric adhesion of rod-shaped bacteria controls microcolony morphogenesis. |
| Q39942552 | Autoradiographic analysis of diaminopimelic acid incorporation in filamentous cells of Escherichia coli: repression of peptidoglycan synthesis around the nucleoid |
| Q47189292 | Bacterial Cell Size: Multifactorial and Multifaceted |
| Q36650535 | Bacterial cell division: the mechanism and its precison |
| Q37636934 | Bacterial cell wall recycling provides cytosolic muropeptides as effectors for beta-lactamase induction |
| Q34474627 | Bacterial cell wall synthesis: new insights from localization studies |
| Q50995827 | Beyond force generation: Why is a dynamic ring of FtsZ polymers essential for bacterial cytokinesis? |
| Q27015700 | Biological consequences and advantages of asymmetric bacterial growth |
| Q28364545 | Cell age dependent concentration of Escherichia coli divisome proteins analyzed with ImageJ and ObjectJ |
| Q36405514 | Cell division and peptidoglycan assembly in Escherichia coli |
| Q37706217 | Cell wall precursors are required to organize the chlamydial division septum. |
| Q42651566 | Classic Spotlight: Cellular Sites of Peptidoglycan Synthesis Revealed |
| Q57910522 | Colocalization and interaction between elongasome and divisome during a preparative cell division phase inEscherichia coli |
| Q39504092 | Constitutive septal murein synthesis in Escherichia coli with impaired activity of the morphogenetic proteins RodA and penicillin-binding protein 2. |
| Q33187415 | Control of cell morphogenesis in bacteria: two distinct ways to make a rod-shaped cell |
| Q47634394 | Cure for a crisis? |
| Q36646537 | Defining the rate-limiting processes of bacterial cytokinesis |
| Q40343553 | Differential effect of mutational impairment of penicillin-binding proteins 1A and 1B on Escherichia coli strains harboring thermosensitive mutations in the cell division genes ftsA, ftsQ, ftsZ, and pbpB. |
| Q38749655 | Differentiation of the bacterial cell division site. |
| Q30541334 | Direct interaction of FtsZ and MreB is required for septum synthesis and cell division in Escherichia coli |
| Q33558045 | Discovery and characterization of three new Escherichia coli septal ring proteins that contain a SPOR domain: DamX, DedD, and RlpA |
| Q39931177 | Epitope mapping of Escherichia coli cell division protein FtsZ with monoclonal antibodies |
| Q54260149 | Escherichia coli inner membrane protein YciB interacts with ZipA that is important for cell division. |
| Q35881824 | Escherichia coli low-molecular-weight penicillin-binding proteins help orient septal FtsZ, and their absence leads to asymmetric cell division and branching. |
| Q50158349 | Excess histidine enzymes cause AICAR-independent filamentation in Escherichia coli. |
| Q39566160 | FtsI and FtsW are localized to the septum in Escherichia coli. |
| Q35949290 | FtsZ directs a second mode of peptidoglycan synthesis in Escherichia coli |
| Q28245159 | FtsZ ring structure associated with division in Escherichia coli |
| Q34110044 | Functional consequences of genome evolution in Listeria monocytogenes: the lmo0423 and lmo0422 genes encode sigmaC and LstR, a lineage II-specific heat shock system |
| Q24671609 | Functional taxonomy of bacterial hyperstructures |
| Q24682585 | Genome diversification in phylogenetic lineages I and II of Listeria monocytogenes: identification of segments unique to lineage II populations |
| Q37232509 | Genomic sequencing reveals regulatory mutations and recombinational events in the widely used MC4100 lineage of Escherichia coli K-12 |
| Q47437200 | Growth and division of Streptococcus pneumoniae: localization of the high molecular weight penicillin‐binding proteins during the cell cycle |
| Q39523292 | Growth of the stress-bearing and shape-maintaining murein sacculus of Escherichia coli. |
| Q34187367 | Hypothesis: membrane domains and hyperstructures control bacterial division |
| Q37191701 | In Escherichia coli, MreB and FtsZ direct the synthesis of lateral cell wall via independent pathways that require PBP 2. |
| Q35954752 | Inactivation of FtsI inhibits constriction of the FtsZ cytokinetic ring and delays the assembly of FtsZ rings at potential division sites |
| Q39960645 | Isogenic variants of Escherichia coli with altered morphology have peptidoglycan with identical muropeptide composition |
| Q33991017 | Localization of FtsI (PBP3) to the septal ring requires its membrane anchor, the Z ring, FtsA, FtsQ, and FtsL |
| Q41815173 | LytM-domain factors are required for daughter cell separation and rapid ampicillin-induced lysis in Escherichia coli. |
| Q50775806 | Maturation of the Escherichia coli divisome occurs in two steps. |
| Q34009977 | Morphogenesis of Escherichia coli |
| Q34545818 | MreB, the cell shape-determining bacterial actin homologue, co-ordinates cell wall morphogenesis in Caulobacter crescentus |
| Q39845464 | Murein segregation in Escherichia coli |
| Q39706148 | New insights into the developmental history of the bacterial cell division site |
| Q43242802 | Nutrient requirements for growth of the extreme oligotroph 'Candidatus Pelagibacter ubique' HTCC1062 on a defined medium |
| Q58699719 | Outer membrane lipoprotein RlpA is a novel periplasmic interaction partner of the cell division protein FtsK in Escherichia coli |
| Q44272835 | Penicillin-binding protein PBP2 of Escherichia coli localizes preferentially in the lateral wall and at mid-cell in comparison with the old cell pole |
| Q98158728 | Penicillin-binding proteins regulate multiple steps in the polarized cell division process of Chlamydia |
| Q39950701 | Peptidoglycan synthesis during the cell cycle of Escherichia coli: composition and mode of insertion |
| Q39927963 | Plasmolysis bays in Escherichia coli: are they related to development and positioning of division sites? |
| Q35098282 | Probing the catalytic activity of a cell division-specific transpeptidase in vivo with beta-lactams |
| Q30781116 | Relative Rates of Surface and Volume Synthesis Set Bacterial Cell Size |
| Q35949337 | Role of peptidoglycan amidases in the development and morphology of the division septum in Escherichia coli |
| Q34141103 | Site-directed fluorescence labeling reveals a revised N-terminal membrane topology and functional periplasmic residues in the Escherichia coli cell division protein FtsK |
| Q88909032 | Surface Area to Volume Ratio: A Natural Variable for Bacterial Morphogenesis |
| Q36930465 | Synthesis of the cell surface during the division cycle of rod-shaped, gram-negative bacteria |
| Q35625462 | Temperature shift experiments with an ftsZ84(Ts) strain reveal rapid dynamics of FtsZ localization and indicate that the Z ring is required throughout septation and cannot reoccupy division sites once constriction has initiated |
| Q40565200 | The Escherichia coli amidase AmiC is a periplasmic septal ring component exported via the twin-arginine transport pathway |
| Q34305324 | The Escherichia coli cell division protein FtsW is required to recruit its cognate transpeptidase, FtsI (PBP3), to the division site. |
| Q41750914 | The biophysics of the gram-negative periplasmic space |
| Q36182316 | The constrained hoop: an explanation of the overshoot in cell length during a shift-up of Escherichia coli |
| Q37081660 | The different shapes of cocci |
| Q42912642 | 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 |
| Q34672738 | The tubulin ancestor, FtsZ, draughtsman, designer and driving force for bacterial cytokinesis |
| Q72759264 | The two-competing site (TCS) model for cell shape regulation in bacteria: the envelope as an integration point for the regulatory circuits of essential physiological events |
| Q39497047 | Timing of FtsZ assembly in Escherichia coli |
| Q33728893 | Visualization of penicillin-binding proteins during sporulation of Streptomyces griseus |
| Q36276314 | ZipA is required for FtsZ-dependent preseptal peptidoglycan synthesis prior to invagination during cell division. |
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