| The Sacculus after Four Decades - Seen from Some Distance | p. 1 |
| Biochemical and Biophysical Studies on the Fine Structure of the Sacculi from Escherichia coli and Staphylococcus aureus | p. 9 |
| New Mass Spectrometric Methods for Peptidoglycan Analysis | p. 23 |
| H.P.L.C. and [superscript 252]Cf Plasma Desorption-Mass Spectrometry of Muropeptides Isolated from Escherichia coli | p. 31 |
| Structure Elucidation of Peptidoglycan Monomers by Fast Atom Bombardment - and Electrospray Ionization Tandem-Mass Spectrometry | p. 39 |
| Investigations on the Structure and Biosynthesis of Cyanelle Murein from Cyanophora paradoxa | p. 47 |
| New Methods in Electron Microscopy Help Elucidate the Structure of the Murein Sacculus and the Distribution of Penicillin-Binding Proteins | p. 57 |
| Synthesis of [alpha] and [beta] Anomers of UDP-N-Acetylmuramic Acid | p. 71 |
| The Muropeptide Composition of the Peptidoglycan of Staphylococcus aureus Determined with Reversed-Phase High Performance Liquid Chromatography | p. 77 |
| Distribution of O-Acetylation in the Peptidoglycan from Proteus mirabilis 19 | p. 83 |
| Murein Structure of Three Different Species of Chemolithothrophic Sulphur Bacteria: Thiobacillus tepidarius, Thiobacillus neapolitanus, and Thiobacillus versutus | p. 91 |
| Phenotypic, Biochemical, and Structural Analysis of S-layer Mutants from Thermus thermophilus HB8 | p. 99 |
| Crystalline Bacterial Cell Surface Layers and their Application Potentials | p. 105 |
| An Overview of the Assembly, Turnover and Recycling of the Murein Sacculus | p. 119 |
| Variations in the Metabolism of Peptidoglycan Prior to Polymerization | p. 127 |
| Identification of the murI and murB Genes Coding for Cytoplasmic Peptidoglycan Synthetases in the 90-Min Region of the E. coli Chromosome | p. 139 |
| Amino Acids as Useful Tools in the Study of Murein Metabolism in Escherichia coli | p. 147 |
| Peptidoglycan Synthesis in Salmonella typhimurium | p. 161 |
| Biosynthesis of Peptidoglycan in Gaffkya homari: Regulation of Transpeptidation by Acceptor Peptide | p. 169 |
| Apparent Obligatory Dependence of Peptidoglycan Synthesis on Phospholipid Synthesis Studied in Ether Treated Escherichia coli | p. 177 |
| Does PBP 2 Regulate Cell Division in E. coli? | p. 183 |
| Peptidoglycan Synthesis During Hyphal Elongation in Streptomyces antibioticus | p. 189 |
| The Role of the envM Genes of Escherichia coli and Salmonella typhimurium in Cell Membrane Biosynthesis | p. 197 |
| Biosynthesis of Pseudomurein and Other Methanobacterial Cell Walls | p. 205 |
| Peptidoglycan (Murein) Hydrolases: Unusual Enzymes for Unusual Substrates | p. 213 |
| Is Muramidase-2 of Enterococcus hirae a Penicillin-Binding Protein? | p. 229 |
| Specific Binding of the Soluble Lytic Transglycosylase to the Murein Sacculus of Escherichia coli | p. 235 |
| Inhibition of an Autolysin Together with PBP3 Causes the Formation of Bulges: Identification of the Soluble Lytic Transglycosylase in E. coli as the Specific Target of Bulgecin | p. 241 |
| The Cell Wall of Bacillus subtilis is Protonated During Growth | p. 245 |
| Searching for the Evolutionary Design of the Pneumococcal Cell Wall Lytic Enzymes | p. 253 |
| Molecular Characteristics of the Cell Wall Lytic Enzymes Coded by Pneumococcal Phages | p. 261 |
| Molecular Cloning, Overexpression of Rz Lysis Gene of Phage [lambda] and Subcellular Localization of its Protein Product | p. 269 |
| Pathway of [Phi]X174 Protein E Mediated Lysis of Escherichia coli | p. 277 |
| Genetic Control of Fungal Cell Wall Autolysis | p. 285 |
| The use of a Mercury-Penicillin V Derivative to Localize Penicillin-Binding Proteins in Escherichia coli | p. 295 |
| A Far Upstream Region Is Required for Expression of the ftsI Gene Coding for Penicillin-Binding Protein 3 of Escherichia coli | p. 303 |
| Involvement of the NH[subscript 2]- and COOH-Terminal ends of PBP3 of Escherichia coli on [beta]-Lactam Binding, Membrane Localization, and Function of the Protein | p. 309 |
| Modular Design of the Bi(Multi?)-Functional Penicillin-Binding Proteins | p. 319 |
| Penicillin-Binding Proteins 1A and 3 in Streptococcus pneumoniae: What Are Essential PBP's? | p. 335 |
| Disturbance of Peptidoglycan Synthesis by Glycine and D-Methionine Creates a Signal for the ampG-Mediated Induction of ampC-[beta]-Lactamase in Escherichia coli | p. 341 |
| In Enterobacter Cloacae Alterations Induced by Glycine and D-Amino Acids in the Composition and Structure of Peptidoglycan Are Accompanied by Induction of Chromosomal [beta]-Lactamase. A Model Involving ftsZ and Septation | p. 347 |
| FtsZ Rings, Polar Morphology and Cell Lysis | p. 355 |
| Stability of the Components of the Escherichia coli Septator | p. 363 |
| Construction of a Triple Deletion of Penicillin-Binding Proteins 4, 5, and 6 in Escherichia coli | p. 369 |
| Deformations in the Cytoplasmic Membrane of Escherichia coli Direct the Repair of Peptidoglycan | p. 375 |
| Wall Teichoic Acid, Peptidoglycan Synthesis and Morphogenesis in Bacillus subtilis | p. 385 |
| Penicillin Induced Bacteriolysis of Staphylococci as a Post-Mortem Consequence of Murosome-Mediated Killing Via Wall Perforation and Attempts to Imitate the Perforation Process without Applying Antibiotics | p. 393 |
| Regulation of the Morphogenetic Cycle of Escherichia coli: 1992 | p. 409 |
| "Three for One" - a Simple Growth Mechanism that Guarantees a Precise Copy of the Thin, Rod-Shaped Sacculus of Escherichia coli | p. 419 |
| Stresses on the Surface Stress Theory | p. 427 |
| Growth and Control of the Cell Wall: A Mechanical Model for Bacillus subtilis | p. 443 |
| Cellular Growth without a Murein Sacculus - the Nucleoid-Associated Compartmentation Concept | p. 453 |
| Contributors | p. 465 |
| Index | p. 469 |
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