LYSOZYME SENSITIVITY OF THE CELL WALL OF PSEUDO-MONAS AERUGINOSA: FURTHER EVIDENCE FOR THE ROLE OF THE NON-PEPTIDOGLYCAN COMPONENTS IN CELL WALL RIGIDITY

1966 ◽  
Vol 12 (1) ◽  
pp. 105-108 ◽  
Author(s):  
K. Jane Carson ◽  
R. G. Eagon
Keyword(s):  
Pseudomonas Aeruginosa ◽  
Cell Wall ◽  
Electron Micrographs ◽  
Cell Walls ◽  
Gram Negative Bacteria ◽  
Normal Cells ◽  
Thin Sections ◽  
Gram Negative ◽  
Cell Wall Rigidity

Electron micrographs of thin sections of normal cells of Pseudomonas aeruginosa showed the cell walls to be convoluted and to be composed of two distinct layers. Electron micrographs of thin sections of lysozyme-treated cells of P. aeruginosa showed (a) that the cell walls lost much of their convoluted nature; (b) that the layers of the cell walls became diffuse and less distinct; and (c) that the cell walls became separated from the protoplasts over extensive cellular areas. These results suggest that the peptidoglycan component of the unaltered cell walls of P. aeruginosa is sensitive to lysozyme. Furthermore, it appears that the peptidoglycan component is not solely responsible for the rigidity of the cell walls of Gram-negative bacteria.

Fine Structure and Radiation Resistance in Acinetobacter: Studies on a Resistant Strain

1968 ◽  
Vol 3 (2) ◽  
pp. 273-294
Author(s):  
MARGARET J. THORNLEY ◽  
AUDREY M. GLAUERT
Keyword(s):  
Cell Wall ◽  
Fine Structure ◽  
Radiation Resistance ◽  
Cell Walls ◽  
Proteolytic Enzymes ◽  
Gram Negative Bacteria ◽  
Intact Cells ◽  
Thin Sections ◽  
Gram Negative ◽  
Isolated Cell

An electron-microscope study of thin sections and negatively stained preparations of intact cells and isolated cell walls of a bacterium which is moderately resistant to ionizing radiation, Acinetobacter strain 199A, showed that it is similar to other Gram-negative bacteria except for its mode of division and for the fine structure of some of the surface layers. During division the cells form a fairly thick septum similar to those observed in Gram-positive bacteria. An examination of the appearance and chemical composition of isolated cell walls before and after treatment with enzymes, detergents and lipid solvents revealed that three layers, each with a characteristic fine structure, are present in the cell wall: (1) an outer membrane with an array of peg-like subunits; (2) a layer of wrinkled material which is digested by proteolytic enzymes; and (3) a smooth, rigid layer, which contains the mucopeptide components of the cell wall. These observations are compared with the results of other workers for various Gram-negative bacteria. From comparisons with the structure of more radiation-sensitive strains of Acinetobacter, it appears that layer (2) may be associated with the radiation resistance of the organism.

scholarly journals MexAB-OprM Efflux Pump Interaction with the Peptidoglycan of Escherichia coli and Pseudomonas aeruginosa

2021 ◽  
Vol 22 (10) ◽  
pp. 5328
Author(s):  
Miao Ma ◽  
Margaux Lustig ◽  
Michèle Salem ◽  
Dominique Mengin-Lecreulx ◽  
Gilles Phan ◽  
...  
Keyword(s):  
Escherichia Coli ◽  
Pseudomonas Aeruginosa ◽  
Cell Division ◽  
Membrane Proteins ◽  
Outer Membrane ◽  
Efflux Pump ◽  
Gram Negative Bacteria ◽  
Gram Negative ◽  
Active Efflux

One of the major families of membrane proteins found in prokaryote genome corresponds to the transporters. Among them, the resistance-nodulation-cell division (RND) transporters are highly studied, as being responsible for one of the most problematic mechanisms used by bacteria to resist to antibiotics, i.e., the active efflux of drugs. In Gram-negative bacteria, these proteins are inserted in the inner membrane and form a tripartite assembly with an outer membrane factor and a periplasmic linker in order to cross the two membranes to expulse molecules outside of the cell. A lot of information has been collected to understand the functional mechanism of these pumps, especially with AcrAB-TolC from Escherichia coli, but one missing piece from all the suggested models is the role of peptidoglycan in the assembly. Here, by pull-down experiments with purified peptidoglycans, we precise the MexAB-OprM interaction with the peptidoglycan from Escherichia coli and Pseudomonas aeruginosa, highlighting a role of the peptidoglycan in stabilizing the MexA-OprM complex and also differences between the two Gram-negative bacteria peptidoglycans.

scholarly journals FINE STRUCTURE OF THE GRAM-NEGATIVE BACTERIUM ACETOBACTER SUBOXYDANS

1964 ◽  
Vol 20 (2) ◽  
pp. 217-233 ◽  
Author(s):  
G. W. Claus ◽  
L. E. Roth
Keyword(s):  
Cell Wall ◽  
Plasma Membrane ◽  
Cell Walls ◽  
Negative Staining ◽  
Homogeneous Layer ◽  
Physical Treatment ◽  
Thin Sections ◽  
Gram Negative ◽  
Acetobacter Suboxydans ◽  
Negative Cell

The morphological features of the cell wall, plasma membrane, protoplasmic constituents, and flagella of Acetobacter suboxydans (ATCC 621) were studied by thin sectioning and negative staining. Thin sections of the cell wall demonstrate an outer membrane and an inner, more homogeneous layer. These observations are consistent with those of isolated, gram-negative cell-wall ghosts and the chemical analyses of gram-negative cell walls. Certain functional attributes of the cell-wall inner layer and the structural comparisons of gram-negative and gram-positive cell walls are considered. The plasma membrane is similar in appearance to the membrane of the cell wall and is occasionally found to be folded into the cytoplasm. Certain features of the protoplasm are described and discussed, including the diffuse states of the chromatinic material that appear to be correlated with the length of the cell and a polar differentiation in the area of expected flagellar attachment. Although the flagella appear hollow in thin sections, negative staining of isolated flagella does not substantiate this finding. Severe physical treatment occasionally produces a localized penetration into the central region of the flagellum, the diameter of which is much smaller then that expected from sections. A possible explanation of this apparent discrepancy is discussed.

scholarly journals The extraction of cell walls of Pseudomonas aeruginosa with aqueous phenol. The insoluble residue and material from the aqueous layers

1967 ◽  
Vol 105 (2) ◽  
pp. 759-765 ◽  
Author(s):  
K. Clarke ◽  
G. W. Gray ◽  
D. A. Reaveley
Keyword(s):  
Pseudomonas Aeruginosa ◽  
Cell Wall ◽  
Cell Walls ◽  
Lipid A ◽  
Diaminopimelic Acid ◽  
Insoluble Residue ◽  
Muramic Acid ◽  
Gram Negative ◽  
Gram Negative Organisms ◽  
Residue Fraction

1. The insoluble residue and material present in the aqueous layers resulting from treatment of cell walls of Pseudomonas aeruginosa with aqueous phenol were examined. 2. The products (fractions AqI and AqII) isolated from the aqueous layers from the first and second extractions respectively account for approx. 25% and 12% of the cell wall and consist of both lipopolysaccharide and muropeptide. 3. The lipid part of the lipopolysaccharide is qualitatively similar to the corresponding material (lipid A) from other Gram-negative organisms, as is the polysaccharide part. 4. The insoluble residue (fraction R) contains sacculi, which also occur in fraction AqII. On hydrolysis, the sacculi yield glucosamine, muramic acid, alanine, glutamic acid and 2,6-diaminopimelic acid, together with small amounts of lysine, and they are therefore similar to the murein sacculi of other Gram-negative organisms. Fraction R also contains substantial amounts of protein, which differs from that obtained from the phenol layer. 5. The possible association or aggregation of lipopolysaccharide, murein and murein sacculi is discussed.

The effects of phospholipid depletion on the cleavage pattern of the cell walls of frozen Gram-negative bacteria

1973 ◽  
Vol 19 (8) ◽  
pp. 1056-1057 ◽  
Author(s):  
A. Forge ◽  
J. W. Costerton
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Cytoplasmic Membrane ◽  
Gram Negative Bacteria ◽  
Cleavage Pattern ◽  
Gram Negative ◽  
Whole Cells ◽  
The Cross ◽  
Double Track ◽  
Chloroform Methanol

Extraction of whole cells of the marine pseudomonad (B-16) with chloroform–methanol causes the disappearance of the cleavage planes, and the cross-sectioned profile of both the cytoplasmic membrane and the double-track layer of the cell wall.

Electron Microscopic Observations on the Effects of Polymixin B Sulfate to Cell Walls of Chlamydia Organisms

1972 ◽  
Vol 30 ◽  
pp. 326-327
Author(s):  
Akira Matsumoto
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Present Report ◽  
Bactericidal Effect ◽  
Chlamydia Psittaci ◽  
Gram Negative Bacteria ◽  
Electron Microscopic ◽  
Cell Content ◽  
Gram Negative ◽  
Reticulate Body

Cell walls of the both types of bodies, mature elementary body(EB) and developmental reticulate body(RB) of Chlamydia psittaci appear the triple layered membrane in thin section. However, in the preparations shadowcast or stained negatively EB cell wall shows hexagonally arrayed structure composed of subunits, 180A in diameter on the inside surface, whereas RB cell wall does not have this structure. Chemical analysis demonstrated that EB cell wall contained a similar amino acid composition with the cell walls of gram-negative bacteria, such as E.coli. The bactericidal effect of polymixin group against gram-negative bacilli is understood that the drug affects to the cell wall and destroys its osmotic regulation. Electron microscopy on the effects of the drug against the gram-negative bacteria revealed the formation of numerous number of projections on the cell wall surface and leakage of cell content through the projections. The present report is concerned with further studies on the fine structure of EB cell walls based on the observation on their response to polymixin B sulfate.

scholarly journals THE FINE STRUCTURE OF STALKED BACTERIA BELONGING TO THE FAMILY CAULOBACTERACEAE

1964 ◽  
Vol 23 (3) ◽  
pp. 587-607 ◽  
Author(s):  
Jeanne L. Stove Poindexter ◽  
Germaine Cohen-Bazire
Keyword(s):  
Cell Wall ◽  
Fine Structure ◽  
Cell Membrane ◽  
Multilayered Structure ◽  
Gram Negative Bacteria ◽  
Thin Sections ◽  
Gram Negative ◽  
Cytoplasmic Region ◽  
The Core ◽  
The Family

The fine structure of a series of stalked bacteria belonging to the genera Caulobacter and Asticcacaulis has been examined in thin sections. The cell wall has the multilayered structure typical of many Gram-negative bacteria, and continues without interruption throughout the length of the stalk. The core of the stalk, continuous with the cytoplasmic region of the cell, is enclosed in an extension of the cell membrane, and contains a system of internal membranes: it is devoid of ribosomes and nucleoplasm. A membranous organelle occupies the juncture of stalk and cell, separating the ribosomal region from the core of the stalk. Typical mesosomes also occur in the cell, being particularly frequent at the plane of division. The secreted holdfast is located at the tip of the stalk in Caulobacter, and at the pole of the cell adjacent to the stalk in Asticcacaulis.

Metal fixation by bacterial cell walls

1985 ◽  
Vol 22 (12) ◽  
pp. 1893-1898 ◽  
Author(s):  
T. J. Beveridge ◽  
W. S. Fyfe
Keyword(s):  
Cell Wall ◽  
Metal Binding ◽  
Bacterial Cell ◽  
Cell Walls ◽  
Nucleation And Growth ◽  
Gram Negative Bacteria ◽  
Gram Positive ◽  
Gram Negative ◽  
Element Transport ◽  
Cell Wall Polymers

All biomass contains a significant quantity of metallic constituents, and mineralization in living and dead biodebris may contribute to element transport from the hydrosphere into sediments. The anionic cell walls of bacteria are remarkable in their ability to fix metals and provide sites for nucleation and growth of minerals. Results presented show the types of cell wall polymers that are responsible for metal binding in walls of Gram-positive and Gram-negative bacteria.

A THREE-DIMENSIONAL COMPUTER MODEL OF THE TRACHEID CELL WALL AS A TOOL FOR INTERPRETATION OF WOOD CELL WALL ULTRASTRUCTURE

IAWA Journal ◽  
2001 ◽  
Vol 22 (3) ◽  
pp. 213-233 ◽  
Author(s):  
L.A. Donaldson
Keyword(s):  
Cell Wall ◽  
Electron Micrographs ◽  
Cell Walls ◽  
Three Dimensional ◽  
Transmission Electron Micrographs ◽  
Direct Result ◽  
Thin Sections ◽  
Transmission Electron ◽  
Wall Ultrastructure ◽  
Random Patterns

Three-dimensional computer models were used to simulate transmission electron micrographs in order to determine the effects of changes in microfibril orientation and arrangement on the appearance of ultrastructural images based on thin sections. It is shown that the tangential fibrillar texture commonly associated with wood cell walls results not from individual microfibrils arranged in tangential lamellae but from overlapping of adjacent microfibrils irrespective of their arrangement. The tangential lamellae observed in transmission electron micrographs of wood cell walls do not necessarily reflect the underlying nanostructure of the wall. Tangential textures can occur irrespective of the arrangement of microfibrils in tangential, radial or random patterns as a direct result of the helical organisation of the cell wall. Comparison between model images and high resolution micrographs suggests that microfibrils are arranged randomly in weakly defined clusters, with perhaps varying amounts of tangential or radial organisation.

scholarly journals Antimicrobial Properties of the Polyaniline Composites against Pseudomonas aeruginosa and Klebsiella pneumoniae

2020 ◽  
Vol 11 (3) ◽  
pp. 59 ◽  
Author(s):  
Moorthy Maruthapandi ◽  
Arumugam Saravanan ◽  
John H. T. Luong ◽  
Aharon Gedanken
Keyword(s):  
Pseudomonas Aeruginosa ◽  
Cell Wall ◽  
Klebsiella Pneumoniae ◽  
Cell Walls ◽  
Antimicrobial Properties ◽  
Cell Lysis ◽  
Antimicrobial Activities ◽  
Sonochemical Method ◽  
Gram Negative ◽  
Polyaniline Composites

CuO, TiO2, or SiO2 was decorated on polyaniline (PANI) by a sonochemical method, and their antimicrobial properties were investigated for two common Gram-negative pathogens: Pseudomonas aeruginosa (PA) and Klebsiella pneumoniae (KP). Without PANI, CuO, TiO2, or SiO2 with a concentration of 220 µg/mL exhibited no antimicrobial activities. In contrast, PANI-CuO and PANI-TiO2 (1 mg/mL, each) completely suppressed the PA growth after 6 h of exposure, compared to 12 h for the PANI-SiO2 at the same concentration. The damage caused by PANI-SiO2 to KP was less effective, compared to that of PANI-TiO2 with the eradication time of 12 h versus 6 h, respectively. This bacterium was not affected by PANI-CuO. All the composites bind tightly to the negative groups of bacteria cell walls to compromise their regular activities, leading to the damage of the cell wall envelope and eventual cell lysis.

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