Keeping DNA Out, Letting It In

2019 ◽  
pp. 183-196
Author(s):  
Janet R. Gilsdorf

All three meningitis bacteria (meningococci, Haemophilus influenzae, and pneumococci) are able to soak up DNA from their environments; thus, they all exhibit substantial genetic diversity. Those whose cell walls stain Gram negative (meningococci and H. influenzae) use DNA uptake signal sequences to take up the DNA, while pneumococci, which stain Gram positive and thus possess a different kind of cell wall, use a unique and less well understood mechanism. Although these interesting and important scientific discoveries have little to do with the clinical management of meningitis, they reveal a lot about the basic biology of H. influenzae and other meningitis-causing bacteria. By using the molecular tools that permit bacteria to acquire new DNA from their environments, H. influenzae bacteria are able to refashion themselves. In this way, at least a few of the bacteria in the enormous population of bacteria that live in humans are able to cope with whatever challenging environment they happen to fall into, including their transit from the throat, where they normally live, to the blood and meninges, where they cause meningitis.

1964 ◽  
Vol 20 (2) ◽  
pp. 217-233 ◽  
Author(s):  
G. W. Claus ◽  
L. E. Roth

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.


1967 ◽  
Vol 105 (2) ◽  
pp. 759-765 ◽  
Author(s):  
K. Clarke ◽  
G. W. Gray ◽  
D. A. Reaveley

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.


1966 ◽  
Vol 12 (1) ◽  
pp. 105-108 ◽  
Author(s):  
K. Jane Carson ◽  
R. G. Eagon

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.


1973 ◽  
Vol 19 (8) ◽  
pp. 1056-1057 ◽  
Author(s):  
A. Forge ◽  
J. W. Costerton

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.


1998 ◽  
Vol 180 (3) ◽  
pp. 746-748 ◽  
Author(s):  
M. L. Gwinn ◽  
R. Ramanathan ◽  
H. O. Smith ◽  
J.-F. Tomb

ABSTRACT Haemophilus influenzae Rd is a gram-negative natural transformer. A mutant strain, RJ248, that has normal DNA uptake and translocation but whose transformation frequency is 300 times lower than that of wild-type H. influenzae and whose phage recombination is 8 times lower was isolated. The affected gene,comM, is induced during competence development in wild-typeH. influenzae but not in RJ248.


2021 ◽  
pp. 1-12
Author(s):  
Isabel Hottmann ◽  
Marina Borisova ◽  
Christina Schäffer ◽  
Christoph Mayer

<i>Tannerella forsythia</i> is an anaerobic, fusiform Gram-negative oral pathogen strongly associated with periodontitis, a multibacterial inflammatory disease that leads to the destruction of the teeth-supporting tissue, ultimately causing tooth loss. To survive in the oral habitat, <i>T. forsythia</i> depends on cohabiting bacteria for the provision of nutrients. For axenic growth under laboratory conditions, it specifically relies on the external supply of <i>N</i>-acetylmuramic acid (MurNAc), which is an essential constituent of the peptidoglycan (PGN) of bacterial cell walls. <i>T. forsythia</i> comprises a typical Gram-negative PGN; however, as evidenced by genome sequence analysis, the organism lacks common enzymes required for the <i>de novo</i> synthesis of precursors of PGN, which rationalizes its MurNAc auxotrophy. Only recently insights were obtained into how <i>T. forsythia</i> gains access to MurNAc in its oral habitat, enabling synthesis of the own PGN cell wall. This report summarizes <i>T. forsythia</i>’s strategies to survive in the oral habitat by means of PGN salvage pathways, including recovery of exogenous MurNAc and PGN-derived fragments but also polymeric PGN, which are all derived from cohabiting bacteria either via cell wall turnover or decay of cells. Salvage of polymeric PGN presumably requires the removal of peptides from PGN by an unknown amidase, concomitantly with the translocation of the polymer across the outer membrane. Two recently identified exo-lytic <i>N</i>-acetylmuramidases (Tf_NamZ1 and Tf_NamZ2) specifically cleave the peptide-free, exogenous (nutrition source) PGN in the periplasm and release the MurNAc and disaccharide substrates for the transporters Tf_MurT and Tf_AmpG, respectively, whereas the peptide-containing, endogenous (the self-cell wall) PGN stays unattached. This review also outlines how <i>T. forsythia</i> synthesises the PGN precursors UDP-MurNAc and UDP-<i>N</i>-acetylglucosamine (UDP-GlcNAc), involving homologs of the <i>Pseudomonas</i> sp. recycling enzymes AmgK/MurU and a monofunctional uridylyl transferase (named Tf_GlmU*), respectively.


Author(s):  
Akira Matsumoto

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.


1968 ◽  
Vol 3 (2) ◽  
pp. 273-294
Author(s):  
MARGARET J. THORNLEY ◽  
AUDREY M. GLAUERT

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.


1985 ◽  
Vol 22 (12) ◽  
pp. 1893-1898 ◽  
Author(s):  
T. J. Beveridge ◽  
W. S. Fyfe

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.


2020 ◽  
Vol 11 (3) ◽  
pp. 59 ◽  
Author(s):  
Moorthy Maruthapandi ◽  
Arumugam Saravanan ◽  
John H. T. Luong ◽  
Aharon Gedanken

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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