Literature DB >> 9561823

The biophysics of the gram-negative periplasmic space.

A L Koch1.   

Abstract

When subject to an osmotic 'up-shock', water flows outward from bacterial cytoplasm of the bacterium. Lipid bilayers can shrink very little in area and therefore must wrinkle to accommodate the smaller volume. The usual consequence is that all the layers of the cell envelope must become wrinkled together because they adhere to each other and must now cover a smaller surface. Plasmolysis spaces are formed if the cytoplasmic membrane (CM) separates from the other components of the wall. However, because the CM bilayer is essentially an incompressible two-dimensional liquid, this constraint restricts the location and shape of plasmolysis spaces. With mild up-shocks they form at the pole and around constricting regions in the cell. Elsewhere their creation requires the formation of endocytotic or exocytotic vesicles. The formation of endocytotic vesicles occurs in animal and plant cells as well as in bacterial cells. With stronger up-shocks tubular structures (Bayer adhesion sites), or other special geometric shapes (e.g., Scheie structures) allow the bilayer to surround an irregular shaped cytoplast. Periosmotic agents, that is, those that extract water from the periplasm as well as the cytoplasm, are molecules such as poly-vinyl-pyrrolidone and alpha-cyclodextrin that are too large to pass through the porins in the outer membrane. They were found to significantly inhibit the formation of plasmolysis spaces. Presumably, they inhibit the plasmolysis process, which requires that extracellular fluid enter between the CM and the outer membrane (OM). In the extreme case, with the dehydrating action of both osmotic agents and periosmotic agents, periplasmic space formation tends to be prevented and a new kind of space develops within the cytoplasm. We have designated these as 'cytoplasmic voids'. These novel structures are not bounded by lipid bilayers, in contrast to the endocytotic vesicles. These new spaces appear to result from the negative turgor pressure generated by the application of the combination of osmotic and periosmotic agents causing bubble formation. Several ideas in the literature about the wall biology (periseptal annuli, leading edge, osmotic pressure in the periplasm) are presented and critiqued. The basic criticism of these is that much of the phenomena can be explained because of the physics of the phospholipid bilayers and osmotic forces and thus does not imply the existence of a special control mechanism to regulate growth and division.

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Year:  1998        PMID: 9561823     DOI: 10.1080/10408419891294172

Source DB:  PubMed          Journal:  Crit Rev Microbiol        ISSN: 1040-841X            Impact factor:   7.624


  17 in total

Review 1.  Structures of gram-negative cell walls and their derived membrane vesicles.

Authors:  T J Beveridge
Journal:  J Bacteriol       Date:  1999-08       Impact factor: 3.490

2.  Damage of the bacterial cell envelope by antimicrobial peptides gramicidin S and PGLa as revealed by transmission and scanning electron microscopy.

Authors:  Mareike Hartmann; Marina Berditsch; Jacques Hawecker; Mohammad Fotouhi Ardakani; Dagmar Gerthsen; Anne S Ulrich
Journal:  Antimicrob Agents Chemother       Date:  2010-06-07       Impact factor: 5.191

3.  Constitutive expression of the maltoporin LamB in the absence of OmpR damages the cell envelope.

Authors:  Sylvia A Reimann; Alan J Wolfe
Journal:  J Bacteriol       Date:  2010-12-03       Impact factor: 3.490

4.  Phage shock proteins B and C prevent lethal cytoplasmic membrane permeability in Yersinia enterocolitica.

Authors:  N Kaye Horstman; Andrew J Darwin
Journal:  Mol Microbiol       Date:  2012-06-12       Impact factor: 3.501

5.  Crowding and confinement effects on protein diffusion in vivo.

Authors:  Michael C Konopka; Irina A Shkel; Scott Cayley; M Thomas Record; James C Weisshaar
Journal:  J Bacteriol       Date:  2006-09       Impact factor: 3.490

6.  Surface viscoelasticity of individual gram-negative bacterial cells measured using atomic force microscopy.

Authors:  Virginia Vadillo-Rodriguez; Terry J Beveridge; John R Dutcher
Journal:  J Bacteriol       Date:  2008-04-11       Impact factor: 3.490

7.  Adaptor protein mediates dynamic pump assembly for bacterial metal efflux.

Authors:  Ace George Santiago; Tai-Yen Chen; Lauren A Genova; Won Jung; Alayna M George Thompson; Megan M McEvoy; Peng Chen
Journal:  Proc Natl Acad Sci U S A       Date:  2017-06-12       Impact factor: 11.205

Review 8.  Popping the cork: mechanisms of phage genome ejection.

Authors:  Ian J Molineux; Debabrata Panja
Journal:  Nat Rev Microbiol       Date:  2013-02-04       Impact factor: 60.633

9.  Distribution of mechanical stress in the Escherichia coli cell envelope.

Authors:  Hyea Hwang; Nicolò Paracini; Jerry M Parks; Jeremy H Lakey; James C Gumbart
Journal:  Biochim Biophys Acta Biomembr       Date:  2018-09-29       Impact factor: 3.747

10.  Cytoplasmic protein mobility in osmotically stressed Escherichia coli.

Authors:  Michael C Konopka; Kem A Sochacki; Benjamin P Bratton; Irina A Shkel; M Thomas Record; James C Weisshaar
Journal:  J Bacteriol       Date:  2008-10-24       Impact factor: 3.490

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