Cell envelope

The cell envelope comprises the inner cell membrane and the cell wall of a bacterium. In gram-negative bacteria an outer membrane is also included.^[1] This envelope is not present in the Mollicutes where the cell wall is absent.

Bacterial cell envelopes fall into two major categories: a gram-positive type and a gram-negative type, distinguished by Gram staining. Either type may have an enclosing capsule of polysaccharide for extra protection. As a group these are known as polysaccharide encapsulated bacteria.

Contents

• 
  1 Function
  


• 
  2 Types of bacterial cell envelopes
  
  
  
  • 
    2.1 The gram-positive cell wall
    
  
  
  • 
    2.2 The gram-negative cell wall
    
  
  
  • 
    2.3 Mycobacteria (Acid-fast bacteria)
    
  
  
  • 
    2.4 Bacteria lacking cell wall
    
  
  
  
  


• 
  3 See also
  


• 
  4 References
  

Function

As in other organisms, the bacterial cell wall provides structural integrity to the cell. In prokaryotes, the primary function of the cell wall is to protect the cell from internal turgor pressure caused by the much higher concentrations of proteins and other molecules inside the cell compared to its external environment. The bacterial cell wall differs from that of all other organisms by the presence of peptidoglycan (poly-N-acetylglucosamine and N-acetylmuramic acid), which is located immediately outside of the cytoplasmic membrane. Peptidoglycan is responsible for the rigidity of the bacterial cell wall and for the determination of cell shape. It is relatively porous and is not considered to be a permeability barrier for small substrates. While all bacterial cell walls (with a few exceptions e.g. intracellular parasites such as Mycoplasma) contain peptidoglycan, not all cell walls have the same overall structures. This is notably expressed through the classification into gram positive and gram negative bacteria.

Types of bacterial cell envelopes

The gram-positive cell wall

Schematic of typical gram-positive cell wall showing arrangement of N-Acetylglucosamine and N-Acetylmuramic acid; Teichoic acids not shown.

The gram-positive cell wall is characterised by the presence of a very thick peptidoglycan layer, which is responsible for the retention of the crystal violet dyes during the Gram staining procedure. It is found exclusively in organisms belonging to the Actinobacteria (or high %G+C gram-positive organisms) and the Firmicutes (or low %G+C gram-positive organisms). Bacteria within the Deinococcus-Thermus group may also exhibit gram-positive staining behaviour but contain some cell wall structures typical of gram-negative organisms. Imbedded in the gram-positive cell wall are polyalcohols called teichoic acids, some of which are lipid-linked to form lipoteichoic acids. Because lipoteichoic acids are covalently linked to lipids within the cytoplasmic membrane they are responsible for linking the peptidoglycan to the cytoplasmic membrane. Teichoic acids give the gram-positive cell wall an overall negative charge due to the presence of phosphodiester bonds between teichoic acid monomers.

Outside the cell wall, many Gram-positive bacteria have an S-layer of "tiled" proteins. The S-layer assists attachment and biofilm formation. Outside the S-layer, there is often a capsule of polysaccharides. The capsule helps the bacterium evade host phagocytosis. In laboratory culture, the S-layer and capsule are often lost by reductive evolution (the loss of a trait in absence of positive selection).

The gram-negative cell wall

Schematic of typical gram-negative cell wall showing arrangement of N-Acetylglucosamine and N-Acetylmuramic acid and the outer membrane containing lipopolysaccharide.

Unlike the gram-positive cell wall, the gram-negative cell wall contains a thin peptidoglycan layer adjacent to the cytoplasmic membrane, which is responsible for the cell wall's inability to retain the crystal violet stain upon decolourisation with ethanol during Gram staining. In addition to the peptidoglycan layer the gram-negative cell wall also contains an additional outer membrane composed by phospholipids and lipopolysaccharides which face into the external environment. The highly charged nature of lipopolysaccharides confer an overall negative charge to the gram -negative cell wall. The chemical structure of the outer membrane lipopolysaccharides is often unique to specific bacterial strains (i.e. sub-species) and is responsible for many of the antigenic properties of these strains.

As a phospholipid bilayer, the lipid portion of the outer membrane is largely impermeable to all charged molecules. However, channels called porins are present in the outer membrane that allow for passive transport of many ions, sugars and amino acids across the outer membrane. These molecules are therefore present in the periplasm, the region between the plasma membrane and outer membrane. The periplasm contains the peptidoglycan layer and many proteins responsible for substrate binding or hydrolysis and reception of extracellular signals. The periplasm is thought to exist as a gel-like state rather than a liquid due to the high concentration of proteins and peptidoglycan found within it. Because of its location between the cytoplasmic and outer membranes, signals received and substrates bound are available to be transported across the cytoplasmic membrane using transport and signalling proteins imbedded there.

In nature, many uncultivated Gram-negative bacteria also have an S-layer and a Capsule (microbiology). These structures are often lost during laboratory cultivation.

Mycobacteria (Acid-fast bacteria)

The Mycobacteria have a cell envelope which is not typical of gram-positives or gram-negatives. The mycobacterial cell envelope does not consist of the outer membrane characteristic of gram-negatives, but has a significant peptidoglycan-arabinogalactan-mycolic acid wall structure which provides an external permeability barrier. Therefore, there is thought to be a distinct 'pseudoperiplasm' compartment between the cytoplasmic membrane and this outer barrier. The nature of this compartment is not well understood.^[2]Acid-fast bacteria, like Mycobacteria, are resistant to decolorization by acids during staining procedures. The high mycolic acid content of Mycobacteria, is responsible for the staining pattern of poor absorption followed by high retention. The most common staining technique used to identify acid-fast bacteria is the Ziehl-Neelsen stain or acid-fast stain, in which the acid fast bacilli are stained bright red and stand out clearly against a blue background.

Bacteria lacking cell wall

The obligate intracellular bacteria in family Chlamydiaceae are unique in their morphology as they do not contain detectable amounts of peptidoglycans.^[3] However, the extracellular forms of these gram-negative bacteria maintain their structural integrity because of a layer of disulfide bind cross-linked layer of cysteine-rich proteins, which is located between cytoplasmic membrane and outer membrane in a manner analogous to peptidoglycan layer in other gram-negative bacteria.^[4] In the intracellular forms of the bacterium the disulfide cross linkage is not found, which confers this form more mechanically fragile.

The cell envelopes of the bacterial class of mollicutes do not have a cell wall.^[5] The main pathogenic bacteria in this class are mycoplasma and ureaplasma.^[5]

L-form bacteria are strains bacteria that lack cell walls derived from bacteria that normally possess cell walls.^[6]

See also

Viral envelope

References

1. 
   ^ "envelope" at Dorland's Medical Dictionary
   
   


2. 
   ^ IC Sutcliffe, DJ Harrington.Lipoproteins of mycobacterium tuberculosis: an abundant and functionally diverse class of cell envelope components. FEMS Microbiology Reviews 28 (2004) 645-759
   


3. 
   ^ Chopra I, Storey C, Falla TJ, Pearce JH. Antibiotics, peptidoglycan synthesis and genomics: the chlamydial anomaly revisited. Microbiology. 1998 144 ( Pt 10):2673-8.
   


4. 
   ^ Hatch TP. Disulfide cross-linked envelope proteins: the functional equivalent of peptidoglycan in chlamydiae? J. Bacteriol. 1996 178:1–5.
   


5. 
   ^ ^ab Rottem S (April 2003). "Interaction of mycoplasmas with host cells". Physiol. Rev. 83 (2): 417–32. doi:10.1152/physrev.00030.2002. PMID 12663864..mw-parser-output cite.citation{font-style:inherit}.mw-parser-output q{quotes:"""""""'""'"}.mw-parser-output code.cs1-code{color:inherit;background:inherit;border:inherit;padding:inherit}.mw-parser-output .cs1-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-limited a,.mw-parser-output .cs1-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration{color:#555}.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration span{border-bottom:1px dotted;cursor:help}.mw-parser-output .cs1-hidden-error{display:none;font-size:100%}.mw-parser-output .cs1-visible-error{font-size:100%}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-format{font-size:95%}.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-right{padding-right:0.2em}
   


6. 
   ^ Leaver M, Domínguez-Cuevas P, Coxhead JM, Daniel RA, Errington J (February 2009). "Life without a wall or division machine in Bacillus subtilis". Nature. 457 (7231): 849–53. doi:10.1038/nature07742. PMID 19212404.
   

v t e Structures of the cell / organelles
Endomembrane system	Cell membrane Nucleus Endoplasmic reticulum Golgi apparatus Parenthesome Autophagosome Vesicle Exosome Lysosome Endosome Phagosome Vacuole Acrosome Cytoplasmic granule Melanosome Microbody Glyoxysome Peroxisome Weibel–Palade body
Cytoskeleton	Microfilament Intermediate filament Microtubule Prokaryotic cytoskeleton Microtubule organizing center Centrosome Centriole Basal body Spindle pole body Myofibril
Endosymbionts	Mitochondrion Plastid Chloroplast Chromoplast Gerontoplast Leucoplast Amyloplast Elaioplast Proteinoplast Tannosome
Other internal	Nucleolus RNA Ribosome Spliceosome Vault Cytoplasm Cytosol Inclusions Proteasome
External	Undulipodium Cilium Flagellum Axoneme Radial spoke Archaellum Cell wall Extracellular matrix

v t e Microbiology: Bacteria
Medical microbiology	infection Coley's toxins Exotoxin Lysogenic cycle Pathogenic bacteria resistance
Biochemistry and ecology	Oxygen preference Aerobic Obligate Anaerobic Facultative Obligate Microaerophile Nanaerobe Aerotolerant Other Extremophile Human flora Gut Lung Mouth Skin Vaginal (In pregnancy) Placental Uterine Salivary Microbial metabolism Nitrogen fixation Microbial ecology Primary nutritional groups Substrate preference Lipophilic Saccharophilic
Shape	Bacterial cellular morphologies Coccus Diplococcus Bacillus Coccobacillus Spiral
Structure	Cell envelope Cell membrane Cell wall: Peptidoglycan NAM NAG DAP Gram-positive bacteria only: Teichoic acid Lipoteichoic acid Endospore Gram-negative bacteria only: Bacterial outer membrane Porin Lipopolysaccharide Periplasmic space Mycobacteria only: Arabinogalactan Mycolic acid Outside envelope Bacterial capsule Slime layer S-layer Glycocalyx Pilus Fimbria Non-motile bacteria Composite Biofilm
Taxonomy	Bacteria (classifications) Bacterial phyla Former groupings: Schizomycetes Monera Prokaryota Gracilicutes Firmicutes Mollicutes Mendosicutes
Book Category Commons Portal

This page is only for reference, If you need detailed information, please check here