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The diagram of the gram-positive cell wall shows alternative NAG (N-acetylglucosamine) and NAM (N-acetylmuramic acid) in a chain; these are shown as alternative red and blue spheres. The chains or red and blue spheres are connected to other chains with smaller yellow spheres in a chain labeled pentapeptide and smaller green spheres labeled tetrapeptide. Each NAG in the chain is connected to the NAG in the chains next to it by both a tetrapeptide connected to a pentapeptide. The diagram of the gram-negative cell wall has the same NAG and NAM chains. But this time they are linked with a kirect line to the chains next to them.
Peptidoglycan is composed of polymers of alternating NAM and NAG subunits, which are cross-linked by peptide bridges linking NAM subunits from various glycan chains. This provides the cell wall with tensile strength in two dimensions.

The Gram staining protocol (see Staining Microscopic Specimens ) is used to differentiate two common types of cell wall structures ( [link] ). Gram-positive cells have a cell wall consisting of many layers of peptidoglycan totaling 30–100 nm in thickness. These peptidoglycan layers are commonly embedded with teichoic acids (TAs), carbohydrate chains that extend through and beyond the peptidoglycan layer. T.J. Silhavy, D. Kahne, S. Walker. “The Bacterial Cell Envelope.” Cold Spring Harbor Perspectives in Biology 2 no. 5 (2010):a000414. TA is thought to stabilize peptidoglycan by increasing its rigidity. TA also plays a role in the ability of pathogenic gram-positive bacteria such as Streptococcus to bind to certain proteins on the surface of host cells, enhancing their ability to cause infection. In addition to peptidoglycan and TAs, bacteria of the family Mycobacteriaceae have an external layer of waxy mycolic acids in their cell wall; as described in Staining Microscopic Specimens , these bacteria are referred to as acid-fast, since acid-fast stains must be used to penetrate the mycolic acid layer for purposes of microscopy ( [link] ).

The gram-positive bacterial cell wall diagram shows a plasma membrane on top of the cytoplasm. The cell wall is shown as a thick layer of peptidoglycans connected to the plasma membrane by techoic acids. The gram-negative cell wall also has a plasma membrane on top of the cytoplasm. On top of the plasma membrane is a thin periplasmic space. On top of that is a thin peptidoglycan cell wall. On top of that is an outer membrane that contains murein lipoproteins that connect the outer membrane to the peptidoglycan cell wall. Lipid A, O antigens, and lipopolysaccharides sit on top of the outer membrane. Proins are tubes that connect the outside of the outer membrane with the region of the peptidoglycan cell wall.
Bacteria contain two common cell wall structural types. Gram-positive cell walls are structurally simple, containing a thick layer of peptidoglycan with embedded teichoic acid external to the plasma membrane. B. Zuber et al. “Granular Layer in the Periplasmic Space of Gram-Positive Bacteria and Fine Structures of Enterococcus gallinarum and Streptococcus gordonii Septa Revealed by Cryo-Electron Microscopy of Vitreous Sections.” Journal of Bacteriology 188 no. 18 (2006):6652–6660 Gram-negative cell walls are structurally more complex, containing three layers: the inner membrane, a thin layer of peptidoglycan, and an outer membrane containing lipopolysaccharide. (credit: modification of work by “Franciscosp2”/Wikimedia Commons)
A) A diagram of gram-positive acid-fast bacteria. The plasma membrane is shown on top of the cytoplasm and a thick layer of peptidoglycan makes up the cell wall outside the plasma membrane. Teichoic acids connect the peptidoglycans to the plasma membrane. On top of the peptidoglycans are mycolic acids, lipomannan and arabinoglycans. B) A micrograph of red cells labeled acid fast bacteria.
(a) Some gram-positive bacteria, including members of the Mycobacteriaceae, produce waxy mycolic acids found exterior to their structurally-distinct peptidoglycan. (b) The acid-fast staining protocol detects the presence of cell walls that are rich in mycolic acid. Acid-fast cells are stained red by carbolfuschin. (credit a: modification of work by “Franciscosp2”/Wikimedia Commons; credit b: modification of work by Centers for Disease Control and Prevention)

Gram-negative cells have a much thinner layer of peptidoglycan (no more than about 4 nm thick L. Gana, S. Chena, G.J. Jensena. “Molecular Organization of Gram-Negative Peptidoglycan.” Proceedings of the National Academy of Sciences of the United States of America 105 no. 48 (2008):18953–18957. ) than gram-positive cells , and the overall structure of their cell envelope is more complex. In gram-negative cells , a gel-like matrix occupies the periplasmic space between the cell wall and the plasma membrane, and there is a second lipid bilayer called the outer membrane , which is external to the peptidoglycan layer ( [link] ). This outer membrane is attached to the peptidoglycan by murein lipoprotein. The outer leaflet of the outer membrane contains the molecule lipopolysaccharide (LPS) , which functions as an endotoxin in infections involving gram-negative bacteria, contributing to symptoms such as fever, hemorrhaging, and septic shock. Each LPS molecule is composed of Lipid A, a core polysaccharide, and an O side chain that is composed of sugar-like molecules that comprise the external face of the LPS ( [link] ). The composition of the O side chain varies between different species and strains of bacteria. Parts of the O side chain called antigens can be detected using serological or immunological tests to identify specific pathogenic strains like Escherichia coli O157:H7 , a deadly strain of bacteria that causes bloody diarrhea and kidney failure.

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Source:  OpenStax, Microbiology. OpenStax CNX. Nov 01, 2016 Download for free at http://cnx.org/content/col12087/1.4
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