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.
The Gram-positive cell wall is characterized 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.
Bacteria within the Deinococcota group may also exhibit Gram-positive staining behavior but contain some cell wall structures typical of Gram-negative organisms.
In laboratory culture, the S-layer and capsule are often lost by reductive evolution (the loss of a trait in absence of positive selection).
As a phospholipid bilayer, the lipid portion of the outer membrane is largely impermeable to all charged molecules.
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.
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.
The obligate intracellular bacteria in the family Chlamydiaceae are unique in their morphology as they do not contain detectable amounts of peptidoglycan in the cell wall of their infectious forms.
[3] Instead, the extracellular forms of these Gram-negative bacteria maintain their structural integrity by relying on a layer of disulfide bond cross-linked cysteine-rich proteins, which is located between cytoplasmic membrane and outer membrane in a manner analogous to the peptidoglycan layer in other Gram-negative bacteria.