The plasma membrane or
bacterial cytoplasmic membrane is composed of a phospholipid bilayer and thus
has all of the general functions of a cell membrane such as acting as a
permeability barrier for most molecules and serving as the location for the
transport of molecules into the cell. In addition to these functions,
prokaryotic membranes also function in energy conservation as the location
about which a proton motive force is generated. Unlike eukaryotes, bacterial
membranes (with some exceptions e.g. Mycoplasma and methanotrophs) generally do
not contain sterols. However, many microbes do contain structurally related
compounds called hopanoids which likely fulfill the same function. Unlike
eukaryotes, bacteria can have a wide variety of fatty acids within their
membranes. Along with typical saturated and unsaturated fatty acids, bacteria
can contain fatty acids with additional methyl, hydroxy or even cyclic groups.
The relative proportions of these fatty acids can be modulated by the bacterium
to maintain the optimum fluidity of the membrane (e.g. following temperature
change).
As a phospholipid bilayer,
the lipid portion of the outer membrane is impermeable to 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 cytoplasmic and outer membranes. 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 in 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.
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