Bi110 Cell Concepts-1
Bi110 Cell Concepts-1
• Resolving power
– is the ability of the microscope to reveal fine detail
of the specimen
• Resolving power is determined by:
– The wavelength of light, power of the objective and
ocular lenses
• Therefore, microscopes are essential tools for
studying cell structures
• transmission electron microscope (TEM)
designed to reveal internal structures of the
specimen.
1. Multicellularity.
• All prokaryotes are fundamentally single-celled
in comparison to multicellular eukaryotes
• 2. Cell size - Most prokaryotic cells are only 1
micrometer or less in diameter. Most
eukaryotic cells are well over 10 times that size.
• 3. Chromosomes - Eukaryotic cells have a
membrane-bound nucleus containing
chromosomes made up of both nucleic acids
and proteins. Prokaryotes do not have
membrane-bound nuclei. Instead, their naked
circular DNA is localized in a zone of the
cytoplasm called the nucleoid.
• 4. Cell division and genetic recombination -
Cell division in eukaryotes takes place by
mitosis and involves spindles made up of
microtubules. Cell division in prokaryotes
takes place mainly by binary fission
Binary Fission in Prokaryotes
Mitosis in Eukaryotes
• 5. Internal compartmentalization. In
eukaryotes, the enzymes for cellular
respiration are packaged in mitochondria. In
bacteria, the corresponding enzymes are not
packaged separately but are bound to the cell
membranes. The cytoplasm of prokaryotes,
unlike that of eukaryotes, contains no internal
compartments or cytoskeleton and no
organelles except ribosomes.
• 6. Flagella. Prokaryote flagella are simple in
structure, composed of a single fibre of the
protein flagellin, spinning like propellers.
Eukaryotic flagella are complex have a whip-like
motion.
• 7. Metabolic diversity. Only one kind of
photosynthesis occurs in eukaryotes, and it
involves the release of oxygen. Prokaryotes have
several different patterns of anaerobic and
aerobic photosynthesis, involving the formation of
end products such as sulphur, sulphate, and
oxygen
BACTERIA
• all bacteria may be classified into two types
based on differences in their cell walls
detected by the Gram staining procedure.
• Danish microbiologist Hans Christian Gram,
who developed the procedure to detect the
presence of certain disease-causing bacteria.
• Two types of bacteria can be identified using a
staining process called the Gram stain, hence
their names.
• Most bacteria are encased by a strong cell
wall composed of peptidoglycan, which
consists of a carbohydrate matrix (polymers of
sugars)
• Gram-positive bacteria have a thick, single-
layered cell wall that retains a violet dye from
the Gram stain procedure, causing the stained
cells to appear purple under a microscope.
• whereas the Gram-negative bacteria contain
less peptidoglycan and do not retain the
purple-coloured dye.
• These gram-negative bacteria can be stained
with a red counter-stain and then appear dark
pink
Gram stain test
• Gram stain testing is a method for classifying bacteria based on their cell
wall. It allows scientists to determine whether an organism is gram-
positive or gram-negative. The test, which uses a microscope, was created
by Hans Christian Gram in 1884.
1. Gently flood the smear with crystal violet and leave for 1 minute.
Tilt the slide slightly and gently rinse with tap water or distilled
water.
2. Gently flood the smear with Gram’s iodine and leave for 1
minute. Tilt the slide slightly and gently rinse with tap water or
distilled water. The smear will now appear purple.
Decolorizer dehydrates the peptidoglycan layer, shrinking and tightening it. In Gram
positive bacteria, the large crystal violet-iodine complexes are then unable to
penetrate and escape the thick peptidoglycan layer, resulting in purple stained cells.
However, in Gram negative bacteria, the outer membrane is degraded, the thin
peptidoglycan layer is unable to retain the crystal violet-iodine complexes and the
color is lost.
4. Gently flood with safranin counterstain and leave for 45 seconds. Tilt the
slide slightly and gently rinse with tap water or distilled water.
Safranin is weakly water soluble and will stain bacterial cells a light red, enabling
visualization of Gram negative cells without interfering with the observation of the
purple of the Gram positive cells.
5. Blot the slide dry on filter paper then view the smear using a light-
microscope under oil-immersion.
• Though both groups of bacteria can cause
disease, they require different treatments. If
you have a bacterial infection, the Gram stain
will determine what kind of medication you
need.
• The major difference is the outer lipid membrane. It’s
difficult to penetrate, which gives gram-negative
bacteria extra protection. Gram-positive bacteria don’t
have this feature.
• Because of this difference, gram-negative bacteria are
harder to kill. This means gram-positive and gram-
negative bacteria require different treatments.
• Though gram-negative bacteria are harder to destroy,
gram-positive bacteria can still cause problems. Many
species result in disease and require specific antibiotics.