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Miss Estruch
Topic 2
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Cell membrane
function:
Selectively permeable
barrier
controls passage of substances in and out the cell
barrier between internal and external cell environments
Nucleus
Structure:
Nuclear
pores,
nucleolus
, DNA and
nuclear
envelope
Nucleus
Function:
Site of
transcription
& premRNA splicing - mRNA production
site of
DNA replication
nucleolus makes
ribosomes
nuclear pore allows movement of substances to/from
cytoplasm
Mitochondria
Function:
Site of
aerobic
respiration
produces
ATP
Chloroplast
structure:
Thylakoid
membranes stacked to form
grana
, linked by
lamellae
stroma
contains enzymes
contains
starch
granules, small circular
DNA
and 70S ribosomes
Chloroplast
function: Chlorophyll absorbs light for
photosynthesis
to produce organic molecules (glucose)
Organisms containing chloroplasts:
Plants
and
algae
Golgi
apparatus stucture:
Fluid-filled, membrane-bound sacs (
horseshoe
shaped)
vesicles
at edge
Lysosome structure: Type of
Golgi vesicle
containing
digestive enzyme
Lysosome
function:
Contains
digestive enzymes
e.g
lysozymes
to hydrolyse pathogens/cell waste products
Rough endoplasmic reticulum function:
Site of
protein synthesis
folds
polypeptides
to secondary & tertiary structures
packaging into
vesicles
to transport to Golgi
Smooth endoplasmic reticulum
function:
Synthesises
and
processes lipids
Ribosome
function: Site of translation in
protein synthesis.
Rough
endoplasmic reticulum structure:
System of
membranes
with bound ribosomes
continuous with
nucleus
Smooth
endoplasmic reticulum structure: System of membranes with
no bound ribosomes
Cell wall
structure:
In
plant
,
fungal
and
bacterial
cells
plants - made of
microfibrils
of
cellulose
fungi - made of
chitin
bacteria -
murein
Contrast prokaryotic & eukaryotic cells:
Prokaryotic cells are
smaller
prokaryotes have no
membrane bound organelles
prokaryotes have smaller
70S
ribosomes
prokaryotes have
no
nucleus - circular DNA not associated with histones
prokaryotic cell wall made of
murein
instead of
cellulose
/
chitin
Occasional features of prokaryotes:
Plasmids
- loops of DNA capsule surrounding
cell wall
- helps agglutination + adds protection
flagella
for
movement
Cell vacuole function:
Makes cells
turgid
-
structural support
temporary store of
sugars
,
amino acids
coloured pigments
attract
pollinators
Protein carriers:
Bind
with a molecule, e.g. glucose, which causes a change in the
shape
of the protein
this change in shape enables the molecule to be
released
to the other side of the membrane
Features of
viruses
:
Non
living
and
acellular
contain genetic material, capsid and attachment proteins
some (HIV) contain a
lipid
envelope + enzymes (reverse transcriptase)
3 types of microscopes:
Optical
(light) microscopes
Scanning electron
microscopes (SEM)
Transmission electron
microscopes (TEM)
Magnification
: How many times
larger
the image is compared to the object
Optical microscopes
:
Beam of
light
used to create image
glass lens
used for focusing
2D coloured
image produced
Evaluate
optical microscopes:
Poorer resolution
as long wavelength of light - small organelles not visible
lower
magnification
can view
living
samples
simple
staining method
vaccum
not required
Transmission electron microscopes:
Beam of
electrons
passes through the sample used to create an
image
focused using
electromagnets
2D
,
black
&
white
image produced
can see
internal ultrastructure
of cell
structures
absorb electrons
and appear
dark
Evaluation TEMs:
Highest
resolving power
high
magnification
extremely
thin
specimens required
complex
staining method
specimen must be
dead
vaccum
required
Scanning electron microscopes:
Beam
of
electrons pass
across
sample
used to create
image
focused using
electromagnets
3D
,
black
and
white image
produced
electrons scattered
across
specimen
producing
image
Evaluation SEM:
High
resolving power
high
magnification
thick
specimens usable
complex
staining method
specimen must be
dead
vaccum
required
Scanning electron microscopes:
Beam of
electrons
pass across sample used to create image
focused using
electromagnets
3D
,
black
and
white
image produced
electrons
scattered
across specimen producing image
Why calibrate eyepiece graticule?
Calibration of the eyepiece is required each time the objective
lens
is changed
Calibrate to work out the
distance
between each
division
at that magnification
Purpose of cell fractionation:
Break open cells
& remove cell debris
so
organelles
can be studied
Homogenisation conditions:
Cold
reduces enzyme activity preventing organelle digestion
Isotonic
prevents movement of water by osmosis - no
bursting
/ shrivelling of organelles
Buffered resists pH changes preventing organelle + enzyme damage
Ultracentrifugation
:
Homogenate solution
filtered
to remove cell debris
solution
placed in a
centrifuge
which
spins
at a low speed initially
then increasingly faster speeds to separate organelles according to their
density
Differential
centrifugation
:
Supernatant first out (spun at lowest speed) is most
dense
=
nuclei
spun at higher speeds
chloroplasts -> mitochondria -> lysosomes -> RER/SER ->
ribosomes
(least dense)
Binary Fission:
Involves
circular
DNA &
plasmids
replicating
cytokinesis
creates two daughter nuclei
each daughter cell has one copy of
circular
DNA and a variable number of
plasmids
Cell cycle:
Interphase
(G1, S, G2)
Nuclear division
- mitosis or meiosis
Cytokinesis
Interphase
:
Longest
stage in the cell cycle
when DNA replicates (S-phase) and organelles duplicate while cell grows (G1&G2-phase)
DNA replicates and appears as
two sister
chromatids
held by
centromere
Mitosis
:
One round of cell division
two
diploid
, genetically
identical
daughter cells
growth and
repair
(e.g. clonal expansion)
comprised of
prophase
,
metaphase
,
anaphase
and
telophase
Prophase
:
Chromosomes
condense
and become
visible
nuclear envelope
disintegrates
in animals - centrioles separate &
spindle fibre
structure forms
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