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What are the distinguishing features of eukaryotic cells?
cytoplasm containing membrane-bound organelles
so DNA enclosed in a nucleus
Describe the general structure of eukaryotic cells
cell surface membrane
mitochondrion
nucleus
ribosomes
roughendoplasmic reitculum
smooth endoplasmic reticulum
golgi apparatus
lysosome
plant only: chloroplast, cell wall, cell vacuole
Describe the structure of the cell-surface membrane
hydrophilic phosphate heads
point to / are attracted to water
hydrophobic fatty acid tails
point away from / are repelled from water
form a phospholipid bilayer
protein may span the width of the bilayer, or only partially
Describe the function of the cell-surface membrane
selectively permeable → enables control of passage of substances in / out of the cell
molecules / receptors / antigens on surface → allow cell recognition / signalling
Describe the structure of the nucleus
Nuclear envelope:
double membrane
has nuclear pores
Nucleoplasm
Nucleolus (dense region)
Protein / histone bound linear DNA
chromatin = condensed
chromosome = highly condensed
Describe the function of the nucleus
holds / stores genetic information which codes for polypeptides
site of DNA replication
site of transcription, producing mRNA
nucleolus makes ribosomes / rRNA
Describe the structure of a ribosome
made of ribosomal RNA and protein (2 subunits)
not a membrane bound organelle
Describe the function of a ribosome
site of protein synthesis (translation)
Describe the structure of rER and sER
system of membranes
rER has ribosomes
Describe the function of rER
ribosome on surface synthesise proteins
proteins processed / folded / transported inside rER
Describe the function of sER
synthesises and processes lipids
e.g. cholesterol and steroid hormones
Describe the structure of Golgi apparatus and Golgi vesicles
apparatus: flattened membrane sacs
vesicle: small membrane sac
Describe the function of Golgi apparatus
modifies protein, e.g. adds carbohydrates to produce glycoproteins
modifies lipids, e.g. add carbohydrates to make glycolipids
packages proteins / lipids into Golgi vesicles
produces lysosomes (a type of Golgi vesicle)
Describe the function of Golgi vesicles
transports proteins . lipids to their required destination
e.g. moves to and fuses with cell-surface membrane
Describe the structure of lysosomes
membrane
hydrolytic enzymes
Describe the function of lysosomes
release hydrolytic enzymes (lysozymes)
to break down / hydrolyse pathogens or worn-out cell components
Describe the structure of mitichondria
outer membrane
cristae - inner membrane fold
matrix, containing
small 70s ribosomes
circular DNA
Describe the function of mitochondria
site of aerobic respiration
to produce ATP for energy release
e.g. for protein synthesis / vesicle movement / active transport
Describe the structure of chloroplasts in plants and algae
double membrane
stroma, containing:
thylakoid membrane
small / 70s mribosomes
circular DNA
starch granules / lipid droplets
lamella- thylakoid linking grana
grana - stacks of thylakoid
Describe the function of chloroplasts in plants and algae
absorbs light energy for photosynthesis
to produce organic substances e.g. carbohydrates / lipids
Describe the structure of the cell wall in plants, algae and fungi
● Composed mainly of cellulose (a polysaccharide) in plants / algae
● Composed of chitin (a nitrogen-containing polysaccharide) in fungi
Describe the function of the cell wall in plants, algae and fungi
● Provides mechanical strength to cell
● So prevents cell changing shape or bursting under pressure due to osmosis
Describe the structure of the cell vacuole in plants
tonoplast membrane
cell sap
Describe the function of the cell vacuole in plants
● Maintains turgor pressure in cell (stopping plant wilting)
● Contains cell sap → stores sugars, amino acids, pigments and any waste chemicals
Name the three groups eukaryotic cells are organised into in complex multicellular organisms
tissues
organs
organ systems
Describe a tissue
Group of specialised cells with a similar structure working together to perform a specific function, often with the same origin.
Describe an organ
Aggregations of tissues performing specific functions.
Describe an organ system
Group of organs working together to perform specific functions
Describe how you can apply your knowledge of cell features / organelles to explain adaptations of eukaryotic cells
General answer format:
● [Named cell] has many [named organelle, eg. ribosomes]
● To [link organelle function to cell function eg. increase rate of protein synthesis, making many antibodies]
What are the distinguishing features of prokaryotic cells?
● Cytoplasm lacking membrane-bound organelles
● So genetic material not enclosed in a nucleus
Describe the general structure of prokaryotic cells
Always present:
cell-surface membrane
cell wall - contain murein, a glycoprotein
cytoplasm
small ribosomes
circular DNA
free in cytoplasm
not associated with proteins
Sometimes present
capsule
plasmids - small rings of DNA
flagella
Compare and contrast the structure of eukaryotic and prokaryotic cells
membrane bound organelles: E has them, P does not
nucleus: E has one, P does not
shape of DNA: E has long, straight and linear with associated histones, P has short and circular with no associated histones
ribosomes: E has larger 80s in cytoplasm, P only has smaller 70s
cell walls: E only in plants, algae, and fungal cells and contains cellulose or chitin, P always has a cell wall containing murein
plasmids/ capsule: E never has these, P sometimes does
flagella: both E and P sometimes have this
size: E is larger, P is much smaller
Explain why viruses are described as acellular and non-living
● Acellular - not made of cells, no cell membrane / cytoplasm / organelles
● Non-living - have no metabolism, cannot independently move / respire / replicate / excrete
Describe the general structure of a virus particle
1. Nucleic acids surrounded by a capsid
(protein coat)
2. Attachment proteins allow attachment
to specific host cells
3. No cytoplasm, ribosomes, cell wall,
cell-surface membrane etc.
4. Some also surrounded by a lipid
envelope eg. HIV
Describe the difference between magnification and resolution
● Magnification = number of times greater image is than size of the real (actual) object
○ Magnification = size of image / size of real object
● Resolution = minimum distance apart 2 objects can be to be distinguished as separate objects
describe the principles and limitations of an optical microscope
light focused using glass lenses
light passes through specimen, different structure absorb different amount & wavelengths of light
generates a 2D image of a cross-section
low resolution due to long wavelength of visible light
can’t see internal structure of organelles or ribosomes
specimen = thin
low magnification (x 1500)
can view living organisms
simple preparation
can show colour
describe the principles and limitations of a transmission electron microscope
electrons focused using electromagnets
electrons pass through specimen, denser parts absorb more and appear darker
generates a 2D image of a cross-section
very high resolution due to short wavelength of electrons
can see internal structures of organelles and ribosomes
specimen = very thin
high magnification (x 1,000,000)
can only view dead / dehydrated specimens as uses a vacuum
complex preparation so artefacts often present
does not show colour
describe the principles and limitations of a scanning electron microscope
electrons focused using electromagnets
electrons deflected / bounce off specimen surface
generates a 3D image of surface
high resolution due to short wavelength of electrons
can’t see internal structures
specimen does not need to be thin
high magnification (x1,000,000)
can only view dead / dehydrated specimens as it uses a vacuum
complex preparation so artefacts are often present
does not show colour
List the steps in calculation involving magnification, real size, and image size
note formula . rearrange if necessary
convert units if necessary - image and actual size must be in the same unit
calculate answer and check units required or if standard form etc. is required
Describe hoe the size of an object viewed with an optical microscope can be measured
Line up scale of eyepiece with scale of stage micrometre
Calibrate eyepiece graticule - use stage micrometre to calculate size of divisions on eyepiece graticule
Take micrometre away and use graticule to measure how many divisions make up an object
calculate size of object by multiplying number of divisions by size of division
Recalibrate eyepiece graticule at different magnification
Describe the principles of cell fractionation and ultracentrifugation as used to separate cell components
homogenise tissue / use a blender
Place in a cool, isotonic, buffered solution
filter homogenate
ultracentrifugation - separates organelles in order of density / mass
Explain homogenising samples in cell fractionation
disrupts cell membrane, breaking open cells and releasing contents / organelles
Explain using a cold, isotonic, buffered solution in cell fractionation
cold to reduce enzyme activity → so organelles are not broken down / damaged
isotonic so water doesn’t move in or out of organelles by osmosis → so they don’t burst
buffered to keep pH constant → so enzymes don’t denature
Explain why the homogenate is filtered in cell ultracentrifugation
removes large, unwanted debris e.g. whole cells, connective tissue
Explain what ultracentrifugation does as a step in cell fractionation
centrifuge homogenate in a tube at a high speed
remoe pellet of heaviest organelle and respin supernatant at a higher speed
repeat at increasing speeds until separated out, each time pellet is made of lighter organelles
nuclei → chloroplasts / mitochondria → lysosomes → ER → ribosomes