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AQA Bio
Paper 1 - AQA Biology
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Cards (250)
Eukaryotes
Cells that have a
nucleus
and
membrane-bound
organelles
Prokaryotes
Cells that lack a
nucleus
and
membrane-bound
organelles
Components
of animal and plant cells
Cell membrane
Cytoplasm
Nucleus
containing
DNA
Components of bacterial cells
Cell
wall
Cell
membrane
Cytoplasm
Single circular strand of
DNA
and
plasmids
Orders of magnitude
Used to understand how much
bigger
or
smaller
one object is from another
Prefixes
Centi
(0.01)
Milli
(0.001)
Micro
(0.000,001)
Nano
(0.000,000,001)
Structures in animal and plant cells
Nucleus
Cytoplasm
Cell membrane
Mitochondria
Ribosomes
Additional structures in plant cells
Chloroplasts
Permanent vacuole
Cell wall
Structures
in
bacterial cells
Cytoplasm
Cell membrane
Cell wall
Single circular strand
of
DNA
Plasmids
Sperm cells
Streamlined head and long tail to aid
swimming
Many
mitochondria
to supply
energy
Acrosome with
digestive enzymes
to break down egg cell
membrane
Nerve
cells
Long
axon
to transmit impulses
Many
dendrites
for branched connections
Mitochondria
to supply
energy
for neurotransmitter production
Muscle
cells
Proteins
(myosin and actin) that slide over each other to cause
contraction
Many
mitochondria
to provide
energy
Can store
glycogen
for
respiration
Root
hair cells
Large
surface area for
water
and mineral ion uptake
Large
vacuole affects
water
movement speed
Mitochondria
provide energy for
active transport
Xylem
cells
Lignin
deposition
makes cells
hollow
and joined to form continuous tubes
Lignin
spirals help withstand
water pressure
Phloem
cells
Sieve plates
allow movement of substances between
cells
Companion cells provide
energy
through their
mitochondria
Cell differentiation
Process where stem cells switch
on/off
genes to produce different
proteins
and acquire specialised structures
In animals, most cells
differentiate
early and lose ability, but some like red blood cells are replaced by adult stem
cells
In plants, many cell types retain ability to
differentiate
throughout life
Light
microscope
Has two lenses (objective and eyepiece), illuminated from underneath, max magnification x2000, resolving power
200nm
Electron
microscope
Uses electrons instead of light, can be scanning (3D) or transmission (2D), max magnification x2,000,000, resolving power 10nm (SEM) and
0.2nm
(TEM)
Calculating magnification of light microscope
Magnification of
eyepiece lens
x
magnification
of objective lens
Calculating size of object
Size of
image
/
magnification
=
size
of object
Standard form
Multiplying a number by a power of
10
to represent very large or small numbers, with the 'number' between 1 and
10
Components
of culture medium
Carbohydrates
Minerals
Proteins
Vitamins
Growing
microorganisms in nutrient broth
Make suspension of
bacteria
, mix with sterile nutrient broth, stopper with
cotton wool
, shake regularly
Growing
microorganisms on agar plates
Spread bacteria suspension on
agar plate
,
seal
, incubate, colonies form
Standard
form
Multiplying a certain number by a power of
10
to make it bigger or smaller, with the 'number' being between 1 and
10
Standard form examples
1.5 x 10^
-5
=
0.000015
3.4
x 10^3 =
3400
Culturing
microorganisms
Growing many microorganisms in the lab using
nutrients
Components
of culture medium
Carbohydrates
Minerals
Proteins
Vitamins
Growing microorganisms in nutrient broth
1. Make
suspension
of
bacteria
2.
Mix
with
sterile
nutrient broth
3. Stopper flask with
cotton wool
4.
Shake
regularly
Growing
microorganisms on agar gel plate
1. Pour hot sterilised agar jelly into sterilised Petri dish
2. Allow to cool and set
3. Inoculate with microorganism using sterilised loop
4. Tape lid on and
incubate
Reasons
for sterilisation steps
Prevents
contamination
with other microorganisms
Prevents competition for
nutrients
and
space
Prevents introduction of
harmful
microorganisms
Reasons for other culturing steps
Inoculating
loops sterilised to kill
unwanted
microorganisms
Petri
dish lid sealed but not completely to allow
oxygen
Petri dish stored
upside
down to prevent
condensation
Incubated at
25°C
to prevent growth of
harmful
bacteria
Binary fission
One bacterial cell splitting into
two
Calculating bacterial population growth
1. Bacteria at
beginning
x 2^(number of divisions) = bacteria at
end
2. Number of divisions =
time
left /
mean
division time
Inhibition zone
Clear area around
antibiotic disc
where bacteria have
died
Testing antibiotic effectiveness
1. Soak paper discs in
antibiotics
and place on agar plate with
bacteria
2. Leave plate to
incubate
3. Measure size of
inhibition zones
Calculating
cross-sectional
areas involves using the formula πr^
2
Chromosomes
Contain
coils
of
DNA
and carry genes
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