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Cards (76)
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
of mineral ions
Xylem cells
Hollow tubes with
lignin
deposits to withstand
water
pressure
Lignin
deposited in spirals for
structural
support
Phloem
cells
Sieve plates
allow movement of substances between cells
Rely on
mitochondria
in companion cells for
energy
Cell differentiation
Process where stem cells switch
on/off
genes to become
specialised
cells
In animals, most cells
differentiate
early and lose ability to
differentiate
further
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
Expressing very large or small numbers by multiplying by a power of
10
, 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
Standard form
Useful when working with very
large
or
small
numbers
Using standard form
1.
Multiply
a certain number by a power of
10
to make it bigger or smaller
2. The
'number'
being multiplied needs to be 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
for
energy
Minerals
Proteins
Vitamins
Growing microorganisms in nutrient broth
1. Make a
suspension
of
bacteria
2. Mix with
sterile
nutrient broth
3. Stopper flask with
cotton wool
4.
Shake
regularly to provide
oxygen
Growing microorganisms on
agar gel plate
1. Pour hot sterilised
agar jelly
into sterilised
Petri
dish
2. Leave to
cool
and set
3. Use inoculating loops to spread
bacteria
over
agar
4.
Tape lid
on and
incubate
for a few days
Petri
dishes and culture media must be
sterilised
before use
Reason for sterilisation
To prevent
contamination
from other microorganisms that could compete for
nutrients
and space, or be harmful
Inoculating loops must be
sterilised
by passing through a
flame
Reason for sealing Petri dish lid
To stop airborne microorganisms from
contaminating
the culture, but not completely sealed to allow
oxygen entry
Reason for storing Petri dish upside down
To prevent
condensation
from the
lid
landing on the agar surface and disrupting growth
Reason for incubating at
25
degrees
To prevent
growth
of bacteria harmful to humans, whose optimum temperature is nearer
37
degrees
Testing antibiotic effectiveness
1. Soak paper discs in different
antibiotics
and place on agar plate with
bacteria
2. Leave control disc soaked in
sterile water
3. Measure size of
inhibition zone
around discs after
2
days
Inhibition zone
The clear area left when
bacteria
die, indicating
antibiotic
effectiveness
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