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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
Branched
dendrites
to form
connections
Many
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
from root hairs
Large permanent
vacuole
Mitochondria
to provide energy for
active transport
of mineral ions
Xylem cells
Lignin
deposited
to form hollow tubes
Lignin
deposited
in spirals to withstand
water pressure
Phloem cells
Sieve plates
allow movement of substances
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
Culture medium
Contains
carbohydrates
, minerals, proteins and
vitamins
to grow microorganisms
Growing microorganisms in nutrient broth
Make suspension of bacteria, mix with sterile nutrient broth, stopper with
cotton wool
,
shake regularly
Standard form
Multiplying
a certain number by a power of
10
to make it bigger or smaller
To be able to compare the size of numbers while using standard form, the 'number' which being multiplied by a power of
10
needs to be between 1 and
10
Standard form
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 solution
1. Make
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. Dip
inoculating loops
in microorganism solution and spread over agar
4.
Tape lid
on and
incubate
for a few days
Petri dishes
and culture media must be
sterilised
before use, often done by an autoclave or UV light
If this sterilisation step does not take place, they are likely to be
contaminated
with other
microorganisms
Inoculating loops must be
sterilised
by passing them through a
flame
The lid of the
Petri
dish should be
sealed
(but not completely) with tape
The Petri dish should be stored
upside down
The culture should be incubated at
25
degrees
Binary fission
One cell splitting into
two
Calculating number of bacteria after a certain time
1. Bacteria at
beginning
x 2^(number of divisions) = bacteria at
end
2. To calculate number of divisions, divide time by
mean
division time
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