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Biology paper 1
Cell biology
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Cards (136)
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
A way to understand how much bigger or smaller one object is compared to another
Prefixes to show multiples of units
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
Cell specialisation
The process where cells gain new sub-cellular structures to be suited to their role
Specialised animal cells
Sperm cells
Nerve cells
Muscle cells
Specialised plant cells
Root hair cells
Xylem cells
Phloem cells
Cell differentiation
The process where stem cells switch on/off genes to produce different proteins and acquire new sub-cellular structures
In animals, most cells differentiate early and lose ability to differentiate, 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
, two types (scanning and transmission), 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
A way to represent 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 solution
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, with the 'number' being between 1 and
10
Culturing microorganisms
Microorganisms
are very small, so scientists need to grow many of them in the lab using
nutrients
Components of culture medium
Carbohydrates
for
energy
Minerals
Proteins
Vitamins
Growing microorganisms in the lab
1. In
nutrient
broth solution
2. On an
agar
gel plate
Steps for making an agar gel plate
Autoclave
An oven used to sterilise
Petri
dishes and
culture
media before use
If Petri dishes and culture media are not sterilised
They are likely to be contaminated with other microorganisms
Inoculating loops are sterilised by passing through a flame
This kills unwanted microorganisms
The lid of the Petri dish is sealed but not completely
This stops airborne microorganisms from contaminating the culture, but allows oxygen to enter
The Petri dish is stored upside down
This prevents condensation from the lid landing on the agar surface and disrupting growth
The culture is incubated at 25 degrees
This prevents bacteria that could be harmful to humans from growing, as their optimum temperature is nearer 37 degrees
Bacteria can multiply by binary fission as fast as every 20 minutes
Formula to calculate number of bacteria
Bacteria at beginning x 2^(number of divisions) = bacteria at end
The number of bacteria at the end of the growth period can be very large, so it is common to leave it in standard form
Testing the effects of antibiotics on bacteria
1. Soak paper discs in different
antibiotics
and place on an
agar plate
with bacteria
2. Leave the plate at
25
degrees for
2
days
3. Measure the zone of
inhibition
around each disc
The bigger the zone of inhibition, the more
bacteria
are killed and the more effective the
antibiotic
is
To calculate cross-sectional areas (of colonies or inhibition zones), the formula is πr^2 where r is the radius
Chromosome
Contains coils of DNA, with each chromosome carrying many genes
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