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Biology Chapter 1
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Cards (67)
Eukaryotes
Cells that have a
nucleus
and
membrane-bound
organelles
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Prokaryotes
Cells that lack a
nucleus
and
membrane-bound
organelles
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Components of animal and plant cells
Cell membrane
Cytoplasm
Nucleus
containing
DNA
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Components of bacterial cells
Cell wall
Cell membrane
Cytoplasm
Single circular strand
of DNA and
plasmids
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Organelles
Structures
in a cell that have
different
functions
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Orders of magnitude
Used to understand how much
bigger
or
smaller
one object is from another
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Prefixes
Centi
(0.01)
Milli
(0.001)
Micro
(0.000,001)
Nano
(0.000,000,001)
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Structures in animal and plant cells
Nucleus
Cytoplasm
Cell membrane
Mitochondria
Ribosomes
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Additional structures in plant cells
Chloroplasts
Permanent vacuole
Cell wall
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Structures in bacterial cells
Cytoplasm
Cell membrane
Cell wall
Single circular strand
of
DNA
Plasmids
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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
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Nerve cells
Long
axon
to transmit impulses
Many
dendrites
to form branched connections
Mitochondria
to supply energy for
neurotransmitter
production
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Muscle cells
Proteins
(myosin and actin) that slide over each other to cause
contraction
Many
mitochondria
to provide
energy
Can store
glycogen
for
respiration
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Root hair cells
Large surface area
from root hairs
Large permanent vacuole
affects
water movement
Mitochondria
to provide energy for active transport of
mineral ions
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Xylem cells
Lignin
deposited to form
hollow tubes
for water/mineral transport
Lignin
deposited in spirals to withstand
pressure
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Phloem cells
Sieve plates
allow
movement
of substances between cells
Rely on
mitochondria
in companion cells for
energy
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Cell differentiation
Process where stem cells acquire new
sub-cellular structures
to become
specialised
cells
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In animals, most cells
differentiate
early and lose ability to
differentiate
further
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In plants, many cell types retain ability to
differentiate
throughout life
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Light microscope
Has
two
lenses (objective and eyepiece) to magnify and
direct
image to eye
Maximum magnification of
x2000
and resolving power of
200nm
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Electron microscope
Uses
electrons
instead of
light
to form image
Scanning
type creates 3D images,
transmission
type creates 2D images of organelles
Magnification up to
x2,000,000
and resolving power of
10nm
(SEM) and 0.2nm (TEM)
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Calculating magnification of light microscope
Magnification of
eyepiece lens x magnification of objective lens
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Calculating size of object
Size of image / magnification =
size
of
object
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Standard form
Multiplying
a number by a power of
10
to represent very large or small numbers
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Culture medium
Contains
carbohydrates
, minerals, proteins and
vitamins
to grow microorganisms
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Growing microorganisms in nutrient broth
Make suspension of
bacteria
and mix with sterile nutrient broth, stopper with
cotton wool
, shake regularly
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Growing microorganisms on agar plates
Spread
bacteria suspension
on agar plate,
seal
and incubate
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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
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Standard form examples
1.5 x 10^
-5
=
0.000015
3.4
x 10^3 =
3400
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Culturing microorganisms
Microorganisms
are very small, so scientists need to grow many of them in the lab using
nutrients
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Components of culture medium
Carbohydrates
for
energy
Minerals
Proteins
Vitamins
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Growing microorganisms in the lab
1. In
nutrient
broth solution
2. On an
agar
gel plate
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Making an
agar gel plate
involves pouring hot sterilised
agar jelly
into a sterilised Petri dish, letting it cool and set, inoculating with a wire loop, and incubating
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Sterilisation
Petri dishes and culture media must be sterilised before use, often by
autoclave
or
UV light
, to prevent contamination
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Inoculating loops
Wire loops that are sterilised by passing through a
flame
to
kill
unwanted microorganisms
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Sealing Petri dish
Lid
should be sealed but not completely, to prevent airborne contamination while allowing
oxygen entry
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Storing
Petri
dish
Upside down to prevent
condensation
from the
lid
disrupting growth
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Incubation temperature
25
degrees, to prevent growth of bacteria
harmful
to humans
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Testing
antibiotic
effectiveness
Soak paper discs in antibiotics, place on agar plate with
bacteria
, measure
inhibition
zone after incubation
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Calculating
cross-sectional
areas of colonies or inhibition zones involves using the formula πr^2, where r is the
radius
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