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what makes a good biological drawing
a to scale, clean, accurate and unshaded line drawing that shows structural features
methylene blue
stains the nucleus of animal cells blue
iodine
turns starch (usually in plant cells) blue/black
eosin
stains cytoplasm in plant cells pink
acetic orcein
stains DNA chromosomes red/ purple
how many micrometers in a milimeter
1mm= 1000µm
advantages of a light microscope
can see living plant and animal cells
relatively cheap and accessible
light and portable
disadvantages of a light microscope
preservation and staining can impact results
limited magnifying and resolving powers
Scanning electron microscopes (SEM)
electron microscope that bounces a beam of electrons across the surface to create a detailed 3D image of its external features
transmission electron microscope (TEM)
a high-resolution microscope that passes a beam of electrons through a specimen to create a 2D image
TEMs vs SEMs microscopes
Transmission electron microscopes | Scanning electron microscopes |
Electrons pass through the specimen | Electrons scan the surface |
2D flat image | 3D surface image |
Shows sub-cellular organelles | External surface shape |
Higher resolution | Lower resolution |
Why do electron microscopes have a greater resolution than light microscopes
electron beams have much smaller wavelength than light waves
how are cells organised in complex organisms
cells ->tissues ->organs -> organ systems -> organism
how to adjust the condenser
1- get a sharp pencil and place it over the light source (lamp or mirror)
2-look through the slide; if the pencil is clear the condenser is set right
condenser is adjusted by a small lever
how to calculate the magnification of a microscope image
multiply eyepiece power by objective lens power
how to measure the size of an object under a microscope
1- place stage micrometer on stage and bring line into focus
2- move stage micrometer until it collides with lines on eyepiece graticule
3- see how many graticule lines fit in the stage micrometer fit in 1mm eg. 40
4- 1mm=1000µm so 1000/40= 25µm
5- take stage micrometer away and look at specimen again. Eg if it covers 2 graticles its 50µm.
how to prepare a microscope slide
1- use a scalpel to remove a thin layer of tissue (so light can pass through)
2- pipette a drop of water on the clean glass slide to mount the sample
3- use clean forceps to place the sample flat on the water
4- add a drop of suitable stain to the specimen to increase contrast
5- place the coverslip on at a 45 degree angle using forceps
light microscope
beam of light (lamp or mirror source) through the object. Objective lens + eyepiece lens magnify and focus the specimen to be observed. course focus is adjusted to focus smaller magnification fine focus focuses higher magnification
magnification
how much bigger the image is compared to the actual size
magnification equation
magnification= image size/ actual size
resolution
how far apart 2 points can be before they are seen as 1
cell theory
all living things are made of cells formed by the division of pre-existing cells all chemical reactions of life take place in cells
Eukaryote
a cell with a nucleus and membrane bound organisms (except ribosomes)
Prokaryotes
a cell with no nucleus and non-membrane bound organelles
structure of the nucleus
double membrane, nuclear envelope, nuclear pores
function of the nucleus
stores DNA and allows substances and mRNA in/out
structure of the nucleolus
dense non-membrane area in the nucleus
function of the nucleolus
produces rRNA and makes ribosomes
structure of 80s ribosomes
40s and 60s sub-units, free or attached to RER
function on 80s ribosomes
site of protein synthesis/ translation
structure of rough endoplasmic reticulum (RER)
membrane bound flattened sacs with ribosomes attached
funtion of rough endoplasmic reticulum (RER)
synthesises folds and transports proteins for secretion, membrane/ lysosomes
structure of smooth endoplasmic reticulum (SER)
membrane bound flattened sacs, no ribosomes
function of smooth endoplasmic reticulum (SER)
lipid synthesis
structure of mitochondria
double membrane- inner folded in cristae. matrix has enzymes, mitochondrial DNA and 70s ribosomes
function of mitochondria
aerobic respiration and ATP production
structure of cetnrtioles
pair of cylindrical structures composed of microtubules
function of centrioles
organises micro tubules for spindle during cell division
structure of lysosomes
single membrane containing hydrolytic/ digestive enzymes
function of lysosomes
digests worn out organelles
structure of golgi apparatus
stack of flattened membrane bound sacs with vesicles
function of golgi apparatus
modifies, sorts and packages proteins and lipids into vesicles to be transported to and from the apparatus
structure of plant cell wall
fully permeable. made of cellulose, middle lamella binds cellulose layers together
function of a plant cell wall
supports cell, maintains shape. strong cellulose fibres prevents bursting
structure of chloroplast
double membrane, thykaloids stacked into grana, has chloroplast DNA and 70s ribosomes
function of chloroplast
grana has large surface area to take in light for photosynthesis
structure of vacuole
membrane bound sac contains water and cell sap
function of vacuole
maintains rigidity and stores water and sap
structure of tonoplast
membrane surrounding the vacuole
function of tonoplast
controls movement of water and cell sap in/out the vacuole
what is ultracentrification
spinning a sample fast to separate organelles (slow= biggest organelles, fast= smallest organelles)
what is supernatant
the fluid left over after a sample is obtained from ultracentrification ready to be spun again at a higher speed to separate the next organelle
structure of a nucleoid
region of cytoplasm in prokaryote where DNA resides. no membrane
function of a nucleoid
prokaryote- contains main genetic information, controls cell activity
structure of plasmids
small circular DNA
function of plasmids
carry additional genes giving bacteria its characteristics
structure of 70s ribosomes
made of rRNA and protein. 30s and 50s subunits
function of 70s ribosomes
site of protein synthesis/ translation
structure of prokaryote cell wall
prokaryote- rigid layer outside the cell
function of a prokaryotic cell wall
maintains cell shape and prevents bursting due to osmosis
fuction of slime coat
prevents desiccation and protects from hosts immune system
structure of slime coat/ protein capsid
sits outside cell wall
Gram positive
thick peptidoglycon layer. no outer membrane. holds crystal violet
gram negative
thin peptidoglycon layer. doesn’t hold crystal violet. does hold sasfranin (red)
plasmodesmata
small channels passing through cell walls joining plant cytoplasm together
gram stain process
1- flood sample with crystal purple
2- wash sample with alcohol
3- counter stain with safranin (red)
gram positive takes up purple- thick peptidoglycon layer absorbs it.
gram negative membrane lets in alcohol doesn’t absorb crystal violet, does absorb safranin
how are viruses classified
structure
type of nucleic acid (DNA or RNA)
DNA nucleic acid
DNA acts as a template for new DNA and mRNA to make viral proteins in host cell. Eg. lambda phage
RNA nucleic acid
contains RNA to make new RNA, no DNA
Positive single stranded RNA viruses
RNA acts as mRNA and is translated at ribosomes of the host. Eg. tobacco mosaic
Negative single stranded RNA viruses
RNA is transcribed into mRNA and translated at the ribosomes of the host. Eg. ebola
RNA retroviruses
converts RNA into double DNA using reverse transcriptase enzyme. DNA then integrated in the cells DNA. Eg. HIV
what is a virus
infectious particle made up of nucleic acid surrounded by a protein coat
viruses are not cells but are classes as living organisms because they change and evolve.
lytic cycle
1- virus attaches itself to host
2-virus uses protein and enzymes in host to replicate viral DNA
3-assembles all viral components to form virus
4- host cell bursts (lysis) and virus spreads
lysogenic/ latency cycle
1- viral DNA in the genome to form a provirus
2-viral DNA replicated when host cell divides (virus is dormant)
3-trigger eg. stress can activate viral DNA
4- then enters lytic cycle and bursts releasing virus
antivirals
inhibit virus replication:
blocking binder receptor prevents the virus from entering the host
inhibiting assembly viral components cannot reassemble
how and why to control viruses
its important to control viruses as they’re hard to treat.
control by:
preventing transmission
identify cases
isolation
appropriate infection control
Ebola 2014 outbreak
RNA virus (needs a host)
spread through guinea, liberia, sierra leone
28000 cases, 11000 deaths
How is ebola transmitted
bodily fluids:
saliva
blood
diarrhoea
why did ebola spread so much in 2014
infected people went to uninfected places
healthcare workers transmit between patients
limited heathcare resources
Ethical implications of using untested drugs during an outbreak
Strengths
may save lives
allows treatment to be tested quickly
Weaknesses
unknown risks
may feel forced to consent
what features of a virus attach to the host
spikes, bacteriophages, tail fibres, glycoproteins
function of slime coat/ protein capsid
prevents desiccation
helps bacteria stick to surfaces
protects the virus from the host´s immune system
why are antibiotics not used to treat a virus
because antibiotics inhibit bacterium´s cell wall and viruses do not have cell walls