B1 Flashcards
kg=g
kg=x1000=>g
mm=µm=nm
mm=x1000=>µm=x1000=>nm
m^3=dm^3=cm^3
m^3=x1000=>dm^3=x1000=>cm^3
What is the equation for magnification?
Magnification=Imange size/actual size
MIA
What is the method for microscopy?
1) Clip slide to stage
2)Select lowest powered objective lens
3)Coarse adjustment knob = to move stage to below objective lense.
4)Look down eyepiece =>objective knob=move stage downwards=roughly in focus.
5)Fine adjustment knob= clear image
6)Greater magnification= swap higher-powered objective lense= refocus
Describe Binary Fission.
What is the diffrence between Plasmids + Large circular strands of DNA
-Happens in** Prokaryotic** cell (bacteria )
-since in single celled orgainism it’s (asexula) reproduction (1=>2)
1)Circular DNA + plasmid replicate.
2)The cell=bigger+circular DNA strands move to opposit ‘poles’ of cell.
3)Cytoplasm=divide=new cell wall=form
4)Cytoplasm divid into 2x daughter cells. Each= i copy of circular DNA ( varies number of copies of plasmids).
Large circular strands of DNA- important genes
Plasmids- Non-essential
What are the optimum conditions for Bactera divison?
What else may vary the mean division time?
Warm+lots of nutrients+ moist
Species of bacteria
What is the fastest Bacteria can divide?
20mins if in right conditions if in unfavourable condtions will stop dividing+ begin to die.
A bacterial cell has a mean division time of 30 mins. How many cells will it have produced after 2.5 h
2.5h x 60=150 min
150min/30 mins= 5 divisions
2^5=32
Number of bacteria =2^n
Number of bacteria =2^n
Time there is / mean divition time=x
yX2^x=ANS
Beggining bac amount=y
What enzyme is produced in the salivary glands?
-Amylase (in saliva)
What enzyme is produced in the Liver glands?
-Where bile is produced
-Bile=neutralises stomach acid+ emulsifies fats
What is stored + prodouced in the gall bladder?
-Bile= stored
-Released=small intestine
What is the function of the Large intestine?
-Excess water= absorbed
How do you calculate the inhibition zone?
Full area of circul including disk
ikppp
What 3 things are done when making microscope slide?
- Specimin must be thin so light can pentrate so individual cells can be seen.
- Apply stain (e.g. Iodine) to see sub cellular structures
- lower slip at an angle= prevents air bubbles wich disrupt view of specimin.
What is the diffrence in a plant and animal cell?What kind of cell are they?
-Eurkryotic
Both have:
* Nucleus
* cytoplasm
* Cell menbrane
* Mitochondria
* Ribosomes
Plants also have:
* Rigid cell wall- made of cellulose supports + strenthens cell
* Permaaent vacule- cell sap(weak sloution of sugar+salt).
* Chloroplasts
What structures may a Bacterai have what kind of cell are they?
-Prokaryotes
* Cell membrane
* Cell wall
* Cytoplasm
* Single starnd of DNA
* Plasmids
* No chloroplast/ mitocondria
What is the diffrence between a light microscope and an electron microscope?
What is resolution and magnifiction?
Light microscope:
* Uses ligh + lenses
* Can see large cells + some lare subcellular structures ( nuclei)
Electron microscope:
* Use electrons to form image
* Higher magifiction than light microscopes.
* Higher resolution than light microscopes=> can see in mitocondria subcellular
Ability to distingus ebetween 2 points sharper image/clarity
How do you prepare a slide for the microscope?
What is a stain?
1)Add water drop to middle of clean slide.
2)cut onion + seperat into layers, use twezer to peel of some of the epidermal tissue from bottem of some of the layers.
3)Place emidermal tissue on slide via tweezers.
4)(if you want) add drop of iodine solution.
5)Place cover slip over.Tilt and lowr carfuly to stop air buble witch could obstruct view.
Stain can highlight obeject by adding colour.
How shoud you draw your microscope observations?
1)Draw with a sharp pencil
2)Make it take up half the space, draw with clear unbrocken lines.
3)No colouring/shading
4)Subcellular structures draw in proportion
5)Include a title of what obsevation is of + magnification
6)Straite lines to lable important features.