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- Temperature
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- The pH/temperature where the enzyme works best at
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- Catalase
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- Celery
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- Hydrogen peroxide
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- This would change the shape of the enzyme
- It would no longer join with the substrate
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- The amount of foam produced in 2 minutes
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- To allow foam to be produced
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- Product
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- Catalase
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- Celery
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- Hydrogen peroxide
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- Proteins
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- 3D
- Folded
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- Used the same buffers
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- Use different beakers with different temperatures
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- Catalase
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- Hydrogen peroxide
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- Boil celery in 100 degrees celsius for 10 minutes
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- There was no foam produced after 2 minutes
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- To keep the pH at an optimum rate so it wont affect the experiment
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- When an enzyme stops working
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- Biological catalyst that speeds up chemical reactions without being used up in the reaction
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- Unboiled celery
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- When an enzyme is fixed in an inert substance
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- Enzyme can be reused
- A purer product
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- Sodium alginate gel
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- Calcium chloride
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- Sucrase
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- Yeast
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- Sucrose solution
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- Mix sodium alginate with water in a beaker
- Mix yeast and water in another beaker
- Add yeast solution to sodium alginate and mix well
- Prepare a calcium chloride solution in a beaker
- Using syringe, add yeast + alginate mixture to calcium beaker
- Leave to sit for 10 minutes
- Remove beads and wash with distilled water
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- Yeast is respiring
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- Boiled glucose solution and let it cool to drive out any oxygen or other gases present
- Used a fermentation lock
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- Half filled with limewater
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- Milky due to CO2
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- Prevent the entry of contaminants
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- Bubbles of CO2
- Froth in the conical flask
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- No more CO2 bubbles produced
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- Iodoform test
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- Added potassium iodide solution and sodium hypochlorite solution to both test tubes
- Then heated the test tubes for 4-5 minutes
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- Formation of yellow crystals
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- Create anaerobic conditions
- Create glucose solution, boil and let it cool
- Add 250cm cubed of glucose solution to two different conical flasks
- Into one flask add 5g of yeast
- No yeast is added to the other (control)
- Add fermentation lock
- Add limewater to fermentation lock
2. Breakdown of glucose
- Add both vessels into water bath set at 25-30 degrees celcius
- Leave overnight for 24 hours
3. Test for alcohol (Ethanol)
- After 24 hours remove the fermentation lock and filter the contents
- Add some of the test filtrate into one test tube
- Add some of the control filtrate into another test tube
- Perform iodoform test (added potassium iodide solution and sodium hypochlorite solution to both test tubes)
- Warm both in water bath for 4-5 minutes
- Allow to cool and note results
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- To protect the objective lens
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- Eyepiece magnification X Objective lens magnification = total magnification
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- Adjust the lamp
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- The actual diameter will be smaller than the magnified diameter
- The total magnification is 10 x 40 = 400
- 0.8/400 = 0.002mm diameter
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- Look through the eyepiece lens
- Use the coarse focus wheel to make the class visible
- Use the fine focus wheel to sharpen the image
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- Test for the presence of protein
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- Sodium hydroxide
- Copper sulfate
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- Test for the presence of reducing sugars
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- Fats will leave a permanent/translucent stain on brown paper
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- Test for reducing sugars / benedicts test
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- Control used - benedicts added to water
- Colour - blue
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- Iodine
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- Purple
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- Stayed blue
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- Brick red
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- Stayed blue
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- Blue/black
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- Red/yellow
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- Fat (butter) left a permanent/translucent stain on brown paper
- Water did not
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- Add water to a test tube
- Add milk to another test tube
- Add biuret reagent to both test tubes
- Swirl test tubes
- Note colour change
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- Add water to test tube
- Dissolve glucose in water, in another test tube
- Add equal amounts of benedict's solution to both test tubes
- Heat both test tubes in beaker of boiling water
- Note colour change
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- Add water to a test tube
- Add starch solution to another test tube
- Add iodine to both test tubes
- Note colour change
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- Rub butter on brown paper
- Rub water on another piece of brown paper
- Leave to dry
- Note the stains left by both the water and fat
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- Used cotton swab
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- Used iodine to stain plant cell to see nucleus
- Used methylene blue to stain animal cell to see nucleus
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- Applied at a 45 degree angle to prevent air bubbles
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- To protect the cell
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- Prevent the cell from drying out
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- The nucleus was more visible when stained
- Darker in colour
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- Breaks down the lipids in the phospholipid bilayer
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- TO ensure DNA is insoluble
- If DNA was room temp it would be soluble
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- Clumps together the DNA
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- To denature the enzymes that breakdown DNA
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- Breakdown proteins that surround DNA
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- Pineapple juice
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- Kiwi
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- Chop up kiwi
- To breakdown cell wall and membrane
‣
- An enzyme that breaks down proteins into amino acids
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- Slid down the side of test tube using a pipette
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- To further breakdown cell walls and membrane
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- If used for any longer it would destroy the DNA
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- Prevent the breakdown of DNA
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- Large cellular debris
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- DNA and protein
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- To act as a semi-permeable membrane
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- The final mass of the visking tubing was heavier than the initial mass
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- Cut 2 pieces of visking tubing
- Tie one end of both
- Fill one with sucrose solution (sugar) and water
- Fill other with water
- Use weighing scales to get initial mass
- Place each in separate beakers
- After 20 mins remove, dry and re-weigh for final mass
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- Visking tubing with sucrose solution increased in size by osmosis
- Final mass increased when compared to initial mass
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- Chloroplast
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- Because it doesn't require light
‣
- Elodea
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- It can survive under water
- Produces bubbles of oxygen gas
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- The number of bubbles counted every minute
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- Catalase
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- Celery
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- Move the lamp closer or further from the elodea
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- As the light increases, the rate of photosynthesis increases
- The rate levels off due to light saturation
- The plant has reached its maximum rate of photosynthesis
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- Supply carbon to produce glucose
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- To supply protons and electrons
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- Carbon dioxide levels
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- Saturate the water with sodium bicarbonate
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- Temperature
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- Used a water bath
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- Miscounting
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- Recount
- Double check answer with another person counting also
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- Monitors for biodiversity
- Detects any potential problems such as pollution
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- Habitat - where an organism lives
- Ecosystem - organisms interacting with their environment
‣
- A key
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- Dasies
- Grass
- Clover
- Dock leaves
- Nettles
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- Ladybirds
- Greenfly
- Spider
- Slug
- Mice
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- Used to suck organisms into a jar
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- Spiders
- Insects
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- Placed under a bush/hedge/tree
- Shake bush/hedge/tree
- Note insects that fall onto the tray
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- Spiders
- Insects
- Caterpillars
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- Hole is made in the ground
- Covered to stop rain entering
‣
- Insects
- Snails
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- Bait is placed in a box
- Has a trap door which allows animals in but not out
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- Shrews
- Mice
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- A piece of wood / log is placed on the ground and left for some time
- Collects animals that prefer dark or moist conditions
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- Slugs
- Snails
- Worms
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- Species - Daisies (or any flora)
- Throw a pencil over your shoulder for random selection
- Place a quadrant where the pencil lands and count the number of daisies
- Repeat this process 9 more times to get an average
- Put results into a table and graph the percentage cover of the daisies
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- Line Transect Experiment
- A rope is marked at intervals
- Each interval is known as a station
- The type of plant touching each station along the rope is recorded
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- Capture-recapture Method
- Species - Snail
- Set up a pitfall trap
- Leave for 24 hours (overnight)
- Come back and count the snails present in the pitfall trap
- Mark the snails with a non-toxic paint and release them
- Return the following day and count the snails again
- Count and record the amount of new snails and previously marked snails
- Use the formula Count 1 x Count 2 to find the total population of snails
Already marked on count 2
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- Any of the following :
- Rainwater
- Wind
- Light
- Water
- pH
‣
- Water
- Used a rain gauge
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- Rhizopus
‣
- Rhizopus is multicellular, yeast is unicellular
- Rhizopus has hyphea, yeast does not
‣
- Wash lab bench with disinfectant
- Flame tweezers
- Wear gloves
‣
- Malt agar
‣
- Stored the correct side up for 24 hours
- Then upside down in an incubator at 25 degrees for 5 days
‣
- Pink colonies
‣
- Sycamore leaf
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- Unopened petri dish
‣
- The time of year
- Leaf yeast is more plentiful in the summer months than in the winter
- This is due to temperature conditions being warmer in the summer for optimum enzyme activity
‣
- Malt
‣
- Flame tweezers to sterilise
- Attach the leaf to lid using vaseline
- Replace the lid
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- Eukaryotic
‣
- A source of nutrients
‣
- Soaked in disinfectant
‣
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- Between the right atrium and the right ventricle
‣
- Cut through the right side of the heart using a scalpel
‣
- At the base of the aorta and pulmonary artery
‣
- Thoracic cavity
‣
- Heart muscle doesn't tire
‣
- Identify the front and the back
- Wearing gloves - use a scalpel to cut the righthand side to view the right atrium and right ventricle
- Cut the left hand side to view the left atrium and left ventricle
‣
- It can shorten, or contract
‣
- Left ventricle
- Because this chamber pumps blood around the entire body (except the lungs)
‣
- Prevent the backflow of blood into the heart
‣
- At the aorta
‣
‣
- The expansion of an artery
‣
- The arteries are near the surface
‣
- The resting pulse rate
‣
- For comparison
‣
- Immediately start counting the pulse after the exercise
- Measure the length of time until resting rate is reached
‣
‣
- Two seed leaves present
‣
- Celery
‣
- To allow light to pass through in order to view the cells clearly
‣
- Use a scalpel
- Cut away from the body
‣
- Use a paintbrush or tweezers
‣
- Fine focus wheel
‣
‣
- Monocots vascular bundles are scattered, dicots are circular
‣
- It is softer, making it easier to cut
‣
‣
- To make different concentrations of IAA
‣
- To measure the shoot and root growth more accurately
‣
- Expose seeds to different concentrations of IAA
- Have one set of seeds with no IAA (control group)
- Leave for 5 days
- Measure the growth
- Compare to control
‣
- The higher the IAA concentration - the greater the shoot growth
- The lower the IAA concentration - the greater the root growth
‣
- IAA
‣
- A growth response to a stimulus
‣
- Controls the growth of a plant
‣
- Raddish seeds
‣
- Water or no IAA
‣
- Auxin
‣
- Auxin
‣
- Use gloves and goggles
‣
‣
- Put oil over the boiled and cooled water
‣
- Roots and shoots were observed
‣
- Three fatty acids and a glycerol
‣
- A period of low metabolism in which little or no growth activity occurs
‣
- Cotyledon or endosperm
‣
- Water
- Oxygen
- Suitable temperature
‣
- To kill any microorganisms
‣
- Removed oxygen (using boiled water and oil) and compare to seeds with oxygen
‣
- The growth of a seed
‣
‣
- To make nutrients soluble for the embryo
‣
- Amylase
‣
- To soften the testa and metabolic activity
‣
- To kill all microorganisms
‣
- To expose the enzyme to the substrate (starch)
‣
- No clear areas
- Blue/black present everywhere
‣
- The enzyme (amylase) had been denatured