Key concepts of Biology Flashcards
What is the difference between a eukaryotic and prokaryotic cell?
Prokaryotes cell divide by binary fission
DNA single molecule found in the cytoplasm no mitochondria
Most are 0.2 ūm-2ūm
Eukaryotes divide by mitosis have a nucleus 5ūm-100ūm
Prokaryote is a single cell
Function of sub cellular structures in an animal cell and how many it contains
Nucleus: contains genetic material which controls activities of the cell
Cytoplasm:jelly like material containing nutrients dissolved sugar and salts it is where many of the chemical reactions happen
Cell membrane:permeable to some substances not all so controls what goes in and out
Mitochondria:enzymes for respiration where most of energy is released in respiration
Ribosome:protein synthesis
What extra sub cellular features does a plant cell have?
Cell wall:made from cellulose to protect the cell
Chloroplast:contains chlorophyll which absorbs light energy for photosynthesis and the enzymes needed for photosynthesis
Permanent Vacuole:filled with cell sap to keep the cell swollen
Sub cellular features of bacteria
Chromosomal DNA:found loose in the cytoplasm w out nucleus
Plasmid DNA:small circles of DNA that can move between bacterium to another to give variation
Flagella: these rotate to or move to move the bacteria
Cell wall:protection only plant made from cellulose
Cell membrane
Ribosomes
How is a sperm cell adapted to its function
Haploid nucleus sex cell contains one set of chromosomes acrosome in the head has enzymes so that the sperm can digest the egg middle piece packed with mitochondria for energy needed to swim and fertilise the egg.tail to swim
How is an egg adapted to its function
Cytoplasm has nutrients for the early embryo to grow.haploid nucleus.cell membrane changes after fertilisation so no more sperm can enter
How is the ciliated epithelial cell adapted to its function
Cilia on the surface beat to move fluids and particles up the trachea
How have changes in the microscope helped us see sub cellular structures better and given us a better understanding
Electron microscopes were invented and instead of using light like the light microscope they fire electrons at samples they have a higher magnification and resolution so they let us see much smaller things in closer detail which has given us a better understanding
Calculations microscope
Magnification is how many times bigger the image is
Total mag=eyepiece lens mag x objective lens mag
If you don’t know which lenses were used you can still work out the mag by
Mag=image size DIVIDE real size
Convert the units Know then in order of size
Millimetres x10 to the -3
Micrometer um x10 to the -6
Nanometer -9
Picometer -12
How do you use a microscope?
1)Place the slide on the stage
2)Set to the lowest magnification
3)Look through the eyepiece lens
4)Turn focusing wheel to increase resolution
5)Increase mag if you want
6)Increase focusing wheel if you want
How do you prepare the microscope slide
1)place slide specimen on slide
2)stain with iodine so the organelles are visible
3)add water to prevent drying out
4)put on a coverslip so the specimen keeps flat and in place
How do enzymes catalyse reactions(speed up)
Enzymes have an active site with a high specificity for a substrate so the substrate fits into the active site if the shape doesn’t fit the reaction won’t be catalysed
How can enzymes be denatured?
Temperature: increases rate at first but if it gets to hot some of the bonds holding the enzyme together will break leads to change in active site substrate won’t fit any more
pH:interfere with bonds all enzymes have an optimum pH
Substrate:higher the faster Because it’s more likely that the enzyme will meet up and react but then the enzymes run out with all active sites full adding more won’t make a difference
Describe how to investigate the effect of pH on the enzyme amylase
Place 1 drop of iodine onto each well in the spotting tile iodine turns blue black if starch is present
Then we get ons test tubes 2cm of starch amylase 2cm of buffer solution ph5 then we put it in a water bath for 10 mins to allow it to reach the correct temperature then we get a pipette and place a drop every 30 seconds to the spotting tile until the colour no longer turns blue/black which means starch is no longer present then you can try with diff buffers like pH 6 or 7