movement, repsiration, sensitivity, growth, reproduction, excretion, Nutrition, DNA (MRSGREND)
eukaryotic
prokaryotic
prokaryotic
prokaryotic
plasma membrane
controls movement of molecules in/out of cell
intracellular fluid with dissolved materials (ions/water/proteins/molecules)
cytoplasm is not in prokaryotic but cytosol in both
protein production (made or rRNA)
processes/packs proteins/lipids
provides support/structure/protection
site of photosynthesis
site of aerobic cellular respiration (production of ATP)
chloroplast/mitochondria originates as microbes engulfed by another organism and gradually formed mitochondria/chloroplast
maintains integrity of DNA, controls cell activity
contains genetic information for cell growth/division/function
helix w/ phosphate sugar backbone w/ nitrogenous base
instructions (genes) needed to make cellular respiration (RNA/proteins)
passive (no specialised structure needed and no energy required) and active (specialised structures and requires energy
greater metabolism required(importing nutrients/exporting waste)
determines exchange of materials from cell/environment
smaller SA:V ratio and this less efficient
more photosynthesis
active boundary where substances transpoted between internl/external enviro
plasma membrane is semi permeable (selective)
integral proteins (embedded in, carbs can attach (glycoproteins)) and peripheral proteins (anchored to exterior, done by bondibg w/lipids)
TRACIE, transport, reception, anchorage, cell identity (glycolipids on cell allow for cell recognision), intracellular joining (joins cells together for communication) and enzyme activity(acts as catalyst)
hydrophilic head (ohosphate group) and hydrophobic tails (fatty acid chain) with proteins, carbs and cholesterol
regulates temp of phospholipid bilayer
diffusion for water (high to low concentration)
high to low concentration
high to low, no energy
low to high (up), movement kf larger particles
facilitated (both no energy and down but one needs channel/carrier proteins other doesnt)
isotonic (in/out), hypERtonic (water concentrated in (going out)) snd hypOtonic (concentrated out (going in))
actuve transport (enzyme function aids transport
phagocytosis (eating), pinocytosis (drinking)
asexual parent essentially cloning (no combination of DNA, exchange of gametes snd one parent) creates two identical daughter cells
growth, repair, procreation
simple mitosis in prokaryotic cells where shit replicated
replication (dna chromosome, cell gets bigger), migration (two chromosomes formed, each migrate to opposite ends of cell) and the split (pinches into two with septum, stretches away in middle and creates two cells)
interphase (dna replicates), mitosis, cytokenisis
gap 1 stage (growth of cytosol, proteins are synthesised, mitochondria and chloroplast divide) then synthesis (DNA synthesises/replicated) parent cell contains two identical copies of DNA) and then gap 2 stage (doubles in size, proteins sunthesised form microtubules of spindle)
G1 (dna damage before replication), G2 checkpoint (checks for DNA replications errors after S stage) and M checkpoint (checks during metaphase of all chromosomes)
proto oncogenes (initate cell cycle, signal production of proteins, turns off to stop excessive cell production, mutstions cause cancer) and tumour suppressing genes (make proteins to signal cell stop dividing, can also repair DNA,, mutations lead to cancer)
adulthood
rate of death
cell death
end of cells life, damges/diseased cells or excessive cells
in cell, due to damage/infection, assesses itsslf
p53 interacts w/ mitochondria
creates and informs apoptosome
enzymes (proteins) tell each other until apoptosis occurs (caspase cascade)
immune system sends signal to the cell which the carbohydrate chain picks up
FADD receieves this
enzymes (proteins) send signal to eachother until apoptosis occurs (caspase cascade)
sometimes rate of renewal/production>rate of death
cancer cells
alzeihmers, multiple sclorisis (bad stuff)
uncontrolled cell cucles (breakdown from regular)
mass produces cells (tumours) (malignant cells break off and migrate)
no contact inhibition (crowded/multiple unorganised layers), unlimited, still divide after damaged (which creates abnormal cells/errors in DNA)
there are many different sites
in roots and shoots
when cells become specialised to perform specific functions
cells that have not undergone differentiation (specialisation)
nope
protein oct4
so that they can renew/divide over long periods of time
by their potency (how many diff types of cells they can become)
totipotent
pluripotent
multipotent
oligopotent
unipotent
the most powerful stem cell
can produce all cell types!
can generate fully functional living organisms
toti and pluri
the second most powerful
can become many diff types of cells
can be made in labs
by harvesting less potent stem cells and treating them
pluripotent as toti is too controversial
multipotent
oligopotent
unipotent
can self renew and differentiate into specific range of cell types (families)
similar to multipotent but further resiricted (closely related cell types only)
least potent
can only become the same type of cell
a cell derived from inner mass cells of an earky embryo at blastoctyst stage (early in fertilisation)
can be obtained via IFV
it destroys the embryo to take the cells
an unfertilised egg
can be artificially stimulated to begin development but not capable of becoming human
adult stemm cells
can be obtained crom various sources in the body (such as bone marrow)
induced pluripotent stem cells
specialised adult somatic cells
can be genetically reprogrammed
created by addition of four genes that encode proteins that keep stem cells undifferentiated
within the cell division, one stem cell is produced to become the parent cell and one cell is produced to differentiate
also skin cells at the surface fill with keratin and die
located in bone marrow (somatic)
divide to give rise to different cells of the blood family
stem cells used fo repair tissues/fix organs anomalies etc
-patient needs help
-disease free cells taken from patient
-enucleation (removal of nucleus) of egg
-fusion of egg and cell (IVF)
-zap with hella electricity
-embryo cultured (artificially made) and stem cells removed
-put in disc, treated/programmed for cell types
the creation of an embryo through somatic nucleur transfer to obtain stem cells that treat patient
this provides a genetic match
complete genetic match
this means there is not immune respone
also less ethical issues than embryonic stem cells
gap 1 stage (growth of cytosol, proteins are synthesised, mitochondria and chloroplast divide)
synthesis (DNA synthesises/replicated) parent cell contains two identical copies of DNA)
gap 2 stage (doubles in size, proteins sunthesised form microtubules of spindle)
the theory regarding how eukaryotic cells have membrane bound organelles
a prokaryotic cell absorbed a prokaryotic cell and the cell inside was able to maintain life, creating a cell inside of a cell, meaning it could uave membrane bound organelles as the cell could not be labelled as much more complex, creating a eukaryotic cell
the mitochondria and chloroplast having their own DNA and membrane
fluid mosaic model
with big cells
transport using pumps