passive transport
does not require energy because it moves with the concentration gradient, (high to low)
active transport
requires energy, goes from low to high concentration so against the concentration gradient
diffusion
molecules move from more (high) to less(low) concentrated area until equilibirium is reached, small nonpolar molecules
osmosis
diffusion of water through a selectivly permeable membrane
osmotic pressure
pressure due to water
facilitated diffusion
diffusion with the help of carrier/channel proteins aka selective transport, hydrophilic and ions t pass through membrane
ex of passive transport
diffusion, osmosis, facilitated diffusion (selective transport)
ex of active transport
sodium pottasium pump, proton pump, exocytosis, endocytosis
exocytosis
large molecules transported out, vesicle fuses with cell membrane
endocytosis
large molecules transported in, vesicle forms from cell membrane
invaginating
the cell membane pushing into the cell to accept the molecule (in exocytosis and endocytosis)
pinocytosis
cell drinking, molecules takeninto cell wall with large amounts of liquid with it
phagocytosis
solid molecules taken in by cell (bacteria engulfed by white blood cells)
receptor mediated endocytosis
receptor proteins figure out the need the molecules floating around and they attach to the recpetor protein and are brought intot he cell through endocytosis
passive transport can be
both directions in and out of the cell
active transport is goes only 1 way because
cells smart why spend energy bringing it in or pushing it out j to do the opposite and spend more energy
voltage channel proteins
sensing electrical signals, how nerve cells communicate
chemical channel proteins
sensing chemical signals, ex. liver cells sensing blood glucoe levels high so they open channel proteins
cell size doesnt change bc of movement of solute but because of
movement of water
water always moves
high water to low water
low solute to high solute
$100(atm)→$1000(bank)→$50000(savings)
atp→carbs→lipids
the 1-2 phosphate bond is
the highest energy bond so it breaks causing atp to change to adp when energy is needed
atp and adp have a
reversible process changing back and forth based on whats needed
enzymes are
biocatalysts
endergonic
energy being absorbed from enviornment, (endothermic with thermal energy)
exergonic
energy being released (exothermic with thermal energy)
subrate saturation is where
the reaction time plateus and no longer increases because the solution is saturated with subrates and adding more will no longer increase reaction rate
catalytic site is also
the active site
allosteric enzymes
have an active site and then an allosteric site where teh product of the active site fits and then after the reaction happens in the allosteric sit ehte active site changes shape so that the enzyme is inactive, when all of the product is used up the enzyme becomes active again and changes the shape of the active site back to what the subrate fits into
biochemical pathway
a→b
b→c
c→d
d→e
if b→c stops working them the chain of reactions stops happening and the biochem pathway goes away and there will be excess b but not c,d, or e
b,c,d are intermediates while a is the reactant and e is the product
multienzyme complex
multiple enzymes working on biochem pathway
cooperativity-process
1 ezyme with mulitple active sites that does the entire biochem pathway
contratransport
secondary active transport, uses energy from electrochemical gradient, transport 2 diff ions across membrane through proteins
symport
2 diff ions same direction
antiport
2 diff ions diff directions
membranes can become ______________ from ions
polarized
electrochemical gradient
type of concentration gradient, electrical difference across membrane
electrical potential
electrical potential diff(voltage) across membrane
osmolarity
total solute concentration
aquaporins
help large quantities of water move via aquaporins
tonicity
mesaurement of the relative concentrations of solute b/w 2 solutions (inside and outside of cell)
hypertonic
more solute less solvent
hypotonic
less solute more solvent
enviornmental hypertonicity
cell shrinks
enviornemental hypotonicity
cell swell
lyses
when cell bursts
water potential
tendency water to move through osmosis
small amounts of polar molecules can
pass through the membrane
endosymbiosis
free living aerobic prokaryote engulfed by anaerobic cell through endocytosis but it didnt get ingested and it eventually lost its independence, origin of mitocondria and chloroplast, they both have double membrane and their own copies of dna and ribosomes
origin of er and nuclues
plasma membrane folding
activation energy
intial starting energy, lowered by enzymes
net releases
typically require less activation energy
net absorption
typically require more
conformational shape
tertiary shape
why does reaction rate increase
inreased speed of molecular movement
increased frequency of enzyme subtrate collisions
decrease in temperature does not denature but instead
decreases reaction time bc less substrate enzymes collisions
enzymes do denature due to increase or decrease in
pH
why does the reaction rate plateu once the concentration is saturated with substrates
themore subrate the more product and once there isalot of product it takes up space so lower chance of enzyme substrate collion
competetive inhibitor
molecules can bind reversibly or irrversibly to the active site of the enzymes, competes with the normal substrate for enzymes active site
what happens if the competetive inhibitors outnumber the substrates
the reactions are slow
if inhibitor binding is irreversile then
the enzymes function is prevented
noncompetetive inhibitors
bind to allosteric site, not active site which causes the enzyme to change shape of the original active site preventing enzyme function
autotrophs capture energy from
physical or chemical sources that are changed into somthing usable
2nd law of thermodynamics
every energy transfer increases disorder
living cells are never at equilibrium there is always a constant flow of materials in and out
cells manage energy resources by energy coupling, energy releasing processes drive energy storing processes
cofactors
inorganic nonprotein helpers (Fe, Zn, Cu)
coenzymes
organic helpers (vitamins)
first law of thermodymanics
energy can neither be created nor destroyed only changed
if the cell needs some of the sodium it pushed out using active transport and a sodium pottassium pump then it will
use couled channel proteins to bring it back in using facilited diffusion
chemiosmosis
chem energy from transport, cell wont spend energy to bring back protons diffuse back in with atp
flaccid
plant cell in isotonic solution
turgid
plant cell in hypotonic solution but doesnt lyse or burst bc of cell wall (turgor pressure)
cells are usually in ________ solute of NaCl so thats whats pumped into u when ur dehyrdated
0.851, (saline)
root pressure
how water is forced up xylem
transpiration
water loss through xylem
trasnlocation
transport of sugar through the phloem
guttation
small drops of sap (water and minerals) ooze from the leaf tip due to root pressure
cuticle
helps prevent water loss, small hair on leaf and leaf surface
what controls the opening of the stoma
guard cells
water moves from ________ psi to
high, low psi
solute ___________ psi
decreases
pressure _____________ psi
increases