a singular metabolic reaction
occurs continually in living cells
the energy cycle between ATP (usable nrg) and other organic compounds (non-usable)
basically endothermic
uses ATP
to produce macromolecules from smaller molecules
break down macromolecules into smaller molecules
release nrg in form of ATP
the sum of all reactions in living organism
must occur fast to adapt to environment
interocnnected biochemical reactions
form multistep biochem pathways
NEEDS specific enzyme in all of the many steps, must be exactly complimentary
reactants (starting molecules) chemically changed to form products
each reactions needs an enzyme
the substrates for a particular enzyme
light change in substrate to fit the enzyme
substrate changes back afterwards
endothermic basically
build complex molecules from smaller ones
net input of nrg
thus energy requiring (endergonic)
nrg of products>reactants
exothermic basically
breaks down complex molecules into simple, smaller
nrg releasing or exergonic
nrg of reactants>products
all reactions require input of nrg
enzymes lower activation nrg
key enzyme in photosynthesis
acts on just 3-10 substrate per second (high conc combats this)
catalyses fixation of atmospheric CO2
complimentary to substrate
sunlight (glucose) -> energy based upon:
- prescence of chlorophyll in plant cells
- CO2 and H20
- enzymes (rubisco)
generation of energy to usable forms (ATP)
active site caused by tertiary structure
hence if loses structure, no active site
additional non-protein molecules
needed for enzyme activity and stability
some inorganic, thus no carbon
organic cofactors needed for enzyme activity (stability)
carries something necessary
used in cellular respiration/photosynthesis
form bonds at active site of enyzyme (also bonds w/substrate)
hence substrate temp held in position which is required for enzyme function
look at diagram for this please
prosthetic groups:
- cofactors tightly bound to an ezyme
- essential to its function as a catalyst
NADPH (loaded) -> NADP+ (unloaded)
ATP -> ADP + Pi
donate H+ ions and electrons and transfer energy
thus it an unload
NADH -> NAD+
FADH2 -> FAD+
both loaded->unloaded
both carry protons and electrons
transferring of atoms or groups of atoms
enegry transfers
e.g. NADH
can donate hydrogen ions/electrons and transfer energy
high energy
oxidises
formed from unloaded enzyme using high energy electrons (uptake of radient energy of sunlight)
receiver of electrons/hydrogen ions
reduces
lower energy
increase temp
increase conc of reagents
increase surface area of reagents
add catalyst
uses enzymes
increase temp (kinetic energy)
ideal pH
substrat/enzyme conc (enzyme doesnt plataue if enzyme conc>substrate conc as must dissociate before another can bind)
bind to site, blocks substrate
slow rate of reaction but eventually same ror
binds at allosteric site
causes conformation change, no longer complimentary
has more of an effect, lowers reaction rate as increase in substrate conc
substrate perma blocked
combines w/another section perma, changes its shape
prevent waste
prevent build up in cells of products to harmful levels
prevent depletion of substrate
slowing or stopping activity of enzymes
inversing activity of specific enzyme
conformational changes of active site
caused by regulator molecules binding to allosteric site
reversible
allosteric inhibitor:
binding produces change of enzyme shape
which stops enzyme activity
allosteric activators:
shape change resulting from binding
produces increase in enzyme activity
eg trp repressor protein
abundance of the end product acts as an inhibitor of key enzyme of first step of pathways
eg trp (activates repressor proteins)
organisms that consume other organisms for energy
organisms that produce own food using light (photoautotrophs) or chem energy (chemoautotrophs)
initial radiation energy captured by autotrophs cannot be used
thus must be transformed into sugars (glucose)
thuse chemical energy
sugars stored as starch (plants) or glycogen (animals)
6CO2 + 6H2O ->C6H12O6 + 6O2
(light+ chlorophyll)
location of photosynthesis
contains chlophyll in internal membranes
enables plants to capture radiant energy of sunlight
green pigment in internal membranes
cells w/this only in mesophyll cell layer
stroma (liquid)
thylakoid membranes/grana (individual blobs)
granum (groups of grana)
inner and outer membrane
fluid inside chloroplast
contains enzymes involved in light-dependant stage (calvin cycle)
enzyme in light-dependant stage of photosynthesis in thylakoid membranes
provide large surface area for capture of sunlight by chlorophyll
transform light energy captured by chlorophyll into chem energy of loaded coenzymes
change simple inorganic carbon dioxide molecules into more complex organic glucose
needs high energy coenzymes
transforms sunlight energy captured by chlorophyll
into chem energy of loaded coenzymes
thylakoid membranes
through ETC (electron transport chain) pathway
series of proteins embedded in thylakoid membranes
thus NADP+ and ADP become loaded
H20 -> O2 (waste product (specifically the O2 not ATP)
ADP + Pi -> ATP
NADP+ -> NADPH
also must include that sunlight is catalyst of these
1. radiant energy from sun absorbed by chlorophyll
2. water becomes 'excited', splits, producing electrons, H+ protons and O2
3. electrons + H+ loaded onto NADP + forms NADPH
-NADP+ + H+ + 2e- ->NADPH
4. energy used to pump protoms from stroma -> inside thylakoid which creates proton gradient
1. radiant energy from sun absorbed by chlorophyll
2. water becomes 'excited', splits, producing electrons, H+ protons and O2
3. electrons + H+ loaded onto NADP + forms NADPH
-NADP+ + H+ + 2e- ->NADPH
4. energy used to pump protoms from stroma -> inside thylakoid which creates proton gradient
assemble simple inorganic CO2 -> glucose molecules
in the stoma of chloroplast
rubisco which is vital in carbon fixation
ATP -> ADP + Pi
NADPH -> NADP
CO2 -> C6H12O6 (important)
known as the CO2 enters
1. CO2 converted to 3-carbon molecule through CARBON FIXATION
2. loaded NADPH coenzymes donate H+ and e-
-bc molecules reduced to higher energy levels
3. ATP supplied energy for anabolic steps of cycle
4. glucose formed as an output
have bundle sheath cells where the majoirt of the cholorplast is (thus photosynthesis)
separate carbon fixation and Calvian cycle by cell type
bundle sheath cells do calvin cycle after the mesophyll cell does carbon fixation
separate carbon fixation and calvin cycle by day and night
night is carbon fixation
day is calvin cycle
minimises photorespiration which would occur in the warm weather that the C4 plants live in
this is done as diff enzyme is used instead of Rubisco in carbon fixation which means that Oxygen cannot be preferntially binded to as the enzyme cannot bind to Oxygen
CO2 can be taken in at night, which in its dry and hot climate, prevents the water loss that would occur if the stomata opened during the day
CO2 enters the mesophyll cell through the stomata
calvin cycle occurs
glucose is produced and exits the cell
CO2 enters the mesophyll cell
transformed into C4
this enters the bundle sheath cells
goes back into CO2 and performs calvin cycle
glucose is produced and exits the cell
CO2 enters mesophyll at night, goes to C4 and then during day CO2 goes into Calvin cycle which produces glucose withought the CO2 entering during the day
when plants uptake O2 and not CO2
this is less efficient and produces CO2 instead of glucose
it can bring bind with both CO2 and O2
thus O2 is a competetive inhibitor
when rubisco binds with oxygen, photorespiration occurs
rubisco fixed O2 more often
this is because CO2 is LESS SOLUBLE
thus more O2 available in mesophyll
if prolonged then rate of photorespiration faster that photosynthesis (death)
stomata prevents H2O loss
blocks entry of CO2
limits exit of O2 produced in light-dependant
more O2 and less CO2
thus rubisco binds more O2 than CO2 and photorespiration rates increase
stage one (in mesophyll)
carbon dioxide ->malic acid
use of PEP Carboxylase to fix carbon
PEP can only bind to CO2 which means no photorespiration
Stage two (in bundle sheath cells)
glucose production via calvin cycle
malic acid convrted into pyruvate and CO2
steady CO2 production
thus Rubisco preferentially binds to the CO2, not O2
CO2 is taken in (optimal)
carbon fixation occurs when stomata open
reaction catalysed by PEP carboxylase
malic acid stored in vacuoles in plant cell for daytime
calvin cycle occurs during the day (needs water to be excited by radient sunlight)
stomata is closed (no water loss)
steady production of CO2
thus Rubisco has affinity for CO2
photoresp reduced
as light intensity increase - photosynthesis rate increases
- until maximum point (similar to substrate conc graph)
further increase has no effect
this point is called the light saturation point
plants can close stomata quick to preventfurther water loss
prevents gas exchange (bad)
lack of supply of CO2 to mesophyll cells (no calvin cycle -> no photosynthesis)
no H2O for long time mean death
roots need O2 to grow
lack of O2 due to excess H2O in air spaces
thus ASPHYXIATION
plant root cells unable to respire
same graph as enzymes as that is what it is
low temp ->lack of kinetic energy
high temp -> denaturisation
has optimal point
as it increases, photo- increases
until limited by limiting factors
- rubisco working at max rate (enzyme conc)
- lack of coenzymes (such as NADPH)
they do not act in isolation
amt of CO2 limits max rate of ps at optimal light intesity (light saturation point)
temp also limits this and others
produces ATP (necessary for life)
protein synthesis
extretory processes (removes metabolic waste)
production of antibodies
anaerobic respiration (some bacteria use)
aerobic respiratio (almost all use this)
fermentation (some bacteria/yeast use this)
C6H12O6 + 6O2 ->6CO2 + 6H2O
ADP+Pi->ATP
in cytosol
first stage
Glucose-> -> ->2 Pyruvate (half of glucose)
2ADP+Pi->2ATP
2NAD+->2NADH
No O2 required
if confusing check book
2 ATP and 2 NADH
per molecule of glucose
Pyruvate cannot enter Krebs
thus pyruvate oxidation occurs
2 Pyruvate ------>2 acetyle CoA + 2CO2
2NAD->2NADH+H+
mitochondrial matrix
Inputs Outputs
Acetyl CoA -> CO2 (x6)
ADP + Pi -> ATP (x2)
NAD+ -> NADH
FAD+ -> FADH2
2 ATP
NADH
FADH2
Inputs Outputs
O2 -> H2O
ADP + Pi -> ATP
NADH -> NAD+
FADH2 -> FAD+
inner membrane in mitochondria
1.NADH and FADH2 drop off e- and H+
2.e- pass through each complex
3.provides energy to pump proteins into intermembrane space
-thus H+ gradient created
4.H+ flows down gradient through ATP synthase
-provides energy for ATP
load as many coenzymes and produce as much ATP for the ETC
26-28 ATP
H+ cannot naturally pass through the membrane as it is not permeable
thus an enzyme must be used
temp (same as temp for enzyme graph)
glucose conc (substrate graph)
oxygen conc (also substrate graph)
glucose and oxygen both increase rate until other limiting factors prevent their increase in rate
when organisms live in oxygen-deficient enviro and neep ATP (do this or anaerobic respiration
net ATP of 2
when supply of O2 to cells by aerobic cellular respiration cannot keep up w/ATP demand
intense athletic performances
can only last a few minutes in humans
indefinetely without interruption
in humans only a few mins
for us they are effectively the same thing
cytosol
anaerobic conditions
lactic acid fermentation (animals)
alcohol (ethanol) fermentation (yeast)
