two molecules of ATP provide twophosphates which are attached to a glucose molecule to form hexose biphosphate
Glycolysis Step 2: Lysis
the molecule is destabilised by the phosphorylation and then splits into two triosephosphate molecules
Glycolysis Step 3: Phosphorylation:
another phosphate group is added to each triose phosphate to form triose biphosphate
the phosphates come from free inorganic phosphate ions located in the cytoplasm
Glycolysis Step 4: Dehydrogenation
the triose biphosphate molecules are oxidised by the removal of hydrogen atoms to form two pyruvate molecules
NAD coenzymes accept the hydrogens and are reduced
the phosphates are used to form fourATP molecules
matrix: contains enzymes for Krebs cycle and link reaction; also contains mitochondrial DNA
outermitochondrial membrane: separates contents of mitochondrion from rest of cell, creating a cellular compartment with ideal conditions for aerobic respiration
inner mitochondrial membrane: contains electron transport chains and ATP synthase
cristae: projections of inner membrane which increase the SA available for oxidative phosphorylation
intermembrane space: proteins are pumped into this space by the electron transport chain. The space is small so the conc. builds up quickly
Link reaction/Oxidativedecarboxylation:
pyruvate enters the mitochondrial matrix by active transport
pyruvate then undergoes oxidativedecarboxylation where carbon dioxide is removed along with hydrogen
the hydrogen atoms are accepted by NAD which is reduced
the remaining acetyl group is bound to coenzymeA to form acetyl-coenzyme A
Acetyl CoA delivers the acetyl group to the Krebs cycle
Krebs cycle Step 1:
Acetyl CoA delivers acetyl to the Krebs cycle
the acetyl group combines with oxaloacetate (4C) to form citrate (6C)
Krebs cycle Step 2:
the citrate molecule undergoes decarboxylation and dehydrogenation to produce one reduced NAD and carbon dioxide
a five carbon compound is formed
Krebs cycle Step 3:
the 5C compound undergoes further decarboxylation and dehydrogenation reactions, eventually regenerating oxaloacetate
the cycle continues
Oxidative Phosphorylation:
the hydrogen atoms collected by NAD and FAD are delivered to the electron transport chains in the cristae
hydrogen atoms dissociate into H+ and e-
the high energy electrons move into the ETC and reduce/oxidiseelectroncarriers
energy is released as the electrons move along the transport chain
this energy is used to create a proton gradient leading to the diffusion of protons through ATPsynthase, resulting in the synthesis of ATP
Substrate level phosphorylation: production of ATP involving the transfer of a phosphate group from a highly reactive intermediate. It is different to oxidative phosphorylation.
Lactate fermentation
pyruvate acts as a hydrogen acceptor, taking in hydrogen from reduced NAD, catalysed by lactate dehydrogenase
pyruvate is converted into lactate and NAD is regenerated
glycolysis continues so small quantities of ATP are synthesised
the reduced quantity of ATP would not be able to maintain vital processes for long enough
the accumulation of lactic acid causes a fall in pH leading to proteins denaturing
Anaerobic respiration:
there is no oxygen to act as the final electron acceptor after the ETC so the flow of electrons stops
ATP synthesis through chemiosmosis stops
reduced NAD and FAD are no longer oxidised so they cannot be regenerated as NAD and FAD
the Krebs cycle comes to a halt as there are no coenzymes available
Alcoholic fermentation:
irreversible
can occur indefinitely
pyruvate is converted to ethanal by pyruvate decarboxylase
ethanal accepts a hydroen from reduced NAD to become ethanol
NAD continues to act as a coenzyme
RQ = CO2 produced/ O2 consumed
RQcarbohydrates = 1
RQProteins = 0.9
RQLipids = 0.7
lipids contain a greater proportion of carbon-hydrogen bonds than carbs so they produce much more ATP in respiration. They also require more oxygen to break them down, and release less CO2