glucose is oxidized through a series of redox reactions (aka cellular respiration)
cellular respiration completely oxidizes glucose, while fermentation doesn’t
cellular respiration harvests more energy (more efficient)
process of cellular respiration:
glycolysis — glucose → 2 pyruvate, ATP is produced, NAD+ → NADH
occurs in cytosol of eukaryotes and prokaryotes
pyruvate processing — pyruvate → CO2 + CoA, NAD+ → NADH
occurs in matrix of mitochondria or cytosol of prokaryotes
citric acid cycle — CoA → 2 CO2, ATP and NADH produced, FAD → FADH2
occurs in matrix of mitochondria or cytosol of prokaryotes
electron transport chain and oxidative phosphorylation — electrons from NADH and FADH2 go through a series of redox reactions, creating a proton gradient across the inner membrane of mitochondria, used to make ATP
occurs in inner membrane of mitochondria or plasma membrane of prokaryotes
glycolysis — process of turning glucose into pyruvate
glycolysis is a sequence of 10 reactions in cytosol
starts by using 2 ATP molecules, termed the energy-investment phase
steps 6-10 are the energy payoff phase
for each molecule of glucose, the net yield is 2 NADH, 2 ATP, and 2 pyruvate
substrate-level phosphorylation — enzymes catalyze transfer of phosphate from phosphorylated substrate to ADP, creating ATP
high levels of ATP inhibit phosphofructokinase which catalyzes synthesis of fructose-6-phosphate to fructose-1,6-biphosphate
it has 2 binding sites for ATP, one active site and one regulatory site
the breakdown of glucose to CO2 and H2O
transforms the energy from food to ATP
can’t extract anymore biologically usable energy from CO2 and H2O
multiple reactions in 3 distinct pathways or “phases”
glycolysis
pyruvate oxidation and Krebs cycle
oxidative phosphorylation (electron transport and chemiosmosis)
phase 1 in the path of making ATP from glucose
“glyco” (sugar) + “lysis” (splitting)
starts with a 6-carbon sugar (glucose), ends with two 3-carbon molecules (pyruvate)
this pathway is actually endergonic up to production of first 3-carbon molecules (uses cell’s store of ATP)
the beginning of glycolysis is endergonic
occurs in the cytoplasm of all living cells
2 steps are endergonic (coupled with ATP → ADP + Pi)
steps 1, 3
ATP “pays for” these steps by being hydrolyzed into ADP and attaching a phosphate group to the molecules
3 steps are exergonic
steps 6, 7, 10
step 6 (so exergonic) — coupled with the reduction (endergonic) of 2 NAD+ → 2 NADH
step 7 — coupled with 2 ADP + 2 Pi → 2 ATP
step 10 — coupled with 2 ADP + 2 Pi → 2 ATP
glycolysis: glucose + 2 ATP → 2 pyruvate + 2 ATP + 2 NADH + 2 H2O + 2 H+
problems at the end of glycolysis
molecules still are not at their lowest energy state
some of our energy is being held in NADH
NAD+ is being used up and not replaced
it depends on the presence or absence of oxygen (O2) or other terminal electron acceptor
if oxygen is present, cells will undergo aerobic respiration
if oxygen is absent but an alternative terminal electron acceptor exists, cells will undergo anaerobic respiration
only difference is the last electron acceptor
if oxygen is absent and no terminal electron acceptor exists, cells might be able to undergo fermentation
carbon source (2 molecules of pyruvate) completely converted to carbon dioxide
pyruvate molecules first converted to acetyl-CoA, which then enters the Krebs (or Citric Acid) Cycle
all C-H bonds converted to C-O bonds (releasing 6 CO2)
more energy transferred to NAD+ and FAD (making more NADH and FADH2)
another substrate-level phosphorylation (SLP) reaction in Krebs cycle (GTP is ATP analog)
occurs in mitochondria of eukaryotes; cytoplasm and plasma membrane of prokaryotes
matrix
where krebs cycle occurs
Krebs enzymes
DNA and ribosomes
inner membrane
folds/tubes
principle site of ATP generation
>70% protein (no porins aka channels)
impenetrable to ions and small molecules except by transporters
cristae
sacs of inner membrane joined to the rest of the inner membrane by short tubes
the more cristae, more electron transport chains
intermembrane space (IMS)
composition of ions and small molecules is the same as the cytoplasm (same pH) because of porins
outer membrane
typical protein 50%, lipid 50%
has porins
like a straw
open channel, completely unregulated except by diameter