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regeneration of NAD+
glycolysis makes NADH but needs NAD+ to run
NADH must be turned back into NAD+
if NAD+ runs out, glycolysis stops → no atp
fermentation
turns NADH → NAD+
happens when there’s no oxygen to keep glycolysis running
its the backup system to restore NAD+
pyruvate → ethanol
enzyme involved in fermentation
alcohol dehydrogenase
redox balance In alcoholic fermentation
keeps NAD+/NADH balanced
restores NAD+ by making ethanol
alternative pathway for regenerating NAD+
lactate fermentation
pyruvate → lactate
happens in muscles when oxygen is low
enzyme in lactic acid fermentation
lactate dehydrogenase
Entry points in glycolysis for galactose and fructose
galactose (G-6P) and fructose (F-6P) adipose tissue
enzymes that control glycolysis
hexokinase
PFK
pyruvate kinase
control sites
irreversible steps in glycolysis
regulation of glycolysis In muscle
muscles adjust glycolysis based on energy needs
long slow run (glycolysis slows down)
co2 and h2o is made from pyruvate
oxygen is more abundant
sprint (glycolysis speeds up)
lactate is made to regenerate NAD+ to keep glycolysis running
oxygen is not abundant you need more
PFK (phosphofructokinase)
most important enzyme in glycolysis
inhibited by: ATP (high energy) stop
activated by: AMP (low energy) go
has 2 ATP binding sites: active site and regulatory site
the allosteric regulation of PFK
when atp is low, more PFK is made at a faster rate. when atp is high, PFK is able to generate and accumulate less and slower
fructose 2,6-BP
strong activator of PFK
pushes glycolysis forward even if ATP is present/high
pyruvate dehydrogenase
enters mitochondria under aerobic conditions (oxygen present)
gets turned into Acetyl CoA (irreversible)
enzyme: pyruvate dehydrogenase complex
acetyl CoA
fuel for citric acid cycle
the link between glycolysis and the citric acid cycle
aka pyruvate processing (pyruvate → acetyl coa)
mitochondria
where pyruvate processing happens
citric acid cycle happens in the matrix
E1
oxidative decarboxylation of pyruvate
E2
transfer of acetyl group to CoA
E3
regeneration of the oxidized form of lipoamide
3 enzymes involved in the synthesis of acetyl coa from pyruvate
E1, E2, E3
5 coenzymes involved in the synthesis of acetyl coa from pyruvate
TPP
lipoamide
CoA
FAD
NAD+
memory trick: TLC Friday Night
3 steps for pyruvate → acetyl coa
decarboxylation
oxidation
transfer to coa
coenzyme A
the activated carrier for acyl groups
activated carrier: universal, reusable currency that can do different reactions
decarboxylation (step 1)
E1 catalyzes decarboxylation (CO2 removed)
uses TPP coenzyme to combine with pyruvate
oxidation (step 2)
electrons transferred
forms acetyllipoamide on E2
catalyzed by E1
formation of acetyl coa (step 3)
acetyl group transferred to coa
transfer is catalyzed by E2
to participate in another reaction cycle of pyruvate processing
dihydrolipoamide must be re-oxidized
reaction is catalyzed by E3
FAD → FADH2
NAD+ → NADH
big picture pf pyruvate processing
pyruvate → Acetyl CoA + CO2 + NADH
Pyruvate dehydrogenase complex is regulated by two mechanisms
pyruvate → acetyl coa is IRREVERSIBLE
Acetyl coa can either be metabolized in the citric acid cycle OR made into fatty acids
Response of the pyruvate dehydrogenase complex to the energy charge
high energy charge (atp, nah) → inhibit PDH (slow down)
low energy charge → activate PDH (speed up)
what 2 enzymes regulate the pyruvate dehydrogenase complex
PDH kinase and PDH phosphatase
how does PDH kinase regulate the pyruvate dehydrogenase complex
turns off PDH (phosphorylation)
how does PDH phosphatase regulate the pyruvate dehydrogenase complex
turns on PDH (dephosphorylation)