Exam Three Flashcards
hexokinase replaced by
G6Pase
PFK replaced with
FBPase
gluconeogenesis
fructose biphosphate and G6Pase (must be tightly controlled) happens in LIVER
free G6Pase
would deplete all ATP in the cell making tight 2 enzyme cycle w/ hexokinase
cori cycle ATP cost in liver
6
cori cycle ATP cost in muscle
2
CAC is ___ compared to glycolysis
strongly oxidative (connected to glycolysis via pyruvate DH complex)
CAC takes place in
matrix (vs. glycolysis in cytoplasm)
products of CAC
NADH and FADH2 (fee electrons into oxidative phosphorylation yielding ATP)
E3
Pyruvate DH Complex
succ DH
inner membrane/membrane bound
irreversible steps
citrate synthase, pyr DH complex, isocitrate DH, alpha KGDH complex
electron transport directly produces
protein gradient (drive ATP synthesis)
malate aspartate shuttle
heart liver kidney
ATP/ADP translocase
ATP out to cytoplasm ADP come in (antiport)
coupling
at rest rate of O2 goes down bc ATP is high
uncoupling
abnormal state can be induced by various things(UCPI, 2,4 DNP) symptoms: hot, rapid breathing, feel weak, burning tops of fuel but not making ATP bc ATP synthesis is uncoupled from O2 use
complex I inhibitor
retenone, amytal
complex III inhibitor
antimycin A
complex IV inhibitor
cyanide, azide, carbon monoxide
PPP makes
NADPH and ribose
30 carbon rxn
want sugar but no NADPH: non ox branch
fixed ratio of 2 NADPH for every Ribose 5P
oxidative branch
only NADPH and no ribose 5P
part of oxidative and non ox (resembles CAC)
glutathione
“redox” buffer to protect cells against oxidation
Wenicke Korsakoff syndrome
lack of thiamine can’t saturate enzymes mut in transketolase
Calvin cycle
rxn from gluceoneo and PPP
“hitting the wall”
depleting glycogen (need 8 pieces of bread, big piece of cake, or banana split)
“a” form of glycogen phosphorylase
added phosphates, normally “on”, LIVER
“b” form of glycogen phosphorylase
no phosphates, “off” (can be turned on allosterically by AMP low E charge) MUSCLE (turned on during exercise)
F-2,6-BP signals
plenty of glucose
pyruvate carboxylase works perfectly in absence of
NAD+
pyruvate DH complex - FAD is attached to
E3
2 enzymes with FeS cluster
succinate DH, aconitase
not inhibited by ATP and NADH
malate DH
C3 of pyruvate labelled one turn of CAC
C2 and C3
isocitrate lyase is important in
glyoxylate cycle
cyto c is located in
intermemb space
pamaquine induced hemolytic anemia
G6PDH deficiency, RBC membrane cross links get brittle
calvin cycle
PPP + gluconeogenesis
transkeltolase
covalent attachment of substrate to thiamine phosphate
F1
contains catalytic sites for ATP synth, contains alpha beta gamma subunits, mostly matrix
F0
proton channel, spans inter mito membrane, contains a b c subunits
TPP at active site
E1
C1 labelled 1 turn of CAC
none lost as CO2
substrate level phosphorylation in CAC catalyzed by
succinyl CoA synthase
ubiquinone
linked btwn electron transport and proton pumping moving H+ across mito membrane
“sugar can make you fat but not sweet” not true for
glyoxalate cycle
glycerol phosphate shuttle
glycerol phosphate + DHAP
C2 labelled after 1 turn of CAC
C4 is labelled
succ DH does not catalyze
oxidative decarboxylation
gamme subunit of Racker’s Knob
camshaft
ox of 1 mole of Acetyl CoA produces
10 ~P
cofactor of transketolase
TPP
ketone bodies do NOT include
alpha KG and OAA
anaplerotic rxns in mammals
convert pyruvate in OAA
cori cycle
responsible for lactate and glucose in blood
ATP formed when electrons from FADH2 are transported to O2 via MET
1.5
transaldolase rxn
Sedo7P + G3P = E4P + F6P
transketolase
Eryth4P + Xylulose 5P = Fru6P + Gly3P