TCA cycle Flashcards
Different names for TCA cycle
- krebs cycle
- citric acid cycle
TCA cycle definition
-the final pathway where the catabolism of carbohydrates, amino acids, and fatty acids (inorganic molecules) converge and their carbon skeletons are converted to CO2
Interactions with catabolic pathways
-the breakdown of some amino acids provides certain TCA cycle intermediates
Interactions with anabolic pathways
- some TCA cycle intermediates feed into biosynthetic pathways
- synthesis of certain amino acids
ETC interactions
- TCA cycle provides energy carried by NADH and FAD2 for the production of ATP in the ETC
- ETC couples reduced carriers with ATP by ovidative phosphorylation
- TCA cycle located in mitochondrial matrix to be close to the ETC
Linear metabolic pathway VS cycle
- linear: Starts with one metabolite and ends with a different one (glycolysis)
- cycle: Starts with a certain metabolite that undergoes certain steps to form different intermediates, but in the end the same metabolite is regenerated and there is no net loss or gain of intermediates
Oxidative decarboxylation of pyruvate
- pyruvate transferred into the mitochondria by mitochondrial pyruvate carrier or simple diffusion
- converted into acetly coA by pyruvate dehydrogenase complex (PDH)
- 1 carbon is released as CO2 and NADH is produced
- IRREVERSIBLE STEP
PDH structure
- protein aggregate of 3 enzymes (E1, E2, E3)
- five different coENZYMES(organic)
- Thiamine pyrophosphate (TTP): from thiamine and vitamin B1
- Lipoamide(requires lipoic acid)
- CoA(pantothenic acid and vitamin B5)
- FAD(riboflavin and vitamin B12)
- NAD+(nicotinamide, vitamin B3/niacin)
Regulation of PDH
- phosphorylation deactivates (PDH kinase)
- dephosphorylation activate(PDH phosphatase)
- pyruvate inhibits kinase, so activater
- NAD+,ADP,Ca2+,CoA=activates
- acetyl coA, NADH, ATP=deactivate
“regulated by substrate activation and product inhibition”
Step 1: synthesis of citrate from acetyl coA and oxaloacetate
- reaction of condensation 2 carbons molecule fuses with a 4 carbon molecule to form 6-CARBON CITRATE
- citrate is a precursor for fatty acid synthesis and an inhibitor for PFK-1 in glycolysis
- enzyme: Citrate Synthase
- regulation: substrate activation or product inhibition
Step 2: Isomerization of Citrate
Enzyme: Aconitase
- reversible
- iron-sulfur protein
- inhibited by fluoroacetate (results in a build up of citrate so its a suicide inhibitor)
Step 3: Oxidative dearboxylation of isocitrate
-IRREVERSIBLE STEP
-RATE LIMITING
-yields first NADH
-releases 1 CO2
Enzyme: isocitrate dehydrogenase
-regulation: allosterically
-ATP and NADH INHIBIT
-ADP and Ca2+ ACTIVATE
“regulation by energy status of the cell”
Step 4: Oxidative decarboxylation of alpha-ketoglutarate
-IRREVERSIBLE STEP
-yields the second NADH
-releases 1 CO2
Enzyme: alpha-ketogutarate dehydrogenase complex
-3 different enzymes
-Same coenzymes required as PDH
Regulation:
-inhibited by its products
-activated by Ca2+
Vitamin deficiencies
- alpha-ketoglutarate dehydrogenase complex and PDH require multiple coenzymes derived by vitamins
- deficiency of niacin or thiamine can cause central nervous system problems
Arsenic poisoning
- alpha-ketoglutarate dehydrogenase and PDH both require lipoic acid
- arsenic poisoning forms a stable thiol with the group in lipoic acid making it unavailable to serve as a coenzyme
- neurological disturbances and death