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Glycolysis and gluconeogenesis are opposing metabolic pathways vital for glucose metabolism. Glycolysis, mainly in muscle and brain, breaks down glucose into pyruvate, producing ATP and NADH. Gluconeogenesis, primarily in the liver, synthesizes glucose from non-carbohydrate precursors like pyruvate, lactate, glycerol, and amino acids. This overview highlights key enzymes, regulatory mechanisms, and conditions under which each pathway operates, emphasizing their roles in maintaining blood glucose homeostasis during starvation, exercise, and low-carbohydrate diets. It details pyruvate conversion to phosphoenolpyruvate, including pyruvate carboxylase and phosphoenolpyruvate carboxykinase, and biotin's role as a CO2 carrier. It further explains how animals produce glucose from sugars and proteins but not fatty acids, and plants' and bacteria's ability to convert CO2 to carbohydrates via the Calvin cycle.
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Glycolysis occurs^ mainly in^ the^ muscle^ +^ brain^ Glucose, Jose Gluconeogenesis occurs^ mainly^ in^ the^ liver^
(^2) pyruvate + 4 ATP + 2 GTP + 2 NADH + 2H^ + (^4) H,0 ->^ Glucose +4^ ADP+2GDP+6Pi+2 NAD Opposing pathways thatare^ both^ thermodynamically favorable irbtusb
Operate in^ opposite direction the End (^) productof one Is the (^) starting compound of^ the other phosphate
stores are^ depleted -> starvation
No ATP^ generated during gluconeogenesis (^) aclds (^) (no (^) fatty acids)
Irreversible reaction of^ glycolysis ->^ bypassed in (^) gluconeogenesis I
Differentenzymes in differentpathways necessary:Brain, nervous system, and^ red^ blood^ cells Gifferentialsregulateeventoffutileare vertegnose
Metabolic (^) pathway;results in (^) generation of (^) glucose from certain
Animals (^) produce (^) glucose from (^) sugars/proteins (^) Blood Animals (^) cannot produce (^) glucose from (^) fatty colds Ubiquitous process ->^ plants,^ animals, fungi,^ bacteria^ +^ other microorganisms Process occurs (^) during periods of (^) fasting, starvation, (^) low-carbohydrate
Mammals -> (^) gluconeogenesis is believed to be restricted to the (^) liver, the (^) kidney,the (^) Intestine,muscle. New evidence (^) suggests thatit occurs in (^) astrocytes of^ the brain
Begins in^ mitochondrial^ Intermediate^ of
path from (^) pyruvate to (^) phosphoenolpyruvate leads (^) through oxaloacetate (^) I Any compound^ thatcan^ be^ converted^ to^ either^ pyruvate^ or^ oxaloacetate^ can^ Pyruvate amino therefore serve as^ starting material^ for^ gluconeogenesis (alanine^ +^ aspartate)^ ā
Glycerol
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yield 3 or^4 carbon^ fragments (^) glycerols fixation
Steps 1+^2 Pyruvate to^ Phosphoenolpyruvate
Bicarbonate (^) Pyruvate
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Carbon is added^ - immediately removed^ from^ structure Blotin Is a (^) CO2 Carrier Guanosine attentionerat
Long (^) CO2blotinyl-Lys from site^ tether 1 to (^) site^ moves 2 HC05 - pyruvate carboxyminera at app isa cat.at I pyruvate carboxylase 0 - P0?
CH2 =C-C00-^ Pyruvate Carboxylase Reaction: Phosphoenolpyruvate FirstGluconeogenic Steps cofactor (^) blottn (^) covalently attached to (^) enzyme (^) through amide (^) linkage to s amino^ group of^ Lys residue^ forming bloting/enzyme Travel (^) through Mitochondria cytosolic S
Catalytic Site^ 1,^ bicarbonate^ on^ is^ converted^ to^ Co, atthe^ expense of^ ATP CO2 reacts^ with^ biotin^ (forms^ carboxybloting-enzyme). Long arm^ composed minerariesministrar isa biotinanocossidechain cattained^ then^ carriesconotcurbobiotingienee
Lactate Flexible arms -> Intermediates between (^) enzyme active^ sites Selectively permeable ->^ Inner^ mitochondrial^ membrane^ Blotin-^ dependentcarboxylation reactions^ (those^ catalyzed by proplony Malate, PEP+^ pyruvate (permeable) (^) CoA (^) carboxylase + acetyl-CoA carboxylase) Oxaloacetate cannotescape Oxaloacetate (^) can be utilized in citric acid (^) cycle (Krebs (^) cycle) * Pathways depend on the (^) availability oflactate or (^) pyruvate + the^ * oxaloacetate can be converted to^ PEP^ or malate^ to^ allow^ cytosolic requirements^ for^ NADHfor^ gluconeogenesis