2.1 Intro to Metabolism Flashcards
Metabolic hub- responsible for the distribution of nutrients that enter the body
Liver
Only substances that can pass through the blood brain barrier
Glucose and ketone bodies
General pathway of aerobic glycolysis
Glucose–>pyruvate–>acetyl coa
Product of anaerobic glycolysis
Lactate
Phosphorylation of molecules is done through
Oxidation reduction reactions
Explain substrate level phosphorylation
Phosphorylation of ADP involves a dehydrogenation reaction coupled with the dehydrogenation of an organic substrateATP is not the donor. The substrate PEP becomes pyruvate via phosphorylation by pyruvate kinase taking an inorganic phosphate from cellular cytosol
Explain oxidative phosphorylationGive products
Products are water and atpHydrokysis of the anhydride releases energy
Central molecule of all oxidative pathways for cellular respiration/oxidation
Acetyl CoA
Metabolic regulation depends largely on two concepts: __ and __
Enzymatic controlAvailability of substrate
Amino acids synthesized during 1st days of starvation, and their path of action
Alanine—> liver for gluconeogenesisGlutamine—> kidney for ammoniagenesisis; or gut to be converted to alanine which goes to the liver for gluconeogenesis
Catalyzes phosphorylation reactions
Protein Kinases
Catalyzes dephosphorylation reaction
Protein Phosphatase
3 principles of metabolism:
Fuels are degraded and large molecules are constructed in a series of linked reactionsATP liks energ-releasing pathways with energy requiring pathwaysMetabolic pathways are highly regulated
Amount of ATP circulating in the body is
100 g
Phosphorylation of molecules is done primarily through
Redox Reactions
Main fuel source of metabolism
Carbohydrates
General path of ATP production using carbohydrates
Carbohydrates> simple sugars (glucose) > Acetyl CoA
General path of ATP production using proteins
Proteins > amino acids > Acetyl CoA
General path of ATP production using fats
Fats > fatty acids + glycerol > Acetyl Coa
Fate of excess glucose
Converted to glycogen and stored in liver or muscles
Fate of amino acids
Excreted in the form of urea
Fate of triacylglycerol
Stored in the adipose tissue
Type of inhibition where the end product of a pathway controls its own rate of synthesis
Feedback inhibition
A type of activation where a metabolite produced early in the pathway activates an enzyme that catalyzes a reaction further down the pathway
Feedforward inactivation