Metabolic Biochem 1,2 Flashcards
Enzyme types
Aminotransferase- transfer amino acids
Dehydrogenase- removes hydrogen, electron carrier
Isomerase- convert one isomer to another
Kinase- transfer phosphate from one group to another
Lipase- breaks down lipid
Mutase- transfer phosphate to a different c in same substrate
Phosphorylase- adds phosphate from free
Reductase- electron transfer without hydrogen
Key intermediates- glucose-6-phosphate
Has 4 major gates
- convert to fructose-6-phosphate
- convert to glucose
- convert to/ from glycogen
- pentose phosphate pathway (building block for RNA)- also make NADP form fag
Key intermediates- pyruvate
Has 5 major fates:
- lactate
- alanine
- enter mitochondrial membrane to form Acetyl coA
- mitochondrial membrane to form oxaloacetate
- ethanol
Key intermediates- Acetyl CoA
Has 6 major fates:
- in mitochondrial matrix
- citrate
- ketone bodies
- fatty acids
- ketogenic AAs
- citrate exit mitochondria - Acetyl coA- FAs or cholesterol
Key intermediates- oxaloacetate
4 major functions
- citrate in m.m to produce malate, pyruvate then produced PEP
- can produce ASP
- can produce a Malays
Compartmentalisation: Cystolic pathways and key intermediates
- cytosol Glucogenesis Glucogenolysis Glycolysis Gluconeogenesis Lactate alanine etc - mitochondria ETC Urea cycle - 1/2 cytosol TCA cycle
Metabolism of a sprinter
100m
Approx 10 secs
Total ATP used: 1.5mol
Metabolic fuels used: muscle ATP, creatine phosphate and muscle glycogen
Average velocity of ATP production: 39-73mmol/sec
Major pathways for energy production: glycogenolysis anaerobic glycolysis
Major metabolic products: increased lactate and decreased blood pH
Metabolism of a marathon runner
42.2km
2-21/2 hours
Total ATP required: 150mol
Major metabolic fuels used: glycogen and fatty acids
Average velocity of ATP production: 6.2-16.7 mmol/sec
Major pathways of energy production: glycogenolysis and fatty acid oxidation
Major metabolic products: CO2, H2O and heat
Metabolism of an ironman triathlete
226.3km
8-10 hours
Total ATP required: 600-800mol
Major metabolic fuels used: glycogen, fatty acids, ketone bodies, amino acids - can deplete up to 25% of muscle protein during an ironman event
Average velocity of ATP production: 6-10mmol/ sec
Major pathways for energy production: glycogenolysis and FA, KB, and AA oxidation
Major metabolic products: CO2, H2O and heat
Allosteric regulation
Of or involving a change in he shape and activity of an enzyme that results from the binding of a regulatory molecule at a site other than the active site
Allosteric regulation in glycolysis- hexokinase
Km (glucose)= 0.1mM
Hexokinase inhibited by own product- to ensure it maintains same level of blood sugar
Glucokinase is not regulatory enzyme, it is regulated by direct blood glucose levels (meals)
Allosteric regulation in glycolysis- phsophofructokinase
Activates AMP2, ADP3, F-2-6-bisP to active to increase ATP
Inhibits- ATP, Invreased H+, cottage to stop energy production, also don’t want cells to become acidic. High citrate in cells indicates efficient glucose in cell.
Bind to allosteric site which makes cell relaxed when not bound- tense.
Low ATP - higher binding affinity
Sigmoidality- allosteric regulation
To the right- allosteric regulation
Allosteric regulation in glycolysis - pyruvate kinase
Liver -LPK- muscle- MPK
Activates F-1-6-bisP- upstream product, returns and activates
Inhibits ATP5, alanine. ATP product of late reaction, prevents too much ATP
Tissue Specificity - brain
Brain: fuel source- glucose- brain can adapt to ketone bodies during starvation (>3 days) and danger occurs when glucose <2.2mM. Does not store, relies on constant supply of blood glucose via GLUT3 Km- 1.0mM.
In resting conditions- brain consumes 60% of total glucose- 120g/day (1.76MJ) in resting state.
Tissue specificity - adipose and liver
Adipose
Fuel sources: required glucose to perform major task of synthesising and storing triacylglycerol, which is mobilised during fasting.
Fuel stores: in a 70kg person, adipose stores >80% of total available energy
Resting conditions: Highly active during starvation (decreased insultin activates hormone sensitive lipase which breaks down TAH)