Biochem Review Flashcards
(9 cards)
Cellular Respiration Overview
- Glycolysis: Glucose –> 2 Pyruvate (NADH and ATP)
- Pyruvate Processing: Pyruvate –> Acetyl CoA (CO2 and NADH)
- Citric Acid: Acetyl CoA –> CO2 (NADH, FADH2 and ATP/GTP)
- ETC/Chemiosmosis: proton gradient –> ATP, O2 and H2O
Glucose CANNOT be generated from FA (true if reversed)
> Acetyl-CoA is not a substrate for gluconeogenesis in animals
Pyruvate dehydrogenase rxn is irreversible (Acetyl-CoA cannot return to pyruvate)
Pyruvate dehydrogenase complex: Pyruvate –> Acetyl-CoA (CoA-SH/NAD+ in with TPP/lipoate/FAD; NADH out)
No net production of oxaloacetate: 2C acetyl-CoA enters TCA via condensing with 4C oxaloacetate and releasing 2 CO2 to regenerate oxaloacetate
Glucose can be generated from AA
Protein –> AA –>
> NH4 –> AA + amines –> urea cycle –> nirogen and urea product
> Alpha-ketoglutarate –> TCA (CO2, H2O and ATP made) –> oxaloacetate –> glucose made via gluconeogenesis
Transaminase and Deamination (NH4+ –> urea)
- Alanine + alpha-keto –> pyruvate + glutamate
2. Glutamate –> alpha-keto (H2O in and NADPH out; by glutamate dehydrogenase)
Gluconeogenesis
- Phosphoenolpyruvate (2) –> pyruvate (2) via pyruvate kinase
- Pyruvate (2) –> Oxaloacetate (2) via pyruvate carboxylase
- Oxaloacetate (2) –> Phosphoenolpyruvate (2) via PEP carboxykinase
FA Synthesis
- OAA + Acetyl CoA –> Citrate
- Acetyl CoA –> Malonyl CoA via Acetyl-CoA carboxylase + CO2
- Malonyl CoA –> Palmitate (C16:0) via FA synthase + NADPH
B Vitamins, Cofactor and Deficiency Consequences
- Thiamine (B1):
> Thiamine Pyrophosphate (TPP); transfer aldehyde; heart problems - Riboflavin (B2):
> Flavin Adenine Dinucleotide (FAD); Redox; mouth lesions - Pyridoxine (B6):
> Pyridoxal Phosphate; group transfer of AA; depression/convulsions - Nicotinic acid/Niacin:
> Nicotinamide adenine Dinucleotide (NAD); Redox; depression/dermatitis - Biotin:
> Biocytin; ATP-dep carboxylation/carboxyl transfer; rashes - Folic Acid:
> Tetrahydrofolate (THF); transfer of 1C/thymine synth; anemia - B12:
> Cobalamin; methyl transfer; anemia/acidosis
Glucogenic AA
- Degraded back to alpha-keto acids and then to glucose
> Involves pyruvate and oxaloacetate in TCA
> Alanine, glycine, serine, tyrosine, threonine
Ketogenic AA
- Can be degraded directly into Acetyl-CoA (ketone bodies)
> Leucine, lysine, phenylalanine, tryptophan