Biochem Review Flashcards

1
Q

Cellular Respiration Overview

A
  1. Glycolysis: Glucose –> 2 Pyruvate (NADH and ATP)
  2. Pyruvate Processing: Pyruvate –> Acetyl CoA (CO2 and NADH)
  3. Citric Acid: Acetyl CoA –> CO2 (NADH, FADH2 and ATP/GTP)
  4. ETC/Chemiosmosis: proton gradient –> ATP, O2 and H2O
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2
Q

Glucose CANNOT be generated from FA (true if reversed)

A

> 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

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3
Q

Glucose can be generated from AA

A

Protein –> AA –>
> NH4 –> AA + amines –> urea cycle –> nirogen and urea product
> Alpha-ketoglutarate –> TCA (CO2, H2O and ATP made) –> oxaloacetate –> glucose made via gluconeogenesis

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4
Q

Transaminase and Deamination (NH4+ –> urea)

A
  1. Alanine + alpha-keto –> pyruvate + glutamate

2. Glutamate –> alpha-keto (H2O in and NADPH out; by glutamate dehydrogenase)

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5
Q

Gluconeogenesis

A
  1. Phosphoenolpyruvate (2) –> pyruvate (2) via pyruvate kinase
  2. Pyruvate (2) –> Oxaloacetate (2) via pyruvate carboxylase
  3. Oxaloacetate (2) –> Phosphoenolpyruvate (2) via PEP carboxykinase
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6
Q

FA Synthesis

A
  1. OAA + Acetyl CoA –> Citrate
  2. Acetyl CoA –> Malonyl CoA via Acetyl-CoA carboxylase + CO2
  3. Malonyl CoA –> Palmitate (C16:0) via FA synthase + NADPH
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7
Q

B Vitamins, Cofactor and Deficiency Consequences

A
  1. Thiamine (B1):
    > Thiamine Pyrophosphate (TPP); transfer aldehyde; heart problems
  2. Riboflavin (B2):
    > Flavin Adenine Dinucleotide (FAD); Redox; mouth lesions
  3. Pyridoxine (B6):
    > Pyridoxal Phosphate; group transfer of AA; depression/convulsions
  4. Nicotinic acid/Niacin:
    > Nicotinamide adenine Dinucleotide (NAD); Redox; depression/dermatitis
  5. Biotin:
    > Biocytin; ATP-dep carboxylation/carboxyl transfer; rashes
  6. Folic Acid:
    > Tetrahydrofolate (THF); transfer of 1C/thymine synth; anemia
  7. B12:
    > Cobalamin; methyl transfer; anemia/acidosis
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8
Q

Glucogenic AA

A
  1. Degraded back to alpha-keto acids and then to glucose
    > Involves pyruvate and oxaloacetate in TCA
    > Alanine, glycine, serine, tyrosine, threonine
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9
Q

Ketogenic AA

A
  1. Can be degraded directly into Acetyl-CoA (ketone bodies)

> Leucine, lysine, phenylalanine, tryptophan

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