L8+9 biochem Flashcards

1
Q
  • conversion of pyruvic acid (end product of glycolysis) irreversibly to Acetyl-CoA, catalyzed by PDH complex (not a component of TCA)
  • known as the link reaction between glycolysis and citric acid cycle.
  • pyruvate transported into mitochondria via pyruvate transporter
A

Oxidative decarboxylation of Pyruvic acid

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2
Q

Pyruvate dehydrogenase complex
E1: needs TPP thiamine pyrophosphate as coenzyme
E2: needs lipoic acid (firmly attached=prosthetic group) and CoASH (free)
E3: need FAD (firmly attached to the enzyme) and NAD (free)

A

E1: Pyruvate decarboxylase (pyruvate dehydrogenase)
E2: Dihyrolipoyl transacetylase
E3: Dihyrolipoyl dehydrogenase

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3
Q

conversion of pyruvate to acetyl CoA via three steps:
a) Decarboxylation (E1)
B) Transfer of acetyl group to CoA (E2)
C) Oxidation (E3)

*End result: ___ NADH and __ ATP

A

*2 NADH used by ETC to produce 6 ATP

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4
Q
  • more toxic than pentavalent form(replaces Pi)
  • mechanism: forms a stable complex with thiol (SH) groups of lipoic acid leading to inhibition of enzymes that require lipoic acid as a coenzyme
  • NEGATIVELY affects the brain and leads to DEATH
A

Triavalent arsenite

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5
Q

A)allosteric regulation
1-PDH complex is inhibited by its own product _____ and ____

B)covalent modification
1-PDH kinase: inhibits PDH complex by _____ of E1 (pyruvate dehydrogenase)
2-PDH kinase can also be regulated allosterically by high ATP, NADH, Acetyl CoA which ____ PDH kinase activity, WHILE high ADP and pyruvate will ___ PDH kinase activity

A

B1-phosphorylation
B2-induce, inhibit

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6
Q
  • rare disorder
  • **most common biochemical cause of congenital lactic acidosis
    symptoms: neurodegeneration, muscle spasticity, neonatal (early)death
A

Pyruvate dehydrogenase deficiency (PDCD)

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7
Q
  • occurs primarily in liver (90%), (10% in kidney) in fasting
  • happens 50% during prolonged starvation
  • in cytosol and mitochondria
  • importance: maintain blood glucose level during fasting for more than 18 hours
  • 6 ATP is consumes
A

Gluconeogenisis

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8
Q

during Anaerobic glycolysis in skeletal muscle, pyruvate is reduced to ______ by _______
this reaction serves 2 critical functions:
1- the LDH reaction requires ___ and yields NAD+ for use of glycolysis
2- the lactate produced will go to the blood, then liver where its converted to glucose then returned to blood for use of muscle this is called the ________

A

Lactate, LDH (lactate dehydrogenase)

1-NADH
2- Cori cycle

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9
Q

glycerol kinase is present only in ___ and ___ (not present in adipose tissue) + it catalyzes glycerol to DHAP

A

Liver and Kidney

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10
Q

glucogenic amino acids are the building units for _____

-they are deaminated giving pyruvate and oxaloacetate (Krebs cycle)

A

Protein (mainly muscle protein)

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11
Q

all amino acids can give glucose except ____ and ___

A

Leucine and lysine

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12
Q

***Q: any reaction with Acetyl CoA as the end product is ALWAYS _____

A

irreversible

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13
Q

***Q: the FA that contributes to gluconeogenesis?

A

odd chain FA only

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14
Q

the enzymes that are irreversible and require** 4 **enzymes unique to gluconeogenesis foe their reversal:
1- ________
2-________
3-________

A

1- PK
2- PFK1
3- glucokinase (hexokinase)

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15
Q

reversal of PK reaction by 2 enzymes :
1- __________ (in metabolism)
2-__________ (in cytosol)

A

1- pyruvate carboxylase

2- phosphoenolpyruvate carboxykinase (PEPCK)

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16
Q

reversal of PFK reaction by ________

A

Fructose 1,6-bisphosphate

17
Q

reversal of glucokinase (hexokinase) reaction by ______

-this enzyme is present in liver and kidney but NOT muscle

A

Glucose 6-phosphatase

18
Q

fructose 1,6-bisphosphate in the liver abd kidney is :
1- allosteracally inhibited by _________ and ____
2- stimulated by ____

A

1- fructose 2,6-bisphosphate, AMP

2- ATP

19
Q

during fasting acetyl coA comes from the ____

A

Liver

20
Q

glucagon increases the synthesis of _____ while insulin decreases it

A

PEPKC