Glycolysis Flashcards

1
Q

What are the four major fates for glucose in cell:

A
  1. Synthesis of structural polymers: ECM and cell wall polysaccharides
  2. Oxidation via pentose phosphate pathway: ribose 5-phosphate
  3. Storage: Glycogen, starch, sucrose
  4. Oxidation via glycolysis: Pyruvate
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2
Q

What are the products in glycolysis

A
  1. 2 pyruvate
  2. 2 NADH
  3. 2 H+
  4. 2 ATP
  5. 2 H2O
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3
Q

Glycolysis is divided into two reactions:

A
  1. Glucose + 2 NAD+ = 2 pyruvate + NADH + 2H+

2. 2 ADP + 2Pi = 2 ATP + 2 H2O

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4
Q

We always have to regenerate ___ for glycolysis to continue

A

NAD+

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5
Q

There is a net gain of how many ATPS

A

2

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6
Q

Production of ATP is:

A

endergonic

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7
Q

Glycolysis is ___under standard conditions

A

irreversible

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8
Q

Glycolysis occurs in the

A

cytosol

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9
Q

Glycolysis is anaerobic.

A

True

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10
Q

Committed steps have a lot of ___modifiers and ___inhibitors

A

allosteric ; feedback

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11
Q

Glycolysis deals with ___reactions divided into ___phases

A

10; 2 (5+5)

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12
Q

What is the first phase of glycolysis

A

Invest energy (from ATP) to break bonds and create two “high energy” 3 carbon compounds

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13
Q

What is the second phase of glycolysis

A

Oxidize these two compounds to pyruvate:

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14
Q

More energy is released in the ___phase than used in the ___first phase

A

second; first

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15
Q

What are the steps of the first (investment) phase of glycolysis

A
  1. Phosphoralate glucose via hexokinase
  2. Rerrangement of enzymes –>phosphohexose isomerase
  3. Phosphorlate again: Fructose 6 -phosphate into fructose 1,6 biphosphate via phosphofructokinsae 1. This is the committed step!
  4. Aldolase Cleaves fructose 1.6 bisphosphate into 2 -3 carbon phosphoralated compounds: Glyceraldehyde 3-phosphate and Dihydroxyacetone phosphate which gets rerragnged back to glyceraldehyde 3 phosphate which is the only one that continues in the cycle
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16
Q

What are the steps of the second (payoff) phase of glycolysis

A
  1. Glyceraldeyhe 3 phosphate gets phosphoralated via G3P dehydrogenase with inorganic phosphate to 1, 3 bisphosphate. This is the step that converts NAD+ to NADH. The enzyme that does this is a dehydrogenase!
  2. Taking off phosphate group via phosphoglycerate kinase (execption!) 1-3 Bisphosphoglycerate; dephosphoralate and make 1 ATP for each G3P.
  3. Arrange 3 phosphoglycerate to 2 phosphoglycerate via phosphoglucomutase.
  4. Enolase dehydrates 2 phosphoglycerate to form phosphoenolpyruvate (PEP). 5. Pyruvate kinase converts PEP to Pyruvate which generates ATP.
17
Q

Make ___ATPS per glucose. But net gain of

A

4; 2

18
Q

A negative delta G tells you

A

its not a reversible reaction

19
Q

What are hexokinase isozymes

A

Hexokinase 1: main enzyme in brain and RBC; have highest affinity for glucose
Hexokinase II: Main enzyme in muscle
Hexokinase IV (Glucokinase): found in liver. Cooperatively reg. by glucose. Reaction rate is glucose limited so acts as a glucose sensor. Much higher Km.

20
Q

If ADP and AMP levels are high it signals:

A

an increase in glycolytic pathway

21
Q

Pyruvate is not the endpoint bc

A

we need to regenerate NAD+

22
Q

What are the fates of pyruvate

A
  1. Lactate
  2. Acetyl CoA –>citric acid cycle
  3. Anabolism; oxaloacetate; alanine
  4. Fermentation to ethanol in yeast
23
Q

Conversion to lactate is irreversible, but it can be reversible if you

A

take away product

24
Q

What is the Cori cycle

A

Under anaerobic conditions we convert glucose into lactate which diffuses into bloodstream taken up by liver and used as a starting point for gluconeogenesis using lactate as its starting point during recovery send glucose back into bloodstream where it gets taken up by skeletal muscle and reconverted into glycogen.

25
Q

When can you get lactic acidosis

A
  1. strenous exercise
  2. hypoxia
  3. CN poisoning
  4. alcohol intoxication
  5. Mitochondrial disorders
  6. leukemia
26
Q

How does lactic acidosis relate to the eyes

A

in CL wearers; you get hypoxic conditions. Hypoxia creates lactic acid buildup in cornea which starts impairing function of endothelial cells. You get corneal swelling and clouding

27
Q

What are some defects in fructose metabolism

A

Deficiences in frutokinase are benign and deal with elevated urine frcutose. Deficiencies in Fructose 1 phosphate aldolase deals with hepatomegaly.

28
Q

What are the 2 routes fructose can enter glycolysis

A
  1. hexokinase

2. fructokinase

29
Q

What is galactose catalized by

A

galactokinase; makes galactose 1 phosphate

30
Q

How is galactose metabolism

A

UDP glucose and galactose intermediate.

31
Q

What is UDP

A

Uridine diphosphate. Found in RNA. Helps with extra binding interactions that help with binding energy that decreases catalytic delta G and brings down activation energy.

32
Q

What is GALT deficiency

A

Classical galactosemia; Buildup of Gal 1-P which damages liver and brain.

33
Q

Conversion to galactitol by aldose reductase in lens causes

A

cataracts

34
Q

Oral bacteria are ___anaerobes. An ex is strep mutans

A

facultative. Can live with or without oxygen

35
Q

Porphyromonas gingivalis is an _____anerobe

A

obligate; periodontal disease deep in pocket.

36
Q

Strep mutans are

A

homofermentative or homolactic fermenter (produce > 90% lactate)

37
Q

Sufficient local acid production leads to ion product of ____

A

calcium