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Glycolysis

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Glycolysis

For this activity, refer to the figure on next page to complete the table below.
Use BLUE INK PEN. Due on March 08 (TTh Classes) and March 09 (MWF and WF classes)

Step | Reactant | Product | Enzyme | Type of Reaction | 1 | | | | | 2 | | | | | 3 | | | | | 4 | | | | | 5 | | | | | 6 | | | | | 7 | | | | | 8 | | | | | 9 | | | | | 10 | | | | |

Identification:

1. 2. Two steps in glycolysis that use ATP 3. Steps in glycolysis where molecule is split. 4. Two steps in glycolysis that produce ATP. 5. # of NADH produced: _____ 6. # of carbons found in the glucose: _____ 7. # of carbons found in each pyruvate molecule: _____ 8. # of ADP produced: _____ 9. # ATP produced: _____ 10. Net total of ATP produced: _____ 11. Which product of glycolysis is used in liver for synthesis of triglycerides?

Glycolysis - occurs in the cytoplasm that converts glucose into two pyruvates * can be aerobic or anaerobic (erythrocytes and exercising skeletal muscles) *
Step 1
Step 1
Step 10
Step 10
Step 9
Step 9
Step 8
Step 8
Step 7
Step 7
Step 6
Step 6
Step 5
Step 5
Step 4
Step 4
Step 3
Step 3
Step 2
Step 2

Citric Acid Cycle/Tricarboxylic acid Cycle (TCA)/ Krebs Cycle * occurs in the mitochondria * Function: oxidation of Acetyl-CoA to carbon dioxide

* Citrate may leave the mitochondria (citrate shuttle) to deliver acetyl-CoA into the cytoplasm for fatty acid synthesis * Succinyl-CoA can be used for heme synthesis * Malate can leave the mitochondria (malate shuttle) for gluconeogenesis

Additional Notes:

Galactose Metabolism
-galactokinae deficiency galactose accumulation galactosemia OR galactose accumulation in lens galactitol cataracts

Fructose Metabolism

Hereditary Fructose Intolerance – deficiency in fructose 1-P aldolase (aldolase B) causing accumulation liver damage

Glycogen – storage form of glucose found in liver and skeletal muscles * glycogen in liver mobilized during hypoglycaemia * glycogen in muscles reserved for muscle contraction * white muscle fibers (fast-twitch) : glucose lactate * red muscle fibers (slow-twitch) : glucose is completely oxidized

Glycogenesis - GLYCOGEN SYNTHESIS
Glycogen synthase – forms glycosidic bond to form linear glucose chains

Glycogenolysis – GLYCOGEN METABOLISM
Glycogen phosphorylase - breaks the glycosidic bond

Glycogen Storage Disease 1. von Gierke Disease – deficiency in glucose-6-phosphatase causing severe hypoglycemia, hepatomegaly 2. Pompe Disease – deficiency in glucosidase causing cardiomegaly, muscle weakness, death by 2 years 3. McArdle Disease – deficiency in muscle glycogen phosphorylase causing muscle cramps and weakness on excercise

The liver maintains glucose levels in blood during fasting through either glycogenolysis or gluconeogenesis

Gluconeogenesis
Substrates for gluconeogenesis 1. glycerol 3-phosphate (from trigylcerides in adipose) 2. lactate (anaerobic glycolysis) 3. gluconeogenic amino acids (proteins from muscle)

The Cori Cycle: lactate from RBC glucose in liver

Alcohol Metabolism and Hypoglycemia

High NADH formed favors the formation of: 1. lactate from pyruvate 2. malate from OAA in the cytoplasm 3. glycerol 3- phosphate from DHAP

This can also lead to lipid accumulation in alcoholic liver diease.

Pentose Phosphate Pathway or Hexose Monophosphate (HMP) Shunt

Functions: 1. NADPH production 2. source of ribose 5-phosphate for nucleotide synthesis

Function of NADPH 1. biosynthesis 2. maintenance of a supply of reduced glutathione to protect against reactive oxygen species (ROS) 3. bactericidal activity of polymorphonuclear leukocytes (PMN)

Glucose 6-phosphate Dehydrogenase (G6PDH) Deficiency * primary cause of hemolytic anemia

G6PDH Deficiency ROS precipitated HgB (Heinz bodies) membrane lipids weakens hemolysis

Triglyceride Synthesis

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