fructose/galactose/pentose phosphate pathways Flashcards
Describe the dietary sources of fructose
In the diet, the main sources of fructose are honey and high fructose corn syrup. Fruit contain sucrose, a disaccharyde of glucose and fructose
Describe the two major functions of the pentose phosphate pathway
Generation of NADPH + H+ The reducing power of NADPH is used for: fatty acid synthesis cholesterol synthesis nucleotide synthesis oxidation of toxins by cytochrome P450 enzymes generation of reduced glutathione
Generation of five carbon sugars
Five carbon sugars are used primarily for synthesizing nucleotides.
compare the two phases of the pentose phosphate pathway
The oxidative phase:
converts glucose to ribulose 5-phosphate
generates NADPH + H+
reactions are not reversible
The regenerative phase:
converts ribulose 5-phosphate to the glycolysis intermediates fructose 6-phosphate and glyceraldehyde 3-phosphate
is reversible– glycolysis intermediates can be used to generate five carbon sugars for nucleotide synthesis
the key enzymes are transketolase and transaldolase; their reactions are reversible
xylulose 5-phosphate is a key metabolic regulator
essential fructosuria
benign deficiency in fructokinase
hereditary fructose intolerance
deficiency in aldolase B, fructose 1-phosphate builds up in liver, not benign
galactose 1-phosphate uridyl transferase deficiency
“classical galactosemia”; autosomal recessive; very serious early onset (1-2 weeks old) jaundice, hepatomegaly, hypoglycemia, lethargy, FTT treatment: eliminate galactose from diet; prognosis is poor
galactokinase deficiency
galactose accumulates, is converted to galactitol through polyol pathway -> catacts
treatment is to eliminate lactose from diet; good prognosis
uridine diphosphate galactose 4-epimirase deficiency
benign form: only affects leukocytes and erythrocytes
serious form: all tissues; symptoms similar to transferase deficiency
treatment: A galactose restricted diet
glucose 6-phosphate dehydrogenase deficiency
If people with glucose 6-phosphate dehydrogenase deficency are exposed to xenobiotics which are detoxified by NAPDH consuming enzymes, their capacity to regenerate NAPDH through the pentose phosphate pathway is limited, and NAPDH is rapidly depleted.
This leads to severe oxidative stress; red blood cells are particularly affected. 50% or more of a person’s red blood cells may be destroyed– this condition is called hemolytic anemia
rate limiting step of glycolysis
fructose 6-phosphate -> fructose 1,6-bis-phosphate. Fructose metabolism bipasses this