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29 Cards in this Set

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GLUT 2

found in the liver (for glucose storage) and pancreatic β-islet cells (as part of the glucose sensor which causes release of insulin)




not responsive to insulin




it has a high Km (15 mM) so it can't be saturated under normal physiological conditions

GLUT 4

found in adipose tissue and muscle and is stimulated by insulin




its has low Km (5mM) so it is saturated when glucose levels are only slightly above 5 mM

glycolysis

occurs in the cytoplasm of all cells, and does not require oxygen. It yields 2 ATP per molecule of glucose

important glycolytic enzymes include

glucokinase


hexokinase


phosphofructokinase-1 (PFK-1)


phosphofructokinase-2 (PFK-2)


glyceraldehyde-3-phosphate dehydrogenase


3-phosphoglycerate kinase


pyruvate kinase

glucokinase

phosphorylates glucose to form glucose 6-phosphate, "trapping" glucose in liver and pancreas cells




it is present in the pancreatic β-islet cells as part of the glucose sensor (along with GLUT 2)




in liver cells, it is induced by insulin




it is irreversible

hexokinase

phosphorylates glucose to form glucose 6-phosphate in peripheral tissues, "trapping" glucose in the cell




it is inhibited by glucose 6-phosphate




it is irreversible

phosphofructokinase-1 (PFK-1)

phosphorylates fructose 6-phosphate to fructose 1,6-biphosphate using ATP in the rate-limiting step of glycolysis




activated by AMP,fructose 2,6-bisphosphate (F2,6-BP) and insulin




it is inhibited by ATP, citrate and glucagon




it is reversible

phosphofructokinase-2 (PFK-2)

produces the F2,6-BP that activates PFK-1




it is activated by insulin and inhibited by glucagon

glyceraldehyde-3-phosphate dehydrogenase

produces NADH (which can feed into the electron transport chain) while phosphorylating glyceraldehyde 3-phosphate to 1,3-bisphosphoglycerate




it is reversible

3-phosphoglycerate kinase

performs substrate-level phosphorylation, placing an inorganic phosphate (Pi) from 1,3-bisphosphoglycerate onto ADP to form ATP and 3-phosphoglycerate




it is reversible

pyruvate kinase

performs substrate-level phosphorylation, placing an inorganic phosphate (Pi) from phosphoenolpyruvate (PEP) onto ADP to form ATP and pyruvate




it is activated by fructose 1,6-bisphosphate




it is irreversible

the enzymes that catalyze irreversible reactions

glucokinase/hexokinase


PFK-1


pyruvate kinase

mitochondrial electron transport chain

when oxygen is present, oxidizes the NADH produced in glycolysis

cytoplasmic lactate dehydrogenase

if oxygen or mitochondria are absent, oxidizes the NADH produced in glycolysis




examples include:


red blood cells


skeletal muscle (during short, intense bursts of exercise)


any cell deprived of oxygen

galactose

comes from lactose in milk




it is trapped (due to phosphorylation) in the cell by galactokinase




it is converted to glucose 1-phosphate via galactose-1-phosphate uridyltransferase and an epimerase (this link galactose metabolism to glycolysis because the product can feed directly into glycolysis)

fructose

comes from honey, fruit and sucrose (common table sugar)




it is trapped in the cell (due to phosphorylation) by fructokinase (with a small contribution from hexokinase) and then cleaved by aldolase B to form glyceraldehyde (which can be phosphorylated to form glyceraldehyde 3-phosphate) and dihydroxyacetone (DHAP), which are glycolytic intermediates thus linking the pathways

pyruvate dehydrogenase (PDH) complex

refers to a complex of enzymes that converts pyruvate to acetyl-CoA




it is stimulated by insulin and inhibited by acetyl-CoA




reactants:


pyruvate


NAD+


CoA




products:


acetyl-CoA


NADH


CO2

glycogenesis

glycose synthesis




the production of glycogen using two main enzymes: glycogen synthase and branching enzyme

glycogen synthase

creates α-1,4 glycosidic links between glucose molecules




it is activated by insulin in liver and muscle

branching enzyme

moves a block of oligoglucose from one chain and adds it to the growing glycogen as a new branch using an α-1,6 glycosidic link

glycogenolysis

the breakdown of glycogen using two main enzymes: glycogen phosphorylase and debranching enzyme

glycogen phosphorylase

removes single glucose 1-phosphate molecules by breaking α-1,4 glycosidic links




in the liver, it is activated by glucagon to prevent low blood sugar




in exercising skeletal muscle, it is activated by epinephrine and AMP to provide glucose for muscle itself

debranching enzyme

moves a block of oligoglucose from one branch and connects it to the chain using an α-1,4 glycosidic link




it also removes the branchpoint, which is connect via an α-1,6 glycosidic link, releasing a free glucose molecule

gluconeogenesis

occurs in both the cytoplasm and mitochondria, predominantly in the liver




there is a small contribution from the kidneys




most is simply the reverse of glycolysis, using the same enzyme

pyruvate carboxylase

converts pyruvate into oxaloacetate, which is converted to phosphoenolpyruvate by phosphoenolpyruvate carboxykinase (PEPCK)




together, these two enzymes bypass pyruvate kinase




pyruvate carboxylase is activated by acetyl-CoA from β-oxidation




PEPCK is activated by glucagon and cortisol

fuctose-1,6-bisphosphatase

converts fructose 1,6-bisphosphate to fructose 6-phosphate, bypassing phosphofructokinase-1




this is the rate limiting step of gluconeogenesis




it is activated by ATP directly and glucagon indirectly (via decreased levels of fructose 2,6-bisphosphate)




it is inhibited by AMP directly and insulin indirecly (via increased levels of fructose 2,6-bisphosphate)

glucose-6-phosphatase

converts glucose 6-phosphate to free glucose, bypassing glucokinase




it is found only in the endoplasmic reticulum of the liver

pentose phosphate pathway (PPP)

also known as hexose monophosphate (HMP) shunt




occurs in the cytoplasm of most cells, generating NADPH and sugars for biosynthesis (derived from ribulose 5-phosphate)

glucose-6-phosphate dehydrogenase

the rate-limiting enzyme of the pentose phosphate pathway




activated by NADP+ and inhibited by NADPH and insulin