Biochemistry Flashcards
2 parts of glycogen
glycogenin
multiple glucose molecules bonded together in chains
bonds found in glycogen molecules
alpha 1-4 straight
alpha 1-6 branches
process which produces glycogen
glycogenesis
UDP-glucose role
activated intermediate
rate limitng enzyme of glycogen production
hexakinase
gluconeogenesis produces glucose from 3 molecules
amino acids
lactate
glycerol
what is the cori cycle
recycles lactate formed by anaerobic respiration
where is the cori cycle
in liver
energy cost of cori cycle
6 ATP
break down of glycogen
inverse reaction of glycogenesis
fates of the monomer subunits of glycogen breakdown
glucose in blood
glycolysis in muscles
3 types of lipid
simple
compound
steroid
what are lipids soluble in
insoluble in water
2 components in triglycerides
3 fatty acids
glycerol backbone
products of beta oxidation
using triglycerides 1 acetyl CoA 1 FADH2 1 NADH +H2 1 fatty AcylCoA - 2 carbons
4 step synthesis of fatty acid occurs
condensation
reduction
dehydration
reduction and release
lipogenesis
de novo synthesis of fatty acids
insulin promotes storage
glucagon signals breakdown
citrate is allosteric
liver glycogen
is a storage system to maintain the blood glucose between meals
muscles glycogen
provides a source of energy to muscle tissue during exercise
what is gluconeogenesis powered by
oxidation of lipids
glucose-6-phosphate in the liver
is converted to glucose
glucose-6-phosphate in muscles
provides energy - glycolysis etc
carnitine shuttle
transport fats into mitochondria
converting to acetyl CoA
energy level of beta oxidation
each acetyl-CoA makes 1 FADH2, 3NADH, 1 GTP
FADH2 - 1.5 ATP
NADH - 2.5 ATP
GTP - 1 ATP
ketones
are produced in the mitochondria of the liver
diffuse out to the peripheries and used in the heart and kidneys and converted back to acetyleCoA
fatty acid synthesis
a starter chain is attached to ACP
acetylCoA and malonylCoA are used to add 2 C atoms per cycle, this consumed NADPH
synthesis of triglycerides
glycerol-3-phosphate and 3 fatty acids form a triglyceride through esterification
break down of amino acids
produce NH3 and NH4 both are toxic
amino acid absorption
proteolytic enzymes in the stomach/intestine produce single amino acids
absorbed into intestinal cells and released into the blood
amino acid protein turnover
tightly regulated
multiple different rates
damaged proteins have to be removed
transamination
moving the amino group from an amino acid to an alpha keto acid
happens in all tissues
uses a TCA intermediate
these are transported to the liver
deamination
conversion of amino groups to free ammonium ions
synthesis of urea
uses water
happens in the mitochondrial matrix
way of making the toxic NH4 through less toxic products to urea that can be excreted
2 types of amino acids
ketogenic - degraded to acetylCoA and can form ketone bodies
glucogenic - degraded to pyruvate