metabolism
the sum processes of chemical changes in living cells by which energy and nutrients are provided for vital processes and activities and new materials are assimilated
anabolism
the constructive part of metabolism involving synthesis (creating new compounds)
catabolism
the destructive part of metabolism involving the release of energy and breakdown of complex materials
oxidation
loss of electrons
reduction
gain of electrons
Glycolysis
anaerobic (no O2) occurs in cytosol
Kreb's Cycle (TCA)
aerobic (needs O2) occurs in mitochondria
Oxidative phosphorylation
aerobic (needs O2) occurs in mitochondriaS
Stage 1 of Glycolysis
priming = uses 2 ATP Hexokinase (takes P from ATP to make Glucose-6-P) Phosphofructokinase (takes P from ATP to make Fructose 1,6-P)
Stage 2 of Glycolysis
production 4 ATP produced per glucose (total output of 2 ATP) generates 2 ATP, 2 NADH, and 2 pyruvate pyruvate kinase
NADH
electron transport yields 3 ATP per NADH
FADH2
electron transport yields 2 ATP per FADH2
Kreb's Cycle
pyruvate converted to acetyl-CoA (takes place for each pyruvate) produces 3 NADH, 2 FADH2, 1 GTP, 12 ATP for each acetyl-CoA (24 ATP total for 2 acetyl-CoA)
mitochondrion
function in the synthesis of ATP, major source of energy electron transport chain is on the inner membrane
oxidative phosphorylation
multi-enzyme complexes located in inner membrane inner membrane is impermeable to NAD, NADH, ATP and ADP proton-motive force
proton-motive force
build up of protons in the inter membrane space that drives ATP synthesis down a concentration gradient
ATP synthesis
ATP synthase catalyzes formation of ATP from ADP and P achieved from flow of protons form inter membrane space matrix NADH moves 10 protons FADH2 moves 6 protons 10 protons are needed for one full turn and will make 3 ATP
insulin
increases uptake of glucose, increases fat storage stimulates the formation of glycogen
Glycagon
Decrease uptake of glucose stimulates conversion of amino acids to glucose
Glucocorticoids
increases blood glucose (stress response)
Epinephrine
increases blood glucose decreases fat storage
Glycogenesis
process of making glycogen muscle and liver happens immediately following a meal caused by insulin
Glycogenolysis
breaking down glycogen caused by glucagon (increases glycogenolysis, increases blood glucose)
Gluconeogenesis
making glucose from non-CHO sources (the reverse of glycolysis) liver and kidney very important in ruminants (very little glucose is absorbed; propionate converted to glucose)
Simple lipids
makes up the largest % of lipids fats, oils, waxes
saturated lipids
single bonds only (as many H as possible)
unsaturated lipids
double bonds
gastric lipase
found in stomach; not very active in mature animals, functional in young animals
pancreatic liapse
primary fat digestion enzyme secreted with pancreatic juice secreted in an inactive form activated by Ca in lumen of SI
Bile
produced by liver and stored in gall bladder secreted in duodenum emulsification of fat arrange triglycerides for hydrolysis of lipase
lipase
cleaves fatty acid from glycerol backbone which exposes the hydrophilic heads
Micelle
free fatty acids and bile salt can interact with brush border and is the form which lipids are absorbed
chylomicron
made up of triglycerides, proteins, phospholipids, and cholesterol
fatty acid metabolism
oxidation to CO2 for ATP make glycolipids, phospholipids, and cell membranes lung alveolar integrity solubilize ADEK prostaglandin, sex hormones, adrenal hormones energy
cortisol
decreases fat storage
glucagon
decreases fat storage
growth hormone
decreases fat storage
fatty acid synthesis
produced from acetyl-CoA from CHO, proteins, VFAs, degraded fats occurs in cytosol fats are made 2 C at a time; process continues until fatty acid is 16 C long fatty acid synthase
B-oxidation
stepwise removal of 2C from fatty acids to make acetyl-CoA (2C) 16C = 8 acetyl CoA occurs in mitochondria
Ketosis
occurs when an animal has high energy demand increases fat catabolism = increases acetyl CoA which overloads Krebs cycle and it backs up converts acetyl CoA to acetoacetic acid (toxic), b-hydroxybutyric acid, and acetone blood pH decreases = metabolic acidosis
essential amino acids
phenylalanine valine threonine tryptophan isoleucine methionine histidine arginine leucine lysine
glucogenic amino acids
glycine, alanine, threonine, cystine, methionine converted to krebs cycle intermediates and converted to glucose
ketogenic amino acids
lysine, leucine converted to acetyl CoA and then to ketones
functions of absorbed proteins
nonessential amino acid synthesis tissue synthesis synthesis of enzymes and hormones deamination transaminiation
Protein synthesis
complex, involves many systems in body requires 20 ATP per peptide bond nucleic acids needed
protein turnover/degradation
constant process since there isn't a storage for amino acids combination of synthesis and degradation
Deamination
excess AA not needed for protein synthesis are catabolized break off NH3 from carbon skeleton
Urea
made with 2 ammonia (NH3) and carbon skeletonf
feeding experiment
feed feedstuff/nutrient, compare with standard source/control, measure production response answers: will they consume it and how well do animals perform questions: nutrient utilization
Digestion experiment
feed feedstuff/nutrient, sample feed and collect feces, analysis of feed and feces, calculate apparent digestibility coefficient (same equation as percent error) answers: nutrient absorption in GI tractme
metabolism experiment
feed feedstuff/nutrient, sample feed and collect feces, analysis of feed and feces, collect urine and analyze, calculate nutrient balance ((intake-(fecal+urine))/intake) x 100 answers: nutrients retained
How many total ATP are used in glycolysis?
2 ATP
What process breaks down glycogen?
Glycogenolysis
What enzymes control glycolysis?
hexokinase, phosphofructokinase, pyruvate kinase
Which pathway is responsible for the breakdown of glucose?
glycolysis
Urea is considered a non-protein nitrogen source.
true
What is a function of the stomach during fat digestion?
produce small droplets of fat
What is acetate converted to and what can it then be used to make?
acetyl CoA; ketones
What are the 2 products of deamination of amino acids?
NH3 and carbon skeleton
Microbes can use urea by aminiating then using the NH3 and carbon skeleton to make MCO protein.
true
Where does glycolysis occur?
cytosol
where does the kreb's cycle occur?
mitochondria
Goats require fatty acids in their diet
false
What must be continuously regenerated for glycolysis to continue?
NAD
After a carbohydrate heavy meal, what would you expect insulin and glucagon to do?
insulin decreases and glucagon increases
After a carbohydrate heavy meal, what would you expect gluconeogenesis and glycogenolysis to do?
stop
glycogen synthesis/glycogenesis will occur after a carbohydrate heavy meal.
true
What would be a route that nitrogen can be recycled back to the rumen?
saliva and bloodstream
what hormone would you expect to increase fat catabolism?
epinephrine
What do carbohydrate, fat, and protein metabolism have in common?
acetyl-CoA
What enzyme produces ATP from NADH, located on the inner mitochondrial membrane?
ATP synthase
What describes the over process of fat catabolism?
B-oxidation
What is produced by the liver, stored in the gall bladder, and secreted into the duodenum to aid in fat digestion?
Bile
What is a chylomicron composed of?
triglycerides, cholesterol, phospholipids, proteins
How is butyrate produced?
2 pyruvate -> 2 acetyl-CoA -> butyrate