1/74
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai | Chat |
|---|
No analytics yet
Send a link to your students to track their progress
what is glycolysis
breakdown of glucose to produce ATP and pyruvate, which can be shuttled to the Krebs cycle
what is Gluconeogenesis
pathway that synthesizes glucose from various molecules
what is the Pentose Phosphate Pathway
produces NADPH and ribose-5 phosphate, and is a major regulator of cellular redox and shunts carbons back to glyolytic and gluconeogenic pathways
what is B oxidation
cells use to breakdown fatty acids into acetyl-CoA, which can enter into the Krebs cycle to produce energy
what is the Krebs Cycle
also known as the citric acid cycle and the TCA cycle, series of enzyme catalyzed chemical reactions that release stored energy by the oxidation of acetyle-CoA
what is the mitochondria
organelle within the eukaryotic cell that generate most of the cellular energy needed by cells
what is electron transport
series of reactikons that shuttle electrons from NADH to FADH2 to molecular oxygen. results in the pumping of protons from the mitochondrial matrixinto the mitochondrial intermembrane space and oxygen is reduced to form water. the H ions (protons) are pumped into the mitochondrial matric via the ATP synthase enzyme, which uses the force to phsphorylate ADP making ATP (oxidative phosphorylation)
what is amino acid oxidation
process by which amino acids are converted into end products that are utilized by other metabolic pathways
what is the urea cycle
pathway for detoxifying excess nitrogen in the form of ammonia by converting it into uric acid or urea
what is a catabolic process
process that breaks down molecules
what is an anabolic process
process that build complex molecules
what is an amphibolic process
pathway that does both catabolism and anabolism
what are the 3 enzymes of glycolysis in order
hexokinase, phosphofructokinase, pyruvate kinase
what is the end product of glycolysis
net yield of 2 atp and 2 pyruvate
ATP is energy ______ molecules
storage
what is the first step of glycolysis
glucose → glu-6-phosphate
what enzymes catalyse the first step of glycolysis
hexokinase and glucokinase
what type of enzyme if hexokinase
regulatory, it is inhibited by the product that it makes and functions at normal concentrations of glucose
what does glucokinase do
only phosphorylates glucose, and is found predominately in the liver, requires a much higher concentration of glucose to become fully active
what are the 2 key regulatory steps of glycolysis
fru-6-phosphate → fru-1,6- bisphosphate, and phosphoenolpyruvate→pyruvate
what enzyme catalyzes fru-6-phosphate → fru-1,6- bisphosphate
phosphofructokinase
what enzyme catalyzes phosphoenolpyruvate→pyruvate
pyruvate kinase
when is phosphofructokinase inhibited
high concentrations of ATP, citrate and long-chain fatty acids
when is pyruvate kinase inhibited
ATP, AMP, citrate, long chain fatty acids, acetyl-coa, and alanine
when is pyruvate kinase stimulated
middle energy states
where does electron transport take place
inner mitochondrial membrane
where does the pentose phosphate pathway occur
cytosol, especially in the liver and adipose cells
what is the pentose phosphate pathway controlled by
glucose-6-phosphate dehydrogenase, inhibited by high levels of NADPH and fatty acid intermediates
what does the PPP produce NADPH for
fatty acid and steroid synthesis
what does the PPP produce ribose for
nucleotide synthesis
what are the different fates of glucose
storage, oxidation via glycolysis, oxidation via PPP
what does glucose turn into if it is used for storage
glycogen, starch, sucrose
what does glucose turn into if its oxidized in glycolysis
pyruvate
what does glucose turn into it if it oxidized using the PPP
Ribose- 5- phosphate
______ is the synthesis of glucose from noncarbohydrate precursors
gluconeogenesis
where does gluconeogensis occur
liver and kidneys
what are the 3 precursors for gluconeogenesis
amino acids, lactic acids, glycerol
what is not a precursor for gluconeogenesis
fatty acids
pyruvate to glucose is
gluconeogenesis
glucose to glycogen is
glycogenesis
glycogen to glucose is
glycogenolysis
glucose to pyruvate is
glycolysis
what is the site of oxidative phosphorylation
mitochondria
where do all mitochondria come from
mom
where does glycolysis occur
cytoplasm
what does the krebs cycle do
generates citrate from pyruvate
what are the start and end points of the electron transport chain
NADH→ Nad+ + 2H, Fadh2 → FAD + 2H, [ 2H + 1/2O2 + 2e- → h20] x2
Glycolysis net energy yeilds
2 atp, 2 nadh
citric acid cycle net energy yeilds
2 atp, 8 nadh, 2fadh2
how many atp can a singular molecule of glucose produce
30-32
what are free fatty acids transported by
albumin
what is the main storage for of fatty acids
triglycerides
where are chylomicrons formed
small intestines
what do chylomicrons transport
triglycerides, phospholipids, cholesterol, and proteins
where is VLDL made
liver
what do VLDL transport
triglycerides, phopholipids, cholesterol, and cholesterol esters
saturated fatty acids
contain no double bonds
monounsaturated fatty acids
one double bound
polyunsaturated fatty acids
more than one double bond
cis unsaturated fatty acids
the hydrogens are located on the same side
trans unsaturated
hydrogens are located on the opposite sides
is B oxidation a catabolic or anabolic process
catabolic
whre does oxidation of fatty acids take place
mitochondria
what is the carnitine transport system used for
getting fatty acids into the mitochondria (active transport)
which amino acids are oxidized into pyruvate and the acetyl-CoA
alanine, threonine, glycine, serine, cysteine
which amino acids are oxidized into oxaloacetate
aspartate and asparagine
which amino acids are oxidized into fumarate
phenylalanine and tyrosinw
which amino acids are oxidized into glutamate then a-ketoglutarate
arginine histidine, glutatmine, proline
which amino acids are oxidized into succinyl-CoA (that also yeilds acetyl-CoA)
Isoleucine, methionone, valine
which amino acids can be oxidized to acetoacetyl-CoA then Acetyl-CoA
phenylalanine, tyrosine, lysine, leucine,tryptophan
which amino acids can e directly oxidized to acetyle- CoA
leucine, Tryptophan
what links the citric acid cycle and the urea cycle
fumarate
what is the urea acid cycle
amino acid catabolism that gets rid of excess nitrogen (NH3)
where does the urea acid cycle occur
liver mitochondira cytosol