Interconversion Flashcards
How is Glucose stored in liver, and released
As G6P, and dephosphorlyated to form Glucose. G6P can be further reacted to form glycogen
How is TAG stored in adipose tissue
FFA (binded to albumin) in blood and TAG binded to chylemicron(–> VLDL in liver) is transported to WAT
TAG in VLDL is broken into FFA and glycerol
While the latter one is sent to liver while FFA becomes FA Co-A
Glucose is converted to DHAP then G3P, which combines with FA Co-A to form TAG
How abt in Liver?
It is converted to liver lipid directly
How is excess amino acid stored
It is nvr stored
So how to cope with them
They are removed by deamination where their amino group is removed as urea and carbon skeleton as carbs
How can Glucose used to release ATP
It forms pyruvate then acetyl Co-A and enters TCA cycle then ETC
How can Lipid release ATP. Where?
At liver, skeletal muscles and Cardiac muscles
FFA undergoes Beta oxidation to release ATP, NADH and Acetyl Co-A
Acetyl Co-A forms Ketone body which travels in blood and can be converted to Acetyl Co-A
NADH enters ETC
how to release energy by Amino acid
In deamination, the carbon skeleton of Alanine is used to synthesize pyruvate, which can be converted to glucose via gluconogenesis or enter TCA cycle
How to convert Glucose to TAG (iN LIVER)
Glucose forms acetyl Co-A, which is converted into cholesterol and FA by citrate
FA combines with glycerol to form TAG
TAG –> Glucose (In liver)
FA forms Acetyl Co-A which enters TCA cycle or export as ketone bodies.
Acetyl Co-A forms oxaloacetate to make PEP/pyruvate , which then forms glucose by gluconegenesis
Glycerol form glucose via gluconogenesis
Amino acid–>Carbs
Via deamination
Become G6P then glucose via gluconogenesis
Form acetyl Co-A and forms glucose via oxaloacetate then PEP
Carbs –> amino acid
Glucose enters TCA cycle to form oxaloacetate and a-ketoglutarate
Oxaloacetate can form TATA SCGP (Trp, Asp, Tyr, Asn, Ser. Cys, Gly, Phe
a-Ketoglutarate –> Glu–> Glu, Pro, Arg
How to form nucleotides
Glu can be used to form purines
Asp and Asn (derived from oxalacetate) can form pyramidines
How to replenish TCA intermediates
Oxaloacetate (In liver and kidney)
Pyruvate +HCO3-+ ATP
–> (pyruvate carboxylase)
Oxaloacetate + ADP+ Pi
In heart and skeletal muscle
Phosphoenolpyruvate +NAD(P)H
–> (carboxykinase)
Oxaloacetate +GTP
In most eukaryotes and bacteria
Pyruvate + HCO3- +NAD(P)H
–> (malic enzymes)
Malate + NAD(P)
Why we have to regulate the catabolism and anabolism
It is wasteful to simultaneously synthesize and degrade some substances