5. PROTEINS
âProteins are the most abundant organic compounds that
constitute a major part of the body dry weight (10-12kg).
âOur body gets sufficient amount of proteins from food
sources such as fishes, milk , egg , mixed nuts etc .
âProtein metabolism is more appropriately learnt as amino
acid metabolism.
âEach of the 20 amino acids undergoes its own metabolism
and perform specific functions.
9. TRANSAMINATION
âThe transfer of an amino group from an amino acid to a
keto acid is known as tansamination.
âThe energy (keto acid) that we get from transamination is
has various fates.
â Utilised to generate energy .
â Used for the synthesis of glucose.
â For the formation of ketone bodies.
â For the production of non-essential amino acids.
11. â All transaminases require pyridoxal phosphate (PLP), a
co enzyme which is derived from vitamin B6
âHere the transfer of amino group from Alanine is
trasferred to the co enzyme pyridoxal phosphate to form
pyridoxamine phosphate.
âThe amino group of pyridoxamine phosphate is then
transferred to the keto acid (alpha keto glutarate) to
produce a new amino acid (Glutamate) and the ezyme
pyrodoxal phosphate (PLP) is regenerated.
âThe transamination process is reversible.
âThere is no free ammonia (NH3) is liberated,only the
transfer of amino group occurs.
15. DE CARBOXYLATION
âDe carboxylation is the removal of CO2 from the
carboxyl group of amino acid and converts it to
corresponding amine.
âIt requires the enzyme decarboxylase, which is present in
liver,microorganisms of intestinal tract etc.
âPyridoxal phosphate acts as a co-enzyme here.
16. UREA - CYCLE
âAmmonia which is synthesised during amino acid
metabolism is higly toxic. This toxic susbstance is
converted to non toxic urea and excreted from our body
through urine.
âThis can be explained through Urea-cycle which was
elucidated by Hans Krebs and Kurt Henseleit, hence it is
also called Krebs-Henseleit cycle.
âThe cycle takes place in mitochondria and cytoplasm of
the cell.