AMINO ACID METABOLISM. Metabolic relationship of amino acids BODY PROTEINS Proteosynthesis Degradation AMINO ACIDS DIETARY PROTEINS GLYCOLYSIS KREBS CYCLE.

AMINO ACID METABOLISM

Metabolic relationship of amino acids

BODY PROTEINS

Proteosynthesis Degradation

AMINO ACIDSDIETARYPROTEINS

GLYCOLYSISKREBS CYCLE

Digestion

Transa

mination

NONPROTEINDERIVATIVESPorphyrinsPurinesPyrimidinesNeurotransmittersHormonesComplex lipidsAminosugars

UREA NH3Con

vers

ion

(Carb

on

skele

ton

)

250 – 300 g/day

ACETYL CoAGLUCOSE CO2 KETONBODIES

Endopeptidases – hydrolyse the peptide bond inside a chain: pepsin, trypsin, chymotrypsinExopeptidases – split the peptide bond at the end of a protein molecule: aminopeptidase, carboxypeptidasesDipeptidases

Enzymes cleaving the peptide bond

pepsin (pH 1.5 – 2.5) – peptide bond derived from Tyr, Phe,bonds between Leu and Glu

trypsin (pH 7.5 – 8.5) – bonds between Lys a Arg

chymotrypsin (pH 7.5 – 8.5) – bonds between Phe a Tyr

Gamma-glutamyl cycle

Essential amino acids in humans

Arginine* Histidine* Isoleucine Leucine Valine

Lysine Methionine Threonine Phenylalanine Tryptophan

*Required to some degree in young growing period and/or sometimes during illness.

Non-essential and nonessential amino acids in humans

Alanine Asparagine Aspartate Glutamate Glutamine

Glycine Proline Serine Cysteine (from Met*) Tyrosine (from Phe*)

* Essential amino acids

Can be formed from -keto acids by transamination and subsequent reactions.

C

O

R COO-

+ NH4+

deamination

transamination C

O

R COO-

CH

NH2

R COO-

CH

NH2

R COO-

General reactions of amino acid catabolism

The fate of the amino group during amino acid catabolism

Transamination reaction

The first step in the catabolism of most amino acids is removal of a-amino groups by enzymes transaminases

or aminotransferases

All aminotransferases have the same prostethic group and the same reaction mechanism.

The prostethic group is pyridoxal phosphate (PPL), the coenzyme form of pyridoxine (vitamin B6)

Biosynthesis of amino acid: transamination reactions

amino acid1 keto acid2 amino acid2 +-keto acid1

NH3+

-O2CCH 2CH2CHCO 2-

Glutamate

OR-CCO 2

-+

O-O2CCH 2CH2CCO 2

-

-Ketoglutarate

NH2

R-CHCO 2-

+

Pyridoxal phosphate (PLP)-dependent aminotransferase

Keto-acid

Amino acid

Active metabolic form of vitamin B6

Mechanism of transamination reaction: PPL complex with enzyme accept an amino group to form pyridoxamine phosphate, which can donate its amino group to an -keto acid.

All amino acids except threonine, lysine, and proline can be transaminated

Transaminases are differ in their specificity for L-amino acids. The enzymes are named for the amino group donor.

Clinicaly important transaminases

ALT

Alanine--ketoglutarate transferase ALT(also called glutamate-pyruvate transaminase – GPT)

Aspartate--ketoglutarate transferase AST(also called glutamate-oxalacetate transferase – GOT)

Important in the diagnosis of heart and liver damage caused by heart attack, drug toxicity, or infection.

Glucose-alanine cycle

Ala is the carrier of ammonia and of the carbon skeleton of pyruvate from muscle to liver.The ammonia is excreted and the pyruvate is used to produce glucose, which is returned to the muscle.

Alanine plays a special role in transporting amino groups to liver.

According to D. L. Nelson, M. M. Cox :LEHNINGER. PRINCIPLES OF BIOCHEMISTRY Fifth edition

Glutamate releases its amino group as ammonia in the liver

The amino groups from many of the a-amino acids are collected in the

liver in the form of the amino group of L-glutamate molecules.

Glutamate undergoes oxidative deamination catalyzed by L-glutamate

dehydrogenase. Enzyme is present in mitochondrial matrix. It is the only enzyme that can use either NAD+ or NADP+ as the acceptor of reducing

equivalents. Combine action of an aminotransferase and glutamate dehydrogenase referred to as

transdeamination.

Ammonia transport in the form of glutamine

Glutamine synthetase

Excess ammonia is added to glutamate to form glutamine.

Glutamine enters the liver and NH4+

is liberated in mitochondria by the enzyme glutaminase.

Ammonia is remove by urea synthesis.

Relationship between glutamate, glutamine and -ketoglutarate

-ketoglutarate glutamate glutamine

NH3

NH3

NH3

NH3

glutamate + NAD+ + H2O -ketoglutarate NH3+ + NADH

glutamate NH3+ glutamine

ATP ADP

glutamine H2O+ glutamate NH3+

A. Glutamate dehydrogenase

B. Glutamine synthetase (liver)

C. Glutaminase (kidney)

From transamination reactions

To urea cycle

Oxidative deamination

Amino acids FMN H2O+ +

keto acids FMNH2 NH3

L-amino acid oxidase

A. Oxidative deamination

FMN H2O2

H2O O2+

+ +

O2

catalse

B. Nonoxidative deamination

serine

pyruvate

threonine

-ketobutirateNH3+

+

NH3

Serin-threonin dehydratase

•L-amino acid oxidase produces

ammonia and -keto acid directly,

using FMN as cofactor.

•The reduced form of flavin must be

regenerated by O2 molecule.

•This reaction produces H2O2

molecule which is decompensated by

catalase.

Is possible only for hydroxy amino acids

CARBAMOYL PHOSPHATE

Ornithine

Citrulline

Argininosuccinate

Fumarate

Arginine +

UREA

UREACYCLE

Aspartate

+

Urea Cycle

REGULATION OF THE UREA CYCLE

Acute: N-acetylglutamate, allosteric effector, up regulates CPS I

N-Acetylglutamate is synthesized from glutamate and acetyl-CoA by a mitochondrial NAG synthase.

Argininosuccinicacidemia

Citrullinemia

Arginase Deficiency

Hyperammonemia:

Type I

Type II

Metabolic Diseases of the Urea Cycle

Disorders present in infants:Symptoms: Lethargy, swelling of the brain

leads to mental retardation/brain damage

Diagnosis: Low blood urea nitrogen (BUN) levels-high levels of ammonia in the blood

elevated circulating glutamine -other metabolites that accumulate depend on the specific enzyme defect

Treatment:Long term, dietary restriction.

Low protein diet. Supplemented with Arginine

Metabolic Diseases of the Urea Cycle

Excessive ammonia is toxic to the

central nervous system.

Alternative pathway therapy:

Sodium benzoate to produce

hippuric acid

Sodium phenylacetate or phenyl-

butyrate to produce

phenylacetylglutamine

Amino acid metabolism and central metabolic pathways

20 amino acids are converted

to 7 products:

pyruvate

acetyl-CoA

acetoacetate

-ketoglutarate

succynyl-CoA

oxalacetate

fumarate

Glucogenic Amino Acids

formed: -ketoglutarate, pyruvate, oxaloacetate, fumarate, or succinyl-CoA

Aspartate Asparagine Arginine Phenylalanine Tyrosine Isoleucine

Methionine Valine Glutamine Glutamate Proline Histidine

Alanine Serine Cysteine Glycine Threonine Tryptophan

Ketogenic Amino Acids

formed acetyl CoA or acetoacetate

Lysine

Leucine

Both glucogenic and ketogenic amino acids

formed: -ketoglutarate, pyruvate, oxaloacetate, fumarate, or succinyl-CoA in

addition to acetyl CoA or acetoacetate

IsoleucineThreonineTryptophanPhenylalanineTyrosine

Glycogenic and KetogenicAmino Acids

Glycogenic Alanine, Arginine Asparagine, Aspartate Cysteine, Glutamate Glutamine, Glycine

Glycogenic and Ketogenic Isoleucome Phenytolanine Tryptophen Tyrosine

Ketogenic

Leucine Lysine

Histidine, Methionine Proline, Serine

Threonine, Valine

1.Glucogenic: converted to glucose via pyruvate2.Ketogenic: converted to ketone bodies 3.Some are both

4.During fasting when FA are the major fuel FA cannot be converted to glucose therefore AA → glucose & ketone bodies (especially for brain) -AA → pyruvate → liver → glucose -keto AA + FA → ketone bodies (acetoacetate & 3 hydroxybutyrate)

Asparagine, Aspartate

The C4 family: aspartate and asparagine are converted into oxalacetate

Aspartic acid Asparagine

Oxalacetate

Glutamine, and Glutamate

The C5 family: several amino acids are converted into -ketoglutarate through glutamate

Glutamine

Proline

Histidine

Arginine

ketoglutarate

Alanine

Serine

Cysteine

Threonine

The C3 family: alanine, serine, cysteine and threonine are converted to pyruvate

Pyruvate

Interconversion of amino acids and intermediates of carbohydrate metabolism and Krebs cycle

Metabolism of some selected amino acids

Tryptophan catabolism

Tryptophan has complex catabolic pathway: 1. the indol ring is ketogenic2. the side chain forms the glucogenic productsKynurenate and xanthurenate are excrete in the urine.

Glycine biosynthesis from serine

Reaction involves the transfer of the hydroxymethyl group from serine to the cofactor tetrahydrofolate (THF), producing glycine and N5,N10-methylene-THF.

Copy from: http://themedicalbiochemistrypage.org/amino-acid-metabolism.html

Glycine oxidation to CO2

Glycine produced from serine or from the diet can also be oxidized by glycine decarboxylase (also referred to as the glycine cleavage complex, GCC) to yield a second equivalent of N5,N10-methylene-tetrahydrofolate as well as ammonia and CO2.

Copy from: http://themedicalbiochemistrypage.org/amino-acid-metabolism.html

The sulfur for cysteine synthesis comes from the essential amino acid methionine.

SAM serves as a precurosor for numerous methyl transfer reactions (e.g. the conversion of norepinephrine to epinenephrine).

Cysteine and methionine are metabolically related

Condensation of ATP and methionine yield S-adenosylmethionine (SAM)

SAM

Cysteine synthesis

Copy from: http://themedicalbiochemistrypage.org/amino-acid-metabolism.html

1. Conversion of SAM to homocysteine.

2. Condensation of homocysteine with serine to cystathione.

3. Cystathione is cleavaged to cysteine.

Conversion of homocysteine back to Met. N5-methyl-THF is donor of methyl group.

*

*folate + vit B12

Genetic defects for both the synthase and the lyase.

Missing or impaired cystathionine synthase leads to homocystinuria.High concentration of homocysteine and methionine in the urine.

Homocysteine is highly reactive molecule.

Disease is often associated with mental retardation, multisystemic disorder of connective tissue, muscle, CNS, and cardiovascular system.

Homocystinuria

Cysteine catabolism

Biosynthesis of Tyrosine from Phenylalanine

Phenylalanine hydroxylase is a mixed-function oxygenase: one atom of oxygen is incorporated into water and the other into the hydroxyl of tyrosine. The reductant is the tetrahydrofolate-related cofactor tetrahydrobiopterin, which is maintained in the reduced state by the NADH-dependent enzyme dihydropteridine reductase

Hyperphenylalaninemia - complete deficiency of phenylalanine hydroxylase (plasma level of Phe raises from normal 0.5 to 2 mg/dL to more than 20 mg/dL).The mental retardation is caused by the accumulation of phenylalanine, which becomes a major donor of amino groups in aminotransferase activity and depletes neural tissue of α-ketoglutarate. Absence of α-ketoglutarate in the brain shuts down the TCA cycle and the associated production of aerobic energy, which is essential to normal brain development. Newborns are routinelly tested for blood concentration of Phe.The diet with low-phenylalanine diet.

Phenylketonuria

Alternative pathways of phenylalaninecatabolism in phenylketonuria

Homogentisic Acid Formation

CH2CHCO2-

NH3+

HO

OH

OH

CH2CO2-

Transamination

Tyrosine p-Hydroxyphenyl-pyruvate

Homogentisate

p-Hydroxyphenyl-pyruvatedioxygenase(ascorbate-dep.)

O2

CO2

CH2CCO2-

O

HO

Homogentisatedioxygenase

O2

Cleavage of aromatic ring

Fumarate + acetoacetate

Deficient in alkaptonuria

Alkaptonuria

• First defect to which inborn error of metabolism applied – Sir Archibald Garrod in early 1900’s• Homogentisate appears in urine• Deposited in cartilage and elsewhere polymerization (black)

• Deficiency of homogentisate dioxygenase• Urine turns dark on standing• Oxidation of homogentisic acid • Asymptomatic in childhood• Tendency toward arthritis in adulthood

valine isoleucine leucine

-ketoglutarate glutamate (transamination)

-ketoisovalerate -keto--methylbutyrate -ketoisokaproate

oxidative decarboxylationDehydrogenase of -keto acids*

CO2

NAD+

NADH + H+

isobutyryl CoA -methylbutyryl CoA isovaleryl CoA

Dehydrogenation etc., similar to fatty acid -oxidation

propionyl CoA acetyl CoA

acetoacetate

acetyl CoA

propionyl CoA+ +

Catabolism of branched amino acids

Branched-chain aminoaciduria

Disease also called Maple Syrup Urine Disease (MSUD) (because of the characteristic odor of the urine in affected individuals).

Deficiency in an enzyme, branched-chain α-keto acid dehydrogenase leads to an accumulation of three branched-chain amino acids and their corresponding branched-chain α-keto acids which are excreted in the urine.

There is only one dehydrogenase enzyme for all three amino acids.

Mental retardation in these cases is extensive.

Essential & Non-essential AA

Conditionally essential(i) ARG:can be made, but not enough(ii) HIS: controversial (essential for growth in children)(iii) PHE essential, TYR can be made from PHE but when enzyme is missing (phenyl- ketonuria) then PHE > TYR; Therefore TYR is essential(iv) MET CYS; Similarly, if MET > CYS then CYS essential

Even with excess, important in excretion NH4

+ therefore continue to be made

Serine biosynthesis from glycolytic intermediate 3-phosphoglycerate

Copy from: http://themedicalbiochemistrypage.org/amino-acid-metabolism.html

Formation of alanine

Asparagine synthetase reaction

The glutamate dehydrogenase

Ammonia transport in the form of glutamine

Glutamine synthetase

Excess ammonia is added to glutamate to form glutamine.

Glutamine enters the liver and NH4+

is liberated in mitochondria by the enzyme glutaminase.

Ammonia is remove by urea synthesis.

Biosynthesis of proline from glutamate

Conversion of methionine to propionyl-CoA.

The phenylalanine hydroxylase reaction

Conversion of Amino Acids

to Specialized Products

Catecholamine Biosynthesis

CH2CHCO2-

NH3+

HO

CH2CHCO2-

NH3+

HO

HO

CH2CH2NH2

HO

HO

CHCH2NH2

HO

HO

OH

CHCH2NHCH3

HO

HO

OH

Tyr hydroxylase

O2

Tyrosine Dihydroxyphenylalanine (DOPA)

Dopamine

DOPAdecarboxylase CO2

Dopaminehydroxylase

Norepinephrine

Catechol

Epinephrine(Adrenaline)

SAM

S-Adenosyl-homocysteine

Methyl transferase

DOPA, dopamine, norepinephrine,and epinephrine are all neurotransmitters

Histidine Metabolism: Histamine Formation

N

NH

CH2CHCO2-

NH3

+

N

NH

CH2CH2NH2

Histidine Histamine

Histidinedecarboxylase

CO2

Histamine: Synthesized in and released by mast cells

Mediator of allergic response: vasodilation, bronchoconstriction

Tryptophan Metabolism: Serotonin Formation

NH

CH2CHCO2-

NH3

+

NH

CH2CHCO2-

NH3

HO

+

NH

CH2CH2NH2

HO

Tryptophan(Trp)

Indole ring

Trphydroxylase

O2

5-Hydroxy-tryptophan

Decarboxylase

CO2 5-Hydroxy-tryptamine (5-HT);Serotonin

Serotonin Metabolism: Melatonin

NH

CH2CH2NHCOCH3

H3CO

NH

CH2CH2NH2

HO2 Steps

Serotonin Melatonin

Melatonin:• Formed principally in pineal gland• Synthesis controlled by light, among other factors• Induces skin lightening• Suppresses ovarian function• Possible use in sleep disorders

Creatine and Creatinine

NH3+NH2

+H2N=C-HNCH2CH2CH2CHCO 2

-

Arginine Glycine Ornithine

Arginine-glycinetransamidinase

(Kidney)NH2

H2N=C-HNCH2CO 2-

+

Guanidoacetate

NHPO3-2

CH3

+H2N=C-NCH2CO 2

-

GuanidoacetateMethyltransferase

(Liver)

SAM + ATP

S-Adenosyl-homocysteine + ADP

Phosphocreatine

N

NH

CH3

HN

O

Creatinine(Urine) Non-enzymatic

(Muscle)

NH2

CH3

H2N=C-NCH2CO 2-

+

Creatine kinase(Muscle)

ATP

Creatine ADP + Pi

Biosynthesis and metabolism of creatine and creatinine

β-Alanyl Dipeptides

Biosynthesis of hippurate

Polyamines: Conversion of spermidine to spermine

Nitric Oxide

glutathione

Carnitine

GABA

Formation of S-adenosylmethionine

Biosynthesis of epinephrine and norepinephrine