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METABOLISME KARBOHIDRAT
Carbohydrate metabolism I
Carbohydrates
Carbohydrates

computing

composed of carbon, hydrogen and oxygen only
in the ratio C6H12O6

esentation copyright © 2002 David A Bender and some images copyright © 2002 Taylor & Francis Ltd


Carbohydrates
• Contain carbon, hydrogen, and oxygen
• Their major function is to supply a source of
cellular food
• Examples:
– Monosaccharides or simple sugars

Figure 2.13a
Carbohydrates
• Disaccharides or double sugars

Figure 2.13b
Carbohydrates
• Polysaccharides or polymers of simple sugars

Figure 2.13c
Nutritionally important
disaccharides - 1
Nutritionally important disaccharides

esentation copyright © 2002 David A Bender and some images copyright © 2002 Taylor & Francis Ltd

computing


α-1,4-binding

β-1,4-binding

Figuur 11. De α-1,4-binding en de β-1,4-binding die in polysacchariden voorkomen.
α-1,6-binding

Figuur 12. De α-1,6-binding zoals deze in amylopectine voorkomt.
Nutritionally important
disaccharides - 2
Nutritionally important disaccharides

computing

CH2OH

CH2OH

CH2OH

O

O

O

HO

OH

OH

OH
O

OH

OH
OH
maltose (glucosyl-glucose)

HO

O
OH
CH2
isomaltose

esentation copyright © 2002 David A Bender and some images copyright © 2002 Taylor & Francis Ltd

O
OH
HO

OH
OH


Branched structure of starch
and glycogen
The branched structure of starch and glycogen

CH2OH

CH2OH

O

α1→6 links: branch points in
amylopectin and glycogen

O

OH

computing

OH

O

O

O
OH

OH
CH2OH

CH2

O

CH2OH
O

OH

O

OH

O

O

OH

OH

O

O
OH

CH2OH

OH

esentation copyright © 2002 David A Bender and some images copyright © 2002 Taylor & Francis Ltd

O
OH

O
OH


Hydrolysis of starch
Hydrolysis by alpha-amylase formation of dextrins, computing
of starch by
in saliva and pancreatic juice results in
then:
amylase
glucose
maltose
isomaltose

CH2OH

CH2OH

O

α1→6 links: branch points in
amylopectin and glycogen

O

OH

OH

O

O

O
OH

OH
CH2OH

CH2

O

CH2OH
O

OH

O

OH

O

O

OH

OH

O

O
OH

CH2OH

OH

esentation copyright © 2002 David A Bender and some images copyright © 2002 Taylor & Francis Ltd

O
OH

O
OH


The major types of non-starch
Major types ofpolysaccharide
non-starch
polysaccharides

computing

cellulose - glucose polymer linked β1→4
CH2OH

CH2OH

O

O

CH2OH

O

OH

O

CH2OH

O

OH

O

O

OH

O

OH

O

inulin - fructose polymer linked β2→1
O

OH

OH

OH

OH

CH2

HOCH2 O
OH

chitin - N-acetylglucosamine polymer linked β1→4
CH2OH

CH2OH

O
O

O
CH2OH

O

OH

O

CH2OH

O

OH

O

OH
HOCH2 O

O

OH

O

CH2
OH

OH

O

O
OH

HN

C

CH3

HN

O

C

HN

CH3

HN

C CH3

O

O

O

C CH3

OH

pectin - galacturonic acid polymer linked α1→4, partially methylated;
some glactose and/or arabinose branches
COOH
O
O

OH

OH

O

O

O
O

O
OH

O

OH

O

OH

CH2

HOCH2 O

COOH

CO CH3

COOH

CH2

HOCH2 O

OH
O

O
OH

OH

OH

OH

OH

esentation copyright © 2002 David A Bender and some images copyright © 2002 Taylor & Francis Ltd


Glycaemic and noncomputing
Glycaemic index
The extent to which a test dose of a carbohydrate increases blood 1
glycaemic carbohydrates - glucose
compared with an equivalent amount of glucose
Glycaemic and non-glycaemic carbohydrates

Dietary starches can be classified as:
 rapidly digested (hence high glycaemic index)
 slowly digested (lower glycaemic index)
 not all digested in small intestine
 amylose is hydrolysed more slowly than amylopectin
 resistant starch (low glycaemic index)
 only hydrolysed to a limited extent in small intestine
 starch may be resistant because:
 it is crystalline and resistant to amylases
 it is enclosed in plant cell walls that are not digested
some resistant starch is fermented by bacteria in the large intestine

esentation copyright © 2002 David A Bender and some images copyright © 2002 Taylor & Francis Ltd


Carbohydrates

• Serve as primary source of energy in the cell
• Central to all metabolic processes
Glucose
Cytosol - anaerobic
Hexokinase
Pentose
Phosphate
Shunt

Glucose-6-P
glycolysis

Pyruvate

Glc-1- phosphate

glycogen
cytosol
mitochondria
(aerobic)

Pyruvate
Aceytl CoA
FATTY ACIDS

Krebs
cycle
AMINO
ACIDS

Reducing
equivalents

Oxidative
Phosphorylation
(ATP)
insulin
IR
P
Protein Kinase B
(inactive)

Glycogen synthase kinase
(active)

P
Glycogen synthase
(inactive)

OH

P

Protein Kinase B
(active)

OH

synthase
P Glycogen(inactive) kinase

OH
Glycogen synthase
(active)

Glycogen formation
GLYCOGENOLYSIS
glycogen
glucose-6-phosphate
GLYCOGEN SYNTHESIS

glucose
( 6 carbons)

GLYCOLYSIS

GLUCONEOGENESIS

Overview of metabolism

computing

pyruvate
(3 carbons)

lactate
triacylglycerols

CO2
FATTY ACID SYNTHESIS
acetyl CoA
fatty acids
(2 carbons) FATTY ACID OXIDATION

ketones
KETOGENESIS

oxaloacetate

LIPASE

citrate

CITRIC ACID CYCLE

CO2
CO2

esentation copyright © 2002 David A Bender and some images copyright © 2002 Taylor & Francis Ltd


Glycolysis pathway
[Tri-carboxylic Acid (TCA) cycle]
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Metabolisme Karbohidrat

  • 2.
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  • 4.
  • 6. Carbohydrates Carbohydrates computing composed of carbon, hydrogen and oxygen only in the ratio C6H12O6 esentation copyright © 2002 David A Bender and some images copyright © 2002 Taylor & Francis Ltd 
  • 7. Carbohydrates • Contain carbon, hydrogen, and oxygen • Their major function is to supply a source of cellular food • Examples: – Monosaccharides or simple sugars Figure 2.13a
  • 8. Carbohydrates • Disaccharides or double sugars Figure 2.13b
  • 9. Carbohydrates • Polysaccharides or polymers of simple sugars Figure 2.13c
  • 10. Nutritionally important disaccharides - 1 Nutritionally important disaccharides esentation copyright © 2002 David A Bender and some images copyright © 2002 Taylor & Francis Ltd computing 
  • 11. α-1,4-binding β-1,4-binding Figuur 11. De α-1,4-binding en de β-1,4-binding die in polysacchariden voorkomen.
  • 12. α-1,6-binding Figuur 12. De α-1,6-binding zoals deze in amylopectine voorkomt.
  • 13. Nutritionally important disaccharides - 2 Nutritionally important disaccharides computing CH2OH CH2OH CH2OH O O O HO OH OH OH O OH OH OH maltose (glucosyl-glucose) HO O OH CH2 isomaltose esentation copyright © 2002 David A Bender and some images copyright © 2002 Taylor & Francis Ltd O OH HO OH OH 
  • 14. Branched structure of starch and glycogen The branched structure of starch and glycogen CH2OH CH2OH O α1→6 links: branch points in amylopectin and glycogen O OH computing OH O O O OH OH CH2OH CH2 O CH2OH O OH O OH O O OH OH O O OH CH2OH OH esentation copyright © 2002 David A Bender and some images copyright © 2002 Taylor & Francis Ltd O OH O OH 
  • 15. Hydrolysis of starch Hydrolysis by alpha-amylase formation of dextrins, computing of starch by in saliva and pancreatic juice results in then: amylase glucose maltose isomaltose CH2OH CH2OH O α1→6 links: branch points in amylopectin and glycogen O OH OH O O O OH OH CH2OH CH2 O CH2OH O OH O OH O O OH OH O O OH CH2OH OH esentation copyright © 2002 David A Bender and some images copyright © 2002 Taylor & Francis Ltd O OH O OH 
  • 16. The major types of non-starch Major types ofpolysaccharide non-starch polysaccharides computing cellulose - glucose polymer linked β1→4 CH2OH CH2OH O O CH2OH O OH O CH2OH O OH O O OH O OH O inulin - fructose polymer linked β2→1 O OH OH OH OH CH2 HOCH2 O OH chitin - N-acetylglucosamine polymer linked β1→4 CH2OH CH2OH O O O CH2OH O OH O CH2OH O OH O OH HOCH2 O O OH O CH2 OH OH O O OH HN C CH3 HN O C HN CH3 HN C CH3 O O O C CH3 OH pectin - galacturonic acid polymer linked α1→4, partially methylated; some glactose and/or arabinose branches COOH O O OH OH O O O O O OH O OH O OH CH2 HOCH2 O COOH CO CH3 COOH CH2 HOCH2 O OH O O OH OH OH OH OH esentation copyright © 2002 David A Bender and some images copyright © 2002 Taylor & Francis Ltd 
  • 17. Glycaemic and noncomputing Glycaemic index The extent to which a test dose of a carbohydrate increases blood 1 glycaemic carbohydrates - glucose compared with an equivalent amount of glucose Glycaemic and non-glycaemic carbohydrates Dietary starches can be classified as:  rapidly digested (hence high glycaemic index)  slowly digested (lower glycaemic index)  not all digested in small intestine  amylose is hydrolysed more slowly than amylopectin  resistant starch (low glycaemic index)  only hydrolysed to a limited extent in small intestine  starch may be resistant because:  it is crystalline and resistant to amylases  it is enclosed in plant cell walls that are not digested some resistant starch is fermented by bacteria in the large intestine esentation copyright © 2002 David A Bender and some images copyright © 2002 Taylor & Francis Ltd 
  • 18.
  • 19. Carbohydrates • Serve as primary source of energy in the cell • Central to all metabolic processes Glucose Cytosol - anaerobic Hexokinase Pentose Phosphate Shunt Glucose-6-P glycolysis Pyruvate Glc-1- phosphate glycogen
  • 21. insulin IR P Protein Kinase B (inactive) Glycogen synthase kinase (active) P Glycogen synthase (inactive) OH P Protein Kinase B (active) OH synthase P Glycogen(inactive) kinase OH Glycogen synthase (active) Glycogen formation
  • 22. GLYCOGENOLYSIS glycogen glucose-6-phosphate GLYCOGEN SYNTHESIS glucose ( 6 carbons) GLYCOLYSIS GLUCONEOGENESIS Overview of metabolism computing pyruvate (3 carbons) lactate triacylglycerols CO2 FATTY ACID SYNTHESIS acetyl CoA fatty acids (2 carbons) FATTY ACID OXIDATION ketones KETOGENESIS oxaloacetate LIPASE citrate CITRIC ACID CYCLE CO2 CO2 esentation copyright © 2002 David A Bender and some images copyright © 2002 Taylor & Francis Ltd 
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