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metabolismofcarbohydrates.ppt for nusring students
Carbohydrate Metabolism
An Overview of
Metabolism
The study of synthesis (Anabolism)
and degradation (catabolism) of
biomolecules is biochemically termed as
metabolism.
Metabolism of carbohydrate
 Structural maintenance
 Support of growth
 Production of secretions
 Building of nutrient reserves
Anabolism
 Breakdown of nutrients to provide energy (in the
form of ATP) for body processes
 Nutrients directly absorbed
 Stored nutrients

Cells break down excess carbohydrates first, then lipids, finally
amino acids if energy needs are not met by carbohydrates and fat
 40% of the energy released in catabolism is captured in ATP, the
rest is released as heat
Catabolism
Carbohydrate Metabolism
 Primarily glucose
 Fructose and galactose enter the pathways at various points
 All cells can utilize glucose for energy production
 Liver is central site for carbohydrate metabolism
Glucose Metabolism
 Four major metabolic pathways:
 Immediate source of energy
 Pentose phosphate pathway
 Glycogen synthesis in liver/muscle
 Precursor for triacylglycerol synthesis
Glucose
Utilization
Glucose
Pyruvate
Ribose-5-phosphate
Glycogen
Energy
Stores
Pentose
Phosphate
Pathway
Glycolysis
Adipose
Glucose
Utilization
Glucose
Pyruvate
Ribose-5-phosphate
Glycogen
Energy
Stores
Pentose
Phosphate
Pathway
Glycolysis
Adipose
Glycolysis
 Sequence of reactions that converts
glucose into pyruvate
 Relatively small amount of energy produced
 Glycolysis reactions occur in cytoplasm
 Does not require oxygen
Glucose  2 Pyruvate
Lactate (anaerobic)
Acetyl-CoA (TCA cycle)
 Glycolysis pathway:
 Oxidation of glucose to Pyruvate +water+
NADH2 in steps wise (10 steps).
 It take place in all cells, for the break
down of glucose to provide energy.
 *Glycolysis pathway occurs in most cell in
the presences of oxygen and called
(aerobic glycolysis)
 An-aerobic glycolysis: occurs in the
completely absent of oxygen or partial
deficiency of oxygen.
 An aerobic glycolysis found in:
 1- Red blood cells (no mitochondria)
 2-Labor (partial deficiency of oxygen)
 3-Exercise muscle (partial deficiency of
oxygen)
 4-Cancer cells
Glycolysis
Glucose + 2 ADP + 2 Pi
2 Pyruvate + 2 ATP + 2 H2O
First Reaction of Glycolysis
Traps glucose in cells (irreversible in muscle cells)
Glycolysis - Summary
Glucose (6C)
2 Pyruvate (3C)
2 ATP
2 ADP
4 ADP
4 ATP
2
NAD
2 NADH + H
Pyruvate Metabolism
 Three fates of pyruvate:
 Conversion to lactate (anaerobic)
 Conversion to alanine (amino acid)
 Entry into the TCA cycle via pyruvate
dehydrogenase pathway (create ATP)
Pyruvate Metabolism
 Three fates of pyruvate:
 Conversion to lactate (anaerobic)
 Conversion to alanine (amino acid)
 Entry into the TCA cycle via pyruvate
dehydrogenase pathway
Anaerobic
Metabolism of
Pyruvate to Lactate
 Problem:
 During glycolysis, NADH is formed from NAD+
 Without O2, NADH cannot be oxidized to NAD+
 No more NAD+
 All converted to NADH
 Without NAD+
, glycolysis stops
Anaerobic
Metabolism of
Pyruvate
 Solution:
 Turn NADH back to NAD+
by making lactate (lactic
acid)
COO
C O
CH3
COO
HC OH
CH3
Lactate
Pyruvate
Lactate dehydrogenase
NADH + H+
NAD+
(oxidized) (reduced)
(oxidized)
(reduced)
Anaerobic
Metabolism of
Pyruvate
 ATP yield
 Two ATPs (net) are produced during the
anaerobic breakdown of one glucose
 The 2 NADHs are used to reduce 2 pyruvate
to 2 lactate
 Reaction is fast and doesnt require
oxygen
 Lactate can be transported by blood to liver and
used in gluconeogenesis
Cori Cycle
Lactate is converted
to pyruvate in the
liver
Pyruvate Metabolism
 Three fates of pyruvate:
 Conversion to lactate (anaerobic)
 Conversion to alanine (amino acid)
 Entry into the TCA cycle via pyruvate
dehydrogenase pathway
Pyruvate metabolism
 Convert to alanine and export to blood
COO
C O
CH3
COO
HC NH3
+
CH3
Alanine amino transferase
(AAT)
Alanine
Pyruvate
Glutamate -Ketoglutarate
Keto acid Amino acid
Pyruvate Metabolism
 Three fates of pyruvate:
 Conversion to lactate (anaerobic)
 Conversion to alanine (amino acid)
 Entry into the TCA cycle via pyruvate
dehydrogenase pathway
Pyruvate Dehydrogenase
Complex (PDH)
 Prepares pyruvate to enter the TCA cycle
Electron
Transport
Chain
TCA Cycle
Aerobic Conditions
TCA Cycle
 In aerobic conditions TCA cycle links pyruvate
to oxidative phosphorylation
 Occurs in mitochondria
 Generates 90% of energy obtained from food
 Oxidize acetyl-CoA to CO2 and capture
potential energy as NADH (or FADH2) and
some ATP
 Includes metabolism of carbohydrate, protein, and
fat
metabolismofcarbohydrates.ppt for nusring students
TCA Cycle -
Summary
Acetyl CoA
3
NAD
3 NADH + H
1 FAD
1 FADH2
1 ADP
1 ATP
2 CO2
 Electron transport chain (E.T.C):
This pathway is found in inner mitochondria
matrix, energy rich molecules, such as
glucose or fatty acids are metabolized by
series of oxidation reaction ultimately
yielding co2 and H20.
Electron Transport Chain
Total ATP from Glucose
 Anaerobic glycolysis  2 ATP
 Aerobic metabolism  glycolysis + TCA
38 ATP from 1 glucose molecule
 Energy production from complete oxidation of glucose :-
 2 ATP (glycolysis) 2 ATP
 2NADH2 (glycolysis) 23 = 6 ATP
2NADH2 (Pyruvate dehydrogenase) E.T.C 23 = 6 ATP
2 Acetyl-coA(212 ATP) 24 ATP
Net energy from aerobic glycolysis:
2 ATP + 6 ATP + 6 ATP + 24 ATP = 38 ATP
Glucose
Utilization
Glucose
Pyruvate
Ribose-5-phosphate
Glycogen
Energy
Stores
Pentose
Phosphate
Pathway
Glycolysis
Adipose
Pentose Phosphate Pathway
 Secondary metabolism of glucose
 Produces NADPH

Similar to NADH

Required for fatty acid synthesis
 Generates essential pentoses

Ribose

Used for synthesis of nucleic acids
Glucose
Utilization
Glucose
Pyruvate
Ribose-5-phosphate
Glycogen
Energy
Stores
Pentose
Phosphate
Pathway
Glycolysis
Adipose
Energy Storage
 Energy from excess carbohydrates
(glucose) stored as lipids in adipose tissue
 Determined by ATP:ADP ratios

High ATP, acetyl-CoA goes to fatty acid synthesis

Low ATP, acetyl CoA enters TCA cycle to generate
MORE ATP
Glucose
Utilization
Glucose
Pyruvate
Ribose-5-phosphate
Glycogen
Energy
Stores
Pentose
Phosphate
Pathway
Glycolysis
Adipose
Glycogenesis
 Liver
 Use glycogen to export glucose to the
bloodstream when blood sugar is low
 Glycogen stores are depleted after
approximately 24 hrs of fasting (in humans)
Glycogenesi
s
Glycogenesis
 Skeletal muscle
 More muscle than liver, therefore
more glycogen in muscle, overall
 Use glycogen (i.e., glucose) for energy
only (no export of glucose to blood)
 Use already-made glucose for synthesis
of glycogen
Fates of Glucose
 Fed state
 Storage as glycogen
 Liver
 Skeletal muscle
 Storage as lipids
 Adipose tissue
 Fasted state
 Metabolized for energy
 New glucose synthesized
Synthesis and
breakdown occur at
all times
The relative rates of
synthesis and
breakdown change
Fasting Situation
 Where does required glucose come from?

Glycogenolysis
Lipolysis
Proteolysis
 Breakdown or mobilization of glycogen stored by glucagon
 Glucagon - hormone secreted by pancreas during times of fasting
 Mobilization of fat stores stimulated by glucagon and epinephrine
 Triglyceride = glycerol + 3 free fatty acids
 Glycerol can be used as a glucose precursor
 The breakdown of muscle protein with release of amino acids
 Alanine can be used as a glucose precursor
Low Blood Glucose
Proteins Broken
Down
Insulin
Pancreas
Muscle
Adipose
Cells
Glycogen
Glycerol, fatty acids
released
Glucose released
In a fasted state, substrates for glucose synthesis
(gluconeogenesis) are released from storage
Gluconeogenesis
 Necessary process
 Glucose is an important fuel

Central nervous system

Red blood cells
 Not simply a reversal of glycolysis
 Insulin and glucagon are primary
regulators
Gluconeogenesis
 Synthesis of glucose from non-carbohydrate
precursors during fasting.
 Glycerol
 Amino acids
 Lactate
 Pyruvate
 Propionate
There is no glucose synthesis from fatty acids
Supply carbon skeleton
Thank for listening
metabolismofcarbohydrates.ppt for nusring students

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metabolismofcarbohydrates.ppt for nusring students