I. Carbohydrate Chemistry: Structure, Function and Classification
I. Carbohydrate Chemistry: Structure, Function and Classification
I. Carbohydrate Chemistry: Structure, Function and Classification
Arcilla, Edward Ashley T., Adao, Celine O., Boado, Kathleen Joyce O., De Guzman, Margaret Alexa C., Gandola,
Kherson P., Marquez, Mark Christian E., Ong, Jehiel Karsten H., San Luis, Pia Lorraine F., Tañas, Trisha Joy M.
4C-Biochemistry
OUTLINE______________________________
I. Carbohydrate Chemistry: Structure, Function 2. Protein sparer
and Classification - since Carbohydrates is the primary source of
II. Carbohydrate Nutritional Processes ATP, it spares glucogenic amino acid from
III. Glucose Metabolism degradation to produce ATP.
IV. Molecular Conditions for galactosemia, lactose 3. Regulator of fat metabolism
intolerance, diabetes and hypoglycemia - too much carbohydrate intake generates too
much pyruvate in which it will be converted
LEARNING OUTCOMES____________________ into acetyl coa. These acetyl coa will be used
● Recognize the chemical nature of as backbone for triacylglycerides (TAG)
carbohydrates production as well as cholesterol synthesis.
● Describe carbohydrate consumption, sources - in mevalonate pathway, acetyl coa is used as
and recommendations substrate
● Classify carbohydrates and discuss its functions 4. Sole energy source for the brain and nerve
and transformations tissues
● Explain the carbohydrate nutritional processes 5. Storage form of energy as glycogen in animal
● Illustrate the body’s use of glucose tissues
● Examine the molecular conditions for 6. Regulator of intestinal peristalsis and provider
galactosemia, lactose intolerance, diabetes and of bulk
hypoglycemia
NON-ENERGY RELATED FUNCTIONS_________
I. Carbohydrate Chemistry: Structure, Function
and Classification 1. important constituents of tissue antigens
2. important constituents of ribonucleic acids
CARBOHYDRATE________________________ 3. important constituents of interstitial fluid
matrix in the form of glycoprotein
- In general, carbohydrates are foods that refer 4. important constituents of brain and nerve
to starches and sugars. tissues in the form of
- They furnish the major source of energy and
form the bulk of the diet around the world. CLASSIFICATIONS_______________________
o 50-60% in developed countries
o 75-80% in the Philippines and other Carbohydrates are classified into two – Simple
oriental countries carbohydrates and Complex Carbohydrates:
- major sources of carbohydrates are from
plants, liver glycogen, milk and processed
foods.
- in photosynthesis, carbohydrates specifically
glucose are synthesized from the Calvin cycle
which happens in the stroma.
DEFINITION_________________----______--
2. Fructose
- sweetest of all
sugars and is found - α(1,2) glycosidic bonds
pre-formed in honey, - known as cane sugar or table sugar but also
ripe fruits and some abundant in in molasses, maple syrup,
vegetables sorghum
- hydrolyzed from - most common form in cooking and table
sucrose and inulin serving
- also known as - hydrolyzed into glucose and fructose
levulose. (it is (invert sugar)
named as levulose since in terms of
polarimetry, it spins levorotatory) 2. Maltose
3. Galactose
CARBOHYDRATE DIGESTION______________
The objective of carbohydrate or starch
digestion is to separate all disaccharides and
complex starches into monosaccharides for
absorption, in spite of the fact that not all are totally
absorbed in the small intestine (e.g., fiber).
b. POLYSACCHARIDES
- are long chains of monosaccharide units (>10
CHO units) that may extend to a number of
hundreds or even thousands
- major polysaccharides of interest in
nutrition:
• Animal tissues: glycogen
• Plant: starch and cellulose
Examples of polysaccharides:
1. Starch
- world’s most abundant In the Mouth
and cheap form for carbohydrate Carbohydrate absorption starts in the mouth.
- storage form of The salivary glands in the mouth discharge salivation,
carbohydrate in plants which saturates the food. The food is then bitten while
- have two components: the salivary glands additionally discharge the protein
amylose and amylopectin salivary amylase, which starts the process towards
- Amylose has α(1,4) separating the polysaccharides in the carbohydrate
glycosidic bonds and are linear food.
while amylopectin has α(1,4)
and α(1,6) glycosidic bonds and
are branched.
- partial hydrolysis: dextrin and maltose;
complete hydrolysis: glucose
In the Stomach Summary
After the carbohydrate food is bitten into little
pieces and blended with salivary amylase and other
salivary juices, it is gulped and gone through the
throat. The mixture enters the stomach where it is
known as chyme. There is no further absorption of
chyme, as the stomach produces corrosive which
destroys microscopic organisms in the food and stops
the activity of the salivary amylase.
ACTIVE TRANSPORT
- Requires energy as ATP
- Glucose binding site is not available
unless the transport protein has already
bound a Na+
- Na+/K+ ATPase then “pumps” the Na ions
back out of the cell
- 3 Na+ for 2 K+
- Sodium binds to transporter
- Induce conformational change, glucose
can bind and go to the cell via symport
mechanism.
Sodium-Glucose Transporter 1 (SGLT1) Features of transporter protein:
- Transports glucose and galactose ● has a specific site for the molecule being
to enterocyte transported
- Symporter: Na+ and glucose or galactose ● undergoes a conformational change upon
- Mutation in the SGLT1 gene is associated with binding the molecule: allow translocation
glucose-galactose malabsorption ● has the ability to reverse the
conformational changes
(a) Active Transport - Goes back to its original form in order to
be reused
GLUT2
- Low affinity
- Predominant expression in the Beta-cells of the
pancreas, liver, small intestine, and kidney
- Rate of transport is highly dependent upon the
blood glucose concentration
- In the pancreas, GLUT2 appears to be the
sensitive indicator of blood glucose level
GLUT3
- High-affinity glucose transporter with
predominant expression in those tissues that
are highly dependent upon glucose, such as
the brain and neurons
- Major site of expression: Brain (neurons)
- Sugar as primary substrate, constant
uptake
FACILITATED TRANSPORT GLUT4
- Insulin-dependent glucose transporter in
Glucose transporters (GLUT) muscle and adipose tissue
- Protein carriers involved in the transport - Other cells and tissues do not express GLUT4
of glucose and other monosaccharide units and not dependent upon insulin for glucose
- Total of 14 individual glucose transport uptake
proteins - Major site of Expression: Muscle, Heart, brown
- 28% of the amino acid sequences are and white adipocytes
common within the family - Require high energy
- Each GLUT is an integral protein - Once insulin is bound, it phosphorylates and
- 12 transmembrane alpha-helix segments then there is a cascade of reactions that
undergo phosphorylation. This aid in
translocation of GLUT4 into the membrane to
accept more glucose molecules
GLUT5
- Specific for transport of fructose and will not
transport of glucose
(b) and (c) Facilitated transport insulin. When insulin is formed, it binds to the
receptors found in the cell membrane of muscle cells
and adipocytes; to allow GLUT4 to be translocated
across the cell membrane. When glucose is transported
and blood glucose levels have normalized, production
of insulin stops.
In addition, as the body’s cell utilizes glucose,
blood glucose level decreases which therefore
stimulates the α-cell of the pancreas to release
glucagon to the bloodstream. Glucagon will now
stimulate the liver cells to breakdown glycogen and
release glucose in the blood which results to increase
in blood glucose level.
CARBOHYDRATE DISTRIBUTION____________
- also referred to as carbohydrate transport.
Overview:
General scheme:
↑Glucose level → GLUT2 triggers production of
insulin by the pancreas → Insulin binds to membrane
receptors → Translocation of GLUT4.
INSULIN ACTION_______________________
FATE OF GLUCOSE________________________
Low GI 0-55
EXAMPLE: Carrots have a GI of 47 and 5 g CHO per
serving
Moderate GI 56-69
The GL of carrots is: (47 × 5) ÷ 100 = 2.4
High GI ≥70
Glycemic Load Value
1. Type of Starch
a. Amylose
- absorbs less water molecules
- forms tight clumps
- slower rate of digestion
- lower GI
- example: kidney bean
b. Amylopectin
- absorbs more water
- more open
- faster rate of digestion
- higher GI
- example: Russet potato
Examples:
Lower GI– Al dente spaghetti (boiled 10 to 15 minutes)
Higher GI– Over-cooked spaghetti (boiled 20 minutes)
enzymes, caused by mutations in different
Summary: Low GI carbohydrates allow for larger genes
portions while regulating the blood glucose levels. It - since it is a genetic disorder, there is no
will typically prompt a moderate rise or increase in the treatment. Proper management and control on
blood glucose level. Whereas carbohydrates having galactose intake is needed
higher GI require smaller portions but causes the blood Galactose
glucose level to increase above the optimal level. - a monosaccharide
- C-4 epimer of glucose
GLUCOSE TOLERANCE_____________________
TYPES OF GALACTOSEMIA:
- determined by the rate at which the inherent
mechanisms for removing excess glucose from
the blood perform their functions Deficient
Type Name Gene
- measured by following blood glucose Enzyme
concentrations 2 hr after an oral load of
50-100 g glucose (given after fasting Galactose-1-ph
Classic
overnight) Type I osphate uridyl GALT
Galactosemia
- the observation is determined by the following: transferase
● the capacity of the body to secrete
adequate amounts of insulin Galactokinase
Type II galactokinase GALK1
● the availability of other nutritional deficiency
factors necessary for insulin binding
and effectiveness UDP-Galactose
Type UDP-galactose-
● the rate of insulin catabolism -4-epimerase GALE
III 4-epimerase
● the presence of insulin antagonists deficiency
● the release of counter regulatory
factors i.e., glucagon to halt
continuing fall of glucose after effect of
insulin has been accomplished
- normal levels of blood glucose: 70-105 mg/dl
TYPE 1 Galactosemia
- more prevalent type compared to other two
types
- Galactose-1-phosphate uridyl transferase is the
deficient enzyme in which this functions for
Diabetic person:
gradually increases plasma glucose level as time after transferring uridyl phosphate to galactose
oral glucose intake increases TYPE 2 Galactosemia
- There is a galactokinase deficiency which is
IV. Molecular Conditions for Galactosemia, responsible for the phosphorylation reaction of
Lactose Intolerance, Diabetes and Hypoglycemia galactose
TYPE 3 Galactosemia
- deficient in the UDP-galactose-4-epimerase in
GALACTOSEMIA __________----____________
which UDP-galactose cannot be further
converted to UDP-glucose
- refers to a group of inherited disorders that
impair the body's ability to process and
produce energy from a sugar called SYMPTOMS:
galactose
Type I
- genetic metabolic disorder following an
autosomal recessive mode of inheritance - most common and severe type
- cognitive impairment
- consumption of galactose will lead to its build
- dysmetria (a type of Ataxia)
up in the blood
- galactose is present in many foods, including - ataxia (incoordination of voluntary muscles)
- hepatic failure (accumulation of galactitol)
dairy products and some fruits and vegetables
- renal failure
- impaired ability to process galactose can
be due to the deficiency of any of 3 - cataracts
Type II MECHANISM OF ACTION
- typically causes only cataracts
Type III
- symptoms and severity depends on whether
the deficiency is confined to certain types of
blood cells or is present in all tissues
- symptoms may be similar to type classic
galactosemia
INHERITANCE:
Lactose Intolerant
- Due to the deficiency with the enzyme lactase,
Autosomal Recessive the lactose was not cleave
- two copies of an abnormal gene must be - The lactose was transferred to the small
present in an individual in order for the disease intestine and to the large intestine
or trait to develop - The microbiome found in the large intestine
will ferment the lactose, producing acid and
LACTOSE INTOLERANCE__________----______ gases
- This acid and gases produced will cause
- Also called lactose deficiency or irritation to the colon which yields to the
hypolactasia different symptoms of lactose intolerance
- Different from galactosemia, because the
lactose here was not degraded by the TYPES OF LACTASE DEFICIENCY
enzyme lactase ● Primary lactase deficiency
- It is the inability of the body to digest and - It is a genetically determined absence or
metabolize lactose decrease in the enzyme is noted
● Secondary, acquired or transient lactase
Lactose deficiency
- is a disaccharide of ß – D – galactose and ß – D - This deficiency is due to the small intestinal
– glucose in ß(1,4) linkage. mucosal disease, abnormalities of brush border
- Human milk contains 200 mmol/L of lactose cells and transport processes.
- It is digested by the enzyme lactase to form - It causes abrasion in colon and problems in
glucose and galactose in the brush border of intestinal microflora
the intestine.
SYMPTOMS:
Lactase - Abdominal bleeding and cramps
- an enzyme that cleaves the ß(1,4) linkages of - Flatulence
glucose and galactose found in the lactose. - Diarrhoea
- Nausea
NOTE: Lactose intolerance is not an allergy because it - Borborygmi (rumbling stomach)
is not an immune response but instead it is caused by - Vomiting (particularly in adolescents)
lactase deficiency.
DIABETES MELLITUS---------------------------------
- group of metabolic disorders characterized by
an elevated blood glucose concentration
and disordered insulin metabolism
(defects in secretion, action or both).
FEATURES OF TYPE 2 DIABETES:
● Prevalence in diabetic population: 90% to
95% of cases
● Age of Onset: >45 yrs. old
● Associated conditions: Obesity, aging,
inherited factors
● Major defect: Insulin resistance, Insulin
Deficiency
● Insulin Secretion: Varies; may be normal,
increased or decreased
● Requirement of Insulin Therapy:
Sometimes
● Other names: Adult-onset diabetes, Non
insulin-dependent diabetes mellitus,
Ketosis-resistant diabetes
SYMPTOMS:
- Frequent Urination (Polyuria)
- Dehydration, Dry mouth
- Increased thirst (Polydipsia)
- Blurred vision
- Increased infections
- Weight loss
- Increased hunger (Polyphagia)
- Fatigue
TYPES OF DIABETES
Galectin 3
- binds to insulin receptor → insulin resistance
TYPE 1 Diabetes - a genetic disorder and an - chemotaxis marker for macrophage
autoimmune disease where immune cells attack beta - if insulin binds, it is unstable and do not cause
cells cascade series of reactions → no GLUT 4 → no glucose
TYPE 2 Diabetes - acquired from lifestyle
Gestational - occurs in pregnant and lactating
Examples of anti-diabetic drugs:
women. Hormones affect the binding of insulin
receptor → no GLUT 4 → no glucose
Drug Mode of action
FEATURES OF TYPE 1 DIABETES:
● Prevalence in diabetic population: 5% to Alpha-glucosidase Delay carbohydrate
10% of cases absorption
● Age of Onset: <30 yrs. old
● Associated conditions: Autoimmune Amylin analogs Suppress glucagon
diseases, viral infection, inherited factors secretion, delay stomach
● Major defect: Destruction of Pancreatic Beta emptying, suppress
Cells, Insulin Deficiency appetite
● Insulin Secretion: Little or none
● Requirement of Insulin Therapy: Always Biguanides Inhibit liver glucose
● Other names: Juvenile-onset diabetes, production, improve
Insulin-dependent diabetes mellitus, glucose utilization
Ketosis-prone diabetes
D-phenylalanine Stimulate insulin
derivatives secretion by pancreas
Non-nutritive sweeteners
- use of NSS has the potential to reduce overall
calorie sweeteners without compensation on
intake of additional calories from other food
sources