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Rt-Control; Lt-Test
Which of the following carbohydrate would not be present in this
sample?
A. glucose
B. fructose
C. lactose
D. trehalose
A. D. trehalose
Except for sucrose and trahalose, the end of these sugars contain
free anomeric carbon, called the reducing end. Therefore, these two
sugars can not participate in the oxidation-reduction reactions
characteristic of reducing sugars(ie Benedicts test).
The principle of Benedict's test is that when reducing sugars are
heated in the presence of an alkali, they get converted to powerful
reducing compounds known as enediols. Enediols reduce the cupric ions
(Cu2+) present in the Benedict's reagent to cuprous ions (Cu+) which get
precipitated as insoluble red copper(I) oxide(Cu2O).
A. D. Protein primer
The center of granule contains a protein known as glycogenin, which
acts a primer for glycogen synthesis.
A. D. Chitin
Heteropolysaccharides are polysaccharides containing more than
one type of monosaccharide unit. They include glycosaminoglycans(GAG
or mucopolysaccharides) in humans, agar, gum & pectin in plants
Chitin is a homopolysaccharide of N acetyl glucosamine.
A. B. Hyaluronic acid
Only GAG to be devoid of sulfate groups is hyaluronic acid. HA is
found in synovial tissue and forms stem cell niche.
A. B. Carbohydrate
Proteoglycans are large molecules made up of 90%
carbohydrate(heteropolysaccahride) and 10% proteins(core protein &
linker protein).
Q. Which MPS out of the options mentioned below will have least
clinical symptoms?
A. MPS IH
B. MPS IS
C. MPS IH-S
D. MPS II
A. B. MPS IS
Scheie syndrome is a subtype of Hurlers syndrome with less clinical
manifestations.
Q. All of the following mucopolysaccharidosis (MPS) syndromes are
autosomal recessive in inheritance except:
A. MPS IH
B. MPS III
C. MPS IH-S
D. MPS II
A. D. MPS II
All except MPS II, Hunters syndrome are autosomal recessive.
Hunters syndrome is X-linked recessive in inheritance.
A. C. Hunters syndrome
Hunters syndrome is MPS II, which is X-linked in inheritance. It is
characterized by deficiency of iduronidase enzyme and excess
accumulation of heparin sulfate and dermatan sulfate.
A. A. It is a C2 epimer of mannose.
Mannose is an epimer of glucose at C2. The ring form of glucose is
pyranose and for fructose it is furanose.
All the carbohydrates exist in D isomeric form and amino acid in the
L-isomeric form.
Glucose is an aldose sugar,wherease fructose is an keto sugar.
C. Isomaltase
D. Sucrase
A. B. Lactase
Deficiency of lactase enzyme causes lactose intolerance, which is
characterized by non absorption of lactose from milk & milk products. This
lactose in colon gets acted upon by bacteria and gets converted into
hydrogen , CO2 and methane, which leads to bloating. Also, unabsorbed
lactose and its products increase the osmotic pressure of intestinal
contents and cause diarrhea. Hydrogen breath test can be diagnostic.
C. GLUT-3
D. GLUT-4
A. D. GLUT-4
GLUT proteins transport glucose and related hexoses. Each glucose
transporter isoform plays a specific role in glucose metabolism determined
by its pattern of tissue expression, substrate specificity, transport kinetics,
and regulated expression in different physiological conditions. To date, 13
members of the GLUT/SLC2 have been identified. On the basis of
sequence similarities, the GLUT family has been divided into three
subclasses :
Class I : GLUT 1,2,3,4
Class II : GLUT 5,7,9,11
Class III : GLUT 6,8,10,12
GLUT 1: mainly present in erythrocytes ;important for basal
uptake of glucose
GLUT 2: present in pancreatic beta cells (acting as glucose sensor),
renal tubular cells, liver, intestine(transports glucose, galactose &
fructose). It is a bidirectional pump.
GLUT 3: present in neurons for basal uptake of glucose
GLUT 4: adipose tissue, skeletal muscle and cardiac muscle; only
insulin responsive glucose transporters; peripheral uptake of glucose
GLUT 5: present in all tissues for fructose transport.
D. adrenal cortex
A. B. skeletal muscle
GLUT 4 present in adipose tissue, skeletal muscle and cardiac
muscle is the only insulin responsive glucose transporters, which would
decrease in fasting.
A. D. Migitilol
Acarbose, Migitilol & are alpha-glucosidase/maltase inhibitors ,which
slow the production of glucose from dietary carbohydrates, and thus
decrease postprandial glucose concentration.
A. C. GLUT-5
GLUT-5, which is a fructose transporter is present in testes and
small intestine.
Q. Glycolysis- a central pathway in carbohydrate metabolismincorrect statement isA. it is an anabolic pathway occurring in cytosol.
B. it involves complete oxidation of glucose to CO2
C. 10 reactions are divided into 2 phases
D. oxygen concentration has no effect on glycolysis
A. B. it involves complete oxidation of glucose to CO2
Glycolysis is simply conversion of glucose to pyruvate. Further fate
of pyruvate depends on the presence or absence of oxygen or the energy
requirement.
Glycolysis has two phases : priming phase and energy yielding
phase.
Glycolysis can occur both in aerobic as well as anaerobic conditions
It occurs in cytoplasm of the cell
A. Step1
B. Step2
C. Step3
D. Step4
D. Step6
C. iP
D. UTP