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Key Biochemistry Concepts and Disorders

This document provides a list of 135 items related to biochemistry concepts. It covers topics like vitamins and cofactors, metabolic pathways, enzyme deficiencies, amino acids, lipids, carbohydrates, and other biochemical processes and structures in the human body. Each item concisely lists a concept and the associated term or process. The list appears to be intended as a study guide or review of key biochemistry topics.

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100% found this document useful (1 vote)
535 views19 pages

Key Biochemistry Concepts and Disorders

This document provides a list of 135 items related to biochemistry concepts. It covers topics like vitamins and cofactors, metabolic pathways, enzyme deficiencies, amino acids, lipids, carbohydrates, and other biochemical processes and structures in the human body. Each item concisely lists a concept and the associated term or process. The list appears to be intended as a study guide or review of key biochemistry topics.

Uploaded by

sk
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
  • Cover Page: Cover page displaying the title and related information of the document.
  • Biochemistry One Liners: Provides a list of single-line statements on various biochemistry topics relevant for exams like FMGE and NEET PG.
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  • More Biochemistry One Liners: Continues the list of biochemistry one liners, covering additional topics and facts.
  • MCQs: Contains multiple-choice questions related to biochemistry covering essential exam topics.
  • Contact Information: Provides contact details and further information about DMA, the publisher of the content.

Davinci Medical Academy

BIOCHEMISTRY

1. In starvation there is an - Increase in Pyruvatekinase


2. Musty odour urine is seen in - Phenylketanuria
3. Vitamin necessary for post transitional modification - Vit.K
4. Decarboxylation needs - Vit.B6
5. Power house of the cell - Mitochondria
6. Protein synthesis takes place in - Endoplasmic reticulum
7. Daily secretion of bile by liver is amount of - 500-1000ml
8. Haemorhagic disease of Newborn is seen due to deficiency of - Vit.K
9. Acrodermatitis enteropathica is due to - Zinc deficiency
10. Molybdenum is necessary for - Xanthine oxidase
11. Hartnup disease is due to deficiency of - Tryptophan
12. Alkaptonuria is due to deficiency of - homogentisic acid oxidase
13. In alkaptonuria,the deposition of substance - Homocysteine
14. Vitamin used to correct neurological symptoms is - Cynocobalamine B12
15. Wernicke-korsakoff psychosis /Beriberi caused by defeciency of - Thiamine B1
16. Pellagra is caused by defeciency of - Niacin B3
17. Burning foot syndrome is caused by defeciency of - Pantothenic
18. Megaloblastic anemia/Neural tube defect caused by defeciency of - Folic acid
19. Pernicious anemia caused by defeciency of - B12
20. Sebhoric dermatitis caused by defeciency of - Riboflavin B2
21. IHD is associated with which type of cholesterol - LDL
22. Seen in chronic starvation - insulin decreases/glucagon & growth hormone
increases/free fatty acids increases/glucose tolerance decreases.
23. Southern blot test is used to detect - DNA
24. Northern Blot test - RNA
BIOCHEMISTRY

25. Western Blot test - Protein


26. Vitamin used for inhibiting lactation - B6
27. Wernicke’s encephalopathy is caused by defeciency of - B1
28. Vitamin K dependant clotting factors are - fac.2,7,9,10
29. Enzyme defecient in marfan’s syndrome is - Lysyl oxidase
30. Reactions takes place in Mitochondria - krebs cycle,urea cycle,electron trans-
fer,fatty acid cycle
31. Melatonin is synthesised from - Tryptophan
32. Amino acids excreted in the urine in cystinosis - cystine,ornithine,argi-
nine,lysine

Biochemistry
33. In maple syrup urine dis. the aminoacids excreted n urine r -leucine,isoleu-
cine,valine
34. Sulphur containing amino acids -cysteine & methionine
BIOCHEMISTRY
35. Conjugated hyperbillirubinemia s seen -Dubin jhonson synd.
36. In Hartnup’s disease excreated in urine is- Tryptophan
37. Bile contains - cholic acid,chenodeoxycholic,deoxycholic,lithocolic acids
38. Cofactor for transamination is - Pyridoxine
39. Vitamin essential for transamination - B6
40. Phenyl pyruvic acid in the urine is detected by - Guthrie’s test
41. In alkaptonuria the urine contains - Homogentisic acid
42. Insulin has - 51 amino acids
43. Von gierke’s disease is due to defeciency of - galactose-1-phosphate uridyl-
transferase
44. Essential fatty acids are - linoleic,linolenic & arachidonic acid
45. Iron is absorbed actively in the - Duodenum
46. vit.B12 is absorbed in the - Terminla ileum
47. Highest content of triglycerides is seen in - Chylomicrons
48. Atherosclerosis is due to - Apo protein E defeciency
49. Triglyceride synthesis is increased by - Insulin
50. Which is an essential amino acid - phenylalanine,lysine,leucine
51. Insulin acts on which enzyme in glycolysis - Glucokinase
52. Present in cerebroside - Sphingosine,galactose
53. Melatonin is derived from - Tryptophan
54. Liver produces - albumin,fibrinogen,prothrombin & not gamma globulin
55. Bile acids are formed from - cholesterol
56. Heme in hemoglobin is in the - Hydrophobic pocket
57. 17-Alpha hydroxylase defeciency causes - decreased testosterone
58. Substance that does not cross blood brain barrier - Insulin
59. Anti infective vitamin is - vitamin A1
60. Tissue with highest glycogen content - Liver
61. Detoxification of drugs is controlled by - cytochrome P450
62. Anti atherosclerotic lipoprotein is - HDL
63. MC enzyme defeciency in man is - glucose-6-phosphate dehydrogenase
64. Largest amounts of prostaglandins are seen in - Seminal fluids
65. Sulphonamides are conjugated by - Glucoronic acid
66. Which amino acid causes Hypoglycemia - Leucine
67. Vitamin present in co-enzyme A is - pantothenic acid
68. Insulin resistance is seen in - hypothyroidism,acromegaly
69. Fatty acid not synthesised in the body is - linoleic acid

Davinci Medical Academy


Biochemistry
70. Albinism results from deficiency of - Tyrosinase
71. Enzymes stored in muscle is- CPK
72. Secondary hyper parathyroidism is caused by - CRF
BIOCHEMISTRY

73. Abnormal Urinary constituents are - albumin, ketone, glucose


74. Urinary constituents - amino acids, urea, creatinine
75. Polyuria is seen in - DM,diabetes insipidus,recovery from acute nephritis
76. Polypeptide hormones are - insulin,angiotensin,growth hormones
77. Physiological constituents of urine - urea,creatinine
78. Major site of action of insulin - muscle,adipose tissue liver
79. Semi essential aminoacids are - Arginine,histidine
80. Ratio of adrenaline to noradrenaline - 85:15
81. Examples of monounsaturated fatty acids are - oleic acid
82. Acidic amino acids are - asparagine,glutamine
83. Basic amino acids are - arginine,lysine
84. Aromatic amino acids are - tryptophan,tyrosine,phenylalanine
85. Total body iodine stores are about - 50mg
86. vit.C is present in largest amount in the body in - Adrenal cortex
87. Tetany can be caused by - hypocalcemia,hypomagnesemia
88. Ketone bodies are - Acetoacetate
89. Bile acids are derived from - cholesterol
90. Which is completely dependant on glucose as fuel - Retina
91. Immediate precursor of nor epinephrine is - Dopamine
92. Uric acid levels are increased in - pre-eclampsia,hodgkins lymphoma,leukemia
93. Metal in vit.B12 is - Cobalt
94. Ammonia in the brain is converted into - Glutamine
95. Dopamine synthesis in brain is increased by - Carbidopa
96. Calcium binding protein is - Troponin-C
97. Metabolite of epinephrine is - Metanephrine
98. End product of purine metabolism is - Uric acid
99. Vitamin A overdosage causes injury to - Lysosomes
100. Myocardium normally utilises - Fatty acid
101. Max. amount of serum cholesterol is found in - LDL
102. Vitamin that is useful in cancer is vitamin - A
103. Enzyme acetylcholine esterase is synthesised in - Liver
104. Urea in the Brain is derived from - Glutamine
105. Non-essential aminoacid is - Tyrosine
106. Enzyme primarily responsible for protein degradation in stomach - Pepsin
107. Increased anion gap is seen in - renal failure, lactic acidosis, DKA
108. Cholesterol from the liver is transported to the tissues mainly by the - VLDL

Davinci Medical Academy


109. Precursor of steroid - cholesterol
110. Maple syrup urine disease is due to the deficiency of - Decarboxylation
111. Amino acid that can be converted into vitamin is - tryptophan
112. Main function of mitochondria is - electron transfer
113. Histamine is produced by - decarboxylation
114. Glutathione is a - tripeptide
115. Ketone body formation takes place in - liver
116. Xantheurenic acid is a product of metabolism of - Tryptophan
117. Neurotransmitter is - Glutamine
118. DNA double helix is bound by - Hydrogen bond
119. Glucose-6-phosphate dehydrogenase deficiency is seen in - vongierke’s disease
120. Which is not seen in starvation - hypercholesterolemia
121. Muscle glycogen is mainly used for supplying energy to - heart
122. Enzyme marker of electron transport system is - cytochrome reductase
123. Major contribution towards gluconeogenesis is by - Alanine
124. Conversion of prothrombin to thrombin requires - factors-7,10,5 & Ca2+
125. Which does not inhibit platelet aggregation - Thromboxane A2
126. Conversion of proline to hydroxyproline is by - vit.C mediated hydroxylation
127. Ketone body which is maximum in DKA - Acetoacetic acid
128. Biotin is essential for - carboxylation
129. Ketoacidosis without glycosuria is seen in - prolonged starvation

Biochemistry
130. Protein synthesis takes place in - Endoplasmic reticulam
131. NADPH is required in - lipogenesis
132. Dietary fibre is rich in - Pectin
BIOCHEMISTRY

133. Lipid which accumulates in fatty liver is - Triglycerides


134. Gluconeogenesis occurs in the- liver & Kidney
135. Germ oil has high content of vitamin - E
136. Melanin is synthesised from - phenylalanine
137. Obesity is associated with - decreased insulin response
138. Glycerol is converted to glucose in - Liver
139. vit.K plays an essential role in - biosynthesis of prothrombin & proconvertin
140. Preservative used in urine samples for chemical analysis is - Thymol
141. Heart muscle in comparison to skeletal muscle has - high carnosine
142. pH of normal sweat is - 4.5
143. Urea is mainly formed in liver & to small extent in - Brain
144. Pantothenic acid acts on - CoA
145. Fluoride ions act by inhibiting - Enolase
146. Deficiency of which vitamin is not known in newborn - E
147. Toad skin is seen in deficiency of vitamin - A
148. Resting membrane potential is close to the isoelectrical potential of - Cl
149. Infant’s gastric juice pH is - 5.0
150. Enzyme diagnostic of MI in acase of hypothyroidism - CPK-MB
151. Transaminase an enzyme is most abundant in - Heart
152. White hair is due to - deficiency of melanin
153. Anticoagulant used for preserving blood for PT estimation is - sodium citrate
154. Biotin deficiency is characterised by - muscular pain, nausea, dermatitis
155. Zinc is a component of - carbonic anhydrase,insulin,carboxypeptidase
156. Respiratory quotient of fat, protein & carbohydrate are - 0.70-0.80-1.0
157. In glycolysis which of the ions is most important - Mg
158. Prostaglandins - are acyclic fatty acid derivatives
159. Thiouracil inhibits thyroid function by - inhibition of thyroxine synthesis
160. Cytochromes are - iron-porphyrin proteins
161. Vitamin acts as a respiratory catalyst - vit.C
162. Histidine decarboxylase is present in - liver & kidney
163. Dietary changes are not required in - wilsons disease
164. Codon consists of - 3 consecutive nucleotide units
165. Coenzymes are - non-protein organic compounds
166. Hair is rich in amino acid - Cystine
167. Component of co-enzyme A - pantothenic acid,adenylic acid,sulphydryl group
168. Renin is present in - stomach

Davinci Medical Academy


169. Methionine is important in - formation of choline
170. Actinomycin D interferes with enzyme induction by combining with - DNA
171. Ketone bodies are by products of metabolism of - Fats
172. Lactate dehydrogenase is - Isozyme
173. Creatinine is formed metabolically from - Arginine
174. Blood brain barrier is maximally permeable to - CO2
175. Which of the following vitamin is destroyed by heat - Biotin
176. Daily normal excretion of ketone bodies - 1.0mg
177. Hexokinase is a - Transferase
178. Which is the by product of the urea cycle - Fumarate
179. False positive reaction of glucose is seen with - Aspirin
180. Which of the following is not a trace element - Ca+
181. Chitin is a - Polysachride
182. Biuret test is mainly done for - Protein
183. In metabolic acidosis, true about urinary change is - increase in Ammonia
184. Monoclonal electrophoresis is useful in the diagnosis of - Multiple myeloma
185. Basic structural unit from which fatty acids are derived - Acetyl Co A
186. Precursor of cholesterol synthesis is - Acetyl CoA
187. Whole wheat is an excellent source of - Thiamine
188. Siderophyllin is - transferrin
189. Which of the following is not a phospholipid - cerebroside
190. Triglycerides in serum are transported by -VLDL
191. Which of the following is a initiating amino acid for protein synthesis - Methi-
onine
192. In mammalian cells protein sequence takes place chiefly at the - nucleolus
193. Insulin resistance may be due to - Acromegaly
194. Cytochromes are - iron-porphyrin proteins
195. Which of the following is seen in obstructive jaundice - excess of bile salts in
the urine
196. Which of the following cannot be metabolized in the body - sucrose
BIOCHEMISTRY

197. High threshold substance is - glucose


198. Million’s test is used for detection of - Tyrosine
199. HMP shunt great importance in cellular metabolism because it produces - NA-
DPH
200. Urea is produced by the enzyme - Arginase
201. Actinomycin D interferes with enzyme induction by combining with - DNA
202. A bi-lipid layer is most permeable to - Urea
203. The lactate dehydrogenase levels are increased in - Glycine
204. The most direct precursor of taurine is - Cysteine
205. Aromatic ring is present in - phenylalanine

Biochemistry
206. A substance having affinity but no intrinsic activity is - Antagonist
207. Ferritin an inactive form of iron is stored in - liver
208. First product of glycogenolysis is - glucose-1-phosphate
BIOCHEMISTRY

209. C-AMP increases glycogenolysis by - contributing phosphate


210. Bohr effect is - effect of PCO2 on oxyhemoglobin dissociation
211. Tea and coffee contains - tannin
212. Specific dynamic action is- energy expenditure on consumption of foods
213. Ingestion of benzoic acid in man results in an increase in urinary- hippuric acid
214. An essential amino acid in man is- L- methionine
215. The mucopolysaccharide hyaluronic acid is found primarily in - vitreous hu-
mor
216. An amino acid not involved in urea synthesis is- histidine
217. The most abundant protein in the human body is - collagen
218. Sorbitol is- sugar alcohol
219. Dicumarol is an antimetabolite of- vit K
220. Inhibition of glycolysis by O2 is known as- Pasteur effect
221. In human body which of the following trace element in next to iron- Cu++
222. Which of the following is a dietary essential- linoleic acid
223. Patients with severe renal disease may not be able to use normal dietary sourc-
es of vitamin- D
224. Winslow test is used to estimate serum or urinary- amylase
225. PH is maximum in- pancreatic secretion
226. Dawn phenomenon refers to -after breakfast hypoglycemia
227. Ehrlich’s test done to detect- urobilinogen
228. Benzidine test is positive with the enzyme- peroxidase
229. Cyanide is toxic because it- inhibits cytochrome oxidase

Davinci Medical Academy


230. The substance essential for transfer fatty acids across mitochondrial mem-
brane-
231. carnitine
232. Which of the following organs can’t use ketone bodies- liver
233. Lipid from tissues is carried to liver by - HDL
234. Unsaturated fatty acids are converted to - Prostaglandins
235. Vitamin necessary for CoA synthesis - Pantothenic acid
236. Lamin is present in - inner nuclear membrane
237. NADPH is used in - Fatty acid synthesis
238. People eating only maize as staple diet develop niacin deficiency due to - high
leucine
239. Thromboxane is mostly produced by - Platelet
240. Alcohol-uric jaundice is caused by - hemolytic jaundice
241. Triple helix is seen in - collagen
242. Urinary protein is detected by - Barfoed test
243. Glutathione peroxidase contains - selenium
244. Cholesterol is a - steroid
245. Saturated fatty acid is present in high quality - coconut oil
246. Keratin is chemically - cystine
247. Untreated diabetes leads to - tissue use fatty acids as main fuel
248. MCC of lactic acidosis - Circulatory failure
249. Not a cause of metabolic acidosis - climbing to high altitudes
250. Vitamin also acting as hormone - Vit D
251. Proteins binding to DNA has - Zinc
252. DNA fragments are separated by - agarose gel electrophoresis
253. Ferritin stores are present in sites - intestine/liver/spleen but not in - bone
254. Osmolarity is - moles per liter of solvent
255. In Beri-Beri which enzyme activity is measured - Transketolase
256. An exclusive protein meal intake will cause - Hypoglycemia
257. Heart uses one of the following as energy source during starvation - Acetoace-
BIOCHEMISTRY

tate
258. In Maple syrup urine absence FeCl3 test with urine gives colour - Blue
259. Carnitine is formed from - Lysine
260. Arthritis occur in - Alkaptonuria
261. Norepinephrine is converted to epinephrine by - N-methylation
262. Most important compensatory mechanism in metabolic acidosis - Hyperventi-
lation
263. Translation occurs at - Ribosome
264. The reaction inhibited in thiamine defeciency is - pyruvate to acetyl CoA
265. Skeletal muscle is deficient in - glucose -6-phosphate

Biochemistry
266. Familial hypercholesterolemia is - deficient of LDL receptors
267. Cholesterol maximally carried in - LDL
268. Most abundant collagen in body is - Type-1
BIOCHEMISTRY

269. What is the technique by which DNA can be amplified - polymerase chain reac-
tion
270. Null mutation is - mutation which produces no functional gene product
271. Which one is non sense codon- UAG,UGA
272. Which of the following amino acid ss assoc. with increased risk of MI - Homo-
cysteine
273. Glutathione peroxidase contains - selenium
274. Which one of the following enzyme use NADP as co-enzyme - G6PD
275. Fatty acids of cholesterol are mainly - palmitic & stearic acid
276. Shortest peptide is - encephalin
277. FIGLU is a metabolite of - Histidine
278. Which is a fructosan - Inulin
279. Saponification means hydrolysis of fats by - Alkali
280. In pregnancy amount of glucose used in GTT - 100mg
281. Total number of genes in a human being is - 50,000
282. Naturally occuring amino acid - hydroxyproline
283. Northern blot is - amplification of mRNA
284. Source of ammonia in urine is - Glutaminase
285. Bilirubin is produced from - hemoglobin/myoglobin
286. Pyruvate utilization in tissues is decreased in - Beri-Beri
287. Amino acid used in the synthesis of purines - Glycine
288. In porphyria cutanea tarda the type of porphyrin excreted in urine is -type 1&3
uroporphyrins

Davinci Medical Academy


289. Chromosomal nomenclature is based on - position of centromere
290. Not seen in - thiamine deficiency - cerebellar dysfunction
291. Warm auto antibodies are seen in - SLE
292. Xeroderma pigmentosum is produced as a result of defect in - DNA ligase
293. Fatty acids does not produce glucose due to absence of -phosphophenolpyru-
vatekinase
294. Best indicator of iron deficiency - serum ferritin
295. Chylomicrons belong to group - Apo-B
296. In the fasting state glucose is obtained from - muscle glycogen
297. Steroid biosynthesis occur at - smooth endoplasmic
298. Ketone bodies are formed in the - Liver
299. New DNA synthesis occurs in - interphase
300. Membrane phospholipid that does not contain glycerol is - Sphingomyelin
301. Antioxidants - vit A,C,E
302. End-product of the action of salivary amylase is – Maltose
303. Severe muscular exercise causes - Lactic acidosis
304. Vitamin A is stored mainly as retinol esters in - liver
305. Idiopathic nyctalopia is due to a hereditary - absence of rod function

Biochemistry
MCQ’s
1. “All enzymes are not proteins.” This state- A. Chemical methods
ment is justified by: B. Physical methods
A. All enzymes do not follow the Michaelis C. Chemiosmotic methods
Menten hypothesis D. Conformational changes
B. RNAs act as ribozymes Ans. C
C. Antibodies take part in the catalysis of
many reactions 5. Thiamine level is best monitored by:
D. Metals are involved in attachment to A. Transketolase level in RBC
enzymes and catalysts B. Thiamine level in blood
Ans. B C. G-6-PD activity
D. Reticulocytosis
2. Enzymes mediating transfer of one mole- Ans. A
cule to another are:
A. Transferases 6. Vitamin B12 and folic acid supplementation
B. Oxidases in megaloblastic anemialeads to the im-
C. Lysases provement of anemia due to:
D. Peptidases A. Increased DNA synthesis in bone
Ans. A marrow
B. Increased hemoglobin production
3. In which of the following reactions is mag- C. Erythroid hyperplasia
nesium required: D. Increased iron absorption
A. Na+K+ ATPase Ans. A
B. Dismutase
C. Phosphatase 7. Nitric oxide synthase:
D. Aldolase A. Is inhibited by Ca++
Ans. A B. Catalyses a dioxygenase reaction
C. Accepts electrons from NADH
4. In oxidative phosphorylation, the ATP pro- D. Requires NADH, FAD, FMN & heme iron
duction and respiratory chain are linked by: Ans. D

Davinci Medical Academy


8. Phenylalanine is the precursor of all the fol- A. Histidine
lowing, except: B. Keratin
A. Tyrosine C. Lysine
B. Epinephrine D. Cysteine
C. Thyroxine Ans. B
D. Melatonin
Ans. D 15. In dividing cells, spindle is formed by:
A. Ubiquitin
9. In a well fed state, acetyl CoA obtained from B. Tubulin
diet is least used in the synthesis of: C. Laminin
A. Palmity CoA D. Keratin
B. Citrate Ans. B
C. Acetoacetate
D. Oxalosuccinate 16. Entropy in a biological system is constant
Ans. C because:
A. It is an open system
10. Substrate level phosphorylation in citric B. It is a closed system
acid cycle is seen in the conversion of: -ke- C. It is a governed by vitalism
toglutaratea D. Has exothermic-endothermic reactions
A. Acetoacetate to Ans. D
B. Succinyl CoA to succinate
C. Fumarate to malate 17. Which of the following is true regarding a
D. Succinate to fumarate system which favours oscillatory responses:
Ans. B A. Has proportional component
B. Has a greater gain
11. Apo B48 and apo B100 are expressed as C. Has a lesser gain
two different apo-proteins because of dif- D. Positive FEEDBACK system
ference in: Ans. D
A. RNA editing
B. RNA splicing 18. Highest binding of iron is seen with:
C. Chromosomal loci A. Transferrin
D. Apo-B gene B. Ferritin
Ans. A C. Haemoglobin
D. Ceruloplasmin
12. All the following can be used to detect mu- Ans. C
tation, except:
A. Single strand conformational 19. The main enzyme responsible for activation
polymorphism of xenobiotics is:
B. Ligase chain reaction A. Cytochrome P-450
C. Polymerase chain reaction B. Glutathione S-transferase
D. DNA sequencing C. NADPH cytochrome P-450-reductase
Ans. B D. Glucoronyl transferase
Ans. A
13. Which of the following is true regarding hy-
droxy ethyl starch: 20. The primary defect which leads to sickle
A. It is an anesthetic agent cell anemia is:
B. It is a plasma expander A. An abnormality in prophyrin part of
C. It is a crystalloid hemo-globin.
D. Used as a nutritional agent #NAME?
Ans. B #NAME?
D. Substitution of -chain of HbA.avaline by
14. Elasticity of the corneal layer of SKIN is due glutanmate in the
to the presence of: Ans. B
Biochemistry
21. Decreased glycolytic activity impairs oxy- 26. The buffering capacity of a buffer is maxi-
gen transport by hemoglobin due to: mum at pH equal to:
A. Reduced energy production A. 0.5 pKa
B. Decreased production of 2,3- B. pKa
biphospho-glycerate C. pKa+1
C. Reduced synthesis of hemoglobin D. 2pKa
D. Low level of oxygen Ans. B
Ans. B
27. Which of the following is present intracellu-
22. The primary role of chaperones is to help lary in muscle cells:
in: A. Insulin
A. Protein synthesis B. Corticosteroid
B. Protein degradation C. Epinephrine
C. Protein denaturation D. Glucagon
D. Protein folding Ans. B
Ans. D
28. Which of the following is not a post tran-
23. The conversion of an optically pure iso- scriptional modification of RNA?
mer (enantiomer) into a mixture of equal A. Splicing
amounts of both dextro and levo form is B. 5 capping polyadenylation
called as: C. 3
A. Polymerization D. Glycosylation
B. Stereoisomerization Ans. D
C. Racemization
D. Fractionation 29. Serum total lactate dehydrogenase level
Ans. C will NOT be raised in:
A. Muscle crush injury
The protein rich in basic amino acids, which B. Stroke
functions in the packaging of DNA in chromo- C. Myocardial infarction
somes, is: D. Hemolysis
A. Histone Ans. B
B. Collagen
C. Hyaluronic acid binding protein 30. Porphobilinogen in urine produces pink co-
D. Fibrinogen lour with:
Ans. A A. Fouchet’s reagent.
B. Benedict’s reagent.
24. An enzyme involved in the catabolism of C. Sodium nitropruside.
fructose to pyruvate in the liver is: D. Ehrlich’s aldehyde reagent.
A. Glyceraldehyde-3-phosphate Ans. D
dehydrogenase
B. Phosphoglucomutase 31. The collagen triple helix structure is not
C. Lactate dehydrogenase found in:
D. Glucokinase A. Cytoplasm.
Ans. A B. Golgi apparatus.
C. Lumen of endoplasmic reticulum.
25. -oxidation of odd-chain fatty acids pro- D. Intracellular vesicles.
duces:bQ 34. Ans. A
A. Succinyl CoA
B. Propionyl CoA 32. Basic amino acids are:
C. Acetyl CoA A. Aspartate and glutamate
D. Malonyl CoA B. Serine and glycine
Ans. B C. Lysine and arginine

Davinci Medical Academy


D. None of the above B. Multiple carboxylase deficiency
Ans. C C. Maple syrup urine disease
D. Urea cycle enzyme deficiency
33. Amino acid with dissociation constant clos- Ans. B
est to physiological pH is:
A. Serine 37. Force not acting in an enzyme substrate
B. Histidine complex:
C. Threonine A. Electrostatic
D. Proline B. Covalent
Ans. B C. Van der Wall
D. Hydrogen
34. Sources of the nitrogen in urea cycle are: Ans. C
A. Aspartate and ammonia
B. glutamate and ammonia 38. Cellular oxidation is inhibited by:
C. Arginine and ammonia A. Cyanide
D. Uric acid B. Carbon dioxide
Ans. A C. Chocolate
D. Carbonated beverages
35. If urine sample darkens on standing: the Ans. A
most likely condition is:
A. Phenylketonuria 39. Q 31. Triple bonds are found between which
B. Alkaptonuria base pairs:
C. Maple syrup disease A. A-T
D. Tyrosinemia B. C-G
Ans. B C. A-G
D. C-T
36. A baby presents with refusal to feed, SKIN Ans. B
lesions, seizures, ketosis organic acids in
urine with normal ammonia; likely diagno- 40. Which of the following RNA has abnormal
sis is: purine bases:
A. Propionic aciduria A. tRNA

Biochemistry
B. mRNA
C. rRNA 44. Which of these fatty acids is found exclu-
D. 16SRNA sively in breast milk:
Ans. A A. Linolaete
B. Linolenic
41. False regarding gout is: C. Palmitic
A. Due to increased metabolism of D. d-hexanoic
pyrimidines Ans. A
B. Due to increased metabolism of purines
C. Uric acid levels may not be elevated 45. Blood is not a newtonian fluid because:
D. Has a predilection for the great toe A. Viscosity does not changing with veloc-
Ans. A ity
B. Viscosity changes with velocity
42. All of the following statements are true re- C. Density does not change with velocity
garding lipoproteins except: D. Density changes with velocity
A. VLDL transports endogenous lipids Ans. B
B. LDL transports lipids to the tissues.
C. Increased blood cholesterol is associat- 46. The predominant isozyme of LDH in cardiac
ed muscle is:
with increased LDL receptors A. LD-1
D. Increased HDL is associated with B. LD-2
decreased risk of coronary disease C. LD-3
Ans. C D. LD-5
Ans. A
43. A destitute woman is admitted to the hos-
pital with altered sensorium and dehydra- 47. All of the following hormones have cell sur-
tion; urine analysis shows mild proteinuria face receptors except:
and no sugar; what other test would be de- A. Adrenalin
sirable: B. Growth hormone.
A. Fouchet C. Insulin
B. Rothera D. Thyroxine.
C. Hays Ans. D
D. Benedict’s
Ans. B

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48. Fluoride, used in the collection of blood 50. The amino acid residue having an imino
samples for glucose estimation, inbibits the side chain is:
enzyme: A. Lysine.
A. Glucokinase. B. Histidine.
B. Hexokinase. C. Tyrosine.
C. Enolase. D. Proline.
D. Glucose-6-phosphatase. Ans. D
Ans. C

49. Enzymes that move a molecular group from


one molecule to another are known as:
A. Ligases.
B. Oxido-reductases.
C. Transferases.
D. Dipeptidases.
Ans. C

Biochemistry
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