Q28
MCQ • 2M
Mass transfer in bioprocesses (kLa)
Match the entries in Group I with those in Group II. Group I Group II P. MTT 1. Dihydrofolate reductase Q. Annexin V 2. Succinate dehydrogenase R. Methotrexate 3. Microtubules S. Taxol 4. Phosphatidylserine (A) P-3, Q-1, R-4, S-2 (B) P-2, Q-4, R-1, S-3 (C) P-2, Q-3, R-4, S-1 (D) P-4, Q-2, R-1, S-3
Q31
MCQ • 2M
Biomolecules, enzyme kinetics
Match the terms in Group I with the ploidy in Group II. Group I Group II P. Disome 1. 2n + 1 Q. Monosome 2. 2n - 1 R. Nullisome 3. n - 1 S. Trisome 4. n + 1 (A) P-4, Q-2, R-3, S-1 (B) P-4, Q-3, R-1, S-2 (C) P-2, Q-3, R-4, S-1 (D) P-1, Q-4, R-3, S-2
Q33
MCQ • 2M
Biomolecules, enzyme kinetics
Match the products in Group I with the applications in Group II. Group I Group II P. Digoxin 1. Muscle relaxant Q. Stevioside 2. Anti-cancer agent R. Atropine 3. Cardiovascular disorder S. Vinblastine 4. Sweetener (A) P-1, Q-4, R-3, S-2 (B) P-3, Q-2, R-1, S-4 (C) P-3, Q-4, R-1, S-2 (D) P-2, Q-3, R-1, S-4
Q37
MCQ • 2M
Mass transfer in bioprocesses (kLa)
Match the entries in Group I with the process parameters in Group II. Group I Group II P. Clark electrode 1. Liquid level Q. Redox probe 2. Dissolved oxygen concentration R. Load cell 3. Vessel pressure S. Diaphragm gauge 4. pH (anaerobic process) (A) P-2, Q-1, R-3, S-4 (B) P-4, Q-2, R-3, S-1 (C) P-2, Q-4, R-1, S-3 (D) P-2, Q-1, R-4, S-3
Q38
MCQ • 2M
Bioreactor types, scale-up
Match the downstream processes in Group I with the products in Group II. Group I Group II P. Solvent extraction 1. Lactic acid Q. Protein-A linked affinity chromatography 2. Penicillin R. Extractive distillation 3. Monoclonal antibody S. Salting out 4. Lipase (A) P-2, Q-3, R-1, S-4 (B) P-4, Q-1, R-2, S-3 (C) P-4, Q-1, R-3, S-2 (D) P-2, Q-4, R-1, S-3
Q41
MCQ • 2M
Downstream processing (chromatography, filtration)
Match the organisms in Group I with the entries in Group II. Group I Group II P. Clostridium 1. Rods with teichoic acid in the cell wall Q. Escherichia 2. Rods with endospores R. Vibrio 3. Helical rods with flagella S. Bacillus 4. Rods with LPS in the outer membrane 5. Curved rods with polar flagella (A) P-2, Q-4, R-5, S-1 (B) P-2, Q-1, R-5, S-4 (C) P-5, Q-4, R-2, S-3 (D) P-3, Q-2, R-1, S-4
Q42
MCQ • 2M
Bioreactor types, scale-up
Match the entries in Group I with the methods of sterilization in Group II. Group I Group II P. Serum 1. Autoclave Q. Luria broth 2. Membrane filtration R. Polypropylene tubes 3. UV irradiation S. Biological safety cabinets 4. Gamma irradiation 5. Dry heat (A) P-5, Q-3, R-1, S-4 (B) P-1, Q-4, R-5, S-3 (C) P-2, Q-1, R-4, S-3 (D) P-4, Q-1, R-3, S-5
Q43
MCQ • 2M
Biomolecules, enzyme kinetics
Match the high energy compounds in Group I with the biosynthetic pathways for the molecules in Group II. Group I Group II P. GTP 1. Fatty acid Q. UTP 2. Phospholipid R. CTP 3. Protein S. Acyl coenzyme A 4. Peptidoglycan (A) P-3, Q-2, R-4, S-1 (B) P-2, Q-4, R-3, S-1 (C) P-4, Q-3, R-1, S-2 (D) P-3, Q-4, R-2, S-1
Q44
MCQ • 2M
Biomolecules, enzyme kinetics
Match the vitamins in Group I with the processes/reactions in Group II. Group I Group II P. Pantothenic acid 1. Electron transport Q. Vitamin B2 2. Transfer of 1-C units R. Vitamin B6 3. Decarboxylation S. Folic acid 4. Fatty acid metabolism 5. Hydrolysis (A) P-5, Q-2, R-4, S-1 (B) P-4, Q-1, R-3, S-2 (C) P-4, Q-2, R-1, S-3 (D) P-2, Q-1, R-3, S-5 2012 BIOTECHNOLOGY - BT
Q45
MCQ • 2M
Probability and Statistics
Consider the data set 14, 18, 14, 14, 10, 29, 33, 31, 25. If you add 20 to each of the values, then (A) both mean and variance change (B) both mean and variance are unchanged (C) the mean is unchanged, variance changes (D) the mean changes, the variance is unchanged
Q46
MCQ • 2M
Biomolecules, enzyme kinetics
An enzymatic reaction is described by the following rate expression: v = (Vmax * [S]) / (Km + [S] + [S]^2 / Ki). Given Vmax = 10 µmol/(min.mg), Km = 1 mM, and Ki = 4 mM, the substrate concentration [S] at which the reaction velocity achieves its maximum value is ________ mM.
Q47
MCQ • 2M
Downstream processing (chromatography, filtration)
A bacterial culture (200 l containing 1.8 × 109 cells) was treated with an antibiotic Z (50 g per ml) for 4 h at 37˚C. After this treatment, the culture was divided into two equal aliquots. Set A: 100 l was plated on Luria agar. Set B: 100 l was centrifuged, the cell pellet washed and plated on Luria agar. After incubating these two plates for 24 h at 37˚C, Set A plate showed no colonies, whereas the Set B plate showed 0.9 × 109 cells. This experiment showed that the antibiotic Z is (A) bacteriostatic (B) bacteriocidal (C) bacteriolytic (D) apoptotic Common Data Questions Common Data for Questions 48 and 49 : In a muscle, the extracellular and intracellular concentrations of Na + are 150 mM and 12 mM, and those of K+ are 2.7 mM and 140 mM, respectively. Assume that the temperature is 25 oC and that the membrane potential is -60 mV, with the interior more negatively charged than the exterior. (R = 8.314 J mol -1 K-1; F = 96.45 kJ mol-1 V-1)
Q50
MCQ • 2M
Biomolecules, enzyme kinetics
The fold purification for each step is (A) P-0.1, Q- 0.66, R-0.84, S- 1.26 (B) P-1.0, Q-0.52, R-0.67, S-0.8 (C) P-1, Q-6.6, R-8.4, S-12.6 (D) P-100, Q-66, R-84, S-12
Q51
MCQ • 2M
Biomolecules, enzyme kinetics
The yield (%) for each step is (A) P-10, Q-7.2, R-4.5, S-2.0 (B) P-34, Q-24, R-15, S-1 (C) P-3.4, Q-2.4, R-1.5, S-0.1 (D) P-100, Q-71, R-44, S-29 Linked Answer Questions Statement for Linked Answer Questions 52 and 53: An E. coli cell of volume 10 -12 cm3 contains 60 molecules of lac -repressor. The repressor has a binding affinity (Kd) of 10-8 M and 10-9 M with and without lactose respectively, in the medium.