Q11
MCQ • 1M
DNA replication, transcription, translation
Phylum proteobacteria is subdivided into -, -, -, - and -proteobacteria based on (A) G+C content (B) 23S rRNA sequences (C)tRNA sequences (D)16S rRNA sequences 2013 BIOTECHNOLOGY - BT
Q26
MCQ • 2M
Mass transfer in bioprocesses (kLa)
Match the commercial microbial sources in Group I with the products in Group II. Group I Group II P. Corynebacteriumlilium 1. 2,3-Butane di-ol Q. Klebsiellaoxytoca 2. Poly- β-hydroxybutyric acid R. Aspergillusniger 3. Glutamic acid S. Alcaligeneseutrophus 4. Citric acid (A) P-3,Q-1,R-2,S-4 (B) P-3,Q-1,R-4,S-2 (C) P-1,Q-3,R-2,S-4 (D) P-1,Q-3,R-4,S-2
Q27
MCQ • 2M
Calculus
Match the entries in the Group I with the elution conditions in Group II. Group I Group II P. Ion-exchange chromatography 1. Isocratic solvent Q. Hydrophobic column chromatography 2. Ampholytes R. Gel filtration chromatography 3. Increasing gradient of salt S. Chromatofocusing 4. Decreasing gradient of polarity (A) P-4,Q-1,R-2,S-3 (B) P-4,Q-3,R-1,S-2 (C) P-3,Q-4,R-1,S-2 (D) P-3,Q-4,R-2,S-1 2013 BIOTECHNOLOGY - BT
Q29
MCQ • 2M
Biomolecules, enzyme kinetics
Match the cell structures in Group I with the organismsin Group II. Group I Group II P. Endospores 1. Methanobacterium Q. Bipolar flagella 2. Treponema R. Pseudomurine in cell wall 3. Spirillum S. Periplasmic flagella 4. Clostridium (A) P-4, Q-3, R-1, S-2 (B) P-4, Q-3, R-2, S-1 (C) P-3, Q-4, R-1, S-2 (D) P-4, Q-1, R-3, S-2
Q30
MCQ • 2M
DNA replication, transcription, translation
Match the antibioticsinGroup Iwith the targets inGroup II. Group I Group II P. Sulfonamide 1. Peptidoglycan synthesis Q. Quinolones 2. Peptide chain elongation R. Erythromycin 3. Folic acid biosynthesis S. Cephalosporin 4. Topoisomerase (A) P-3, Q-4, R-1, S-2 (B) P-2, Q-4, R-3, S-1 (C) P-4, Q-1, R-2, S-3 (D) P-3, Q-4, R-2, S-1
Q32
MCQ • 2M
Biomolecules, enzyme kinetics
Match the entries inGroup I with the enzymes inGroup II. Group I Group II P. NAD+ 1. Glutathione peroxidase Q. Selenium 2. Nitrogenase R. Pyridoxal phosphate 3. Lactate dehydrogenase S. Molybdenum 4. Glycogen phosphorylase (A) P-3, Q-2, R-4, S-1 (B) P-4, Q-1, R-3, S-2 (C) P-3, Q-1, R-4, S-2 (D) P-3, Q-4, R-2, S-1 2013 BIOTECHNOLOGY - BT
Q33
MCQ • 2M
Biomolecules, enzyme kinetics
Match the herbicides in Group Iwith the target enzymesin Group II. Group I Group II P. Glyphosate 1. Nitrilase Q. Bromoxynil 2. Acetolactatesynthetase R. Sulphonylureas 3. Dehalogenase S. Dalapon 4. 5-Enolpyruvyl shikimate3-phosphate synthase (A) P-4, Q-1, R-2, S-3 (B) P-2, Q-1, R-4, S-3 (C) P-4, Q-3, R-2, S-1 (D) P-3, Q-2, R-4, S-1
Q35
MCQ • 2M
Biomolecules, enzyme kinetics
Match the entries in Group Iwith the entries in Group II. Group I Group II P. RNAse P 1. Polyadenylation Q. RNase H 2. Splicing R. snRNAs 3. Ribozymes S. CstF 4. DNA-RNAhybrids (A) P-3, Q-4, R-2, S-1 (B) P-4, Q-3, R-2, S-1 (C) P-3, Q-2, R-1, S-4 (D) P-2, Q-4, R-1, S-3
Q37
MCQ • 2M
Biomolecules, enzyme kinetics
Match the entries in the Group Iwith the entries inGroup II. Group I Group II P. Threading 1. Gene duplication Q. FASTA 2. Fold prediction R. Profile 3. HMM S. Paralogs 4. k-tuple (A) P-2, Q-1, R-3, S-4 (B) P-2, Q-4, R-3, S-1 (C) P-3, Q-4, R-2, S-1 (D) P-1, Q-4, R-3, S-2
Q42
MCQ • 2M
CRISPR-Cas9 gene editing
A complete restriction digestion of a circular plasmid (5000bp) was carried out with HindIII,BamHIandEcoRIindividually. Restriction digestion yielded following fragments. Plasmid + HindIII→ 1200bp and3800bp Plasmid + BamHI→5000bp Plasmid + EcoRI→ 2500bp The number of sites for EcoRI,BamHIandHindIIIpresent on this plasmid are (A)EcoRI-2, BamHI-1, HindIII-2 (B) EcoRI-1, BamHI-1, HindIII-2 (C)EcoRI-3, BamHI-2, HindIII-1 (D) EcoRI-2, BamHI-2, HindIII-1 2013 BIOTECHNOLOGY - BT Q. 43 - Q. 47 are of numerical answer type.
Q47
NAT • 2M
Biomolecules, enzyme kinetics
A fed batch culture was operated with intermittent addition of glucose solution at a flow rate of 200 ml h-1. The values of K s, m and D are 0.3 g l -1, 0.4 h-1 and 0.1 h-1, respectively. Determine the concentration of growth limiting substrate (gl-1) in the reactor at quasi-steady state. ____________ Common Data Questions Common Data for Questions 48 and 49: A solution was prepared by dissolving 100 mg of protein X in 100 ml of water. Molecular weight of protein X is 15,000 Da; Avogadro's number = 6.022x 10 23.