| Column-I | Column-II | ||
| i. | Alu I | a. | Bacillus amyloliquefaciens H |
| ii. | Bam HI | b. | H. influenza RD |
| iii. | Eco RI | c. | Arthobacter luteus |
| iv. | Hind II | d. | Escherichia coli Ry 13 |
| Column I (Restriction Enzyme) |
Column II (Recognition sequence) |
||
| i. | AluI | P. | \(5'---G- \downarrow-A-T-C-C---3'\\3'---C-C-T-A-G-\uparrow-G---5'\) |
| ii, | BamHI | Q. | \(5'---A-G-\downarrow-C-T---3'\\ 3' ---T-C- \uparrow -G-A---5' \) |
| iii. | EcoRI | R. | \(5'--G-T-C- \downarrow - G-A-C--3' \\ 3'--C-A-G-\uparrow-C-T-G--5'\) |
| iv. | HindII | S. | \(5'---G- \downarrow-A-A-T-T-C---3'\\ 3'--- C-T-T-A-A-\uparrow-G---5'\) |
| Column-I | Column-II | ||
| (a) | DNA fragmentation | (i) | ssDNA gets embedded in nylon membrane |
| (b) | Electrophoresis | (ii) | Sample DNA and probe DNA from double stranded DNA |
| (c) | Southern blotting | (iii) | DNA fragmentation move to positive pole |
| (d) | Hybridization | (iv) | Fragments of DNA with variable length are formed |
| Column-I | Column-II | ||
| (a) | Gel electrophosis | (i) | To combine genes from two organisms |
| (b) | cDNA | (ii) | To make a copy of DNA from mRNA |
| (c) | Genetic Engineering | (iii) | Separate the DNA fragments |
| (d) | PCR | (iv) | Gene multiplication in vitro |
| Column-I | Column-II | ||
| (a) | Heat denaturation | (i) | 70-75°C |
| (b) | Annealing | (ii) | 90-98°C |
| (c) | Primer extension | (iii) | 40-60°C |
| Column-I | Column-II | ||
| (a) | Amplifications of gene of interest | (i) | Downstream processing |
| (b) | Large scale production of plants in short duration | (ii) | Polymerase chain reaction |
| (c) | Separation and purification of desired product | (iii) | Transformation |
| (d) | Insertion of rDNA into host | (iv) | Micro propagation |
| Column-I | Column-II | ||
| (a) | Alu I | (i) | Bacillus amyloliquefaciens H |
| (b) | Bam HI | (ii) | H. influenza Rd. |
| (c) | Eco RI | (iii) | Arthobacter luteus |
| (d) | Hind RI | (iv) | Escherichia coli Ry 13 |
| Column-I | Column-II | ||
| (a) | Heat denaturation | (i) | addition of nucleotides on template |
| (b) | Annealing | (ii) | separation of two strands of DNA |
| (c) | Primer Extension | (iii) | paring of primer to complementary sequence in DNA |
| Column-I | Column-II | ||
| (a) | Gel electrophoresis | (i) | Chrimeric DNA |
| (b) | Restriction endonuclease | (ii) | In vitro DNA multiplication |
| (c) | rDNA technology | (iii) | Palindrome |
| (d) | PCR | (iv) | Separation of DNA fragments |
| Assertion (A): | A piece of DNA, if needed to be propagated during recombinant DNA procedures, requires a vector. |
| Reason (R): | The vectors provide the origin of replication. |
| 1. | Both (A) and (R) are True but (R) does not correctly explain (A). |
| 2. | (A) is False but (R) is True. |
| 3. | (A) is True but (R) is False. |
| 4. | Both (A) and (R) are True and (R) correctly explains (A). |