| 1. | Janus green followed by exposure to gamma radiation |
| 2. | Acetocarmine followed by exposure to infrared radiation |
| 3. | Ethidium bromide followed by exposure to UV radiation |
| 4. | Methylene blue followed by exposure to X-rays |

| 1. | Increases the length of the gene of interest |
| 2. | Produces identical and complementary ends on both DNAs, allowing them to join |
| 3. | Ensures the ligase functions only on source DNA |
| 4. | Prevents the gene of interest from undergoing transcription |
| 1. | They provide better control over pH, temperature, and nutrient supply during fermentation. |
| 2. | They are simpler and more cost-effective than shake flasks. |
| 3. | They are only suitable for small-scale culture experiments. |
| 4. | They do not require continuous monitoring or adjustments. |
| 1. | Because they randomly degrade all DNA molecules inside a cell. |
| 2. | Because they attach new DNA segments to a target sequence during genetic recombination. |
| 3. | Because they cut DNA at specific recognition sequences, allowing precise genetic modifications. |
| 4. | Because they unwind and separate DNA strands during replication. |
| 1. | It provides a binding site for ribosomes to initiate translation. |
| 2. | It serves as the site where DNA replication begins, allowing the foreign DNA to replicate along with the host genome. |
| 3. | It facilitates the transcription of the alien DNA into mRNA for protein synthesis. |
| 4. | It acts as a recognition site for restriction enzymes to cut and insert new DNA segments. |
| 1. | Genus name of the source organism |
| 2. | Species name of the source organism |
| 3. | Strain designation of the source organism |
| 4. | Order of discovery in the species |
| 1. | Defend against viral invasion by cleaving non-methylated DNA sequences |
| 2. | Degrade foreign RNA molecules within their cytoplasm |
| 3. | Facilitate horizontal gene transfer through transformation |
| 4. | Repair mismatched DNA during replication |