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Recombinant DNA
| Question | Answer |
|---|---|
| Name one way of altering a wild microbe | 1. mutagenesis 2. Recombinant DNA technology |
| Define mutagenesis | Deliberately exposing microbes to UV light to induce an advantageous mutation |
| Explain why mutagenesis of wild microbes occurs | To try to create an improved strain of microbe through advantageous mutations |
| Define recombinant DNA technology | Plant/animal genes inserted into microbes to produce plant/animal proteins |
| Describe the role of endonuclease | Same endonuclease is used to cut open plasmid and cut gene from chromsome |
| Explain why the same restriction endonuclease is used | To create complementary sticky ends between gene and plasmid |
| Explain the role of ligase | To seal gene into plasmids |
| Name the process when plasmids are inserted into bacterial cells | Transformation |
| Explain why yeast vectors are preferable over bacterial plasmids | Only yeast vectors can fold the protein correctly making protein active |
| Define a vector | DNA molecule used to carry foreign genetic material into a cell. |
| Name the two types of vectors | 1. plasmids 2. artificial chromosomes |
| Which vector is preferable when inserting a larger gene | Artificial chromosomes |
| Explain the role of ORI | self replication of the plasmid |
| Explain the role of regulatory sequences | Control gene expresssion |
| Give an example of a selectable marker | 1. Antibiotic resistance 2. fluorescence |
| Explain the process by which only transformed bacteria can be detected using an antibiotic resistance selectable marker | Expose all bacteria to antibiotics & only those that have been selectively transformed have resistance and survive |
| If a selectable marker has been interrupted will it still confer antibiotic resistance to the bacteria | No - gene not functional and protein cant be made |