Explain the meaning of biotechnology.
Biotechnology refers to the use of organisms, biological systems or processed to produce goods or provide services.
State the definition of genetic engineering.
Genetic engineering refers to the changing of the genetic make-up of an organism by direct manipulation of DNA.
Name a commonly used vector in recombinant DNA technology.
A plasmid, which is a small ring of extrachromosomal DNA found naturally in bacteria.
Outline the main steps of recombinant DNA technology.
Explain the source of the DNA fragments in recombinant DNA technology.
They are obtained from donor cells, which can be any nucleated cells.
List two purposes with examples which recombinant plasmids can serve when introduced into host cells.
Explain the original purpose of restriction enzymes.
Restriction enzymes are part of the natural defence mechanisms of bacteria against viruses. When DNA of infecting viruses enters the bacterial cells, the restriction enzymes cut the DNA into pieces and defend the bacteria against viruses.
Name two uses of recombinant DNA technology in the medicine industry.
List 5 pharmaceutical products which are produced using recombinant DNA technology and explain their uses.
State the method of obtaining human insulin in the past and list 4 disadvantages of this method.
Insulin for injection was usually extracted from the pancreas of cattle or sheep.
Problems:
1. The extraction required a long time and was expensive.
2. Only small amounts of insulin were obtained in each extraction.
3. The insulin from cattle or sheep has an amino acid sequence slightly difference from that of human insulin. They may be rejected by the immune system.
4. If the cattle or sheep are infected by pathogens, pathogens may be passed from the cattle or sheep to the patients, resulting in a higher risk of infections.
List 4 advantages of producing insulin using recombinant DNA technology.
Name 3 uses of recombinant DNA technology in the agricultural industry.
List 4 examples in which recombinant DNA technology is used to increase the productivity of crops and animals.
List 2 examples in which recombinant DNA technology is used to improve the nutritional value of foods.
Explain the meaning of selective breeding.
Selective breeding is done by selecting the plants or animals having the desirable characteristic to breed for many generations.
State the definition of gene pool.
Gene pool is the total of all the alleles of all the genes in a population at a given time.
Explain why selective breeding reduces the range of alleles in the gene pool.
In selective breeding, the alleles for the desirable characteristic become more and more widespread in the population. The alleles for the undesirable characteristic may be eliminated in a population eventually.
List 3 advantages of recombinant DNA technology to produce crops or farm animals instead of using selective breeding.
List and explain 4 examples in which recombinant DNA technology is used industrially.
Enzymes for industrial use can be produced using recombinant DNA technology. Genes for the enzymes are introduced into bacteria, allowing larger amounts of enzymes to be produced by the bacteria in a shorter time and at a lower cost.
Examples:
1. Digestive enzymes in biological washing powders
2. Proteases in meat tenderisers
3. Enzymes used in cheese production
4. Enzymes used in beer production
List and explain an example in which recombinant DNA technology is used for environmental protection.
Oil-eating bacteria can help clean up oil spills. They work by breaking down hydrocarbons in the oil into harmless substances. Using recombinant DNA technology, these bacteria can be genetically modified so that they break down a wider range of hydrocarbons.
Outline the major steps of DNA fingerprinting (by restriction fragment length polymorphism analysis).
State the tissues which can be used for DNA extraction and list 3 examples.
Any tissue of a person can be used because they contain the same DNA. Common examples are blood, semen, and hairs.
Explain the working principle of gel electrophoresis.
Gel electrophoresis makes use of an electric field to drive DNA fragments across a gel slab. DNA fragments are negatively charged during to the presence of phosphate groups. Under an electric field, they migrate towards the positive terminal. There are pores in the gel slab which allow shorter DNA fragments to move faster than the longer ones. In a fixed period of time, shorter fragments can travel further, separating DNA fragments according to their size.
Explain the need of staining in gel electrophoresis (for direct observation of DNA fragments in the gel slab).
The DNA bands produced in the gel slab are invisible. Staining is required before the bands can be seen. It is commonly done using a fluorescent dye and the pattern of bands on the cell slab can be viewed under ultraviolet light.