27: Biotechnology Flashcards

(39 cards)

1
Q

Explain the meaning of biotechnology.

A

Biotechnology refers to the use of organisms, biological systems or processed to produce goods or provide services.

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2
Q

State the definition of genetic engineering.

A

Genetic engineering refers to the changing of the genetic make-up of an organism by direct manipulation of DNA.

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3
Q

Name a commonly used vector in recombinant DNA technology.

A

A plasmid, which is a small ring of extrachromosomal DNA found naturally in bacteria.

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4
Q

Outline the main steps of recombinant DNA technology.

A
  1. Obtain DNA fragments containing the gene of interest.
  2. Obtain vectors (eg. plasmids).
  3. Cut DNA fragments and plasmids with a restriction enzyme.
  4. Join DNA fragments and plasmids together using a DNA ligase.
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5
Q

Explain the source of the DNA fragments in recombinant DNA technology.

A

They are obtained from donor cells, which can be any nucleated cells.

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6
Q

List two purposes with examples which recombinant plasmids can serve when introduced into host cells.

A
  1. Producing GMOs that possess new characteristics, eg. producing fruits that do not turn brown when they are cut.
  2. Producing proteins of other species, eg. producing human insulin by bacteria.
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7
Q

Explain the original purpose of restriction enzymes.

A

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.

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8
Q

Name two uses of recombinant DNA technology in the medicine industry.

A
  1. Production of pharmaceutical products
  2. Gene therapy
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9
Q

List 5 pharmaceutical products which are produced using recombinant DNA technology and explain their uses.

A
  1. Human insulin, used to treat patients with type 1 diabetes.
  2. Human growth hormone, used to treat patients with growth hormone deficiency.
  3. Hepatitis B vaccine, used to prevent hepatitis due to viral infection.
  4. Human blood clotting factor VIII, used to treat haemophilia.
  5. Human interferons, used to treat cancer.
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10
Q

State the method of obtaining human insulin in the past and list 4 disadvantages of this method.

A

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.

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11
Q

List 4 advantages of producing insulin using recombinant DNA technology.

A
  1. Insulin can be produced in a shorter time with lower extraction cost.
  2. The product yield is much higher.
  3. The insulin produced is structurally the same as human insulin. It is not rejected by the immune system.
  4. The insulin produced is pure and the risk of causing infections is low.
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12
Q

Name 3 uses of recombinant DNA technology in the agricultural industry.

A
  1. Increasing the productivity of foods
  2. Improving the nutritional value of foods
  3. Reducing pollution caused by agriculture (eg. by using chemical pesticides)
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13
Q

List 4 examples in which recombinant DNA technology is used to increase the productivity of crops and animals.

A
  1. A fast-growing GM salmon grows to a marketable size in a shorter time, increasing the productivity of fish farming.
  2. A pest-resistant GM maize plant produces a pest-resistant toxin to kill certain pests, reducing crop loss due to the pests.
  3. A virus-resistant GM papaya plant can help reduce crop loss due to viral infection.
  4. A herbicide-resistant GM soya bean plant can help reduce crop loss due to the use of herbicides.
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14
Q

List 2 examples in which recombinant DNA technology is used to improve the nutritional value of foods.

A
  1. Golden rice is a GM rice of which the grains are rich in β-carotene, which can be converted to vitamin A in our body, strengthening vision and immunity.
  2. Pigs can be genetically modified to increase the levels of unsaturated fatty acids. Eating their meat may help prevent heart disease.
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15
Q

Explain the meaning of selective breeding.

A

Selective breeding is done by selecting the plants or animals having the desirable characteristic to breed for many generations.

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16
Q

State the definition of gene pool.

A

Gene pool is the total of all the alleles of all the genes in a population at a given time.

17
Q

Explain why selective breeding reduces the range of alleles in the gene pool.

A

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.

18
Q

List 3 advantages of recombinant DNA technology to produce crops or farm animals instead of using selective breeding.

A
  1. Recombinant DNA technology is a quicker method.
  2. Only one or several genes are involved at the same time. The results are more predictable.
  3. Recombinant DNA technology can be used to transfer genes between unrelated species.
19
Q

List and explain 4 examples in which recombinant DNA technology is used industrially.

A

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

20
Q

List and explain an example in which recombinant DNA technology is used for environmental protection.

A

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.

21
Q

Outline the major steps of DNA fingerprinting (by restriction fragment length polymorphism analysis).

A
  1. DNA is extracted from the sample of tissues collected.
  2. DNA fragments containing the selected regions from the DNA sample (eg. highly variable regions) are obtained by cutting the DNA with restriction enzymes and amplifying (eg. using PCR).
  3. The DNA fragments are separated according to their lengths using gel electrophoresis.
  4. The pattern of bands obtained is called a DNA fingerprint, which is unique to each individual except identical twins.
22
Q

State the tissues which can be used for DNA extraction and list 3 examples.

A

Any tissue of a person can be used because they contain the same DNA. Common examples are blood, semen, and hairs.

23
Q

Explain the working principle of gel electrophoresis.

A

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.

24
Q

Explain the need of staining in gel electrophoresis (for direct observation of DNA fragments in the gel slab).

A

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.

25
List an advantage of DNA fingerprinting.
The DNA fingerprint is **unqiue to each individual**, except for identical twins. It is a very reliable method to identify an individual.
26
List 7 applications of DNA fingerprinting.
Forensic science, parentage tests, victim identification, authentication of foods and Chinese medicine, protection of endangered animals, tracking the source of infectious diseases, screening for genetic diseases
27
Explain how DNA fingerprinting can be used to establish family relationships in parentage tests.
It is based on the fact that half of the genetic material of an individual comes from the father and the other half from the mother. Therefore, half the bands in the DNA fingerprint of an individual can be found in the DNA fingerprint of the father, and the remaining half can be found in the DNA fingerprint of the mother.
28
Explain how DNA fingerprinting can be used in victim identification.
Identification can be done by comparing the DNA fingerprint of the dead body with that of the suspected victim, by obtaining DNA samples from the personal items of the suspected victims or their family members.
29
Explain how DNA fingerprinting can be used in authentication of foods and Chinese medicines.
Authentication of Chinese medicine can be done by comparing the DNA fingerprint of an unknown sample with that of the genuine medicine. The composition of foods can also be tested by DNA fingerprinting, by producing a DNA fingerprint of a meat product and comparing the band pattern with those of different types of meat identifies the types of meat present in the meat product.
30
Explain how DNA fingerprinting can be used in conservation of endangered elephants.
**Elephant dung** at different locations across Africa are collected and DNA fingerprints for elephants from different populations are produced. Then, DNA fingerprinting can be used to identify the **origin of ivory products** and find out the country in which the elephants were killed by comparing DNA fingerprints of the product with the DNA fingerprints of elephant dung. This helps authorities arrest illegal hunters.
31
Explain how DNA fingerprinting can be used to study the parentage of wild animals.
DNA fingerprinting can be used to ensure **unrelated animals** are used in breeding programmes of endangered species. This increases the genetic variations between individuals in the population, increasing the chance of survival of the species.
32
Explain how DNA fingerprinting can be used in tracking the source of infectious diseases.
DNA fingerprinting can be used to identify the strains of bacteria causing infectious diseases quickly, allowing preventive measures to be taken.
33
List 6 diseases which can be screened using DNA fingerprinting.
Cystic fibrosis, haemophilia, Huntington's disease, Alzheimer's disease, sickle-cell anaemia, thalassemia.
34
Describe how DNA fingerprinting can be used to test for sickle-cell anaemia.
Copies of DNA fragments containing the gene associated with sickle-cell anaemia can be obtained by PCR and cut using a specific **restriction enzyme**. Due to mutation, the diseased allele has a single base difference from the normal allele. This leads to a **loss of restriction site** in the DNA fragment containing the diseased allele. As a result, different patterns of bands appear after the DNA fragments are separated using gel electrophoresis.
35
State the definition of genome.
A genome is the base sequence of the complete set of DNA.
36
List 5 goals of the human genome project.
1. To determine the base sequence that makes up the human genome. 2. To locate all genes (**gene mapping**) in the human genome 3. To store the information in a database which is open to the public 4. To develop related new technologies and improve tools for data analysis. 5. To address the ethical, legal, and social issues that may arise.
37
Outline a timeline for the human genome project.
1990: HGP started in the US, involving scientists from 18 countries. The first gene for breast cancer is mapped. 1996: Sequencing of year genome completed, mapping of mouse genome completed. 1999: Sequencing of first human chromosome completed. 2000: Draft version of human genome sequence completed, sequencing of fruit fly genome completed. 2003: Finished version of human genome sequence completed, all goals of the HGP are achieved.
38
List 2 limitations of the HGP.
1. The functions of many genes are **still unknown** although the base sequences and locations have been found. 2. The data obtained are still **not enough to understand some biological processes**.
39
List 3 benefits of the HGP.
1. Better understanding of genetics 2. Improved diagnoses and treatment of diseases 3. Better understanding of evolution