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Cloning and Biotechnology

Kayla Price AS Biology AS - Level English 5.0Average rating 5.0 out of 5 (1 rating) 63 cards

Cloning and Biotechnology

Cards in this deck (63)

  1. 1What does natural plant cloning occur in?Bulbs, runners, rhizomes and stem tubers
  2. 2What are rhizomes?A specialised horizontal stem running underground, often swollen with stored food.
  3. 3How is natural plant cloning exploited in horticulture?Splitting up bulbs, removing young plants from runners etc. to increase plant numbers and produce plants with the same characteristics as parent
  4. 4What are the advantages and disadvantages of natural plant cloning?Faster than planting seeds, guaranteed quality
    Lack of genetic variation - more susceptible to disease
  5. 5What is micropropagation?The process of making large numbers of genetically identical offspring from a single parent plant using tissue culture techniques
  6. 6When is micropropagation used?When the plant does not readily produce seeds, doesn't respond well to natural cloning, is rare, has been genetically modified or selectively bred with difficulty, is susceptible to pathogens
  7. 7How are plants kept sterile outside of a sterile lab?using sodium dichloroisocyanurate tablets
  8. 8How is micropropagation carried out?Take a small sample of plant tissue, sterilise by immersing in sterilising agents (bleach, ethanol, sodium dichlorisocyanurate), place the explant in a sterile culture medium containing plant hormones to stimulate mitosis, the cells proliferate forming a callus, the callus is divided up and placed into a different mixture of hormones to stimulate the development of plantlets, they are then potted and grown into crops
  9. 9What are the advantages of micropropagation?Rapid production of desired characteristics, disease free plants produced, reproduces genetically modified plants, produces seedless plants, a way of growing plants which are difficult to reproduce, increases numbers of rare plants.
  10. 10What are the disadvantages of micropropagation?Monoculture more susceptible to disease, expensive, if the source material is infected all the clones will become infected.
  11. 11What is the main form of vertebrate cloning?The formation of monozygotic twins - when the early embryo splits to form two separate embryos.
  12. 12What is artificial twinning?the process of producing monozygotic twins artificially
  13. 13How is artificial twinning carried out in cattle?1) A cow with desirable traits is treated with hormones to make her super-ovulate
    2) The ova are fertilised by a bull with desirable traits
    3) When the cells are still totipotent, the cells are split to produce several smaller embryos
    4) The embryos are implanted into surrogate mothers
    5) Several identical calves are born
  14. 14What is somatic cell nuclear transfer?The cloning of an adult animal by transferring the nucleus of an adult somatic cell to an enucleated egg cell (oocyte)
  15. 15How is somatic cell nuclear transfer carried out?1) The nucleus is removed from both a somatic cell and mature ovum from a different female
    2) The nucleus from the somatic cell is placed into the enucleated ovum and given a mild electric shock so it fuses and begins to divide.
    3) The embryo is transferred into the uterus of another female and develops to term
    The embryo will have the same DNA as the adult the somatic cell came from, but the mitochondrial DNA of the egg cell
  16. 16What are the advantages of somatic cell nuclear transfer?Enables GM embryos to be replicated and develop (important in pharming), allows specific animals to be cloned, rare or extinct animals can be reproduced.
  17. 17What are the disadvantages of somatic cell nuclear transfer?Inefficient because many eggs required to produce a single clone, rarely successful births, clones have shortened lifespans
  18. 18What are the advantages of artificial twinning?Produces more offspring than normal reproduction, more offspring guaranteed to have desirable traits
  19. 19Define biotechnologyApplying biological organisms or enzymes to the synthesis, breakdown or transformation of materials in the service of people
  20. 20Define bioremediationThe use of microorganisms to breakdown pollutants in soil and water
  21. 21Why are microorganisms ideal for biotechnological processes?No welfare issues, large range of microorganisms that can carry out many different functions, can be genetically engineered to carry out synthesis reactions they don't do naturally (insulin), short life cycle and rapid rate of growth, simple and relatively cheap nutrient requirements, provide their own catalysts, work at relatively low temperatures.
  22. 22What are the disadvantages for using microorganisms in indirect food production?Conditions ideal for other dangerous microorganisms to grow and contaminate the food so conditions have to be sterile, some microorganisms are genetically engineered which has ethical issues
  23. 23Describe how yeast is used in bakingIt is mixed with sugar and water to respire aerobically and produces carbon dioxide which makes the bread/cake rise
  24. 24How is beer made?1) Malting - barley germinates producing enzymes that break starch molecules down to sugars. Seeds are then killed by slow heating but enzyme activity retained to produce malt
    2) Mashing - malt is mixed with hot water (55-60 degrees) and enzymes break down starches to produces wort. Hops are added and the wort is sterilised and cooled
    3) Fermentation - wort is inoculated with yeast, which respires anaerobically. Eventually the yeast is inhibited by falling pH, build up of ethanol and lack of oxygen
    4) Maturation - the beer is conditioned for 29 days at temperatures of 2-6 degrees
    5) Finishing - the beer is filtered, pasteurised and bottled
  25. 25How is cheese made?1) Milk is pasteurised by heating it to 95degrees for 20 seconds, and homogenised to disperse fat droplets throughout the milk.
    2) Bacterial cultures and sometimes chymosin enzymes are added and left unti solid curds and liquid whey
    3) The curds are left to dry and mature - the bacteria continue to act.
  26. 26How is yoghurt made?1) Milk is pasteurised, homogenised and cooled to about 47degrees.
    2) It is then mixed with equal amounts of Lactobacillus bulgaricus and Streptococcus thermophilus and incubated
  27. 27What fungus is Quorn made from?Fusarium venetatum
  28. 28What is SCP?Single-celled protein - protein produced from microorganisms
  29. 29What are the advantages of using microorganisms in direct food production?Produce protein faster than animals and plants, high protein low fat, microorganisms can use a wide variety of waste materials which can reduce costs, can be genetically modified to produce specific proteins, continuous process, no welfare issues, flavours can be added
  30. 30What are the disadvantages of using microorganisms in direct food production?Some microorganisms can produce toxins if conditions not maintained, food is processed, needs sterile conditions which adds to cost, concerns about eating GM food, people put off by eating microorganisms, needs additives to make it taste better
  31. 31What is the fungus that is commercially used as penicillin?Penicillium chrysogenum
  32. 32How is penicillin produced?In the first stage the fungus grows and in the second stage it produces penicillin. The drug is then extracted and purified.
  33. 33What conditions are required in the production of penicillin?- Small fermenters are used to make it easier to maintain high levels of oxygenation
    - Mixture stirred continuously to keep it oxygenated
    - Rich nutrient medium
    - Growth medium contains a buffer that keeps the pH at 6.5
    - Temperature of 25-27degrees
  34. 34What are the two possible approaches to biomediation?Using natural organisms or GM organisms
  35. 35What are natural organisms used for in biomediation?Breaking down organic material
  36. 36What are GM organisms used for in biomediation?Breaking down contaminants the microorganisms don't usually encounter eg. mercury
  37. 37Why is it important to culture microorganisms in strictly controlled conditions?There is always a risk of mutation making the strain pathogenic and there may be contamination from the environment
  38. 38What is the difference between a nutrient broth and agar?Broth is a liquid form of nutrient medium and agar is solid
  39. 39How is broth inoculated?1) Make a suspension of the bacteria to be grown
    2) Mix a known volume with the sterile nutrient broth
    3) Stopper the flask with cotton wool to prevent contamination from the air
    4) Incubate at a suitable temperature, shaking regularly to aerate the broth
  40. 40How is agar inoculated?1) A wire inoculating loop is sterilised by holding it in a flame until it glows red hot.
    2) The loop is dipped in the bacterial suspension and spread across the surface of the agar.
    3) The lid of the agar plate is sealed with tape but not completely - so oxygen can get in.
  41. 41Describe the growth curve of a bacterial population in a closed systemLag phase - when bacteria are adapting to the environment, they don't reproduce but grow and synthesise enzymes they need
    Log/exponential growth phase - when the rate of bacterial reproduction is close to or at it's theoretical maximum.
    Stationary phase - when total growth rate is zero and the number of new cells forming is equal to the number of cells dying
    Death phase - when death rate becomes larger than rate of reproduction
  42. 42What are the limiting factors for growth of bacteria?Nutrients available, oxygen levels, temperature, build-up of waste, change in pH
  43. 43Draw a graph to show the concentrations primary and secondary metabolites during the growth of a bacterial culture in a closed systemDraw a graph to show the concentrations primary and secondary metabolites during the growth of a bacterial culture in a closed system
  44. 44What is the difference between primary and secondary metabolites?Primary are essential metabolites of the normal functioning of a microorganism, secondary are non-essential to normal growth but are still used
  45. 45How is batch fermentation carried out?As growth of microorganisms in bioreactor takes place, nutrients are used up, and biomass and waste products build up. As the culture reaches stationary phase, the microorganisms often begin to form the desired end products. The process is then stopped before the death phase and products harvested. The whole system is then sterilised and a new culture started up.
  46. 46How is continuous culture carried out?Sterile nutrient medium is continually added to the culture once it reaches exponential growth. Culture broth is also continually removed, keeping the culture volume constant.
  47. 47What is the process of separating a culture broth to obtain the useful part called?Downstream processing
  48. 48What factors are important to ensure the growing conditions in a bioreactor are at optimum?Temperature, nutrients, oxygen, making sure the mixture is stirred continuously, sterile conditions
  49. 49Draw and label a diagram of a bioreactorDraw and label a diagram of a bioreactor
  50. 50What are the advantages of isolated enzymes?Less wasteful - no microorganisms using up substrate by growing and reproducing
    More efficient - enzymes can be given ideal conditions that may not be ideal for the microorganism's growth
    More specific - only the enzymes required present, no wasteful side reactions
    Less downstream processing - Pure product produced so isolating desired product less difficult
  51. 51Why are extracellular enzymes easier to isolate than intracellular?Extracellular are secreted, microorganisms produce relatively few extracellular enzymes making the desired enzyme easier to identify, extracellular more robust so adapted to greater changes in temperature and pH
  52. 52What are the advantages of immobilised enzymes?Reusable, easily separated from reaction mixture so less downstream processing, greater temperature tolerance, easily manipulated to fit a particular process
  53. 53What are the disadvantages of using immobilised enzymes?Less efficient as immobilising can reduce its activity rate, higher initial costs of materials and bioreactor, more complicated process
  54. 54What are the four methods of immobilising enzymes?Adsorption to an inorganic carrier, entrapment in a matrix, forming covalent or ionic bonds to an inorganic carrier or encapsulating in a microcapsule.
  55. 55What are the advantages of surface immobilisation by adsorption to inorganic carriers?Simple, inexpensive, can be used in many different processes, enzymes very accessible to substrate
  56. 56What are the disadvantages of surface immobilisation by adsorption to inorganic carriers?Enzymes can be lost from carrier relatively easily
  57. 57What are the advantages of surface immobilisation by forming covalent or ionic bonds to an inorganic carrier?Enzymes strongly bound so unlikely to be lost, enzymes very accessible to substrate, pH and substrate concentration have little effect on enzyme activity.
  58. 58What are the disadvantages of surface immobilisation by forming covalent or ionic bonds to an inorganic carrier?Active site may be modified in process
  59. 59What are the advantages of entrapment in a matrix?Can be used in many different processes
  60. 60What are the disadvantages of entrapment in a matrix?Expensive, difficult to entrap, slow diffusion rate to and from enzyme
  61. 61What are the advantages of entrapment in microcapsules?Simple, small effect on enzyme activity, can be used in many different processes.
  62. 62What are the disadvantages of entrapment in microcapsules?Expensive, slow diffusion rate to and from enzyme
  63. 63—

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AS - Level AS Biology Flashcards on Cloning and Biotechnology, created by Kayla Price on 29/05/2017.
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Kayla Price
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