22 Biotechnology Flashcards

1
Q

What is biotechnology?

A

Biotechnology is the industrial use of biological organisms or enzymes to produce food, drugs and other products.

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2
Q

Why are microorganisms ideal for biotechnology?

A
  • No welfare issues to consider
  • can be genetically engineered, allowing us to artificially manipulate microorganisms to carry out synthesis reactions e.g producing human insulin
  • Microorganisms have a very short life cycle and rapid growth rate so huge quantities can be produced in a short time. Reproduce quickly
  • Nutrient requirements are simple and cheap, they can grow on unwanted food/nutrients
  • conditions needed are low temp and pressure, so its cheaper and safer to maintain
  • microorganisms provide their own catalysts in form of enzymes so CHEAP
  • products are pure / easy to separate (little downstream processing)
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3
Q

What microorganism is involved in baking?

A

Yeast.

  • It is mixed with sugar and water to respire aerobically
  • Carbon dioxide bubbles expand when cooked in hot oven making the bread rise.
  • Yeast cells are killed during cooking.
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4
Q

What microorganism is involved in brewing?

A

Yeast.

  • Respires anaerobically to produce ethanol.
  • GM yeasts ferment at lower temperatures so cheaper
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5
Q

What are the advantages of using microorganisms to produce human food?

A

Microorganisms:

  • Reproduce fast and produce protein faster than animals and plants.
  • Have a high protein content with little fat.
  • Can use a wide variety of waste materials including human and animal waste, reducing costs.
  • Can be genetically modified to produce the protein required.
  • Can be made to taste like anything.
  • Have no welfare issues when growing
  • Are not dependent on weather, breeding cycles etc. so can be increased or decreased to match demand.
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6
Q

What microorganism is involved in cheese-making?

A

Bacteria.

- Feed on lactose in milk, changing the texture and taste, and inhibiting the growth of bacteria which make milk go off.

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7
Q

What are the disadvantages of using microorganisms to produce human food?

A
  • Some microorganisms can produce toxins if the conditions aren’t maintained at the optimum.
  • Need carefully controlled sterile conditions which adds to the costs.
  • Has little natural flavour and needs additives
  • Often involve GM organisms and many people have concerns about eating GM food.
  • The protein has to be purified to ensure it contains no toxin or contaminants.
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8
Q

What microorganism is involved in yoghurt-making?

A

Bacteria.

- They produce extracellular polymers that give yoghurt its smooth, thick texture.

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9
Q

How is penicillin produced?

A
  • The process uses relatively small fermenters because it’s difficult to maintain high levels of oxygenation in very large bioreactors.
  • The mixture is continuously stirred to keep it oxygenated.
  • There is a rich nutrient medium.
  • The growth medium contains a buffer to maintain pH at around 6.5.
  • The bioreactors are maintained at about 25-27 degrees.
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9
Q

How is insulin produced?

A

Via genetic engineering.

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10
Q

What is bioremediation?

A

Bioremediation is the use of microorganisms to break down pollutants and contaminants in soil or water.

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11
Q

What are the different approaches to bioremediation?

A

1) Using natural organisms: Nutrients can be added to encourage microbial growth so microorganisms can break down the pollutants.
2) GM organisms: Scientists are trying to develop GM bacteria which can break down contaminants that they would usually not encounter.

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12
Q

What forms can the nutrient medium exist in?

A
  • Liquid form: BROTH

- Solid form: AGAR

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13
Q

How is broth inoculated?

A

1) Make a suspension of the bacteria to be grown.
2) Mix a known volume with the sterile nutrient broth in the flask.
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 providing oxygen for the growing bacteria.

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14
Q

How is agar inoculated?

A

1) The wire inoculating loop must be sterilised by holding it in a Bunsen flame until it glows red hot.
2) Dip the sterilised loop in the bacterial suspension. Remove the lid of the Petri dish and make a zig zag streak across the surface of the agar.
3) Replace the lid of the Petri dish holding it down with tape so oxygen can get in. Incubate at a suitable temperature.

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15
Q

What is the first stage of the bacterial growth curve?

A

The lag phase.

  • This is when bacteria are adapting to their new environment.
  • They are growing, synthesising the enzymes they need, and are not yet reproducing at their maximum rate.
16
Q

What is the second stage of the bacterial growth curve?

A

The log or exponential phase.

- This is when the rate of bacterial reproduction is close to or at its theoretical maximum.

17
Q

What is the third stage of the bacterial growth curve?

A

The stationary phase.

  • This occurs when the total growth rate is zero
  • The number of new cells formed by binary fission is cancelled out by the number of cells dying.
18
Q

What is the fourth stage of the bacterial growth curve?

A

The decline or death stage.

- This comes when reproduction has almost ceased and the death rate of cells is increasing.

19
Q

What limiting factors prevent exponential growth in a culture of bacteria?

A
  • NUTRIENTS AVAILABLE: As microorganisms multiply exponentially the nutrient level will become insufficient to support further growth and reproduction. Therefore provide nutrients via a nutrient medium (usually a liquid broth/agar gel)
  • OXYGEN LEVELS: As population rises, the demand for oxygen increases so oxygen levels can become limiting. Aerobic respiration is needed so O2 levels need to be controlled
  • TEMPERATURE: If temperature gets too high, the enzymes denature, killing the microorganisms. So there is a need to maintain the optimum temperature for enzyme controlled reactions like aerobic respiration.
  • BUILD UP OF WASTE: as bacterial numbers rise, anaerobic respiration may occur leading to the build-up of toxic materials like lactic acid/ethanol which may inhibit further growth and can even poison and kill the microorganisms in the culture
  • CHANGE IN PH: As carbon dioxide produced by respiration increases, the pH of the culture falls and affects enzyme activity which inhibits population growth. Therefore use a ph buffer.
20
Q

What are two of the main ways of growing microorganisms?

A
  • Batch fermentation

- Continuous fermentation

21
Q

What occurs in batch fermentation?

A
  • The microorganisms are inoculated into a fixed volume of medium.
  • As growth takes place, nutrients are used up and both new biomass and waste products build up.
  • As the culture reaches the stationary phase, overall growth ceases but during this phase the microorganisms often carry out biochemical changes to form the desired end products.
  • The process is stopped before the death phase and the products are harvested. The whole system is then cleaned and sterilised and a new batch culture started up.
  • ideal for secondary metabolites as they have higher production in stationary phase and batch fermentation maintains culture in stationary phase
22
Q

What occurs in continuous culture?

A
  • Microorganisms are inoculated into sterile nutrient medium and start to grow.
  • Sterile nutrient medium is added continually to the culture once it reaches the exponential point of growth.
  • Culture broth is continually removed- the medium, waste products, microorganisms, and product- keeping the culture volume in the bioreactor constant.
23
Q

What factors need to be controlled into bioreactors?

A

1) TEMPERATURE: If temp too low, microorganisms won’t grow quickly enough. If temp too high, enzymes start to denature and microorganisms are destroyed.
2) NUTRIENTS AND OXYGEN

24
Q

What are the advantages of using isolated enzymes instead of whole microorganisms?

A
  • Less wasteful: Whole microorganisms use up substrate growing and reproducing, producing biomass rather than product. Isolated enzymes don’t.
  • More efficient: Work at much higher concentrations
  • More specific: No wasteful side reactions take place
  • Less downstream processing: Isolated enzymes produce pure product, whereas whole microorganisms give a variety of products in the broth, making isolation of the desired product expensive.
  • more resistant to temp and ph changes
25
Q

Why are extracellular enzymes used?

A
  • Extracellular enzymes are more robust than intracellular enzymes- they are adapted to cope with greater variations of temperature and pH
  • Each microorganism produces few extracellular enzymes so the required enzyme is easy to identify and isolate.
26
Q

What are immobilised enzymes?

A

Immobilised enzymes are attached to an inert support system, so because it is held stationary it can be recovered from the reaction mixture and reused.

27
Q

What are the advantages of immobilised enzymes?

A
  • Can be reused so cheaper
  • Reduced downstream processing so cheaper
  • Greater temperature tolerance
28
Q

What are the disadvantages of immobilised enzymes?

A
  • Reduced efficiency
  • Higher initial costs of materials
  • Higher initial costs of bioreactor
  • More technical issues
29
Q

why is aseptic techniques needed for fermentation ? (for example when penicillin is made in batch fermentation)

A
  • to avoid unwanted microbe entry that would compete for nutrients,
  • so no contamination of , batch/product
  • yield of product is not decreased
  • so conditions in fermenter remain unchanged
30
Q

batch culture features vs continuous culture features :

A

batch :

  • less efficient than continuous as fermenter is not in operation all the time
  • batch is useful for production of secondary metabolites whilst continuous for primary
  • batch is easier to set up and maintain
  • growth rate is slower in batch as nutrient levels decrease over time whilst in continuous culture nutrients constantly added to tank
  • if contamination occurs only one batch is affected in batch whilst in continuous large volume of product may be lost