Biotechnology Flashcards

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0
Q

What are the main areas of biotechnology?

A

Health care and medical processes
Agriculture
Industry
Food science

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1
Q

What is biotechnology?

A

The industrial use of living organisms to produce foods, drugs or other useful products.

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2
Q

Biotechnology in Medical processes

A

Production of drugs from microorganisms.
Pharming (geneticaly modifying animals to produce medicines.
Gene therapy to treat some disorders.

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3
Q

Biotechnology in agriculture

A

Micripropagation of plants and the development of geneticaly modified crops.

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4
Q

Biotechnology in industry.

A

Genetically modify organisms to produce enzymes to catalyse reactions for the production of specific products.

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5
Q

Biotechnology in food science.

A

Microorganisms used to produce cheese, yoghurt or beer.

The development of foods with improved taste, nutrition and texture.

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6
Q

Advantages of using microorganisms in biotechnology.

A

Rapid growth rate in favourable conditions.
Most proteins produced are extracellular so can be harvested easily.
Simple genetics for easy manipulation.
Grow at low temperatures compared to chemical engineering.
Purer products.
Growth non climate dependent.
Can be grown on a cheap medium.
No ethical concerns.

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7
Q

Why use aseptic technique?

A

To prevent infection.
Prevent environmental contamination.
Prevent contamination of specimen!

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8
Q

Aseptic procedure.

A

Wash hands with antibacterial soap, to prevent hands contaminating culture.
Sterilise working area by burning ethanol on the desk.
Flame sterilise necks of bottles and glasses to prevent cross-contamination.
Work within 50cm of flame ( convection currents prevent bacteria from landing on plates).

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9
Q

Bacterial growth curve.

A

Lag phase,
Log phase,
Stationary phase,
Death phase.

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10
Q

Lag phase.

A

Bacteria acclimatising to the environment.
Synthesising new cell components,
Taking in water,
Synthesising enzymes.

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11
Q

Log phase.

A

Population doubles with every generation,
No competition for food or space,
Growth not limited,
Dependent on time taken to reproduce.

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12
Q

Stationary phase.

A

Cell division slows due to limiting factors:
CO2,
Build up of waste,
Food accessibility
Death rate increases until equal to new cell division.

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13
Q

Death phase.

A

Death rate greater than cell division
Increased levels of toxic waste products,
Lack of food,
In a closed system all microbes will eventually die.

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14
Q

Fermentation definition.

A

The culturing of organisms in fermentation tanks. The substances generated by the growth of the culture are separated and purified to produce useful products.

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15
Q

Metabolism.

A

This refers to all of the chemical reactions that occur in an organism.
New cells
Enzymes and hormones
Waste products.

16
Q

What is a primary metabolite?

A

Substances produced by an organism as part of normal growth (amino acids, proteins, enzymes…)
All microorganisms produce primary metabolites.
Their production matches the growth curve of the organism.

17
Q

What is a secondary metabolite?

A

Substances produced by the organism when it reaches the stationary phase only.
E.g some fungi produce antibiotics as a survival mechanism.
Only some microorganisms produce secondary metabolites.

18
Q

Batch culture

A

Conditions are set up and not changed once the fermentation starts.
The process is stopped once sufficient product is made.
The contents are removed, product isolated.
Microorganisms discarded.
Fermenter cleaned for fresh batch.

19
Q

Continuous culture

A

Continuous operation over many weeks.
Nutrients added at the same rate they are used.
Overflow harvested and product purified.

20
Q

Advantages of batch culture

A

Less specialised, can be used for more processes,
Suitable for production of secondary metabolites,
Easier to set up and run,
Less labour demand.

21
Q

Disadvantages of batch culture

A

Environment changes and becomes unfavourable as time goes on,
Turnaround time between batches can be prolonged wasting production time.

22
Q

Advantages of continuous culture

A

Optimum growth rate is maintained,
Greater productivity,
Higher yields,
More control over environmental conditions.

23
Q

Disadvantages of continuous culture

A

No production of secondary metabolites,
More specialised fermenters needed,
Greater risk of contamination.

24
Q

Enzyme imobilisation.

A

Enzyme molecules are bound to a surface and not allowed to dissolve in solution with substrate.
Substrate added to enzyme ESC forms, product released.
Product leaves enzyme and can be easily colected.

25
Q

Advantages of enzymes in industry

A

Enzymes are specific to the desired reaction so only produce the desired product.
Biodegradable and produce less pollution.
Work at moderate temperatures and pressures.

26
Q

Adsorption.

A

Enzymes mixed with porous material (carbon, clay, glass beads)
Form hydrophobic interactions and ionic links

Leakage can occur along with change of the active site.

27
Q

Entrapment

A

Enzymes trapped in gel beads or cellulose fibres,
Active site not effected

Harder for substrate to reach active site
Slower reaction rate.

28
Q

Covalent bonding

A

Enzymes covalently bound to insoluble support using a cross linking agent.
Strong bonds, little leakage.

29
Q

Membrane separation.

A

Semi-permeable membrane separates mixture,

Substrate and products can move across membrane, enzymes cant.

30
Q

Advantages of immobilised enzymes.

A

Can reuse enzymes,
Enzymes are more stable,
Purification costs are low as enzymes are not mixed with product.

31
Q

Disadvantages of immobilised enzymes.

A

Reduced rate of reaction,
Lower yield,
Time consuming to set up,
Contamination ruins whole process.