biotechnology Flashcards

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1
Q

what is biotechnology

A

use of living organisms or parts of living organisms in industrial process - could be to produce food, drug or to remove toxic materials = bioremediation. Biotechnology also encompasses gene technology, genetic modification, selective breeding, cloning, use of enzyme in industry and immunology.

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2
Q

why must we ensure, that we prevent the growth of unwanted bacteria?

A
  • they will compete, with culture m/o for nutrients and space and therefore reduce yield of useful product.
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3
Q

why do we not wanted unwanted bacteria?

A
  • produce toxins and chemical and which may contaminate the product, destroy cultured m/o and their products. In food/ medicine if contamination occurs waste/toxic products must be discarded.
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4
Q

what are primary metabolites?

A

e.g. alcohol from saccharomyces cerevisiae.

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5
Q

what is continuous fermentation

A
  • used when primary metabolite is the required product -> this is a product synthesised in normal metabolism when the m/o is actively dividing.
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6
Q

describe the process of continuous

A
  • sterile nutrient medium is continually added to the culture, once it reaches the exponential point of growth.
  • culture broth is continually removed. (medium, m/o, waste and desired product) so culture volume in fermenter is constant.
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7
Q

what are secondary metabolites

A

e.g. antibiotics from penicillium Crysogenum

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8
Q

what is batch fermentation

A
  • when secondary metabolites is required product = product synthesised only when there is limited nutrients availability in stationary phase.
  • m/o are inoculated into a small. volume of sterile medium.
  • as growth takes place, nutrients are used up and both new biomass and waste products, build up.
  • as the culture reaches stationary phase overall growth ceases, but during this phase the m/o often produce the desired end products as secondary metabolites.
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9
Q

know the comparasion, between batch and continuous production , of bread

A

yeast

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10
Q

name the type of m/o used to produce cheese

A

lactoballiclus (bacteria)

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11
Q

name the type of m/o used to produce human insulin

A

coli. (Bacteria)

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12
Q

name the type of m/o used to produce penicillin

A

fungus

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13
Q

name the type of m/o used to produce beer

A

yeast

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14
Q

what happens during the process of malting

A

barley grains, germinate and starch is broken down in maltose

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15
Q

what happens during the process of rising (proving)

A

carbon dioxide is produced

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16
Q

what happens during the process of fermentation

A

yeast, added to cooled wort (anaerobic respiration) , which produces ethanol and carbon dioxide.

17
Q

bioremediation

A

removal of toxic materials, from polluted sources. e.g. heavy metals + breakdown of hydrocarbons in crude oil, petrol.

18
Q

understand the aseptic techniques on page 15

A
19
Q

what is an immobilised enzyme

A

enzymes are held in place, are not free to diffuse through the solution.

20
Q

what are the 4 methods of immobilised enzyme

A
  • adsorption.
  • surface immobilisation.
  • entrapment.
  • encapsulation.
21
Q

what is adsorption

A
  • enzyme bound to supporting surface by a combination of hydrophobic and ionic links.
  • suitable surfaces include, clay, porous carbon, glass beads and resin.
22
Q

what is surface immobilisation

A
  • enzymes are bonded to supporting surface such as clay using covalent or ionic bonds. Enzymes are bonded using a cross linking agent which may also link them in a chain.
23
Q

what is surface entrapment

A
  • enzymes are trapped in a matrix. e.g. polysaccharides (cellulose mesh) that does not allow free movement.
  • calcium alginate beads are often used in school.
24
Q

what is encapsulation

A
  • encapsulation in microcapsules made of semi permeable membrane. (membrane separation).
25
Q

what are the advantages of adsorption.

A
  • simple, + cheap to set up.
  • enzyme active site, is exposed + accessible to the substrate.
26
Q

what are the disadvantages of adsorption

A
  • enzyme molecules, can detach from matrix or carrier easily.
  • active site distorted by bonds connecting the enzymes to the carrier.
27
Q

what are the advantages of surface immobilisation

A

enzyme molecules are much less likely to detach from matrix.

28
Q

what are the disadvantages of surface immobilisation

A
  • more expensive to set up, compared to adsorption.
  • stronger covalent bonds, distort, active site.
29
Q

what are the advantage of entrapment

A
  • enzyme shape, unaffected by entrapment.
30
Q

what are the disadvantages entrapment

A
  • substrate must diffuse in + products, must diffuse out.
  • only works with small reactant or products.
31
Q

what are the advantages of encapsulation

A
  • easy to setup/ cheap to set up.
  • membrane, has no effect, on shape of enzyme.
32
Q

what are the disadvantages of encapsulation

A
  • substrate. must diffuse in + products must diffuse out.
  • slow
    substrate diffusion, into bed through membrane, is limited by presence of product.
33
Q
A