The industrial use of microorganisms Flashcards

1
Q

What are the three stages of the production process?

A
  • Stage 1; Upstream processing - preparation of liquid medium, separation of particulate and inhibitory chemicals from the medium, sterilisation, air purification
  • Stage 2; Fermentation - conversion of substrate to desired product by bacteria, yeast or mammalian cells
  • Stage 3; Downstream processing - separation of cells from fermentation broth, purification and concentration of desired product and waste disposal or recycling
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2
Q

In upstream processing, there is medium preparation. What happens here?

A
  • Medium is formulated and optimised for host to get optimum product yield at minimum cost.
  • Separation of particulate and inhibitory chemicals from medium
  • Medium sterilisation and air purification
  • Sterilisation of bioreactor so that you don’t contaminate the reactor vessels
  • Adequate supply of producer cells (cell banking and maintenance).
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3
Q

How do cell banking systems work? How are the cultures of newly constructed production cell line aliquoted? First tier is called?
Second tier is called?

A

The production cell lines are stored in a two tiered cell bank. This ensures long term availability of producer cell lines.
Aliquoted into 5 ampoules.
Master cell bank
Working cell bank

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4
Q

Stage 2; Fermentation - How is the volume of medium increased?

A

Start of with contents of single ampule of working cell bank.
Next is lab scale starter culture; where there are few 100ml of medium.
Next is production scale starter culture; where there is a small bioreactor with several litres/ tens of litres of medium.
Lastly there is production scale bioreactor; several thousands/ tens of thousands of litres of medium
PROGRESSIVELY, LARGER VOLUMES OF MEDIUM ARE INOCULATED.

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5
Q

Name some properties and function of bioreactors.

A
  • high grade stainless steel, fully sterilisable
  • jacketed for temp control
  • impeller ensures even distribution of nutrients and cells
  • Air/gas sparger (supplies oxygen)
  • Ports contain: probes for pH, temp. Ports also allow pH adjustment and addition of nutrients,
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6
Q

What are some other types of bioreactor?

A

airlift, fluidised bed, packed bed, hollow fibre and membrane bioreactors

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7
Q

What does the impeller do?

A

Impeller blades smash bubbles to very small size, increasing dissolution rate of oxygen.
Bubbles rise to surface but have tortuous flow due to blades - increasing residence time.

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8
Q

Dissolved oxygen is important for what kind of bacteria? Oxygen is very insoluble in _____ systems. Solubility decreases with ______ in temp and dissolved solutes.

A

Aerobic
aqueous
increased

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9
Q

What component of bioreactor provides oxygen?

A

Air/ Gas sparger

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10
Q

Dissolution of oxygen depends on

A

Size of air bubbles

Residence time in fermenter

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11
Q

What sterilisers the bioreactor vessels?

A

Steam

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12
Q

Which type of bioreactor does not have an impeller?

A

Air lift. It only has a sparger

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13
Q

Which type of bioreactor does not have an liquid medium?

A

Fluidised bed

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14
Q

Fermentations can only be carried out in cell types that grow in _______. i.e. most _______, some simple ______ (e.g yeasts).
Only a few mammalian cells can grow in suspension, most are “______-________” i.e. they need to grow attached to solid surfaces. Mammalian cells are wall-less and more _______ (weak).

A
suspension
prokaryotes
eukaryotes
anchorage-dependent 
fragile
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15
Q

Mammalian cell culture reactors use? Are these cheap?

A

Airlift

EXPENSIVE!

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16
Q

Expand on downstream processing.

A

Normally carried out in a pharmaceutical clean room.
Operators use Grade A laminar flow.
Filling process is automated to prevent contamination between operator and product.

17
Q

What are the three downstream processing steps?

A
  1. Cell harvesting and recovery of crude product
  2. (Concentration if necessary and) Purification
  3. Final formulation
18
Q

During cell harvesting and recovery of crude product:

Once fermented, if protein is expressed intracellularly..

A
  • Recovery of producer cells (centrifugation or filtration)
  • Cellular disruption (homogenisation)
  • Removal of cellular debris (centrifugation or filtration)
19
Q

During cell harvesting and recovery of crude product:

Once fermented, if protein is expressed extracellularly..

A

Removal of cells from media (centrifugation or filtration)

20
Q

Following fermentation, if protein is expressed intracellularly, the product needs to be recovered from?

A

producer cells

21
Q

Following fermentation, if protein is expressed extracellularly, the product needs to be recovered from?

A

culture medium

22
Q

During purification: if protein is expressed intracellularly:

A

Initial purification/ concentration (ultrafiltration/precipitation) AND THEN chromatographic purification (usually 2-4 chromatographic steps)

23
Q

During purification: if protein is expressed extracellularly:

A

concentration (ultrafiltration/precipitation) AND THEN chromatographic purification (usually 2-4 chromatographic steps)

24
Q

During final product formulation: What happens after 2-4 chromatographic steps?

A

Adjustment of potency and addition of excipients
Sterile filtration and aseptic filling
THEN either:
(freeze drying –> powder preparation –> sealing of final product container, labelling and packaging)
OR
(liquid preparation –> sealing of final product container, labelling and packaging)

25
Q
Analysis of final product. 
Presence of following impurities may have what medical consequences?
a) microorganisms
b) viral particles
c) pyrogenic substances
d) DNA
e) contaminating proteins
A

a) microbial infection, septicaemia
b) viral infection
c) fever
d) possible immune reaction
e) immune reaction/ unwanted biological activity