Block C Lecture 3: Exploiting Fungi Flashcards

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1
Q

What are intermediates and end products of anabolism used as?

A

Cell building blocks or converted to co-enzymes
(Slide 7)

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2
Q

What are products of catabolism related to?

A

Substrate consumption and breakdown
(Slide 7)

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3
Q

What is citric acid widely used for?

A

In the food industry, drinks, sweets, baking and used to treat metal contamination in detergents as a replacement for phosphate
(Slide 8)

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4
Q

When was an A. niger citric acid producing strain isolated, and when did production begin?

A

It was isolated in 1917 and production began in 1919
(Slide 10)

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5
Q

Why does industrial production of citric acid by A. niger need a production media which is iron deficient?

A

As A. niger secretes large amounts of citric acid for use as an iron chelator to scavenge extracellular iron
(Slide 11)

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6
Q

What must the stainless steel fermenter vessels used in industrial production of citric acid by A. niger be?

A

They must be glass lined
(Slide 11)

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7
Q

What 2 pathways is citrate produced from in the fungi A. niger?

A

Glycolysis and the TCA cycle
(Slide 13)

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8
Q

How is citrate purified?

A

By the addition of CaO to the culture broth
(Slide 14)

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9
Q

How does the addition to CaO to the culture broth purify citrate?

A

As it precipitates the citrate as calcium citrate
(Slide 14)

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10
Q

After the calcium citrate precipitates are filtered, what is it treated with?

A

Sulfuric acid
(Slide 14)

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11
Q

What 2 things does treating calcium citrate with sulfuric acid yield?

A

CaSO4 and citric acid
(Slide 14)

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12
Q

What occurs after the CaSO4 is filtered out in citric acid product isolation?

A

The citric acid is crystalised by evaporation
(Slide 14)

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13
Q

What are fungi from the Penicillium genus used to ripen?

A

A variety of cheeses
(Slide 15)

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14
Q

What cheese are penicillum roqueforti and penicillum glaucum involved in the production of?

A

Blue cheese
(Slide 15)

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15
Q

What cheeses are Penicillium candidum and Penicillium camemberti used in the production of?

A

Brie and camembert
(Slide 15)

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16
Q

What is quorn?

A

A meat alternative made of the fungus fusarium venenatum which is grown by fermentation
(Slide 16)

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17
Q

What fungi does marmite contain?

A

Saccharomyces cerevisiae
(Slide 17)

18
Q

What does fermentation do to make bread?

A

It helps the dough rise
(Slide 18)

19
Q

What does yeast turn sugar into?

A

Alcohol
(Slide 19)

20
Q

What can Saccharomyces be used to produce?

A

Ethanol
(Slide 20)

21
Q

What has Saccharomyces yeast been genetically engineered to ferment?

A

Xylose
(Slide 20)

22
Q

What is the formation of secondary metabolites dependant on?

A

Growth conditions and media components
(Slide 21)

23
Q

What are secondary metabolites often associated with?

A

The sporulation process
(Slide 21)

24
Q

What reactions occur to form secondary metabolites?

A

A number of enzymatic reactions
(Slide 23)

25
Q

During what phase do reactions which form secondary metabolites not occur?

A

The growth phase
(Slide 23)

26
Q

Where are the starting materials to form secondary metabolites derived from?

A

Primary metabolism
(Slide 23)

27
Q

What are the best known type of secondary metabolites?

A

Antibiotics
(Slide 23)

28
Q

Where does the fermentation of antibiotics generally occur in?

A

Aerobic vessels up to 500,000 litres (though usually 100-150K)
(Slide 24)

29
Q

What is generally automatically controlled in the industrial fermentation of antibiotics?

A

pH conditions
(Slide 24)

30
Q

What are antibiotics in the industrial fermentation of antibiotics usually grown as?

A

Fed-batch cultures
(Slide 24)

31
Q

What is the ß-lactam antibiotics class comprised of?

A

Penicillin and its relatives
(Slide 25)

32
Q

What 2 ways can ß-lactam antibiotics be obtained?

A

Natural or semi-synthetic
(Slide 25)

33
Q

Why are the semi-synthetic ß-lactam antibiotics preferred?

A

As they have more desirable pharmaceutical properties as they are more acid stable and resistant to ß-lactamases
(Slide 25)

34
Q

What is flucloxacillin used to treat?

A

Staphylococcal infections
(Slide 26)

35
Q

What do penicillins target?

A

Most gram-positive bacteria and some gram-negative cocci
(Slide 26)

36
Q

What is the mechanism of action of penicillins?

A

They bind to the active sites of PBPs (Penicillin binding proteins) and inactive them, preventing the formation of new peptidoglycan cross-links and weaken the existing cell wall structure
(Slide 26)

37
Q

When are penicillins produced by fungi?

A

When the carbon source becomes exhausted
(Slide 28)

38
Q

The addition of what 2 things during the production phase of penicillin can extend the phase?

A

Carbon and nitrogen
(Slide 28)

39
Q

What occurs at the end of the penicillin production process?

A

Cells are removed by filtration, the pH of the medium is lowered and penicillin is extracted in a solvent and crystallised
(Slide 28)

40
Q

What do Aspergillus terreus and Penicillium citrinum produce?

A

Statins (lovastatin and mevastatin respectively)
(Slide 29)

41
Q

What produces cyclosporine?

A

Tolypocladium inflatum
(Slide 29)

42
Q

What is cyclosporine used to treat?

A

Rheumatoid arthritis, psoriasis, Crohn’s disease, nephrotic syndrome and in organ transplants (to prevent rejection as it’s an immunosuppressant)
(Slide 29)