L1 Flashcards

1
Q

What are 2 industrial microorganisms?

A

Fungi
Bacteria

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2
Q

What are properties of industrial strains?

A

Produce substance of interest
Large scale culture (inexpensive)
non-pathogenic, spore former
Amenable to genetic engineering

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3
Q

What is the difference between primary & secondary metabolites?

A

Primary - essential for growth of the organisms eg aas
secondary - not essential for growth eg antibiotics

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4
Q

What are secondary metabolites production dependent on?

A

Growth conditions

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5
Q

Define fermentation.

A

Any large-scale microbial process - not necessarily biochemical

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6
Q

What is monosodium glutamate (MSG)?

A

Food additive

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7
Q

How was MSG formerly produced?

A

produced formerly by acid hydrolysis of plant protein

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8
Q

What microorganism produces large scale MSG?

A

Corynebacterium glutamicum

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9
Q

What are 3 pros of using Corynebacterium glutamicum?

A

Less expensive
1000,000t produced per annum
biotin-limited medium (auxotroph)

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10
Q

What is an auxotroph?

A

Strain that cannot produce a key nutrient itself

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11
Q

What is in the biotin limited medium?

A

carbohydrate
ammonia
minerals
aerobic
100g glutamate

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12
Q

What is a key enzyme in the glutmate production?

A

Glutamate dehydrogenase

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13
Q

What is the efflux of glutamic acid through?

A

MscCG specialized mechanoreceptor

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14
Q

When happened to alpha ketoglutarate in low biotin levels?

A

Activity suppressed

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15
Q

When happened to alpha ketoglutarate in presence of penicillin?

A

Decreased levels

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16
Q

What is alpha ketoglutarate activity regulated by?

17
Q

What happens to OdhI in biotin-limiting conditions?

A

Unphosphorylated

18
Q

What is the gene DtsR a component of?

A

Biotin-containing protein in fatty acid metabolism

19
Q

What happens if dtsR is knocked out?

A

Consititutive overproduction of glutamate

20
Q

What is replacing screening of strains?

A

Rational strategies

21
Q

What are 6 ways to increase valine production?

A

Amplification of biosynthesis pathway enzymes
Reduction of by-product formation
Release of feedback regulation of key enzymes
Increase supply of reducing equivalents
Reduce metabolic fluxes to TCA cycle
Increase in export

22
Q

How do you grow antbiotics?

A

Isolate antibiotic producers from environment -> purify -> toxicity testing, clinical trails -> improve yield

23
Q

What are 2 ways to improve yield?

A

Optimize conditions
isolate high producing strains

24
Q

What is depelication?

A

Keep finding same antibiotics

25
What are 4 ways to discover new antibiotics?
Unexplored environments investigating 'unculturable' m/o genome mining activation of silent gene clusters
26
What are unculturable m/o?
Majority of strains cannot be cultured in lab conditions
27
What is genome mining?
Bypass cultivation & just sequence DNA to find biosynthetic gene clusters coding for enzymes that produce antibiotics
28
How do you make an iChip?
dip central plate into suspension of cells mixed with molten agar Single cell trapped in well Unit assembled with semi-permeable membrane to cover wells
29
What antibiotic was discovered due to i Chip?
Teixobactin
30
Where do m/o grow in the iChip?
Series of wells - approx. one cell per well
31
What is the MoA of teixobactin?
Inhibits cell wall biosynthesis (binds lipid II)
32
Is there resistance to Teixobactin?
No resistant pathogens
33
What type of antibiotic is Teixobactin?
Non-ribosomal peptide