16 - Biological Control of Foodborne Bacteria Flashcards

1
Q

what is biopreservation?

A

use of microorganisms, their metabolic products, or both to preserve foods

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2
Q

is fermentation a form of biopreservation

A

usually not

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3
Q

what is controlled acidification?

A

acid is produced by the controlled growth of LAB “in situ” for temperature-abused foods

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4
Q

what examples of biopreservation are there?

A
  • controlled acidification
  • use of bacteriocins
  • use of bacteriophages
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5
Q

what’s MicroGARD?

A

family of products that can be added to refrigerated food; contains fermentable CHO and bacterial culture; offers customizable protection

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6
Q

when is MicroGard effective?

A

only when food temperature is abused

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7
Q

what are the benefits of using MicroGard?

A
  • protect shelf life
  • maintain organoleptic qualities in food
  • meet consumers’ demand for natural products
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8
Q

what factors affect MicroGard’s effectiveness?

A
  • pH
  • buffering capacity
  • target spoilage microorganisms
  • concentration of fermentable CHO
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9
Q

describe the original experiment that determined the effectiveness of MicroGard

A

on “chicken a la king”

  • one sample was innoculated with LAB (L. bulgaricus and lactis)
  • the other was not
  • conditions simulated temp abuse
  • the one without LAB became toxic after 5 days
  • the one with LAB saw only 3/16 samples become toxic
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10
Q

what’s the wisconsin process?

A

pertains to bacon, which is normally preserved with nitrites. nitrites were found to produce carcinogenic derivatives.

this process replaces some nitrites with LAB, which makes the product less toxic

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11
Q

what are bacteriocins?

A

antimicrobial peptides of bacterial origin that are lethal to some bacteria but not to the native host

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12
Q

true or false: bacteriocins are antibiotics

A

false; bacteriocins are not antibiotics

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13
Q

what is one concern regarding the use of bacteriocins?

A

development of bacteriocin-resistant pathogens

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14
Q

what 4 classes can bacteriocins be divided into?

A
  • Class I
  • Class II
  • Class III
  • Class IV
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15
Q

describe class I bacteriocins

A

contain unusual amino acids produced by posttranslational modification

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16
Q

what are some of the weird amino acids found in class I bacteriocins?

A
  • dehydroalanine
  • dehydrobutyrine
  • lanthionine
  • methyllanthione
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17
Q

what’s a lantibiotic?

A

bacteriocin containing lanthionine rings (class I)

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18
Q

what’s nisin?

A
  • best-characterized LAB bacteriocin
  • obtained from L. lactis.
  • used in processing of cheese, meats, beverages, and more
  • extends shelf life by suppressing Gram-negative spoilage and pathogenic bacteria
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19
Q

what’s subtilin?

A
  • class I bacteriocin
  • a lantibiotic
  • effective protease that can be used in food, laundry detergent and contact lens cleaners
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20
Q

describe class II bacteriocins

A

small, heat-stable proteins with a consensus leader sequence that signals to the producing cell that the protein must be exported

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21
Q

what are the 3 subclasses of class II bateriocins?

A

IIa: active against listeria monocytogenes
IIb: require 2 different peptides for activity
IIc: require reduced cysteine for activity

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22
Q

describe class III bacteriocins

A

> 30 kDa, heat liable antimicrobial proteins

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23
Q

describe class IV bacteriocins

A

have lipid or CHO moieties and function of these non-protein portions are unknown

24
Q

how are bacteriocins discovered?

A
  • overlay colony of bacteriocin producer over target bacteria
  • bacteriocin producers will form a sharp inhibitions zone
  • fuzzy edges are due to organic edges
  • zones with no colony in the center are due to bacteriophages
25
Q

what causes the formation of inhibition zones?

A
  • bacteriocins
  • organic acids
  • bacteriophage
  • H2O2
26
Q

how do you verify that a colony produces bacteriocins?

A

add protease to inactivate bacteriocin, enabling bacteria to grow in the zone it was originally inhibited

27
Q

how do bacteriocins work?

A
  • disrupt integrity of cytoplasmic membrane
28
Q

what does the addition of bacteriocins to vegetative cells do?

A

results in rapid, non-specific efflux of prea-accumulated ions, amino acids, and ATP molecules

29
Q

the efflux of pre-accumulated ions, AAs and ATP molecules does what to a cytoplasmic membrane?

A

rapidly dissipates chemical and electrical gradients; leads to cell inhibition and death

30
Q

true or false: ALL bacteriocins functions by the same mechanism

A

true

31
Q

most bacteriocins have ____ ____ ____ which allow for insertion into the membrane and permeabilization

A

amphiphilic cationic peptides

32
Q

what 2 models are proposed for bacteriocins to enter a cell?

A
  • pore formation model

- membrane solubilization model

33
Q

describe the pore formation model

A

bacteriocins bind, insert into the membrane, and oligomerize to form a pore

34
Q

describe the solubilization model

A

bacteriocins act as detergents resulting in lysis of the cell

35
Q

how do bacteriocins interact with spores?

A
  • allows (maybe encourages) spores to germinate
  • inhibits outgrowth of pre emergent spore
  • pre emergent spore is less resistant to environmental stresses than the spore
36
Q

what are colicins?

A

proteins produced by and are toxic to some strains of E. coli

37
Q

what does the plasmid bearing the genetic determinants for colicin production contain??

A
  • colicin synthesis
  • immunity
  • release
38
Q

colicin expression in under ….

A

SOS regulation, then released into extracellular medium

39
Q

what is the first step for a colicin to exert lethal action?

A
  • bind to specific receptors (outer membrane protein used for entry)
40
Q

how do colicins enter a membrane?

A

translocation through outer membrane and transit through the periplasm by either Tol or TonB system

41
Q

how do colicins reach/act their lethal target?

A
  • forming voltage-dependent channel into the inner membrane

- using endonuclease activity on DNA, rRNA, or tRNA

42
Q

how are colicins categorized?

A
  • enzymatic

- pore-forming

43
Q

what are some mode of actions for enzymatic colicins?

A
  • peptidoglycan synthesis block [M]
  • protein synthesis block by cleavage of tRNA [D and E5]
  • protein synthesis block by cleavage of 16S rRNA [E3, E4, and E6]
  • DNA degradation [E2, and E7 to E9]
44
Q

how are bacteriocins added to food?

A
  • bacteriocins added directly
  • bacteriocinogenic cultures can be added to non-fermented food products, bacteriocins are produced in situ
  • starter cultures that encode for bacteriocins can be chosen for fermentation reactions
45
Q

what bacteriocin is added directly to food?

A

Nisin (dairy products, canned foods, smoked fish, mayo, and baby foods)

  • anti-listerial properties
  • sensitizes spores to heat
  • used in foods where botulism is a concertn
46
Q

true or false: nisin is sufficient to add on its own

A

false: it’s usually added as part of a multiple-barrier inhibitory system; MAP storage
- delay toxin production by C. botulinum
- delay/stop growth of L. monocytogenes

47
Q

what bacteriocin is added to non-fermented food products?

A

Pediocins

48
Q

what do pediocins do?

A
  • active against VEGETATIVE monocytogenes cells (not spores)

- used in weiners

49
Q

what increases inhibition using bacteriocins?

A
  • lower temps

- greater anaerobic conditions

50
Q

which bacteriocin is added to fermentation products

A
  • pediocin in fermented sausage

- nisin in LAB strain in cheddar cheese

51
Q

how do bacteria become resistant to bacteriocins?

A

changes in membrane permeability. also:

  • destruction
  • modification
  • altered receptors
  • membrane composition
52
Q

how is bacteriocin resistance avoided?

A

use in combination with other hurdles

53
Q

true or false: nisin resistance is well studied

A

false

54
Q

what can bacteriophages do?

A

control growth of salmonella, e. coli, and listeria

55
Q

problem with using bacteriophages?

A
  • possible resistance

- low numbers of bacteria in food (phage needs 10^5 or 6 to be actively growing)

56
Q

how is resistance to bacteriophages developed?

A

changes in bacteriophage receptor site (proteins, LPS, or lipoproteins)

57
Q

how should be bacteriophages be administered?

A

as a cocktail containing several different strains and types