Key points on MLF Flashcards

1
Q

11 factors contributing to MLF

A
  1. pH (most important)
  2. S02
  3. Nutrient Composition
  4. Oxygen
  5. CO2
  6. Alcohol
  7. Temperature
  8. Organic Acids
  9. Phenolics or phenolic acids
  10. Presence of other LAB
  11. Bacteriophage
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2
Q

MLF inhibited by (7)

A
  1. Use of SO2 (should be used after)
  2. Early racking (it likes solids)
  3. Downward pH adjustment
  4. Low temp
  5. Filtration/Fining
  6. Addition of Fumaric acid (only outside EU)
  7. Bacteriocin (lysozyme) addition (egg whites and are the best additive to prevent MLF)
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3
Q

How to inhibit MLF (4)

A
  1. Add SO2
    - 0.8 mg/L molecular pH adjusted
  2. Temperature
    - Below 18°C and as low as 13°C
  3. High ethanol does not always inhibit because often coupled with high pH
  4. Acidity
    - Adding tartaric acid (better than malic acid) will help but may not stop it
    - Wines pH 3.3 and below need to be stimulated while wines greater than 3.3 will be difficult to stop
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4
Q

Inhibition 2 (3)

A
  1. Elimination of viable bacteria
  2. Sterile filtration and sterile bottling
  3. Chemical inhibitors
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5
Q

Lysozyme

A

Egg whites that are used as an antimicrobial agent. When we use this we need to avoid adding close to bottling it is a protein and is capable of combining tannins

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6
Q

Importance of Lysozyme

A

It is included among wine additives able to control fermentation processes and avoid spoilage during wine making. Because it is an animal product its not vegan.

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7
Q

Amount of Lysozyme added

A

The amount of lysozyme added normally ranges between 25 and 50 g/hL.

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8
Q

Organic acids that can be added (3)

A
  1. Fumarate inhibitory at low concentrations
  2. Fatty acids (C8 and C10 released by yeasts)
    can also be inhibitory
  3. Malate stimulates growth prior to malolactic fermentation
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9
Q

Oxygen (3)

A
  1. Stimulatory to growth
  2. Affects spectrum of end products
  3. Can produce more energy (and acetic acid) in presence of oxygen (TCA cycle, via citrate a/o by pentose phosphate pathway –> Eterof. LAB)
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10
Q

Carbon Dioxide (2)

A
  1. Stimulatory to malolatic fermentation
  2. Mechanism unknown
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11
Q

Bacteriophage

A
  1. Bacterial “viruses” that can be spread from one bacterium to another and that cause cell death
  2. Not known if this is a problem in wine production or not; it is a problem in other lactic acid bacteria fermentations
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12
Q

Presence of Other Lactic Acid Bacteria positive

A
  1. Mixed cultures may yield “better” complexity
  2. Can be stimulatory
    - Increase in pH (Difficult to start MLF below 3.3-3.4 pH)
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13
Q

Presence of Other Lactic Acid Bacteria Negative

A

Can be inhibitory
- Bacteriocin production (Lysozyme)
- Competition for nutrients

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14
Q

Nutrient Composition (4)

A
  1. Lactic acid bacteria are fastidious: numerous growth requirements
  2. Aging on yeast lees increases micronutrient content via autolysis
  3. Extended skin contact enhances lactic acid bacteria
  4. Higher solids or a less clarification degree enhance lactic acid bacteria

Remember Red wines have more nutirents because they offer more solids

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15
Q

Yeast and Bacteria interaction (Metabolization)

A

Yeast and bacteria are competing for nutrients
( Yeast are mainly interested in sugars
and are able to metabolize amino acids)

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16
Q

Yeast and Bacteria interaction (bacteria growth)

A

Yeast can both inhibit and stimulate bacterial growth

17
Q

What inhibits bacterial growth

A

Formation of ethanol, bisulfite and fatty acid by yeast

18
Q

What else stimulates bacterial growth

A

SO2 binding and the products of yeast autolysis after “sur lies” aging

19
Q

Death Phase

A

Bacteria can stimulate death phase in yeast

20
Q

Choice of strain of Bacteria and yeast (5)

A
  1. compatibility
  2. Production of desirable characteristics
  3. Ability to complete MLF
  4. Vigor
  5. Availability of freeze dried inoculum
21
Q

Inoculated MLF (4)

A
  1. Better control over both timing and organisms present
  2. Difficult to maintain inocula
  3. Starter culture must be “pure”
  4. Percent inoculation: 1-50% depending upon vigor of culture
22
Q

Inoculum prep (4)

A
  1. Start culture from a medium supporting good growth of organism
  2. Inoculate “diluted” juice (with water) with starter and addition of nutrients
  3. Use #2 to inoculate full strength wine or juice with addition of nutrients
  4. Use #3 to inoculate the rest of wine
23
Q

Spontaneous MLF (3)

A
  1. Uncontrolled timing of process
  2. Risk of unwanted species/strains
  3. Off-characters can be produced if MLF when undesired
24
Q

Timing of MLF (4 options)

A
  1. Prior to yeast fermentation
  2. Simultaneous with yeast fermentation
  3. Mid-way through yeast fermentation
  4. After yeast fermentation
25
Q

Pre Ferm Inoculum (2)

A
  1. Decreases yeast nutrients
    - Stuck/sluggish fermentation
    - Production of off-characters
  2. May lead to production of inhibitory compounds (acetic acid) due to presence of oxygen
26
Q

Simultaneous yeast inoculation (3)

A
  1. See increase in acetic acid
  2. See a decrease in viability of both yeast and bacteria
  3. Yeast “rebound” better than bacteria
27
Q

Mid Ferm inoculation (4)

A
  1. Nutrients left for bacteria
  2. Ethanol low and not inhibitory
  3. Yeast-produced SO2 may be inhibitory
  4. May lead to arrest of yeast fermentation
28
Q

Post Ferm Inoculation (4)

A
  1. Nutrients have been depleted
  2. Ethanol concentration high
  3. Concentration of other yeast inhibitory compounds also high
  4. Better temperature control