2. Fermentation

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9 Terms

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Different types of processes by secreted enzymes acting on substrate

  • Proteolysis: digestibility, flavor and taste

  • Lipolysis: flavor

  • Amylolysis: digestiblity, acid formation

  • Pectinolysis: digestibility

  • Cellulolysis: digestibility

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What kind of metabolites do microorganisms produce?

  • Flavor compounds

    • acids, alcohol, esters, acetoin

  • Coloring substnaces

    • Carotenoids

  • Vitamins

    • B-vitamins

    • Yeast extract

  • Antimicrobial compounds

    • Acids, alcohols, carbon dioxide

    • Hydrogen peroxide

    • Reuterin, bacteriocins, killer-toxins

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Conversion of carbohydrates into lactic acid

Produces:

  • yoghurt

  • cheese

  • vegetables

  • sausages

not efficient; not all the substrate is used

<p>Produces:</p><ul><li><p>yoghurt</p></li><li><p>cheese</p></li><li><p>vegetables</p></li><li><p>sausages</p></li></ul><p></p><p>not efficient; not all the substrate is used</p><p></p>
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Types of lactic acid bacteria

  1. Homofermentative: can switch between the following types of fermentation

    • Homolactic fermentation → only produces lactate as an end product.

    • Mixed acid fermentation

  2. Heterofermentative

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Homo-fermentation vs. heterofermentation

no CO2 in homo

<p>no CO2 in homo</p>
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How to ferment alcohols

Use yeast

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Steps of alcoholic fermentation

  1. EM pathway: common glycolysis.

    • EM pathway is found in: bacteria & yeast.

    • Net yield: 2ATP, 2NADH, 2pyruvate

  2. EtOH production: pyruvate reduction

    • Net yield: 2CO2, 2NAD+, 2ethanol

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Fusel alcohols

  • Alcohols with a higher number of C atoms

  • Whisky, brandy, and rum rely on fusel alcohols (and their esters) for depth, body, and fruity/spicy notes.

  • Isoamyl alcohol → used to make isoamyl acetate (“banana oil”) for flavorings and fragrances.

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How are fusel alcohols made?

  • Following the Ehrlich pathway

    • Transamination
      → The amino acid loses its nitrogen (–NH₂) group.
      → This turns it into a keto acid.

    • Decarboxylation
      → The keto acid loses a carbon (as CO₂).
      → What’s left is an aldehyde.

    • Reduction
      → The aldehyde is reduced (adds hydrogen) using NADH.
      → That turns it into a fusel alcohol.