Yttrium2
Perpetual Question Machine
Posts: 1104
Registered: 7-2-2015
Member Is Offline
|
|
products produced through yeast fermentation
whats been produced since sugar to alcohol, and who studies , or knows how to deal with producing products through yeast fermentation. Can other
microorganisms also
|
|
j_sum1
Administrator
Posts: 6320
Registered: 4-10-2014
Location: At home
Member Is Online
Mood: Most of the ducks are in a row
|
|
Ethanol and carbon dioxide are the main products. But this varies. Not all microorganisms metabolise the same way. And not all behave the same
under all conditions (availability of oxygen being one of the chief variables.)
Other products can include lactic acid, acetone, butyric acid, hydrogen gas and probably a bunch of other things. Then, given a but of oxidation you
can have acetaldehyde and acetic acid which then lead to a bunch of byproducts: esters included.
Of course in the world of fermentation it is not just sucrose that is used and then you have whole fields of possible products which give a variety of
flavours to your beverages.
Any yes, other organisms can be used for fermentation including some bacteria and various other non-yeast fungi.
Big field. I'm no expert. I'll shut up now.
|
|
Ubya
International Hazard
Posts: 1247
Registered: 23-11-2017
Location: Rome-Italy
Member Is Offline
Mood: I'm a maddo scientisto!!!
|
|
a few weeks ago i was intrested in butanol production using fermentation,
https://en.wikipedia.org/wiki/Acetone%E2%80%93butanol%E2%80%... this is just an idea of what can be done
---------------------------------------------------------------------
feel free to correct my grammar, or any mistakes i make
---------------------------------------------------------------------
|
|
markx
National Hazard
Posts: 646
Registered: 7-8-2003
Location: Northern kingdom
Member Is Offline
Mood: Very Jolly
|
|
Even the most common bakers yeast fermentation of simple sugars produces a whole collection of different substances besides the ethanol and carbon
dioxide being the main components:
Acetone, methanol, aldehydes, ethyl acetate (also acetate esters of higher alcohols), amyl alcohols (pentanol isomers), furfural, organic
acids....just to name some.
The main problem is that one needs a very good fractionating column to separate just some of them out the main stew and it is quite a complicated mix.
For example a quite reasonably pure ethyl acetate fraction can be separated from the heads of a distillation run.
Methanol content is usually very low (but remarkable in products that are fermented using apples).
Amyl alcohols can be separated from congener fraction (tails) and furfural from the very end of the tail fraction if grains are used as the source of
sugars. It is a lot of work and usually not worth doing on small scale, but for the fun of it I have separated the amyl alcohol fraction, concentrated
it by leaching out the residual water with a saturated brine and used it to produce a sample of amyl acetate. Quite a flavorful ester....smells of
pears, banana, and a whole lot of something else that I really can't place.
Exact science is a figment of imagination.......
|
|
Yttrium2
Perpetual Question Machine
Posts: 1104
Registered: 7-2-2015
Member Is Offline
|
|
why does the yeast produce those compounds though?
|
|
macckone
Dispenser of practical lab wisdom
Posts: 2168
Registered: 1-3-2013
Location: Over a mile high
Member Is Offline
Mood: Electrical
|
|
Ethyl acetate is nearly impossible to separate from ethanol.
Ethyl acetate has a bp of 77C
Ethanol has a bp of 78C
Yes given enough reflux and enough runs you can get it out but it isn't easy. It is easier to decompose it with sodium carbonate or sodium hydroxide.
If you are making ethyl acetate, the usual method is absolute ethanol and acetic acid over sulfuric acid or sodium bisulfate at reflux with an acid
water scavenger (sulfuric acid acts as a scavenger).
|
|
unionised
International Hazard
Posts: 5126
Registered: 1-11-2003
Location: UK
Member Is Offline
Mood: No Mood
|
|
Quote: Originally posted by macckone | Ethyl acetate is nearly impossible to separate from ethanol.
Ethyl acetate has a bp of 77C
Ethanol has a bp of 78C
Yes given enough reflux and enough runs you can get it out but it isn't easy. It is easier to decompose it with sodium carbonate or sodium hydroxide.
If you are making ethyl acetate, the usual method is absolute ethanol and acetic acid over sulfuric acid or sodium bisulfate at reflux with an acid
water scavenger (sulfuric acid acts as a scavenger). |
The azeotrope boils at 71.8C
|
|
Fulmen
International Hazard
Posts: 1716
Registered: 24-9-2005
Member Is Offline
Mood: Bored
|
|
It's food. In the absence of oxygen they extract energy from converting sugars into other compounds.
We're not banging rocks together here. We know how to put a man back together.
|
|
macckone
Dispenser of practical lab wisdom
Posts: 2168
Registered: 1-3-2013
Location: Over a mile high
Member Is Offline
Mood: Electrical
|
|
Unionized, yes ethanol and ethyl acetate form an azetrope as well. But I can assure you that if you have significant ethyl acetate in your ethanol
the only way to get it out is by using sodium hydroxide or carbonate.
And it is undrinkable if there is too much ethyl acetate.
|
|