Whew back to mashing 101.
Now this is just off the top of my head without checking any numbers - so basic principals only OK.
There are something like a dozen enzymes in malt that do/may play a role in brewing there are probably hundreds more that we as brewers dont care about.
The two we talk about the most are Alpha and Bets Amylase. They have a range of conditions in which they are happy but let's say I create conditions biased for Alpha Amylase.
Say 73C and less acidic say around pH of 6
About an hour later I would have a mash that tests Starch Free (lets come back to this)
I would also have a mash that was rich in Dextrins because Alpha Amylase attacks the middle of a starch chain.
But there are rules; it can only break a chain about 7 or more sugars in from the end, so you get lots of 7-12 long rows or chains of glucose these are non fermentable and the resulting brew would be thick as glue and have next to no alcohol.
Conversely if I created the optimum conditions for Beta Amylase activity
Say 62-3 C and more acid say pH 5 and a bit
It would probably take all day to test starch free; because Beta can only bite 2 glucose molecules off the end of a chain, and there arent many ends for the enzymes to nibble on.
The resulting brew would be super dry and highly alcoholic.
At around 65C and a pH of 5.2-5.5
There is a balance, the Alpha is splitting long chains into smaller parts and providing lots of ends for the Beta to chew on. So we get a fairly fast conversion and a beer that has a balance of alcohol and body.
These processes go on after the mash tests Iodine normal!
There were some questions being asked recently about the possibility of shorter mash times.
Just because the starch has been reduced to dextrins doesn't mean that there is the right ratio of fermentable and un-fermentable components in the wort.
You have to leave the enzymes active until the desired ratio is achieved; this takes time
Now why would we want to change what the brewer created when the malt extract profile was designed?
Because Malt is expensive, even more expensive when you process it in a brewhouse then concentrate the wort to make Malt Extract.
In an attempt to get as much beer made with every Kg of malt as possible; as quickly as possible the brewer will be biasing the product toward dextrin production (higher Alpha activity then we would use as mash brewers) - in anticipation of you adding fermentables to restore the balance
If you want to use extract and change the ratio of fermentable components you need to add enzymes. Specifically enzyme that will tackle 12 glucose chains and shorter (primarily Beta Amylase)
To do this; if you milled up some malt, warmed the wort (extract and water) to 62-65 C, stirred the malt into the wort and left it for an hour or so the enzymes will get to work chopping up any dextrins they can.
There is another enzyme "Limit Dextrinase"
It can tackle lots of what would usually be residual dextrins; peak activity is 50-60 C (it breaks the 1.6 bonds as well as 1.4 bonds) Limit Dextrinase will break up dextrins that Beta Amylase wont touch.
Playing with this enzyme will make big changes to the fermentability of your wort.
It's going to be important to boil the wort for 2 reasons -
To sterilise the wort, there is lots of Lacto on the malt.
To kill all the enzymes, if you dont they can keep working; some even in the fermenter and you will have a super dry beer.
MHB
Sorry to ramble, but it's an interesting idea