The Theory of Mashing
Mashing is the process in which the milled grain is mixed with water. This activates enzymes that were already present in the barley seed or have been formed during the malting process. These enzymes work best in particular temperature and pH ranges. By varying the temperature of the mash, the brewer has control over the enzyme activity. In essence, mashing needs to been seen as an extension of the malting process. The following sections describe the enzymes that are more or less important for the mashing process.
Starch conversion enzymes
(Beta Amylase, Alpha Amylase, Limit Dextrinase)
Starch conversion is the most important aspect of mashing. In barley starch makes up 63% - 65% of the dry weight. Starch is a polysaccarid (very large chains of glucose) which is insoluble in water. Brewer's yeast, however, can only ferment monosacharides (glucose, ???), disacharides (maltose, ???) and trisacharides (matotriose, ???). The latter can only be completely fermented by lager yeast strains (s. uvarum).
In order for that starch to be converted into water soluble sugars (fermentable and unfermentable), two processes need to happen. First the starch is gelatenized to become water soluble. For starch found in barley and malt this happens above 140 *F (60 *C). Other starches (rice for example) gelatinizes only above 194 *F (90 *C) and requires boiling (see cereal mash) before it can be converted by enzymes. Secondly the activity of the amylase enzymes break the long chained starch molecules into shorter chains.
The starch found in malt is composed from Amylose and Amylopectin. Amylase is a single chain of glucose molecules liked between their 1st and 4th carbon atom (called 1-4 link). 17-24% of barley starch is Amylose [Narziss, 2005] the remaining 76-83% is Amylopectin. Amylopectin has a branched structure. These branches are formed by bonds between the 1st and 6th carbon atom of 2 glucose rings (called 1-6 link).
Beta amylase produces Maltose, the main wort sugar, by splitting 2 glucose molecules from the non-reducing end of a glucose chain. It is therefore able to completely convert Amylose. But since it cannot get past the branch joins, Amylopectin cannot completely be converted by beta amylase. The optimal pH range for beta amylase between 5.4 and 5.6 and the optimal temperature range is between 140 *F (60 *C) and 150 *F (65 *C). Above 160 *F (70*C) beta amylase is quickly deactivated [Narziss, 2005].
Alpha Amylase is able to split 1-4 links within glucose chains. By doing so, it exposes additional non-reducing ends for the beta amylase. This allows for the further conversion of Amylopectin. The optimal pH range is between 5.6 and 5.8 and the optimal temperature range is between 162 *F (72 *C) and 167 *F (75 *C). Above 176 *F (80 *C) alpha amylase is quickly deactivated [Narziss, 2005]
Limit dextrinase is able to split the 1-6 links that are found in Amylopectin. It is therefore able to reduce the amount of limit dextrins (glucose chains containing a 1-6 link) which are left over by alpha and beta amylase activity. Its optimal pH is 5.1 and the otimal temperature range is between 133 *F (55 *C) and 140 *F (60 *C). Above 149 *F (65 *C) this enzyme is quickly deactivated [Narziss 2005]. Because of an optimal temperature well below the commonly used saccrification rest temperature for single temperature saccrification rests, this enzyme plays only a mior role in most mashing schedules. Extended rests in the lower and upper 130s *F (upper 50s *C) benefit a higer fermentability of the wort.
During mashing the starch conversion to fermentable and unfermentable sugars is mostly done though beta and alpha amylase activities.
- After completed mashing the mash and the resulting wort needs to test negative with iodine (i.e. conversion has been completed). This is the case for linear dextrines shorter than 9 glucose molecules and branched dextrines with less than 60 glucose molecules.
- The fermentability should match the targeted style of beer [Narziss, 2005].
If a single temperature rest for starch conversion is chosen, it needs to allow for sufficient beta and alpha amylase actitiy. This is given at temperatures between 140 *F (60 *C) and 160 *F (70 *C), but only temperatures between 148 *F (65 *C) and 158 *F (69 *C) are commonly used. The higher the temperature the lower the limit of attenuation (fermentability) of the resulting wort will be. The following is a table that lists the relation between temperature and fermentability [Narziss, 2005]:
|Temperature||140 *F (60 *C)||149 *F (65 *C)||160 *F (70 *C)||167 *F (75*C)|
|apparent limit of attenuation||87.5%||86.5 %||76.8%||54.0 %|
The rests were held until conversion was complete. It should also be noted that the exact fermentability will depend on more than the temperature. The fermentability is mainly determined by the time the beta amylase was active. The higher the temperatiure, the quicker the beta amylase is deactivated. This results in less maltose production.
While temperature has the biggest impact, the following factors also determine the achieved fermentability:
- pH - a given pH may favour one enzyme over the other
- time - A longer mash will give the enzymes more time to break down starch and dextrines
- water/grist ratio - a thicker mash protects the beta amylase, giving it more time to produce maltose. Thus the fermentability is increased
- crush - a finer crush makes the starches accessible more quickly thus giving the beta amylase more time to work on their conversion before it is deactivated. The results is increased fermentability
- mash-schedule. The chosen mash schedule has a very significant impact. Dough-in at temperatures well below the optimum for beta and alpha amylase allow the starches to be hydrated before the amylase enzymes are activated. Again, this gives the beta amylase more time to work on starch conversion, thus increasing the fermantability. Decoction mashing does the same, even better. The boiling of the mash gelatinizes the starch and makes it available immediately. This is important for the bata amylase because at its optimal temperature barley starch is just starting to gelatenize. Though this effect does increases the fermentability, the inactivation of enzymes during the mash depletes the number of available enzymes.
- enzymatic power of the mash - This heavily depends on the grist. If large amounts of highly kilned base malts (like Munich) or large amounts of adjuncts (which are unmalted grains that do not contain a significant amount of enzymes) are used, the mash will have a lower enzymatic strength. Thus less maltose is produced and the fermentability suffers. This needs to be counteracted with a lower rest temperature and/or a more intensive mashing schedule.
German brewers commonly apply a multi step saccrification rest to achieve better fermentability. As noted above, the genatinization of barley starch happens between 140 *F (60 *C) and 150 *F (65 *C) [Palmer, 2006]. This means that at the optimal temperature for beta-amylase not not all starch may have gelatenized and is accessible to the enzymes. A multi step saccrification rest would employ a first rest between 140 *F (60 *C) and 150 *F (65 *C) which gives the beta amylase plenty of time to produce maltose from the accessible starches. Due to the limit dextrinase and already existing alpha amylase activity, the 1-6 links of amylopectin don't pose a limit for the beta amylase. This rest is commonly known as maltase rest. The lower the temperature of this rest, the longer the beta amylase will last and the more maltose is produced which increases the fermentability. Since the mash is generally not completely converted after the 30-60 min maltose rest, a second conversion rest, called saccrification or dextrinization rest is employed. This rest is held between 160 *F (70 *C) and 164 *F (72 *C) which is well above the gelatinization temperatuere for barley starch and within the optimal temperature range for alpha Amylase which will quickly convert the remaining starches. This rest is usually held until conversion of the mash is complete. An other benefit of this rest is the formation of foam positive glyco proteins [Fix, 1999]
If even better fermentability is desired, multiple rests within the beta and alpha amylase temperature range are possible. Such a mash schedule is used by Anheuser Bush to brew Bud Light without the use of enzyme additions in the mash. In order to leave as little dextrines as possible, their saccrification "rest" takes 2 hours while they slowly step the mash from 140 *F (60 *C) to 160 *F (70 *C) [source ??]. Such a mash schedule could be used by home brewers to brew highly attenuated styles like Belgian Saisons.
Protein converting enzymes
proteinase and peptidase
The protein conversion is another aspect of mashing. Other than the starch conversion, a significant part of the protein conversion could have already happened during malting. This need to be considered when choosing a mashing schedule for a particular malt.
The goal of malting and mashing is not the complete conversion of the malt's protein content, but the creation of a balanced mix of short (amino acids) and medium chained proteins. These become water soluble and, because they don't coagulate during the boil, will be carried over into the cast-out wort (the wort that is later fermented to beer). Amino acids are a necessary yeast nutrient and low FAN (free amino nitrogen) levels can lead to sluggish and unhealthy fermentations. Medium chained proteins are important for the perception of body in the beer as well as the foam stability.
In contrast to the starch conversion there is no simple set of enzymes or substrate that needs to be converted. Generally, when a protein rest is held in a mash, it is held between 122ºF (50ºC) and 133ºF (55ºC) where protoelytic activity shows a maximum. But even at higher temperatures, and in the starch conversion range is significant protein conversion happening [Narziss, 2005].
Rest temperatures closer to 122ºF (50ºC) tend to produce more short chained proteins (amino acids) while depleting the long and medium chained proteins. In sufficiently modified malts, this depletion of medium chained proteins can lead to a loss of body and head retention.
Rest temperatures closer to 155ºF (55ºC) emphasize the formation of medium chained proteins. Such a rest is better suited for most modern European lager malts. A dough at this temperature also benefits the fermentability if the mash lacks enzymatic strength.
Because of the protective effect of a ticker mash on the protoelytic enzymes, a protein rest benefits from a thicker mash. This works out well for step mash schedules where the temperature increase is achieved by hot water infuions.
Overmodified malts (like English or American Pale malts) do not require a protein rest. Since the protein conversion has been driven to a fairly advanced point during the malting process a protein rest may actually hurt by depleting the head and body positive medium chained proteins. For such malts a dough-in above the protein rest range or a simple single infusion mash is best.
Other mash enzymes
Maltase converts maltose into glucose. It is therefore an important enzyme for the yeast. But it is also present in malt. But since its temperature optimum is between 95 *F (35 *F) and 104 *F (40 *C) [Narziss, 2005] and it is being deactivated above 115 *F (45 *C), this enzyme does not play any significant role in most mashing schedules since higher temperature rests are necessary to genate glucose for this enzyme.
It is however used in a masching schedule developed by Markus Hermann from the Weihenstephan brewing school in Germany. This mash converts half the mash to get a large amount of glucose. After that conversion is complete, it is mixed with the remaining mash to achieve a rest temperature of 95 *F (35 *F) where the maltase converts the now existing maltose to glucose. After that the whole mash is again run through a regular mashing schedule to convert the remaining starch to matose and dextrins. The result is a wort with a very high glucose content (about 40% of the fermentable sugars). Yeast fermenting such a wort will generate more esters, a property that can be used to produce German wheat beers with a high ester content.
- [Narziss, 2005] Prof. Dr. agr. Ludwig Narziss, Prof. Dr.-Ing. habil. Werner Back, Technische Universitaet Muenchen (Fakultaet fuer Brauwesen, Weihenstephan), Abriss der Bierbrauerei. WILEY-VCH Verlags GmbH Weinheim Germany, 2005
- [Fix, 1999] George J. Fix Ph.D, Principles of Brewing Science, Brewers Publications, Boulder CO, 1999
- [foodnews.ch] www.foodnews.ch/x-plainmefood/index.html
- [Palmer, 2006] John J. Palmer, How to Brew, Brewers Publications, Boulder CO, 2006
- [TU Vienna] www.vt.tuwien.ac.at/scripts/172942/172942_Brauerei_04.pdf