Proprietary Enzymes Blend in for Grain based distillery
Grain-based distilleries (corn, sorghum, wheat, barley, broken rice, etc.) need enzyme blends tailored to starch liquefaction β saccharification β fermentation. Unlike molasses, the raw material here is starch-heavy, so the focus is on Ξ±-amylase, glucoamylase, and debranching enzymes, with optional add-ons (protease, cellulase, phytase) to improve yield and fermentation performance.
1) Core Enzymes in Grain-Based Distilleries
EnzymeRoleTypical Process StageThermostable Ξ±-AmylaseBreaks long starch chains β dextrins (liquefaction step at high temp 85β95 Β°C).Jet cooker / slurry tank β liquefaction.Glucoamylase (amyloglucosidase)Hydrolyzes dextrins β glucose.Saccharification tank or simultaneous with fermentation (SSF).Pullulanase (Debranching enzyme)Cuts Ξ±-1,6 bonds in amylopectin, exposing more sites for glucoamylase β boosts glucose yield.Co-dosed with glucoamylase during saccharification.Protease (optional)Hydrolyzes grain proteins β releases amino acids/peptides as yeast nutrients, reduces viscosity/foaming.Slurry / fermentation.Cellulase / Hemicellulase (optional)Breaks down non-starch polysaccharides in husk/bran β reduces viscosity, increases sugar release.Saccharification.Phytase (optional)Hydrolyzes phytic acid β releases phosphorus (nutrient) for yeast.Pre-fermentation nutrient boost.
2) Typical Blend Formulations
A. Standard 3-enzyme blend (minimum effective)
Thermostable Ξ±-Amylase (liquefaction)
Glucoamylase (saccharification)
Pullulanase (for full debranching)
Gives higher glucose yields and lowers residual dextrins β 2β5% more ethanol.
B. Performance-enhanced blend
Standard 3-enzyme blend +
Protease β better FAN (free amino nitrogen) for yeast β faster, more complete fermentations.
Cellulase / Hemicellulase β reduces viscosity of whole stillage β easier DDGS handling.
Phytase (optional, for nutrient economy).
3) Process Flow with Enzyme Blends
Slurry preparation
Grind grains to fine meal.
Adjust solids (28β35% DS typical).
pH adjusted (~5.5β6.0).
Liquefaction
Heat to ~85β95 Β°C.
Add thermostable Ξ±-amylase (often in split doses).
Dextrinization occurs β viscosity drops.
Saccharification
Cool to ~55β65 Β°C.
Add glucoamylase + pullulanase.
Hold for 30β120 min (or proceed SSF directly).
Fermentation (SSF option)
Pitch yeast + saccharification enzymes together.
Protease, phytase, and optional cellulase can be added here.
Maintain ~30β35 Β°C for yeast.
4) Performance Gains from Blends
Ξ±-Amylase + Glucoamylase alone β baseline ethanol yield.
+ Pullulanase β 1β3% ethanol yield gain, lower residual starch.
+ Protease β faster fermentation, 10β20% higher FAN, reduced stuck fermentations.
+ Cellulase/Hemicellulase β lower mash viscosity, improved solids separation.
+ Phytase β reduced need for added nutrients (P, Zn).
β Bottom line:
At minimum, Ξ±-amylase + glucoamylase are essential.
For performance gains (higher ethanol yield, better plant runnability), add pullulanase and protease.
Extra cellulase/hemicellulase/phytase are optional but beneficial depending on feedstock & process bottlenecks.
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