Abstract
Barley β-glucans present in wort reduce beer filtrability and cause hazes and precipitates in the finished beer. The endo-β-1,4-glucanase enzyme, EGI, found in the filamentous fungus Trichoderma reesei, is capable of efficiently hydrolyzing these β-glucans. The cDNA copy of the eg11 gene, which codes for the EGI enzyme, was coupled to yeast regulatory sequences and transferred to a brewer's yeast using the yeast copper chelatin gene CUP1 as a selection marker in the transformation. The eg11 gene was transferred to the yeast both on a multicopy plasmid and on an integrating plasmid. In both cases, highly glycosylated, active EGI enzyme was secreted into the medium. Barley β-glucans present in wort were efficiently hydrolyzed by the recombinant brewer's yeast.
| Original language | English |
|---|---|
| Pages (from-to) | 413-420 |
| Journal | Current Genetics |
| Volume | 12 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 1 Oct 1987 |
| MoE publication type | A1 Journal article-refereed |
Keywords
- Chromosomal integration
- Endo-β-1,4-glucanase
- Glucanolytic brewer's yeast
- Saccharomyces cerevisiae
- Transformation