Abstract
Most Saccharomyces spp. cannot degrade or ferment dextrin, which is the second most abundant carbohydrate in wort for commercial beer production. Dextrin-degrading brewer’s bottom and top yeasts expressing the glucoamylase gene (GAM1) from Debaryomyces occidentalis were developed to produce low-carbohydrate (calorie) beers. GAM1 was constitutively expressed in brewer’s yeasts using a rDNA-integration system that contained yeast CUP1 gene coding for copper resistance as a selective marker. The recombinants secreted active glucoamylase, displaying both α-1,4- and α-1,6-debranching activities, that degraded dextrin and isomaltose and consequently grew using them as sole carbon source. One of the recombinant strains expressing GAM1 hydrolyzed 96 % of 2 % (w/v) dextrin and 98 % of 2 % (w/v) isomaltose within 5 days of growth. Growth, substrate assimilation, and enzyme activity of these strains were characterized.
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Jin-Yeong Park was supported by the second stage of the Brain Korea 21 Project.
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Park, JY., Lee, JY., Choi, SH. et al. Construction of dextrin and isomaltose-assimilating brewer’s yeasts for production of low-carbohydrate beer. Biotechnol Lett 36, 1693–1699 (2014). https://doi.org/10.1007/s10529-014-1530-5
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DOI: https://doi.org/10.1007/s10529-014-1530-5