机构地区: 山东农业大学食品科学与工程学院食品科学系
出 处: 《食品与发酵工业》 1995年第6期33-38,共6页
摘 要: GYNB培养基中肉桂酸浓度达到100μg/ml时,酿酒酵母(Sacchqromyes cervisiaepof-sta)的生长受到抑制,而糖化酵母(Sacchromyes dlastaticus POF1STA)能够生长。用紫外线诱变糖化酵母,在GYNBSCA100培养基平板上检出pof-糖化酵母营养缺陷株。经糊精发酵试验、模拟啤酒发酵试验CO2失重试验及糖化酶活性比较。 Cinnamic acid(100μg/ml)incorporated in GYNBCA100 medium inhibited the growth of brewing strains(pof-) of Saccharomyces cervisiae while permitting the growth of Saccharomyces diastaticus(POF1).Ultraviolet rays eliminated POF1 gene of Saccharomyces diastaticus haploids haploids(a or α) which produce glucoamylase. pof- nutritional deficiency strains of Sac.diasdtaticus were selected on GYNBSCA100 Soild medium. After dextrin fermentation test, imitating beer fermentation trial,CO_2 loss in weight experiment and comparing glucoamylase activity test,three strains(pof- STA) were chosed which possess greater glucoamylase activity,ferment rapid and have no phenolic-off-flavour when fermented hopped wort.