Alloue-Boraud Wazé Aimée Mireille, N'Guessan Kouadio Florent, Djeni N'Dédé Théodore, Hiligsmann Serge, Djè Koffi Marcellin, Delvigne Franck
Centre Wallon de Biologie Industrielle (CWBI) Unité de Bio-industries, Université de Liège, Gembloux Agrobio-Tech, Passage des Déportés 2, 5030 Gembloux, Belgium ; Laboratoire de Biotechnologie et Microbiologie des Aliments, UFR-STA, Université Nangui Abrogoua, 02 BP 801, Abidjan 02, Côte d'Ivoire.
Laboratoire de Biotechnologie et Microbiologie des Aliments, UFR-STA, Université Nangui Abrogoua, 02 BP 801, Abidjan 02, Côte d'Ivoire.
J Food Sci Technol. 2015 Aug;52(8):5236-42. doi: 10.1007/s13197-014-1526-0. Epub 2014 Aug 31.
Saccharomyces cerevisiae C8-5 and Candida tropicalis F0-5 isolated from traditional sorghum beer were tested for kinetic parameters on barley malt extract, YPD (863 medium) and for alcohol production. The results showed that C. tropicalis has the highest maximum growth rate and the lowest doubling time. Values were 0.22 and 0.32 h(-1) for maximum growth rate, 3 h 09 min and 2 h 09 min for doubling time respectively on barley malt extract and YPD. On contrary, glucose consumption was the fastest with S. cerevisiae (-0.36 and -0.722 g/l/h respectively on barley malt extract and YPD). When these two yeasts were used as starters in pure culture and co-culture at proportion of 1:1 and 2:1 (cell/cell) for barley malt extract fermentation, we noticed that maltose content increased first from 12.12 g/l to 13.62-16.46 g/l and then decreased. The highest increase was obtained with starter C. tropicalis + S. cerevisiae 2:1. On contrary, glucose content decreased throughout all the fermentation process. For all the starters used, the major part of the ethanol was produced at 16 h of fermentation. Values obtained in the final beers were 11.4, 11.6, 10.4 and 10.9 g/l for fermentation conducted with S. cerevisiae, C. tropicalis, C. tropicalis + S. cerevisiae 1:1 and C. tropicalis + S. cerevisiae 2:1. Cell viability measurement during the fermentation by using flow cytometry revealed that the lowest mean channel fluorescence for FL3 (yeast rate of death) was obtained with C. tropicalis + S. cerevisiae 2:1 after 48 h of fermentation.
对从传统高粱啤酒中分离出的酿酒酵母C8 - 5和热带假丝酵母F0 - 5进行了关于大麦麦芽提取物、YPD(863培养基)的动力学参数测试以及酒精产量测试。结果表明,热带假丝酵母具有最高的最大生长速率和最短的倍增时间。在大麦麦芽提取物和YPD上,最大生长速率值分别为0.22和0.32 h⁻¹,倍增时间分别为3小时09分钟和2小时09分钟。相反,酿酒酵母消耗葡萄糖最快(在大麦麦芽提取物和YPD上分别为 - 0.36和 - 0.722 g/l/h)。当将这两种酵母以1:1和2:1(细胞/细胞)的比例用于大麦麦芽提取物发酵的纯培养和共培养时,我们注意到麦芽糖含量先从12.12 g/l增加到13.62 - 16.46 g/l,然后下降。使用热带假丝酵母 + 酿酒酵母2:1作为起始发酵剂时麦芽糖含量增加最多。相反,葡萄糖含量在整个发酵过程中都下降。对于所有使用的起始发酵剂,大部分乙醇在发酵16小时时产生。用酿酒酵母、热带假丝酵母、热带假丝酵母 + 酿酒酵母1:1和热带假丝酵母 + 酿酒酵母2:1进行发酵,最终啤酒中获得的乙醇含量分别为11.4、11.6、10.4和10.9 g/l。在发酵过程中使用流式细胞术测量细胞活力,结果显示发酵48小时后,热带假丝酵母 + 酿酒酵母2:1的FL3(酵母死亡率)平均通道荧光最低。