酒精不管做為能源還是食物一直以來是人類依賴的重要產物,如何產酒以及增加產酒效率一直以來是工業中的課題之一。 在過往的研究中,學家利用Methylnitronitrosoguanidine(MNNG)或Ethyl Methane Sulfonate(EMS)藥劑與UV突變法對酵母菌BY4742菌株進行基因突變,更有利用Global transcription machinery engineering (gTME)基因工程的方式轉換細胞基因,期望利用改變原有基因配置能增加酵母菌在高醣高酒精的環境下酒精生產的效率。 本實驗採UV突變法並以3000、4000、5000μJ/cm2強度進行照射突變,再藉由高濃度葡萄糖與高濃度酒精的培養條件,對已隨機突變過的菌株進行連續液態篩選,初步篩選出具有高醣高酒精耐受性的菌種。
Alcohol has always been an important product of human dependence, whether it is energy or food. How to produce wine and increase the efficiency of wine production has always been one of the topics in the industry. In previous studies, scientists used Methylnitronitrosoguanidine (MNNG) or Ethyl Methane Sulfonate (EMS) agents and UV mutations to genetically mutate the yeast BY4742 strain, furthermore, converted the genes of the cells by using Global transcription machinery engineering (gTME), expected to use the altered original gene configuration that can increase the efficiency of yeast production in high concentration of glucose and alcohol environments. In our experiment, UV mutation method was used to irradiate mutations with intensity of 3000, 4000 and 5000 μJ/cm2, and the strains with random mutations were subjected to continuous liquid screening by high-concentration glucose and high-concentration alcohol culture conditions. In order to find a strain with high sugar and high alcohol tolerance.