Pichia pastoris gene expression system is a second generation expression system in yeast after the s . cerevisiae 甲醇毕赤酵母pichiapastoris表达系统是继酿酒酵母之后的第二代酵母表达系统。
Biological function of intracellular trehalose of s . cerevisiae in the alcoholic fermentation was briefly evaluated in the study 在试验中对酿酒酵母细胞内海藻糖在整个酒精发酵过程中的生物功能作了简要的评价。
Material : 1 . 1 strains ; saccharomyces cerevisiae s288c was provided by microbiology research institute of china science academy , regular culture 实验材料1 1材料：酿酒酵母s288c菌株由中国科学院微生物研究所提供，常规培养。
The amino acids sequence of pgl29 is 44 % identical to lst8p from s . cerevisiae and four wd40 domains found in its entire amino acids sequence 在pgl29的编码蛋白中，共有4个wd40结构域。其全长氨基酸序列与模式生物酿酒酵母中的lst8p有440的问源性。
Using pomegranate as raw material , pomegranate fruit wine was produced by saccharomyces cerevisiaes fermentation and added with sugar to adjust sugar content after pulping or juicing 摘要以石榴果为原料，经榨汁并调整糖度后，采用优良酿酒酵母进行发酵，酿制出石榴果酒。
This paper studied the technological process of fermenting cellulose to fuel ethanol by saccharomyces cercvisiae yt318 which was obtained through uv mutation 本文研究了酿酒酵母( saccharomycescercvisiaeyt318 )发酵纤维素物质(以玉米秸秆为原料)转化为燃料酒精的工艺过程，通过紫外线诱变法选育高产菌株yt318 。
Our aim was to investigate the effect of carcinogen mms on dna and telomerase activity of s . cerevisiae s288c and provide some scientific foundation for the relation between telomerase and cancer 本研究旨在观察致癌剂mms对酿酒酵母s288c细胞dna损伤反应以及对端粒酶活性的影响，为端粒酶与恶性肿瘤的关系提供科学依据。
Recent reports showed that telomerase activity in s . cerevisiae cells could be significantly up - regulated after exposure to some dna - damaging agents , which may be related with dna - damage repair 端粒酶与细胞生长、繁殖、衰老及肿瘤的发生密切相关。近来研究发现，酿酒酵母经dna损伤剂作用后端粒酶活性升高，可能与端粒dna损伤后修复机制有关。
5 statistic treatment with spss soft . results after treatment with mms at various ( 0 . 01 ~ immol / l ) concentration for 72h , we examined s . cerevisiae s288c cells for dna - damage situation and changes in telomerase activity 5统计学处理结果将不同浓度的mms ( 0 . 01一1 ~ fl )作用于酿酒酵母5288c细胞72h后，分别检测其dna损伤程度及端粒酶活性变化。
When cotransforming pgbd - nifa and ad fusion genomic library into saccharomyces cerevisiae pj69 - 4a , 109 candidates interacting with nifa had been selected by testing for the expression of the his3 , ade2 and lacz reporter genes 诱饵质粒和文库质粒共转化酿酒酵母( saccharomycescerevisiae ) pj69 - 4a ，通过检测报告基因his3 、 ade2及lacz的表达进行筛选，初筛得到109个阳性酵母菌落。
