Murakami Kiriko, Tao Eriko, Ito Yuki, Sugiyama Minetaka, Kaneko Yoshinobu, Harashima Satoshi, Sumiya Takahiro, Nakamura Atsushi, Nishizawa Masafumi
Department of Microbiology and Immunology, School of Medicine, Keio University, Shinjuku, Tokyo, 160-8582, Japan.
Appl Microbiol Biotechnol. 2007 Jun;75(3):589-97. doi: 10.1007/s00253-007-0859-2. Epub 2007 Mar 8.
Saccharomyces cerevisiae, for centuries the yeast that has been the workhorse for the fermentative production of ethanol, is now also a model system for biological research. The recent development of chromosome-splitting techniques has enabled the manipulation of the yeast genome on a large scale, and this has allowed us to explore questions with both biological and industrial relevance, the number of genes required for growth and the genome organization responsible for the ethanol production. To approach these questions, we successively deleted portions of the yeast genome and constructed a mutant that had lost about 5% of the genome and that gave an increased yield of ethanol and glycerol while showing levels of resistance to various stresses nearly equivalent to those of the parental strain. Further systematic deletion could lead to the formation of a eukaryotic cell with a minimum set of genes exhibiting appropriately altered regulation for enhanced metabolite production.
几个世纪以来,酿酒酵母一直是发酵生产乙醇的主力军,如今它也是生物研究的一个模式系统。染色体分裂技术的最新发展使得大规模操纵酵母基因组成为可能,这使我们能够探索具有生物学和工业相关性的问题,如生长所需的基因数量以及负责乙醇生产的基因组组织。为了解决这些问题,我们相继删除了酵母基因组的部分区域,并构建了一个突变体,该突变体丢失了约5%的基因组,其乙醇和甘油产量增加,同时对各种胁迫的抗性水平与亲本菌株几乎相当。进一步的系统删除可能会导致形成一个具有最小基因集的真核细胞,该基因集表现出适当改变的调控以提高代谢产物的产量。