Ohto Chikara, Muramatsu Masayoshi, Obata Shusei, Sakuradani Eiji, Shimizu Sakayu
Bio Research Lab., Toyota Motor Corporation, 1 Toyota-cho, Toyota, 471-8572, Japan.
Appl Microbiol Biotechnol. 2009 Apr;82(5):837-45. doi: 10.1007/s00253-008-1807-5. Epub 2008 Dec 16.
To develop microbial production method for prenyl alcohols (e.g., (E,E)-farnesol (FOH), (E)-nerolidol (NOH), and (E,E,E)-geranylgeraniol (GGOH)), the genes encoding enzymes in the mevalonate and prenyl diphosphate pathways were overexpressed in Saccharomyces cerevisiae, and the resultant transformants were evaluated as to the production of these alcohols. Overexpression of the gene encoding hydroxymethylglutaryl (HMG)-CoA reductase was most effective among the genes tested. A derivative of S. cerevisiae ATCC 200589, which was selected through screening, was found to be the most suitable host for the production. On cultivation of the resultant transformant, in which the HMG-CoA reductase gene was overexpressed, in a 5-liter bench-scale jar fermenter for 7 d, the production of FOH, NOH, and GGOH reached 145.7, 98.8, and 2.46 mg/l, respectively.
为开发用于生产异戊烯醇(如(E,E)-法尼醇(FOH)、(E)-橙花叔醇(NOH)和(E,E,E)-香叶基香叶醇(GGOH))的微生物生产方法,将甲羟戊酸途径和异戊烯基二磷酸途径中的酶编码基因在酿酒酵母中过表达,并对所得转化体的这些醇类产量进行评估。在所测试的基因中,编码羟甲基戊二酰(HMG)-CoA还原酶的基因过表达最为有效。通过筛选选出的酿酒酵母ATCC 200589的一个衍生物被发现是最适合生产的宿主。将过表达HMG-CoA还原酶基因的所得转化体在5升实验室规模的罐式发酵罐中培养7天,FOH、NOH和GGOH的产量分别达到145.7、98.8和2.46毫克/升。