Yazawa Hisashi, Iwahashi Hitoshi, Kamisaka Yasushi, Kimura Kazuyoshi, Aki Tsunehiro, Ono Kazuhisa, Uemura Hiroshi
National Institute of Advanced Industrial Science and Technology, AIST Tsukuba Central 6, Higashi 1-1-1, Tsukuba, Ibaraki 305-8566, Japan.
Appl Environ Microbiol. 2007 Nov;73(21):6965-71. doi: 10.1128/AEM.01008-07. Epub 2007 Sep 14.
To make dihomo-gamma-linolenic acid (DGLA) (20:3n-6) in Saccharomyces cerevisiae, we introduced Kluyveromyces lactis Delta12 fatty acid desaturase, rat Delta6 fatty acid desaturase, and rat elongase genes. Because Fad2p is able to convert the endogenous oleic acid to linoleic acid, this allowed DGLA biosynthesis without the need to supply exogenous fatty acids on the media. Medium composition, cultivation temperature, and incubation time were examined to improve the yield of DGLA. Fatty acid content was increased by changing the medium from a standard synthetic dropout medium to a nitrogen-limited minimal medium (NSD). Production of DGLA was higher in the cells grown at 15 degrees C than in those grown at 20 degrees C, and no DGLA production was observed in the cells grown at 30 degrees C. In NSD at 15 degrees C, fatty acid content increased up until day 7 and decreased after day 10. When the cells were grown in NSD for 7 days at 15 degrees C, the yield of DGLA reached 2.19 microg/mg of cells (dry weight) and the composition of DGLA to total fatty acids was 2.74%. To our knowledge, this is the first report describing the production of polyunsaturated fatty acids in S. cerevisiae without supplying the exogenous fatty acids.
为了在酿酒酵母中合成二高-γ-亚麻酸(DGLA,20:3n-6),我们导入了乳酸克鲁维酵母Δ12脂肪酸去饱和酶、大鼠Δ6脂肪酸去饱和酶和大鼠延长酶基因。由于Fad2p能够将内源性油酸转化为亚油酸,这使得无需在培养基中添加外源脂肪酸就能进行DGLA的生物合成。我们研究了培养基组成、培养温度和培养时间以提高DGLA的产量。通过将培养基从标准合成缺陷培养基改为氮限制基本培养基(NSD),脂肪酸含量得以增加。在15℃下生长的细胞中DGLA的产量高于在20℃下生长的细胞,而在30℃下生长的细胞中未观察到DGLA的产生。在15℃的NSD培养基中,脂肪酸含量在第7天之前增加,在第10天之后下降。当细胞在15℃下于NSD中培养7天时,DGLA的产量达到2.19微克/毫克细胞(干重),DGLA占总脂肪酸的比例为2.74%。据我们所知,这是第一份描述在不供应外源脂肪酸的情况下酿酒酵母中多不饱和脂肪酸生产情况的报告。