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Heterologous Production of Dihomo-γ-Linolenic Acid in Saccharomyces cerevisiae▿

机译:酿酒酵母中异源产γ-亚麻酸

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摘要

To make dihomo-γ-linolenic acid (DGLA) (20:3n-6) in Saccharomyces cerevisiae, we introduced Kluyveromyces lactis Δ12 fatty acid desaturase, rat Δ6 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°C than in those grown at 20°C, and no DGLA production was observed in the cells grown at 30°C. In NSD at 15°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°C, the yield of DGLA reached 2.19 μg/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.
机译:为了在酿酒酵母中制备二高-γ-亚麻酸(DGLA)(20:3n-6),我们引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伸酶基因。由于Fad2p能够将内源性油酸转化为亚油酸,因此可以进行DGLA生物合成,而无需在培养基上提供外源脂肪酸。检查培养基组成,培养温度和孵育时间以提高DGLA的产量。通过将培养基从标准的合成辍学培养基更改为限氮基本培养基(NSD),可以增加脂肪酸含量。在15℃下生长的细胞中DGLA的产生高于在20℃下生长的细胞中的DGLA的产生,并且在30℃下生长的细胞中未观察到DGLA的产生。在15°C的NSD中,脂肪酸含量一直增加到第7天,而在第10天后降低。当细胞在15°C的NSD中生长7天时,DGLA的产量达到2.19μg/ mg细胞(干重) )和DGLA占总脂肪酸的比例为2.74%。据我们所知,这是第一份描述酿酒酵母中不提供外源脂肪酸的多不饱和脂肪酸生产的报告。

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