Li Mingji, Kildegaard Kanchana R, Chen Yun, Rodriguez Angelica, Borodina Irina, Nielsen Jens
The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, 2970 Hørsholm, Denmark.
Department of Biology and Biological Engineering, Chalmers University of Technology, SE-41296 Gothenburg, Sweden; The Novo Nordisk Foundation Center for Biosustainability, Chalmers University of Technology, SE-41296 Gothenburg, Sweden.
Metab Eng. 2015 Nov;32:1-11. doi: 10.1016/j.ymben.2015.08.007. Epub 2015 Sep 4.
Resveratrol is a natural antioxidant compound, used as food supplement and cosmetic ingredient. Microbial production of resveratrol has until now been achieved by supplementation of expensive substrates, p-coumaric acid or aromatic amino acids. Here we engineered the yeast Saccharomyces cerevisiae to produce resveratrol directly from glucose or ethanol via tyrosine intermediate. First we introduced the biosynthetic pathway, consisting of tyrosine ammonia-lyase from Herpetosiphon aurantiacus, 4-coumaryl-CoA ligase from Arabidopsis thaliana and resveratrol synthase from Vitis vinifera, and obtained 2.73 ± 0.05 mg L(-1) resveratrol from glucose. Then we over-expressed feedback-insensitive alleles of ARO4 encoding 3-deoxy-D-arabino-heptulosonate-7-phosphate and ARO7 encoding chorismate mutase, resulting in production of 4.85 ± 0.31 mg L(-1) resveratrol from glucose as the sole carbon source. Next we improved the supply of the precursor malonyl-CoA by over-expressing a post-translational de-regulated version of the acetyl-CoA carboxylase encoding gene ACC1; this strategy further increased resveratrol production to 6.39 ± 0.03 mg L(-1). Subsequently, we improved the strain by performing multiple-integration of pathway genes resulting in resveratrol production of 235.57 ± 7.00 mg L(-1). Finally, fed-batch fermentation of the final strain with glucose or ethanol as carbon source resulted in a resveratrol titer of 415.65 and 531.41 mg L(-1), respectively.
白藜芦醇是一种天然抗氧化化合物,用作食品补充剂和化妆品成分。到目前为止,白藜芦醇的微生物生产是通过添加昂贵的底物对香豆酸或芳香族氨基酸来实现的。在此,我们对酿酒酵母进行工程改造,使其通过酪氨酸中间体直接从葡萄糖或乙醇生产白藜芦醇。首先,我们引入了生物合成途径,该途径由来自橙色滑柱菌的酪氨酸解氨酶、来自拟南芥的4-香豆酰辅酶A连接酶和来自葡萄的白藜芦醇合酶组成,并从葡萄糖中获得了2.73±0.05毫克/升的白藜芦醇。然后,我们过表达了编码3-脱氧-D-阿拉伯庚酮糖酸-7-磷酸的ARO4和编码分支酸变位酶的ARO7的反馈不敏感等位基因,从而以葡萄糖作为唯一碳源生产出4.85±0.31毫克/升的白藜芦醇。接下来,我们通过过表达乙酰辅酶A羧化酶编码基因ACC1的翻译后去调控版本来改善前体丙二酰辅酶A的供应;该策略进一步将白藜芦醇产量提高到6.39±0.03毫克/升。随后,我们通过对途径基因进行多重整合来改进菌株,从而使白藜芦醇产量达到235.57±7.00毫克/升。最后,以葡萄糖或乙醇作为碳源对最终菌株进行补料分批发酵,白藜芦醇产量分别达到415.65和531.41毫克/升。