The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Lyngby, DK-2800 Kgs, Denmark.
Biotrend-Inovação e Engenharia em Biotecnologia SA, Cantanhede, 3060-197, Portugal.
ACS Synth Biol. 2020 Mar 20;9(3):634-646. doi: 10.1021/acssynbio.9b00477. Epub 2020 Feb 14.
Muconic acid is a potential platform chemical for the production of nylon, polyurethanes, and terephthalic acid. It is also an attractive functional copolymer in plastics due to its two double bonds. At this time, no economically viable process for the production of muconic acid exists. To harness novel genetic targets for improved production of -muconic acid (CCM) in the yeast , we employed a CCM-biosensor coupled to GFP expression with a broad dynamic response to screen UV-mutagenesis libraries of CCM-producing yeast. Via fluorescence activated cell sorting we identified a clone Mut131 with a 49.7% higher CCM titer and 164% higher titer of biosynthetic intermediate-protocatechuic acid (PCA). Genome resequencing of the Mut131 and reverse engineering identified seven causal missense mutations of the native genes (, , , , , , and ) and a duplication of two CCM biosynthetic genes, encoding dehydroshikimate dehydratase and catechol 1,2-dioxygenase, which were not recognized as flux controlling before. The Mut131 strain was further rationally engineered by overexpression of the genes encoding for PCA decarboxylase and AROM protein without shikimate dehydrogenase domain (Aro1p), and by restoring prototrophy. The resulting engineered strain produced 20.8 g/L CCM in controlled fed-batch fermentation, with a yield of 66.2 mg/g glucose and a productivity of 139 mg/L/h, representing the highest reported performance metrics in a yeast for CCM production to date and the highest production of an aromatic compound in yeast. The study illustrates the benefit of biosensor-based selection and brings closer the prospect of biobased muconic acid.
衣康酸是一种有潜力的平台化学品,可用于生产尼龙、聚氨酯和对苯二甲酸。由于其两个双键,它也是塑料中具有吸引力的功能共聚物。目前,还没有经济可行的生产衣康酸的工艺。为了利用新型遗传靶标来提高酵母中 - 衣康酸(CCM)的生产,我们采用了 CCM 生物传感器与 GFP 表达相结合的方法,该传感器对 CCM 生产酵母的 UV 诱变文库进行了广泛的动态筛选。通过荧光激活细胞分选,我们鉴定出一个克隆 Mut131,其 CCM 滴度提高了 49.7%,生物合成中间体 - 原儿茶酸(PCA)的滴度提高了 164%。Mut131 的基因组重测序和反向工程确定了七个导致天然基因(,,,,,,和)发生错义突变的原因,以及两个 CCM 生物合成基因的重复,编码脱氢莽草酸脱水酶和儿茶酚 1,2-双加氧酶,这两个基因在以前不被认为是通量控制基因。Mut131 菌株通过过表达 PCA 脱羧酶和没有莽草酸脱氢酶结构域的芳香族化合物 ARO 蛋白(Aro1p),以及恢复原养型,进一步进行了理性工程改造。在控制补料分批发酵中,工程菌株产生了 20.8 g/L 的 CCM,葡萄糖得率为 66.2 mg/g,生产率为 139 mg/L/h,这是迄今为止酵母中报道的最高 CCM 生产性能指标,也是酵母中芳香族化合物的最高产量。该研究说明了基于生物传感器选择的优势,并使生物基衣康酸的前景更加接近。