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油脂酵母解脂耶罗维亚酵母中脱落酸的生产。

Production of abscisic acid in the oleaginous yeast Yarrowia lipolytica.

机构信息

The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kemitorvet 220, 2800 Kgs Lyngby, Denmark.

Department of Biotechnology and Biomedicine, Technical University of Denmark, Søltofts Plads 223, 2800 Kgs Lyngby, Denmark.

出版信息

FEMS Yeast Res. 2022 Apr 8;22(1). doi: 10.1093/femsyr/foac015.

DOI:10.1093/femsyr/foac015
PMID:35274684
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8992728/
Abstract

Abscisic acid (ABA) is a phytohormone with applications in agriculture and human health. ABA can be produced by Botrytis cinerea, a plant pathogenic filamentous fungus. However, the cultivation process is lengthy and strain improvement by genetic engineering is difficult. Therefore, we engineered the oleaginous yeast Yarrowia lipolytica as an alternative host for ABA production. First, we expressed five B. cinerea genes involved in ABA biosynthesis (BcABA1,BcABA2,BcABA3,BcABA4 and BcCPR1) in a Y. lipolytica chassis with optimized mevalonate flux. The strain produced 59.2 mg/L of ABA in small-scale cultivation. Next, we expressed an additional copy of each gene in the strain, but only expression of additional copy of BcABA1 gene increased the ABA titer to 168.5 mg/L. We then integrated additional copies of the mevalonate pathway and ABA biosynthesis encoding genes, and we expressed plant ABA transporters resulting in an improved strain producing 263.5 mg/L and 9.1 mg/g dry cell weight (DCW) ABA. Bioreactor cultivation resulted in a specific yield of 12.8 mg/g DCW ABA; however, surprisingly, the biomass level obtained in bioreactors was only 10.5 g DCW/L, with a lower ABA titer of 133.6 mg/L. While further optimization is needed, this study confirms Y. lipolytica as a potential alternative host for the ABA production.

摘要

脱落酸(ABA)是一种具有农业和人类健康应用的植物激素。ABA 可以由植物病原丝状真菌 Botrytis cinerea 产生。然而,其培养过程漫长,且通过遗传工程进行菌株改良较为困难。因此,我们将产油酵母 Yarrowia lipolytica 工程化为 ABA 生产的替代宿主。首先,我们在优化的甲羟戊酸通量的 Y. lipolytica 底盘中表达了参与 ABA 生物合成的五个 B. cinerea 基因(BcABA1、BcABA2、BcABA3、BcABA4 和 BcCPR1)。该菌株在小规模培养中产生了 59.2 mg/L 的 ABA。接下来,我们在该菌株中额外表达了每个基因的一个拷贝,但只有额外表达 BcABA1 基因的拷贝数增加了 ABA 的滴度至 168.5 mg/L。然后,我们整合了额外的甲羟戊酸途径和 ABA 生物合成编码基因的拷贝数,并表达了植物 ABA 转运蛋白,使改良菌株产生了 263.5 mg/L 和 9.1 mg/g 干细胞重量(DCW)的 ABA。生物反应器培养产生了 12.8 mg/g DCW ABA 的特异性产率;然而,令人惊讶的是,生物反应器中获得的生物量水平仅为 10.5 g DCW/L,ABA 的滴度为 133.6 mg/L。虽然需要进一步优化,但本研究证实 Y. lipolytica 是 ABA 生产的潜在替代宿主。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6862/8992728/aec31f67a891/foac015fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6862/8992728/21b2efb1433b/foac015fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6862/8992728/078e218ef44c/foac015fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6862/8992728/ee6116c0d82f/foac015fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6862/8992728/ac8613bb3d23/foac015fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6862/8992728/aec31f67a891/foac015fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6862/8992728/21b2efb1433b/foac015fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6862/8992728/078e218ef44c/foac015fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6862/8992728/ee6116c0d82f/foac015fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6862/8992728/ac8613bb3d23/foac015fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6862/8992728/aec31f67a891/foac015fig5.jpg

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