Tan Shih-I, Ng I-Son, Zhao Huimin
Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana Champaign, Champaign, Illinois, USA.
Department of Chemical Engineering, National Cheng Kung University, Tainan, Taiwan.
Biotechnol Bioeng. 2025 Feb;122(2):415-423. doi: 10.1002/bit.28877. Epub 2024 Nov 6.
Biological production of 5-aminolevulinic acid (5-ALA) has received growing attention over the years. However, there is the tradeoff between 5-ALA biosynthesis and cell growth because the fermentation broth will become acidic due to the production of 5-ALA. To address this limitation, we engineered an acid-tolerant yeast, Issatchenkia orientalis SD108, for 5-ALA production. We first discovered that the cell growth rate of I. orientalis SD108 was boosted by 5-ALA and its endogenous ALA synthetase (ALAS) showed higher activity than those homologs from other yeasts. The titer of 5-ALA was improved from 28 mg/L to 120-, 150-, and 300 mg/L, by optimizing plasmid design, overexpressing a transporter, and increasing gene copy number, respectively. After redirecting the metabolic flux using the pyruvate decarboxylase (PDC) knockout strain (SD108ΔPDC) and culturing with urea, we increased the titer of 5-ALA to 510 mg/L, a 13-fold enhancement, proving the importance of the newly identified IoALAS with higher activity and the strategic selection of nitrogen sources for knockout strains. This study demonstrates the acid-tolerant I. orientalis SD108ΔPDC has a high potential for 5-ALA production at a large scale in the future.
多年来,5-氨基乙酰丙酸(5-ALA)的生物生产受到了越来越多的关注。然而,5-ALA生物合成与细胞生长之间存在权衡,因为5-ALA的产生会使发酵液变酸。为了解决这一限制,我们构建了一种耐酸酵母东方伊萨酵母SD108用于生产5-ALA。我们首先发现5-ALA可提高东方伊萨酵母SD108的细胞生长速率,并且其内源的ALA合成酶(ALAS)比其他酵母的同源酶具有更高的活性。通过优化质粒设计、过表达一种转运蛋白以及增加基因拷贝数,5-ALA的产量分别从28 mg/L提高到了120 mg/L、150 mg/L和300 mg/L。在使用丙酮酸脱羧酶(PDC)基因敲除菌株(SD108ΔPDC)重定向代谢通量并使用尿素培养后,我们将5-ALA的产量提高到了510 mg/L,提高了13倍,证明了新鉴定的具有更高活性的东方伊萨酵母ALAS(IoALAS)以及为基因敲除菌株战略性选择氮源的重要性。本研究表明,耐酸的东方伊萨酵母SD108ΔPDC在未来大规模生产5-ALA方面具有很高的潜力。