Li Xiaowei, Wang Yanyan, Chen Xin, Eisentraut Leon, Zhan Chunjun, Nielsen Jens, Chen Yun
Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, China.
Department of Life Sciences, Chalmers University of Technology, Gothenburg, Sweden.
Nat Commun. 2025 May 16;16(1):4551. doi: 10.1038/s41467-025-59966-x.
The tightly regulated central carbon metabolism in Saccharomyces cerevisiae, intricately linked to carbon sources utilized, poses a significant challenge to engineering efforts aimed at increasing the flux through its different pathways. Here, we present a modular deregulation strategy that enables high conversion rates of xylose through the central carbon metabolism. Specifically, employing a multifaceted approach encompassing five different engineering strategies-promoter engineering, transcription factor manipulation, biosensor construction, introduction of heterologous enzymes, and expression of mutant enzymes we engineer different modules of the central carbon metabolism at both the genetic and enzymatic levels. This leads to an enhanced conversion rate of xylose into acetyl-CoA-derived products, with 3-hydroxypropionic acid (3-HP) serving as a representative case in this study. By implementing a combination of these approaches, the developed yeast strain demonstrates a remarkable enhancement in 3-HP productivity, achieving a 4.7-fold increase when compared to our initially optimized 3-HP producing strain grown on xylose as carbon source. These results illustrate that the rational engineering of yeast central metabolism is a viable approach for boosting the metabolic flux towards acetyl-CoA-derived products on a non-glucose carbon source.
酿酒酵母中受到严格调控的中心碳代谢与所利用的碳源紧密相连,这给旨在增加其不同途径通量的工程改造工作带来了重大挑战。在此,我们提出了一种模块化的去调控策略,该策略能够通过中心碳代谢实现木糖的高转化率。具体而言,我们采用了一种多方面的方法,涵盖五种不同的工程策略——启动子工程、转录因子操纵、生物传感器构建、异源酶的引入以及突变酶的表达,在遗传和酶促水平上对中心碳代谢的不同模块进行工程改造。这导致木糖向乙酰辅酶A衍生产物的转化率提高,在本研究中3-羟基丙酸(3-HP)作为一个代表性例子。通过实施这些方法的组合,所构建的酵母菌株在3-HP产量上表现出显著提高,与我们最初优化的以木糖为碳源生长的3-HP生产菌株相比,产量提高了4.7倍。这些结果表明,对酵母中心代谢进行合理工程改造是一种可行的方法,可用于提高在非葡萄糖碳源上向乙酰辅酶A衍生产物的代谢通量。