Liu Changshuo, Juvonen Vilja, Meriläinen Ella, Efimova Elena, Luo Jin, Salmela Milla, Santala Suvi, Santala Ville
Faculty of Engineering and Natural Sciences, Tampere University, Hervanta Campus, PO Box 527, Tampere, FI-33014, Finland.
Microb Cell Fact. 2025 Jul 2;24(1):150. doi: 10.1186/s12934-025-02780-3.
,-muconic acid (ccMA), an important platform chemical, can be produced from lignin related molecules (LRM) via a specific two-branch catabolic route known as the β-ketoadipate pathway, which is present in certain soil bacteria. This pathway enables high production yields because ccMA is a native intermediate in one of its branches. However, commonly obtained LRM, such as -coumaric and ferulic acid, are typically metabolized through the branch that lacks the ccMA intermediate. To redirect these LRM toward ccMA production, the two branches must be functionally integrated. This is usually achieved by introducing a non-native enzymatic activity, specifically protocatechuate decarboxylase (PCADC), which catalyzes the conversion of protocatechuate to catechol. Nevertheless, this conversion often represents the rate-limiting step in the production process.
Here, we established a growth-coupled selection system for screening PCADCs using the soil bacterium ADP1 as the host. In this system, cell growth depends on the in vivo performance of PCADC, thereby enabling the selection of the optimal candidate for further ccMA production. In total, five PCADC candidates were screened. AGDC1, a gallic acid decarboxylase from the yeast , was selected for production studies. In fed-batch cultivations, the engineered strain expressing AGDC1 achieved an 83% molar yield of ccMA from ferulate and -coumarate, that were found in lignin hydrolysate derived from straw.
In this study, we established a growth-based selection system for PCADCs. The outcome of the selection system was further validated in production cultivations using an engineered ADP1 strain. This study not only confirms the feasibility of AGDC1 in ccMA production in bacterial systems but also provides a practical screening system for future improvements.
The online version contains supplementary material available at 10.1186/s12934-025-02780-3.
己二酸(ccMA)是一种重要的平台化学品,可通过特定的双分支分解代谢途径从木质素相关分子(LRM)中产生,该途径称为β-酮己二酸途径,存在于某些土壤细菌中。由于ccMA是其一个分支中的天然中间体,因此该途径能够实现高产率。然而,常见的LRM,如对香豆酸和阿魏酸,通常通过缺乏ccMA中间体的分支进行代谢。为了将这些LRM重定向用于ccMA生产,必须对这两个分支进行功能整合。这通常通过引入非天然酶活性,特别是原儿茶酸脱羧酶(PCADC)来实现,该酶催化原儿茶酸转化为儿茶酚。然而,这种转化通常是生产过程中的限速步骤。
在这里,我们建立了一种生长偶联选择系统,以土壤细菌ADP1为宿主筛选PCADC。在该系统中,细胞生长取决于PCADC的体内性能,从而能够选择用于进一步ccMA生产的最佳候选物。总共筛选了五个PCADC候选物。选择了来自酵母的没食子酸脱羧酶AGDC1进行生产研究。在补料分批培养中,表达AGDC1的工程菌株从木质素水解产物中发现的阿魏酸和对香豆酸中获得了83%的ccMA摩尔产率。
在本研究中,我们建立了一种基于生长的PCADC选择系统。选择系统的结果在使用工程化ADP1菌株的生产培养中得到了进一步验证。本研究不仅证实了AGDC1在细菌系统中生产ccMA的可行性,还为未来的改进提供了一个实用的筛选系统。
在线版本包含可在10.1186/s12934-025-02780-3获取的补充材料。