Engineering of 1,4-Butanediol and Adipic Acid Metabolism in Pseudomonas taiwanensis for Upcycling to Aromatic Compounds

IF 5.2 2区 生物学
Leonie Op de Hipt, Yannic S. Ackermann, Hannah de Jong, Tino Polen, Benedikt Wynands, Nick Wierckx
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引用次数: 0

Abstract

The overwhelming amount of plastic produced is an unprecedented challenge for humanity due to the lack of end-of-life solutions for heterogeneous plastic wastes. One possibility is feedstock recycling of mixed plastics and complex polymers with subsequent biological funnelling and upcycling. Major depolymerisation products of common plastics such as polyurethanes, polyesters and polyamides include aliphatic dicarboxylic acids or diols such as adipic acid (AA) and 1,4-butanediol (BDO), which can be metabolised by engineered Pseudomonas putida strains. However, the spectrum of upcycled compounds that can be produced from these monomers is still limited. Therefore, we extended the substrate spectrum of an aromatics-overproducing Pseudomonas taiwanensis strain to AA and BDO. Adaptive laboratory evolution (ALE) followed by genome sequencing was used to identify and reverse engineer key growth-enabling mutations. In this context, we observed a conflict between the dual objectives of fast growth on AA and efficient aromatics production, which materialised in the form of mutations in the ribosomal protein-encoding gene rpmE. These mutations promote faster growth on AA at the cost of aromatics production. In contrast to P. putida KT2440, knockout of the repressor gene psrA regulating expression of genes involved in β-oxidation had no positive effect on growth of P. taiwanensis on AA. Evolution for growth on BDO revealed several point mutations that affect expression of multiple oxidoreductases, with an identified key role for the dehydrogenase encoded by PVLB_10545. This dehydrogenase likely catalyses the initial oxidation of BDO, thus substituting for PedE, which is present in P. putida but absent in P. taiwanensis. Integration of RpcTAL into the Tn7 site enabled de novo production of 4-coumarate with a yield of 14.4% ± 0.1% (Cmol/Cmol) from BDO and 11.5% ± 0.3% (Cmol/Cmol) from AA. Thereby, the potential of these P. taiwanensis strains for upcycling plastic hydrolysates to value-added compounds was successfully demonstrated.

Abstract Image

Abstract Image

台湾假单胞菌对1,4-丁二醇和己二酸的代谢工程
由于缺乏对异质塑料废物的报废解决方案,大量生产的塑料对人类来说是一个前所未有的挑战。一种可能性是混合塑料和复杂聚合物的原料回收,随后进行生物漏斗和升级回收。常见塑料(如聚氨酯、聚酯和聚酰胺)的主要解聚产物包括脂肪族二羧酸或二醇,如己二酸(AA)和1,4-丁二醇(BDO),它们可以被工程恶臭假单胞菌菌株代谢。然而,可以从这些单体中产生的升级循环化合物的光谱仍然有限。因此,我们将过量产生芳香的台湾假单胞菌的底物光谱扩展到AA和BDO。适应性实验室进化(ALE)和基因组测序被用于鉴定和逆向工程关键的生长促进突变。在这种情况下,我们观察到AA快速生长和高效芳烃生产的双重目标之间的冲突,这以核糖体蛋白编码基因rpmE突变的形式实现。这些突变促进了AA上更快的生长,以牺牲芳香烃的产生为代价。与恶臭p.p . putida KT2440相比,敲除调节β-氧化相关基因表达的抑制基因psrA对台湾p.p . ensis在AA上的生长没有积极影响。BDO的生长进化揭示了几个影响多种氧化还原酶表达的点突变,其中PVLB_10545编码的脱氢酶发挥了关键作用。这种脱氢酶可能催化了BDO的初始氧化,从而取代了蜈蚣藻中存在但在台湾蜈蚣藻中不存在的蜈蚣藻。将RpcTAL整合到Tn7位点后,BDO和AA的产率分别为14.4%±0.1% (Cmol/Cmol)和11.5%±0.3% (Cmol/Cmol)。因此,这些台湾p.s ainensis菌株将塑料水解物升级为增值化合物的潜力已被成功证明。
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来源期刊
Microbial Biotechnology
Microbial Biotechnology Immunology and Microbiology-Applied Microbiology and Biotechnology
CiteScore
11.20
自引率
3.50%
发文量
162
审稿时长
1 months
期刊介绍: Microbial Biotechnology publishes papers of original research reporting significant advances in any aspect of microbial applications, including, but not limited to biotechnologies related to: Green chemistry; Primary metabolites; Food, beverages and supplements; Secondary metabolites and natural products; Pharmaceuticals; Diagnostics; Agriculture; Bioenergy; Biomining, including oil recovery and processing; Bioremediation; Biopolymers, biomaterials; Bionanotechnology; Biosurfactants and bioemulsifiers; Compatible solutes and bioprotectants; Biosensors, monitoring systems, quantitative microbial risk assessment; Technology development; Protein engineering; Functional genomics; Metabolic engineering; Metabolic design; Systems analysis, modelling; Process engineering; Biologically-based analytical methods; Microbially-based strategies in public health; Microbially-based strategies to influence global processes
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