Abstract

Background3-Phenylpropanol with a pleasant odor is widely used in foods, beverages and cosmetics as a fragrance ingredient. It also acts as the precursor and reactant in pharmaceutical and chemical industries. Currently, petroleum-based manufacturing processes of 3-phenypropanol is environmentally unfriendly and unsustainable. In this study, we aim to engineer Escherichia coli as microbial cell factory for de novo production of 3-phenypropanol via retrobiosynthesis approach.ResultsAided by in silico retrobiosynthesis analysis, we designed a novel 3-phenylpropanol biosynthetic pathway extending from l-phenylalanine and comprising the phenylalanine ammonia lyase (PAL), enoate reductase (ER), aryl carboxylic acid reductase (CAR) and phosphopantetheinyl transferase (PPTase). We screened the enzymes from plants and microorganisms and reconstructed the artificial pathway for conversion of 3-phenylpropanol from l-phenylalanine. Then we conducted chromosome engineering to increase the supply of precursor l-phenylalanine and combined the upstream l-phenylalanine pathway and downstream 3-phenylpropanol pathway. Finally, we regulated the metabolic pathway strength and optimized fermentation conditions. As a consequence, metabolically engineered E. coli strain produced 847.97 mg/L of 3-phenypropanol at 24 h using glucose-glycerol mixture as co-carbon source.ConclusionsWe successfully developed an artificial 3-phenylpropanol pathway based on retrobiosynthesis approach, and highest titer of 3-phenylpropanol was achieved in E. coli via systems metabolic engineering strategies including enzyme sources variety, chromosome engineering, metabolic strength balancing and fermentation optimization. This work provides an engineered strain with industrial potential for production of 3-phenylpropanol, and the strategies applied here could be practical for bioengineers to design and reconstruct the microbial cell factory for high valuable chemicals.

Highlights

  • ObjectivesWe aim to engineer Escherichia coli as microbial cell factory for de novo production of 3-phenypropanol via retrobio‐ synthesis approach

  • Using RetroPath 2.0 [33], an automated retrosynthesis workflow, we predicted potential pathways based on enormous amount of generative reactions in public databases [34], and two potential pathways were generated extending from the native l-phenylalanine metabolism in E. coli (Fig. 2, pathways I and II)

  • The results indicated that the endogenous alcohol dehydrogenases (ADHs) or aldo–keto reductases (AKRs) actively worked as previous reports [13, 43] and that the enoate reductase (ER), carboxylic acid reductase (CAR) and phosphopantetheinyl transferase (PPTase) were essential for biosynthesis of 3-phenylpropanol when they were expressed in E. coli

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Summary

Objectives

We aim to engineer Escherichia coli as microbial cell factory for de novo production of 3-phenypropanol via retrobio‐ synthesis approach. Retrobiosynthetic design of 3‐phenylpropanol biosynthetic pathway Due to the lack of characterization for the natural pathway in plants and limited knowledge on established pathway for 3-phenylpropanol biosynthesis, we aimed to enumerate possible 3-phenylpropanol pathways from a retrobiosynthesis viewpoint

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