Abstract

BackgroundPhenylpropanoids represent a diverse class of industrially important secondary metabolites, synthesized in plants from phenylalanine and tyrosine. Cyanobacteria have a great potential for sustainable production of phenylpropanoids directly from CO2, due to their photosynthetic lifestyle with a fast growth compared to plants and the ease of generating genetically engineered strains. This study focuses on photosynthetic production of the starting compounds of the phenylpropanoid pathway, trans-cinnamic acid and p-coumaric acid, in the unicellular cyanobacterium Synechocystis sp. PCC 6803 (Synechocystis).ResultsA selected set of phenylalanine ammonia lyase (PAL) enzymes from different organisms was overexpressed in Synechocystis, and the productivities of the resulting strains compared. To further improve the titer of target compounds, we evaluated the use of stronger expression cassettes for increasing PAL protein levels, as well as knock-out of the laccase gene slr1573, as this was previously reported to prevent degradation of the target compounds in the cell. Finally, to investigate the effect of growth conditions on the production of trans-cinnamic and p-coumaric acids from Synechocystis, cultivation conditions promoting rapid, high density growth were tested. Comparing the different PALs, the highest specific titer was achieved for the strain AtC, expressing PAL from Arabidopsis thaliana. A subsequent increase of protein level did not improve the productivity. Production of target compounds in strains where the slr1573 laccase had been knocked out was found to be lower compared to strains with wild type background, and the Δslr1573 strains exhibited a strong phenotype of slower growth rate and lower pigment content. Application of a high-density cultivation system for the growth of production strains allowed reaching the highest total titers of trans-cinnamic and p-coumaric acids reported so far, at around 0.8 and 0.4 g L−1, respectively, after 4 days.ConclusionsProduction of trans-cinnamic acid, unlike that of p-coumaric acid, is not limited by the protein level of heterologously expressed PAL in Synechocystis. High density cultivation led to higher titres of both products, while knocking out slr1573 did not have a positive effect on production. This work contributes to capability of exploiting the primary metabolism of cyanobacteria for sustainable production of plant phenylpropanoids.

Highlights

  • Phenylpropanoids represent a diverse class of industrially important secondary metabolites, synthesized in plants from phenylalanine and tyrosine

  • We searched the literature for available kinetic data on purified phenylalanine ammonia lyase (PAL) proteins, and from available data choose a set of genes with different origins and characteristics

  • Selected candidates for pal genes were from two plant species, Petroselinum crispum (Pc) [34] and Arabidopsis thaliana (At) [35], and two filamentous cyanobacteria Nostoc punctiforme (Np), Anabaena variabilis (Av) [18]

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Summary

Introduction

Phenylpropanoids represent a diverse class of industrially important secondary metabolites, synthesized in plants from phenylalanine and tyrosine. Aromatic amino acids (AAA) and their derivatives phenylpropanoids, represent a large group of plant secondary metabolites that includes flavonoids, coumarins, Kukil and Lindberg Microbial Cell Factories (2022) 21:8 stilbensenes, lignols, and catechin. These compounds are widely applicable as food additives, fragrances, cosmetics, nutraceuticals, and for production of antibacterial, antitumor, antiviral drugs and other pharmaceuticals [1,2,3,4]. The pathway starts from the condensation of erythrose-4-phosphate (E4P) and phosphoenolpyruvate (PEP), derived from C­ O2 fixation in central carbon metabolism, to form the first compound in the shikimate pathway, 3-deoxy-d-arabinoheptulosonate 7-phosphate synthase (DAHP) This first step is catalyzed by the enzyme DAHP synthase. PAL and TAL are widely spread in nature, in bacteria

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