Rational Engineering of Phenylalanine Accumulation in Pseudomonas taiwanensis to Enable High-Yield Production of Trans-Cinnamate

Microbial biocatalysis represents a promising alternative for the production of a variety of aromatic chemicals, where microorganisms are engineered to convert a renewable feedstock under mild production conditions into a valuable chemical building block. This study describes the rational engineering of the solvent-tolerant bacterium Pseudomonas taiwanensis VLB120 toward accumulation of L-phenylalanine and its conversion into the chemical building block t-cinnamate. We recently reported rational engineering of Pseudomonas toward L-tyrosine accumulation by the insertion of genetic modifications that allow both enhanced flux and prevent aromatics degradation. Building on this knowledge, three genes encoding for enzymes involved in the degradation of L-phenylalanine were deleted to allow accumulation of 2.6 mM of L-phenylalanine from 20 mM glucose. The amino acid was subsequently converted into the aromatic model compound t-cinnamate by the expression of a phenylalanine ammonia-lyase (PAL) from Arabidopsis thaliana. The engineered strains produced t-cinnamate with yields of 23 and 39% Cmol Cmol−1 from glucose and glycerol, respectively. Yields were improved up to 48% Cmol Cmol−1 from glycerol when two enzymes involved in the shikimate pathway were additionally overexpressed, however with negative impact on strain performance and reproducibility. Production titers were increased in fed-batch fermentations, in which 33.5 mM t-cinnamate were produced solely from glycerol, in a mineral medium without additional complex supplements. The aspect of product toxicity was targeted by the utilization of a streamlined, genome-reduced strain, which improves upon the already high tolerance of P. taiwanensis VLB120 toward t-cinnamate.


INTRODUCTION
Trans-cinnamate is an aromatic compound naturally occurring in plants, where it serves as central intermediate for the biosynthesis of a large number of substances, including coumarins, flavonoids, and phenylpropanoids (Chemler and Koffas, 2008;Vogt, 2010). It is widely used in industry for flavoring, pharmaceuticals, and cosmetics (Fausta et al., 1999;De et al., 2011;Vargas-Tah and Gosset, 2015) and can serve as precursor for bio-based drop-in chemicals such as styrene (McKenna and Nielsen, 2011) or for value-added chemicals such as the stilbene pinosylvin (van Summeren-Wesenhagen and Marienhagen, 2015). Commercial production currently happens from petroleum-based, non-renewable feedstocks in processes that demand high amounts of energy and release toxic by-products (Bruckner, 2010;Tietze et al., 2015). This comes along with increasing apprehension on global climate change and depleting aromatic fossil resources. Hence, there are both environmental and economic drivers for alternative synthesis routes.
Microbial production by whole-cell biocatalysis represents a less environmentally demanding alternative to the common and well-established petrochemical processes (Hatti-Kaul et al., 2007;Becker and Wittmann, 2012;Cho et al., 2015;Kallscheuer et al., 2019). Herein, microbes can be supplied with renewable feedstocks (e.g., glucose, glycerol, or lignin, Kohlstedt et al., 2018;Johnson et al., 2019), and metabolic conversion enables the synthesis of diverse products under mild production conditions, either via native enzymes (Hosseinpour Tehrani et al., 2019) or by heterologous expression of foreign genes (Kallscheuer et al., 2019). In plants, t-cinnamate is formed through deamination of the amino acid L-phenylalanine by phenylalanine ammonialyase (PAL) (Cochrane et al., 2004;Huang et al., 2010), and can be further converted into the cis-isoform by photoisomerization (Salum and Erra-Balsells, 2013). While only the trans-isoform is involved in biosynthesis pathways in plants (Salum and Erra-Balsells, 2013), cis-cinnamate displays higher anti-bacterial activities (Chen et al., 2011). The heterologous synthesis of this enzyme in various microorganisms, including Escherichia coli Bang et al., 2018) or Streptomyces lividans (Noda et al., 2011) enabled t-cinnamate production. Product toxicity is a limiting factor for the efficiency of many microbial production process with these hosts (McKenna and Nielsen, 2011). From a biochemical engineering perspective, it is important to "begin with the end in mind" when developing microbial production strains (Straathof et al., 2019), and product toxicity is one important aspect for this.
Bacteria of the genus Pseudomonas are considered as promising alternative host to produce aromatics such as t-cinnamate. Their robust growth behavior and metabolic versatility recently enabled the synthesis of many different industrially relevant compounds, including a variety of aromatics (Nijkamp et al., 2007;Kuepper et al., 2015;Wynands et al., 2018), rhamnolipids (Tiso et al., 2017), terpenes (Mi et al., 2014), or prodiginines (Domröse et al., 2015). This is in particular due to their high stress tolerance, which has been extensively investigated in the past (Kusumawardhani et al., 2018). Pseudomonads are able to thrive under both endogenous and exogenous oxidative stress, enabled by their particular central carbon metabolism architecture (Chavarría et al., 2013;Nikel et al., 2015). Furthermore, they are equipped with a variety of native tolerance mechanisms that allow growth in the presence of highly toxic compounds (Sardessai and Bhosle, 2002;Segura et al., 2012). For this, Pseudomonads are able to adapt the composition of the inner and outer membrane to lower the permeability for substrates and they can increase their production of energy to fuel energy-consuming tolerance mechanisms (Isken and de Bont, 1998;Ramos et al., 2002;Belda et al., 2016). Some strains of Pseudomonas additionally express solvent efflux pumps that can actively extrude toxic compounds from the inner membrane (Kieboom et al., 1998) and degrade solvents such as toluene (Ramos et al., 2002) or styrene (Velasco et al., 1998). Additional transporters confer higher resistance to further aromatic molecules like p-hydroxybenzoate or pcoumarate (Verhoef et al., 2010;Calero et al., 2018). The native capabilities of Pseudomonas species thus form a strong basis for a biocatalytic process for t-cinnamate synthesis by expanding process options due to reduced product toxicity.
To further exploit its potential as industrial production strain, we recently enhanced the bioprocess features of the solventtolerant strain Pseudomonas taiwanensis VLB120 by successive feature reduction . The deletion of redundant genomic elements such as proviral segments, genes for biofilm formation and flagella expression and the megaplasmid pSTY resulted in strains with 15% enhanced growth rates and increased biomass yields, thereby improving the overall performance of the strain under bioprocess conditions. In addition, genes encoding for the efflux pump TtgGHI located on the pSTY plasmid were re-integrated into the chromosome of the genome-reduced chassis (GRC) strains to maintain tolerance enabled by this efflux pump. These modifications, in combination with inherent tolerance traits, make the engineered strains promising hosts to efficiently synthesize aromatic compounds like t-cinnamate, as well as potential hydrophobic derivatives such as styrene or stilbenes.
The potential of Pseudomonas species for t-cinnamate production has been demonstrated in a strain of P. putida S12 by the expression of PAL from Rhodosporidium toruloides (Nijkamp et al., 2005). Here, enhanced precursor supply was realized by mutagenesis and subsequent selection on the toxic analog m-fluoro-phenylalanine, leading to the production of 5 mM tcinnamate with a yield of 6.7% Cmol Cmol −1 . However, although genomic analysis of this strain provided leads to enhance the flux through the shikimate pathway in P. taiwanensis VLB120 , the genetic rearrangements enabling the enhanced flux specifically toward L-phenylalanine have not been determined. We recently reported a study on phenol production from L-tyrosine in P. taiwanensis VLB120, where 22 mutations in 50 different strains delivered a comprehensive insight on the rational engineering of L-tyrosine accumulation . In the most productive strain, five genes involved in the degradation of aromatic intermediates and the gene pykA were deleted to increase the precursor supply for the synthesis of aromatic amino acids. The flux through the shikimate pathway was further enhanced by genomic modifications of genes at their native chromosomal locus resulting in a strain able to accumulate up to 2.8 mM of L-tyrosine from 20 mM glucose.
The aim of this study was to build on this knowledge to redirect the enhanced flux to L-tyrosine in P. taiwanensis GRC3 5 pykA-tap (Wynands, 2018) toward L-phenylalanine, given the close relation of their biosynthesis pathways, and thereby expanding the potential product range. Furthermore, the superior tolerance of the streamlined P. taiwanensis GRC toward high concentrations of t-cinnamate was assessed. Routes involved in L-phenylalanine degradation were deleted, leading to L-phenylalanine accumulation. Titers were further increased by an additional overexpression of feedback-resistant versions of the bottleneck enzymes AroG and PheA. Heterologous expression of a PAL from Arabidopsis thaliana in the engineered strains then enabled the production of t-cinnamate. In a completely minimal medium, the plasmid-free chassis strains produced up to 6.3 mM of t-cinnamate from glycerol, which corresponds to a yield of 48% Cmol Cmol −1 . Cultivation in fed-batch fermentations resulted in titers of around 33.5 mM, which is the highest reported titer of microbially produced t-cinnamate in a cultivation medium without complex supplements. The engineered strains can further serve as efficient platform to produce various products from L-phenylalanine and t-cinnamate, including styrene, benzoate, or plant polyphenols such as pinosylvin.

Bacterial Strains, Plasmids, and Cultivation Conditions
Strains and plasmids used in this study can be found in Tables 1, 2. For cloning purposes, E. coli and Pseudomonas cells were cultivated at 37 or 30 • C, respectively, either in liquid LB medium containing 5 g L −1 sodium chloride or on solid LB agar plates [additionally containing 1.5% (w/v) agar]. After tri-or four-parental mating procedures, Pseudomonads were isolated on cetrimide agar (Sigma Aldrich) plates supplemented with 10 mL L −1 glycerol. Kanamycin (50 µg mL −1 ) or gentamicin (20 µg mL −1 ) was added to cultures or plates when necessary.
During production and toxicity experiments in shake flasks and well plates, liquid cultures of P. taiwanensis were grown in mineral salt medium (MSM) adapted from Hartmans et al. (1989) at pH 7.0 without the addition of antibiotics. The medium's standard phosphate buffer capacity was increased to 5-fold (111.5 mM K 2 HPO 4 and 68 mM NaH 2 PO 4 ). Glucose or glycerol were added as sole carbon source at indicated concentrations. Main cultures were inoculated at an OD 600 of 0.2, from seed cultures grown in MSM containing glucose as carbon source. Production experiments were performed in 500 mL Erlenmeyer flasks with a culture volume of 50 mL, which were cultivated in a rotary shaker with a frequency of 200 rpm and a throw of 50 mm. Toxicity assays were performed in 96-round low-well plates with a filling volume of 200 µL in the System Duetz R cultivation system (EnzyScreen, Leiden, Netherlands) with a shaking frequency of 225 rpm. OD 600 values were calculated from the measured green values using a calibration. Phenylalanine accumulation was analyzed in 24-square deep-well plates with a filling volume of 5 mL and a shaking frequency of 225 rpm, and growth was monitored in the Growth profiler R system.

Plasmid Construction and Genomic Modification
For plasmid construction, DNA fragments were PCR amplified using the Q5 high-fidelity polymerase (New England Biolabs, New Ipswich, USA) with corresponding overhangs to enable subsequent Gibson assembly (Gibson et al., 2009) with the HiFi DNA assembly master mix (New England Biolabs, New Ipswich, USA). Primers were ordered from Eurofins Genomics (Ebersberg, Germany). The gene sequences for aroG fbr (from E. coli K12 W3110) and AtPAL (from A. thaliana) were codonoptimized for P. taiwanensis VLB120 using the online tool OPTIMIZER (Puigbo et al., 2007) and ordered as synthetic DNA fragments from Thermo Fisher Scientific (Waltham, USA). The gene pheA T310I was amplified from genomic DNA of strain P. putida S12palM12. pEMG-based plasmids were transformed into E. coli DH5α λpir cells, pBG-based plasmids were transformed into E. coli PIR2. Correct plasmid assembly was verified by Sanger sequencing performed by Eurofins Genomics (Ebersberg, Germany). Integration at the attTn7-site was achieved by patch-mating of the E. coli donor strain holding the respective pBG-plasmid, the helper strain E. coli HB101 pRK2013, DH5α λpir pTNS1 providing the required transposase and the recipient Pseudomonas taiwanensis strain as described by Wynands et al. (2018). After the mating procedure, Pseudomonas were isolated on Cetrimide agar containing gentamicin and correct integration was confirmed by colony PCR using the OneTaq Quick-Load Master Mix (New England Biolabs, New Ipswich, USA).
Genomic deletions and point mutations were realized using the I-SceI-based method developed by Martínez-García and de Lorenzo (2011) using a streamlined protocol adapted by Wynands et al. (2018). Successful deletions were verified by colony PCR using the OneTaq quick-Load Master Mix (New England Biolabs, New Ipswich, USA).

Fed-Batch in Controlled Bioreactors
Fermentations were carried out in fed-batch operation mode in DASbox R mini-bioreactors using the DASware control software (Eppendorf, Hamburg, Germany). The reactors were set up of 385 ml glass vessels, two Rushton-type impellers driven by direct overhead drives, feeding lines for acid, base, and carbon source, a temperature sensor, an EasyFerm Plus K8 120 pH-sensor (Hamilton Company, Reno, NV, USA) and an InPro R 6800 series O 2 sensor (Mettler-Toledo International Inc., Columbus, OH, USA). The starting volume was 100 mL and the temperature was maintained at 30 • C. Gas supply was provided via headspace with a starting gas flow rate of 6 sL h −1 . The initial agitation frequency was 500 rpm. The dO 2 was controlled with a cascade, keeping the concentration of diluted oxygen at 35% by first increasing the agitation speed up to 1,200 rpm, then increasing the oxygen concentration in the air supply to a maximum of 80% and subsequently increasing the gas flow rate. pH 7 was maintained by automatic addition of 5% NH 3 or 1 M H 2 SO 4 . Cells were grown in MSM according to Hartmans et al. (1989), where the addition of mineral salts stock was increased by 2-fold (MgCl 2 .6H 2 O 0.2 g L −1 , ZnSO 4 .7H 2 O 0.004 g L −1 , CaCl 2 .2H 2 O 0.002 g L −1 , FeSO 4 .7H 2 O 0.01 g L −1 , Na 2 MoO 4 .2H 2 O 0.0004 g L −1 , CuSO 4 .5H 2 O 0.0004 g L −1 , CoCl 2 .6H 2 O 0.0008 g L −1 , MnCL 2 .2H 2 O 0.002 g L −1 ). The initial batch medium contained either 20 mM of glucose or 40 mM of glycerol as sole carbon source. The reactors were operated in a dO 2 -controlled fed-batch mode. When glucose or glycerol was depleted, the dO 2 signal rapidly increased as a result of metabolic arrest. A dO 2 signal >70 triggered a feed pump, resulting in a feed shot of 5 mM of glucose or 10 mM of glycerol per trigger initiation.

Analytical Methods
Optical densities of liquid cultures were measured at 600 nm using an Ultrospec 10 Cell Density Meter (GE Healthcare, Illinois, USA). Samples taken from the cultures were centrifuged at 13,000 rpm for 2-5 min and the supernatant was analyzed by HPLC. Aromatics quantification was performed using a Beckman System Gold 126 Solvent Module with a 168 diode 201 array detector (Beckman Coulter, Brea, USA) and an ISAspher 100-5 C18 BDS reversed-phase 202 column (ISERA, Düren, Germany) at 30 • C and a flow rate of 0.8 mL min −1 . Elution took place with a gradient starting at 90% H 2 O containing 0.1% (v/v) TFA and 10% methanol. This ratio was held for 2 min, followed by gradual increase to 100% methanol over the course of 8 min. After 2 min at 100% methanol, initial ratios were reached again within 1 min and held constant for further 2 min. UV detection was conducted at a wavelength of 245 nm. L-phenylalanine and L-tyrosine quantification shown in Figure 3 was performed with the same column and elution setup as mentioned before, in a Dionex Ultimate 3000 HPLC system, where detection took place with a Corona Veo charged aerosol detector (Thermo Fisher Scientific, Waltham, MA, USA). Glucose, gluconate and glycerol analysis was performed using a Beckman System Gold 126 Solvent Module with a System Gold 166 UV-detector (Beckman Coulter, Brea, USA) and Smartline RI Detector 2300 (KNAUER, Berlin, Germany) on a MetabAAC column (ISERA, Düren, Germany). Elution took place with 5 mM H 2 SO 4 at an isocratic flow of 0.5 mL min −1 and a temperature of 30 • C for 20 min. Glucose and glycerol were analyzed using the RI detector, gluconate concentrations were determined with the UV detector at a wavelength of 210 nm. Due to co-elution of glucose and gluconate, glucose concentrations were determined by subtraction of the gluconate concentration.
These problems can be avoided by the utilization of robust, natively stress-resistant host strains such as Pseudomonas taiwanensis VLB120. As shown in Figure 1A, the wildtype can grow in the presence of 30 mM (4.4 g L −1 ) t-cinnamate in MSM with a rate of 0.24 ± 0.01 h −1 . P. taiwanensis VLB120 is equipped with particular mechanisms that enable this superior tolerance toward a variety of toxic compounds. While RNDtype efflux pumps mainly act on hydrophobic aromatic solvents and a number of antibiotics (Terán et al., 2003;Köhler et al., 2013;Volmer et al., 2014), an ABC transporter (Ttg2ABC) was recently identified as crucial for p-coumarate tolerance, the hydroxylated derivative of t-cinnamate (Calero et al., 2018). Furthermore, chaperone upregulation is observed as response to protein misfolding (Segura et al., 2012).
To further exploit the native potential of P. taiwanensis VLB120 as microbial cell factory, we recently engineered a genome-reduced variant of this strain which exhibited higher growth rates and enhanced biomass formation . The benefit of genome reduction for potential aromatics production strains is underlined by the tolerance test in the presence of 30 mM t-cinnamate ( Figure 1A). The streamlined strains GRC1 and GRC3 had a reduced lag phase in the presence of high t-cinnamate concentrations, while the growth rate remains similar to the wildtype. In addition, the GRC strains reached higher final OD 600 values compared to the wildtype. This is particularly important to improve the efficiency of a microbial production process by reducing the overall process time and lowering the amount of substrate needed to generated and maintain the biomass. The only exception is strain P. taiwanensis GRC2, which grew slower and with a longer lag phase than the wildtype. In contrast to GRC1 and 3, GRC2 constitutively expresses ttgGHI genes that encode a solvent-efflux pump. Although this constitutive expression greatly increases the fitness of GRC2 in the presence of hydrophobic solvents such as toluene, it causes a fitness reduction in the absence of solvents . This drawback is absent in the other two strains, where the whole ttg operon is absent (GRC1), or the regulatory genes ttgVW are included to induce the pump in response to solvents (GRC3). The similar performance of GRC1 and GRC3 in the presence of t-cinnamate indicates that this aromatic acid does not induce expression of the ttgGHI, nor does the TtgGHI pump contribute to cinnamate tolerance. Given this similar performance, and in light of the potential to use a t-cinnamate-producing strain as platform for a variety of further industrially relevant hydrophobic aromatics, the strain GRC3 was chosen as host to maintain the possibility of solvent efflux by TtgGHI. As shown in Figure 1B, P. taiwanensis GRC3 can grow in the presence of t-cinnamate concentrations of up to 50 mM (7.4 g L −1 ), which is 10-fold higher than MIC for E. coli. The native tolerance potential of P. taiwanensis VLB120 in combination with improved bioprocess features obtained by streamlining of this strain hence set an ideal starting point for an efficient microbial production process of t-cinnamate.
pyruvate, thereby increasing the precursor pool for the shikimate pathway. An introduction of these mutations in the genomereduced strains of P. taiwanensis VLB120 led to the efficient production of phenol from L-tyrosine . As shown in Figure 3, the strain P. taiwanensis GRC3 5 pykAtap accumulates 2.85 ± 0.02 mM of tyrosine from 20 mM of glucose, which is comparable to the non-genome-reduced strain. Three genes involved in phenylalanine catabolism were subsequently deleted from the chromosome of P. taiwanensis GRC3 5 pykA-tap: (i) phhAB encoding for phenylalanine-4-monooxygenase involved in the conversion of phenylalanine to tyrosine (Herrera et al., 2010), (ii) PVLB_10925, putatively encoding an aromatic-L-amino-acid decarboxylase responsible for the decarboxylation into phenylethylamine, and (iii) katG, putatively coding for a catalase-peroxidase which converts phenylalanine into phenyl acetamide (Figure 2).
Pseudomonads possess a variety of transporters that allow export and import of aromatic amino acids. Transcriptome analysis of a Pseudomonas putida strain with increased flux toward tyrosine revealed that upon increased intracellular aromatic amino acid levels, amino acid exporters are upregulated, while uptake systems are downregulated (Wierckx et al., 2008). Aromatics accumulation shown in Figure 3 displays extracellular concentrations, indicating enhanced efflux of both tyrosine and phenylalanine.
The deletion of phhAB led to the accumulation of 2.22 ± 0.02 mM of phenylalanine and 0.29 ± 0.01 mM tyrosine after 50 h (Figure 3). This indicates that about 88% of L-tyrosine FIGURE 3 | L-phenylalanine and L-tyrosine accumulation of P. taiwanensis GRC3 5 pykA-tap and subsequent mutants with deletions to prevent L-phenylalanine degradation and additional overexpression of AroG fbr and PheA T310I . The strains were cultivated in MSM containing 20 mM glucose in a System Duetz ® shaker. Error bars represent the standard error of the mean (n = 3).
accumulating due to the enhanced flux toward prephenate in strain P. taiwanensis GRC3 5 pykA-tap is stemming from Lphenylalanine. In most microorganisms, L-phenylalanine cannot be converted into L-tyrosine in which case it is solely synthesized from prephenate (Guroff and Ito, 1965). In Pseudomonas however, the pathway via L-phenylalanine seems to be a major route for L-tyrosine formation under the given conditions (Wierckx et al., 2009). As described for other Pseudomonas species, Xanthomonads and Alcalignes (Ahmad et al., 1990), this diversity of aromatic amino acid metabolism account for the flexibility of the organism to cope with a variety of end product analogs (Fiske et al., 1983). The concentration of L-phenylalanine in the culture of P. taiwanensis GRC3 5 pykA-tap phhAB was slightly reduced after 70 h, indicating that other pathways involved in L-phenylalanine degradation were still active in this strain. The subsequent deletion of gene PVLB_10925 prevented this degradation, resulting instead in a further increase of the final titer to 2.62 ± 0.00 mM L-phenylalanine. The deletion of katG had no influence on phenylalanine accumulation and the strain shows a similar production pattern as the strain without a deletion. Indeed, as the progenitor strain P. taiwanensis GRC3 5 pykA-tap was already not able to grow on Lphenylalanine and L-tyrosine , this confirms that catabolic pathways are either not active (katG) or not connected to the central carbon metabolism (PVLB_10925) under the applied conditions, even though this strain contains the genetic inventory for the full degradation of the resulting 2phenylacetamide and phenylethylamine. This is underlined by similar observations in an L-phenylalanine overproducing strain of P. putida DOT-T1E (Molina-Santiago et al., 2016).
L-Tyrosine and L-phenylalanine production could be increased further by the additional overexpression of AroG fbr , a feedback inhibition resistant versions of the DAHP synthase from E. coli K12 W3110 (Kikuchi et al., 1997) and PheA T310I from P. putida S12palM12 (Nijkamp et al., 2005). The coding genes were integrated chromosomally at the attTn7-site and expressed under the control of the constitutive promoter P 14g (Zobel et al., 2015). Overexpression in the tyrosine-accumulating strain P. taiwanensis GRC3 5 pykA-tap led to tyrosine titers of about 3.5 ± 0.11 mM after 70 h. Transient L-phenylalanine accumulation was observed with this strain, further underlining the high flux through PhhAB. Upon overexpression of aroG fbr and pheA T310I in strains with deletions of phhAB, katG and PVLB_10925, the resulting strain GRC3 8 pykA-tap attTn7::P 14d -aroG fbr -pheA AT31I ( 8 = eight deletions of pathways involved in aromatics degradation) accumulated 3.0 ± 0.07 mM of L-phenylalanine after 70 h. Also, L-tyrosine production was reduced, likely due to PheA T310I increasing the flux of prephenate toward L-phenylalanine.

Production of t-cinnamate From Glucose and Glycerol in Shake Flasks
The L-phenylalanine-accumulating strain P. taiwanensis GRC3 8 pykA-tap was subsequently used as host for the production of t-cinnamate. The deamination of L-phenylalanine into t-cinnamate was achieved using the PAL2 enzyme from A. thaliana. While four genes encoding PAL have been identified in A. thaliana (Cochrane et al., 2004), PAL2 displayed the highest specific activity when expressed in E. coli (McKenna and Nielsen, 2011). In addition, it has no activity on L-tyrosine as a substrate, in contrast to a variety of other yeast PALs (Cui et al., 2008). As overexpression of aroG fbr and pheA T310I improved L-phenylalanine yields by 15% (Figure 3), combinatorial expression with PAL on the Tn7 transposon under the control of P 14g was applied for t-cinnamate production in the strain P. taiwanensis GRC3 8 pykA-tap attTn7::P 14g AtPAL-aroG fbr -pheA T310 . The strain was cultivated in shake flasks in MSM containing either 20 mM of glucose or 40 mM of glycerol as sole carbon source. Glycerol is a promising alternative as feedstock for microbial production processes as abundant by-product of the bio-diesel production (Zambanini et al., 2016). When cultivated on glucose, the strain accumulated 3.80 ± 0.20 mM t-cinnamate, corresponding to a yield of 25.9 ± 0.1% Cmol Cmol −1 , with a volumetric productivity of 0.10 ± 0.00 mM h −1 (Figure 4). From glycerol, the t-cinnamate titer was further increased to 6.33 ± 0.12 mM, corresponding to a yield of 47.5 ± 0.9% Cmol Cmol −1 . As observed for the production of phenol and p-hydroxybenzoate Lenzen et al., 2019), metabolism of glycerol is highly beneficial for enhanced titers and yields of compounds derived from aromatic amino acids, likely due to metabolic rearrangements favoring the supply of PEP and E4P (Nikel et al., 2014;Poblete-Castro et al., 2019). The volumetric productivity on glycerol is slightly lower compared to glucose (0.09 ± 0.01 mM h −1 ), as a result of the reduced growth rate. While this strain has a very high yield, its reliable application as a production host was problematic. When the experiment described above was repeated, the cultures displayed varying growth behavior in terms of lagphase, growth rates, and productivity ( Figure S1), even though the cultivation procedure remained identical. Re-transformation of the Tn7-transposon bearing the overexpression constructs and culturing of single colonies yielded the same unstable phenotype. Sequencing of the attTn7-regions of theses strains revealed no mutations in this sequence and verified correct integration. Likely, a combination of the extreme drain on carbon posed by the high t-cinnamate yield, the burden of heterologous overexpression of genes, and the production of a mildly toxic compound provide a strong selection for suppressor mutations. This impairs the reproducibility and renders the strain P. taiwanensis GRC3 8 pykA-tap attTn7::P 14g AtPAL-aroG fbr -pheA T310 unsuitable as reliable production host in its current form.
In contrast, P. taiwanensis GRC3 8 pykA-tap attTn7::P 14f AtPAL, harboring only the PAL for L-phenylalanine deamination under the control of the weaker P 14f promoter, showed reliable growth and production patterns. This strain still carries feedback-resistant aroF-1 P148L , pheA T310I , but only in their native context. The lack of in trans overexpression of aroG fbr and pheA T310I reduced t-cinnamate titers and yields slightly, with 3.34 ± 0.07 mM produced from glucose and 5.25 ± 0.22 mM from glycerol, which corresponds to yields of 22.8 ± 0.5 and 38.9 ± 1.6% Cmol Cmol −1 , respectively. To the best of our knowledge, these are still the highest yields of t-cinnamate produced in a microbial process using a mineral medium without the addition of complex supplements. This strain furthermore reached higher final biomass and exhibited improved volumetric productivity on glucose (0.13 ± 0.00 mM h −1 ) and glycerol (0.11 ± 0.00 mM h −1 ) compared to the strain additionally expressing aroG fbr and pheA T310I . In the course of the cultivations, no accumulation of L-phenylalanine was observed. This indicates that PAL activity is not inhibited by the concentrations of t-cinnamate reached in these cultures, in contrast to observations in other hosts and with PALs from different organisms (Nijkamp et al., 2005;McKenna and Nielsen, 2011;Molina-Santiago et al., 2016). Furthermore, no L-tyrosine accumulation was observed, in contrast to the phenylalanine-producing equivalent that does not express PAL (Figure 3), likely due to a reduction of product inhibition of the upstream metabolic enzymes as a result of efficient conversion to t-cinnamate.
FIGURE 5 | dO 2 -stat fed-batch fermentations of t-cinnamate producing strains of P. taiwanensis. Cultivations were performed in MSM, where the initial batch medium contained either glucose or glycerol as sole carbon source and the subsequent feeding solution contained solely the respective carbon source. The top graphs show growth (black lines) and t-cinnamate accumulation (blue lines) during fermentation of P. taiwanensis GRC3 8 pykA-tap attTn7::P 14g AtPAL-aroG fbr -pheA T310 on glucose (A) and glycerol (B). The glycerol figure (B) displays data of a single reactor. The bottom graphs represent growth (black lines) and t-cinnamate accumulation (green lines) during fermentation of P. taiwanensis GRC3 8 pykA-tap attTn7::P 14f AtPAL on glucose (C) and glycerol (D). The error bars represent the standard error (n = 2).

Production in Controlled Bioreactors
In order to assess higher-level t-cinnamate production under more industrially relevant conditions, the strains were cultivated in fed-batch fermentations in controlled bioreactors. The fermenters were operated in a dO 2 -stat fed-batch mode where carbon depletion and the resulting increase of the dO 2 due to metabolic arrest triggered the initiation of a pulse feed of either 5 mM glucose or 10 mM glycerol (Johnson et al., 2016(Johnson et al., , 2019. This feeding protocol allows controlled addition of carbon source throughout the whole fermentation process, independent from time-varying carbon demands of the cell, thereby preventing excess carbon surplus (Johnson et al., 2016). The resulting feeding trends of single reactors are exemplarily shown in Figure S3. Cultivation took place at pH 7 in a mineral medium without the addition of complex supplements.
Under these conditions, the strain P. taiwanensis GRC3 8 pykA-tap attTn7::P 14g AtPAL-aroG fbr -pheA T310 accumulated 17.2 ± 0.28 mM of t-cinnamate from glucose, corresponding to a yield of 11.2 ± 0.6% (Cmol Cmol −1 ) and a volumetric productivity of 0.19 ± 0.20 mM h −1 . As shown in Figure 5A, the culture reaches a final OD 600 of 12.7 after around 65 h. At this point, a decrease in biomass concentration was observed. Furthermore, there was no significant increase in t-cinnamate titers from this point on, in spite of the fact that the base strain GRC3 tolerated higher concentrations of t-cinnamate up to 50 mM (Figure 1). It is possible that several factors impact the lowered growth performance of the production strains in the presence of t-cinnamate. One factor is the overexpression of heterologous genes which leads to lowered growth rates and impaired fitness as observed in shake flask experiments (Figure 4). Especially the overexpression of AroG and PheA appears to lead to increased cellular stress, which in turn also lowers the growth performance in the presence of toxic compounds. Furthermore, experiments regarding styrene toxicity have demonstrated a crucial difference in tolerance depending on whether a compound is added exogenously to the medium or produced intracellularly (Lian et al., 2016).
Fed-batch fermentations using glycerol as carbon source further underline complications using the phenotypically unstable strain P. taiwanensis GRC3 8 pykA-tap attTn7::P 14g AtPAL-aroG fbr -pheA T310 (Figure 5B; Figure S2). During fermentations, cultures in duplicate reactors showed different growth behavior while stemming from the same preculture. The cultures showed differences in lag-phase, growth rate and productivity. The final titers remained comparable, likely as a result of product inhibition as described before. Figure 5B shows a single fermentation on glycerol as an example. Here, the strain produced up to 19.8 mM t-cinnamate, with a yield 3 | Comparison of t-cinnamate titer, yield, and volumetric productivity of strains P. taiwanensis GRC3 8 pykA-tap attTn7::P 14g AtPAL-aroG fbr -pheA T310 and GRC3 8 pykA-tap attTn7::P 14f AtPAL in shake flask cultivations and fed-batch fermentations. As observed for shake flask cultivations, reproducibility and stable production was restored in a strain overexpressing solely PAL for L-phenylalanine conversion. The strain P. taiwanensis GRC3 8 pykA-tap attTn7::P 14f AtPAL produced up to 33.2 ± 2.4 mM t-cinnamate from glucose ( Figure 5C) and 33.5 ± 2.7 mM from glycerol ( Figure 5D) in a fed-batch fermentation. While the productivity throughout the whole cultivation of P. taiwanensis GRC3 8 pykA-tap attTn7::P 14f AtPAL on glucose was 0.30 ± 0.02 mM h −1 , increasing concentrations of tcinnamate impaired the strain's fitness and productivity. The volumetric productivity within the first 25 h is 0.55 ± 0.08 mM h −1 , which is reduced after 38 h to 0.16 ± 0.04 mM h −1 . At the same time, a drop in OD 600 was observed at concentrations above 20 mM t-cinnamate. As production continued and cells were still viable at this point as indicated by the ongoing substrate consumption, this drop in OD 600 values hints toward an increased cumulative burden on the cell. The drop in OD 600 was not caused by biofilm formation, likely due to the deletion of the biofilm-associated lap genes in the GRC3 strain. Membrane adaptation is a key mechanisms of Pseudomonas to cope with environmental stress. Membrane active substances and certain environmental conditions cause adaptations such as cis-to trans-isomerization of fatty acids to increase membrane rigidity and lead to the formation of outer membrane vesicles to facilitate biofilm formation (Eberlein et al., 2018). In addition, many porins as well as import and export pumps are differentially expressed under stress, altering membrane permeability (Volkers et al., 2006;Ramos et al., 2015). The importance of membrane structure on similar compounds such as p-coumarate has recently been demonstrated (Calero et al., 2018) and can likely be partially be transferred to t-cinnamate tolerance.
As enzyme inhibition of different PALs by t-cinnamate has been observed in various studies (Nijkamp et al., 2007;McKenna and Nielsen, 2011), the decrease in productivity could also be linked to this effect. However, no L-phenylalanine accumulation was observed over the course of the fermentations, indicating that the precursor was completely converted by the PAL. Furthermore, no L-tyrosine accumulation was observed during fermentations.
In contrast to the strain overexpressing AroG fbr and PheA T310I , experiments with strain P. taiwanensis GCR3 8 pykA-tap attTn7::P 14f AtPAL are highly reproducible. While an additional expression of AroG fbr and PheA T310I led to higher yields in shake flasks, solely PAL expression in the L-phenylalanine-overproducing chassis strains enables both higher titers and volumetric productivities in fed-batch fermentations ( Table 3). To the best of our knowledge, these are the highest t-cinnamate yields reported for a microbial production process. While titers of 6.5 g L −1 (43.9 mM) have been reported in fed-batch fermentations of t-cinnamate-producing strains of E. coli (Bang et al., 2018), these processes required the addition of yeast extract in the initial batch medium and casamino acid in the feeding solution. The utilization of these engineered P. taiwanensis GRC strains enables growth without the addition of complex supplements. However, tolerance mechanisms for t-cinnamate remain to be further investigated and exploited to enhance titers and thus the feasibility of microbial t-cinnamate synthesis.

CONCLUSION
In this study, we describe the rational engineering of P. taiwanensis VLB120 towards efficient t-cinnamate production. The plasmid-free strain bearing no auxotrophies synthesized t-cinnamate from glucose or glycerol, with yields of up to 48% Cmol Cmol −1 in shake flask cultivations. Titers were increased up to 33.35 mM in fed-batch fermentations using glycerol as sole carbon source. As product titers achieved in this study impair fitness and productivity of the chassis strains, the native tolerance features of Pseudomonas allowing enhanced t-cinnamate tolerance require further investigation and enhancement to increase process efficiency. One promising target is the ABC transporter Ttg2ABC, an extrusion pump involved in p-coumarate tolerance (Calero et al., 2018). An overexpression of this pump might deliver enhanced tolerance toward t-cinnamate, its regulation however remains to be investigated. Fine-tuning of additional aroG and pheA overexpression, e.g., by using weaker or inducible promoters, could furthermore avoid the observed growth defects while still maintaining the high yields achieved with this setup. Overall, the results underline the high potential of Pseudomonas species to produce chemical building blocks using aromatic amino acids as precursors. The establishment of efficient microbial production of the model compound t-cinnamate will in future serve as foundation to expand the product collection of this versatile species, ranging from bulk chemicals such as styrene  to specialty compounds such as stilbenes (van Summeren-Wesenhagen and Marienhagen, 2015).

DATA AVAILABILITY STATEMENT
All datasets generated for this study are included in the article/Supplementary Material.

AUTHOR CONTRIBUTIONS
NW conceived and supervised the study with the help of LB. MO and MF performed the experiments with support of BW and CL. BW provided the GRC strains with deletions for L-tyrosine accumulation and deletion vectors. MO wrote the manuscript with the help of BW and NW. All authors read and approved the manuscript.

FUNDING
MO, BW, CL, and NW were funded by the German Research Foundation (DFG) through the Emmy Noether program (WI 4255/1-1).