Native LCI has been previously produced in E. coli using the signal sequence of OmpA (OmpAss), but the low yield of secreted protein and plasmid instability precluded any development requiring large-scale production 9. We decided to investigate several expression parameters in order to improve the production of LCI in the periplasm of E. coli. The gene encoding the mature LCI protein (LCI_N), as determined from the medical leech Hirudo medicinalis 9, contains 7 codons that are used at a frequency below 8 per 1000 in E. coli 11. We hypothesized that a biased codon usage might limit its expression level. Since other non-optimal codons for E. coli are also present in LCI_N, a whole synthetic coding sequence with codon usage optimized for E. coli was designed. The resulting LCI_O sequence contains 44 codon changes over the 66 codons (figure 1). Both LCI_N and LCI_O were subcloned under the control of the tightly regulated araB promoter from the pLCB vector encoding chloramphenicol resistance. This expression vector, derived from the pBAD33 plasmid 12, was constructed for achieving high cell density cultures. In a first attempt, we retained the original OmpAss to evaluate the effect of codon optimization. Next, we investigated whether the limiting expression levels were only governed by its mature sequence, and tested the production of LCI_N and LCI_O fused either to the signal sequence of DsbA (DsbAss) or MalE (MalEss), two well-studied periplasmic proteins of E. coli. We chose these signal sequences because there are known to direct co- and post-translational export of heterologous precursors through the SRP- and Sec-dependent pathways, respectively 5. Besides translocation modes, it was recently shown that a biased codon usage in signal sequences may also play a role in the coupling of translation to protein export, by slowing down the translation rate 13. Therefore, we decided to use the natural signal sequences of E. coli for targeting the various LCI precursors (preLCI) to the SecYEG translocase.

All expression vectors were transformed into the LMG194 strain in which arabinose is not catabolized because of a deletion encompassing most of the araBAD operon 12. The corresponding cells were cultured at 37°C in LB media supplemented with chloramphenicol. After 2 h of induction, LCI expression appeared to slow down cell growth progressively (figure 2). When growth stops, a higher density was achieved for cells expressing LCI fused to MalEss or DsbAss than for those expressing LCI fused to OmpAss, independent of codon optimization. This observation suggested that the physiological state of the corresponding cells could be affected. We took advantage of the carboxypeptidase inhibitory activity of LCI as a reliable indicator of active protein to detect its presence in both whole cell lysates and culture supernatants. Indeed, it was previously reported that periplasmic LCI could be released into the growth medium 9, as frequently observed for small exported proteins 14. Table 1 shows the distribution of active LCI between cells and culture supernatants determined from the six expression vectors. Cells expressing LCI fused either to DsbAss or MalEss displayed higher levels of activity than those expressing LCI with OmpAss (Table 1). If the LCI protein is unable to fold within the reductive environment of the cytoplasm 15, these data could reflect differences in the efficiency of export of the different LCI precursors (see below). However, active LCI was found in the culture supernatants when cells expressed the E. coli optimized gene, suggesting also a translational effect. To assess the steady-state production and cellular location of LCI, cells were fractionated from spheroplasts. Regardless of the signal sequence used, figure 3 shows the accumulation of large amounts of preLCI for all expression vectors. In addition, expression from LCI_opt was markedly higher than from LCI_N, consistent with increased translation rate. Nevertheless, for cells expressing LCI fused to OmpAss, little or no protein was detectable in the periplasmic fractions while preLCIs were correctly produced. This result indicated that LCI export did not occur to any significant extent when OmpAss was used, and also confirmed previous findings 9. It is noteworthy that growth of the corresponding cells was severely inhibited. The relative amounts of precursor (p) and mature (m) LCI were assessed, and export efficiency (m/p) evaluated for each expression vectors (Table 2). To ensure that all periplasmic contents were released during spheroplast preparation, we compared m/p ratios determined from whole cell extracts to those determined from subcellular fractions (Table 2). Because both values are similar, it can be concluded that: (i) a complete release of the periplasmic mature LCI had been attained, and (ii) all preLCIs remained in the soluble cytoplasmic fractions. Besides OmpAss, our results indicated that the two other preLCIs with optimized E. coli codons could give rise to a high level of periplasmic expression (figure 3C). The highest export efficiency was observed with LCI_O fused to DsbAss. Interestingly, amounts of LCI in the culture supernatants (Table 1) correlated with their levels in the corresponding periplasmic fractions, suggesting that the presence of extracellular LCI resulted from a direct leakage of the outer membrane. Although the level of LCI when fused to MalEss was somewhat lower than when fused to DsbAss, the efficient export of preLCI may require a co-translocation mode. Since pDsbALCIo seemed to be a good expression vector, we checked its stability on selection pressure. After different cultivation times, bacteria were plated onto solid LB media with and without chloramphenicol in the presence of arabinose. After overnight growth, the number of colony forming units (CFU) determined from these plates indicated no plasmid loss (see below).

The batch production of LMG194 cells transformed with pDsbALCIo was performed at 37°C in the HDM medium, a balanced complex medium previously optimized for high cell density cultures in multiple microfermentors 16. Addition of arabinose was performed at an OD₆₀₀ value of 16, equivalent to 5.5 g dry cell weight (DCW) per liter, and the culture continued to grow during the next 8-h period (figure 4). The level of periplasmic LCI increased up to 5 h after induction, then decreased progressively. In contrast, the level of extracellular LCI increased continuously until a cultivation time of 8 h, resulting in most of the overproduced protein being found in the culture supernatants. This result suggested that a high concentration of periplasmic LCI is required before being released into the growth medium, presumably because of an increased permeability of the outer membrane. Although that the mechanism of this non- or semi-specific 2 protein secretion is still unclear, it was proposed that the high level production of secreted protein could inhibit the synthesis of outer membrane proteins, and compromise the permeability barrier of outer membrane. Therefore, we checked the viability of cells during cultivation in the fermentor, and in parallel experiments we monitored CFU counts for plasmid loss. The data shown in figure 5 indicate that about 90% of cells were still alive and able to form colonies on selective plates. The accumulated LCI in the growth medium during high cell density culture did not result from cell lysis or death. Finally, after 8 h of induction, about 470 mg of active LCI could be purified from 1 liter of culture by a single step reverse-phase chromatography.

The E. coli LMG194 strain [F^- ΔlacX74 galE galK thi rpsL ΔphoA Δara714 leu::Tn10] carrying the araBAD deletion 12 was used as the expression host throughout the experiments. Recombinant DNA manipulations were performed as described in established protocols 22. Plasmid pLCB was constructed in two steps from the pBAD33 expression vector 12. First, the residual bla sequence was deleted by BglI-Tth111I digestion and filling in with Klenow fragment. Second, a DNA fragment which contained the Shine-Dalgarno sequence comprising an ATG start codon within a NdeI site from the pIVEX2.3MCS vector 23 was amplified using 5'-AAGAGCTCGAATTCCATATGTATATCTCCTTGCTAGCCCAAAAAAACGGGTATGG-3' and 5'-GTAACAAAGCGGGACCAAAGCC-3' as primers, and pBAD33 as DNA template. The PCR product was digested with MluI and SacI, and cloned into the same restriction sites of the previous pBAD33 derivative. The structure of the resulting plasmid was confirmed by sequencing and designated as pLCB. The mature LCI sequence was codon optimized for E. coli expression and chemically synthesized by Geneart (Regensburg, Germany). The substitution of malE or dsbA signal sequence was generated by overlap extension PCR as previously described 24.

For shake flask cultures, cells were grown in 100 ml of LB medium supplemented with chloramphenicol (30 μg.ml^-1). Induction of the araB promoter was accomplished by addition of L-arabinose to a final concentration of 0.2%. After 6 h at 37°C, cells were harvested by centrifugation at 6,000 rpm for 15 min. For high cell density cultures, bacteria were grown in a Sartorius Biostat B^® 2-L fermentor at 37°C. The aeration rate and stirrer speed were regulated to keep the dissolved oxygen concentration at 60% of its saturation value. Precultures (80 ml) were prepared in shake flasks at 37°C to mid-log phase, and then added into the fermentor containing 800 ml of the HDM medium 16 supplemented with chloramphenicol (30 μg.ml^-1). Induction was accomplished by addition of L-arabinose (0.5%). Cell biomass was monitored by measuring both the optical density at 600 nm (OD₆₀₀) and dry cell weight (DCW) as previously described 25. Cell viability was determined by using the LIVE/DEAD BacLight kit (Invitrogen) in combination with flow cytometry as described by the manufacturer 26. Plasmid stability was assessed by plating properly diluted amounts of culture samples on LB-agar plates containing 0.5% arabinose without antibiotic and with 30 μg.ml^-1 chloramphenicol. After overnight growth at 37°C the numbers of colony forming unit (CFU) were determined.

Cells carrying the pLCB derivatives, normalized to the same OD₆₀₀, were fractionated by spheroplast preparation as previously described 27. To analyse secreted LCI in the culture media, culture supernatants were applied to SepPak Plus C18 cartridges (Waters) pre-equilibrated by 10% acetonitrile. Then, the columns were washed with 10% acetonitrile, and proteins were eluted by 30% isopropanol. Total protein content was determined by the Bradford assay using bovine serum albumin as a standard. Cellular fractions were separated on 10% Bis-Tris polyacrylamide NuPage gels (Invitrogen), and proteins were visualized by Coomassie blue staining. For quantitative analysis, gels were scanned with Gel Doc XR imaging system (Biorad).

After cultivation, cells were centrifuged as described above and supernatants were filtered through a 0.22 μm syringe filter (Millipore). LCI was purified by reverse phase chromatography using a Ultimate 300 HPLC system (Dionex) and a Vydak C4 column, with a linear gradient ranging from 20 to 80% acetonitrile at a flow rate of 1 ml.min^-1 as previously described 9. To quantify the concentration of native LCI found in periplasmic and culture supernatants, a calibration curve was constructed by using purified active protein as a standard. The LCI activity was assayed using the Carboxypeptidase A assay kit (Sigma Aldrich) in 50 mM Tris-HCl buffer, pH 7.5; containing 100 mM NaCl.