Development of a light-regulated cell-recovery system for non-photosynthetic bacteria
© Nakajima et al. 2016
Received: 1 November 2015
Accepted: 19 January 2016
Published: 15 February 2016
Recent advances in the understanding of photosensing in biological systems have enabled the use of photoreceptors as novel genetic tools. Exploiting various photoreceptors that cyanobacteria possess, a green light-inducible gene expression system was previously developed for the regulation of gene expression in cyanobacteria. However, the applications of cyanobacterial photoreceptors are not limited to these bacteria but are also available for non-photosynthetic microorganisms by the coexpression of a cyanobacterial chromophore with a cyanobacteria-derived photosensing system. An Escherichia coli-derived self-aggregation system based on Antigen 43 (Ag43) has been shown to induce cell self-aggregation of various bacteria by exogenous introduction of the Ag43 gene.
An E. coli transformant harboring a plasmid encoding the Ag43 structural gene under a green light-regulated gene expression system derived from the cyanobacterium Synechocystis sp. PCC6803 was constructed. Ag43 was inserted downstream of the cpcG 2 promoter P cpcG2 , and its expression was regulated by green light induction, which was achieved by the functional expression of cyanobacterial CcaS/CcaR by coexpressing its chromophore synthesis gene cassette in E. coli. E. coli transformants harboring this designed system self-aggregated under green light exposure and precipitated, whereas transformants lacking the green light induction system did not. The green light induction system effectively functioned before the cell culture entered the stationary growth phase, and approximately 80 % of the cell culture was recovered by simple decantation.
This study demonstrated the construction of a cell recovery system for non-photosynthetic microorganisms induced by exposure of cells to green light. The system was regulated by a two-component regulatory system from cyanobacteria, and cell precipitation was mediated by an autotransporter protein, Ag43. Although further strict control and an increase of cell recovery efficiency are necessary, the system represents a novel tool for future bioprocessing with reduced energy and labor required for cell recovery.
Recent advances in the understanding of photosensing in biological systems have permitted the use of photoreceptors as novel genetic tools [1–8]. Photoreceptors are protein machineries that detect and respond to changes in light quality and intensity. Optogenetics, which uses various photoreceptors to control cell behaviors directly via light exposure, has recently attracted attention as a synthetic biology-based bioprocess design.
Cyanobacteria have various light-sensing systems to effectively regulate photosynthesis [9, 10] and avoid photo-inhibition caused by strong or short-wavelength light [11–17]. By exploiting various photoreceptors in cyanobacteria, a green light-inducible gene expression system has been developed. A unicellular cyanobacterium, Synechocystis sp. PCC6803, harbors a green light-sensing system. The expression of a phycobilisome linker gene, cpcG2, is chromatically regulated by a sensor histidine kinase, CcaS, and a cognate response regulator, CcaR . Using the endogenous CcaS/CcaR system, the green light regulation of an exogenously induced gene was achieved using a modified promoter of cpcG2, P cpcG2 , inserted upstream of the target gene on a vector plasmid . In addition, CcaS, CcaR, and P cpcG2 from Synechocystis sp. PCC6803 has been transformed into the marine cyanobacterium Synechococcus sp. NKBG 15041c as an exogenous green light-regulated gene expression system . This system has been applied to the construction of a green light-regulated autolysis system for cyanobacteria that employs a T4 phage-derived lysis system under the control of green light-regulated gene expression .
However, the applications of cyanobacterial photoreceptors are not limited to cyanobacteria but are also available for non-photosynthetic microorganisms. A pioneering study by Tabor et al. achieved the functional expression and utilization of a cyanobacterium-derived green light-sensing system in E. coli . Because phycocyanobilin (PCB), a chromophore of CcaS, is not endogenously synthesized in E. coli, the coexpression of a PCB synthesis gene cassette together with CcaS/CcaR resulted in green light-regulated gene expression in E. coli . Tabor and his coworkers also reported a multichromatic gene expression system employing an engineered CcaS.
In this study, we aimed to construct a novel technology for non-photosynthetic microorganism-based bioprocesses, a light-regulated cell-recovery system. As a light-regulated gene expression system, the cyanobacterium-derived green light-regulated gene expression system controlled by the two-component regulatory system CcaS/CcaR was selected. For the cell recovery technology, the E. coli-derived self-aggregation system was selected. Antigen 43 (Ag43), an autotransporter protein from E. coli, is an essential protein for aggregation and biofilm formation during infection. Ag43 is composed of three domains: a signal peptide for secretion into the periplasmic space, a β domain that forms a selective channel in the outer membrane to transfer the α domain for extracellular display, and an α domain, which is a linker for the self-aggregation. High affinity among the α domains triggers self-aggregation, which leads to cell precipitation [24–28]. Recently, the structure of the α-domain complex of Ag43 has been reported . In the present study, the Ag43 structural gene was inserted downstream of the cpcG 2 promoter, P cpcG2 , and its expression was regulated by green light induction, achieved by the functional expression of cyanobacterial CcaS/CcaR by coexpression of its chromophore synthesis gene cassette in E. coli. E. coli transformants carrying this system self-aggregated under green light exposure and precipitated, whereas transformants lacking the green light-induction system did not. The green light-induction system effectively functioned before the cell culture entered the stationary growth phase, and approximately 80 % of the cell culture was recovered by simple decantation.
Construction of a plasmid encoding a green light-inducible aggregation system
Vector used in this study
V ori, p15A ori
cca cluster with gfpuv instead of cpcG2
cca cluster with ag43 instead of cpcG2
cca cluster with ag43 instead of cpcG2 without ccaS
cca cluster with ag43 instead of cpcG2 without ccaR
cca cluster with ag43 instead of cpcG2 without ccaS, ccaR
original vector used for construction of pBRGLAg
ho1 and pcyA genes for PCB synthesis
original vector used for construction of pSTV28
Construction of a plasmid encoding PCB synthesis genes
A PCB synthesis gene cassette was constructed by assembling P LtetO-1 (BBa_R0040; Registry of Standard Biological Parts ), a ribosomal binding site (RBS) (BBa_B0034; Registry of Standard Biological Parts ), the heme oxygenase gene ho1 from Synechocystis sp. PCC6803 (BBa_I15008; Registry of Standard Biological Parts ), the PCB–thioredoxin oxidoreductase gene pcyA from Synechocystis sp. PCC6803 (BBa_I15009; Registry of Standard Biological Parts ), and a double terminator (BBa_B0015; Registry of Standard Biological Parts ) using three antibiotic assembly and inserted at the EcoRI and PstI sites of the plasmid derived from pSTV28, whose construction has been previously described [32, 33, 34]. This plasmid was named pSTVPCB. In this plasmid, ho1 and pcyA were constitutively transcribed independently following RBS in E. coli DH5α by P Ltete-1 polycistronically (Fig. 1). The components of this plasmid are shown in Table 1.
E. coli cells carrying pBRGLAg, pBRGLAgΔS, pBRGLAgΔR, or pBRGLAgΔSR together with pSTVPCB were cultured in LB broth containing 25 µg/ml chloramphenicol and 100 µg/ml ampicillin in a test tube at 37 °C with shaking at 140 rpm overnight. The prepared pre-cultures were inoculated into fresh 40 ml LB broth containing 0.1 M HEPES (pH 6.6), 0.05 mM aminolevulinic acid, 0.05 mM FeCl3, 100 µg/ml ampicillin, and 25 µg/ml chloramphenicol in 100-ml Erlenmeyer flasks. Cell density was monitored 6 h after the start of culture. Cells were cultured with shaking at 100 rpm and exposed to red light (660 nm, 40 µmol s−1 m2) at 30 °C until the cell density reached OD595 or OD600 = 0.4–0.6. After this period, each transformant was cultured under either of the following two conditions: one culture in triplicate was exposed to green light (520 nm, 40 µmol s−1 m2) instead of red light for 6 h, and the other culture in triplicate was continuously exposed to red light with shaking at 100 rpm and 30 °C. A 10-ml culture was transferred to a 15-ml tube to measure the aggregation-regulation ability of the cells.
The transferred culture in each 15-ml tube was exposed to red light for 2 h. During the incubation, a 100-µl culture was periodically transferred from the tube to a 96-well plate every 10 min, and 200 µl of fresh culture was added to the wells to dilute the culture. Cell density was measured using a plate reader (Thermo Fisher Scientific Inc., MA, USA). Cell density measurements were performed in triplicate. In all aggregation experiments, E. coli DH5α was used.
Transcriptional analysis of ag43 by quantitative reverse transcription PCR
E. coli cells harboring pSTVPCB and pBRGLAg were cultured as described above in the aggregation-regulation assay. During culture, a 1-ml culture was periodically removed.
Total RNA was extracted from the cell pellets from 1-ml cultures taken after centrifugation at 12,000 g for 5 min at 4 °C, using a NucleoSpin® RNA Clean-up kit (Takara Bio Inc., Shiga, Japan). The extracted RNA was treated with DNase to eliminate genomic DNA, and reverse transcription from RNA to cDNA was performed using PrimeScript® RT reagent kit with gDNA Eraser (Takara Bio Inc.). Quantitative PCR was performed to measure the transcriptional level of ag43 and 16S ribosomal RNA (rRNA) (housekeeping genes) with SYBR® Premix Ex TaqTM II (Tli RNaseH Plus) (Takara Bio Inc.). The transcription level was measured using the ΔΔCt method and normalized using the calculated transcription values of 16S rRNA.
Evaluation of cell recovery
Cells harboring the green light-inducible aggregation system were cultured as described above with modification in the timing of the start of exposure to green light.
To determine the timing of gene induction, cultures were induced by green light at different stages of growth. Four separate cultures in triplicate were prepared. For each culture, green light was irradiated at OD595 = 0.7, 1.1, or 1.2 or until 10 h had passed after the cell density reached OD595 = 1.7. Cultures were then exposed to green light (520 nm, 40 µmol s−1 m2) for 2 h.
Cultures diluted to cell density OD595 = 1.0 by the addition of fresh LB broth containing 0.1 M HEPES (pH 6.6), 0.05 mM aminolevulinic acid, 0.05 mM FeCl3, 100 µg/ml ampicillin, and 25 µg/ml chloramphenicol were transferred to a 15-ml tube and exposed to red light for 180 min for cell precipitation. Then, 7.6 ml of the supernatant was sampled and 400 µl of the culture containing precipitated cells was left behind (decantation procedure). The remained cells in 400 µl of the culture was defined as the recovered cells. In order to quantify the amount of recovered cells and unrecovered cells, thus prepared 400 µl of the culture containing precipitated cells and 7.6 ml supernatant were centrifuged. The cell recovery was calculated as the ratio (%) of the wet weight cells of recovered cells and total (recovered and unrecovered) cells.
The results of the aggregation assays and transcriptional analysis indicated that the green light regulated aggregation of E. coli cells was achieved by introducing a green light-sensing two-component regulatory system derived from cyanobacteria and Ag43 gene.
Cells at all growth phases showed precipitation ability, with 2-h exposure to green light resulting in Ag43 expression. Amounts of cells recovered by decantation of the precipitated cells are shown in Fig. 4. From the cells exposed to green light at the early, middle, and late-logarithmic growth phases, >70 % of cells were recovered by decantation. However, for cells exposed to green light at the stationary phase, <50 % of total number of cells was recovered by decantation. Thus, for efficient recovery of engineered E. coli cells harboring pSTVPCB and pBRGLAg, cells should be exposed to green light before growth enters the stationary phase, preferably before the late logarithmic phase. These results demonstrate the construction of a green light-induced cell recovery system for non-photosynthetic microorganisms by the combination of a cyanobacteria-derived green light-sensing system and Ag43 from E. coli.
In this study, we aimed to construct a green light-regulated cell recovery system for non-photosynthetic microorganisms using a green light-regulated gene expression system controlled by a two-component regulatory system from cyanobacteria and using Ag43, an autotransporter protein from E. coli.
Recently, the crystal structure of α-domain of Ag43 has been reported . The crystal structure of this domain shows that the formation of cell aggregates proceeds via a molecular Velcro-like handshake mechanism. Under this mechanism, if Ag43 is expressed on the surface of the outer membrane, cell self-aggregation will occur. The self-aggregation of bacteria using recombinant Ag43 has been previously reported . Exogenously introduced Ag43 led to the self-aggregation of E. coli, Pseudomonas fluorescens, and Klebsiella pneumoniae. Thus, our green light-induced cell recovery system will also be useful in a variety of non-photosynthetic microorganisms if the functional expression of the green light-sensing system is possible with the introduction of the PCB synthesis gene cassette.
Cell precipitation was observed in green light-exposed transformants harboring both pSTVPCB for PCB synthesis and pBRGLAg encoding CcaS/CcaR and Ag43 under P cpcG2 but not in transformants harboring pSTVPCB and with an imperfect green light-regulation system (pBRGLAg∆S, pBRGLAg∆R, or pBRGLAg∆SR) (Fig. 2a–d). However, even in the transformants with pSTVPCB and pBRGLAg, slight precipitation was observed under red light exposure at 70 min of incubation (Fig. 2a). Although the slight precipitation of the cells exposed to red light was observed at 70 min incubation, the expression of Ag43 under red light was not observed by transcriptional analysis (Figs. 2, 3). However, because the increase tendency was observed in the ag43 transcription under red light, the result suggests undetectable level ag43 transcription under red light led to Ag43 expression and precipitation of cells under red light. The difference in the Ag43 expression levels of transformants with pSTVPCB and pBRGLAg under red light was obvious in transformants harboring an imperfect green light-sensing system with ag43. Thus, the expression of Ag43 under red light was not due to the endogenously present P cpcG2 activating factors in E. coli but due to background-level expression under red light in the presence of CcaS/CcaR. It has been reported that CcaS autophosphorylation was repressed under red light. To prevent expression leakage of Ag43 under non-inducing conditions, we cultured E. coli transformants under red light. However, further repression of kinase activity of CcaS is required to achieve tight regulation using this system.
Cell recovery by exposure to green light was achieved when the cells were induced before entry into the stationary phase. However, when cells were exposed to green light even at the early-logarithmic growth phase, 80 % could be recovered by decantation with 20 % remaining in the culture supernatant. Aggregation is strongly dependent on the cell concentration . With decreasing free cell concentration in the supernatant resulting from the precipitation of flocculate from Ag43-mediated aggregation, aggregation may decrease. To overcome this inherent problem of aggregation-mediated cell recovery, an increase in the expression level of Ag43 per cell would enhance cell precipitation.
In conclusion, this study demonstrated the construction of a cell recovery system for non-photosynthetic microorganisms that is induced by the exposure of cells to green light. The system is regulated by a two-component regulatory system from cyanobacteria, and the cell precipitation is mediated by an autotransporter protein, Ag43. Although further strict control and increase of cell recovery efficiency are necessary, the proposed system provides a novel tool for future bioprocessing with reduced energy and labor for cell recovery.
MN; Mitsuharu Nakajima, KA; Koichi Abe, SF; Stefano Ferri, KS; Koji Sode MN conducted the preparation of recombinant cells and experiments throughout this research. KA designed the genes and vectors used in this research. SF and KS designed the plan of this research and performed the data analysis. KS has supervised this study. All authors participated in design and coordination and wrote the manuscript. All authors read and approved the final manuscript.
Financial support was obtained through the Core Research of Evolutional Science & Technology (CREST) program from the Japan Science and Technology Agency (JST).
The authors declare that they have no competing interests.
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