Isolating promoters from Corynebacterium ammoniagenes ATCC 6871 and application in CoA synthesis
Corynebacterium ammoniagenes is an important industrial organism that is widely used to produce nucleotides and the potential for industrial production of coenzyme A by C. ammoniagenes ATCC 6871 has been shown. However, the yield of coenzyme A needs to be improved, and the available constitutive promoters are rather limited in this strain.
In this study, 20 putative DNA promoters derived from genes with high transcription levels and 6 promoters from molecular chaperone genes were identified. To evaluate the activity of each promoter, red fluorescence protein (RFP) was used as a reporter. We successfully isolated a range of promoters with different activity levels, and among these a fragment derived from the upstream sequence of the 50S ribosomal protein L21 (Prpl21) exhibited the strongest activity among the 26 identified promoters. Furthermore, type III pantothenate kinase from Pseudomonas putida (PpcoaA) was overexpressed in C. ammoniagenes under the control of Prpl21, CoA yield increased approximately 4.4 times.
This study provides a paradigm for rational isolation of promoters with different activities and their application in metabolic engineering. These promoters will enrich the available promoter toolkit for C. ammoniagenes and should be valuable in current platforms for metabolic engineering and synthetic biology for the optimization of pathways to extend the product spectrum or improve the productivity in C. ammoniagenes ATCC 6871 for industrial applications.
KeywordsCorynebacterium ammoniagenes Transcriptome Promoter Coenzyme A
Corynebacterium ammoniagenes (formerly known as Brevibacterium ammoniagenes) is a Gram-positive, non-pathogenic soil bacterium with high guanine–cytosine (GC) DNA content. Due to the divergent evolution of C. ammoniagenes, different strains are used to produce different metabolites. For example, C. ammoniagenes ATCC 6872 is used in the production of nucleotides and nucleosides , while C. ammoniagenes ATCC 6871 shows a relatively high synthesis capacity of coenzyme A (CoA), which is a ubiquitous and essential cofactor found in all three domains of life and is involved in numerous metabolic pathways [2, 3, 4].
Sequencing of the C. ammoniagenes genome has helped to identify key enzymes for diverting carbon flow from metabolic pathways to other products [5, 6]. However, a major breakthrough in genetic manipulation to precisely regulate the expression of individual biosynthetic genes is still in process. Progress in the manipulation of C. ammoniagenes genes has been achieved through the development of effective transformation protocols and cloning vectors . Most vectors are based on the related C. glutamicum endogenous cryptic plasmids that have incorporated E. coli elements for transfer between the species [8, 9, 10]. Almost all these vectors have adopted E. coli promoters or C. ammoniagenes native promoters to express foreign proteins in C. ammoniagenes [11, 12, 13]. Although some of these promoters are active in C. ammoniagenes, the activities are quite low .
To efficiently engineer C. ammoniagenes, it is necessary to screen endogenous promoters. Paik and coworkers isolated 22 representative promoters from the genome of C. ammoniagenes ATCC 6872 and the activity of overexpressed chloramphenicol transacetylase from the strongest promoter IJ73 was 2.85 U . Similar studies have been performed by Park and coworkers, where they overexpressed the attenuator binding protein in C. ammoniagenes ATCC 6872 using the endogenous promoter CJ1 . However, the above promoters have not been universally applied in C. ammoniagenes ATCC 6871 (see text), probably due to the divergent evolution of C. ammoniagenes genomes. For instance, the sequence identities of promoters IJ59 and IJ73 from C. ammoniagenes ATCC 6872 with the homologous promoters from C. ammoniagenes ATCC 6871 are 93 and 89%, respectively. Therefore, due to the importance of CoA, it is necessary to find promoters that are effective in C. ammoniagenes ATCC 6871.
Endogenous promoters can be obtained by genomic dissection or promoter trapping et.al . Nonetheless, with the advent of genomics and transcriptomics, we can isolate promoters more rationally. Studies have shown that strong promoters are usually obtained from the promoters of essential genes whose transcription levels are presumed to be high and constant . In addition, we found that some commonly-used strong promoters such as Pdnak in Gluconobacter oxydans and Pgro in Corynebacterium glutamicum are promoters of molecular chaperones [18, 19]. In this study, the promoters for 20 genes with high transcription levels and 6 molecular chaperone-encoding genes are identified by bioinformatic methods and their activities were further examined experimentally. Among them, Prpl21 was found to be the strongest promoter, which was used in the biosynthesis of CoA, increasing the yield by 4.4 times.
Screening promoters and construction of probe-vector
Identified molecular chaperone genes or those with high level expression from RNA-seq data
23S ribosomal RNA
23S ribosomal RNA
Ribosomal subunit interface protein
Universal stress protein
50S ribosomal protein L29
F0F1 ATP synthase subunit gamma
Elongation factor Tu
50S ribosomal protein L21
NarK/NasA family nitrate transporter
Type I glyceraldehyde-3-phosphate dehydrogenase
50S ribosomal protein L10
Antibiotic biosynthesis monooxygenase
Class II fructose-bisphosphate aldolase
50S ribosomal protein L11
ABC transpoter, substrate-binding protein
Molecular chaperone GroEL
Molecular chaperone GroEL
Molecular chaperone DnaJ
Molecular chaperone DnaJ
Molecular chaperone DnaK
Previous studies have shown that most promoters of molecular chaperones exhibit high transcription levels in prokaryotes, so all 6 annotated molecular chaperones in the C. ammoniagenes ATCC 6871 genome (Accession Number: NZ_CP009244) (two GroEL, two DnaJ, one DnaK, and one Co-chaperone GroES) were identified and their promoters were predicted as described in materials and methods. The information of these genes and transcriptomic RPKM values are also listed in Table 1. By predicting the promoter regions, 26 promoters were constructed according to the rules described below and their corresponding RFP expression plasmids were named as pXMJ190-Pn. The sequences of the 26 promoters are listed in Additional file 1: Table S3.
Analysis and comparison of promoters in C. ammoniagenes ATCC 6871
To quantify the activities of the cloned promoters, growth-normalized fluorescence intensities were measured using a microplate assay and the data are shown in Fig. 3b and Additional file 1: Table S2, the results showed that we successfully isolated 20 endogenous promoters with different activities. Among the 20 promoters (PrrlA-Psbp) from genes with high transcription levels, Ptmr, Pnat, PatpG, PgpdI, Pacn are essentially inactive, while PgroELA from the 6 molecular chaperone promoters was also inactive. Meanwhile, four strong promoters, including the Prpl21 with 43,433 RFU/OD intensity and followed by PdnaK (19,125 RFU/OD), PgroELB (8166 RFU/OD) and Prpl10 (6490 RFU/OD) were identified whose fluorescence levels were consistent with those observed on plates. Thus, a range of promoters with different transcriptional activities, including four strong promoters, were identified and can be used directly in further applications. According to the obtained data, only two promoters (Prpl21 and Prpl10) from the 20 genes with high levels of transcription had strong activities, while two promoters (PgroELB and PdnaK) sourced from the six molecular chaperone genes exhibited relatively high activities, which may indicate that isolating promoters from molecular chaperones may be a more efficient strategy. Although most of the promoters identified from the RNA-seq profiles exhibited low level expression or were silent, the red fluorescence intensity of Prpl21 was almost 2.3 times that of the highest promoter (PdnaK) derived from upstream regions of the molecular chaperones. This suggests isolating promoters from genes with high transcription levels may yield strong promoters.
When it comes to the known promoters, the promoter CJ1 had some certain activity (4171 RFU/OD), the IJ59 (2866 RFU/OD) promoter had almost non activity, and the activity of Pgro (5872 RFU/OD) was slightly higher than the Ptac (5683 RFU/OD) promoter but still lower than promoter Prpl10 (6490 RFU/OD). This demonstrates the promoters that work well in one species or homologous strains may not possess the same characteristics in another.
Application of Prpl21 in C. ammoniagenes for improving the production of CoA
It has been reported that CoA, a ubiquitous and essential cofactor in biochemical reactions, can be produced by C. ammoniagenes ATCC 6871 . In the CoA biosynthetic pathway, the committed step catalyzed by pantothenate kinase (coaA) is subject to feedback inhibition by CoA and acyl-CoAs . Bacterial coaA proteins are categorized based on their amino acid sequences into three types, namely type I, II, and III. C. ammoniagenes carries a type I coaA which is highly regulated by CoA and its derivatives. In contrast, type II and III enzymes are insensitive to CoA and its thioesters [27, 28], therefore, in order to reduce feedback inhibition and increase the production of CoA, the type III pantothenate kinase from Pseudomonas putida (PpcoaA) was selected and overexpressed by the control of the strongest promoter Prpl21 in C. ammoniagenes ATCC 6871 [29, 30].
C. ammoniagenes ATCC 6871 is a producer of CoA, however, its genetic operation has been rarely reported, and its industrial application potential still needs to be improved. In order to further increase the production of CoA, endogenous promoters from C. ammoniagenes ATCC 6871 were screened in this study. Firstly, 20 putative promoters based on genes with high transcription levels and 6 promoters upstream of molecular chaperones were identified and characterized for transcriptional activity by using RFP as the reporter gene. Among the 26 putative promoters, 20 with different transcriptional activities were isolated including 15 from the high transcription level genes and 5 from molecular chaperone genes. The output efficiency demonstrates that isolating promoters from molecular chaperones (5/6) might be a more efficient strategy than using RNA-seq (15/20). Therefore, isolating promoters from molecular chaperone genes is more effortless and cost-effective than RNA-seq. These results may ascribe to that the RPKM values of the genes only represent the abundance of RNA and do not equivalent to its promoter activities, which might be caused by multiple factors, such as the codon usage of genes, copy numbers of genes, the half-lives of mRNA and limitations inherent in transcriptomics [22, 23, 24]. It thus, isolating promoters based on RNA-Seq requires further verification by experiments.
Nevertheless, we should note that the red fluorescence intensity of the highest promoter (Prpl21) identified from RNA-seq was almost 2.3 times than the highest promoter (PdnaK) derived from molecular chaperone genes, so isolating promoters based on the genes transcriptional data may be more likely to yield promoters with highest activity. To our best knowledge, Prpl21 from the upstream sequence of the 50S ribosomal protein L21 is the strongest C. ammoniagenes ATCC 6871 promoter reported so far. The promoters obtained in this work will enrich the available promoter toolkit for C. ammoniagenes and should be valuable in current platforms for metabolic engineering and synthetic biology for the optimization of pathways to extend the product spectrum or improve the productivity in C. ammoniagenes ATCC 6871.
To further verify the capacity of Prpl21, the key gene PpcoaA in the biosynthetic pathway of CoA was overexpressed in C. ammoniagenes ATCC 6871 with the aim of reducing the feedback inhibition and increasing the production of CoA. The CoA production of manipulated C. ammoniagenes was approximate 4.4 times to the control, which confirmed that PpcoaA overexpressed and functionalized successfully in C. ammoniagene. These results prove that the selected promoter for the overexpression of foreign genes in C. ammoniagenes could be used as an efficient tool for improving the yield of major products in C. ammoniagenes. However, eliminating the burden of co-expressing RFP only slightly increase the CoA production, possibly due to the undiscovered limitations exist in the CoA synthetic pathway. Thus, more efforts should be focus on the resolving of rate-limiting steps of CoA synthesis in C. ammoniagenes.
In summary, this study provides a rational strategy to isolate endogenous promoters from C. ammoniagenes ATCC 6871, which may be helpful in other similar scientific research. Through this strategy, we successfully isolated a range of promoters with different transcriptional activities and the strongest one was applied to improve the CoA production in C. ammoniagenes ATCC 6871, raising hope for further improving the industrial production level of CoA.
Bacterial strains, media, and growth conditions
The C. ammoniagenes ATCC 6871 was purchased from China General Microbiological Culture Collection Center (CGMCC, Beijing, China). E. coli Top10 (Tsingke, Beijing, China) was cultivated in Luria-Bertani (LB) broth or on LB plates with 2% (w/v) agar at 37 °C as a host for transformation. C. ammoniagenes ATCC 6871 grown in NCM medium at 30 °C was used as the transformation host for E. coli/Corynebacteria vectors used in this study. After transformation by electroporation (1.8 kV), transformants were plated on BHIS plates with 20 μg/mL chloramphenicol at 30 °C. Fermentation medium (glucose 100 g/L, peptone 12 g/L, yeast powder 8 g/L, MgSO4·7H2O 10 g/L, KH2PO4 10 g/L, K2HPO4 10 g/L, urea 7 g/L, pH 7.5–7.8) was used to cultivate strains producing CoA. Cultivation for expression analysis was performed in at least biological duplicates.
Recombinant DNA techniques
C. ammoniagenes genomic DNA was isolated using a genomic DNA isolation kit (Tiangen, Beijing, China). Kits for plasmid isolation, extraction of DNA from agarose gels and PCR product purification were also purchased from Tiangen (Beijing, China). I-5 2 × High-Fidelity Master Mix and Trelief™ SoSoo Cloning Kit were purchased from Tsingke (Beijing, China) and used for routine molecular biology applications.
Construction of probe-vector pXMJ190
The shuttle vector pXMJ19 (a kind gift from Professor Dong, Fig. 2a) was used as the backbone for vectors constructed in this study. To eliminate interference from the promoter already present in pXMJ19, the tac promoter and lac operator were removed. A gene encoding red fluorescent protein (RFP) was inserted into the MCS to form a probe-vector named pXMJ190 (Fig. 2b). Gibson assembly was used to assemble DNA fragments upstream of the reporter gene rfp, resulting in seamless ligation between fragments and the probe-vector [31, 32].
Genetic manipulation of C. ammoniagenes
To increase transformation efficiency, recipients were grown in 100 mL of NCM medium at 30 °C until an OD600 nm of approximately 1.0. Cells were incubated on ice for 20 min and harvested by centrifugation in a polypropylene tube at 4000 rpm for 10 min at 4 °C. After washing twice in cold distilled water and two washes in ice-cold 10% glycerol, cells were resuspended in 1 mL of 10% glycerol. For electroporation, 100 μL of the freshly prepared electro-competent cells were mixed with 3 μL plasmid (50 ng/μL in ddH2O) in a cold sterile electroporation cuvette (1 mm electrode gap) and pulsed immediately with a MicroPulser electroporator (Bio-Rad Laboratories, Inc., Hercules, CA). The electroporator was usually set at a voltage of 1.8 kV. Cells were subsequently resuspended in 0.9 mL of BHIS, heated at 46 °C for 6 min and withdrawn immediately for recovery by incubating for 3 h at 30 °C and then plated for selection of transformants.
Construction and analysis of selected promoters
The transcriptional levels of genes can be estimated by Reads Per Kilobase per Million mapped reads (RPKM), so the genes were ranked by RPKM value based on transcriptional data from C. ammoniagenes and the top 20 genes were selected. All of the genes were identified from the genome and their promoters were predicted as below. Six annotated molecular chaperones in the genome were sorted and their promoters were predicted as outlined below. According to previous studies, the promoter-5′-UTR junction influences mRNA and protein levels [23, 33]. Therefore, we integrated the corresponding 5′-UTR into each promoter.
Promoter sequences were predicted using the Neural Network Promoter Prediction online tool (http://www.fruitfly.org/seq_tools/promoter.html) . The promoter prediction score threshold was set to 0.7. Moreover, due to the possibility of tandem promoters, all eligible promoter sequences within 300 bp upstream of the start codon were considered . For correct transcription initiation, the complete “promoter” consisted of 5′-UTR, predicted promoter region and Shine-Dalgarno sequence, which typically correspond to the region 60 bp upstream of a predicted promoter and 1 bp upstream of the start codon. The 60 bp extension upstream of the promoter accounts for potential UP-elements [36, 37].
Promoters were amplified from C. ammoniagenes ATCC 6871 and C. glutamicum ATCC 13032 genomic DNA with the corresponding primers. Oligonucleotide primers used in this work are listed in Additional file 1: Table S1. PCR products were ligated into the vector pXMJ190 using Gibson assembly as shown in Fig. 2c. All plasmids were constructed in E. coli TOP10 and then transformed into C. ammoniagenes ATCC 6871 for subsequent analysis.
Fluorescence intensity assay
To evaluate RFP expression under the control of the various promoters, C. ammoniagenes strains harboring various vectors were grown overnight on LB plates containing 20 μg/ml chloramphenicol. Fluorescence was observed using a LUYOR-3430 stereo microscope with a fluorescence excitation source (LUYOR, USA) set at 501 nm and matching lenses to detect RFP. Pictures were captured with a camera.
For more accurate comparisons, the fluorescence intensities of bacteria harboring different plasmids were measured using a Synergy H4 microplate reader (BioTek, USA). In order to exclude other interfering factors, harvested cells were washed once with PBS (pH 7.4) and then resuspended in PBS (pH 7.4) at an OD600 nm of approximately 1.0. The excitation wavelength for RFP was set at 554 nm and emission was set at 586 nm. Fluorescence intensities were normalized by OD600 nm and were used to indicate the activities of the promoters. Bacteria harboring pXMJ19-Ptac were induced with 1 mM IPTG.
Construction of the recombinant plasmid pXMJ190-Prpl21-PpcoaA-RFP
To further examine the function of the isolated promoters, a type III pantothenate kinase from P. putida KT2440 (PpcoA) and RFP were co-expressed under the control of the strongest promoter Prpl21. The PpcoaA gene was amplified by PCR from the genomic DNA of P. putida KT 2440, and the Shine-Dalgarno sequence for translation of RFP was calculated using the RBS calculator online tool (https://www.denovodna.com/software/). All primers used in this section are listed in Additional file 1: Table S1. The recombinant plasmid pXMJ190-Prpl21-PpcoaA-RFP was constructed with Gibson assembly and positive colonies were confirmed by DNA sequencing (Tsingke, China). Recombinant plasmids were transformed into C. ammoniagenes ATCC 6871 for further experiments.
C. ammoniagenes strains were precultured in 10 mL LB medium at 30 °C and shaken at 220 rpm for 24 h. Ten percent of the culture was inoculated in a 250 mL shake flask containing 100 mL fermentation medium. After 24 h cultivation, cell samples were harvested by centrifugation at 12,000 rpm for 10 min. Forty micrograms of cell lysate were loaded per lane. The PpcoaA and RFP expression was analyzed by 15% (v/w) polyacrylamide gel electrophoresis (PAGE) with cell-free extract under denaturing conditions. Mini-Protean III Electrophoresis System (Bio-Rad, USA) was utilized to perform the operation. Coomassie Brilliant Blue R-250 (0.2%, w/v) was utilized to stain protein on the gel.
Analysis of CoA production
Coenzyme A content was determined according to the modified phosphotransacetylase method [38, 39]. All reagents were purchased from National Institutes for Food and Drug Control. Briefly, 3.0 mL of Tris buffer (pH 7.6), 0.1 mL of acetyl phosphate dilithium salt (15.2 g/L) and 0.1 mL of the test solution were added into a 1 cm cuvette and mixed. Absorbance at 233 nm was recorded as E0; and then 0.01 mL of the phosphotransacetylase (30–40 U/mL) solution was added, mixed well and the highest absorbance within 3 to 5 min was taken as E1. Finally, another 0.01 mL of phosphotransacetylase solution was added, mixed well and the absorbance was read as E2. The number of CoA units per milliliter was calculated as U = (2E1-E0-E2) × 5.55 × 413.
We are grateful to Professor Zhiyang Dong (Institute of Microbiology, Chinese Academy of Sciences, China) for generously providing the plasmid pXMJ19. This work was supported by Grant from National Natural Science Foundation of China (31570077 to S.W.).
YH, SW, YT designed all the experiments; YH and SC carried out the experiments, YH organized and interpreted the data, and drafted the manuscript. JW, GL, SW and YT contributed to discussion, revised and corrected the manuscript. All authors read and approved the final manuscript.
This study was funded by National Natural Science Foundation of China (31570077). The funding body did not play any role in the design, execution, analysis, and interpretations of data or in writing the manuscript.
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The authors declare that they have no competing interests.
- 9.Santamaria R, Gil JA, Mesas JM, Martin JF. Characterization of an endogenous plasmid and development of cloning vectors and a transformation system in Brevibacterium lactofermentum. J Gen Microbiol. 1984;130(9):2237–46.Google Scholar
- 16.Deaner M, Alper HS. Promoter and terminator discovery and engineering. Adv Biochem Eng Biot. 2018;162:21–44.Google Scholar
- 19.Schafer A, Schwarzer A, Kalinowski J, Puhler A. Cloning and characterization of a DNA region encoding a stress-sensitive restriction system from Corynebacterium glutamicum ATCC 13032 and analysis of its role in intergeneric conjugation with Escherichia coli. J Bacteriol. 1994;176(23):7309–19.CrossRefGoogle Scholar
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