Skip to main content

Construction and application of a CRISPR/Cas9-assisted genomic editing system for Corynebacterium glutamicum


Corynebacterium glutamicum is widely used as microbial cell factory for various bioproducts, but its genomic editing efficiency needs to be improved. In this study, a highly efficient CRISPR/Cas9-assisted genomic editing system for C. glutamicum was constructed. This system mainly involves a plasmid and can be used for both gene insertion and deletion in the chromosome of C. glutamicum. The recombinant plasmid for the target gene containing all the editing elements, and first constructed it in E. coli, then purified and transformed it into C. glutamicum. This temperature-sensitive plasmid was cured at high temperature after the genomic editing was completed in C. glutamicum. Using this genetic editing system, the genetic editing efficiency in C. glutamicum ATCC 13032 could reach 95%. The whole work of editing could be done in 8–9 days and showed most time-saving compared to the reported. Using this system, the native promoter of gdhA1 in ATCC 13032 has been replaced with the strong promoter PtacM, and more than 10 genes in ATCC 13032 have been deleted. The results demonstrate that this CRISPR/Cas9-assisted system is highly efficient and very suitable for genome editing in C. glutamicum.


Corynebacterium glutamicum is an ideal industrial strain on account of high growth velocity and food-safety (Liu et al. 2016). Its traditional utilization in industries are for various amino acids production such as l-glutamic acid (Wada et al. 2016; Wen and Bao 2019), l-threonine (Lv et al. 2012; Wei et al. 2018), branched-chain amino acid (Schwentner et al. 2018; Wang 2019; Wang et al. 2019), l-lysine (Xiao et al. 2020), nonprotein amino acid (Mindt et al. 2019; Shi et al. 2018) and so on. C. glutamicum are one of most important model organisms in microbial cell factories due to decade studies, increasing other bioproducts metabolic pathway have been constructed in C. glutamicum, for example, biofuels (Sasaki et al. 2019; Zhang et al. 2019b), organic acid (Fukui et al. 2019), enzyme preparations (Yang et al. 2019) and other natural compounds (Braga et al. 2018; Cheng et al. 2019; Zha et al. 2018) and so on. The metabolic engineering of C. glutamicum to produce various bioproducts indicated its attractive prospect.

Metabolic engineering studies are most important part of synthetic biology for C. glutamicum. With the development of molecular biology, the cell factories’ establishment was inclined to rational design of metabolic pathway including Design, Construction, Evaluation, and Optimization (Chen et al. 2017). Hence, some more efficient molecular tools must be constructed and used to reestablish metabolic pathway. To date, although there are some gene editing methods of C. glutamicum have been reported, there were some obvious deficiencies like low efficiency and time-consuming. W. Jager et al. (Jager et al. 1992) was the first to report SacB-based genomic editing in C. glutamicum and Tan (Tan et al. 2012) improving this method and successfully constructed plasmid pDXW-3, which is a traceless editing method and needs two-step homologous recombination. Cre/loxP-based recombination system was first found in a plasmid of prophage of bacteriophage P1 (Austin et al. 1981) and Nobuaki Suzuki et al. (Suzuki et al. 2004) first reported the Cre/loxP-based method for editing of C. glutamicum genome, this method was suitable to large region (56 kb) deletion. Jinyu Hu et al. (Hu et al. 2013) constructed multiple-gene-deletion system based on Cre/loxP-mediated method in C. glutamicum, this method need three plasmids to edit genome: pBluescript II SK, pDTW202 and pDTW109, pBluescript II SK was used as vector of homologous arms and kanamycin cassette, pDTW202 was kanamycin cassette carrier (lox66 and lox71 sequence were added to each end of kanamycin resistance gene), temperature-sensitive plasmid pDTW109 was used to delete kanamycin cassette from targeted gene locus in chromosome. This method will leave residual sequence in the genomic loci of interest and require two electrical conversions. These methods above are often show low efficiency (< 5%) and need at least 20 days in C. glutamicum.

Streptococcus pyogenes type II CRISPR/Cas9-assisted genomic editing and CRISPRi technology are generalizable to microbiologic cell factories, such as C. glutamicum (Cameron Coates et al. 2019; Cleto et al. 2016; Liu et al. 2017), Escherichia coli (Jiang et al. 2015; Pyne et al. 2015), Bacillus subtilis (Altenbuchner 2016; Westbrook et al. 2016), Lactobacillus (Oh and van Pijkeren 2014; Song et al. 2017), Aspergillus (Nodvig et al. 2018; Zhang et al. 2016), Saccharomyces cerevisiae (Mitsui et al. 2019; Zhang et al. 2019a). The CRISPR/Cas9 mutation and CRISPRi (Cleto et al. 2016; Gauttam et al. 2019) can fine-tune gene expression level in genome and have been used to study metabolic engineering in C. glutamicum, hence, some strategies for C. glutamicum genomic editing had been documented (Cho et al. 2017; Peng et al. 2017; Wang et al. 2018). Jiang (Jiang et al. 2017) was failed to construct CRISPR/Cas9-assisted genomic editing system, he/she speculated Cas9 protein might toxic to C. glutamicum, and reported Francisella novicida CRISPR/Cpf1-assisted genome editing system, the efficiency of codon saturation mutagenesis reached near 100% while shown low efficiency in large gene deletion (> 1 kb). Peng (Peng et al. 2017) optimized codon of Cas9 and limit its expression in C. glutamicum to make the cells survived in media, he used two plasmids to express Cas9 nuclease and targeted sgRNA separately. The sgRNA vector was constructed as two-step method: link targeted sgRNA (including N20 sequence) and homologous repaired arm to the vector pFST respectively, electroporation for twice to introduce vector pFSC and pFST into C. glutamicum, so the method was tiring and time-consuming in practical usage.

In this research, we succeed in construction of a single-plasmid CRISPR/Cas9-assisted genomic editing for C. glutamicum, all elements including gene cas9, sgRNA and homologous arms were designed in one temperature-sensitive plasmid pCCG1 or pCCG2, the whole editing work could be done in 8–9 days and 5 days for continuous editing. The editing efficiency was about 50%–95% in C. glutamicum ATCC 13032, this method was suitable to both small and large (> 3 kb) targeted gene mutation. Meanwhile, this strategy was extended examined in C. glutamicum ATCC 14067 and C. glutamicum ssp. lactofermentum (Shi et al. 2019) (a strain of C. glutamicum for l-isoleucine production, genomic sequence is similar to C. glutamicum ATCC 13869). Up to now, our strategy demonstrated high efficiency in editing procedure and time-saving compared to the reported.

Materials and methods

Strains, plasmids, and growth conditions

All bacterial strains and plasmids used in this study are listed in Table 1. E. coli DH5α was cloning host for vectors’ construction. C. glutamicum ATCC 13032 are mainly used strain for editing strategy, meanwhile, C. glutamicum ATCC 14067 and C. glutamicum ssp. lactofermentum as supplementary strains used in this study. E. coli DH5α were cultured in Luria–Bertani (LB) media (tryptone 10 g/L, yeast extract 5 g/L, NaCl 10 g/L, pH 7.0–7.2, LB agar supplemented with 15 g/L agar) at 37 °C. C. glutamicum is cultured in LBHIS media (d-sorbitol 91 g/L, tryptone 5 g/L, yeast extract 2.5 g/L, NaCl 5 g/L, brain heart infusion 1.85 g/L, pH 7.2–7.4, LBHIS agar supplemented with 15 g/L agar) at 30 °C. C. glutamicum harboring pCCG1/pCCG2 was cultured at 28 °C, and 37 °C for plasmid curing. Adding kanamycin 30 mg/L for E. coli DH5α and 20 mg/L for C. glutamicum as needed. The seed media (g/L): glucose·H2O 25, corn extract 20, KH2PO4 1, MgSO4·7H2O 0.4, urea 5, pH 7.2–7.4. l-glutamic acid fermentation media (g/L): glucose·H2O 110, corn extract 1, KH2PO4 2, MgSO4·7H2O 0.8, MnSO4·H2O 0.01, FeSO4·7H2O 0.02, pH 7.2–7.4.

Table 1 Bacterial strains and plasmids used in this study

Plasmid construction

The main primers used in this study are given in Table 2. Kanamycin resistance gene (kanr) with its native promoter was amplified from plasmid pEC-XK99E using primers P1/P2; temperature-sensitive replicon pBL1TS in C. glutamicum was amplified from plasmid pDTW109 using primers P3/P4; PUC ori replicon in E. coli was amplified from plasmid pBluescript II SK using primers P5/P6, fused three fragments above to single Fx1 fragment with overlap PCR method, lacIq-cas9-T1T2 terminator fragment (Fx2) was amplified from pFSC using primers P7/P8, the fragment Fx2 contain three units: DNA-binding transcriptional repressor (LacIq), cas9 gene (under inducible promoter Ptrc) and T1T2 terminator. Ligate NotI-ApaI-digested Fx1, NotI-SmaI-digested Fx2 and artificial synthetic PtacM promoter (annealed primers P9/P10) with T4 ligase (Thermo, USA), the products were transformed into E. coli DH5α to obtain plasmid pCCG-zero. Extracted the plasmid pCCG-zero from E. coli DH5α using TIANprep Mini Plasmid Kit (TIANGEN, China), then inserted the synthetic multiple cloning site (MCS, annealed primers P11/P12) between BamHI-SmaI-digested pCCG-zero, the new plasmid was named as pCCG1. Amplified fragment Fx3 from plasmid pCCG1 using primers P13/P14, amplified fragment Fx4 from plasmid pEC-XK99E using primers P15/P16, amplified Fx5 fragment from plasmid pDTW109 using primers P17/18, ligate NotI-XmaJI-digested Fx3, XbaI-XhoI-digested Fx4 and XhoI-NotI-digested Fx5 using T4 ligase, the products were transformed into E. coli DH5α to construct a new plasmid pCCG2. Both plasmids pCCG1 and pCCG2 can utilize to editing genome of C. glutamicum.

Table 2 The main primers used in this study

In this research, tracrRNA and crRNA was fused to a single synthetic guide RNA (sgRNA), which is 82-bp fragment. In order to facilitate the editing procedure, another plasmid pBS-sgRNA was constructed, the procession was as followings: linearized plasmid pBluescript II SK by PCR with primers P19/20, purified the products with SanPrep Column DNA Gel Extraction Kit (Sangon Biotech, China) and digested with XbaI-NcoI, then ligated it with NheI-NcoI-digested sgRNA (artificial synthesis) using T4 ligase, the products were transformed into E. coli DH5α to construct plasmid pBS-sgRNA, which was used as vector for cloning sgRNA fragment.

Genomic editing procedure

The genomic editing relies on two processes: Cas9 nuclease activity and homologous recombination repair activity. For construction of recombinant plasmid to targeted gene, three elements need to be amplified: sgRNA, up and down homologous sequence flanking the deletion target sequence. In this study, several genes were used as candidates to test this method (Table 3). Take poxB deletion as an example, use primers poxBsg-F/sgRNA-R to amplify sgRNA fragment (pBS-sgRNA as template), use primers poxB-U-F/poxB-U-R and poxB-D-F/poxB-D-R to amplify up and down homologous repair arms (C. glutamicum genome as template), fuse sgRNA, up and down homologous repair arms to one strand using primers poxB-F/poxB-D-R. N20 sequence was added at the 5’-end of primer poxBsg-F and vector’s homologous sequence at the 5’-end of primer poxB-F, ligate the fused fragment to the BamHI-AflII-digested pCCG1 by the ClonExpress® II One Step Cloning Kit (Vazyme, China), then use chemical transformation to construct the recombinant plasmid pCCG1-poxB in E. coli DH5α. The sgRNA-homologous arm fragment also can be ligated to pCCG1/pCCG2 with restriction enzyme digestion-T4 ligase method. The design of 20-bp region (N20) with protospacer-adjacent motif (PAM, NGG sequence) matching the targeted gene was programmed artificially or CHOPCHOP/CRISPy-web on net (Blin et al. 2016). In this research, fifteen candidate genes were used to test this strategy, gene knockout: ldh, eutD, gabP, glnA1, glnA2, alaT, argR, gabTD, aceAB, poxB; substitution of gene native promoter: gdhA1; gene insertion at targeted loci of genome: eutD:: speC, gabP:: gadB, eutD:: gdhA, alaT:: gdhA. When insert gene speC, gadB and gdhA into eutD, gabP and eutD, cloning the gene (including promoter PtacM) using primers speC-F/speC-R, gadB-F/gadB-R, gdhA-F/gdhA-R and plasmids pJYW-5-speC, pJYW-5-gadB, pJYW-5-gdhA as template respectively, then ligate the gene between homologous arms to construct the plasmids pCCG1-ΔeutD::speC, pCCG1-ΔgabP::gadB, pCCG1-ΔeutD::gdhA, pCCG1-ΔalaT::gdhA and pCCG2-ΔalaT::gdhA in E. coli DH5α.

Table 3 Gene editing in this study

The recombinant plasmid was purified from E. coli DH5α and electroporated into C. glutamicum. The electrocompetent of C. glutamicum was prepared as reported (Jiang et al. 2017) with modification: inoculate the candidate strain into 4 mL liquid LBHIS media and cultured at 30 °C, 200 rpm for 12–16 h to get pre-culture, 0.5–1 mL of the culture was inoculated into 50 mL media (LBHIS supplemented with Tween-80 1 g/L, l-glycine 25 g/L, l-glycine separately sterilized) and shaking at 30 °C, 200 rpm for 4–5 h until OD562nm reached 0.9–1.0, bath the cells in ice for 15–20 min, centrifugate it at 4000 rpm (~ 3040 g) for 5–10 min to harvest the cells. Wash the cell twice with pre-cooling 10% (vol. / vol.) glycerol, resuspend it in 1 mL 10% glycerol, split to 80 μL per tube, and store at –70 °C.

For electroporation, ~ 1 μg plasmid was mixed with 80 μL electrocompetent, adding the mixture into pre-cooling 1 mm Gene Pulser cuvette, bath it in ice for 10 min and electroporation at 1.8 kV for twice, the cells were immediately recovered in 0.9 mL pre-cooling liquid LBHIS media for 1–1.5 h in shaker at 30 °C, 150 rpm, then spread the cell on LBHIS agar (supplemented with kanamycin 20 mg/L, isopropyl β-d-1-thiogalactopyranoside, IPTG, 0.01 mM) and culture for 2–3 days at 28 °C until obtain proper size colonies. The colonies were examined by colony PCR method.

Plasmid curing

Plasmid pCCG1/pCCG2 harbor temperature-sensitive replicon in C. glutamicum on account of replicase mutation pBL1P47S, when the cultivation temperature higher than 34 °C, the replicase turns to inactivated. For curing the plasmid in positive editing cells, inoculate the cells into 4 mL liquid LBHIS media, shake at 37 °C, 200 rpm for 16 h to obtain proper cell density, plate streaking and cultured at 30 °C for 30–36 h to obtain single colony. Colony PCR or/and kanamycin-resistance LBHIS plates were used to verify plasmid curing, universal primers cas9Test-F (5′-GAAAACCCAATCAACGCATCT-3′)/cas9Test-R (5′-GCTTAGGCAGCACTTTCTCGT-3′) was designed in cas9 region, which are suitable for all plasmids curing examination, the product is 940-bp-sized fragment if the plasmid existed in cells and nothing for correct curing.

Gene gdhA1, glnA1 and glnA2 mutations and l-Glu fermentation

Corynebacterium glutamicum is an important industrial strain for l-glutamic acid and l-Glutamine production. Glutamate dehydrogenase (gdhA1) and glutamine synthase (glnA1 and glnA2) were key genes related to both amino acids’ biosynthesis in C. glutamicum ATCC 13032 (Fig. 2a). In this research, the strong constitutive promoter PtacM and artificial RBS was used to substitute gdhA1 native promoter in C. glutamicum ATCC 13032 chromosome. Amplified targeted sgRNA using primers gdhA1sg-F/sgRNA-R, amplified upstream using primers gdhA1-U-F/gdhA1-U-R, amplified PtacM and downstream using primers gdhA1-D-F/gdhA1-D-R (the plasmid pJYW-5-gdhA1 as template), fused three fragment by overlap PCR, and ligated the fragment with BamHI-AflII-digested pCCG1 by one-step homologous recombinant cloning kit, transformed the ligated product into E. coli DH5α to construct plasmid pCCG1-PtacM-gdhA1, and electroporated the purified plasmid into C. glutamicum ATCC 13032. The new strain called CGG001. The next, the plasmids pCCG1-glnA1 and pCCG1-glnA2 was constructed using similar method to delete gene glnA1 and glnA2, the new strains named as CGN004 and CGN005 respectively. To examine the effect, the strains ATCC 13032, CGG001, CGN004 and CGN005 was cultured in the seed media at 30 °C, 200 rpm for 8–10 h until the OD562nm reached 40 ± 3, inoculate 10% culture in l-glutamic acid fermentation media and fermentation at 30 °C, 200 rpm for 72 h. Supplement urea 4 g/L at 0 h and supplement 2.4 g/L at 10 h, 12 h, 14 h, 17 h and 20 h respectively, the overall additive amount of urea was 16 g/L. The strain CGN004 turns to l-glutamine auxotroph after glnA1 been deleted, so, proper l-glutamine must be supplemented in media to make the cells survive, 100 mg/L l-glutamine was added in seed media, fermentation broths add 100 mg/L l-glutamine twice at 0 h and 24 h. HPLC (Shi et al. 2013) was used to assay the concentration of l-glutamic acid and l-Glutamine in fermentation broths.


Construction of CRISPR/Cas9-assisted system for one-step genomic editing in C. glutamicum

The E. coliC. glutamicum shuttle plasmid of CRISPR/Cas9 vector were constructed and named as pCCG1/pCCG2. The overview diagram of its construction was showed in Fig. 1a. The vector pCCG1 (10077 bp) was first constructed, and then another vector pCCG2 (10147 bp) was following been constructed, both plasmids are functional in genomic editing of C. glutamicum. cas9 expression was designed under the control of inducible promoter Ptrc. sgRNA was under constitutive promoter PtacM to insure its expression level. The construction of recombinant plasmid for targeted gene could utilize the method of restriction enzymes digestion-T4 ligase or homologous recombinant cloning kit. The fragment sgRNA, upstream and downstream homologous repair arms could be fused to single strand with overlap PCR technology to promote the construction efficiency of recombinant plasmids in E. coli. The sequence of artificial multiple cloning sites (MCS) (Fig. 1b) under PtacM promoter was optimized to ensure every restriction site could be efficiently cut by relevant restriction enzymes. Small sgRNA gene fragment was synthesized and ligated with plasmid pBluescript II SK (the new plasmid named as plasmid pBS-sgRNA, Fig. 1a) to facilitate its conservation and cloning. The full sequence of sgRNA (without N20) in pBS-sgRNA was showed in Fig. 1c.

Fig. 1
figure 1

Construction of CRISPR/Cas9-assisted system. a The overview diagram of vectors pCCG1, pCCG2 and pBS-sgRNA construction, E. coliC. glutamicum shuttle expression vector pCCG1 and pCCG2 is kanamycin resistance, Cas9 nuclease gene is under the control of the inducible promoter Ptrc, pBL1TS is temperature-sensitive replicon in C. glutamicum, constitutive promoter PtacM and multiple cloning site (MCS) were artificial synthesis, sgRNA were expressed by promoter PtacM. Small sgRNA sequence was ligated with plasmid pBluescript II SK. sgRNA fragment were amplified from the plasmid pBS-sgRNA when needed. b The sequence of multiple cloning sites, including BamHI, NheI, Asc I, AflII and SmaI (XmaI) restriction enzyme sites. c The full nucleotide sequence of sgRNA fragment (171 bp) in plasmid pBS-sgRNA, the red part is Cas9 nuclease recognition site (82 bp)

Application of the system for genomic editing in C. glutamicum

In order to test our CRISPR/cas9 system, gene ldh, eutD, gabP, glnA1, glnA2, alaT, argR, gabTD, aceAB, poxB were deleted in C. glutamicum ATCC 13032 genome, the results were listed in Table 4. The deletion efficiency of genes was mainly between 26%-90% in C. glutamicum ATCC 13032. gabP was also deleted in C. glutamicum ATCC 14067 and C. glutamicum ssp. lactofermentum genome, the efficiency was 38.4% and 25.0% respectively, lower than 82.6% in C. glutamicum ATCC 13032. Paradoxically, the gene deletion efficiency was great related to gene itself, for example, the deletion efficiency of argR in ATCC 13032 was 60.0% using TCGCGGGCGATGCTATCTAC sequence, nevertheless, the gene cluster argFR deletion efficiency was 0% when with the same N20 sequence.

Table 4 The results of gene editing

In this research, four genes were inserted into targeted genes in C. glutamicum ATCC 13032 genome: eutD:: speC, gabP:: gadB, eutD:: gdhA and alaT:: gdhA, Based on the experimental results, the efficiency of gene insertion was lower than deletion in most cases, meanwhile, the different gene insertion at same locus might show different efficiency even if using the same N20 and homologous repaired arms. In this research, derived from E. coli W3110 gene speC (2261 bp, including promoter) and gdhA (1459 bp, including promoter) were inserted into eutD with same N20 and homologous arms, the efficiency were 34.8% and 69.6% respectively, the editing efficiency was contrary to the size of inserted gene, and lower than eutD deletion (86.4%), the efficiency of gabP:: gadB (30.4%) also lower than gabP deletion (82.6%).

The vector pCCG1 and pCCG2 were both used to insert gdhA into alaT. Gene gdhA was cloned from E. coli W3110 genome and ligated it between alaT up and down homologous arms. The efficiency was 26.1% and 21.7% for pCCG1 and pCCG2 respectively.

Editing of genes gdhA1, glnA1 and glnA2 in C. glutamicum

In this research, the plasmid pCCG1-PtacM-gdhA1 was designed to replace the gdhA1 native promoter using the strong promoter PtacM and artificial RBS, the plasmid profile and agarose gel eletrophoresis was showed in Fig. 2b, pCCG1-glnA1 and pCCG1-glnA2 were used to delete glnA1 and glnA2 from chromosome. The efficiency was 95.7%, 56.5% and 69.6% respectively.

Fig. 2
figure 2

l-Glu and l-Gln biosynthetic pathway and the results of gene editing. a l-Glu and l-Gln biosynthetic pathway. Pyr: pyruvate; Ac-CoA: acetyl-CoA; Cit: Citrate; Aco: cis-aconitate; Icit: isocitate; α-KG: alpha-ketoglutaramate; Suc-CoA: succinyl-CoA; Suc: succinate; Fum: fumarate; Mal: malate; OAA: oxaloacetate. b The first lane is DNA marker and the second lane is the control before editing, the upstream primer of gdhA1 was designed in promoter PtacM, there is no PCR product in negative cells. c The plasmid stability at different temperature. The cells harboring plasmid were cultured at 25 °C, 28 °C, 30 °C and 37 °C respectively, the total number of colonies were counted by cfu per plate

In this research, the plasmid pCCG1-PtacM-gdhA1 was used to study the stability of recombinant plasmid pCCG1/pCCG2 in C. glutamicum. Some cells which harboring plasmid pCCG1-PtacM-gdhA1 was cultured at different temperature, the statistical result was showed in Fig. 2c. The cells showed maximum stability when cultured at 28 °C, while the plasmid will start to loss when the temperature higher than 30 °C, the plasmid curing reached nearly 90% at 37 °C, the stability at 25 °C was similar to 28 °C while the cell growth rate will decrease and editing cycle increase at least one day, so the 28 °C is optimal culture temperature when the cells harboring recombinant plasmid pCCG1/pCCG2.

Comparison of l-Glu and l-Gln production in the mutant strains

The new strains CGG001, CGN004, CGN005 and ATCC 13032 (as control) were cultured in l-Glutamic acid fermentation media, the results were depicted in the Fig. 3. The concentration of the l-Glutamic acid reached maximum at 60 h, the strains CGN004 (22.03 g/L) and CGN005 (20.64 g/L) decreased 20.1% and 25.1% compared to ATCC 13032 (27.57 g/L). The l-glutamine concentration in CGG001 (2.06 g/L) and CGN005 (4.73 g/L) broths increased 30.4% and 199.4% compared to ATCC 13032 (1.58 g/L), there is no l-glutamine could be detected in CGN004 broths. The cell density of ATCC 13032, CGG001 and CGN005 reached maximum at 36 h while CGN004 was increasing in 72 h and 1.21-fold than ATCC 13032. The average glucose consumption rate decreased 42.9% in CGN004 compared to ATCC 13032 in 24 h.

Fig. 3
figure 3

The fermentation results of the strains CGG001, CGN004 and CGN005. C. glutamicum ATCC 13032 was used as control. l-Glu: l-Glutamic acid; l-Gln: l-Glutamine. The results showed the concentration of l-Glu and l-Gln in fermentation broths. Meanwhile, the cell density (OD562nm) and the glucose concentration also been showed in the results. Data was shown as mean ± CI (Confidence Interval), 3 independent experiments for statistics, α = 0.01


In this research, an improved method of CRISPR/Cas9-assisted system for C. glutamicum was established, all elements for the gene editing were designed in one vector pCCG1/pCCG2. Gene editing could be done by electrotrasformation at one time. the recombinant plasmid for targeted gene could be one-step constructed in E. coli DH5α, the overall procedure of genomic editing was showed in Fig. 4, this method demonstrates simplest operation and time-saving compared to the reported, 8–9 days can complete the whole work of genomic editing and 5 days for continuous editing (the next plasmid was prepared before electrotransformation), so this method is highly efficient and suitable for abundant gene mutation in C. glutamicum.

Fig. 4
figure 4

The diagram of genomic editing procedure. a Day 1–3: The recombinant plasmid construction for targeted gene X in E. coli DH5α. Day 4–6, electroporate the plasmid into the electrocompetent cell of C. glutamicum and cultured for 2–3 days at 28 °C, examine the colonies using colony PCR method. N20 sequence at 5′-end of sgRNA was complementary to the targeted gene X, which guide Cas9 to break genome at PAM (NGG) site, the upstream and downstream homologous sequence in plasmid was used to repair the DSBs. Day 7–9, cure the plasmids in positive cells. If continuous editing was needed, make electrocompetent cells of the positive cells, electroporate another plasmid into it for the next editing cycle

Corynebacterium glutamicum is an important industrial microorganism, the studies of metabolic engineering were due to rationally design and optimize the metabolic pathway, these strategies’ implementation often based on high efficient genomic editing tools. The reported genomic editing methods were mainly multiple-plasmid system (Peng et al. 2017; Zhao et al. 2020), or integrated cas9/recET into chromosome before editing targeted gene with traditional method (Cho et al. 2017), the processes of plasmid construction, introduced one by one, and plasmid curing were complex. Wang et al. (Wang et al. 2018) introduced cas9 and recET into chromosome using plasmids pIN-cas9 and pIN-recET in advance, the plasmids were SacB-based method and need two rounds of homologous recombination, so these methods are labor-intensive and gene cas9/recET remain on chromosome after editing, sometimes, the exogenous cas9/recET in chromosome might disturbed certain metabolism of C. glutamicum and not suitable to the studies of metabolic engineering. Our method designed cas9 in plasmid and don’t need introduce any genes or plasmid into chromosome before genomic editing, meanwhile, there was no residual sequence in chromosome after editing, this is another advantage for metabolic engineering research in C. glutamicum. Peng (Peng et al. 2018) constructed two-plasmid system and improved it all-in-one CRISPR/Cas9 system, the chloramphenicol resistant pFSTC is 11.2-kb-sized vector, larger than pCCG1/pCCG2 (10 kb), so pCCG1/pCCG2 have larger loading capacity than pFSTC theoretically. Furthermore, C. glutamicum had higher resistance to kanamycin than chloramphenicol, the incubation time of C. glutamicum harboring pCCG1/pCCG2 on LBHIS plate will decrease 2–3 days than pFSTC, pCCG1/pCCG2 indicated shorter editing cycle and more efficient.

The genomic editing of C. glutamicum was time-consuming and low efficiency, the efficiency of Cas9/Cpf1-based editing were often between 20–90%, The plasmid pCCG1/pCCG2 also have some deficiencies as well, it’s hard to reach 100% might because the lack of typical CRISPR RNA sequence in C. glutamicum (Jiang et al. 2017) or Off-Target effect of Cas9 nuclease (Fu et al. 2013; Shen et al. 2014, 2019). In this research, take poxB deletion in ATCC 13032 as example, N20 sequence of AATCAGCAGATCCGCCTCAT cannot target Cas9 to cut off the genome but GGTCACCGGATACTTCACCG sequence did. Large fragments or genes (> 3 kb) insertion were not suggested due to the size of plasmids, the vector pCCG1/pCCG2 were about 10 kb, the editing efficiency will dramatically decline when the recombinant plasmid larger than 14 kb, 1.6-kb and 3.2-kb fragment integration into gabP, the efficiency was 30.4% and 21.7% respectively (Table 4). So large gene (> 3.5 kb) integration in chromosome was suggested to break the gene into some fragments and insert it one by one. Both of pCCG1 and pCCG2 were effective in C. glutamicum while there were some differences, pCCG1 might have higher efficiency while pCCG2 have higher concentration extract from E. coli DH5α, pCCG1 was mainly used in this research. To compare the pCCG1 and pCCG2, gdhA was inserted into alaT by pCCG1 and pCCG2 with same N20 and repair arms, the efficiency is 26.1% and 21.7% respectively (Table 4), we lack enough data to compare the efficiency of pCCG1 and pCCG2, but both of them were effective in C. glutamicum.

This method was ideal in C. glutamicum ATCC 13032 and ATCC 14067, other strains of C. glutamicum might show lower effective (Table 4), perhaps the replicon pBL1TS was not suitable for these strains. Some recombinant plasmids might impact the growth of E. coli DH5α, the cells’ growth rate and density might lower than regular E. coli DH5α harboring empty vector pCCG1/pCCG2. To solve this problem, E. coli DH5α could be cultured for longer time (16–20 h) or use not less than 5 mL culture to extract recombinant plasmids.

Cas9 nuclease is toxic for C. glutamicum. In this strategy, cas9 were expressed under inducible promoter Ptrc, low concentration IPTG were supplemented in media to limit cas9 expression, 0.01–0.05 mM IPTG was proper concentration and can make the cell survived (0.01 mM was suggested). Cas9 limited-expression can be achieved with two methods: first, supplement 0.01–0.02 mM IPTG in LBHIS agar plates, this method can make cas9 little continuous expression; second, supplement 0.1 mM IPTG in liquid recovery LBHIS media after electroporation and short-time induce cas9 expression for 1–1.5 h, then centrifugate the culture to collect the cell, discard the supernatant to remove IPTG, resuspend the cells in 0.1 mL LBHIS and plate streaking, the first method maybe more convenient. sgRNA fragment was amplified from plasmid pBS-sgRNA, because sgRNA is 82-bp-sized small fragment, we amplified downwards the sequence to obtain about 200-bp-size production (Fig. 1c) to facilitate the later experiment (sgRNA-R was used as universal primer). This CRISPR/Cas9-assisted method needs homology-directed system to repair double-strand breaks (DSBs) (Malyarchuk et al. 2007; Wilson et al. 2003), the proper length of homologous repaired arms were suggested between 500–1000 bp. pCCG1/pCCG2 is temperature-sensitive plasmid in C. glutamicum due to the replicon pBL1P47S mutation, plasmid pCCG1-PtacM-gdhA1 was used to test its stability in C. glutamicum ATCC 13032 (Fig. 2c), the colonies in plates were counted at 25 °C, 28 °C, 30 °C and 37 °C. It’s stable at 25–28 °C and will lost when the temperature ≥ 30 °C. The plasmid curing efficiency will up to 90% at 37 °C. It showed the maximum number of colonies at 28 °C, so 28 °C was utilized to culture the cells harboring recombinant plasmid pCCG1/pCCG2 considering with Cas9 nuclease activity, homologous repaired activity and cell growth velocity. Meanwhile, the incubation time could be decreased one day at 28 °C compared to 25 °C on the LBHIS plates, and revealed higher efficiency for large gene editing (> 2 kb). The cells harboring recombinant plasmid pCCG1/pCCG2 sometimes appeared some extremely big colonies on LBHIS plates after electrotansformation, these colonies were fast-growing (might appeared in one day on plate) compared to regular one on LBHIS plates, it is not correct mutant and not necessary to examine it with colony PCR method, the reasons of this phenomenon are unknown, perhaps related to the replicon itself.

Availability of data and materials

The datasets generated and/or analyzed during the current study are available from the corresponding author on reasonable request.


E. coli :

Escherichia coli


Polymerase chain reaction


Isopropyl β-d-1-thiogalactopyranoside


LB media containing brain heart infusion solution


  1. Altenbuchner J (2016) Editing of the Bacillus subtilis genome by the CRISPR–Cas9 system. Appl Environ Microbiol 82(17):5421–5427.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  2. Austin S, Ziese M, Sternberg N (1981) A novel role for site-specific recombination in maintenance of bacterial replicons. Cell 25(3):729–736.

    CAS  Article  PubMed  Google Scholar 

  3. Blin K, Pedersen LE, Weber T, Lee SY (2016) CRISPy-web: an online resource to design sgRNAs for CRISPR applications. Synth Syst Biotechnol 1(2):118–121.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Braga A, Oliveira J, Silva R, Ferreira P, Rocha I, Kallscheuer N, Marienhagen J, Faria N (2018) Impact of the cultivation strategy on resveratrol production from glucose in engineered Corynebacterium glutamicum. J Biotechnol 265:70–75.

    CAS  Article  PubMed  Google Scholar 

  5. Cameron Coates R, Blaskowski S, Szyjka S, van Rossum HM, Vallandingham J, Patel K, Serber Z, Dean J (2019) Systematic investigation of CRISPR–Cas9 configurations for flexible and efficient genome editing in Corynebacterium glutamicum NRRL-B11474. J Ind Microbiol Biotechnol 46(2):187–201.

    CAS  Article  PubMed  Google Scholar 

  6. Chen X, Gao C, Guo L, Hu G, Luo Q, Liu J, Nielsen J, Chen J, Liu L (2017) DCEO biotechnology: tools to design, construct, evaluate, and optimize the metabolic pathway for biosynthesis of chemicals. Chem Rev.

    Article  PubMed  Google Scholar 

  7. Cheng F, Yu H, Stephanopoulos G (2019) Engineering Corynebacterium glutamicum for high-titer biosynthesis of hyaluronic acid. Metab Eng 55:276–289.

    CAS  Article  PubMed  Google Scholar 

  8. Cho JS, Choi KR, Prabowo CPS, Shin JH, Yang D, Jang J, Lee SY (2017) CRISPR/Cas9-coupled recombineering for metabolic engineering of Corynebacterium glutamicum. Metab Eng 42:157–167.

    CAS  Article  PubMed  Google Scholar 

  9. Cleto S, Jensen JVK, Wendisch VF, Lu TK (2016) Corynebacterium glutamicum Metabolic Engineering with CRISPR Interference (CRISPRi). ACS Synth Biol 5(5):375–385.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  10. Fu Y, Foden JA, Khayter C, Maeder ML, Reyon D, Joung JK, Sander JD (2013) High-frequency off-target mutagenesis induced by CRISPR-Cas nucleases in human cells. Nat Biotechnol 31(9):822–826.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  11. Fukui K, Nanatani K, Nakayama M, Hara Y, Tokura M, Abe K (2019) Corynebacterium glutamicum CgynfM encodes a dicarboxylate transporter applicable to succinate production. J Biosci Bioeng 127(4):465–471.

    CAS  Article  PubMed  Google Scholar 

  12. Gauttam R, Seibold GM, Mueller P, Weil T, Weiß T, Handrick R, Eikmanns BJ (2019) A simple dual-inducible CRISPR interference system for multiple gene targeting in Corynebacterium glutamicum. Plasmid 103:25–35.

    CAS  Article  PubMed  Google Scholar 

  13. Hu J, Tan Y, Li Y, Hu X, Xu D, Wang X (2013) Construction and application of an efficient multiple-gene-deletion system in Corynebacterium glutamicum. Plasmid 70(3):303–313.

    CAS  Article  PubMed  Google Scholar 

  14. Hu J, Li Y, Zhang H, Tan Y, Wang X (2014) Construction of a novel expression system for use in Corynebacterium glutamicum. Plasmid 75:18–26.

    CAS  Article  PubMed  Google Scholar 

  15. Jager W, Schafer A, Puhler A, Labes G, Wohlleben W (1992) Expression of the Bacillus subtilis sacB gene leads to sucrose sensitivity in the gram-positive bacterium Corynebactenium glutamicum but not in Streptomyces lividans. J Bacteriol 174(16):5462–5465

    CAS  Article  Google Scholar 

  16. Jiang Y, Chen B, Duan C, Sun B, Yang J, Yang S (2015) Multigene editing in the Escherichia coli genome via the CRISPR-Cas9 system. Appl Environ Microbiol 81(7):2506–2514.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  17. Jiang Y, Qian F, Yang J, Liu Y, Dong F, Xu C, Sun B, Chen B, Xu X, Li Y, Wang R, Yang S (2017) CRISPR-Cpf1 assisted genome editing of Corynebacterium glutamicum. Nat Commun 8:15179.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Liu X, Yang Y, Zhang W, Sun Y, Peng F, Jeffrey L, Harvey L, McNeil B, Bai Z (2016) Expression of recombinant protein using Corynebacterium Glutamicum: progress, challenges and applications. Crit Rev Biotechnol 36(4):652–664.

    CAS  Article  PubMed  Google Scholar 

  19. Liu J, Wang Y, Lu Y, Zheng P, Sun J, Ma Y (2017) Development of a CRISPR/Cas9 genome editing toolbox for Corynebacterium glutamicum. Microb Cell Fact 16(1):205.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  20. Lv Y, Wu Z, Han S, Lin Y, Zheng S (2012) Construction of recombinant Corynebacterium glutamicum for L-threonine production. Biotechnol Bioproc E 17(1):16–21.

    CAS  Article  Google Scholar 

  21. Malyarchuk S, Wright D, Castore R, Klepper E, Weiss B, Doherty AJ, Harrison L (2007) Expression of Mycobacterium tuberculosis Ku and Ligase D in Escherichia coli results in RecA and RecB-independent DNA end-joining at regions of microhomology. DNA Repair (amst) 6(10):1413–1424.

    CAS  Article  Google Scholar 

  22. Mindt M, Heuser M, Wendisch VF (2019) Xylose as preferred substrate for sarcosine production by recombinant Corynebacterium glutamicum. Bioresour Technol 281:135–142.

    CAS  Article  PubMed  Google Scholar 

  23. Mitsui R, Yamada R, Ogino H (2019) CRISPR system in the yeast Saccharomyces cerevisiae and its application in the bioproduction of useful chemicals. World J Microbiol Biotechnol 35(7):111.

    Article  PubMed  Google Scholar 

  24. Nodvig CS, Hoof JB, Kogle ME, Jarczynska ZD, Lehmbeck J, Klitgaard DK, Mortensen UH (2018) Efficient oligo nucleotide mediated CRISPR-Cas9 gene editing in Aspergilli. Fungal Genet Biol 115:78–89.

    CAS  Article  PubMed  Google Scholar 

  25. Oh JH, van Pijkeren JP (2014) CRISPR-Cas9-assisted recombineering in Lactobacillus reuteri. Nucleic Acids Res 42(17):e131.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  26. Peng F, Wang X, Sun Y, Dong G, Yang Y, Liu X, Bai Z (2017) Efficient gene editing in Corynebacterium glutamicum using the CRISPR/Cas9 system. Microb Cell Fact 16(1):201.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  27. Peng F, Liu X, Wang X, Chen J, Liu M, Yang Y, Bai Z (2018) Triple deletion of clpC, porB, and mepA enhances production of small ubiquitin-like modifier-N-terminal pro-brain natriuretic peptide in Corynebacterium glutamicum. J Ind Microbiol Biotechnol 46(1):67–79.

    CAS  Article  PubMed  Google Scholar 

  28. Pyne ME, Moo-Young M, Chung DA, Chou CP, Kivisaar M (2015) Coupling the CRISPR/Cas9 system with lambda red recombineering enables simplified chromosomal gene replacement in Escherichia coli. Appl Environ Microbiol 81(15):5103–5114.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  29. Sasaki Y, Eng T, Herbert RA, Trinh J, Chen Y, Rodriguez A, Gladden J, Simmons BA, Petzold CJ, Mukhopadhyay A (2019) Engineering Corynebacterium glutamicum to produce the biogasoline isopentenol from plant biomass hydrolysates. Biotechnol Biofuels 12:41.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Schwentner A, Feith A, Munch E (2018) Metabolic engineering to guide evolution – Creating a novel mode for L-valine production with Corynebacterium glutamicum. Metab Eng 47:31–41.

    CAS  Article  PubMed  Google Scholar 

  31. Shen B, Zhang W, Zhang J, Zhou J, Wang J, Chen L, Wang L, Hodgkins A, Iyer V, Huang X, Skarnes WC (2014) Efficient genome modification by CRISPR–Cas9 nickase with minimal off-target effects. Nat Methods 11(4):399–402.

    CAS  Article  PubMed  Google Scholar 

  32. Shen CC, Hsu MN, Chang CW, Lin MW, Hwu JR, Tu Y, Hu YC (2019) Synthetic switch to minimize CRISPR off-target effects by self-restricting Cas9 transcription and translation. Nucleic Acids Res 47(3):e13.

    CAS  Article  PubMed  Google Scholar 

  33. Shi F, Li K, Huan X, Wang X (2013) Expression of NAD(H) kinase and glucose-6-phosphate dehydrogenase improve NADPH supply and L-isoleucine biosynthesis in Corynebacterium glutamicum ssp. lactofermentum. Appl Biochem Biotechnol 171(2):504–521.

    CAS  Article  PubMed  Google Scholar 

  34. Shi F, Luan M, Li Y (2018) Ribosomal binding site sequences and promoters for expressing glutamate decarboxylase and producing gamma-aminobutyrate in Corynebacterium glutamicum. AMB Express 8(1):61.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  35. Shi F, Zhang S, Li Y, Lu Z (2019) Enhancement of substrate supply and ido expression to improve 4-hydroxyisoleucine production in recombinant Corynebacterium glutamicum ssp. lactofermentum. Appl Microbiol Biotechnol 103(10):4113–4124.

    CAS  Article  PubMed  Google Scholar 

  36. Song X, Huang H, Xiong Z, Ai L, Yang S (2017) CRISPR-Cas9(D10A) Nickase-Assisted Genome Editing in Lactobacillus casei. Appl Environ Microbiol 83(22)

  37. Suzuki N, Tsuge Y, Inui M, Yukawa H (2004) Cre/loxP-mediated deletion system for large genome rearrangements in Corynebacterium glutamicum. Appl Microbiol Biotechnol 67(2):225–233.

    CAS  Article  PubMed  Google Scholar 

  38. Tan Y, Xu D, Li Y, Wang X (2012) Construction of a novel sacB-based system for marker-free gene deletion in Corynebacterium glutamicum. Plasmid 67(1):44–52.

    CAS  Article  PubMed  Google Scholar 

  39. Wada M, Sawada K, Ogura K, Shimono Y, Hagiwara T, Sugimoto M, Onuki A, Yokota A (2016) Effects of phosphoenolpyruvate carboxylase desensitization on glutamic acid production in Corynebacterium glutamicum ATCC 13032. J Biosci Bioeng 121(2):172–177.

    CAS  Article  PubMed  Google Scholar 

  40. Wang X (2019) Strategy for improving L-isoleucine production efficiency in Corynebacterium glutamicum. Appl Microbiol Biotechnol 103(5):2101–2111.

    CAS  Article  PubMed  Google Scholar 

  41. Wang B, Hu Q, Zhang Y, Shi R, Chai X, Liu Z, Shang X, Zhang Y, Wen T (2018) A RecET-assisted CRISPR-Cas9 genome editing in Corynebacterium glutamicum. Microb Cell Fact 17(1):63.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  42. Wang Y-Y, Xua J-Z, Zhanga W-G (2019) Metabolic engineering of l-leucine production in Escherichia coli and Corynebacterium glutamicum: a review. Crit Rev Biotechnol 39(5):633–647.

    CAS  Article  PubMed  Google Scholar 

  43. Wei L, Xu N, Wang Y, Zhou W, Han G, Ma Y, Liu J (2018) Promoter library-based module combination (PLMC) technology for optimization of threonine biosynthesis in Corynebacterium glutamicum. Appl Microbiol Biotechnol 102(9):4117–4130.

    CAS  Article  PubMed  Google Scholar 

  44. Wen J, Bao J (2019) Engineering Corynebacterium glutamicum triggers glutamic acid accumulation in biotin-rich corn stover hydrolysate. Biotechnol Biofuels 12:86.

    Article  PubMed  PubMed Central  Google Scholar 

  45. Westbrook AW, Moo-Young M, Chou CP (2016) Development of a CRISPR–Cas9 tool kit for comprehensive engineering of Bacillus subtilis. Appl Environ Microbiol 82(16):4876–4895.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  46. Wilson TE, Topper LM, Palmbos PL (2003) Non-homologous end-joining: bacteria join the chromosome breakdance. Trends Biochem Sci 28(2):62–66.

    CAS  Article  PubMed  Google Scholar 

  47. Xiao J, Wang D, Wang L, Jiang Y, Xue L, Sui S, Wang J, Guo C, Wang R, Wang J, Li N, Fan H, Lv M (2020) Increasing l-lysine production in Corynebacterium glutamicum by engineering amino acid transporters. Amino Acids 52(10):1363–1374.

    CAS  Article  PubMed  Google Scholar 

  48. Yang Z, Pei X, Xu G, Wu J, Yang L (2019) Efficient inducible expression of nitrile hydratase in Corynebacterium glutamicum. Process Biochem 76:77–84.

    CAS  Article  Google Scholar 

  49. Zha J, Zang Y, Mattozzi M, Plassmeier J, Gupta M, Wu X, Clarkson S, Koffas MAG (2018) Metabolic engineering of Corynebacterium glutamicum for anthocyanin production. Microb Cell Fact 17(1):143.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  50. Zhang C, Meng X, Wei X, Lu L (2016) Highly efficient CRISPR mutagenesis by microhomology-mediated end joining in Aspergillus fumigatus. Fungal Genet Biol 86:47–57.

    CAS  Article  PubMed  Google Scholar 

  51. Zhang Y, Wang J, Wang Z, Zhang Y, Shi S, Nielsen J, Liu Z (2019a) A gRNA-tRNA array for CRISPR-Cas9 based rapid multiplexed genome editing in Saccharomyces cerevisiae. Nat Commun 10(1):1053.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  52. Zhang Y, Zhang X, Xiao S, Qi W, Xu J, Yuan Z, Wang Z (2019b) Engineering Corynebacterium glutamicum Mutants for 3-Methyl-1-butanol Production. Biochem Genet 57(3):443–454.

    CAS  Article  PubMed  Google Scholar 

  53. Zhao N, Li L, Luo G, Xie S, Lin Y, Han S, Huang Y, Zheng S (2020) Multiplex gene editing and large DNA fragment deletion by the CRISPR/Cpf1-RecE/T system in Corynebacterium glutamicum. J Ind Microbiol Biotechnol 47(8):599–608.

    CAS  Article  PubMed  Google Scholar 

Download references


We thank Professor Zhonghu Bai from Jiangnan University for providing the plasmid pFSC in this research.


This work is supported by the National Key R&D Program of China (2018YFA0900300), the Key Technology Project of Inner Mongolia Autonomous Region in China (2019GG302), and the National First-class Discipline Program of Light Industry Technology and Engineering (LITE2018-10).

Author information




XW and XH proposed the idea, CY designed the experiments and wrote the first manuscript, XW modified and supervised this manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Xiaoyuan Wang.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no conflict of interest.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Yao, C., Hu, X. & Wang, X. Construction and application of a CRISPR/Cas9-assisted genomic editing system for Corynebacterium glutamicum. AMB Expr 11, 70 (2021).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI:


  • Corynebacterium glutamicum
  • CRISPR/Cas9
  • Metabolic engineering
  • Genomic editing
  • l-Glutamic acid fermentation