A strategy for enhanced circular DNA construction efficiency based on DNA cyclization after microbial transformation
- Ying-Ying Guo†1,
- Zhen-Yu Shi†3,
- Xiao-Zhi Fu1,
- Jin-Chun Chen1,
- Qiong Wu1Email author and
- Guo-Qiang Chen1, 2Email author
© Guo et al.; licensee BioMed Central. 2015
Received: 18 December 2014
Accepted: 28 January 2015
Published: 12 February 2015
With the rapid development of synthetic biology, the demand for assembling multiple DNA (genes) fragments into a large circular DNA structure in one step has dramatically increased. However, for constructions of most circular DNA, there are two contradictions in the ligation/assembly and transformation steps. The ligation/assembly consists of two different reactions: 1) the ligation/assembly between any two pieces of a linear form DNA; 2) the cyclization (or self-ligation) of a single linear form DNA. The first contradiction is that the bimolecular ligation/assembly requires a higher DNA concentration while the cyclization favors a lower one; the second contradiction is that a successful transformation of a ligation/assembly product requires a relatively high DNA concentration again. This study is the first attempt to use linear plasmid and Cyclization After Transformation (CAT) strategy to neutralize those contradictions systematically.
The linear assembly combined with CAT method was demonstrated to increase the overall construction efficiency by 3–4 times for both the traditional ligation and for the new in vitro recombination-based assembly methods including recombinant DNA, Golden Gate, SLIC (Sequence and Ligation Independent Cloning) and Gibson Isothermal Assembly. Finally, the linear assembly combined with CAT method was successfully applied to assemble a pathway of 7 gene fragments responsible for synthesizing precorrin 3A which is an important intermediate in VB12 production.
The linear assembly combined with CAT strategy method can be regarded as a general strategy to enhance the efficiency of most existing circular DNA construction technologies and could be used in construction of a metabolic pathway consisting of multiple genes.
The rapid developing synthetic biology has an increasing need for assembling multiple genes or operons into a large DNA fragment consisting of multiple metabolic pathways [1-4]. At present, three major DNA assembly techniques were commonly used: The first one is the traditional recombinant DNA technology based on the type II restriction endonucleases, BioBrick and BglBrick are two representatives, mutiple DNA fragments with standardized flanking sequences allow assembly to achieve via a simple and standardized restriction/ligation procedure [5,6]. However, the BioBrick and BglBrick techniques cannot be used for seamless assembly due to the use of restriction enzyme(s). The assembly becomes laborious when applied to a pathway involving mutiple genes. The challenge of multiple DNA fragment assembly has led to the emerge of Golden Gate method, a parallel one-pot, one-step 5 min technique to seamless assemble larger constructs [7,8]. Golden Gate method had been successfully used to assemble a 32 kb gene cluster .
The second DNA assembly technique is in vitro recombination method based on single-strand overhangs generated by single-strand exonucleases or incomplete PCR (Polymer Chain Reaction), typically represented by OE-PCR (Overlap Extension-PCR). The method is commonly used in vitro to assemble 0.5 to 5 kb DNA fragment . For multiple DNA assembly by the second method, three more improvements including In-Fusion, SLIC and Gibson have been made [10-12]. All three improvements use a proprietary enzyme mixture to assemble any fragment with 15+ bp sequence overlap. The last common method is USER (uracil-specific excision reagent) cloning, which first introduces at least one uracil in the PCR process, followed by excision of uracil using uracil DNA glycosylase . The resultant abasic site(s) cleaved by an AP-lyase, leaving 30 overhangs annealed with the complementary overhang of a fragment sharing the same overlap sequence .
The third major DNA assembly technique is the in vivo recombination that requires certain recombination systems operating inside the cells [14,15], represented by the yeast homologous recombination developed by J. Craig Venter Institute [16,17]. It can be used to assemble the entire circular synthetic Mycoplasma. genitalium genome in one step from 25 DNA pieces approximately 24 kb in size . For genome-sized assembly, yeast is not the only prefer host; recently the complete assembly of chromosomes was also achieved in Bacillus by Itaya et al. . The 3500 kb of Synechocystis DNA was inserted into B. subtilis from some 100 kb + long starting DNA fragments . Except for the extreme case of blunt ligation, both the first two assembly methods rely on the annealing of single strand DNA overhangs. Some of these technologies were reported to be successful in assembling 4–6 fragments routinely such as the Gibson isothermal assembly . Nevertheless, they suffer from demanding operations and constrains on fragment lengths mentioned in their protocols. Therefore, multiple fragment assembly is still challenging and requires improvement on efficiency.
The current study focuses on finding a solution to the dilemma: if the cyclization step is not in between the other two steps that require a high DNA concentration, the dilemma should be avoided. This solution will have three advantages: there is no by-product if all DNA fragments are mixed at an equal molar ratio when the target ligation/assembly product is linear form DNA with each junction designed to be specific (Figure 1C); secondly, the absence of by-product further allows even higher concentration for ligation/assembly and subsequently for an efficient transformation; thirdly, if an efficient in vivo cyclization after transformation can occur, the transformation will dilute and even separate the DNA physically by cell walls to allow higher yield of in vivo cyclization of linear DNA inserted into the cells with less oligomer by-products than cyclizations performed at a higher ligation concentration.
Alternatively, there is also a way to avoid cyclization if linear plasmids are used. The linear lambdoid phage N15 is one of the best studied E. coli phages due to its unique linear form, whose linear ends are protected by telomerase attached hairpins . A series minimized N15 phages were developed and reported to improve the cloning efficiency of large DNA fragments . They are candidates for constructing plasmids without cyclization.
A linear ligation/assembly with Cyclization after Transformation (CAT) strategy mentioned above could provide a way out of the dilemma, it could be especially useful for multiple fragments DNA ligation/assembly.
Unidirectional linear ligation system and grouped assembly
Since the SLIC and Gibson assembly methods are specific at every single DNA junction unless repetitive DNA is assembled. The first goal of this study was to establish a proper ligation strategy for traditional type II restriction endonucleases based methods.
Although the designed sticky ends created by 5 endonucleases could theoretically be ligated in only one way, unexpected annealing of non-complementary sticky ends were always observed when more than two fragments were mixed together. In a previous study, T to G and A to C mismatches were reported to occur in unidirectional ligation . In our study, similar phenomenon was observed when the incorrectly assembled plasmids were sequenced.
Therefore, a computer program termed StickyEndDesigner was developed to reduce mismatching phenomena during the primer design process. A copy of this software can be freely downloaded from http://stickyenddesigner.codeplex.com/. This software was designed to avoid T or A as the last base in the sticky ends, because the T or A base easily leads to mismatch in the annealing process. With all possibilities considered, the software generates only 8 sets of sticky ends that satisfied the requirements above. Hence, the previous 4 DNA fragment ligation process was modified to use 3 pairs of software-designed triplets. In addition, a grouped ligation procedure was applied with the hope that physical isolation of subgroups may show a better performance in reducing mismatch phenomenon (Figure 2B). Impressively, a denser target band was observed in the electrophoresis for the final round of grouped ligation mixture (Figure 2A, lane 2), indicating a reduced unexpected ligation, this was accompanied by increasing number of correctly constructed plasmids.
Different ligases and buffers were compared during the 4 fragments ligation experiments containing F1 (935 bp), F2 (948 bp), FR (921 bp) and Fk (1598 bp). The 4 fragments were mixed at the same molar concentration with the different ligation systems preapared above. After the 2 h ligation, the ligation efficiency was studied after the mixture was treated with SDS at 75°C for 20 min before electrophoresis. Solution I containing T4 ligase was revealed to be the most suitable for the ligation. In addition, in vitro linear ligation efficiency was also dependent on DNA fragment purity (data not shown). For example, the ligation efficiency was much higher if the DNA fragment was cloned by Phusion polymerase and purified via gel extraction compared with that of its cloned by Pfu polymerase and purified by solution extraction.
Linear plasmid as an alternative choice to avoid cyclization
Two traditional in vitro cyclization strategies
The in vitro linear ligation system was developed in our study to prevent the multimer by-product formation. However, the linear ligation products formed in vitro could not replicate in E. coli due to their linear nature. Therefore, an efficient cyclization strategy must be established. We further evaluated the “in vitro cyclization” by comparing with two traditional strategies.
Number of transformants formed using conventional in vitro circular ligation system, in vitro diluted self-ligation cyclization, in vitro self-recombination cyclization, and CAT , respectively
4 DNA fragments
6 DNA fragments
Conventional in vitro circular ligation system (S17-1λ pir )
In vitro diluted self-ligation cyclization (S17-1λ pir )
In vitro self-recombination cyclization (S17-1λ pir )
CAT strategy (S17-1λ pir∆attB HK022 pAH83CI)
CAT (Cyclization after transformation) strategy
The two traditional in vitro cyclization strategies were not as efficient as expected. Therefore, a new CAT (Cyclization after Transformation) strategy was developed. In CAT, the ligation product E. coli S17-1 λpirΔattB HK022 harboring pAH83CI was transformed with the ligation product (See Bacterial Strains and Mediums) and the ligation product would to be cyclized via the attL-attR in vivo recombination system (Figure 3C). Four and six fragments were assembled based on the CAT strategy above, as a result, 80 in 96 and 36 in 42 clones were demonstrated to be properly assembled via PCR screening of every junction, respectively, and followed by the supporting sequencing results (Table 1). Both transformation yield and DNA assembly accuracy based on the CAT strategy outperformed those of the circular ligation and diluted cyclization. It was demonstrated that the efficiencies of grouped unidirectional ligation coupled with CAT strategy are more efficient and precise than that of the conventional circular ligation, “in vitro diluted self-ligation cyclization” and “in vitro self-recombination cyclization” (Table 1). As expected, less colony numbers containing 6 properly assembled fragments were formed compared with those consisting of 4 fragments assembly. In order to further explore the advantages of this CAT strategy on multiple fragments assembly, nine DNA fragments assembly was performed (Additional file 2: Table S2). The number of successful transformants selected by kanamycin was only 16, and 2 of them were found to be assembled in the correct order via PCR screening and DNA sequencing. Colony PCR was used to study ligation accuracies. 96 randomly selected transformants were investigated if the colony number exceeded 96. After screening by colony PCR, random colonies were selected to do plasmid extraction. The extracted plasmids were analyzed by endonuclease digestion and DNA sequencing. It was found that all the sequencing results were consistent with the colony PCR ones. Also, the incorrect constructed plasmids were sequenced, the sequencing results showed that the incorrect assembly could mainly be contributed to the ligation mismatching.
CAT-Recombinant DNA: Recombinant DNA using CAT
Results of the comparisons between CAT strategy and non-CAT control
Circular Recombinant DNA
CAT - Recombinant DNA
CAT /non- CAT × 4/3
Circular Gibson Assembly
CAT - Gibson Assembly
CAT /non- CAT × 4/3
CAT /non- CAT × 4/3
Circular Golden Gate
CAT - Golden Gate
Golden Gate method has a low overall efficiency when the concentration is low. We repeated 3 times yet were not able to obtain reliable data at 0.5 pM total DNA molar concentration. When the total concentrations are 1 pM and 2 pM, respectively, however, CAT strategy showed exceptional 24.44 times and 19.98 times more efficient compared with the non-CAT controls, respectively (Table 2).
In order to demonstrate that the CAT strategy can truly improve the efficiency for DNA assembly, and it was possible to apply to SLIC method. Similar to the recombinant DNA (ligation) method, the overall efficiency of CAT turned out to be 3.48 times of the non-CAT one at 2 pM total DNA molar concentration (Table 2).
When CAT strategy was applied to Gibson isothermal assembly, similarly, an overall efficiency as 3.48 times high as the non-CAT control was observed at 2 pM total DNA molar concentration (Table 2).
Construction of optimized precorrin-3A production pathway from precursor 5-aminolevulinic acid
Grouped ligation can avoid DNA assembling mismatch
Circular ligation always comes along with the formation of multimer by-products (Figure 1B-D). On the other hand, the absence of multimer by-products indicated no occurrence of circular ligations. Linear ligation offers a possibility to overcome this contradiction (Figure 3C).
As long as every DNA fragment has an equal molar concentration in the mixture, and the ligation yield of every ligation process is 100%, the theoretical ligation yield should be 100%. To precisely address the effect of each fragment on ligation yield, theoretical models (http://www.synthenome.com/StickyEndDesigner.zip) were developed to study effects of concentrations of the DNA fragments in the ligation mixture on linear ligation yield. It was found that over-dose of the first and the last fragments, namely FR and FK did not affect ligation yield, while other DNA fragments in between must have an equal molar ratio to avoid ligation by-products.
However, ligation yield was always below 100% under experimental conditions due to inadequate ligations and unexpected ligations (Figure 2A). Many studies focused on unexpected ligation resulted from mismatching ligation, such as the mismatches of T to G and A to C . It is useful to properly design sticky ends so that unexpected ligation can be significantly reduced. However, the designed sticky ends did not significantly reduce mismatches (data not shown). Therefore, the method of grouped ligation into a linear fragment with a free end was developed. The method was found the most efficient in reducing the ligation mismatches (Figure 2B). As grouped ligation isolates fragments that are not designed to ligate, and thus lead to reduction on unexpected ligations. Furthermore, parts of the unexpected ligation may be attributed to unexpected digestion of the single-strand overhangs . It could be expected that unwanted digestions can be significantly reduced when highly pure reagents were used. The single strand annealing nature determines that unspecific annealing would be also an issue for in vitro the recombination methods such as SLIC and Gibson isothermal assembly. This study also demonstrates that the grouped ligation/assembly can enhance SLIC assembly efficiency.
CAT strategy takes advantages of DNA concentration conditions in both ligation and transformation
Unidirectional ligation/assembly requires a DNA concentration to be high enough to allow efficient bimolecular ligation/assembly, transformation will benefit from a high DNA concentration of the ligation/assembly mixture. However, the challenge for transforming linear ligation products into a host is the difficulty to cyclize them rapidly and efficiently in vivo to form stable and reproducible circular DNA form. In order to obtain a high cyclization efficiency, site-specific recombination was selected as the cyclization strategy, as this attB-attP recombination catalyzed by Int or Int-Xis has very high efficiency (Figure 3C, right hand) . When E. coli DH5 alpha harboring pInt-ts was transformed with plasmid pAH63 , the number of resulting successful transformants could match that of E. coli S17 λpir. That is to say, if the transformation efficiencies of linear and circular DNA are similar, the attB-attP in vivo recombination may be close to 100% (Additional file 3: Figure S1) . Therefore, the in vivo cyclization does not result in decrease in efficiency. During the transformation, the transformed linear ligation products are naturally diluted by competent cell mixtures and finally isolated physically by cell walls. This provides a situation that favors a much higher yield of self-cyclization. Our results demonstrated that circular ligation of six fragments showed a lower efficiency than that of the linear ligation coupled with in vivo cyclization of six fragments (Table 1). Therefore, the grouped ligation coupled with the in vivo cyclization process can take advantages of all procedures including: a close to 100% theoretical yield of linear ligation, a dilution during transformation, and a close to 100% yield on in vivo lambda attachment sequences recombination, as well as a final high self-cyclization yield (Figure 3C, right hand). Furthermore, this strategy showed enhanced efficiency in ligating at least nine fragments (data not shown) than that of the traditional circular approaches.
CAT strategy increases overall construction efficiency for existing circular DNA construction methods
In order to demonstrate that the CAT strategy can improve the efficiency for all known existing circular plasmids construction methods, it was applied to 4 most widely used methods, i.e. Recombinant DNA, Golden Gate, SLIC and Gibson isothermal assembly (Table 2). Since it is a challenge to obtain highly concentrated DNA, a comparison was made using CAT strategy and non-CAT control based on same total DNA concentration to ensure that there is no additional difficulty in preparing DNA for CAT strategy. As a result, the multiplier 4/3 is applied to the CAT/non-CAT number to present the true difference in efficiency. It was found that CAT strategy generated a 3.55 ± 0.13 times correct colonies of the original technologies for all technologies except Golden Gate. And this stable 3.55 times may indicate that there is at least 71.8% by-products in the circular ligation/assembly products for the three fragments when each fragment is 0.67 pM in the ligation/assembly mixture. Another assembly technique including recombination of attL/R for assembling multiple fragments should also benefit from CAT strategy .
CAT strategy is easy to use together with most existing circular construction technology
Any existing circular construction system can easily adopt CAT strategy by splitting the plasmid backbone into 2 fragments and this will not affect the ligation/assembly of the other fragments/inserts. When attP scar is allowed to appear between inserts and plasmid backbone, a 5-time higher efficiency could be possible, which means, the efficiency of the CAT strategy was 5 times as high as the conventional in vitro cyclization (Table 1). Although the CAT strategy requires the in vivo cyclization step, this step is identical to typical electroporation because the recombination occurs in vivo without even the need for heat induction. The only additional in vitro operation is the preparation of an additional fragment. Furthermore, as discussed in the section above, no additional efforts in concentrating DNA is required to adopt CAT strategy.
Synthetic biology often requires the assembly of many fragments at one time. Low concentration and high by-products ratio are the two major challenges for such assembly. Since CAT strategy has a higher tolerance to high DNA concentration without formation of by-products as long as every junction is specific, it should have wide application in multiple-fragments ligation/assembly.
In summary, this study successfully established the CAT strategy to avoid the long-standing concentration dilemma in circular DNA construction. CAT was shown to significantly improve recombinant DNA, SLIC, USER and Gibson isothermal assembly, thus it can be applied to existing circular plasmid construction methods.
Materials and methods
Bacterial strains, media and plasmids
Bacterial strains and plasmids used in this study
Strains and plasmids
Reference(s) and/or derivations
E. coli S17-1λ pir
TpR SmR recA, thi, pro, hsdR-M + RP4: 2-Tc:Mu: Km Tn7 λp
E. coli BL21(DE3)
F−, ompT, hsdS(rb −mb −), gal, dcm(DE3)
E. coli TSA
Host strain fro linear plasmid
A. hydrophila 4AK4
AmpR; Wild type isolated from sewage samples, PHBHHx producing strain
Gram-negative facultative anaerobic bacterium that performs denitrification, producing VB12
Huabei Pharmaceutical Enterprise
HK022 attP site, KmR
pUK derived, attL,attR sequence produced by recombination, KmR
FLP recombinase helper plasmid, ts-rep, AmpR,CmR
pAH83 derived, expression control gene cI was broken by HindIII digesition
pAL2 derived,int under the control of P1 promoter, expression control gene cI AmpR
E.coli Genetic Stock Center
pJAZZOC derived, a fragment containing DraIII recognition site inserted.
P15A replicon, CmR
Qing Lan corporation
pVQL derived, haboring genes hemBCD, cobAI, CmR
In this study, HK022 attL-attR (Additional file 5: Table S4) recombination system was used for in vivo cyclization . Plasmid pUKG (Additional file 6: Figure S2) was used as a template for vector backbone fragments FR, attL-R6K (R6K: R6kγ origin) and FK, attR-Km (Km: kanamycin resistant gene). pUKG was constructed by the following procedures: pUK plasmid  was integrated into E. coli genome with the help of pAH69  by recombination between attB and attP. The resulting attL-R6K–Km-attR fragment in the genome was then amplified by PCR, and self-ligated into a circular plasmid, namely pUKG (Table 3).
Preparation of DNA fragments with sequence of 5 specific non-palindromic restriction endonucleases
In order to ligate N DNA fragments i.e. F1, F2 … FN, two fragments as backbone of the plasmids, namely, FR and FK, were required. Totally N + 2 fragments were produced using PCR. The backbone fragments were different due to the various types of vectors and ligation methods used. In circular ligation, the FR fragment contained R6K (R6kγ replicon) and attL, and the FK fragment consisted of kanamycin resistant gene and attR (attL and attR were the HK022 attL/R recombination system). Five non-panlindromic restriction sites (AlwnI, BglI, DraIII, PflmI and SfiI) for unidirectional ligation (i.e. each junction in the ligation is designed to be specific) were attached to all ends of the N + 2 fragments. For linear ligation, all the N + 2 fragments were the same except for no restriction site added at the attL and attR sides of FR and FK. Furthermore, the N DNA fragments were ligated into the specific linear plasmid pJAZZ-OC-DraIII which was modified on the basis of pJAZZ-OC (Lucigen, USA) by inserting a fragment subcloned from pBBR1MCS2  with two DraIII recognition sites. The two backbone fragments FR and FK were different, they are the two large digestion products of pJAZZ-OC-DraIII: FR contained the linear replication origin, telN: telemorease and one hairpin end, and FK was the chloramphenicol resistant gene linked with the other end of the hairpin . All the fragments were digested by corresponding restriction enzymes, respectively, followed by purification using agarose gel-electrophoresis or solution extraction, and finally they were adjusted to a final molar concentration of 200 fmol/μl.
In vitro ligation
Two ligation systems were adopted. The first one combined all the N + 2 fragments with the same molar concentration into one test tube, followed by the ligation process using the commercial Takara ligation kit. The second one is called “grouped ligation”, in which the linear ligation process was divided into several runs. Taking the group of ligation fragments FR, F1, F2, F3 and FK as an example (Figure 5), FR and F1 were ligated into FR1, F2 and F3into F23 in the first run, and FK was left for the next run. During the second run of ligation, FR1 and F23 were ligated to form FR123, and FK was left for the next round. In the final round, FR123 and FK were ligated to become the final product FR123K. In each run, an equal mole of every two adjacent fragments was assigned in one group and ligated at 16°C for 2 h. This method could reduce unspecific ligation between non-adjacent fragments. After the in vitro ligation process, the circular DNA products that could replicate in E. coli directly were formed in circular ligation system, and E. coli S17-1λpir was transformed with these circular DNA products.
In vitro and in vivo cyclization
In the case of linear ligation system, the linear ligation products need to be cyclized to be able to replicate as circular plasmids in E. coli. In this study, three systems were adopted. The first was in vitro “diluted ligation cyclization”, the ligation products were diluted 10 folds with water in order to ensure self-ligation, and T4 ligase was used to cyclize the ligation products (The first branch from left of Figure 3C); The second one is “in vitro diluted self-recombination cyclization”, LR clonase was applied to cyclize the ligation products. In the case of LR clonase, the HK022 attL and attR in FR and FK were changed to λattL and attR. All the in vitro cyclized products were electroporated into E. coli S17-1 λpir electro-competent cells (The second branch from left of Figure 3C). Transformants were sprayed onto kanamycin agar plates, and then verified by PCR after 18 h of incubation. The last one is the “CAT strategy”, the linear ligation products were directly electroporated into electro-competent cells of E. coli S17-1 λpirΔattB HK022 carrying the corresponding pAH83CI helper plasmid (The right branch of Figure 3C). The pAH83CI could catalyze the recombination reaction of the Hk022 attL/R system.
CAT on Recombinant DNA: Recombinant DNA using CAT
When CAT (Linear assembly - Transformation –in vivo Cyclization) is applied to a Recombinant DNA technology ligation of 3 fragments, the backbone fragment with an attP site is designed as 2 separate fragments with the attL and attR sites respectively for in vivo cyclization. The attL and attR sites will recombine and produce an attP site so that the final product is exactly the same as the expected ligation product from 3 fragment (Figure 4A). The fragments for digestion were all prepared by PCR. In the in vitro linear ligation of the CAT strategy, 4 DNA fragments digested by 5 specific non-palindromic restriction endonucleases were mixed at equal molar ratio to reach final total DNA concentrations of 0.5 pM, 1.0 pM, 2.0 pM, and then ligated into linear form intermediates by grouped ligation. And then the ligation products were directly electroporated into electro-competent cells of E. coli S17-1 λpirΔattB HK022 carrying the corresponding pAH83CI helper plasmid to do the in vivo cyclization step. At the meanwhile, 3 fragments digested by the same set of restriction enzymes were mixed at 0.5 pM, 1.0 pM, 2.0 pM concentrations and directly ligated into circular forms and then electroporated into the same E. coli S17-1 λpirΔattB HK022 competent cells carrying the corresponding pAH83CI helper plasmid to serve as the non-CAT control. The colonies on the Km screening plates from both CAT and non-CAT control sets were counted and verified by PCR and sequencing.
CAT-Golden Gate: Golden Gate Assembly using CAT
Similarly, the CAT strategy was also applied to the Golden Gate methods. DraIII and BglI were used as the cutting enzymes in Golden Gate method. For short, in CAT strategy, 4 PCR fragments were mixed at equal molar ratio with 0.5 μl of DraIII (Fermentas), 0.5 μl of BglI (Fermentas), 5 units of T4 DNA ligase and 1 μl of T4 DNA ligase buffer and finally calibrated to a 10 μl digestion-ligation system with total DNA concentrations at 0.5 pM, 1.0 pM and 2.0 pM. The 3 fragments for non-CAT control were treated in the same way to reach the 0.5 pM, 1.0 pM and 2.0 pM digestion-ligation system, respectively. The digestion-ligations were performed in a thermocycler. Programs consist of the following steps: 1) incubation for 2 minutes at 37°C and 5 minutes at 16°C, both steps repeated 50 times; 2) incubation for 5 minutes at 50°C (final digestion); 3) 5 minutes at 80°C (heat inactivation). Finally, electro-competent cells of E. coli S17-1 λpirΔattB HK022 harboring the corresponding pAH83CI helper plasmid were transformed with the digestion-ligation products to finished the in vivo cyclization step. The colonies of transformants on the Km screening plates were counted and verified by PCR and sequencing.
CAT-SLIC: SLIC using CAT
In a similar manner, CAT was also applied to SLIC. The 4 fragments for CAT-SLIC and 3 fragments for non-CAT control were prepared from the same templates as the recombinant DNA group, but a 40 bp homologous region that could specifically recombine under T4 DNA polymerase and annealing treatments were attached to each end. These PCR products were purified by gel-electrophoresis, and subsequently treated by T4 DNA polymerase for 5 minutes in a thermocycler. T4 DNA polymerase was inactivated at 75°C for 10 minutes, then, 4 fragments for CAT strategy were mixed together in a reaction system containing RecA and T4 ligation buffer at final DNA concentration of 0.5 pM, 1.0 pM and 2.0 pM, respectively. The annealing process was conducted by gradually reducing the temperature from 75°C to 37°C at the rate of 0.1°C/s. The 3 fragments for non-CAT control were treated in the same way. Finally, E. coli S17-1 λpir was transformed with the reaction system and spread on a selective plate containing Km. The colonies of transformants were counted and verified by PCR and sequencing.
CAT-Gibson: Gibson isothermal assembly using CAT strategy
Similar to the CAT-SLIC strategy, the 4 PCR fragments for CAT-Gibson or the 3 fragments for non-CAT Gibson control were mixed at final DNA concentrations of 0.5 pM, 1.0 pM and 2.0 pM in the Gibson Assembly Master Mix (2X). Then electro-competent cells of E. coli S17-1 λpirΔattB HK022 harboring the corresponding pAH83CI helper plasmid were transformed with the Gibson assembly products to complete the in vivo cyclization step. The colonies of transformants on the Km screening plates were counted and verified by PCR and sequencing.
Construction of optimized precorrin-3A synthesis pathway from precursor 5-aminolevulinic acid
The genes for precorrin-3A synthesis pathway from precursor 5-aminolevulinic acid include hemB, hemC, hemD, cobA, and cobI. Among these genes, hemB, hemC, hemD are from Bacillus subtilis. cobA, cobI from P. denitrificans (Table 3). For the expression of these 5 genes in E. coli, codon optimization was conducted. These genes were synthesized chemically. These 5 genes were constructed into one plasmid p15ABCDAI which requires a multiple DNA (in this case, 7) fragments assembly method. These 7 fragments include FR (attL-p15a-T7), F1 (hemB), F2 (hemC), F3 (hemD), F4 (T7-cobA), F5 (cobI) and Fk (Cm-attR).
The FR fragment was prepared by over-extension PCR using the template plasmid pUK and pVQL, the T7 promoter was attached into the primer sequence. The 7 fragments were cloned, digested, and linearly ligated in group according the standard grouped in vitro linear ligation method (Figure 5B). Then, electro-competent cells of E. coli S17-1 λpirΔattB HK022 harboring the corresponding pAH83CI helper plasmid were transformed with the ligation products (The right branch of Figure 3C). Transformants were sprayed onto chloromycetin agar plates, and then verified by PCR after 18 h of growth. The E. coli BL21 (DE3) was transformed with the constructed plasmid p15ABCDAI to from the strain E. coli BL21DE3 (p15ABCDAI). The BL21DE3 (p15ABCDAI) strain was cultured by LB medium with 1 g/L 5-aminolevulinic acid as precursor to test the production of precorrin 3A.
This project was supported by the State Basic Science Foundation 973 (Grant No. 2012CB725201 to GQC, Grant No. 2012CB725204 to QW) and National Natural Science Foundation of China (Grant No. 31430003 and 31270146).
- Ellis T, Adie T, Baldwin GS. DNA assembly for synthetic biology: from parts to pathways and beyond. Integr Biol (Camb). 2011;3:109–18.View ArticleGoogle Scholar
- Lu C, Mansoorabadi K, Jeffries T. Comparison of multiple gene assembly methods for metabolic engineering. Appl Biochem Biotechnol. 2007;137–140:703–10.View ArticleGoogle Scholar
- Zhou XY, Yuan XX, Shi ZY, Meng DC, Jiang WJ, Wu LP, et al. Hyperproduction of poly(4-hydroxybutyrate) from glucose by recombinant Escherichia coli. Microb Cell Fact. 2012;11:54.View ArticleGoogle Scholar
- Rodriguez A, Martinez JA, Flores N, Escalante A, Gosset G, Bolivar F. Engineering Escherichia coli to overproduce aromatic amino acids and derived compounds. Microb Cell Fact. 2014;13:126.Google Scholar
- Smolke CD. Building outside of the box: iGEM and the BioBricks Foundation. Nat Biotechnol. 2009;27:1099–102.View ArticleGoogle Scholar
- Anderson JC, Dueber JE, Leguia M, Wu GC, Goler JA, Arkin AP, et al. BglBricks: a flexible standard for biological part assembly. J Biol Eng. 2010;4:1.View ArticleGoogle Scholar
- Engler C, Gruetzner R, Kandzia R, Marillonnet S. Golden gate shuffling: a one-pot DNA shuffling method based on type IIs restriction enzymes. PLoS One. 2009;4:e5553.View ArticleGoogle Scholar
- Engler C, Marillonnet S. Combinatorial DNA assembly using Golden Gate cloning. Methods Mol Biol. 2013;1073:141–56.Google Scholar
- Bryksin AV, Matsumura I. Overlap extension PCR cloning: a simple and reliable way to create recombinant plasmids. Biotechniques. 2010;48:463–5.View ArticleGoogle Scholar
- Sleight SC, Bartley BA, Lieviant JA, Sauro HM. In-Fusion BioBrick assembly and re-engineering. Nucleic Acids Res. 2010;38:2624–36.View ArticleGoogle Scholar
- Li MZ, Elledge SJ. Harnessing homologous recombination in vitro to generate recombinant DNA via SLIC. Nat Methods. 2007;4:251–6.View ArticleGoogle Scholar
- Gibson DG, Young L, Chuang RY, Venter JC, Hutchison 3rd CA, Smith HO. Enzymatic assembly of DNA molecules up to several hundred kilobases. Nat Methods. 2009;6:343–5.View ArticleGoogle Scholar
- Geu-Flores F, Nour-Eldin HH, Nielsen MT, Halkier BA. USER fusion: a rapid and efficient method for simultaneous fusion and cloning of multiple PCR products. Nucleic Acids Res. 2007;35:e55.View ArticleGoogle Scholar
- Li MZ, Elledge SJ. MAGIC, an in vivo genetic method for the rapid construction of recombinant DNA molecules. Nat Genet. 2005;37:311–9.View ArticleGoogle Scholar
- Shao Z, Zhao H. DNA assembler, an in vivo genetic method for rapid construction of biochemical pathways. Nucleic Acids Res. 2009;37:e16.View ArticleGoogle Scholar
- Gibson DG, Benders GA, Andrews-Pfannkoch C, Denisova EA, Baden-Tillson H, Zaveri J, et al. Complete chemical synthesis, assembly, and cloning of a Mycoplasma genitalium genome. Science. 2008;319:1215–20.View ArticleGoogle Scholar
- Gibson DG, Benders GA, Axelrod KC, Zaveri J, Algire MA, Moodie M, et al. One-step assembly in yeast of 25 overlapping DNA fragments to form a complete synthetic Mycoplasma genitalium genome. Proc Natl Acad Sci U S A. 2008;105:20404–9.View ArticleGoogle Scholar
- Gibson DG, Glass JI, Lartigue C, Noskov VN, Chuang RY, Algire MA, et al. Creation of a bacterial cell controlled by a chemically synthesized genome. Science. 2010;239:52–6.View ArticleGoogle Scholar
- Itaya M, Fujita K, Kuroki A, Tsuge K. Bottom-up genome assembly using the Bacillus subtilis genome vector. Nat Methods. 2008;5:41–3.View ArticleGoogle Scholar
- Itaya M, Tsuge K, Koizumi M, Fujita K. Combining two genomes in one cell: stable cloning of the Synechocystis PCC6803 genome in the Bacillus subtilis 168 genome. Proc Natl Acad Sci U S A. 2005;102:15971–6.View ArticleGoogle Scholar
- Ravin NV. N15: the linear phage-plasmid. Plasmid. 2011;65:102–9.View ArticleGoogle Scholar
- Godiska R, Mead D, Dhodda V, Wu C, Hochstein R, Karsi A, et al. Linear plasmid vector for cloning of repetitive or unstable sequences in Escherichia coli. Nucleic Acids Res. 2010;38:e88.View ArticleGoogle Scholar
- Rieger A, Nassal M. Restriction endonuclease Alw NI is blocked by overlapping Dcm methylation. Nucleic Acids Res. 1993;21:4148.View ArticleGoogle Scholar
- Burger KJ, Schinzel R. Restriction endonuclease BglI as a tool for in vitro reconstruction and recombination of plasmid and bacteriophage genomes. Mol Gen Genet MGG. 1983;189:269–74.View ArticleGoogle Scholar
- Grosskopf R, Wolf W, Kessler C. Two new restriction endonucleases DraII and DraIII from Deinococcus radiophilus. Nucleic Acids Res. 1985;13:1517–28.View ArticleGoogle Scholar
- Qiang BQ, Schildkraut I. A type II restriction endonuclease with an eight nucleotide specificity from Streptomyces fimbriatus. Nucleic Acids Res. 1984;12:4507–16.View ArticleGoogle Scholar
- Heldt D, Lawrence AD, Lindenmeyer M, Deery E, Heathcote P, Rigby SE, et al. Aerobic synthesis of vitamin B12: ring contraction and cobalt chelation. Biochem Soc Trans. 2005;33:815–9.View ArticleGoogle Scholar
- Roessner CA, Park JH, Scott AI. Genetic engineering of Escherichia coli for the production of precorrin-3 in vivo and in vitro. Bioorg Med Chem. 1999;7:2215–9.View ArticleGoogle Scholar
- Tsuge K, Matsui K, Itaya M. One step assembly of multiple DNA fragments with a designed order and orientation in Bacillus subtilis plasmid. Nucleic Acids Res. 2003;31:e133.View ArticleGoogle Scholar
- Minaeva NI, Gak ER, Zimenkov DV, Skorokhodova AY, Biryukova IV, Mashko SV. Dual-In/Out strategy for genes integration into bacterial chromosome: a novel approach to step-by-step construction of plasmid-less marker-less recombinant E. coli strains with predesigned genome structure. BMC Biotechnol. 2008;8:63.View ArticleGoogle Scholar
- Haldimann A, Wanner BL. Conditional-replication, integration, excision, and retrieval plasmid-host systems for gene structure-function studies of bacteria. J Bacteriol. 2001;183:6384–93.View ArticleGoogle Scholar
- Zhang L, Zhao G, Ding X. Tandem assembly of the epothilone biosynthetic gene cluster by in vitro site-specific recombination. Sci Rep. 2011;1:141.Google Scholar
- Simon R, Priefer U, Pühler A. A broad host range mobilization system for in vivo genetic engineering: transposon mutagenesis in gram negative bacteria. Nat Biotechnol. 1983;1:784–91.View ArticleGoogle Scholar
- Meng DC, Shi ZY, Wu LP, Zhou Q, Wu Q, Chen JC, et al. Production and characterization of poly(3-hydroxypropionate-co-4-hydroxybutyrate) with fully controllable structures by recombinant Escherichia coli containing an engineered pathway. Metab Eng. 2012;14:317–24.View ArticleGoogle Scholar
- Zhou Q, Shi ZY, Meng DC, Wu Q, Chen JC, Chen GQ. Production of 3-hydroxypropionate homopolymer and poly(3-hydroxypropionate-co-4-hydroxybutyrate) copolymer by recombinant Escherichia coli. Metab Eng. 2011;13:777–85.View ArticleGoogle Scholar
- Yagil E, Dolev S, Oberto J, Kislev N, Ramaiah N, Weisberg RA. Determinants of site-specific recombination in the lambdoid coliphage HK022. An evolutionary change in specificity. J Mol Biol. 1989;207:695–717.View ArticleGoogle Scholar
- Datsenko KA, Wanner BL. One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. Proc Natl Acad Sci. 2000;97:6640–5.View ArticleGoogle Scholar
- Lee SH, Oh DH, Ahn WS, Lee Y, Choi J, Lee SY. Production of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) by high-cell-density cultivation of Aeromonas hydrophila. Biotechnol Bioeng. 2000;67:240–4.View ArticleGoogle Scholar
- ZY S. Parallel DNA Assembly by Recombination. https://minerva-access.unimelb.edu.au/handle/11343/37429?show=full (2014). Accessed 22 May 2014
- Zhenyu S, Anthony Gordon W, Gras SL. Parallel In Vivo DNA Assembly by Recombination: experimental demonstration and theoretical approaches. PLoS One. 2013;8:e56854.View ArticleGoogle Scholar
- Kovach ME, Elzer PH, Hill DS, Robertson GT, Farris MA, Roop 2nd RM, et al. Four new derivatives of the broad-host-range cloning vector pBBR1MCS, carrying different antibiotic-resistance cassettes. Gene. 1995;166:175–6.View ArticleGoogle Scholar
- Mardanov AV, Ravin NV. Functional characterization of the repA replication gene of linear plasmid prophage N15. Res Microbiol. 2006;157:176–83.View ArticleGoogle Scholar
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