Team:CU-Boulder/Project/Kit/RestrictionEnzymes

From 2013.igem.org

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We ordered 500bp segments of DNA that, when connected through a Gibson Assembly, contained the full sequence of our genes of interest (EcoRI and EcoRI methylase). After Gibson Assembly into plasmids failed to produce any transformants, we attempted to PCR amplify our constructs from linear intermediates in the Gibson Reaction.  These PCR reactions resulted in smearing and unexpected bands (below left).  Finally, we used a PCR purification kit to clean up the Gibson Reactions before PCR amplification. Smearing disappeared and our expected bands became more prominent (below right) although multiple unexpected bands remained.  
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We ordered 500bp segments of DNA that, when connected through a Gibson Assembly, contained the full sequence of our genes of interest (EcoRI and EcoRI methylase). After Gibson Assembly into plasmids failed to produce any transformants, we attempted to PCR amplify our constructs from linear intermediates in the Gibson Reaction.  These PCR reactions resulted in smearing and unexpected bands (below left).  Finally, we used a PCR purification kit to clean up the Gibson Reactions before PCR amplification. Smearing disappeared and our expected bands became more prominent (below right) although multiple unexpected bands remained, most likely due to the DNA blocks in the Gibson Assembly annealing incorrectly, especially in the EcoRI Methylase where three 500bp DNA blocks were required.
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Using PCR with the flanking primers, we isolated and amplified the desired gene from the Gibson Assembly. These primers also included tails that added AgeI and XbaI cut-sites, thereby making our parts Freiburg compatible. Multiple bands appeared during gel electrophoresis, most likely due to the DNA blocks in the Gibson Assembly annealing incorrectly, especially in the EcoRI Methylase where three 500bp DNA blocks were required. To remedy this problem, we gel extracted the band of the correct size to isolate it from the other products. The resulting DNA was at such a low concentration that a second round of PCR was required and a subsequent purification.
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To remedy this problem, we gel extracted the band of the correct size to isolate it from the other products. The resulting DNA was at such a low concentration that a second round of PCR was required and a subsequent purification.
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In order to synthesize a plasmid containing the desired genes, we digested EcoRI, its methylase, and a previously made Freiburge pSB1C3 backbone with XbaI and AgeI. All three DNA sequences were extracted and purified with an extraction kit.
In order to synthesize a plasmid containing the desired genes, we digested EcoRI, its methylase, and a previously made Freiburge pSB1C3 backbone with XbaI and AgeI. All three DNA sequences were extracted and purified with an extraction kit.

Revision as of 03:36, 28 September 2013

Abstract

The main focus of our project was to create the constructs and purification methods necessary to produce and isolate the restriction enzyme EcoRI. EcoRI is commonly used for research and is one of the primary restriction endonucleases used in the Biobrick standard. Synthesizing a plasmid containing the gene for EcoRI and producing a simple purification method would provide a cheaper option for obtaining the enzyme.

Background Information

Bacteria lack an immune system so rely on restriction-modification (R-M) systems for defense against foreign viruses. The first enzyme involved in the system is the restriction endonuclease (REase). It is specific to a single DNA sequence that is typically four to eight nucleotides in length and is usually palindromic. When the REase recognizes this sequence, it will cleave both strands of the DNA at the backbone, resulting in “blunt” or “sticky” ends, depending on the exact function of the specific enzyme. When a bacterial cell is infected by a virus, the REase will bind to and cut its recognition sequence if present in the virus DNA; thereby, hindering or stopping the effects of the virus on the host. But this process is not specific to host or virus DNA.

To protect their own genetic information, bacterial cells also produce a methyltransferase (MTase). This enzyme is specific to the same site as its corresponding REase, but instead of cutting the DNA at this site, it tags the DNA with a methyl group, which sterically inhibits the binding of the REase. In type I R-M systems, the REase and MTase are apart of a single enzyme whereas in the simpler, type II system, they are found as two individual enzymes. When isolated, the REase from a type II system can be used independently of the methylase to digest DNA for analysis and synthesis making these enzymes a valuable tool in synthetic biology.

General Considerations

In order to produce restriction enzymes in vivo, it is necessary to protect the host DNA from auto-restriction and cell death. This is possible by expressing an excess of the MTase in relation to the REase that is being produced within the cell. Since REases form dimers (whereas MTases are monomeric) in their active form there is a natural lag phase before enzymatic activity is observed. This also implies a 2:1 excess of active MTase within the cell if both enzymes are expressed at the same rate. We intend to create a construct that expresses both enzymes on the same promoter in order to test if MTase can effectively protect the cell's DNA through this mechanism alone. It is possible that this will not provide the MTase with the advantage needed to sufficiently protect the host DNA from auto-restriction. In this is the case, it may be possible for the MTase to out compete the REase by simply expressing the MTase on a strong constitutive promoter and the REase on a weak constitutive promoter. Alternatively, it should be possible to express the MTase on a constitutive promoter and use an inducible promoter system to delay the expression of the REase until the host genome is protected.

Methods of Production

We ordered 500bp segments of DNA that, when connected through a Gibson Assembly, contained the full sequence of our genes of interest (EcoRI and EcoRI methylase). After Gibson Assembly into plasmids failed to produce any transformants, we attempted to PCR amplify our constructs from linear intermediates in the Gibson Reaction. These PCR reactions resulted in smearing and unexpected bands (below left). Finally, we used a PCR purification kit to clean up the Gibson Reactions before PCR amplification. Smearing disappeared and our expected bands became more prominent (below right) although multiple unexpected bands remained, most likely due to the DNA blocks in the Gibson Assembly annealing incorrectly, especially in the EcoRI Methylase where three 500bp DNA blocks were required.

To remedy this problem, we gel extracted the band of the correct size to isolate it from the other products. The resulting DNA was at such a low concentration that a second round of PCR was required and a subsequent purification.

In order to synthesize a plasmid containing the desired genes, we digested EcoRI, its methylase, and a previously made Freiburge pSB1C3 backbone with XbaI and AgeI. All three DNA sequences were extracted and purified with an extraction kit.

We then ligated EcoRI into the pSB1C3 backbone and EcoRI methylase into the pSB1C3 backbone at 16C for 12 hours. The ligation products were then transformed into DH10B cells and selected for on Chloramphenicol plates. We received over 200 colonies for EcoRI and about 150 colonies for EcoRI methylase.

The samples with the correct band size on the gel were sequenced. Both EcoRI and EcoRI methylase were sequence confirmed; however, we found a nonsense mutation in the methylase, which rendered it non-functional. At this point, we successfully produced and submitted a Freiburg 1C3 backbone with an EcoRI coding gene.

The Next Step

Continuing with our project, we would like to obtain a functional EcoRI methylase to then express with a promoter RBS. We then would transform plasmids with the expressed EcoRI and EcoRI methylase into bacterial cells and observe any changes in growth rates and to purify out the produced EcoRI protein.

Other restriction endonucleases we would like to express through a plasmid are: ApoI, PstI, SpeI, and XbaI.

ApoI for Malaria Testing

Another application of our project is for testing for antimicrobial resistant malaria strains. Malaria is an infection of Plasmodium falciparum and caused approximately 660,000 deaths in 2010 [1]. Chloroquine, an antimicrobial drug, is widely used to treat malaria; however, an increasing prevalence of chloroquine resistance has complicated malaria treatment. This increased resistance is linked to a mutation in one of the membrane transporters of Plasmodium falciparum (pfmdr-1) where a tyrosine residue is replaced by an arginine residue and a mutation of the transporter pfcrt where lysine is replaced by threonine [2]. The same mutation in pfmdr-1 may also be involved in lumefantrine resistance and serves as a marker for mefloquine vulnerability [3].

In order to treat malaria, the infecting bacteria must be tested for the presence of these mutations. One possible method of testing for and monitoring the spread of malaria strains is by digestion with the enzyme ApoI [4]. In wild-type strains, digestion with ApoI results in two bands during gel electrophoresis; however, chloroquine resistant strains have a mutation that destroys this cut site so only one band is produced [5].

If we applied the same procedure that we did for EcoRI we could produce a plasmid containing the ApoI gene. We could then express it by growing cultures and later harvest the enzyme for uses in restriction digests. If this restriction enzyme could be readily available, in cheap and resource limited conditions, it would make restriction enzyme assay viable for testing for antimicrobial resistance in malaria.

1. Organization WH: World Malaria Report 2012. 2012.
2. H.H. Abruquah FYB, S.C.K. Tay, and B.W.L. Lawson: Resistance-Mediating Polymorphisms of Plasmodium Falciparum Among Isolates from Children with Severe Malaria in Kumasi, Ghana. Ghana Medical Journal 2010, 44:52-58.
3. Laufer MTaM: Resistance to Antimalarial Drugs: Molecular, Pharmacologic, and Clinical Considerations. Pediatric Research 2009, 65:64-70.
4. Durand R, Huart V, Jafari S, Le Bras J: Rapid Detection of a Molecular Marker for ChloroquineResistant Falciparum Malaria. Antimicrobial Agents and Chemotherapy 2002, 46:2684-2686.
5. Abruquah, HH: Resistance-Mediatign Polymorphisms of Plasmodium Falciparum Among Isolates fraom Children with Severe Malaria in Kumasi, Ghana. Ghana Medical Journal 2010.