Team:Rutgers

From 2014.igem.org

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<li><a href="https://static.igem.org/mediawiki/2014/3/35/Rutgers_transformation.png">Chemical Transformation of Competent E. coli cells</a></li>
<li><a href="https://static.igem.org/mediawiki/2014/3/35/Rutgers_transformation.png">Chemical Transformation of Competent E. coli cells</a></li>
<li><a href="https://static.igem.org/mediawiki/2014/4/48/Rutgers_overnight.png">Growing Cell Cultures Overnight and Creating a Glycerol Stock</a></li>
<li><a href="https://static.igem.org/mediawiki/2014/4/48/Rutgers_overnight.png">Growing Cell Cultures Overnight and Creating a Glycerol Stock</a></li>
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<li><a href="https://static.igem.org/mediawiki/2014/f/fe/Rutgers_NEB_gibson.pdf">NEB's Gibson Assembly protocol</a></li>
</ul>
</ul>
</td></tr></table>
</td></tr></table>
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<h2>Chronology</h2>
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<div class="fp"><p>May</p></div>
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<ul class="reglist">
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<li>this and that</li>
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<li>that and this</li>
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</ul>
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<div class="fp"><p>June</p></div>
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<div class="fp"><p>July</p></div>
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<div class="fp"><p>August</p></div>
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<div class="fp"><p>September</p></div>
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<div class="fp"><p>October</p></div>
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Revision as of 00:38, 18 October 2014

The Next Step in DNA Synthesis

De novo DNA Synthesis is extremely important to the world of Synthetic Biology, but the low efficiency of today's DNA Synthesis technology limits us.

We can only synthesize about 150 bases at a time, so new genes have to be stitched together from smaller strands, which adds a lot to the time and cost required. This needs to change.

A Primer on DNA Synthesis

We currently use organic (anhydrous) solvents and reactive amidites to synthesize all custom DNA sequences, whether for antibody/enzyme engineering, multi-gene pathway building, or even genome construction. The process looks something like this:

This is one cycle in the process of DNA Synthesis. A solution of blocked nucleotides (whichever A, C, G, or T comes next in the sequence) is added to a group of immobilized DNA strands, and a single nucleotide is incorporated at the end of each strand. The trouble with this highly unnatural method is that each of the chemicals depicted (trichloroacetic acid, 2-benzylthiotetrazole, acetonitrile) causes some harm to the chemical structure of DNA, and this will limit the yield in a way that gets exponentially worse when building longer and longer pieces of DNA.

The process pictured above typically causes enough side-reactions to chemically "break" 1.5% of the existing DNA strands, in each and every cycle (leaving 98.5% of them intact and with correct sequence). This concept is called coupling efficiency, and it's the reason we can only synthesize up to 130-150 bases at a time (or even 200 bases if you're willing to pay a whole lot extra).

Our Idea: Use Enzymes

We believe that both cost and efficiency could be vastly improved by using enzymes for de novo DNA Synthesis. Enzymes that have evolved alongside nucleic acids for billions of years (polymerases) could be applied to eliminate side-reactions and significantly simplify the process overall. This process simplification could be beneficial on two counts: less complexity in required machinery would reduce capital costs, and less material requirements would reduce operational costs. One way to get huge gains in efficiency for any DNA-related process (see Sequencing, for example) ... With DNA Synthesis, this would mean switching from ... it may be prudent to begin investigating more natural, aqueous environments (that are chemically less harmful to the DNA during synthesis).

This is the enzymatic process that our team has envisioned. Note the

Accomplishments

Over the summer we ran a number of assays to investigate the functionality of TdT in the context of our envisioned DNA Synthesis strategy. We used short, single-stranded primers (composed of 15 thymidine residues each) with 5' fluorescent tags (5'-FAM), and visualized the results on 22% polyacrylamide nondenaturing gels. The images are oriented with the loading wells above, so that the shortest oligos (which travel the fastest) end up furthest down in each lane. Each assay has a Control lane containing only the 15-length primer for reference. All lanes are labeled with neon-green text superimposed over the strange gray blotches of loading dye.


  • Tested the extension of single-stranded primers with TdT
  • This assay established that TdT will add ordinary (not blocked) thymidine triphosphate to the ends of the single-stranded primers. The lanes are labeled with how many minutes the primers were incubated with TdT and dTTP. The 30-minute result has the longest oligos (having traveled the least distance), but it appears more condensed because it had less distance to effectively resolve the differing oligo lengths. In later assays we let the gels run as far as possible to avoid the bunching-up of long oligos.
  • Based on data in the literature, we estimate that a few hundred bases were added to each oligo (on average) under these reaction conditions (see Protocols, under Lab Notebook). A DNA ladder would be prohibitively expensive to create for these short, single-stranded, fluorescent primers, unfortunately.
  • Tested the effect of pH on acetylated thymidine incorporation
  • The lanes, as labeled: "C" is the primer-only control, "6.5" is the reaction carried out with acetylated thymidine in MOPS buffer at pH 6.5 for 10 minutes, "7.0" is the same (at pH 7.0), "7.5" is the same (at pH 7.5), "7.9" is the same (at pH 7.9), and "dTTP+NEB buffer" is the reaction carried out with unmodified thymidine in (NEB-supplied) Tris buffer at pH 7.9 for 10 minutes.
  • This assay demonstrates that TdT adds less 3'-acetylated ("blocked") nucleotides at a lower pH. Aside from lane "7.0" (the anomaly), there is a clean step-ladder effect of longer oligos produced at higher pH. There is still a significant spread of differing oligo lengths in the pH 6.5 lane, which indicates that enough hydrolysis occurs (of the acetyl blocking group) to allow for multiple additions. This contradicts the findings of the later assays (below) that show no such spread of oligo lengths after reaction at pH 6.5. In principle, the rate of hydrolysis depends not only on pH of reaction, but also on the concentration of acetylated thymidine. Another factor influencing hydrolysis is the amount of time that the aliquot of acetylated thymidine sat out at room-temperature (I vaguely remember this assay taking longer to set up). Either way, the next assays (below) lack this hydrolysis-induced multiple-addition spread of oligos in the pH 6.5 lane.
  • In other (unlisted) assays, we established that TdT gets progressively less active at pH lower than 7.9. The "dTTP+NEB Buffer" lane shows the activity of TdT with unmodified nucleotides at pH 7.9. Comparing the activity in this lane with the others shows that acetylated nucleotides cause some truncation throughout the distribution of oligo lengths. Another (unlisted) assay shows that the difference in TdT's activity between NEB's Tris buffer and a homemade MOPS buffer (both at pH 7.9) was indiscernible.
  • Tested the extent of hydrolysis of incorporated acetylated thymidines
  • The lanes are as follows:
  • This assay attempted to show that 3'-blocked nucleotides, once incorporated into a growing oligo, effectively halt the addition of additional non-acetylated nucleotides.

Parts

Name

Type

Decription

Length
  • BBa_K1556000

coding

Mouse TdT

1590
This part was submitted late, and is not eligible for medals and awards.

Students

Kenny Kostenbader

Chem Eng

Scott Lazaro

Cell Bio & Neurosci

Wilson Wong

Mol Bio

Jay Patel

Chem Eng

Faculty

Sagar Khare

P.I.

Andrew Laudisi

Lab Manager

Attributions

Dr Jones is a professor in the Rutgers Chemistry Department who researches modified nucleotides. He gave valuable feedback on our initial project ideas, and suggested a way to create (and characterize) 3'-acetylated thymidine triphosphate in our lab. We attempted this synthesis (involving pyridine and acetic anhydride) and got promising results (via LC/MS), but then we found out that TriLink (below) could simply synthesize and purify it for us for free.

Arun Nayar was on last year's Rutgers iGEM team, so he helped train us with various lab protocols.

All of the pictured results on the Project page represent assays that were designed jointly by the students and Dr Khare, and carried out completely by the undergraduate team members in the Khare lab. Additional help was provided by other Rutgers students as well, namely: Diego Barreto, Wesley Okwemba, Neil Patel, Harsh Patel, and Samantha Ashley. The fluorescent gels were imaged using the "BioRad Gel Doc" machine in the Kalodimos lab (next door). Kenny did the web design and coding.

Trilink Biotech supported the project by custom-synthesizing acetylated thymidine triphosphate, and supplying it free of charge.

NEB Inc supported the project by supplying a Terminal Transferase enzyme kit and a dNTP set, both free of charge.

Gen9 supported the project with a $500 donation.

Protocols

Click to download a copy of each protocol that we followed and/or wrote this summer:

Chronology

May

  • this and that
  • that and this

June

July

August

September

October

  • All lab members underwent Biosafety Level 2 training with the Rutgers Environmental Health & Safety department.
  • We utilized only one organism: Escherichia coli K-12 DH5a
  • Public health and safety would be under little conceivable risk in the event of an accidental release of our biobrick part into the wild (in the form DNA or a transformed colony of cells), because the TdT enzyme expression is very low, and the enzyme is only capable of adding deoxynucleoside triphosphates to the 3' ends of DNA strands. Given that very little TdT would be produced, and that free 3' DNA ends are rare in living systems, we believe that the risk posed by our biobrick part is minimal.
  • Appropriate precautions were taken when casting and using the Polyacrylamide Electrophoresis gels for our various assays. Used gels were disposed of properly in acrylamide waste bins.
  • Our team's safety form can be found here.

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