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Contents 1 Team CRISPR 1.1 July 3 2 Team Cinnamaldehyde 3 Team Caffeine 3.1 June 20 3.2 June 27 3.3 July 4 3.4 July 5 3.5 July 8 3.6 July 9 3.7 July 11 3.8 July 12 3.9 July 15 3.10 July 17 3.11 July 18 3.12 July 19 3.13 July 23 3.14 July 24 3.15 August 12 3.16 August 13 3.17 August 14 3.18 August 15

Team CRISPR

July 3

List of BioBricks that are/will be on the way:

Cas9:

• Cas9 - Joe and Anna
• pTet -
• const. promoter + Cas9 - Joe
• promoter + Cas9 + Leader + R + spacer + R (on Kan)
• L + R + spacer + R

Target:

• tracerRNA
• repeat + spacer + repeat - Vanins*2 + underlings
• leader - Ray, Fisal, Dan

Decoy:

• PAM + spacer (on Amp)

Team Cinnamaldehyde

4-coumarate-CoA ligase:

• PCR worked

Team Caffeine

June 20

Heat-shock competent cells were made today - they are labelled "HS" on the lid and can be found in the top compartment of the -80º Freezer #3 in the freezer room. We will be ordering primers to modify the TU Munich caffeine biosynthesis BioBricks we got in the Distribution Kit. These are found in wells 17H, 17J, and 17L on plate 2.

June 27

Parts 17H/J/L were previously transformed into the above-mentioned competent cells and plated. Today, transformation efficiency was found to be very low - two colonies per plate after more than 18 hours at 37ºC. The three parts were miniprepped, with DNA concentration of 154.3ng/ul, 323.8ng/ul and 117.3ng/ul respectively.

July 4

We ran a confirmation PCR on the miniprepped plasmids with standard Biobrick primers, VF2 and VR, to confirm the presence of an insert in the backbone. Gel confirmation of the PCR products showed a band around 1kb, our expected gene size, for one of the genes only (17J). The other samples did not show any bands. Because the transformation efficiency was very low, unsuccessful transformation was thought to be causing the issues. We decided to retry transformation of the kit parts into "tried and true" cells, and to discard today's plasmids if the new transformation gave different results.

July 5

We acquired aliquots of "good" competent cells from Ray, our grad advisor, and re-tried the transformation of the distribution kit parts.

In order to confirm our parts of interest (17H/J/L) contained the desired insert, we retried PCR, this time with 1 uL of eluted DNA from the distribution kit as template. Even with this low concentration of template, amplification appeared successful. A bright band was seen for 17J and no bands for the other two, validating yesterday's PCR results. As our project depended largely on the manipulation of the inserts in each part, we sent them for sequencing to confirm what PCR told us. The results revealed the correct insert was indeed present in each of the three parts, a "green light" to moving forward.

We designed and ordered primers to remove the "TCACA" yeast consensus sequence found in the TU Munich Biobrick parts, as our goal was to replace this sequence with a bacterial ribosome-binding site. This round of PCR was named "PCR 1" to indicate downstream PCR reactions that would use these products as template.

July 8

Transformation of 17H/J/L with Ray's competent cells was found to be highly efficient, indicating our own heat-shock competent cells were faulty. We received the protocol used to prepare these cells, and a new stock was made today.

July 9

Cultures of 17H/J/L were miniprepped, and with the products, we:

• did a restriction digest with EcoRI and PstI to confirm the presence of an insert
• prepared each plasmid for sequencing to confirm the sequence of the insert (and the presence of the yeast consensus sequence, which we hoped to remove)
• PCR with primers designed to remove the yeast consensus sequence (TCACA)

The confirmation gel for the restriction digest showed there was an insert slightly larger than 1kb for each of the genes, which was desired. However, PCR did not appear to work. Higher molecular weight smears were seen at around 2.5kb, indicating the template was not amplified, likely because there was too much of it. Around 200ng of plasmid template was used, annealing temperature was the lower primer Tm, and no DMSO was used. We will try this PCR again with much less template (10-50 ng per 50 uL reaction), as per NEB's suggestions, and fewer cycles.

July 11

PCR 1 was retried for all three parts, with the amount of template reduced to around 30 ng per 50uL reaction. Phusion HF (high fidelity) buffer was used, in the absence of DMSO. Thermocycling conditions were not changed, except the reduction of number of cycles from 30 to 20. Parts J and L were successfully amplified this time, with bands seen at around 1100-1200 bases on the agarose gel. However, nothing was seen for part H. One option is to try adding DMSO to a final concentration of 3% to hopefully allow amplification of part H.

The amplified products for J and L, as well as pSB1C3 with GFP between the X and S cut sites, were digested with restriction enzymes XbaI and SpeI in preparation for ligation.

July 12

With Ray, we designed and ordered the "stitching" primers that would allow us to assemble our Biobricks easily, by using restriction enzyme cut sites other than the four standard to avoid illegal cut sites. Once digested, two or three genes could be ligated together in a single ligation. This follows the decision to combine the three available (from the kit) caffeine biosynthesis genes and Biobrick them behind a promoter and ribosome-binding site (RBS). We included a bacterial ribosome-binding site in each of the forward primers to allow transcription when each gene is also Biobricked individually. This round of PCR reactions was named "PCR 2."

PCR 2 would ideally yield the following products:

• Part H: ---XbaI---gene H---SpeI---NcoI---
• Part J: ---NcoI---XbaI---gene J---SpeI---BamHI---
• Part L: ---BamHI---XbaI---gene L---SpeI---

Individually and ligated together, these products could be digested by XbaI and SpeI and inserted into a Biobrick vector cut with X and S.

July 15

PCR 1 was re-tried for part H, this time with the addition of DMSO. This was done in duplicate, to be able to compare the Phusion HF and GC buffers. PCR was successful, with bands seen at 1100 bases for both reactions. It appeared using either buffer would yield the same results, so we combined the two products and decided to use the HF buffer for consistency. The product was cut with XbaI and SpeI.

PCR 1 product for parts J and L were cut again with XbaI and SpeI with an increased amount of DNA, as a gel showed very faint bands at the size of the insert.

July 17

July 18

July 19

July 23

July 24

August 12

We transformed three vectors into heat-shock cells: each gene (H/J/L) individually in pSB1C3.

We also set up another massive ligation with the remainder of our X/S-cut PCR 2 products. The goal was to run an gel and gel extract the band at 3kb, which would contain the three-gene ligation we are looking for. The band at 3kb was very faint on the gel, and after extraction the concentration of DNA in the eluted sample was found to be around 10 ng/uL.

August 13

White colonies from yesterday's transformations (with the vector thought to be faulty) were picked and 5mL cultures inoculated for miniprepping tomorrow.

Yesterday's ligations (yielding a 3-gene product), as they had previously been digested with XbaI and SpeI, were ready to ligated into a vector. These were ligated into pSB1C3 (again with GFP between the X and S cut sites) that was freshly cut with X and S in case the vector we had previously been using was faulty. Eight new vectors were created: parts H, J, L individually in pSB1C3 (3 vectors), yesterday's 3-gene product in pSB1C3 with 3:1 and 6:1 insert to vector ratios (2 vectors), and remaining 3-gene product from several days ago also with the different insert:vector ratios (2 vectors). We set up ligation with X/S-cut PCR 2 products into pSB1C3 to create individual biobricks. There was also a "no insert control" to determine how many colonies form from the spontaneous closing of the pSB1C3 cut with X and S. These were all transformed and plated. Tomorrow, we will inoculate cultures with selected white colonies, as well as set up colony PCR to quickly check which colonies may have vectors containing the desired insert.

August 14

Overnight cultures from yesterday were miniprepped (6 samples for each gene).

Then, we digested the miniprepped plasmids with XbaI and SpeI. If the vector contains the insert, we expect two bands - a band at around 1kb (gene size) and a band at 2kb (empty vector). If the vector has our gene but in the wrong direction (thereby creating scars), or if the vector has self-ligated, uncut plasmid pattern on gel is expected.

From yesterday's transformations, we picked 3 white colonies from each plate and set up a colony PCR with VF2 and VR to confirm the presence of insert. Only one of the colonies for plate J (J3) showed amplification at 1kb. Colony J3 was picked and 5mL culture was inoculated.

August 15

Overnight culture (J3) from yesterday was miniprepped and set up for digest with X and P. Digest analysis should tell us whether the insert is in the correct orientation.