Team:Hawaii/Ligation of pRL1383a Parts

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Latest revision as of 03:32, 30 October 2008

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Ligation of Parts

• The BioBrick parts of pRL1383a are to be ligated in a series of experiments.

Methods

Restriction Digest

• Each part is digested with both enzymes. For all cases NEBuffer 2 is used. For a 3-way ligation, the front insert is digested with E and S, the back insert is digested with X and P, and the vector is digested with E,P.

• Reaction Conditions:

• 5ul Buffer
• 1ul Enzyme 1 + 1ul Enzyme 2
• 0.5 ul BSA
• Xul water
• Yul DNA

• Running Conditions: 2 hours at 37°C.

• Check the progress of the reaction by running a 0.8% gel.

Ligation

• Refer to http://openwetware.org/wiki/DNA_ligation for the reasoning behind this.
• The vector will be de-phosphorylated in most cases to prevent self-ligation. As a negative control, this de-phosphorylated vector will be self ligated.

Transformation

• The 3-way ligations usually involve the replacement of the ccdB gene with the insert, so DH5-alpha cells are used for transformation-- any plasmids not containing the correct insert, but containing the original (ccdB) will die in DH5-alpha.
• For the last ligation involving the Base Vector and the insert, DB3.1 cells will be used because the ccdB gene will not be replaced.
• Positive controls will usually be pUC18 to verify that the competent cells used are transformable.
• Negative controls will usually be the competent cell with no plasmid added.

Verification

• Colony PCR

• Reaction conditions: 10ul volume: 5ul green taq, 4ul water, 1ul primers (VF2+VR)+ a sterile poke from a colony.
• Running conditions: 94 hold, [95 30", 62 30", 72 (time varies based on size of verification site)]x 30 cycles, 72 10', 4 hold.

• I decided later that as another verification before sequencing, the plasmid could be restriction digested to verify that BioBrick sites are present.
• In most cases, positive results from colony pcr and restriction digest were sent in for sequencing.

Results

7/27

• A few re-digests and ligations were performed today: oriT + pSB1A3, oriV + pSB1A3, mob + B0024, rep + R0010, aadA(pRL1383a+R0010). Afterwards, the ligation product was transformed to DH5-alpha. Only OriT transformed. I did not check the progress of this experiment with a gel, so I am not sure where this went wrong.
• Next time, a gel will be run after every step.

8/11

Restriction digest from 8/11/08.

Ligation products from 8-11 ligation.

Transformation & Verification PCR

PCR verification of colonies from transformation with plasmids containing rep, P1 lytic region, the aadA (BB&pRL1383a) region, and oriV.

• The only bands corresponding to the correct size are the 4 oriVs and the 4th BB version of aadA.
• The rep region lanes are all either 300 or 600bp when they should be 3.3kb. If the RBS (B0030) ligated back to itself, the band should be 253bp. The bands at 300bp may be explained by this. It is unclear what happened in the latter case. The incorrect aadA bands are also around 300bp which would mean the RBS containing vector ligated back to itself some how. B0030 was cut with SpeI and PstI.

Plasmid Prep

• OriV1-4 and aadA (BB) were cultured over-night in Terrific Broth with amp100 as selection.
• The plasmids were isolated using an Alkaline Lysis Mini-Prep.

8/13

PCR verification of rep, P1lytic, and aadA from pRL1383a from 8/14/08.

PCR verification of aadA from pRL1383a.

• Three ligations were performed today. I checked my math from the last ligation and decided it wasn't totally correct for the rep ligation to B0030.
• P1 lytic was ligated to B0015 (TT), Rep to B0030 with precisely 2:1 insert to vector ratio, and the aadA region from pRL1383a to B0030.
• Unfortunately there is no gel to confirm this ligation.

Transformation

• The ligation products were transformed into DH5-alpha cells with selection on LB amp100 plates. pUC18 was transformed into DH5-alpha cells as a positive control, while no plasmid was used in a transformation as a negative control.
• A lawn of colonies was observed for all three transformations. No colonies grew for either control (need to check pUC18 and see if there are problems with our stock).

PCR Verification

• The rep region, as with the last ligation was not inserted to the vector. The band at 300bp suggest the B0030 vector was amplified by VF2&VR. Another possibility is that some of this plasmid was not digested and the ligation just did not work, so these were the only circular plasmids available for transformation.
• The P1 lytic region is at 400kb while the verification size of B0015 is 445bp...
• aadA from pRL1383a is amplified to several different sizes. One of which is about correct (~1kb), one above 10kb, and one at 0.25kb.

9/2

PCR for size verification for sequencing.

9/6

• 3A-(ish) ligation is going to be used for subsequent ligation reactions.
• The lac promoter and RBS have been synthesized. They were ligated together 1:1.
• The other parts are to be digested out of plasmid or PCR amplified and restriction digested to give the correct over-hangs.
  • Vector: E,P
  • Front part: E,S
  • Back: X,P

9/19/08

• Psuedo- 3A Assembly. This method is the same in that 2 pieces are assembled into a vector at one time, but differs in that the inserts are gel purified, so that the only plasmid involved is the recipient plasmid.

• Protocol:

The restriction digest products are run on a gel and then purified.

Ligation of 2 inserts into pSB1A3:replication proteins with promoter/RBS and promoter/rbs/aadA with terminator.

1. Restriction Digest: front insert (E,S), back insert (X,P), vector (E,P)
2. Purification/Preparation of Parts: the vector is de-phosphorylated with SAP and the inserts are gel purified, with the exception of parts <200bp, which are ligated directly
3. Ligation: at 16°C for 2 hours using T4 ligase.

Colony PCR from 9/20 and 9/21, results described in table.

Colony PCR from 9/20 and 9/21, results described in table.

Transformation of ligation Products

10/6

On 9/29/08, this part was verified by PCR.

• Plac/RBS/rep in pSB1A3

• PCR verification of this part was compared to rep and the size difference determined that further verification was needed. This amplicon was sent in for sequencing using a series of primers for full coverage of sequence. rep was previously sequenced and contained BioBrick sites and no mutations, except for a 50 bp region at 1500 bp. An additional primer was designed to cover this region.

• A glycerol stock of this part was made for long-term storage.

• XbaI and PstI were used to digest Plac/RBS/rep in pSB1A3. This digest was run on a gel and purified.

On 10/3/08, the band around 3478 bp was purified.

• The next step is to ligate this part to oriV.
• Today a plasmid prep of the glycerol stock was prepared to ensure that I have this part in stock and that the re-digest can be replicated.

• Plac/RBS/aadA

9/16/08 the lac promoter and RBS were added to aadA.

• plac/rbs was added to aadA.

9/19/08 the terminator was added to plac/rbs/aadA.

• a terminator was added to plac/rbs/aada. from the gel, it appear that something was added, however after sequencing these two constructs, it was found that the terminator was not added, however the BioBrick cloning sites, the promoter, rbs and aada all have correct sequences.
• a glycerol stock of plac/rbs/aada/terminator was prepared, though now I know there is no terminator in this construct. The final plasmid will have a transcription terminator near the aada region.
• plac/rbs/aada in pSB1A3 was cut with E,S and purified from a gel.

• oriV

10/5 verification of ligation of oriV and plac/rbs/aada + oriT.

• The most recent attempt to clone oriV into pSB1A3. From the gel, one would suspect that the ligation was successful, but the PCR verification of the 4 colonies yielded from the transformation were not amplified by VF2/VR.
• I will attempt the transformation again with the same ligation reaction.

• oriT

• The sequence of this construct has been verified and oriT is stored on pSB1A2 in a glycerol stock.

Assembly of Parts

• oriT + plac/rbs/aada + pSB1A3

• The ligation and transformation were unsuccessful, and after running the two inserts and the pcr verification on a gel, it is clear that the plac/rbs/aada construct was not successfully purified from the gel. The band was visualized before purification, but not afterwards. I have started a culture from the glycerol stock of plac/rbs/aada.

10/10

• Ligations of the oriT to [promoter/rbs/aada] and the oriV to [promoter/rbs/rep], (-) control is the pSB1A3 (E,P, dephosphorylated) self ligation.
• The products of ligation were transformed into DH5-a cells.

• Transformation results on 10/12;

Transformation of ligation Products

• results of colony pcr

• 2/20 colonies from the oriV + [promoter/rbs/rep] transformation were correct size--> 4.2 kb (colony 6 and colony 1)
• 1/20 of the colonies from oriT + [promoter/rbs/aada] were correct size ~1 kb (colony 12)

• These colonies were cultured, plasmid prepped and re-digested.

• only colony 6 from oriV + [promoter/rbs/rep] cut correctly --> sent in for sequencing

• no colony from oriT + [promoter/rbs/aada] cut correctly --> colony PCR more colonies

10/15

• Ligation, followed by transformation into DH5-a

• [promoter/rbs(34)] (E,S) + [rep2] (X,P) + pSB1A3 (de-phosphorylated, E,P)
• [promoter/rbs(30)rep/oriV(6)] (E,S) + [promoter/rbs(34)aada/oriT(A)] (X,P) +pSB1A3 (de-phosphorylated, E,P)
• [promoter/rbs(30)rep/oriV(6)] (S,P) + [promoter/rbs(34)aada/oriT(A)] (X,P)
• [promoter/rbs(30)rep/oriV (6)] (S,P) + [promoter/rbs(34)aada/oriT(B)] (X,P)
• oriV (E,S) + oriT (X,P) + pSB1A7 (E,P)
• pSB1A7 self (did not de-phosphorylate) (E,P)

10/16

• Transformation Results:

Transformation of ligation Products

• Colony PCR: 20 colonies for each construct were verified with PCR

1. [promoter/rbs(30)rep/oriV(6)] (S,P) + [promoter/rbs(34)aada/oriT(A)] (X,P)
2. [promoter/rbs(30)rep/oriV (6)] (S,P) + [promoter/rbs(34)aada/oriT(B)] (X,P)
3. oriV (E,S) + oriT (X,P) + pSB1A7 (E,P)
4. [promoter/rbs(30)rep/oriV(6)] (E,S) + [promoter/rbs(34)aada/oriT(A)] (X,P) +pSB1A3 (de-phosphorylated, E,P)

• Results of Colony PCR: I would expect for 1 and 2 (from the above colony PCR) to be about 5 kb, 3 to be about 850 bp, and 4 to be about 5 kb. These pictures are not available in electronic copy so the results are just reported.

1. 5, 15, 6, 16, 7, 17, 8, 18, 9, 19, 10, and 20 are all about 5 kb.
2. 18 of these colonies are about 5 kb, excluding colony 1 and 11.
3. colonies 2, 4, 24, 6, and 16 are about 850 bp.
4. no bands at 5 kb present.

• colonies 1-5, 1-13, and 1-16, 2-12, 2-5, and 2-20 were cultured in Amp100 overnight with shaking at 37°C.
• They were plasmid prepped and then subjected to restriction digest with EcoRI and SpeI. The restriction digests were then run on a gel.

Lane 1: ladder --> good separation Lane 2: 1-5 (E,S) bands were incorrect size Lane 3: 1-13 (E,S) insert band at 4.8 kb, cut out and purified, amt ~ 13 ng/ul Lane 4: 1-16 (E,S) insert band at 4.8 kb, cut out and purified, amt ~ 13 ng/ul Lane 5: 2-5 (E,S) bands were incorrect size Lane 6: 2-12 (E,S) bands were incorrect size Lane 7: 2-17(E,S) bands were incorrect size Lane 8: 2-20 (E,S) bands were incorrect size

• Both of the correct bands were from the [promoter/rbs(30)rep/oriV(6)] (S,P) + [promoter/rbs(34)aada/oriT(A)] (X,P)ligation.

10/20

• Sequencing of Ligation of [promoter/rbs/rep] came back and the promoter and rbs were not present. While I thought I had the construct [promoter/rbs/rep/oriV/promoter/rbs/aadA/oriT] in pSB1A3, I actually have [rep/oriV/promoter/rbs/aadA/oriT]. I will take the following steps:

• Front ligation of [promoter/rbs]into [rep/oriV/promoter/rbs/aadA/oriT]: cut [promoter/rbs] with E,S and cut [rep/oriV/promoter/rbs/aadA/oriT] with E and X and de-phosphorylate, then Ligate [promoter/rbs] with E,S with [rep/oriV/promoter/rbs/aadA/oriT]E,X,de-phosphorylated using T4 ligase. The negative control for this experiment is [rep/oriV/promoter/rbs/aadA/oriT]E,X,de-phosphorylated self-ligated.

• Results of Transformation:

Transformation of ligation Products

• PCR was used to verify some of the colonies. I used the VF2/VR primers to identify if the correct insert is present. I also used some additional primers to identify whether or not the rbs was present:

Part Existence and Distance Verification

Colony pcr to verify colonies containing the [promoter/rbs/rep/oriV /promoter/rbs/aadA/oriT] construct. The two lanes with ** and *** above them were cultured and further studied.

• Gel results: The lane with (**) above it is an example of the expected results. In the top half of the gel, the colony was verified with VF2/VR primers. For this construct to be correct, we would expect a band at around 5.2 kb.

There is some non-specific binding in the lower kb region, but there is a band (*) that is around 5.2 kb. In the lane directly below this, the same colony was verified using the VF2/VR_B0034 primers. We would expect a band about 200 bp verifying the rbs located in front of the rep genes and a band at around 1 kb verifying that the aadA region has an rbs in front. This is verified by a positive control: the [promoter/rbs/aada] construct in pSB1A3 in a colony, pcr amplified with VF2/VR_B0034 primers. Both of these regions should be the same size because the amplification region should be the Forward verification region (158 bp) + the promoter (~60 bp) = 218 bp. The aadA regions was not amplified in this case, but due to the shortage of colonies containing results near what was expected, this colony, along with the colony designated with 3 * were cultured and plasmid prepped.

• Culture: These two colonies ** = (1-16-22) and *** = (1-16-24), were cultured over night, shaking at 37°C in Terrific broth with antibiotic selection. The colonies were tested for Amp100 resistance in 1 flask and Sp100 resistance in another flask. The amp100 flask lends evidence that the pSB1A3 plasmid is present while the Sp100 flask lends evidence that the aadA construct is present.

10/22

• The construct [promoter/rbs/rep/oriV/promoter/rbs/aadA/oriT] will be ligated to the Base Vector. The Base Vector was previously cut with NheI and de-phosphorylated.

• Results: The next day the flasks were checked and both of them had growth, but the flask containing (1-16-24) in Sp100 had more growth, so it was plasmid prepped using the alkaline lysis mini-prep method. The plasmid was subjected to a restriction digest with SpeI and XbaI in preparation for the ligation to the base vector.

• Ligation was performed:

1. 50 ng of X-[promoter/rbs/rep/oriV/promoter/rbs/aadA/oriT]-S was ligated to 77 ng N-Base Vector-N, or a 1:3 ratio.
2. (-) control Base Vector ligated to self.

• The ligation products were then transformed into DB3.1 cells. This construct does contain the ccdB gene, so must be transformed into a strain resistant to the death protein.

10/23

• Transformation results:

Transformation of ligation Products

I then ran a gel to try to determine why there were no transformants. The size of the plasmid was incorrect.

Discussion

• Ligations into empty vectors seems to be successful, but when adding my part to an existing part, I run into problems.
• As a team we decided to synthesize the Promoters, RBS, and TT.
• The vector was not completed. There is a problem getting the insert into the base vector.

[http://manoa.hawaii.edu/ ][http://manoa.hawaii.edu/ovcrge/ ][http://www.ctahr.hawaii.edu ]

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