Lab notes (9/6 - 9/12)

Flagella Group

Restriction Digest of Gel Extracted FlhDCmut, pSB1C3 and pSB1AK3

Date: 9/12 2010
Done By: Sheila
Protocol: RD1.1
Notes: The restriction digests are made in preperation for two different ligations, the first is the ligation of FlhDCmut into the submission backbone; pSB1C3. The second is the the ligation of FlhDCmut into pSB1AK3. Different restriction enzymes were used in, as shown in the following tables

Restriction Digest mixtures
FlhDCmut and pSB1C3 Restriction digest
FlhDCmut

Ligation of FlhDCmut and pSB1C3

Date: 9/12 2010
Done By: Sheila
Protocol: LG1.2
Notes:
Results:

Ligation of FlhDCmut and pSB1AK3

Date: 9/12 2010
Done By: Sheila
Protocol: LG1.2
Notes:
Results:

Photosensor group

Taq gradient PCR of pKJ606 with PS primers

Date: 9/7 2010
Done By: Maria and Lc
Protocol: CP1.3
Notes:
A gradient PCR was carried out to determine the appropiate annealing temperature of the new PS primers. PCR tubes were marked PSII A-H.

Premix x 9

miniprep of pKJ606 was used as template. 1uL was distrubuted into each tube.
PCR program:

Anealing temperatures:

PCR product was loaded onto a 1.5 agarose gel. gene ruler DNA ladder mix (red) was used as marker.

Results:

Analysis:
Only very weak bands was observed at app. 2000 bp, and very strong bands were observed at app. 4000 bp, indicating that too much template was used in the PCR. An additional PCR was carried out using diluted miniprep as template.
--Tipi 10:27, 21 September 2010 (UTC)

Insertion of PS in pSB1C3 and pSB1AK3

Date: 9/8 - 9/12 2010
Done By: Maria and Lc
Protocol: CP1.1DE1.3RD1.1LG1.2CC1.1TR1.1CP1.3

Pfu PCR amplification of PS (no.1)

Date: 9/8 2010
Done By: Maria and Lc
Protocol:CP1.1
Notes:
5 PCR reactions are prepared. 2uL Miniprep of pKJ606 are diluted in 8uL H2O to reach a 5x dilution, and are used as template. PCR tubes are marked PSIII A-E.
Premix x6:

PCR program:

All of the PCR product was loaded onto a 1.5 agarose extraction gel. Gene ruler DNA ladder mix was used ad marker.

Results:
Analysis:
No bands were visible in the gel, indicating that the PCR reaction had been unsuccessfull. This could be due to the low elongation time, wherefore another PCR reaction with a longer elongation time was carried out.

Pfu PCR amplification of PS (no.2)

Date: 9/9 2010
Done By: Maria and Lc
Protocol:CP1.1
Notes:
5 PCR reactions are prepared. 2uL Miniprep of pKJ606 are diluted in 8uL H2O to reach a 5x dilution, and are used as template. PCR tubes are marked PSIV A-E.
Premix x6:

PCR program:

All of the PCR product was loaded onto a 1.5 agarose extraction gel. Gene ruler DNA ladder mix was used ad marker.

Results:
Analysis:
Bands were observed at app. 2000bp and bands were extracted by gel extraction

Gel extraction of PS

Date: 9/9 2010
Done By: Maria and Lc
Protocol:DE1.3
Notes:
DNA was extracted from gel according to protocol and each sample was diluted in 20uL.

Analysis:
each sample had a concentration of app. 7ng/uL. All 4 samples were pooled and used for restriction digest.

Restriction digest of PS, pSB1C3 and pSB1AK3

Date: 9/9 2010
Done By: Maria and Lc
Protocol:RD1.1DE1.3
Notes:
Restriction mixture pSB1C3:

Restriction mixture pSB1AK3:

Restriction mixture PS (used in pSB1C3):

Restriction mixture PS (used in pSB1AK3):

Digested samples were loaded onto a 1.5% agarose extraction gel. Uncut PS, pSB1C3 and pSB1AK3 were used as controles. Gene ruler DNA ladder mix was used as marker.
Loading scheme:

DNA was extracted from gel according to protocol.

Results:
DNA conc:

Analysis: the purified DNA was used for ligation.

Ligation of PS and pSB1C3 and pCB1AK3

Date: 9/9 2010
Done By: Maria and Lc
Protocol:LG1.2
Notes:
For each of the ligations three ligation mixtures were prepared. vector concentrations of 10ng/uL (pSB1C3) and 15ng/uL (pSB1AK3) respectively was used for each mixture. Appropiate amount of insert was added to reac vector:insert ratios of 1:1, 1:2 and 1:4 respectively.
Ligation mixtures (PS in pSB1C3):

Ligation mixtures (PS in pSB1AK3):

The samples was incubated at 17C ON at used for transformation

Transfomation of ligated plasmin in Top 10 E.coli

Date: 9/10 2010
Done By: Maria and Lc
Protocol:CC1.1TR1.1
Notes:
The compotent cells and transformation was carried out according to protocol. Cells transformed with ligations of PS in pSB1AK3 was plated on kanamycine plates.

Results:
the controle plates were okay, and there was many colonies on plates with cells transformed with ligations of pSB1C3 and PS. There was 10-20 colonies on the plates with cells transformed with ligation of PS and pSB1AK3.

Analysis:
The transformation was successfull and colonies was selected and used in coloni PCR.
--Tipi 13:41, 26 September 2010 (UTC)

Colony PCR of transformation of PS in pSB1C3 and pSB1AK3 in TOP10 E.Coli

Date: 09/11
Done by: LC & Maria
Methods: Colony PCR
Protocols: CP1.3[1]
Notes:
Premix:
45 µl 10xTAQ Buffer
18 µl MgCl2
18 µl VF2
18 µl VR
9 µl dNTP
63 µl H2O
2,25 µl TAQ Polymerase

The chosen colonies were lysed in 15 ul of H20.

PCR Program:

Results: For the ligation into pSB1C3, colonies B, F and H showed bands at the right length. For the other reatcion (in pSB1AK3), colonies A to D showed bands with the correct length. The colonies with bands at the right length will be miniprepped and sent for sequencing.

Control restriction digest of cPCR product of PS in pSB1C3 and pSB1AK3

Date: 09/12
Done by: LC & Maria
Methods: Restriction digest
Protocols: RD1.1[2]
Notes:
The afore mentioned samples (B, F and H of PS in pSB1C3 and A and D in pSB1AK3) were cut with EcoRI and PstI to see if it was 1) possible to cut them at all, thereby confirming the presence of biobrick prefix and suffix and 2) determining if the insert in the plasmid has the right length.
Mix for 1 RD reaction:
12 ul H2O
1 ul PstI
1 ul EcoRI
2 ul Fast digest green buffer
5 ul PCR product

Uncut PCR product and RFP were also loaded on the gel as a control.

Results: All samples pSB1C3 samples were cut as expected (to around 2000 BP), but the restriction digest of pSB1AK3 sample A and D failed, so that one will have to be repeated with sample B and C, as these only showed a cut double terminator without the PS insert.

Second control restriction digest of cPCR product of PS pSB1AK3

Date: 09/12
Done by: LC & Maria
Methods: Restriction digest
Protocols: RD1.1[3]
Since samples A and D fromt he colony PCR gave inadequate results when cut with EcoRI and PstI, we had to repeat the restriction digest with the remaining two samples that were the right length on the cPCR, sample B and C. Samples E, F and G were also cut to confirm that there were no errors in naming the samples that resulted in sample A and D not giving the expected results.
Restriction mixture:
72 ul H2O
6 ul PstI
6 ul EcoRI
12 ul Fast digest green buffer
5 ul PCR product per sample (x6)

Uncut PCR product was loaded on the gel as a control.

Results: Only sample C showed bands at the correct length (around 2180 BP), where as all other bands were at the length of a double terminator (b0015) without the photosensor insert. All samples were properly cut indicating the presence of biobrick pre- and suffix in these. Sample C will be miniprepped and sent off to sequencing.

Second round of colony PCR on PS ligated into pSB1AK3 (containing double terminator

Date: 09/12
Done by: LC & Maria
Methods: Colony PCR
Protocols: CP1.3[4]
Notes:
Since only sample C from the previous colony PCR looked right after a restriction digest we decided to run another round of colony PCR on the photosensor ligated into pSB1AK3, to find more colonys containing the right (ligated!) plamid.
The original samples A - D were also used as a template, now called I, J, K and L. Sample M to Y were new colonies.

Premix:
42,5 µl 10xTAQ Buffer
17 µl MgCl2
17 µl VF2
17 µl VR
8,5 µl dNTP
59,5 µl H2O
2,125 µl TAQ Polymerase

The chosen colonies were lysed in 15 ul of H20.

PCR Program:

Results: Samples K (former C) and Q produced bands at the right length of around 2150 BP, which eans that sample Q will also be miniprepped and send to sequencing together with the previously chosen sample C (now K).

Miniprep and controle digestion of PS in pSB1C3 and pSB1AK3

Date: 9/13 2010
Done By: Maria and Lc
Protocol:MP1.2RD1.1
Notes:
Coloni B, F and H of PS in pSB1C3 and coloni C of PS + double terminator in pSB1AK3 was miniprep'ed according to prtocol. To ensure that the plasmids contains the insert as expected, the miniprep is cut with EcoRI and PstI.
the 2 minipreps of each coloni are diluted in 20uL and 50uL respectively.
Restriction mixture x4:

The digested products are loaded onto a 1% agarose gel. 2.5uL of undigested plasmid are used as controle. Gene ruler DNA ladder mix are used as marker
Loading scheme:

concentrations of miniprep was measured on nanodrop.

Results:
nanodrop:

Analysis:
In the lanes containing the digested pSB1C3 plasmids bands at app. 2000bp are observed corresponding to PS. The lane containing digested pSB1AK3 plasmids shows a band at app. 2100bp corresponding to the size of PS and the double terminator. Miniprep of coloni B, F and C are sent to sequentation.
--Tipi 14:44, 26 September 2010 (UTC)

Miniprep of PS+B0015 sample Q and pSB3T5 containing J13002

Date: 27/7
Methods: ON, Miniprep
Protocol: MP1.1
Experiment done by: LC & Maria
Notes: PS+B0015 sample Q (1) was eluded in 20 ul to get a concentration over 200 ng/ul, so we would directly be able to send it in for sequencing. All other samples were eluded in 50 ul of elution buffer.

Results: The concentrations were as followed:
PS+B0015 (1): 180 ng/ul
PS+B0015 (2): 130 ng/ul
pSB3T5+J13002 (1 and 2): 50 ng/ul

Sample Q did not fulfill DNA technologies sample specifications for sequencing we waited with sending it in, since we were expecting the results from sample C which was sent in earlier. Since those returned positive, sample Q was never sent in, since we just proceeded with sample C.