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Revision as of 22:14, 28 October 2008

August, 16th

Agr A and C ligation to pSB4C5

Ligation was performed using Fermentas Rapid Ligation kit according to their protocol.

After ligation, samples were visualized on a gel, but little product of the correct size was seen.

For agrA we should have gotten a band of size 3700 (3000plasmid + 700 insert)

For agrC we should have gotten a band of size 4300 (3000plasmid + 1300insert)

The bands of appropriate sizes were extracted for transformation.

August, 18th

Check promoters

On Friday, PCR out promoters, we want to check them.

- Run a gel

- Results : good size of bands!!!

Transformation of AgrA and AgrC

AgrA and C gell-extracted ligation was transformed into Top 10 cells using standard protocol. Puc9 was used as a positive control.

August, 19th

Results of AgrA and C transformation

Transformation has failed. No colonies were visible for the plates of Agr A or C. The Puc9 positive control grew. We believe that the problem was in the gel-extraction between ligation and transformation. Most of our plasmid was probably lost in this step. Next time we will directly use the results from the ligation reaction to transform. Although many bands were seen on the previous gel of the ligation reaction, we will check our transformation growth by single colony PCR to confirm transformation of the plasmid with our correct insert.

Lux parts

To make the Lux Receiver, we need 4 different parts ;

R0040, TetR repressible promoter

SO168, luxR + double terminator

R0062, promoter activated by luxR

JO4630 (GFP + double terminator)

All these parts have been transformed into E.coli. We want to test them. R004, R0062 and JO4630 have already been tested, it should be fine. We received from the MIT R0040, R0062 and S068 already transformed into E.coli, so we want to check these stocks (which are certainly fine) and use them. For JO4630, we want to double check our transformation.

- Plate on antibiotic plates and do LB stocks of single colony from the MIT stock (R0040, R0062 and S0168).

- Put on Kan plates 4 different colonies from J04630 (transformation Amp plate) and also incubate these colonies into LB

August, 20th

Check Lux components

- Single colony PCR for :

R0040 (MIT stuff)

R0062 (MIT stuff)

4 different colonies of S0168 (from a transformation plate from 12/08)

4 different colonies of J04630 (from a transformation plate from 12/08)

- Protocol : add 1μL of cells (diluted in water), 10μL of Master Mis, 7μL of SDW, 1μL of VF primer and 1μL of VR primer

- Gel PCR products

Gel 1

Lane2 : Hyperladder1
Lane3 : JO4630, colony 1
Lane4 : JO4630, colony 2
Lane5 : JO4630, colony 3
Lane6 : JO4630, colony 4
Lane7 : HyperladderI

Gel 2

Lane2 : HyperladderI
Lane3 : ECE190 double digest
Lane4 : S0168, colony 1
Lane5 : S0168, colony 2
Lane6 : S0168, colony 3
Lane7 : S0168, colony 4
Lane8 : HyperladderI
Lane9 : R0040
Lane10 : R0062
Lane11 : Ladder 100bp

300px

- Results

R0040 and R0062 : one big band of about 300b (expected size 293), OK!

S0168 : one band of about 400b for the 4 different colonies (expected size 1234!), bad! This plate does not contain S0168

J04630 (colonies 2 and 4) : one band of about 1100b (expected size 1173), OK!

J04630 (colony 1) : one good band plus another band...

J04630 (colony 3) : one band of about 600b, bad!

Ligation

- Materials :

AgrA
AgrB
AgrC
AgrD
Pupp
Pspac
Ppac
Pxyl
RBS S
RBS W
psB4C5

- Double digest of PCR products

- Run vector, AgrA and AgrD on a gel

- DNA clean and concentrator for AgrA, B,C and D, promoters

- Microclean for both RBS

- Nanodrop

	260/280	ng/μL
AgrA	1.66	16.4
AgrB	1.91	23.5
AgrC	1.99	35.9
AgrD	2.13	4.9
Pxyl	1.54	5.6
Ppac	1.49	4.6
Pspc	1.62	9.6
Pupp	1.88	8.5
RBS S	2.44	29
RBS W	1.44	10.7

- Extract plasmid annd Agr from gel and clean

- Ligation

August, 21st

Transformation of ligation products

- Spin chemically competent TOP10, add 100μL of CaCl2 solution

- Add 5μL of DNA (ligation products), and 1μL of PUC9

- Continue the protocol of transformation

J04630

- Plate good colonies from yesterday on Kan25 and put in LB (for plasmid stock for tomorrow)

Plasmid stocks

- Plasmid miniprep R0040 and R0062

August, 22nd

New PCR of promoters

August, 23rd

Check promoters (after PCR from bacillus vectors)

- Gel

Lane1 : Hyperladder 5
Lane2 : Pxyl
Lane3 : Pspac
lane4 : Ppac
Lane5 : Pupp

Size is ok.

August, 27th

New transformation of ligation products

Products : agrD, Pupp, Pspac, RBS W, RBS S (from ligation with biolabs kit)

- Competent top 10 from the freezer

- Add 5μL of ligation products, and 1.2μL of PUC9

August, 28th

Results from transformation of ligation products

- nothing on plate, even on control plate

Reasons ?

- cells non competent anymore (try with fresh competent cells)

- not enough DNA (try with 10μL of DNA)

- very short ligation products

Transformation of ligation products (new)

Products to ligate : Pupp, Pspac, agrD, RBS S and RBS W

- new fresh competent TOP 10

- 5μL of DNA (1.5μL of PUC9)

- 2h30 in the incubator

August, 29th

Results of transformation with our ligation products

Everything grew! Better efficiency with electrop. than with chemical protocol

Single colony PCR to check our transformation

Transformed products	number of picked colonies from chemical transformation	number of picked colonies from electrop. transformation (neat)	number of picked colonies from electrop. transformation (1:10)
Pupp	2	2	0
Pspac	2	2	0
RBS S	3	0	2
RBS W	3	0	2
agrD	3	2	0

- Single colony PCR : 13μL of SDW+cells, 5μL of Master Mix, 1μL of VF and 1μL of VR (and plate each single colony)

- Load a gel (1.3% agarose) : 5μL of PCR products + 1μL of dye (only 1μL of 100b ladder)

In the death plasmid, the VF-VR size is about 280b.

Transformed products	size of the product (with cutting sites)	expected size after PCR (about)
Pupp	255	480
Pspac	125	350
RBS S	56	280
RBS W	56	280
agrD	200	430

Result : nothing, even no ladder, problem with the gel!

- run again on a e-gel

Lane1 :ladder 100bp
Lane2 : Pupp colony 1
Lane3 : Pupp colony 3
Lane4 : Pspac colony 1
Lane5 : Pspac colony 3
Lane6 : RBS S colony 1
Lane7 : RBS S colony 4
Lane8 : RBS W colony 1
Lane9 : RBS W colony 4
Lane10 : agrD colony 1
Lane11 : agrD colony 4
Lane12 : HyperladderI

Result : nothing, just the primers! Problem with our PCR

Plate biobricks from MIT

E0840
B0014
I712007
C0012
B0015
C0061
R0063

September, 2nd

Check transformation in E.coli of our ligated products

- Single colony PCR with VF and VR : add 10μL of SDW, 5μL of MM, 1μL of VF, 1μL of VR and 3μL of cells

inserted products	number of colonies to check (chemical transf.)	number of colonies to check (electrop. transf.)
RBS S	3	2
RBS W	3	2
Pspac	2	2
Pupp	2	2
agrD	3	2

- Gel (3% of agarose)

Result

gel	lane	inserted product (name of the colony)	observation	conclusion
top	3	RBS S (1)	one band (260bp)	size of the insert, RBS too small to see on a gel
top	4	RBS S (2)	one band (260bp)	size of the insert, RBS too small to see on a gel
top	5	RBS S (4)	nothing	?
top	6	RBS S (5)	nothing	?
top	7	RBS W (1)	2 band (260bp + 350bp)	size of the insert, RBS too small to see on a gel + something else?
top	8	RBS W (2)	one band (350bp)	too big
top	9	RBS W (4)	one band (260bp)	size of the insert, RBS too small to see on a gel
top	10	RBS W (5)	one band (260bp)	size of the insert, RBS too small to see on a gel
top	11	Pspac (1)	2 band (260bp + 350bp)	maybe problem with products loaded on gel (exactly the same bands than for RBS W)
top	12	Pspac (2)	one band (450bp)	size of Pupp?
top	13	Pspac (3)	one band (450bp)	size of Pupp?
bottom	3	Pspac (4)	nothing	?
bottom	4	Pupp (1)	one band (400bp)	size of Pspac?
bottom	5	Pupp (2)	one band (400bp)	size of Pspac?
bottom	6	Pupp (3)	one band (slightly lower than 400bp)	size of Pspac?
bottom	7	Pupp (4)	one band (400bp)	size of Pspac?
bottom	8	agrD (1)	2 bands (380 and 450bp)	big band is ok
bottom	9	agrD (2)	2 bands (380 and 450bp)	big band is ok
bottom	10	agrD (3)	no bands	?
bottom	11	agrD (4)	strong band (450bp)	ok
bottom	12	P2	one band (350bp)	ok

September, 3rd

Checking the insert of promoters

We ligated promoters into death vector, and transforned into Top 10. Our transformation worked, but it was hard to say with the result of yesterday if we had the good insert. Moreover, it is possible that we inverted Pupp and Pspac. So we are going to make a new single colony PCR with the primers of promoters (we used the same single colonies than yesterday).

We also want to PCR again all promoters (Pspac, Pxyl, Pupp and Ppac) from plasmids to have more.

Picture of the gel with the different promoters

promoter	colony	primers	name
Pspac	1	Pspac primers	A
Pspac	1	Pupp primers	B
Pspac	2	Pspac primers	C
Pspac	2	Pupp primers	D
Pupp	1	Pupp primers	E
Pupp	1	Pspac primers	F
Pupp	3	Pupp primers	G
Pupp	3	Pspac primers	H

- Single colony PCR : add 10μL of SDW, 5μL of MM, 1μL + 1μL of primers, 3μL of cells

- Gel

lane 3 : hyperladderI
lane 4 : Pspac (colony1) with Pspac primers
lane 5 : Pspac (colony1) with Pupp primers
lane 6 : Pspac (colony2) with Pspac primers
lane 7 : Pspac (colony2) with Pupp primers
lane 8 : Pupp (colony1) with Pupp primers
lane 9 : Pupp (colony1) with Pspac primers
lane 10 : Pupp (colony3) with Pupp primers
lane 11 : Pupp (colony3) with Pspac primers
lane 12 : HyperladderI

- Results

promoter	colony	primers	observation	Conclusion
Pspac	1	Pspac primers	nothing	it is in fact Pupp
Pspac	1	Pupp primers	band (about 280bp)	Pupp OK
Pspac	2	Pspac primers	nothing	it is in fact Pupp
Pspac	2	Pupp primers	band (about 280bp)	Pupp OK
Pupp	1	Pupp primers	nothing	it is in fact Pspac
Pupp	1	Pspac primers	band (about 180bp)	Pspac OK
Pupp	3	Pupp primers	nothing	it is in fact Pspac
Pupp	3	Pspac primers	band (about 180bp)	Pspac OK

Make some stock of our new biobricks

Pupp (colony1) into the death vector, transformed into TOP10
Pspac (colony1) into the death vector, transformed into TOP10
agrD (colony5) into the death vector, transformed into TOP10

- Grow this single colony into 10mL of LB (Cm35)

Transformation of new "biobricks"

- transform into E.coli :

agrA
agrB
agrC
Pxyl

September, 4th

Results of new "biobricks"transformation

- Nothing on our plate, except for the control plate.

New attempt of new "biobricks" transformation

- transform into E.coli these ligated products:

agrA
agrB
agrC
Pxyl

September, 7th

New PCR

- New stocks of Master Mix

- PCR agrA, agrB, Pxyl, Pspac, Ppac and Pupp

September, 8th

Check product of PCR from yesterday

Lane3 : Hyperladder I
Lane4 : agrA
Lane5 : agrB
Lane6 : Pxyl
Lane7 : Pspac
Lane8 : Ppac
Lane9 : Pupp
Lane10 Hyperladder IV

Results : everything is ok

Check transformation from 03/09

After several days of incubation, we have a few colonies on our transformed plates (agrA, B and C).

Single colony PCR

- Add 13μL of cells diluted into SDW, 5μL of MM, 1μL of VF and 1μL of VR

Gel

September, 10th

PCR of GFP+RBS and Promoter+RBS

- PCR

- Run a 1.2% agarose gel with 1μL of sample

Lane 3 : HyperladderI
Lane 4 : GFP + RBS 1A
Lane 5 : GFP + RBS1B
Lane 6 : GFP + RBS 2A
Lane 7 : GFP + RBS 2B
Lane 8 : Pupp + RBS 1
Lane 9 : Pupp + RBS 2
Lane 10: HyperladderIV

Result

RBS screening

5 colonies from chemical transformation + 6 colonies from electroporation transformation for RBS S
5 colonies from chemical transformation + 6 colonies from electroporation transformation for RBS W

- PCR : 11μL of SDW + 5μL of MM + 1+1μL of primers (RBS detect + VR) + 2μL of cells (program iGEM34)

- Gel1

Lane2 : RBSS1
Lane3 : RBS S2
Lane4 : RBS S3
Lane5 : RBS S4
Lane6 : RBS S5
Lane7 : RBS S6
Lane8 : HyperladderIV
Lane9 : RBS S7
Lane10 : RBS S8
Lane11 : RBS S9
Lane12 : RBS S10
Lane13 : RBS S6 with VF and VR primers
Lane14 : RBS S11

- Gel2

Lane2 : RBSW1
Lane3 : RBS W2
Lane4 : RBS W3
Lane5 : RBS W4
Lane6 : RBS W5
Lane7 : RBS W6
Lane8 : HyperladderIV
Lane9 : RBS W7
Lane10 : RBS W8
Lane11 : RBS W9
Lane12 : RBS W10
Lane13 : RBS W6 with VF and VR primers
Lane14 : RBS W11

Result

- Nothing, except for the PCR with VF and VR primers, either our primers are not right, either we have no insert. But the gel is not good enough to see very well, we will try to run a new gel.

@@ Line 528: / Line 528: @@
 * Gel
+=September, 10th=
+==PCR of GFP+RBS and Promoter+RBS==
+- PCR
+- Run a 1.2% agarose gel with 1μL of sample
+*Lane 3 : HyperladderI
+*Lane 4 : GFP + RBS 1A
+*Lane 5 : GFP + RBS1B
+*Lane 6 : GFP + RBS 2A
+*Lane 7 : GFP + RBS 2B
+*Lane 8 : Pupp + RBS 1
+*Lane 9 : Pupp + RBS 2
+*Lane 10: HyperladderIV
+* Result
+[[Image:gel10091pcr.gif|300px|center]]
+==RBS screening==
+*5 colonies from chemical transformation + 6 colonies from electroporation transformation for RBS S
+*5 colonies from chemical transformation + 6 colonies from electroporation transformation for RBS W
+- PCR : 11μL of SDW + 5μL of MM + 1+1μL of primers (RBS detect + VR) + 2μL of cells (program iGEM34)
+- Gel1
+*Lane2 : RBSS1
+*Lane3 : RBS S2
+*Lane4 : RBS S3
+*Lane5 : RBS S4
+*Lane6 : RBS S5
+*Lane7 : RBS S6
+*Lane8 : HyperladderIV
+*Lane9 : RBS S7
+*Lane10 : RBS S8
+*Lane11 : RBS S9
+*Lane12 : RBS S10
+*Lane13 : RBS S6 with VF and VR primers
+*Lane14 : RBS S11
+- Gel2
+*Lane2 : RBSW1
+*Lane3 : RBS W2
+*Lane4 : RBS W3
+*Lane5 : RBS W4
+*Lane6 : RBS W5
+*Lane7 : RBS W6
+*Lane8 : HyperladderIV
+*Lane9 : RBS W7
+*Lane10 : RBS W8
+*Lane11 : RBS W9
+*Lane12 : RBS W10
+*Lane13 : RBS W6 with VF and VR primers
+*Lane14 : RBS W11
+*Result
+[[Image:gel10092pcr.gif|200px|center]]
+- Nothing, except for the PCR with VF and VR primers, either our primers are not right, either we have no insert. But the gel is not good enough to see very well, we will try to run a new gel.
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Team:Cambridge/Signalling/Lab Work