Take glycerinated cultures of C58 Agrobacterium with dsRED from GoldenBraid Collection. Prepare broth culture (5 mL LB + 5 μL kanamycin + 5 μL Rifampin) 1:1000 and incubate overnight at 28°C.

Refresh previously made culture by inoculating 10 μL in a new culture medium.

Agroinfiltration in Nicotiana benthamiana of C58 with dsRED.

• Take from the glycerinates of Goldenbraid Collection:

Prepare liquid culture (3 mL LB + 3 μL antibiotic) 1:1000. Incubate at 37°C overnight.

• Experiment with snails:
• Two experiments: one with infiltrated Nicotiana benthamiana and another with not infiltrated N.benthamiana (negative control). Lettuce leafs haven’t been correctly infiltrated and it seems that the expression level is low.
• Let both N. benthamiana leafs with snails overnight at room temperature in separated boxes. We will observe if snails eat the leafs and if appears fluorescence.

Experiment is over due to snails haven’t eaten leafs enough so we have not been able to see fluorescence.

Orange Clemenules DNA Genome Extraction protocol

• Take from the glycerinates of GoldenBraid Collection:

Miniprep of 35s:Cas9:Tnos with E.Z.N.A ®. Plasmid Mini Kit I, Q(capless) Spin.

Luciferase and nopaline synthase terminator cultures haven’t succeed. Repeat Luc and Tnos cultures.

Primers IG16JUN01 and IG16JUN02 have arrived.

Finish orange DNA Genome Extraction and check DNA concentration with NanoDrop. Concentration is very low so extraction will be done again.

• Miniprep with E.Z.N.A ®. Plasmid Mini Kit I, Q(capless) Spin of:
• Luc in pUPD2
• Tnos in pUPD2

Check orange DNA genome concentration with NanoDrop.

Perform a PCR to bind linker SAGTI with luciferase:

Run electrophoresis gel of Clemenules DNA (agarose 1%). 45 mL agarose gel at 1% 0.45 g of agarose with 45 mL of TAE 1X. Voltage used is 100 V.

Gleva Rice DNA Genome Extraction Protocol

Run electrophoresis gel of Luciferase PCR product. 45 mL agarose gel at 1% 0.45 g of agarose with 45 mL of TAE 1X. Voltage used is 100 V.

Ligation Reaction of SAGTI:Luciferase into a pUPD2.

Transform E. coli DH5α with it. The method that is necessary to carry out this procedure is explained in protocols

Check DNA concentration with NanoDrop.

Run electrophoresis gel of Gleva rice DNA. We have checked that there isn’t DNA.

Repeat: Rice DNA Genome Extraction Protocol

Check DNA concentration with NanoDrop.

Run electrophoresis gel of Gleva rice DNA. It observed that genome extraction is correctly done.

Take glycerinated cultures from Goldenbraid Collection:

• Miniprep with E.Z.N.A ®. Plasmid Mini Kit I, Q(capless) Spin of:
• psgRNA in pUPD2
• U6-26 in pUPD2

Primers IG16JUL01, IG16JUL02, IG16JUL03, IG16JUL04, IG16JUL05, IG16JUL06, IG16JUL07 and IG16JUL08 arrived.

gBlocks of - 35s:5’ region - have arrived.

We perform a PCR of Clemenules Orange and Gleva Rice Genome Extraction following the protocol. We want to obtain a fragment of the gene TFL of the orange DNA extraction and the gene Ga20ox of the rice DNA extraction.

Ligate reaction of 35s:5’ region in pUPD2. Following ligation protocol, BsmbI enzyme is used in this reaction.

Run electrophoresis gel of TFL and Ga20ox PCR products. 45 mL agarose gel at 1 % 0.45 g of agarose with 45 mL of TAE 1X. Voltage used is 120 V.

Transform E. coli with the next part: 35s:5’ region (electroporation 2.5KV). Plating it and incubate overnight at 37°C.

Take glycerinated culture for Georgia collaboration. The part is 35s:GFP:Tnos (α1 and kanamycin).

Miniprep with E.Z.N.A ®. Plasmid Mini Kit I, Q(capless) Spin of 35s:GFP:Tnos

No colonies have grown in the 35s:5’ region petri dishes. Repeat transformation procedure, plating again and incubate overnight at 37°C.

Pick a single E. coli DH5α (35s:5’ region in pUPD2) colony from the plate that has been incubated overnight. Inoculate a starter culture of 4 ml of LB medium with 4 μL of chloramphenicol in a 50 ml tube with the colony and incubate it overnight at 37°C with shaking.

Check Georgia miniprep concentration with NanoDrop (35s:GFP:Tnos)

Targets ligations in pUPD2 (Orange TFL and Rice Ga20ox). Following ligation protocol, BsmbI enzyme is used in this reaction.

Pick a single E. coli DH5α (target Ga20ox in pUPD2 and target TFL in pUPD2) colony from the plate that has been incubated overnight. Inoculate a starter culture of 4 ml of LB medium with 4 μL of chloramphenicol in a 50 ml tube with the colony and incubate it 16 hours at 37°C.

Miniprep with E.Z.N.A ®. Plasmid Mini Kit I, Q(capless) Spin of 35s:5’region in pUPD2

Digestion of minipreps with NotI. Incubate 1 hour at 37°C

Run electrophoresis gel of the following part: 35s:5’ region in pUPD2. We remain the samples 1 and 3.

• Miniprep with E.Z.N.A ®. Plasmid Mini Kit I, Q(capless) Spin of:
• Ga20ox PCR in pUPD2
• TFL PCR in pUPD2

Digestion of minipreps with NotI. Incubate 1 hour at 37°C.

• Run electrophoresis gel of the same part:
• Ga20ox PCR in pUPD2
• TFL PCR in pUPD2

Ligation using Golden Braid assembly of the device 35s:5’region:TFL PCR:Luc:Tnos and 35s:5’region:Ga20oxPCR:Luc:Tnos in α1 plasmid.

E. coli Transformation with the device 35s:5’region:TFL PCR:Luc:Tnos and 35s:5’region:Ga20oxPCR:Luc:Tnos in α1 plasmid.

E. coli plating in plates with Kanamycin (antibiotic). Incubate overnight at 37°C.

Pick a single E. coli DH5α (35s:5’ region) colony from the plate that has been incubated overnight. Inoculate a starter culture of 4 ml of LB medium with 4 μL of chloramphenicol in a 50 ml tube with the colony and incubate it 16 hours at 37°C.

Primers IG16JUL09, IG16JUL10, IG16JUL11, IG16JUL12, IG16JUL13, IG16JUL14, IG16JUL15 and IG16JUL16 arrived.

• Ligation using Golden Braid assembly of the next devices:
• 35s:5’ region:TFL PCR control positive:Luc:Tnos
• 35s:5’ region:Ga20oxPCR control positive:Luc:Tnos
• 35s:5’ region:TFL PCR consensus:Luc:Tnos
• 35s:5’ region:Ga20ox PCR consensus:Luc:Tnos
• U6-26:sgRNA TFL: psgRNA (scaffold)
• U6-26:sgRNA Ga20ox: psgRNA (scaffold)

• Step 1: Annealing of oligonucleotides. Received primers are at 1uM. It is necessary taking to 10 uM.
• Mix in an Eppendorf:
• 8 μL of H₂O milli-Q
• 1 μL forward primer
• 1 μL reverse primer
• Step 2: Ligation reaction

E. coli Transformation with the devices previously explained.

E. coli plating in 6 plates (6 ligation reactions) with Kanamycin (antibiotic). Incubate overnight at 37°C.

• Miniprep with E.Z.N.A ®. Plasmid Mini Kit I, Q(capless) Spin of:
• 35s:5’ region : TFL PCR : Luc : Tnos (3α1)
• 35s:5’ region : Ga20ox PCR : Luc : Tnos (3α1)

Digestion of minipreps with EcoRI. Incubate 1 hour at 37°C

• Ligation using Golden Braid assembly of the next devices:
• 35s:Cas9:Tnos – 35s:5’ region:TFL PCR:Luc:Tnos
• 35s:Cas9:Tnos – 35s:5’ region:Ga20ox PCR:Luc:Tnos

E. coli Transformation with the devices previously explained.

• Run an electrophoresis gel of the products from the digestion of minipreps. The devices are:
• 35s:5’ region:TFL PCR:Luc:Tnos (3α1)
• 35s:5’ region :Ga20ox PCR:Luc:Tnos (3α1)

Sequencing 35s:5’region in pUPD2 → correct

• Transformations in E. coli DH5α with:
• 35s:5’ region:TFL PCR:Luc:Tnos (3α1)
• 35s:5’ region:Ga20ox PCR:Luc:Tnos (3α1)

Plating the last devices in 2 plates with Agrobacterium C58. Incubate 2 days at 28°C.

• Minipreps (2 samples for each device) with E.Z.N.A ®. Plasmid Mini Kit I, Q(capless) Spin of:
• 35s:5’ region:TFL target control positive:Luc:Tnos
• 35s:5’ region:Ga20ox target control positive:Luc:Tnos
• 35s:5’ region:TFL target consensus:Luc:Tnos
• 35s:5’ region:Ga20ox target consensus:Luc:Tnos
• U6-26:sgRNA TFL:psgRNA (scaffold)
• U6-26:sgRNA Ga20ox:psgRNA (scaffold)

• Ligation using Golden Braid assembly of the next devices:
• 35s:Cas9:Tnos – U6:TFL sgRNA:psgRNA (scaffold) (Ω1)
• 35s:Cas9:Tnos – U6: Ga20ox sgRNA:psgRNA (scaffold) (Ω1)

Digestion of the minipreps with EcoRI which have been done before. Incubate 1 hour at 37°C. There is a total of twelve minipreps. It has been followed the Miniprep {digestion protocol path:https://2016.igem.org/Team:Valencia_UPV/Notebook/Protocol].

Run electrophoresis gel of the digestion products.

• Pick a single E. coli DH5α colony from the plates that have been incubated overnight. The devices are:
• 35s:TFL Knock-out:Luc:Tnos (4 samples)
• U6-26:Ga20ox sgRNA:psgRNA (2 samples)

Inoculate a starter culture of 4 ml of LB medium with 4 μL of kanamycin in a 50 ml tube with the colony and incubate it 16 hours at 37°C.

• Transformation in DH5α E. coli with:
• 35s:Cas9:Tnos – U6:TFL sgRNA:psgRNA (scaffold) (Ω1)
• 35s:Cas9:Tnos – U6:Ga20ox sgRNA:psgRNA (scaffold) (Ω1)

Plating E. coli transformations in plates with LB + agar + IPTG + XGal and incubate it overnight at 37°C.

• Miniprep with E.Z.N.A ®. Plasmid Mini Kit I, Q(capless) Spin of:
• U6-26:Ga20ox sgRNA:psgRNA
• 35s:5’ region:TFL Knock-out:Luc:Tnos (3α1)

Digestion of the minipreps with EcoRI which have been done before. Incubate 1 hour at 37°C. There is a total of six minipreps. It has been followed the Miniprep digestion protocol.

Run an electrophoresis gel of the digestion products.

However, despite the fact that electrophoresis gel have correctly run, we have decided to repeat the ligation reactions. We have not get the expected results for a gRNA.

• Ligation using Golden Braid assembly of the next devices:
• 35s:5’ region:TFL target control positive:Luc:Tnos
• 35s:5’ region:Ga20ox target control positive:Luc:Tnos
• 35s:5’ region:TFL target consensus:Luc:Tnos
• 35s:5’ region:Ga20ox target consensus:Luc:Tnos
• U6-26:sgRNA TFL:psgRNA (scaffold)
• U6-26:sgRNA Ga20ox:psgRNA (scaffold)

Transformation in DH5α E. coli with ligation products (consensus targets and knock-out targets of TFL and Ga20ox as well as their gRNAs)

Plating E. coli transformations in plates with LB + agar + IPTG + XGal and incubate it overnight at 37°C.

• Pick a single Agrobacterium C58 colony from the plates that have been incubating since 16/06/2016. The devices are:
• 35s:5’ region:TFL PCR:Luc:Tnos (3α1)
• 35s:5’ region:Ga20ox PCR:Luc:Tnos (3α1)

Incubate it 48 hours at 28°C.

• Pick transformed E. coli colony from the incubated plates. The devices are:
• 35s:5’ region:TFL target control positive:Luc:Tnos
• 35s:5’ region:Ga20ox target control positive:Luc:Tnos
• 35s:5’ region:TFL target consensus:Luc:Tnos
• 35s:5’ region:Ga20ox target consensus:Luc:Tnos
• U6-26: sgRNA TFL:psgRNA (scaffold)
• U6-26: sgRNA Ga20ox:psgRNA (scaffold)

Incubate it overnight at 37°C.

• Miniprep with E.Z.N.A ®. Plasmid Mini Kit I, Q(capless) Spin of:
• 35s:5’ region:TFL target knock-out:Luc:Tnos
• 35s:5’ region:Ga20ox target control knock-out:Luc:Tnos
• 35s:5’ region:TFL target consensus:Luc:Tnos
• 35s:5’ region:Ga20ox target consensus:Luc:Tnos
• U6-26:sgRNA TFL:psgRNA (scaffold)
• U6-26:sgRNA Ga20ox:psgRNA (scaffold)

Digestion of the minipreps with EcoRI which have been done before. Incubate 1 hour at 37°C. There is a total of six minipreps. It has been followed the Miniprep digestion protocol.

Run an electrophoresis gel of the digestion products. We will keep the minipreps with “1”.

• Ligation using Golden Braid assembly of the next devices. Is used the restriction enzyme BsmbI.
• 35s:Cas 9:Tnos – U6-26:TFL sgRNA:psgRNA
• 35s:Cas 9:Tnos – U6-26:Ga20ox sgRNA:psgRNA

• Transformations in E. coli DH5α with:
• 35s:Cas 9:Tnos – U6-26:TFL sgRNA:psgRNA
• 35s:Cas 9:Tnos – U6-26:Ga20ox sgRNA:psgRNA

Incubate 2 hours at 37°C.

Plating E. coli transformation explained before and incubate it at 37°C overnight.

#Agrobacterium C58 transformation with:

• #35s:5’ region:TFL target knock-out:Luc:Tnos
• 35s:5’ region:Ga20ox target control knock-out:Luc:Tnos
• 35s:5’ region:TFL target consensus:Luc:Tnos
• 35s:5’ region:Ga20ox target consensus:Luc:Tnos

Incubate 48 hours at 28°C.

Sequencing reaction:

Ordered the necessary primers to sequence: TFL consensus, TFL knockout, Ga20ox consensus and Ga20ox knockout.

E. coli transformations with 35s:Cas 9:Tnos – U6-26:TFL sgRNA: psgRNA

Plating the last device in plates with Agrobacterium C58. Plates contain spec + IPTG + X-Gal. Incubate 2 days at 28°C.

Pick a single E. coli DH5α (35s:Cas 9:Tnos – U6-26:TFL sgRNA:psgRNA and 35s:Cas 9:Tnos – U6-26:Ga20ox sgRNA:psgRNA) colony from the plates that has been incubated overnight. Inoculate a starter culture of 4 ml of LB medium with 4 μL of spectinomycin in a 50 ml tube with the colony and incubate it overnight at 37°C with shaking.

• #Minipreps (4 samples for each device) with E.Z.N.A ®. Plasmid Mini Kit I, Q(capless) Spin of:
• #35s:Cas 9:Tnos – U6-26:TFL sgRNA:psgRNA
• 35s:Cas 9:Tnos – U6-26:Ga20ox sgRNA:psgRNA

• #35s:Cas 9:Tnos – U6-26:TFL sgRNA:psgRNA
35s:Cas 9:Tnos – U6-26:Ga20ox sgRNA:psgRNA

• #Store the next cultures at -80°C:
• #35s:5’ region in pUPD2 (DH5α) number 1
SAGTI: luciferase in pUPD2 (DH5α) number 2

Pick a single Agrobacterium C58 (35s:Cas 9:Tnos – U6-26:TFL sgRNA:psgRNA in 3Ω1 and 35s:Cas 9:Tnos – U6-26:Ga20ox sgRNA:psgRNA in 3Ω1 ) colony from the plates that has been incubated overnight. Inoculate a starter culture of 5 ml of LB medium with 5 μL of spectinomycin and kanamycin in a falcon tube with the colony and incubate it overnight at 28°C with shaking.

Incubate it 48 hours at 28°C

• #Minipreps of Agrobacterium with E.Z.N.A ®. Plasmid Mini Kit I, Q(capless) Spin of:
• #35s:5’ region:TFL target control positive:Luc:Tnos
35s:5’ region:Ga20ox target control positive:Luc:Tnos
35s:5’ region:TFL target consensus:Luc:Tnos
35s:5’ region:Ga20ox target consensus:Luc:Tnos

• #Minipreps with E.Z.N.A ®. Plasmid Mini Kit I, Q(capless) Spin of:
• #35s:5’ region:TFL PCR:Luc:Tnos in 3α1 plasmid from C58 Agrobacterium
35s:5’ region:Ga20ox PCR:Luc:Tnos in 3α1 plasmid from C58 Agrobacterium

• #Sequencing products have arrived:
• #U6-26:Ga20ox gRNA:psgRNA in α1 - correct
U6-26:TFL gRNA:psgRNA in α1 - correct

• #Minipreps with E.Z.N.A ®.® Plasmid Mini Kit I, Q(capless) Spin of:
• #35s:5’ region: Ga20ox PCR : Luc : Tnos in α1
35s:5’ region: TFL PCR : Luc : Tnos in α1

• #DH5α E. coli transformation with the devices:
• #35S : 5’ region : TFL KO : Luc : Tnos - promoter35s: Renilla:Tnos in Ω2
35S : 5’ region : TFL consensus : Luc : Tnos - promoter35s: Renilla:Tnos in Ω235S : 5’ region : Ga20ox KO : Luc : Tnos - promoter35s: Renilla:Tnos in Ω235S : 5’ region : Ga20ox consensus : Luc : Tnos - promoter35s: Renilla:Tnos in Ω2

• #Minipreps with E.Z.N.A ®.® Plasmid Mini Kit I, Q(capless) Spin of:
• #35s:5’region:TFL PCR:Luc:Tnos in α1
35s:5’region:Ga20oxPCR: Luc: Tnos in α1

1	35S:5’	pUPD2	CAM
2	SAGTI:Luc	pUPD2	CAM
3	35s:5’:TFLPCR:Luc:Tnos	3α1	KAN
4	35s:5’:Ga20PCR:Luc:Tnos	3α1	KAN

Ligate reactions of TFL PCR and Ga20ox PCR with Renilla

Reagent	Volume(μL)
35s:5’region: TFL/Ga20oxPCR: Luc: Tnos	1
Promoter35s: Renilla: Tnos	1
pUPD2	1
BSA10X	1.2
Ligase Buffer	1.2
BsmbI	1
T4 ligase	1
H2O milli-Q	4.6

04Aug

05Aug

Miniprep with E.Z.N.A ®.® Plasmid Mini Kit I, Q(capless) Spin of TMV CDS
Transform DH5 α E. coli with the device 35s : 5’ region: PCR PCR: Luc: Tnos - 35s: Renilla: Tnos. After incubating 2 hours, it must be plated.
Refresh C58 Agrobacterium tumefaciens cultures with the aim of infiltrating in N.benthamiana on 05/08.
Pick a single E. coli DH5α (35S : 5’ region: KO/cons target: Luc:Tnos - promoter35s: renilla: Tnos) colony from the plate that has been incubated overnight. Inoculate a starter culture of 4 ml of LB medium with 4 μL of spectinomycin in a 50 ml tube with the colony and incubate it overnight at 37° with shaking.Sequencing TMV empty vector with the primer D09OCT01 (10 uM). 5μL of Miniprep and 9μL of primer (dilution 1:3). Sequencing code of 210.13.300 and 210.13.301.
Pick a single E. coli DH5α (promoter35s: 5’ region: TFL/Ga20oxPCR: Luc: Tnos - promoter35s: Renilla: Tnos ) colony from the plate that has been incubated overnight. Inoculate a starter culture of 4 ml of LB medium with 4 μL of kanamycin in a 50 ml tube with the colony and incubate it overnight at 37° with shaking.
#Miniprep with E.Z.N.A ®.® Plasmid Mini Kit I, Q(capless) Spin of:
	#35s: 5’ region: TFL PCR: Luc: Tnos - promoter35s: Renilla: Tnos
	35s: 5’ region: Ga20oxPCR: Luc: Tnos - promoter35s: Renilla: Tnos
	35s: 5’ region: Ga20oxconsensus: Luc: Tnos - promoter35s: Renilla: Tnos
	35s: 5’ region: Ga20oxKO: Luc: Tnos - promoter35s: Renilla: Tnos
Digestion of minipreps with EcoRV. Incubate 1 hour at 37°
Run electrophoresis gel of the digestion products: TFLK01, TFLK02, TFLcons01, TFLcons02, GAK01, GAK02, GAcons01, GAcons02.
Prepare the Agroinfiltration with the correct protocol.
Centrifuge the cultures at 3000 rpm during 15 minutes. We discard the supernatant and it is necessary to resuspend in 5mL of Agroinfiltration solution. Let shaking it a RT during 2 hours. OD’s measurement.

device	Volume of culture (mL)	Volume of Agroinfiltration solution (mL)
Cas9 - TFL gRNA	0.7	9.3
Cas 9 - Ga20ox gRNA	0.7	9.3
Cas 9 - XT1: XT2	0.59	9.41
TFL KO	0.67	9.33
TFL PCR	0.73	9.27
Ga20ox consensus	0.71	9.28
Pnos	0.68	9.32
35s : Luc	0.78	9.22
Ga20ox PCR	0.74	9.26
TFL consensus	0.71	9.29
Ga20ox- KO	0.73	9.27

08Aug

09Aug

#Infiltration cultures:
	#35s: Luc: Tnos	Laboratory controls
	Pnos: Luc: Tnos	Laboratory controls
	gTS TFL KO + Cas9 - XT1:XT2	Positive controls
	gTSGa20oxKO + Cas9 - XT1:XT2	Positive controls
	gTS TFL PCR + Cas9 - XT1:XT2	Negative controls
	gTS Ga20oxPCR + Cas9 - XT1:XT2	Negative controls
	gTS TFL PCR + Cas9 - TFLgRNA	Samples
	gTS TFL cons + Cas9 - TFLgRNA	Samples
	gTS Ga20oxPCR + Cas9 - Ga20gRNA	Samples
	gTS Ga20oxcons + Cas9 - Ga20gRNA	Samples
Transplant agroinfiltrated plants (Nicotiana benthamiana)
Pick up 6 disks per each plant in order to carry out the luciferase assay on 09/08
Ligate reaction of:

devices	Volume (μL)
35s : 5’ region: Ga20/TFL KO: Luc: Tnos - 35s: Renilla: Tnos - 35s: hCas9: Tnos: U6: Ga20/TFL gRNA: psgRNA	1
35s : 5’ region: Ga20/TFL cons: Luc: Tnos - 35s: Renilla: Tnos - 35s: hCas9: Tnos: U6: Ga20/TFL gRNA: psgRNA	1
3 α 1 plasmid	1.2
Bsa 10X	1.2
Buffer ligase	1
Bsa I	1
T4 ligase	1
H20 milliQ	4.6

U6:Ga20oxgRNA: psgRNA - 35s: Cas9: Tnos - Miniprep number 2 was empty. We have resuspended it with 40 μL of H20 milliQ and we have checked the DNA concentration with the Nanodrop. The results show us that the DNA concentration in the Eppendorf was 140 ng/ μL so we have used it.

Miniprep with E.Z.N.A ®.® Plasmid Mini Kit I, Q(capless) Spin of 35s: 5’ region: TFL/Ga20oxPCR: Luc: Tnos – 35s: Renilla: Tnos

Transform in C58 Agrobacterium 35s: Renilla : Tnos (3 α2)

Plating promoter35s: Renilla: Tnos (3α2)

Luciferase assay

Promoter35s	pNos
TFLKO	Ga20KO
TFLPCRXT1	Ga20PCRXT1
TFLPCROK	Ga20PCROK
TFLconsOK	Ga20consOK

Transform the products of ligation in DH5 α. Incubate it at 37° during 2 hours.

We store at -80°:

5	35s:5’:Ga20cons:Luc:Tnos	3α1	KAN
6	35s:5’:Ga20KO:Luc:Tnos	3α1	KAN
7	35s:5’:TFLcons:Luc:Tnos	3α1	KAN
8	35s:5’:TFLKO:Luc:Tnos	3α1	KAN
9	35s:5’:Ga20cons:Luc:Tnos-35s:Ren:Tnos	3Ω2	SPEC
10	35s:5’:Ga20KO:Luc:Tnos-35s:Ren:Tnos	3Ω2	SPEC
11	35s:5’:Ga20PCR:Luc:Tnos-35s:Ren:Tnos	3Ω2	SPEC
12	35s:5’:TFLcons:Luc:Tnos-35s:Ren:Tnos	3Ω2	SPEC
13	35s:5’:TFLKO:Luc:Tnos-35s:Ren:Tnos	3Ω2	SPEC
14	35s:5’:TFLPCR:Luc:Tnos-35s:Ren:Tnos	3Ω2	SPEC
15	U6:Ga20sgRNA:psgRNA	3α1	KAN
16	U6:TFLsgRNA:psgRNA	3α1	KAN
17	35s:Cas9:Tnos-U6:Ga20gRNA:psgRNA	3Ω1	SPEC
18	35s:Cas9:Tnos-U6:TFLgRNA:psgRNA	3Ω1	SPEC
19	Ga20PCR	pUPD2	CAM
20	TFLPCR	pUPD2	CAM

10Aug

Run electrophoresis gel of: 35s: 5’ region: TFL/Ga20oxPCR: Luc: Tnos – 35s: Renilla: Tnos. We keep the Miniprep number 1.

Refresh the cultures of TFL PCR (pUPD2) and Ga20oxPCR (pUPD2) because we suspect that these cultures are the correct ones but we are not sure so we want to check them. The cultures that we use to refresh were made on 12/07/2016. It is important to remember that we need them to assemble the gTS with the new linkers.

Miniprep with E.Z.N.A ®.® Plasmid Mini Kit I, Q(capless) Spin of TFL / Ga20oxPCR in pUPD2

Digestion of minipreps with NotI. Incubate 1 hour at 37°

Run electrophoresis gel of Miniprep products. We have made a small gel so we have mix 0.45 g of Agarose with 45 mL of TAE 1X. Voltage used is 100V. Both samples are correct.

Pick a single E. coli DH5α (promoter35s: 5’ region: TFL/Ga20oxcons: Tnos - promoter35s: Renilla: Tnos - 35s: Cas9: Tnos - U6: TFL/Ga20oxgRNA: psgRNA) colony from the plate that has been incubated overnight. Inoculate a starter culture of 4 ml of LB medium with 4 μL of chloramphenicol in a 50 ml tube with the colony and incubate it overnight at 37° with shaking.

We throw out from Golden Braid collection the glycerinate number 1107 (Cas9 - XT1gRNA) and 0549 (35s: TEV: Tnos)

Ligation reaction of 35s: 5’ region: TFL/ Ga20: Tnos - 35s: Renilla: Tnos + 35s: Cas9: Tnos - U6: TFL/Ga20oxgRNA: psgRNA

devices	Volume (μL)
gTS TFL/ Ga20ox- Renilla	1
Cas9 - gRNA	1
3 α 1 plasmid	1.2
Bsa 10x	1.2
Buffer ligase	1
Bsa I	1
T4 ligase	1
H20 milliQ	4.6