Aim: to form a level 1 construct (full transcriptional unit) from level 0 modules in a in a one-pot, one-step, digestion-ligation GoldenGate cloning reaction.

Add relevant DNA to a PCR tube at a 2:1 ratio of insert to acceptor (dilutions may be required depending on starting DNA concentration).

Add enzymes and reaction buffers according to the template shown below.

Make up the reaction mix to 15 µL using distilled water.

Reaction component	Volume (µL)
Level 1 acceptor	Ratio 2:1 (Insert: acceptor)
Insert 1	Ratio 2:1 (Insert: acceptor)
Insert 2	Ratio 2:1 (Insert: acceptor)
Insert 3	Ratio 2:1 (Insert: acceptor)
T4 reaction buffer	1.5
BSA buffer	1.5
BsaI	0.5
T4 DNA Ligase	0.5
Distilled water	Make up to 15 µL

Cycle the reaction mix in a PCR machine according to the program given below.

Step	Temperature (°C)	Time (minutes: seconds)
1	37	0:20
2*	37	3:00
3*	16	4:00
4	50	5:00
5	80	5:00
6	16	∞

*Steps 2-3 cycled x26

Aim: to form a level 2, multigene construct from level 1 modules in a in a one-pot, one-step, digestion-ligation GoldenGate cloning reaction..

Add relevant DNA to a PCR tube at a 2:1 ratio of insert to acceptor (dilutions may be required depending on starting DNA concentration).

Add enzymes and reaction buffers according to the template shown below.

Make up the reaction mix to 15 µL using distilled water.

Reaction component	Volume (µL)
Level 1 acceptor	Ratio 2:1 (Insert: acceptor)
Insert 1	Ratio 2:1 (Insert: acceptor)
Insert 2	Ratio 2:1 (Insert: acceptor)
Insert 3	Ratio 2:1 (Insert: acceptor)
T4 reaction buffer	1.5
BSA buffer	1.5
Bpi1	0.5
T4 DNA Ligase	0.5
Distilled water	Make up to 15 µL

Cycle the reaction mix in a PCR machine according to the program given below.

Step	Temperature (°C)	Time (minutes: seconds)
1	37	0:20
2*	37	10:00
3*	16	10:00
4	37	10:00
5	65	20:00
6	16	∞

*Steps 2-3 cycled x3

PROTOCOL HERE

PROTOCOL HERE

Aim: to get DNA expression in E. coli.

• Remove chemically competent E. coli (DH5-alpha) cells from the -80°C freezer and thaw on ice.
• Take 1-2 µL of DNA and transfer into a clean 1.5 mL tube.
• Add 50 µL of chemically competent E. coli to the DNA and incubate on ice for 30 mins.
• Preheat water bath to 42°C.
• Heat shock the DNA and E. coli tube for 30-60 sec (not more than 60 sec).
• Transfer back onto ice for 5 mins.
• Add 250-500 µL of LB broth to the tube and incubate at 370C with shaking for 2 hrs.
• Spread plate 100 µL onto plates containing the relevant antibiotics and incubate over night at 37°C.

PROTOCOL HERE

Aim: to get DNA expression in Agrobacterium tumefaciens to allow infiltration into Nicotiana Benthamiana.

Remove 50 µL of electrocompetent Agrobacterium GV3101 cells from the -80°C freezer and thaw on ice.

Add 5 µL of DNA and transfer to a clean 1m electroporation cuvette.

Electroporate cells at 1.8kV using a Bio-rad micropulser machine.

Add 500 µL of LB broth to the elctroporated cells and transfer to a clean 1.5 mL Eppendorf tube.

Incubate at 28°C with shaking for 1 hour.

Spread plate 100 µL onto plates containing the relevant antibiotics and incubate over night at 28°C.

Aim: to determine the size (bp) of the DNA expressed by the colony picked

This helps us to check that the construct is what we expected.

Aim

The following protocols were used with QIAGEN QIAprep miniprep kits.

• Create an overnight culture- Pick a single colony from a freshly streaked selective plate and inoculate a culture of 1–5 ml LB medium containing the appropriate selective antibiotic. Incubate for 12–16 h at 37°C with shaking.
• Centrifuge 1-5ml of overnight culture at >8000 for 3 minutes in an Eppendorf tube to form a bacterial pellet; discard the supernatant.
• Re-suspend bacterial pellet in 250µl of P1 Buffer (kept at <5oC).
• Add 250µl of P2 Buffer and invert 4-6 times to mix thoroughly. This reaction is left for no longer than 5 minutes before completing the next step.
• Add 350µl of N3 Buffer and invert 4-6 times to mix thoroughly.
• Centrifuge for 10 minutes at 13,000rpm
• Decant supernatant into a spin column, centrifuge for 30-60 seconds, and discard the flow-through.
• Add 750µl of PE Buffer to the spin column and centrifuge for 30-60 seconds to wash the DNA. Discard the flow-through and centrifuge for a further 1 minute to remove any remaining buffer.
• Remove the top section of the spin column and place in a clean 1.5ml Eppendorf tube. Add 50µl of EB Buffer to the column; let it stand for 1 minute before centrifuging for a further 1 minute to elute the DNA.

Aim: to sequence our DNA in order to check content of our constructs

• Add 5µl of DNA sample at a concentration of 80-100ng/µl of Plasmid DNA (Diluting with sterile water if Plasmid DNA is at a concentration greater than 100ng/µl) to two separate 1.5 ml Eppendorf tubes.
• Add 5µl of primer 1 (Sense) to the first tube at a total concentration of 5µM (5pmol/µl) and 5µl of primer 2 (AntiSense) to the second tube (at a total concentration of 5µM (5pmol/µl)
• Send off both 10µl samples for sequencing.

PROTOCOL HERE

PROTOCOL HERE

The following antibiotic concentrations have been used for antibiotic selection throughout the project. Antibiotics have been added to agar plates and overnight cultures in order to select for bacteria carrying the desired plasmid.

Antibiotic	Use	Stock concentration	µL/ mL required
Chloramphenicol	PSB1C3 constructs	33mg/ml	1.5
Kanamycin	Level 0 constructs	30mg/ml	1
Carbenicillin	Level 1 constructs	100mg/ml	1
Ampicillin	Level 1 constructs	100 mg/ml	1
Spectinomycin	Level 2 constructs
Rifampicin	Agrobacterium tumefaciens	10mg/ml	5
Gentamicin	Agrobacterium tumefaciens	10mg/ml	2