Team:KU Leuven/Protocols

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Latest revision as of 03:58, 29 October 2013

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Protocols

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Index

Aphid population preference
Aphid mobility experiment
Chemically competent E.coli cells: CaCl2 method
Chemically competent E.coli cells: Inoue method
Colony PCR for Streptomyces
Digestion and ligation
DNA extraction from agarose gels
GC-MS analysis
Grow electrocompetent cells
Headspace GC

Isolation of plasmid DNA from E. coli (mini prep)
PCR clean-up
PCR Protocol for Taq DNA Polymerase
Plasmid DNA isolation
Predator attraction to MeS induced aphid infested plants
Predator attraction to Methyl Salicylate
Protein Extraction
qRT-PCR Protocol
Root measurements

Aim: To determine the effect on aphid population on Methyl Salicylate (MeS) induced plants.

Experimental setup: We induced five plants per concentration

Plants: Small potted paprika plants in two ways: via the root or byspraying; 60 in total. Paprika plants don’t make MeS naturally but do produce salicylic acid.
Concentration: 1ng/ml, 0,8ng/ml, 0,4ng/ml, 0.1ng/ml ,0.01ng/ml of MeS (Sigma-Aldrich, ReagentPlus®, ≥99% (GC)) in 97% pure ethanol or water.

Procedure

Induction requires 48h

Induction via the roots

Uproot the plant, clean off the dirt with water because compost can interfere with the uptake of MeS
Wipe off the water before placing the roots in a cup with the desired concentration for 10 minutes. MeSA was first suspended in ethanol before being further diluted to the desired concentration in 50ml water
Re-pot the plant and divide the remainder of the MeSA solution amongst the 5 plants

Induction via the leaf

The desired concentrations were diluted in 15ml ethanol, resulting in 3ml per plant. Ethanol has been shown to have no plant induction properties
Each leaf of the plant is sprayed above and underneath

Place aphids on MeS induced plants 48h post-induction

Place 15 green peach aphids on the head of each induced plant
Take the smallest aphids present on the aphid-infested leaf. To be sure that it is a first generation aphid
Place each plant in a separate net
Plants of the same concentration, induced by spraying or via the roots, are placed in the same row; 10 plants per row. The rows are roughly 1 metre apart

Counting aphids on day 7

Following a form, count how many aphids are on Cotyledon, separate true leafs and the head of the induced plants.
See <a href"> results</a>
There is a possibility of contamination while placing the aphids on the plant, meaning that older aphids and/or flying aphids crawled onto the plant by accident. These were removed from the plant so that the amount of aphids on day 10 would not be tainted

Counting aphids on day 10

We count the aphids for a second time to allow the second generation to develop. This way we investigate whether MeS has an effect on the aphid’s behaviour. That they are encouraged to leave the plant, reproduce less or generate mobile (flying) aphids.
The head of the plant is where the majority of the secondary metabolites gather; hence we expect to see an effect on the distribution of the aphid population.

Aim: To determine the effect of EBF on aphid mobility.

Experimental setup: Leaves infested with aphids were divided in two glass containers (not sealed) randomly (n=3; 3 leaves per group). After 1h plates with bacteria, either control (BL21) or BL21 with EBF construct, were put under each leaf.

Measurement: Aphids that were on the top of each leaf were counted at start and at each time point during the experiment.
At each time point the amount of aphids moving on the leaf were also counted. The time points used were 0, 50, 150 and 200 minutes.

Procedure

Perform every action on ice – also when resuspending your cells!
Do not shock freeze (liqN2) – just transfer from ice to -80°C!
Work sterile!

Inoculate 3 ml growth medium with your cells of choice (DH5alpha or TOP10 for plasmid maintenance & cloning)
Grow overnight at 37°C with sufficient aeration
Inoculate 100 ml LB with 1 ml of overnight culture
Grow at 37°C to an OD 600nm of approx 0.5 to 0.8 (usually 2-3 hrs)
Centrifuge cells (3700-4000 rpm 4°C 12 min – sterile 50ml tube)
Resuspend pellet on ice with FSB to 15 ml (cold) for each 100 ml pellet
Incubate cells 10 min on ice
Centrifuge cells (3700 – 4000 rpm 4°C 10 min)
Re-suspend pellet on ice in 4-8 ml FSB (cold) for each 100 ml pellet
Aliquot cells appropriately (200-400 µl aliquots) and freeze aliquots at -80°C

Buffers and solutions

Risk assessment for pH electrode and preparation of buffers

Growth medium
- LB 25 g/l
Frozen Storage Buffer (FSB)
- 10 mM Potassium Acetate
- 10% glycerol
- 10 mM KCl
- 50 mM CaCl2
- Check pH – must be around 6.2 – if need be adjust with AcAc (HCl) or KOH
- Buffer should be filter-sterilized (0.45 micrometer filter)

Procedure

Perform every action on ice – also when resuspending your cells.
Work sterile

Pick a single colony from a freshly transformed plate (after overnight growth at 37 °C)
Transfer the colony to 25 ml growth medium in a sterile 250 ml erlenmeyer
Incubate the culture at 37°C for 6 – 8 hrs under vigorous shaking (250 – 300 rpm)
Prepare 3 1L flasks with 250 ml growth medium in each
Inoculate the flasks with 10, 4 or 2 ml of the dayculture -> you create 3 different starting optical densities.
Incubate the cultures at 18-22°C overnight under moderate shaking (180 – 220 rpm)
Monitor the OD600nm until it reaches 0.55
Place cells in an ice-water bath to cool them down quickly (-> swirl occasionally, keep them in for approx 10 min)
Centrifuge cells at 4°C for 10 min at 2500 g
Pour off supernatant – make sure all remaining droplets are removed
Resuspend gently (swirl !) in 80 ml icecold inoue transformation buffer
Centrifuge cells at 4°C for 10 min at 2500 g
Pour off supernatant – make sure all remaining droplets are removed
Resuspend gently (swirl !) in 20 ml icecold inoue transformation buffer
Add 1.5 ml 100% DMSO – mix by swirling
Store whole on ice for approx 10 minutes
Aliquot as quickly as possible 100 – 200 µl aliquots into 1.5 ml tubes (precooled on ice) and snapfreeze them into a liquid N2 bath

Buffers and solutions

Growth medium
Inoue transformation buffer

Reagent	Final concentration (mM)	Amount per liter
MnCl2	55	10.88 g (from MnCl2*4H2O)
CaCl2	15	2.20 g (from CaCl2*2H2O)
KCl	250	18.65 g (from KCl)
PIPES	10	20 ml (from 0.5M stock solution)
H2O	to 1 liter

Filter sterilize with a 0.45 µm nalgene filter

Risk assessment for pH electrode and preparation of buffers

Stock 0.5 M PIPES (piperazine-1,2-bis[2-ethanesulfonic acid]) pH 6.7
- Dissolve 15.1 g PIPES in 80ml MilliQ H2O
- Adjust pH to 6.7 with 5M KOH
- Bring volume to 100 ml with MilliQ H2O
- Filter sterilize with a 0.45 µm nalgene filter
- Aliquot (5 times) and store at -20°C

Pretreatment of Streptomyces

Because of the fact that Streptomyces are Gram-positive bacteria with a thick peptidoglycan layer, we performed 4 ways to pretreat the cells for colony PCR (all pretreatments gave positive results in the end):

microwave Streptomyces for 4 mins
mix Streptomyces with water and 0.2% SDS, microwave for 4 mins
mix Streptomyces with 1% SDS, microwave for 4 mins
mix Streptomyces with TE buffer, 0.2% SDS, microwave for 4 mins

PCR mixture

Risk assessment for PCR

Components	Amount
2x fusion master mix (add in the end)	25 µl
forward primer (final conc. 0.5 µM)	1.25µl (of 20 µM stock)
reverse primer (final conc. 0.5 µM)	1.25µl (of 20 µM stock)
template DNA	1 µl
DMSO (recommended for high GC content)	1.5 µl
H2O (PCR certified, no contamination)	add to final volume of 50µl

Keep tubes on ice at all times!
Be sure to put Phusion Master Mix immediately back at -20!

Cycling instruction

Step	Temperature	Time
1	95°C	6'
2 cycle 29x	95°C 55°C 72°C	30" 30" 45"
3	72°C	10'
4	12°C	infinite/hold

Consumables and equipment

Restriction enzymes (EcoRI, Xbal, Spel, Pstl), NEBuffer 2.1
10x T4 DNA ligase Reaction Buffer, T4 DNA Ligase
Keep all enzymes on ice; make sure buffers have no precipitation
H20
Small PCR Tubes or eppendorfs
2 µl, 200 µl pipette tips
Destination plasmid as purified DNA
Upstream and downstream part as purified DNA
2 µl and 20 µl pipette
Heat block 37° and 80°C
Timer
Rack for small PCR tubes
-20°C freezer + freeze box

Digestion

Mark PCR tubes or eppendorfs

   a. U= upstream part : E + S restriction enzymes
   b. D= downstream part : X + P restriction enzymes
   c. P= plasmid (destination) : E + P restriction enzymes
   d. NB: if only one part for insertion insert I= Insert : E + P restriction enzymes

In each tube 500 ng DNA for digestion + H20 until total volume is 43 µl
Add 5 µl of NEBuffer 2.1 to each tube
Add 1 µl of first restriction enzyme
Add 1 µl of the second restriction enzyme TOTAL VOLUME = 50 µl
Mix well by flicking each tube
Incubate at 37°C for 20 min. (officially 15 min)
Incubate at 80°C for 20 min.

   a. OPTIONAL: run 10-20 µl on 1% agarose gel and look for expected bands as confirmation
   b. OPTIONAL: store at -20°C or proceed to ligation immediately

Ligation

Add 13 µl of H2O to a 200 µl PCR tube or eppendorf
Add 2 µl of each part you want to ligate
Add 2 µl of 10X T4 DNA Ligase Reaction Buffer to the tube
Add 1 µl of the T4 DNA Ligase to the tube TOTAL VOLUME = 20 µl
Mix well by flicking each tube
Incubate at room temperature for 10 min

   a. Incubate at 80°C for 20 min. 
   b. Store the ligation mix at -20°C or proceed immediately to the transformation step.

(source: NucleoSpin® Gel and PCR Clean-up - Macherey-Nagel)
Procedure

Excise DNA fragment/solubilize gel slice: take a clean scalpel to excise the DNA fragment from an agarose gel, remove all excess agarose. For each 100mg of agarose gel < 2% add 200µl buffer NTI, for gels containing > 2% agarose, double the volume of buffer NTI. Incubate sample for 5-10 min at 50°C, vortex the sample briefly every 2-3 min until the gel slice is completely dissolved.
Binding DNA: place a PCR clean-up column into a collection tube (2ml) and load up to 700µl sample, centrifuge for 30s at 11000g, discard flow-through and place the column back into the collection tube.
Wash silica membrane: add 700µl buffer NT3 to the column, centrifuge for 30s at 11000g, discard flow-through and place the column back into the collection tube. Repeat the washing again.
Dry silica membrane: centrifuge for 1min at 11000g to remove buffer NT3 completely. Make sure the spin column does not come in contact with the flow-through while removing it from the centrifuge and the collection tube.
Elute DNA: place the column into a new 1.5ml microcentrifuge tube, add 15-30µl buffer NE and incubate at room temperature for 1 min, centrifuge for 1 min at 11000g.

Aim: To detect the production of MeS by our E. coli.

Sample preparation:

At day 0: a preculture was grown at 37°C overnight (BL21 or BBa_K1060003)
The preculture was used to inoculate 500µl into 50ml of fresh LB medium supplemented with or without 0.1 mM salicylic acid and left to grow for overnight. Samples were induced with 0.2 mM IPTG 6 hours post inoculation.
Cultures were then chilled on ice and put at 4°C
Bacterial cells were removed by centrifugation (10’, 4000g, 4°C) and then filter sterilized (0.22µm).
2 ml of this filtersterilized supernatant was then extracted with 1 ml of hexane
Extractions were done in glass tubes with rigorous vortexing for 10 minutes
The upper phase was transferred to a new glass vial
The extraction was repeated twice (total of 3 extractions with 1 ml of hexane)
The resulting ± 3 ml of extract were then reduced by evaporation under a nitrogen flow and redissolved in 50 µl of hexane.

Gas chromatography: GC-MS analyses were carried out using a 7890A Agilent gas chromatograph coupled to a 5977A mass spectrometric detector. The GC was equiped with a HP-5MS capillary column (30m x 0.25 mm x 0.25 µm). 1 µl of each sample was injected using splitless injection at a temperature of 250 °C. The initial oven temperature of 40 °C was held for 1 min., ramped at 6 °C / min. to 124 °C, then ramped at 20 °C / min. to 320 °C and finally kept at this temperature for 5 min. The transfer line and ion source were held at 320 °C and 230 °C, respectively. Mass spectra were taken between masses m/z 30-300 with an ionization potential of 70 eV. Retention indices of standards were determined by co-injection of a C7-C30 n-alkane mixture (Supelco) and were compared with published retention indices.

(source: adapted from openwetware.org)

Materials

GYT (glycerol, yeast extract, tryptone)
- 10%(v/v) glycerol
- 0.125% (w/v) yeast extract
- 0.25% (w/v) tryptone

DI water
10% Glycerol

Special Equipment

Centrifuge
Ice water bath
Liquid nitrogen

Procedure

Important: All steps in this protocol should be carried out aseptically

Inoculate: Prepare flask containing 5 ml of LB medium. Pick up a single colony of cells from plate (using a sterile toothpick) and swirl around inside flask. Incubate the culture overnight at 37°C with vigorous aeration (250 pm in a rotary shaker).

Dilute and incubate: Inoculate two aliquots of 495 ml of prewarmed LB medium in separate 2-liter flasks with 5 ml of the overnight bacterial culture. Incubate the flasks at 37°C with agitation (300 cycles/min in a rotary shaker). Measure the OD-600 every twenty minutes (this step will take around 1.5-2 hrs). (or judge the OD by eyes to avoid always taking the sample to disturb the growth as well as avoiding the contamination)

Rapidly cool culture: Once the OD-600 of the culture reaches 0.6-1.0 (Molecular Cloning recommends 0.4), rapidly transfer the flasks to the pre-made ice-water bath for 15-30 minutes. Swirl the culture occasionally to ensure that cooling occurs evenly. In preparation for the next step, place the centrifuge bottles in the ice-water bath as well.

Note: After this point, do not let your cells warm up past 4°C always keep on ice

Note: When harvesting cells by decanting, be very careful not to disturb the pellet-- this could result in a much lower yield. If necessary, aspirate instead or decant the supernatant. Ask someone to show you how to aspirate. Also, if the pellet seems loose, sometimes it is helpful to re-spin the cells down.

Centrifuge 1: Transfer the cultures to ice-cold centrifuge bottles. Harvest the cells by centrifugation at 1000 g (2500 rpm) for 15 minutes at 4°C. Decant the supernantant and resuspend the cell pellet in 20 ml of ice-cold 10% glycerol. Note: this should be done for each of the two 500ml cultures, i.e this is a 1:1 resuspension rather than a concentration by a factor of 2 BC.

Centrifuge 2 (10% glycerol): Harvest the cells by centrifugation at 1000 g for 20 minutes at 4°C. Decant the supernatant and resuspend the cell pellet in 20 ml ice-cold 10% glycerol.

Centrifuge 3 (10% glycerol): Harvest the cells by centrifugation at 1000 g for 20 minutes at 4°C. Decant the supernatant and resuspend the cell pellet in 10 ml ice-cold 10% glycerol.

Centrifuge 4 (10% glycerol): Harvest the cells by centrifugation at 1000 g for 20 minutes at 4°C. Carefully decant the supernatant and use a Pasteur pipette attached to a vacuum line to remove any remaining drops of buffer.

Resuspend in GYT: Resuspend in 1 ml ice cold GYT. This is best done by gently swirling rather pipetting or vortexing.

Test for arcing: Transfer 40 µl of the suspension to an ice-cold electroporation cuvette and test whether arcing occurs when an electrical discharge is applied. Place the cuvette in the holder attached to the machine. Go to option 4, Pre-set protocols; choose bacterial; choose the correct choice for your size cuvette, probably the first option for a .1 cm cuvette. If arcing occurs, wash the remainder of the cell suspension once more with ice-cold GYT medium to ensure that the conductivity of the bacterial suspension is sufficiently low (<5 mEq). (or check the pulse time, if the pulse time < 4, redo the wash, if the pulse time > 4, it's ok)

Storage: Store cells at -80°C until they are required for use. For storage, dispense 40 µl aliquots of the cell suspension into sterile, ice-cold .5 ml microcentrifuge tubes, drop into a bath of liquid nitrogen and transfer to a -80°C freezer. To remove the tubes from the liquid nitrogen bath, bring out into the hall along with a storage box, and pour the tubes and liquid nitrogen into the box. Once all the tubes are out, close the box most of the way and let the liquid run out into the hallway. Try not to do this in the very center of the walkway!

To use frozen cells: Remove an appropriate number of aliquots of cells from the -80°C freezer. Thaw the tubes on ice.

Aim: To detect the production of MeS by our E. coli.

Sample preparation:

At day 0: a preculture was grown at 37°C overnight (BL21 or BBa_K1060003)
The preculture was used to inoculate 500µl into 50ml of fresh LB medium supplemented with 0 or 0.1 mM of salicylic acid and left to grow for 7 hours.
Cultures were chilled on ice and put at 4°C
Bacterial cells were removed by centrifugation (10’, 4000g, 4°C) and then filterstelized (0.22µm).
Salt was added to 5 ml of this filtersterilized supernatant

Gass chromatography: Samples were analyzed with a calibrated Autosystem XL gas chromatograph with a headspace sampler (HS40; Perkin-Elmer, Wellesley, Mass.) and equipped with a CP-Wax 52 CB column (length, 50 m; internal diameter, 0.32 mm; layer thickness, 1.2 μm; Chrompack; Varian, Palo Alto, Calif.). Samples were heated for 16 min at 72°C in the headspace autosampler. The injection block and flame ionization detector (FID) temperatures were kept constant at 180 and 250°C, respectively; helium was used as the carrier gas. The oven temperature was 75°C held for 6 min and then increased to 110°C at 25°C min−1 and held at 100°C for 3.5 min. Results were analyzed with Perkin-Elmer Turbochrom Navigator software.

(source: NucleoSpin® plasmid - Macherey-Nagel)

Nanodrop protocol

Nanodrop can be used to measure the DNA, RNA and protein Measure the concentration and purity of extracted DNA using absorbance (using the automated nanodrop machine!)

Method:

Log onto computer and select Nanodrop program from the desktop (ND 1000)
To clean Nanodrop machine wipe pedestal and top and add 3 µl of water to nib of pedestal. Press blank.
Wipe the water off, to initialize/equalize the equipment add 3 μl of the elution buffer [EB] used in the sample and press blank. Set to DNA-50 for DNA.
Wipe to remove buffer and apply 3 μl of sample to nib. Press measure.
If dealing with multiple samples, clean the equipment with water at regular intervals (about every 10 samples).
After measurements, clean the equipment with 3 μl of water on the spectrometer and press blank. Wipe and log off.

(source: NucleoSpin® Gel and PCR Clean-up - Macherey-Nagel)

This is used for PCR clean-up as well as DNA concentration and removal of salts, enzymes, etc. from enzymatic reactions (SDS<0.1%)

Adjust DNA binding condition: mix 1 volume of sample with 2 volumes of buffer NTI (eg. mix 100 µl PCR reaction and 200 µl buffer NTI).
Binding DNA: place a PCR clean-up column into a collection tube (2 ml) and load up to 700 µl sample, centrifuge for 30 s at 11000 g, discard flow-through and place the column back into the collection tube.
Wash silica membrane: add 600µl buffer NT3 to the column, centrifuge for 30 s at 11000 g, discard flow-through and place the column back into the collection tube. Repeat the washing again.
Dry silica membrane: centrifuge for 1 min at 11000 g to remove buffer NT3 completely. Make sure the spin column does not come in contact with the flow-through while removing it from the centrifuge and the collection tube.
Elute DNA: place the column into a new 1.5 ml microcentrifuge tube, add 50 µl buffer NE and incubate at room temperature for 1 min, centrifuge for 1 min at 11000 g.

Reaction set up

Risk assessment for PCR
We recommend assembling all reaction components on ice and quickly transferring the reactions to a thermocycler preheated to the denaturation temperature (95°C).

Components	25 μl reaction	50 μl reaction	Final concentration
10X Standard Taq Reaction Buffer	2.5 µl	5 µl	1X
10 mM dNTPs	0.5 µl	1 µl	200 µM
10 µM Forward Primer	0.5 µl	1 µl	0.2 µM (0.05–1 µM)
10 µM Reverse Primer	0.5 µl	1 µl	0.2 µM (0.05–1 µM)
template DNA	variable	variable	<1,000 ng
Taq DNA Polymerase	0.125 µl	0.25 µl	1.25 units/50 µl PCR
Nuclease-free water	to 25 µl	to 50 µl

Notes: Gently mix the reaction. Collect all liquid to the bottom of the tube by a quick spin if necessary. Overlay the sample with mineral oil if using a PCR machine without a heated lid. Transfer PCR tubes from ice to a PCR machine with the block preheated to 95°C and begin thermocycling.

Thermocyclingconditions for a routine PCR

Step	Temperature	Time
Initial denaturation	95°C	30"
30 cycles	95°C 48-65°C 68°C	15-30" 15-60" 1min/kb
Final extension	68°C	5'
Hold	12°C	infinite/hold

Procedure

Risk assessment for plasmid DNA purification kit

Bring 1.5 ml culture in an eppendorf, centrifuge for 1 min with maximum speed
Pour away the supernatant
Bring another 1.5 ml culture into the same eppendorf, centrifuge for 1 min and pour away supernatant
Resuspend the pellet with 200µl GTE-solution we made earlier
Add 4 µl RNase A (10mg/ml)
Add 400 µl premade solution (contains 0.2M NaOH and 1%SDS in sterile water)
Mix them well, place on ice for 5 min
Add 300 µl ice cold 7.5 M ammonium acetate, vortex for 10 s, place on ice for 5 mins
Centrifuge for 5min with 13000 rpm
Bring the supernatant into a new eppendorf
Centrifuge this supernatant for a second time (5 min, 13000 rpm) and bring the supernatant in a new eppendorf
Add isopropanol to the supernatant (60% in volume of the supernatant), leave at room temp. for 5 min
Centrifuge for 10 min with 13000 rpm, immediately remove the supernatant, keep the transparent pellet in the tube, put the tube upside down on a tissue to dry it
Add 1 ml of cold 70% ethanol to the pellet, invert 5 times
Centrifuge 3 min with 13000 rpm
Remove supernatant, the droplet on the tube wall can be removed by tissue
Let the pellet dry
Add 50 µl elution buffer (or sterile water) to the pellet

Buffers and Solutions

GTE-buffer
- 50 mM glucose
- 25 mM Tris-Cl (pH 8.0)
- 10 mM EDTA
- 4 mg/ml lysozyme

IPTG stock solution
- 238 mg in 10 ml AD
- Filter sterilize
- Split into 1 ml aliquots
- Store in -20 freezer

Final concentration/work concentration in agar plates = 0.1mM – 1 mM
Sigma recommends 0.2 mM for blue-white screening
Thermo Scientific recommends 0.1 mM

Aim: To determine the effect on aphid predators’ attraction to Methyl Salicylate (MeS) induced plants.

Experimental setup: We continue with the same plants used in the experiments to determine aphid population preference (see above), this way we try to create an as close as possible in vivo situation. The predators were subjected to choice experiment - cafetaria model.

Predators: Macrolophus adults
Plants: Small potted MeS induced paprika plants in two ways: via the root or via the leaf, 60 in total.
Concentration: 1ng/ml, 0,8ng/ml, 0,4ng/ml, 0.1ng/ml, 0.01ng/ml of MeS (Sigma-Aldrich, ReagentPlus®, ≥99% (GC)).

Cafetaria model

In the cafeteria model shown above, each concentration will be placed, plus the control, randomly in a circle. The plants should not be close to the edge of the cage in which the experiments are carried out. The plants should be placed in rotation with every repeat of the set-up to eliminate other factors.

Releasing the Macrolophus:

10 Macrolophus (adult) are shaken out of the pot and placed in the middle of the cafetaria model (see picture)
We release around 50 Macrolophus (adult) per set-up

Counting the Macrolophus:

After every 45 min from the moment we released the Macrolophus, the amount per plant is counted and recorded
The Macrolophus are then shaken off the plant back into the middle of the circle so that they can make their choice again
We will take 3 recordings

Aim: To determine a working concentration of methyl salicylate (MeS) concentration which attracts predators .

Experimental setup: We continue with the same plants used in the experiments to determine aphid population preference (see above), this way we try to create an as close as possible in vivo situation. The predators were subjected to choice experiment - cafetaria model.

Predators: Adalia bipunctata (ladybugs): adult and larvae
Concentration: 1000ng/ml, 100ng/ml, 10ng/ml, 1ng/ml, 0.1ng/ml, 0.01ng/ml of MeS (Sigma-Aldrich, ReagentPlus®, ≥99% (GC)) in 96% ethanol.

Biobest setup

The predators were subjected to a choice experiment between one of the MeS concentrations and a control (pure EtOH).
We repeated each dilution three times with different ladybugs.
After using the ladybugs, we collected them in a different tube and didn’t use them again.
These experiments were performed in a chemical safety cabinet to prevent the distribution of MeS in the air.

pcfruit setup

The predators were subjected to a choice experiment between one of the MeS concentrations and a control (pure hexane or paraffin oil).
We repeated each dilution three times with different ladybugs.
After using the ladybugs, we collected them in a different tube and didn’t use them again.
These experiments were performed in a chemical safety cabinet to prevent the distribution of MeS in the air.

Aim: To extract proteins from our E. coli for SDS-PAGE analysis.

Sample preparation:

E.coli cells transformed with the indicated plasmids were grown either to mid-exponential phase (OD600nm ~ 1.0 for endpoint assays) or to the indicated optical densities.
Samples were taken and spun down (3min, 4000 rpm, 4°C).
Growth medium was removed and cell pellets frozen (-80 °C)
Cell pellets were thawed on ice and resupended in equal volumes extraction buffer.
Suspensions were incubated on ice for 10min and subsequently sonicated (3X 10” pulses) with ice cooling in between.
Suspensions were spun down (10min, 14000 rpm, 4°C).
Aliquots were mixed with 5X sample buffer and boiled (5min 95°C).
Samples were loaded on precast SDS-PAGE systems (Biorad) according to the manufacturer's instructions.

Extraction buffer :

25mM Tris pH 8.0; 0.1%(v/v) NP40; 5 mM EDTA; 50 mM NaCl; protease inhibitor cocktail (Benzamidine; PMSF; Leupeptin).

General experiment: 3 biological repeats of stationary phase cultures 16 hrs growth.

Sample preparation

Inoculate fresh LB plate with the strain harbouring the MS brick
Isolate plasmid DNA, MS brick
Nanodrop plasmid (minimum concentration 20 ng/µl) = 155 ng/µl
Design primers for pcha/pchb and for bsmt1 using Primer express. Primer sequence can be found in document “Genes_qPCR_primers_IC.docx”.
Inoculate E. Coli with Methylsalicylate brick (MIT 2006) on LB plate.
Add 5 µl of Kanamicin (50 mg/ml) and 10 µl of IPTG (100 mM) to 5 ml of LB medium (tubes).
Incubate 16h at 37 °C under shaking conditions.
Measure OD of 3 cultures.
Account for differences in OD: ex. If you have an OD of 1 take 1 ml of this sample, if you have an OD of 0,8 take 1,2 ml.
Add 1/5 volume of stopsolution (95% ethanol, 5% phenol).
Freeze 5 minutes in liquid Nitrogen.
Centrifuge needed amount of cells.

mRNA isolation

For mRNA isolation use the Promega SV total RNA isolation kit ([http://be.promega.com/resources/protocols/technical-manuals/0/sv-total-rna-isolation-system-protocol/?origUrl=http%3a%2f%2fwww.promega.com%2fresources%2fprotocols%2ftechnical-manuals%2f0%2fsv-total-rna-isolation-system-protocol%2f Promega SV total RNA isolation protocol])

Section 8.C (Isolation of RNA from Gram-positive and Gram-negative bacteria)
Section 4.E (RNA Purification by Centrifugation) We did not do step 4 and 5 (addition of DNase) but instead used the DNase protocol of [http://products.invitrogen.com/ivgn/product/AM2238 Ambion Turbo DNase]

For 100 µl of RNA:

1. Add 10 µl 10x buffer. Add 1 µl Turbo DNase and mix gently.
2. Put on 37 °C for 20 to 30 min.
3. Add 1 µl of Turbo DNase.
4. Put on 37 °C for 20 to 30 min.
5. Add 20 µl of DNase inactivation reagent and mix well.
6. Put on room temperature for 5 min. Mix occasionally by flicking the tube
7. Centrifuge on 10000 g for 2 min.
8. Transfer the RNA to a new tube.

Create cDNA

Use the Fermentas Revert aid H kit ([http://www.thermoscientificbio.com/reverse-transcription-rtpcr-rtqpcr/revertaid-h-minus-first-strand-cdna-synthesis-kit/ Fermentas Revert aid H protocol]) The protocol for RT-PCR (I. First Strand Synthesis) was followed

qPCR

qPCR kit was not yet decided.

Aim: To determine whether the different induction methods or the Methyl Salicylate (MeS) had an effect on plant growth.

Experimental setup: We measured the roots of the same plants used in the experiments to determine aphid population and predator preference (see above).

The plants were cut off at the bottom of the stem and removed from the pot.
After most of the dirt has been removed, they were carefully washed to remove the rest of the dirt.
After using the ladybugs, we collected them in a different tube and didn’t use them again.
The roots were then dried and weighed.

The roots were then measured and recorded.

Team:KU Leuven/Protocols

From 2013.igem.org

Latest revision as of 03:58, 29 October 2013

Secret garden

Journals

Protocols

Safety

Index

Aphid population preference

Aphid mobility experiment

Chemically competent E.coli cells: CaCl2 method

Chemically competent E.coli cells: Inoue method

Colony PCR for Streptomyces

Digestion and ligation

DNA extraction from agarose gels

GC-MS analysis

Grow electrocompetent cells

Headspace GC

Isolation of plasmid DNA from E. coli (mini prep)

PCR clean-up

PCR protocol for Taq DNA polymerase with standard Taq Buffer

Plasmid DNA isolation

Predator attraction to MeS induced aphid infested plants

Predator attraction to methyl salicylate

Protein Extraction

qRT-PCR protocol

Root measurements

@@ Line 1: / Line 1: @@
 {{:Team:KU Leuven/Template:Header}}
+{{:Team:KU Leuven/Template:Style}}
 {{:Team:KU Leuven/Template:Menu}}
+<html>
+<body>
+<div id="container">
+<div class="container">
+<!--LOGOS-->
+<div class="row-fluid">
+ <div class="span4 icon white">
+  <div class="row-fluid">
+   <div class="visible-desktop span3 bg-grey1">
+    <a href="https://2013.igem.org/Team:KU_Leuven/Journal" title="Team:KU_leuven">
+    <i class="livicon activeicon" data-name="calendar" data-color="white"></i></div>
+   <div class="span7 icon-text">
+    <h3>Journals</h3>
+    </a>
+     <p>Follow our activities week-by-week</p>
+   </div>
+  </div>
+ </div>
+ <div class="span4 icon white">
+  <div class="row-fluid">
+   <div class="visible-desktop span3 bg-yellow">
+    <a href="https://2013.igem.org/Team:KU_Leuven/Protocols">
+    <i class="livicon activeicon" data-name="magic" data-color="white"></i></div>
+   <div class="span7 icon-text">
+    <h3>Protocols</h3> </a>
+     <p>You are here!</p>
+   </div>
+  </div>
+ </div>
+ <div class="span4 icon white">
+  <div class="row-fluid">
+   <div class="visible-desktop span3 bg-grey1">
+    <a href="https://2013.igem.org/Team:KU_Leuven/Safety">
+     <i class="livicon activeicon" data-name="biohazard" data-color="white"></i>
+    </div>
+   <div class="span7 icon-text">
+    <h3>Safety</h3>
+    </a>
+     <p>Be careful!</p>
+   </div>
+  </div>
+ </div>
+</div>
+<div class="row-fluid">
+ <div class="span12 white">
+  <h3>Index</h3>
+  <div class="row-fluid">
+   <div class="span6 greytext">
+    <a href="#Aphid population preference">Aphid population preference</a><br>
+    <a href="#Aphid mobility experiment">Aphid mobility experiment</a><br>
+    <a href="#Chemically competent E.coli cells: CaCl2 method">Chemically competent E.coli cells: CaCl2 method</a><br>
+<a href="#Chemically competent E.coli cells: Inoue method">Chemically competent E.coli cells: Inoue method</a><br>
+<a href="#Colony PCR for Streptomyces">Colony PCR for Streptomyces</a><br>
+<a href="#Digestion and ligation">Digestion and ligation</a><br>
+<a href="#DNA extraction from agarose gels">DNA extraction from agarose gels</a><br>
+<a href="#GC-MS analysis">GC-MS analysis</a><br>
+<a href="#Grow electrocompetent cells">Grow electrocompetent cells</a><br>
+<a href="#Headspace GC">Headspace GC</a><br>
+   </div>
+   <div class="span6 greytext">
+    <a href="#Isolation of plasmid DNA from E. coli (mini prep)">Isolation of plasmid DNA from E. coli (mini prep)</a><br>
+    <a href="#PCR clean-up">PCR clean-up</a><br>
+    <a href="#PCR Protocol for Taq DNA Polymerase with Standard Taq Buffer">PCR Protocol for Taq DNA Polymerase</a><br>
+    <a href="#Plasmid DNA isolation">Plasmid DNA isolation</a><br>
+    <a href="#Predator attraction to MeS induced aphid infested plants">Predator attraction to MeS induced aphid infested plants</a><br>
+    <a href="#Predator attraction to Methyl Salicylate">Predator attraction to Methyl Salicylate</a><br>
+    <a href="#Protein Extraction">Protein Extraction</a><br>
+    <a href="#qRT-PCR Protocol">qRT-PCR Protocol</a><br>
+    <a href="#Root measurements">Root measurements</a><br>
+   </div>
+  </div>
+ </div>
+</div>
+</div>
+</div>
+</body>
+</html>
+<!-- TITLE -->
+<html>
+<div id="header" class="row-fluid">
+ <div class="span12">
+<a id="Aphid population preference"> </a>
+  <h3 class="bg-yellow">Aphid population preference</h3>
+ </div>
+</div>
+</html>
+<b>Aim</b>: To   determine   the   effect   on   aphid   population   on   Methyl Salicylate (MeS) induced plants.
+<br/> <br/>
+Experimental setup: We induced five plants per concentration
+*Plants: Small potted paprika plants in two ways: via the root or byspraying;   60   in   total.   Paprika   plants   don’t   make   MeS naturally but do produce salicylic acid.
+*Concentration: 1ng/ml, 0,8ng/ml, 0,4ng/ml, 0.1ng/ml ,0.01ng/ml  of   MeS   (Sigma-Aldrich, ReagentPlus®, ≥99% (GC)) in 97% pure ethanol or water.
+<br>
+<b>Procedure</b>
+Induction requires 48h
+*Induction via the roots
+#Uproot the plant, clean off the dirt with water because compost can interfere with the uptake of MeS
+#Wipe off the water before placing the roots in a cup with the desired concentration for 10 minutes. MeSA was first suspended in ethanol before being further diluted to the desired concentration in 50ml water
+#Re-pot the plant and divide the remainder of the MeSA solution amongst the 5 plants
+[[File:Rootinduction.png|200px|Root induction]]
+*Induction via the leaf
+#The desired concentrations were diluted in 15ml ethanol, resulting in 3ml per plant. Ethanol has been shown to have no plant induction properties
+#Each leaf of the plant is sprayed above and underneath
+[[File:Leafinduction.png|200px|Leaf induction]]
+<br/>
+*Place aphids on MeS induced plants 48h post-induction
+#Place 15 green peach aphids on the head of each induced plant
+#Take the smallest aphids present on the aphid-infested leaf. To be sure that it is a first generation aphid
+#Place each plant in a separate net
+#Plants of the same concentration, induced by spraying or via the roots, are placed in the same row; 10 plants per row. The rows are roughly 1 metre apart
+* Counting aphids on day 7
+#Following a form, count how many aphids are on Cotyledon, separate true leafs and the head of the induced plants.
+#See <a href"> results</a>
+#There is a possibility of contamination while placing the aphids on the plant, meaning that older aphids and/or flying aphids crawled onto the plant by accident. These were removed from the plant so that the amount of aphids on day 10 would not be tainted
+[[File:Howtocountaphids.png|300px|How to count aphids]]
+* Counting aphids on day 10
+#We count the aphids for a second time to allow the second generation to develop. This way we investigate whether MeS has an effect on the aphid’s behaviour. That they are encouraged to leave the plant, reproduce less or generate mobile (flying) aphids.
+#The head of the plant is where the majority of the secondary metabolites gather; hence we expect to see an effect on the distribution of the aphid population.
+<br/>
+<!-- TITLE -->
+<html>
+<div id="header" class="row-fluid">
+ <div class="span12">
+<a id="Aphid mobility experiment"> </a>
+  <h3 class="bg-yellow">Aphid mobility experiment</h3>
+ </div>
+</div>
+</html>
+<br/><b>Aim</b>: To determine the effect of EBF on aphid mobility.
+<br/> <br/>
+<b>Experimental setup</b>: Leaves infested with aphids were divided in two glass containers (not sealed) randomly (n=3; 3 leaves per group). After 1h plates with bacteria, either control (BL21) or BL21 with EBF construct, were put under each leaf.
+<br>
+<b>Measurement</b>: Aphids that were on the top of each leaf were counted at start and at each time point during the experiment.<br/>
+At each time point the amount of aphids moving on the leaf were also counted. The time points used were 0, 50, 150 and 200 minutes.
+<!-- TITLE -->
+<html>
+<div id="header" class="row-fluid">
+<a id="Chemically competent E.coli cells: CaCl2 method"> </a>
+ <div class="span12">
+  <h3 class="bg-yellow">Chemically competent <i>E.coli</i> cells: CaCl2 method</h3>
+ </div>
+</div>
+</html>
-== Chemically competent E.coli cells: CaCl2 method ==
+<b>Procedure</b>
-=== Procedure ===
 '''Perform every action on ice – also when resuspending your cells!''' <br\>
 '''Do not shock freeze (liqN2) – just transfer from ice to -80°C!''' <br\>
@@ Line 15: / Line 186: @@
 #Inoculate '''100 ml LB''' with '''1 ml''' of overnight culture
 #Grow at '''37°C''' to an OD 600nm of approx '''0.5 to 0.8''' (usually '''2-3 hrs''')
-#Centrifuge cells ('''3700-4000 rpm 4°C 12min''' – sterile 50ml tube)
+#Centrifuge cells ('''3700-4000 rpm 4°C 12 min''' – sterile 50ml tube)
 #Resuspend pellet on ice with FSB to '''15 ml''' (cold) for each '''100 ml''' pellet
 #Incubate cells '''10 min''' on ice
-#Centrifuge cells ('''3700 – 4000 rpm 4°C 10min''')
+#Centrifuge cells ('''3700 – 4000 rpm 4°C 10 min''')
 #Re-suspend pellet on ice in '''4-8 ml''' FSB (cold) for each '''100 ml pellet'''
 #Aliquot cells appropriately ('''200-400 µl aliquots''') and freeze aliquots at '''-80°C'''
+<br>
+<b>Buffers and solutions</b>
-=== Buffers and solutions ===
 [https://static.igem.org/mediawiki/2013/1/1b/Risk_assessment_use_of_pH_electrode_and_preparation_of_buffers_KULeuven.pdf Risk assessment for pH electrode and preparation of buffers]
 *Growth medium
-**LB 25g/l
+**LB 25 g/l
 *Frozen Storage Buffer (FSB)
 **10 mM Potassium Acetate
 **10% glycerol
-**10 mMKCl
+**10 mM KCl
 **50 mM CaCl2
 **Check pH – must be around 6.2 – if need be adjust with AcAc (HCl) or KOH
@@ Line 35: / Line 207: @@
 <br/>
-----
+<!-- TITLE -->
+<html>
+<body>
+<div id="header" class="row-fluid">
+<a id="Chemically competent E.coli cells: Inoue method"> </a>
+ <div class="span12">
+  <h3 class="bg-yellow">Chemically competent <i>E.coli</i> cells: Inoue method</h3>
+ </div>
+</div></body>
+</html>
-== Chemically competent E.coli cells: Inoue method ==
+<b>Procedure</b>
-=== Procedure ===
 '''Perform every action on ice – also when resuspending your cells.'''<br/>
 '''Work sterile'''<br/>
-#Pick a single colony from a freshly transformed plate (after overnight growth '''@ 37 °C''')
+#Pick a single colony from a freshly transformed plate (after overnight growth '''at 37 °C''')
 #Transfer the colony to '''25 ml growth medium''' in a sterile '''250 ml''' erlenmeyer
-#Incubate the culture '''@ 37°C''' for '''6 – 8 hrs''' under vigourous shaking ('''250 – 300 rpm''')
+#Incubate the culture '''at 37°C''' for '''6 – 8 hrs''' under vigorous shaking ('''250 – 300 rpm''')
 #Prepare '''3 1L flasks''' with '''250 ml growth medium''' in each
 #Inoculate the flasks with 10, 4 or  2 ml of the dayculture -> you create 3 different starting optical densities.
-#Incubate the cultures @ '''18-22°C overnight''' under moderate shaking ('''180 – 220 rpm''')
+#Incubate the cultures at '''18-22°C overnight''' under moderate shaking ('''180 – 220 rpm''')
 #Monitor the '''OD600nm''' until it reaches '''0.55'''
-#Place cells in an ice-water bath to cool them down quickly (-> swirl occasionally, keep them in for approx 10min)
+#Place cells in an ice-water bath to cool them down quickly (-> swirl occasionally, keep them in for approx 10 min)
-#Centrifuge cells '''@4°C for 10min at 2500g'''
+#Centrifuge cells '''at 4°C for 10 min at 2500 g'''
 #Pour off supernatant – make sure all remaining droplets are removed
 #Resuspend gently (swirl !) in '''80 ml icecold inoue transformation buffer'''
-#Centrifuge cells '''@4°C for 10min at 2500g'''
+#Centrifuge cells '''at 4°C for 10 min at 2500 g'''
 #Pour off supernatant – make sure all remaining droplets are removed
-#Resuspend gently (swirl !) in '''20 ml icecold inoue transformation buffe'''r
+#Resuspend gently (swirl !) in '''20 ml icecold inoue transformation buffer'''
 #Add '''1.5 ml 100% DMSO''' – mix by swirling
 #Store whole on ice for approx '''10 minutes'''
-#Aliquot as quickly as possible '''100 – 200 microliter aliquots''' into '''1.5 ml tubes''' (precooled on ice) and snapfreeze them into a liquid N2 bath
+#Aliquot as quickly as possible '''100 – 200 µl aliquots''' into '''1.5 ml tubes''' (precooled on ice) and snapfreeze them into a liquid N2 bath
+<b>Buffers and solutions</b>
-=== Buffers and solutions ===
 *Growth medium
 *Inoue transformation buffer
@@ Line 66: / Line 247: @@
 | '''Reagent''' || '''Final concentration (mM)'''  || '''Amount per liter'''
 |-
-| MnCl2  || 55  || 10.88g (from MnCl2*4H2O)
+| MnCl2  || 55  || 10.88 g (from MnCl2*4H2O)
 |-
-| CaCl2 || 15  ||  2.20g (from CaCl2*2H2O)
+| CaCl2 || 15  ||  2.20 g (from CaCl2*2H2O)
 |-
-| KCl || 250  ||  18.65g (from KCl)
+| KCl || 250  ||  18.65 g (from KCl)
 |-
-| PIPES || 10  ||  20ml (from 0.5M stock solution)
+| PIPES || 10  ||  20 ml (from 0.5M stock solution)
 |-
 | H2O || to 1 liter  ||
 |}
-Filter sterilize with a 0.45 µmeter nalgene filter
+Filter sterilize with a 0.45 µm nalgene filter
 [https://static.igem.org/mediawiki/2013/1/1b/Risk_assessment_use_of_pH_electrode_and_preparation_of_buffers_KULeuven.pdf Risk assessment for pH electrode and preparation of buffers]
-*Stock 0.5M PIPES (piperazine-1,2-bis[2-ethanesulfonic acid]) pH 6.7
+*Stock 0.5 M PIPES (piperazine-1,2-bis[2-ethanesulfonic acid]) pH 6.7
-**Dissolve 15.1g PIPES in 80ml MilliQ H2O
+**Dissolve 15.1 g PIPES in 80ml MilliQ H2O
 **Adjust pH to 6.7 with 5M KOH
 **Bring volume to 100 ml with MilliQ H2O
-**Filter sterilize with a 0.45 µmeter nalgene filter
+**Filter sterilize with a 0.45 µm nalgene filter
 **Aliquot (5 times) and store at -20°C
 <br/>
-----
-== Plasmid DNA isolation ==
+<!-- TITLE -->
+<html>
+<body>
+<div id="header" class="row-fluid">
+ <div class="span12">
+  <a id="Colony PCR for Streptomyces"> </a>
+  <h3 class="bg-yellow">Colony PCR for <i>Streptomyces</i></h3>
+ </div>
+</div>
+</body>
+</html>
-=== Procedure ===
+<b>Pretreatment of ''Streptomyces''</b>
-[https://static.igem.org/mediawiki/2013/8/8f/Risk_assessment_Plasmid_DNA_Purification_kit_KULeuven.pdf Risk assessment for plasmid DNA purification kit]
-#Bring '''1.5 ml culture''' in an eppendorf, centrifuge for '''1 min with maximum speed'''
-#Pour away the supernatant
-#Bring another '''1.5 ml culture''' into the same eppendorf, centrifuge for '''1 min''' and pour away supernatant
-#Resuspend the pellet with '''200µl GTE-solution''' we made earlier
-#Add '''4µl RNase A (10mg/ml)'''
-#Add '''400µl premade solution''' (contains 0.2M NaOH and 1%SDS in sterile water)
-#Mix them well, place on ice for '''5 min'''
-#Add '''300µl ice cold 7.5 M ammonium acetate''', vortex for 10s, place on ice for '''5 mins'''
-#Centrifuge for '''5min with 13000 rpm'''
-#Bring the supernatant into a new eppendorf
-#Centrifuge this supernatant for a second time ('''5min, 13000rpm''') and bring the supernatant in a new eppendorf
-#Add isopropanol to the supernatant (60% in volume of the supernatant), leave '''@ room temp. for 5 min'''
-#Centrifuge for '''10 min with 13000 rpm''', immediately remove the supernatant, keep the transparent pellet in the tube, put the tube upside down on a tissue to dry it
-#Add '''1 ml of cold 70% ethanol''' to the pellet, invert 5 times
-#Centrifuge '''3 min with 13000 rpm'''
-#Remove supernatant, the droplet on the tube wall can be removed by tissue
-#Let the pellet dry
-#Add '''50 µl elution buffer''' (or sterile water) to the pellet
-=== Buffer and solution ===
+Because of the fact that ''Streptomyces'' are Gram-positive bacteria with a thick peptidoglycan layer, we performed 4 ways to pretreat the cells for colony PCR (all pretreatments gave positive results in the end):
-*GTE-buffer
+*microwave ''Streptomyces'' for 4 mins
-**50 mM glucose
+*mix ''Streptomyces'' with water and 0.2% SDS, microwave for 4 mins
-**25 mM Tris-Cl (pH 8.0)
+*mix ''Streptomyces'' with 1% SDS, microwave for 4 mins
-**10 mM EDTA
+*mix ''Streptomyces'' with TE buffer, 0.2% SDS, microwave for 4 mins
-**4 mg/ml lysozyme
+<br>
+<b>PCR mixture</b>
-*IPTG stock solution
-**238 mg in 10 ml AD
-**Filter sterilize
-**Split into 1 ml aliquots
-**Store in -20 freezer
-Final concentration/work concentration in agar plates = 0.1mM – 1 mM <br/>
-Sigma recommends 0.2mM for blue-white screening <br/>
-Thermo Scientific recommends 0.1mM
-<br/>
-----
-== Colony PCR for Streptomyces ==
-=== Pretreatment of Streptomyces ===
-Because of the fact that Streptomyces is gram negative bacteria, we performed 4 ways to extract its genome:
-*microwave Streptomyces for 4 mins
-*mix Streptomyces with water and 0.2% SDS, 4 min microwave
-*mix streptomyces with 1% SDS, 4 min microwave
-*mix streptomyces with TE buffer, 0.2% SDS, 4 min microwave
-=== PCR mixture ===
 [https://static.igem.org/mediawiki/2013/7/7b/Risk_assessment_PCR_KULeuven.pdf Risk assessment for PCR]
 {| class="wikitable"
 | '''Components''' || '''Amount'''
 |-
-| 2x fusion master mix (add in the end)  || 25µl
+| 2x fusion master mix (add in the end)  || 25 µl
 |-
-| forward primer (final conc. 0.5µM) || 1.25µl (of 20µM stock)
+| forward primer (final conc. 0.5 µM) || 1.25µl (of 20 µM stock)
 |-
-| reverse primer (final conc. 0.5µM) || 1.25µl (of 20µM stock)
+| reverse primer (final conc. 0.5 µM) || 1.25µl (of 20 µM stock)
 |-
-| template DNA || 1µl
+| template DNA || 1 µl
 |-
-| DMSO (recommended for high GC content) || 1.5µl
+| DMSO (recommended for high GC content) || 1.5 µl
 |-
 | H2O (PCR certified, no contamination) || add to final volume of 50µl
@@ Line 161: / Line 310: @@
 '''Be sure to put Phusion Master Mix immediately back at -20!'''
-=== Cycling instruction ===
+<b>Cycling instruction</b>
 {| class="wikitable"
 | '''Step''' || '''Temperature''' || '''Time'''
@@ Line 175: / Line 324: @@
 <br/>
-----
+<!-- TITLE -->
+<html>
+<div id="header" class="row-fluid">
+<a id="Digestion and ligation"> </a>
+ <div class="span12">
+  <h3 class="bg-yellow">Digestion and ligation</h3>
+ </div>
+</div></html>
+<b>Consumables and equipment</b>
-== PCR Protocol for Taq DNA Polymerase with Standard Taq Buffer ==
+* Restriction enzymes (EcoRI, Xbal, Spel, Pstl), NEBuffer 2.1
+* 10x T4 DNA ligase Reaction Buffer, T4 DNA Ligase
+* Keep all enzymes on ice; make sure buffers have no precipitation
+* H20
+* Small PCR Tubes or eppendorfs
+* 2 µl, 200 µl pipette tips
+* Destination plasmid as purified DNA
+* Upstream and downstream part as purified DNA
+* 2 µl and 20 µl pipette
+* Heat block 37° and 80°C
+* Timer
+* Rack for small PCR tubes
+* -20°C freezer + freeze box
+<br>
+<b>Digestion</b>
+* Mark PCR tubes or eppendorfs
+    a. U= upstream part : E + S restriction enzymes
+    b. D= downstream part : X + P restriction enzymes
+    c. P= plasmid (destination) : E + P restriction enzymes
+    d. NB: if only one part for insertion insert I= Insert : E + P restriction enzymes
+* In each tube 500 ng DNA for digestion + H20 until total volume is 43 µl
+* Add 5 µl of NEBuffer 2.1 to each tube
+* Add 1 µl of first restriction enzyme
+* Add 1 µl of the second restriction enzyme		'''TOTAL VOLUME = 50 µl'''
+* Mix well by flicking each tube
+* Incubate at 37°C for 20 min. (officially 15 min)
+* Incubate at 80°C for 20 min.
+    a. OPTIONAL: run 10-20 µl on 1% agarose gel and look for expected bands as confirmation
+    b. OPTIONAL: store at -20°C or proceed to ligation immediately
+<br>
+<b>Ligation</b>
+* Add 13 µl of H2O to a 200 µl PCR tube or eppendorf
+* Add 2 µl of each part you want to ligate
+* Add 2 µl of 10X T4 DNA Ligase Reaction Buffer to the tube
+* Add 1 µl of the T4 DNA Ligase to the tube		'''TOTAL VOLUME = 20 µl'''
+* Mix well by flicking each tube
+* Incubate at room temperature for 10 min
+    a. Incubate at 80°C for 20 min.
+    b. Store the ligation mix at -20°C or proceed immediately to the transformation step.
+<br/>
+<!-- TITLE -->
+<html>
+<div id="header" class="row-fluid">
+ <div class="span12">
+<a id="DNA extraction from agarose gels"> </a>
+  <h3 class="bg-yellow">DNA extraction from agarose gels</h3>
+ </div>
+</div></html>
+(source: NucleoSpin® Gel and PCR Clean-up - Macherey-Nagel)
+<br>
+<b>Procedure</b>
+#Excise DNA fragment/solubilize gel slice: take a clean scalpel to excise the DNA fragment from an agarose gel, remove all excess agarose. For each '''100mg of agarose gel < 2%''' add '''200µl buffer NTI''', for gels containing > 2% agarose, double the volume of buffer NTI. Incubate sample for '''5-10 min''' at '''50°C''', vortex the sample briefly every 2-3 min until the gel slice is '''completely''' dissolved.
+#Binding DNA: place a PCR clean-up column into a collection tube (2ml) and load up to 700µl sample, centrifuge for '''30s''' at '''11000g''', discard flow-through and place the column back into the collection tube.
+#Wash silica membrane: add '''700µl buffer NT3''' to the column, centrifuge for '''30s''' at '''11000g''', discard flow-through and place the column back into the collection tube. Repeat the washing again.
+#Dry silica membrane: centrifuge for '''1min''' at '''11000g''' to remove '''buffer NT3''' completely. Make sure the spin column does not come in contact with the flow-through while removing it from the centrifuge and the collection tube.
+#Elute DNA: place the column into a '''new''' 1.5ml microcentrifuge tube, add '''15-30µl buffer NE''' and incubate at '''room temperature''' for '''1 min''', centrifuge for '''1 min''' at '''11000g'''.
+<br/>
+<!-- TITLE -->
+<html>
+<div id="header" class="row-fluid">
+ <div class="span12">
+<a id="GC-MS analysis"></a>
+  <h3 class="bg-yellow">GC-MS analysis</h3>
+ </div>
+</div></html>
+<br/><b>Aim</b>: To detect the production of MeS by our <i>E. coli</i>.
+<br/><br/>
+<b>Sample preparation</b>:<br/>
+#At day 0: a preculture was grown at 37°C overnight (BL21 or BBa_K1060003)
+#The preculture was used to inoculate 500µl into 50ml of fresh LB medium supplemented with or without 0.1 mM salicylic acid and left to grow for overnight. Samples were induced with 0.2 mM IPTG 6 hours post inoculation.
+#Cultures were then chilled on ice and put at 4°C
+#Bacterial cells were removed by centrifugation (10’, 4000g, 4°C) and then filter sterilized (0.22µm).
+#2 ml of this filtersterilized supernatant was then extracted with 1 ml of hexane
+#Extractions were done in glass tubes with rigorous vortexing for 10 minutes
+#The upper phase was transferred to a new glass vial
+#The extraction was repeated twice (total of 3 extractions with 1 ml of hexane)
+#The resulting ± 3 ml of extract were then reduced by evaporation under a nitrogen flow and redissolved in 50 µl of hexane.
+<br/><br/>
+<b>Gas chromatography:</b>
+GC-MS analyses were carried out using a 7890A Agilent gas chromatograph coupled to a 5977A mass spectrometric detector. The GC was equiped with a HP-5MS capillary column (30m x 0.25 mm x 0.25 µm). 1 µl of each sample was injected using splitless injection at a temperature of 250 °C. The initial oven temperature of 40 °C was held for 1 min., ramped at 6 °C / min. to 124 °C, then ramped at 20 °C / min. to 320 °C and finally kept at this temperature for 5 min. The transfer line and ion source were held at 320 °C and 230 °C, respectively. Mass spectra were taken between masses m/z 30-300 with an ionization potential of 70 eV. Retention indices of standards were determined by co-injection of a C7-C30 n-alkane mixture (Supelco) and were compared with published retention indices.<br/><br/>
+<!-- TITLE -->
+<html>
+<div id="header" class="row-fluid">
+<a id="Grow electrocompetent cells"> </a>
+ <div class="span12">
+  <h3 class="bg-yellow">Grow electrocompetent cells</h3>
+ </div>
+</div></html>
+(source: adapted from openwetware.org)
+<br/>
+<b>Materials</b>
+*GYT (glycerol, yeast extract, tryptone)
+**10%(v/v) glycerol
+**0.125% (w/v) yeast extract
+**0.25% (w/v) tryptone
+*DI water
+*10% Glycerol
+<b>Special Equipment</b>
+*Centrifuge
+*Ice water bath
+*Liquid nitrogen
+<b>Procedure</b>
+Important: All steps in this protocol should be carried out aseptically
+*Inoculate: Prepare flask containing 5 ml of LB medium. Pick up a single colony of cells from plate (using a sterile toothpick) and swirl around inside flask. Incubate the culture overnight at 37°C with vigorous aeration (250 pm in a rotary shaker).
+*Dilute and incubate: Inoculate two aliquots of 495 ml of prewarmed LB medium in separate 2-liter flasks with 5 ml of the overnight bacterial culture. Incubate the flasks at 37°C with agitation (300 cycles/min in a rotary shaker). Measure the OD-600 every twenty minutes (this step will take around 1.5-2 hrs). (or judge the OD by eyes to avoid always taking the sample to disturb the growth as well as avoiding the contamination)
+*Rapidly cool culture: Once the OD-600 of the culture reaches 0.6-1.0 (Molecular Cloning recommends 0.4), rapidly transfer the flasks to the pre-made ice-water bath for 15-30 minutes. Swirl the culture occasionally to ensure that cooling occurs evenly. In preparation for the next step, place the centrifuge bottles in the ice-water bath as well.
+Note: After this point, do not let your cells warm up past 4°C '''always keep on ice'''
+Note: When harvesting cells by decanting, be very careful not to disturb the pellet-- this could result in a much lower yield. If necessary, aspirate instead or decant the supernatant. Ask someone to show you how to aspirate. Also, if the pellet seems loose, sometimes it is helpful to re-spin the cells down.
+*Centrifuge 1: Transfer the cultures to ice-cold centrifuge bottles. Harvest the cells by centrifugation at 1000 g (2500 rpm) for 15 minutes at 4°C. Decant the supernantant and resuspend the cell pellet in 20 ml of ice-cold 10% glycerol. Note: this should be done for each of the two 500ml cultures, i.e this is a 1:1 resuspension rather than a concentration by a factor of 2 BC.
+*Centrifuge 2 (10% glycerol): Harvest the cells by centrifugation at 1000 g for 20 minutes at 4°C. Decant the supernatant and resuspend the cell pellet in 20 ml ice-cold 10% glycerol.
+*Centrifuge 3 (10% glycerol): Harvest the cells by centrifugation at 1000 g for 20 minutes at 4°C. Decant the supernatant and resuspend the cell pellet in 10 ml ice-cold 10% glycerol.
+*Centrifuge 4 (10% glycerol): Harvest the cells by centrifugation at 1000 g for 20 minutes at 4°C. Carefully decant the supernatant and use a Pasteur pipette attached to a vacuum line to remove any remaining drops of buffer.
+*Resuspend in GYT: Resuspend in 1 ml ice cold GYT. This is best done by gently swirling rather pipetting or vortexing.
+*Test for arcing: Transfer 40 µl of the suspension to an ice-cold electroporation cuvette and test whether arcing occurs when an electrical discharge is applied. Place the cuvette in the holder attached to the machine. Go to option 4, Pre-set protocols; choose bacterial; choose the correct choice for your size cuvette, probably the first option for a .1 cm cuvette. If arcing occurs, wash the remainder of the cell suspension once more with ice-cold GYT medium to ensure that the conductivity of the bacterial suspension is sufficiently low (<5 mEq). (or check the pulse time, if the pulse time < 4, redo the wash, if the pulse time > 4, it's ok)
+*Storage: Store cells at -80°C until they are required for use. For storage, dispense 40 µl aliquots of the cell suspension into sterile, ice-cold .5 ml microcentrifuge tubes, drop into a bath of '''liquid nitrogen''' and transfer to a -80°C freezer. To remove the tubes from the liquid nitrogen bath, bring out into the hall along with a storage box, and pour the tubes and liquid nitrogen into the box. Once all the tubes are out, close the box most of the way and let the liquid run out into the hallway. Try not to do this in the very center of the walkway!
+*To use frozen cells: Remove an appropriate number of aliquots of cells from the -80°C freezer. Thaw the tubes on ice.<br/>
+<!-- TITLE -->
+<html>
+<div id="header" class="row-fluid">
+ <div class="span12">
+<a id="Headspace GC"></a>
+  <h3 class="bg-yellow">Headspace GC</h3>
+ </div>
+</div></html>
+<br/><b>Aim</b>: To detect the production of MeS by our <i>E. coli</i>.
+<br/><br/>
+<b>Sample preparation</b>:<br/>
+#At day 0: a preculture was grown at 37°C overnight (BL21 or BBa_K1060003)
+#The preculture was used to inoculate 500µl into 50ml of fresh LB medium supplemented with 0 or 0.1 mM of salicylic acid and left to grow for 7 hours.
+#Cultures were chilled on ice and put at 4°C
+#Bacterial cells were removed by centrifugation (10’, 4000g, 4°C) and then filterstelized (0.22µm).
+#Salt was added to 5 ml of this filtersterilized supernatant<br/><br/>
+<b>Gass chromatography:</b>
+Samples were analyzed with a calibrated Autosystem XL gas chromatograph with a headspace sampler (HS40; Perkin-Elmer, Wellesley, Mass.) and equipped with a CP-Wax 52 CB column (length, 50 m; internal diameter, 0.32 mm; layer thickness, 1.2 μm; Chrompack; Varian, Palo Alto, Calif.). Samples were heated for 16 min at 72°C in the headspace autosampler. The injection block and flame ionization detector (FID) temperatures were kept constant at 180 and 250°C, respectively; helium was used as the carrier gas. The oven temperature was 75°C held for 6 min and then increased to 110°C at 25°C min−1 and held at 100°C for 3.5 min. Results were analyzed with Perkin-Elmer Turbochrom Navigator software.
+<br/>
+<!-- TITLE -->
+<html>
+<div id="header" class="row-fluid">
+<a id="Isolation of plasmid DNA from E. coli (mini prep)"> </a>
+ <div class="span12">
+  <h3 class="bg-yellow">Isolation of plasmid DNA from <i> E. coli</i> (mini prep)</h3>
+ </div>
+</div></html>
+(source: NucleoSpin® plasmid  - Macherey-Nagel)
+<br>
+<b>Nanodrop protocol</b>
+<br><br>
+Nanodrop can be used to measure the DNA, RNA and protein
+Measure the concentration and purity of extracted DNA using absorbance (using the automated nanodrop machine!)
+Method:
+#Log onto computer and select Nanodrop program from the desktop (ND 1000)
+#To clean Nanodrop machine wipe pedestal and top and add 3 µl of water to nib of pedestal. Press blank.
+#Wipe the water off, to initialize/equalize the equipment add 3 μl of the elution buffer [EB] used in the sample and press blank. Set to DNA-50 for DNA.
+#Wipe to remove buffer and apply 3 μl of sample to nib. Press measure.
+#If dealing with multiple samples, clean the equipment with water at regular intervals (about every 10 samples).
+#After measurements, clean the equipment with 3 μl of water on the spectrometer and press blank. Wipe and log off.
+<br/>
+<!-- TITLE -->
+<html>
+<div id="header" class="row-fluid">
+<a id="PCR clean-up"> </a>
+ <div class="span12">
+  <h3 class="bg-yellow">PCR clean-up</h3>
+ </div>
+</div></html>
+(source: NucleoSpin® Gel and PCR Clean-up - Macherey-Nagel) <br/>
+This is used for PCR clean-up as well as DNA concentration and removal of salts, enzymes, etc. from enzymatic reactions (SDS<0.1%)
+#Adjust DNA binding condition: mix '''1 volume of sample''' with '''2 volumes of buffer NTI''' (eg. mix 100 µl PCR reaction and 200 µl buffer NTI).
+#Binding DNA: place a PCR clean-up column into a collection tube (2 ml) and load up to 700 µl sample, centrifuge for '''30 s''' at '''11000 g''', discard flow-through and place the column back into the collection tube.
+#Wash silica membrane: add '''600µl buffer NT3''' to the column, centrifuge for '''30 s''' at '''11000 g''', discard flow-through and place the column back into the collection tube. Repeat the washing again.
+#Dry silica membrane: centrifuge for '''1 min''' at '''11000 g''' to remove '''buffer NT3''' completely. Make sure the spin column does not come in contact with the flow-through while removing it from the centrifuge and the collection tube.
+#Elute DNA: place the column into a '''new''' 1.5 ml microcentrifuge tube, add '''50 µl buffer NE''' and incubate at '''room temperature''' for '''1 min''', centrifuge for '''1 min''' at '''11000 g'''.
+<br/>
+<!-- TITLE -->
+<html>
+<div id="header" class="row-fluid">
+<a id="PCR Protocol for Taq DNA Polymerase with Standard Taq Buffer"> </a>
+ <div class="span12">
+  <h3 class="bg-yellow">PCR protocol for Taq DNA polymerase with standard Taq Buffer</h3>
+ </div>
+</div></html>
+<b>Reaction set up</b>
-=== Reaction set up ===
 [https://static.igem.org/mediawiki/2013/7/7b/Risk_assessment_PCR_KULeuven.pdf Risk assessment for PCR]<br/>
 '''We recommend assembling all reaction components on ice and quickly transferring the reactions to a thermocycler preheated to the denaturation temperature (95°C).'''
 {| class="wikitable"
-| '''Components''' || '''25μl reaction''' || '''50μl reaction''' || '''Final concentration'''
+| '''Components''' || '''25 μl reaction''' || '''50 μl reaction''' || '''Final concentration'''
 |-
-| 10X Standard Taq Reaction Buffer || 2.5µl  || 5µl || 1X
+| 10X Standard Taq Reaction Buffer || 2.5 µl  || 5 µl || 1X
 |-
-| 10 mM dNTPs || 0.5µl || 1µl || 200µM
+| 10 mM dNTPs || 0.5 µl || 1 µl || 200 µM
 |-
-| 10 µM Forward Primer || 0.5µl || 1µl || 0.2 µM (0.05–1 µM)
+| 10 µM Forward Primer || 0.5 µl || 1 µl || 0.2 µM (0.05–1 µM)
 |-
-| 10 µM Reverse Primer || 0.5µl || 1µl || 0.2 µM (0.05–1 µM)
+| 10 µM Reverse Primer || 0.5 µl || 1 µl || 0.2 µM (0.05–1 µM)
 |-
 | template DNA || variable || variable || <1,000 ng
@@ Line 203: / Line 586: @@
 Transfer PCR tubes from ice to a PCR machine with the block preheated to 95°C and begin thermocycling.
-=== Thermocyclingconditions for a routine PCR ===
+<b>Thermocyclingconditions for a routine PCR</b>
 {| class="wikitable"
 | '''Step''' || '''Temperature''' || '''Time'''
@@ Line 217: / Line 600: @@
 <br/>
-----
+<!-- TITLE -->
+<html>
+<div id="header" class="row-fluid">
+<a id="Plasmid DNA isolation"> </a>
+ <div class="span12">
+  <h3 class="bg-yellow">Plasmid DNA isolation</h3>
+ </div>
+</div></html>
-== PCR clean-up ==
+<b>Procedure</b>
-(source: NucleoSpin® Gel and PCR Clean-up) <br/>
-This is used for PCR clean-up as well as DNA concentration and removal of salts, enzymes, etc. from enzymatic reactions (SDS<0.1%)
-#Adjust DNA binding condition: mix '''1 volume of sample''' with '''2 volumes of buffer NTI''' (eg. mix 100µl PCR reaction and 200µl buffer NTI).
-#Binding DNA: place a PCR clean-up column into a collection tube (2ml) and load up to 700µl sample, centrifuge for '''30s''' at '''11000g''', discard flow-through and place the column back into the collection tube.
-#Wash silica membrane: add '''600µl buffer NT3''' to the column, centrifuge for '''30s''' at '''11000g''', discard flow-through and place the column back into the collection tube. Repeat the washing again.
-#Dry silica membrane: centrifuge for '''1min''' at '''11000g''' to remove '''buffer NT3''' completely. Make sure the spin column does not come in contact with the flow-through while removing it from the centrifuge and the collection tube.
-#Elute DNA: place the column into a '''new''' 1.5ml microcentrifuge tube, add '''50µl buffer NE''' and incubate at '''room temperature''' for '''1min''', centrifuge for '''1min''' at '''11000g'''.
-<br/>
+[https://static.igem.org/mediawiki/2013/8/8f/Risk_assessment_Plasmid_DNA_Purification_kit_KULeuven.pdf Risk assessment for plasmid DNA purification kit]
-----
+#Bring '''1.5 ml culture''' in an eppendorf, centrifuge for '''1 min with maximum speed'''
+#Pour away the supernatant
+#Bring another '''1.5 ml culture''' into the same eppendorf, centrifuge for '''1 min''' and pour away supernatant
+#Resuspend the pellet with '''200µl GTE-solution''' we made earlier
+#Add '''4 µl RNase A (10mg/ml)'''
+#Add '''400 µl premade solution''' (contains 0.2M NaOH and 1%SDS in sterile water)
+#Mix them well, place on ice for '''5 min'''
+#Add '''300 µl ice cold 7.5 M ammonium acetate''', vortex for 10 s, place on ice for '''5 mins'''
+#Centrifuge for '''5min with 13000 rpm'''
+#Bring the supernatant into a new eppendorf
+#Centrifuge this supernatant for a second time ('''5 min, 13000 rpm''') and bring the supernatant in a new eppendorf
+#Add isopropanol to the supernatant (60% in volume of the supernatant), leave '''at room temp. for 5 min'''
+#Centrifuge for '''10 min with 13000 rpm''', immediately remove the supernatant, keep the transparent pellet in the tube, put the tube upside down on a tissue to dry it
+#Add '''1 ml of cold 70% ethanol''' to the pellet, invert 5 times
+#Centrifuge '''3 min with 13000 rpm'''
+#Remove supernatant, the droplet on the tube wall can be removed by tissue
+#Let the pellet dry
+#Add '''50 µl elution buffer''' (or sterile water) to the pellet
-== DNA extraction from agarose gels ==
+<b>Buffers and Solutions</b>
-(source: NucleoSpin® Gel and PCR Clean-up)
-#Excise DNA fragment/solubilize gel slice: take a clean scalpel to excise the DNA fragment from an agarose gel, remove all excess agarose. For each '''100mg of agarose gel < 2%''' add '''200µl buffer NTI''', for gels containing > 2% agarose, double the volume of buffer NTI. Incubate sample for '''5-10min''' at '''50°C''', vortex the sample briefly every 2-3min until the gel slice is '''completely''' dissolved.
-#Binding DNA: place a PCR clean-up column into a collection tube (2ml) and load up to 700µl sample, centrifuge for '''30s''' at '''11000g''', discard flow-through and place the column back into the collection tube.
-#Wash silica membrane: add '''700µl buffer NT3''' to the column, centrifuge for '''30s''' at '''11000g''', discard flow-through and place the column back into the collection tube. Repeat the washing again.
-#Dry silica membrane: centrifuge for '''1min''' at '''11000g''' to remove '''buffer NT3''' completely. Make sure the spin column does not come in contact with the flow-through while removing it from the centrifuge and the collection tube.
-#Elute DNA: place the column into a '''new''' 1.5ml microcentrifuge tube, add '''15-30µl buffer NE''' and incubate at '''room temperature''' for '''1min''', centrifuge for '''1min''' at '''11000g'''.
-<br/>
+*GTE-buffer
-----
+**50 mM glucose
+**25 mM Tris-Cl (pH 8.0)
+**10 mM EDTA
+**4 mg/ml lysozyme
-== Nanodrop protocol ==
+*IPTG stock solution
-Nanodrop can be used to measure the DNA, RNA and protein
+**238 mg in 10 ml AD
-Measure the concentration and purity of extracted DNA using absorbance (using the automated nanodrop machine!)
+**Filter sterilize
+**Split into 1 ml aliquots
+**Store in -20 freezer
-Method:
+Final concentration/work concentration in agar plates = 0.1mM – 1 mM <br/>
-#Log onto computer and select Nanodrop program from the desktop (ND 1000)
+Sigma recommends 0.2 mM for blue-white screening <br/>
-#To clean Nanodrop machine wipe pedestal and top and add 3 µl of water to nib of pedestal. Press blank.
+Thermo Scientific recommends 0.1 mM
-#Wipe the water off, to initialise/equalizen the equipment add 3 μl of the elution buffer [EB] used in the sample and press blank. Set to DNA-50 for DNA.
-#Wipe to remove buffer and apply 3 μl of sample to nib. Press measure.
-#If dealing with multiple samples, clean the equipment with water at regular intervals (about every 10 samples).
-#After measurements, clean the equipment with 3 μl of water on the spectrometer and press blank. Wipe and log off.
 <br/>
-----
+<!-- TITLE -->
+<html>
+<div id="header" class="row-fluid">
+ <div class="span12">
+<a id="Predator attraction to MeS induced aphid infested plants"></a>
+  <h3 class="bg-yellow">Predator attraction to MeS induced aphid infested plants</h3>
+ </div>
+</div></html>
+<b>Aim</b>: To determine the effect on aphid predators’ attraction to Methyl Salicylate (MeS) induced plants.
+<br/><br/>
+Experimental setup: We continue with the same plants used in the experiments to determine aphid population preference (see above), this way we try to create an as close as possible in vivo situation. The predators were subjected to choice experiment - cafetaria model.
+*Predators: <i>Macrolophus</i> adults
+*Plants: Small potted MeS induced paprika plants in two ways: via the root or via the leaf, 60 in total.
+*Concentration: 1ng/ml, 0,8ng/ml, 0,4ng/ml, 0.1ng/ml, 0.01ng/ml of MeS (Sigma-Aldrich, ReagentPlus®, ≥99% (GC)).
+<br>
+<b>Cafetaria model</b>
-== Digestion and ligation ==
+[[File:Cafetariamodel.png|100px|Leafinduction]] [[File:Cafetariamodel1.png|200px|Leafinduction]]
-=== Consumables and equipment ===
+<br/>
+In the cafeteria model shown above, each concentration will be placed, plus the control, randomly in a circle. The plants should not be close to the edge of the cage in which the experiments are carried out. The plants should be placed in rotation with every repeat of the set-up to eliminate other factors.
+*Releasing the <i>Macrolophus</i>:
+#10 <i>Macrolophus</i> (adult) are shaken out of the pot and placed in the middle of the cafetaria model (see picture)
+#We release around 50 <i>Macrolophus</i> (adult) per set-up
+[[File:Macrolophus2.png|200px|Leafinduction]]
+*Counting the <i>Macrolophus</i>:
+# After every 45 min from the moment we released the <i>Macrolophus</i>, the amount per plant is counted and recorded
+# The <i>Macrolophus</i> are then shaken off the plant back into the middle of the circle so that they can make their choice again
+# We will take 3 recordings
+<!-- TITLE -->
+<html>
+<div id="header" class="row-fluid">
+<a id="Predator attraction to Methyl Salicylate"></a>
+ <div class="span12">
+  <h3 class="bg-yellow">Predator attraction to methyl salicylate</h3>
+ </div>
+</div></html>
+<b>Aim</b>: To determine a working concentration of methyl salicylate (MeS) concentration which attracts predators .
+<br/><br/>
+Experimental setup: We continue with the same plants used in the experiments to determine aphid population preference (see above), this way we try to create an as close as possible in vivo situation. The predators were subjected to choice experiment - cafetaria model.
+*Predators: <i>Adalia bipunctata</i> (ladybugs): adult and larvae
+*Concentration: 1000ng/ml, 100ng/ml, 10ng/ml, 1ng/ml, 0.1ng/ml, 0.01ng/ml of MeS (Sigma-Aldrich, ReagentPlus®, ≥99% (GC)) in 96% ethanol.
+<br>
+<b>Biobest setup</b>
-* Restriction enzymes (EcoRI, Xbal, Spel, Pstl), NEBuffer 2.1
+[[File:Biobestsetup.png|200px|Biobeststetup]]
-* 10x T4 DNA ligase Reaction Buffer, T4DNA Ligase
+<br/>
-* Keep al enzymes on ice; make sure buffers have no precipitation
+The predators were subjected to a choice experiment between one of the MeS concentrations and a control (pure EtOH).
-* H20
+<br/>We repeated each dilution three times with different ladybugs.
-* Small PCR Tubes or eppendorfs
+<br/>After using the ladybugs, we collected them in a different tube and didn’t use them again.
-* 2ul, 200ul pipr tips
+<br/>These experiments were performed in a chemical safety cabinet to prevent the distribution of MeS in the air.
-* Destination plasmid as purified DNA
-* Upstream and downstream part as purified DNA
-* 2ul and 20 ul pippet
-* Heat block 37° and 80°C
-* Timer
-* Rack for small PCR tubes
-* -20°C freezer +freeze box
+<b>pcfruit setup</b>
-=== Digestion ===
+[[File:Y-tubeolfactormeter.png|200px|Leafinduction]]
+<br/>
+The predators were subjected to a choice experiment between one of the MeS concentrations and a control (pure hexane or paraffin oil).
+<br/>We repeated each dilution three times with different ladybugs.
+<br/>After using the ladybugs, we collected them in a different tube and didn’t use them again.
+<br/>These experiments were performed in a chemical safety cabinet to prevent the distribution of MeS in the air.
-* Mark PCR tubes or eppendorfs
-    a. U= upstream part : E + S restriction enzyme
-    b. D= downstream part : X+ P restriction enzymes
-    c. P= plasmid (destination) : E+ P restriction enzymes
-    d. NB: if only one part for insertion insert I= Insert : E+P restriction enzymes
-* In each tube 500 ng DNA for digestion + H20 until total volume is 43ul
-* Add 5ul of NEBuffer 2.1 to each tube
-* Add 1ul of first restriction enzyme
-* Add 1ul of the second restriction enzyme		'''TOTAL VOLUME = 50ul'''
-* Mix well by flicking each tube
-* Incubate at 37°C for 20 min. (official 15 min)
-* Incubate at 80°C for 20min.
-    a. OPTIONAL: run 10-20ul on 1% agarose gel and look for expected bands as confirmation
-    b. OPTIONAL: store at -20°C or proceed to ligation immediately
-=== Ligation ===
-* Add 13ul of H2O to a 200ul PCR tube or eppendorf
-* Add 2ul form each part you want to ligate
-* Add 2ul of 10X T4 DNA Ligase Reaction Buffer to the tube
-* Add 1ul of the T4 DNA Ligase to the tube		'''TOTAL VOLUME = 20ul'''
-* Mix well by flicking each tube
-* Incubate at room temperature for 10min
-    a. Incubate at 80°C for 20min.
-    b. Store the ligation mix at -20°C or proceed immediately to the transformation step.
+<!-- TITLE -->
+<html>
+<div id="header" class="row-fluid">
+ <div class="span12">
+<a id="Protein Extraction"></a>
+  <h3 class="bg-yellow">Protein Extraction</h3>
+ </div>
+</div></html>
+<br/><b>Aim</b>: To extract proteins from our <i>E. coli</i> for SDS-PAGE analysis.
+<br/><br/>
+<b>Sample preparation</b>:<br/>
+#E.coli cells transformed with the indicated plasmids were grown either to mid-exponential phase (OD600nm ~ 1.0 for endpoint assays) or to the indicated optical densities.<br/>
+#Samples were taken and spun down (3min, 4000 rpm, 4°C).<br/>
+#Growth medium was removed and cell pellets frozen (-80 °C)<br/>
+#Cell pellets were thawed on ice and resupended in equal volumes extraction buffer.<br/>
+#Suspensions were incubated on ice for 10min and subsequently sonicated (3X 10” pulses) with ice cooling in between.<br/>
+#Suspensions were spun down (10min, 14000 rpm, 4°C).<br/>
+#Aliquots were mixed with 5X sample buffer and boiled (5min 95°C).<br/>
+#Samples were loaded on precast SDS-PAGE systems (Biorad) according to the manufacturer's instructions.
+<br/>
+<b>Extraction buffer </b>:<br/>
+: 25mM Tris pH 8.0; 0.1%(v/v) NP40; 5 mM EDTA; 50 mM NaCl; protease inhibitor cocktail (Benzamidine; PMSF; Leupeptin).
 <br/>
-----
-== Grow electrocompetent cells ==
+<!-- TITLE -->
-(source: openwetware.org) <br/>
+<html>
+<div id="header" class="row-fluid">
+ <div class="span12">
+<a id="qRT-PCR Protocol"></a>
+  <h3 class="bg-yellow">qRT-PCR protocol</h3>
+ </div>
+</div></html>
+General experiment: 3 biological repeats of stationary phase cultures 16 hrs growth.
-=== Materials ===
+<b>Sample preparation</b>
-*GYT (glycerol, yeast extract, tryptone)
+# Inoculate fresh LB plate with the strain harbouring the MS brick
-**10%(v/v) glycerol
+# Isolate plasmid DNA, MS brick
-**0.125% (w/v) yeast extract
+# Nanodrop plasmid (minimum concentration 20 ng/µl) = 155 ng/µl
-**0.25% (w/v) tryptone
+# Design primers for pcha/pchb and for bsmt1 using Primer express. Primer sequence can be found in document “Genes_qPCR_primers_IC.docx”.
+# Inoculate E. Coli with Methylsalicylate brick (MIT 2006) on LB plate.
+# Add 5 µl of Kanamicin (50 mg/ml) and 10 µl of IPTG (100 mM) to 5 ml of LB medium (tubes).
+# Incubate 16h at 37 °C under shaking conditions.
+# Measure OD of 3 cultures.
+# Account for differences in OD: ex. If you have an OD of 1 take 1 ml of this sample, if you have an OD of 0,8 take 1,2 ml.
+# Add 1/5 volume of stopsolution (95% ethanol, 5% phenol).
+# Freeze 5 minutes in liquid Nitrogen.
+# Centrifuge needed amount of cells.
-*DI water
+<b>mRNA isolation</b>
-*10% Glycerol
-=== Special Equipment ===
+For mRNA isolation use the Promega SV total RNA isolation kit ([http://be.promega.com/resources/protocols/technical-manuals/0/sv-total-rna-isolation-system-protocol/?origUrl=http%3a%2f%2fwww.promega.com%2fresources%2fprotocols%2ftechnical-manuals%2f0%2fsv-total-rna-isolation-system-protocol%2f Promega SV total RNA isolation protocol])
-*Centrifuge
+# Section 8.C (Isolation of RNA from Gram-positive and Gram-negative bacteria)
-*Ice water bath
+# Section 4.E (RNA Purification by Centrifugation) We did not do step 4 and 5 (addition of DNase) but instead used the DNase protocol of [http://products.invitrogen.com/ivgn/product/AM2238 Ambion Turbo DNase]
-*Liquid nitrogen
+For 100 µl of RNA:
+## Add 10 µl 10x buffer. Add 1 µl Turbo DNase and mix gently.
+## Put on 37 °C for 20 to 30 min.
+## Add 1 µl of Turbo DNase.
+## Put on 37 °C for 20 to 30 min.
+## Add 20 µl of DNase inactivation reagent and mix well.
+## Put on room temperature for 5 min. Mix occasionally by flicking the tube
+##	Centrifuge on 10000 g for 2 min.
+## Transfer the RNA to a new tube.
-=== Method ===
+<b>Create cDNA</b>
-Important: All steps in this protocol should be carried out aseptically
+Use the Fermentas Revert aid H kit ([http://www.thermoscientificbio.com/reverse-transcription-rtpcr-rtqpcr/revertaid-h-minus-first-strand-cdna-synthesis-kit/ Fermentas Revert aid H protocol])
+The protocol for RT-PCR (I. First Strand Synthesis) was followed
-*Inoculate: Prepare flask containing 5 ml of LB medium. Pick up a single colony of cells from plate (using a sterile toothpick) and swirl around inside flask. Incubate the culture overnight at 37°C with vigorous aeration (250 pm in a rotary shaker).
+<b>qPCR</b>
-*Dilute and incubate: Inoculate two aliquots of 495 ml of prewarmed LB medium in separate 2-liter flasks with 5 ml of the overnight bacterial culture. Incubate the flasks at 37°C with agitation (300 cycles/min in a rotary shaker). Measure the OD-600 every twenty minutes (this step will take around 1.5-2 hrs). (or judge the OD by eyes to avoid always taking the sample to disturb the growth as well as avoiding the contamination)
+qPCR kit was not yet decided.
-*Rapidly cool culture: Once the OD-600 of the culture reaches 0.6-1.0 (Molecular Cloning recommends 0.4), rapidly transfer the flasks to the pre-made ice-water bath for 15-30 minutes. Swirl the culture occasionally to ensure that cooling occurs evenly. In preparation for the next step, place the centrifuge bottles in the ice-water bath as well.
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+<a id="Root measurements"></a>
+  <h3 class="bg-yellow">Root measurements</h3>
+ </div>
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+<b>Aim</b>: To determine whether the different induction methods or the Methyl Salicylate (MeS) had an effect on plant growth.
+<br/><br/>
+Experimental setup: We measured the roots of the same plants used in the experiments to determine aphid population and predator preference (see above).
+<br/>
+[[File:Uppot.png|200px|Uppot]]
+[[File:Wash.png|200px|Root wash]]
+[[File:Dryandweigh.png|200px|Dry roots]]
-Note: After this point, do not let your cells warm up past 4°C
+<br/>
+The plants were cut off at the bottom of the stem and removed from the pot.
-Note: When harvesting cells by decanting, be very careful to not disturb the pellet-- this could result in a much lower yield. If necessary, aspirate instead of decant the supernatant. Get someone to show you how to aspirate. Also, if the pellet seems loose, sometimes it is helpful to re-spin the cells down.
+<br/>After most of the dirt has been removed, they were carefully washed to remove the rest of the dirt.
+<br/>After using the ladybugs, we collected them in a different tube and didn’t use them again.
-    Centrifuge 1: Transfer the cultures to ice-cold centrifuge bottles. Harvest the cells by centrifugation at 1000g (2500 rpm) for 15 minutes at 4°C. Decant the supernantant and resuspend the cell pellet in 500 ml of ice-cold DI water. Note: I think this should be done for each of the two 500ml cultures, i.e this is a 1:1 resuspension rather than a concentration by a factor of 2 BC.
+<br/>The roots were then dried and weighed.
+<br>
-    Centrifuge 2 (water): Harvest the cells by centrifugation at 1000g for 20 minutes at 4°C. Decant the supernatant and resuspend the cell pellet in 250 ml ice-cold DI water.
+[[File:Rootmeasurement.png|200px|Root measurement]]
+[[File:Rootmeasurement1.png|200px|Root measurement 1]]
-    Centrifuge 3 (water): Harvest the cells by centrifugation at 1000g for 20 minutes at 4°C. Decant the supernatant and resuspend the cell pellet in 10 ml ice-cold 10% glycerol.
+<br/>The roots were then measured and recorded.
-        To spin down your pellet in 10 ml, it might be helpful to use 15-ml Falcon tubes instead of the round-bottom tubes. KC
-    Centrifuge 4 (glycerol): Harvest the cells by centrifugation at 1000g for 20 minutes at 4°C. Carefully decant the supernatant and use a Pastteur pipette attached to a vacuum line to remove any remaining drops of buffer.
-    Resuspend in GYT: Resuspend in 1 ml ice cold GYT. This is best done by gently swirling rather pipetting or vortexing.
-    Measure OD: Measure the OD-600 of a 1:100 dilution of the cell suspension. (In the cuvette, mix 0.99 mL water and 0.01 mL cell suspension).
-Note: The desired concentration is 2.5 \times 10^{11} cells per mL, giving 1\times 10^{10} cells per 40 μL. This corresponds to an OD-600 (after 100x dilution) of roughly 3.75. It is difficult to reach this value, but it is still important to know the concentration of cells to calculate efficiencies.
-    Dilute the cell suspension to a concentration of 2 x 10^10 to 3 x 10^10 cells/ml (1.0 OD600 = approx. 2.5 x 10^8 cells/ml) with ice-cold GYT medium.
-    Test for arcing: Transfer 40 ul of the suspension to an ice-cold electroporation cuvette (0.1-0.2 cm gap, on middle shelf next to electroporator) and test whether arcing occurs when an electrical discharge is applied. Place the cuvette in the green holder attached to the machine. Go to option 4, Pre-set protocols; choose bacterial; choose the correct choice for your size cuvette, probably the first option for a .1 cm cuvette. If arcing occurs, wash the remainder of the cell suspension once more with ice-cold GYT medium to ensure that the conductivity of the bacterial suspension is sufficiently low (<5 mEq).
-    Storage: Store cells at -80°C until they are required for use. For storage, dispense 40 ul aliquots of the cell suspension into sterile, ice-cold .5 ml microcentrifuge tubes, drop into a bath of liquid nitrogen and transfer to a -80°C freezer. To remove the tubes from the liquid nitrogen bath, bring out into the hall along with a storage box, and pour the tubes and liquid nitrogen into the box. Once all the tubes are out, close the box most of theh way and let the liquid run out into the hallway. Try not to do this in the very center of the walkway!
-To use frozen cells: Remove an appropriate number of aliquots of cells from the -80°C freezer. Thaw the tubes on ice.
+<br/><br/>