Team:Edinburgh/Project/Notebook

From 2013.igem.org

Revision as of 15:18, 23 July 2013

Chronological notebook

• 27th of June:

B. subtilis (strain: 168) culture inoculated into 10 ml LB medium. Overnight incubation in 37 deg.C

Preparation of metal ion stock solutions: Ni - 0.1M; Zn - 0.1M; Fe - 0.5M; Cu - 0.5M; Co - 0.1M; Mn - 1M (Aleksandra, Harry and Jan)

• 28th of June:

0.5 ml units of O/N culture diluted to 50ml (x100 dilution in LB medium). 3 ml of diluted culture aliquots poured into universal bottles (enables adequate aeration of the culture). Those were inoculated with 30 ul of differently concentrated metal ion solutions giving final concentrations of:

Ni - 1mM; 0.75 mM; 0.5 mM and 0.25mM; Zn - 1mM; 0.75 mM; 0.5 mM and 0.25mM; Fe - 5mM; 3.75mM; 2.5mM and 1.25mM; Cu - 5mM; 3.75mM; 2.5mM and 1.25mM; Co - 1mM; 0.75 mM; 0.5 mM and 0.25mM; Mn - 10mM; 7.5mM; 5mM; 2.5mM; 1.25mM and 0.625mM

0.4 ml of O/N culture diluted to 40ml (x100 dilution in 2xLB medium). 3 ml of diluted culture aliquots poured into universal bottles (enables adequate aeration of the culture). Those were inoculated with 1ml of differently concentrated ethanol solutions giving final concentrations of:

2%; 4%; 6%; 8%; 10%; 15%; 20% and 25%

The initial Absorbance readings at OD600 for diluted cultures were taken. Following 7h. incubation in 37 deg.C absorbance of each sample was measured and compared to samples inoculated only with H2O (Kyle, Harry, Aleksandra, Dainius and Jan).

• 1st of July:

B. subtilis EtOH resistance assay was continued in a narrow concentration range (Jan).

E. coli (DH5alpha) cells were transformed using BioBricks required for EtOH production (Aleksandra).

O/N cultures of E. coli and B. subtilis were set up to continue with the experiments tomorrow (Harry).

• 2nd of July:

Transformation was successful. Four colonies were selected and propagated into 5ml LB bottles supplemented with adequate antibiotic (Jan). After 8h incubation in 37 deg. C cells were pelleted and plasmids were extracted using Qiagen MiniPrep Kit (Aleksandra). Concentration and quality of DNA was measured using NanoDrop.

E. coli cells plated for competitors were harvested and propagated into 50 ml LB medium. Following 4h incubation they were used to make competent cells for future transformations (Aleksandra and Jan).

B. subtilis resistance to heavy metals experiment was continued in a narrow metal ion concentration range (Harry).

• 3rd of July:

Since we propose using B. subtilis as a chassis for our waste water treatment bacteria, we first set about determining the concentration of different metal ions that the non genetically altered chassis can cope with. We initially observed cell density of cultures after 8 hours incubation with varying metal concentrations. Following this we recorded culture density every hour to obtain growth data for appropriate concentrations of metals, as indicated by the initial 8 hour cultures. These experiments continue... (Harry, Danius, Hugo)

• 4th of July:

The competent E. coli cells were tested by transforming them with parts for ethanol production. The negative control was performed to confirm that cells have no indigenous antibiotic resistance and that prepared antibiotic plates have antibacterial properties (Aleksandra and Jan).

Time-lapse measurements of B. subtilis growth in specified metal concentrations (based on previous data) were performed (Harry, Hugo, Dainius and Kyle)

Team started preparing poster (Kyle) and presentation (Dainius and Hugo) for the Young Synthetic Biologist meeting held in London over the next weekend: 12-14/07/2013

• 5th of July:

Outcome of the transformation was positive with the negative control showing no growth (as expected). Four colonies were collected and grown in 5ml LB supplemented with adequate antibiotic. Following 7h incubation the entire culture was pelleted and plasmid was purified using Qiagen MiniPrep Kit. NanoDrop was used to measure the DNA concentration (Harry and Jan)

Time-lapse measurements of B. subtilis growth in specified metal and ethanol concentrations (based on previous data)were performed (Harry, Hugo, Dainius and Jan).

• 8th of July:

Two PCR reactions were set up to clone out genes of interest from B. subtilis (Harry and Hugo; Dainius and Kyle).

The ethanol production part was combined with a promoter - overnight ligation(Jan)

• 9th of July:

The PCR product was run on the gel to confirm the presence of the desired product (Aleksandra, Dainius, Jan)

The ligation product was transformed into the competent E. coli cells. Those were plated on the KAN+IPTG+X-gal plates (Aleksandra, Jan).

B. subtilis genomic DNA was purified from the O/N culture for the use in the future PCR reaction (Harry)

• 10th of July:

DNA gel electrophoresis of the PCR product was performed once more due to inconclusive results from 9/07/2013 (Jan). Bands of expected size were observed. Additional PCR was set up to obtain more DNA (Harry and Hugo). Following gel electrophoresis resulting products were restricted using correct enzyme and an O/N ligation reaction was set-up (Aleksandra and Jan)

The transformation using the EdiBrick and ethanol production parts ligation product was successful - numerous blue colonies were obtained. Two colonies were selected and propagated into 5ml LB +KAN medium. Two more colonies (4 in total) were propagated onto LB+KAN+X-gal plates and incubated O/N in 37 deg.C (Aleksandra, Jan)

• 11th of July:

The ligation products of vector and two transcription factors amplified using PCR were transformed into E. coli and plated on LB+AMP+X-gal+IPTG plates (Harry and Weike)

• 15th of July:

The transformation done using the ligation product gave negative results. The restriction of SinR; Fur and AmpR vector was repeated. O/N ligation was set up using new restriction products (Harry, Weike and Jan)

Cells from four different plates of the EdiBrick_pET ligation were resuspended in 5 ml LB medium + KAN and grown in 37 deg.C. The plasmid was purified following 4 hours of incubation using Qiagen MiniPrep Kit (Aleksandra and Jan)

• 16th of July:

The DNA resulting from ligation was used for transformation of competent E. coli. Cells were plated on LB+AMP+IPTG (20 ul) plates (Weike and Hugo)

The EdiBrick_pET DNA was restricted using XbaI and PstI in CutSmart buffer. 2 h. incubation in 37 deg. C was used for restriction reaction.The resulting proucts were run on the gel (15ul product + 3ul loading dye). Three out of four DNA samples showed correct band sizes (Aleksandra).

Reagents required for ethanol assay were prepared and a sample data for 0; 0.5 mM and 1 mM were obtained in order to plot a standard curve. O/N cultures of E. coli with pET and EdiBrick_pET were set up in order to analyse those tomorrow (Aleksandra and Jan).

Timelapse analysis of B. subtilis growth in varying concentrations of three different heavy metals was performed (Harry and Dainius)

2xLB was prepared to perform the time-lapse analysis of B. subtilis growth in higher EtOh concentrations (Jan).

• 17th of July:

Due to negative results of ligation all DNA involved in the process was analysed using DNA gel electrophoresis to identify the faulty step (Kyle, Dainius and Hugo)

Supernatant of the pET and EdiBrick_pET O/N cultures was subjected to the ethanol assay. Due to encouraging results the pET plasmid was isolated and restricted using XbaI and PstI to confirm it definitely has the correct insert (Aleksandra and Jan)

• 18th of July:

B. subtilis growth in higher [EtOH] was analysed (Aleksandra and Jan)

PCR reaction was set up to obtain the DNA fragments required to perform deletions in the B. subtilis sporulation pathway (Dainius and Kyle)

PCR reaction for the MABEL based fusion of adhB and pdc was performed. Product was analysed on a gel. An O/N blunt-end ligation reaction was set up to obtain the plasmid with fusion proteins(Aleksandra and Jan)

Restriction of the Fur and SinR PCR products was performed using an enhanced protocol with an O/N incubation in 37 deg. C (Dainius)

• 19th of July:

Due to low amount of product obtained second PCR reaction was set up to amplify the DNA fragments required to perform deletions in the B. subtilis sporulation pathway (Dainius and Kyle)

The O/N restriction product was purified from the reaction mix. This was used for two separate ligation reactions using different ligant-to-vector ratios and [vactor] (Hugo and Dainius)

New GenBrick linkers were prepared to be tested over the next week (Aleksandra)

• 20th of July:

The ligation products were used for transformation of super-competent E. coli cells (Hugo and Dainius)

• 22nd of July:

The transformation result was positive. Four colonies per insert were selected and subjected to colony PCR. Moreover, those were propagated into 5ml LB + AMP cultures. Cultures were grown for 7 h and entire 5 ml was used for plasmid purification using the Qiagen MiniPrep kit. The resulting DNA was quantified using NanoDrop (Hugo and Dainius)

The MABEL blunt end ligation product was transformed into competent E. coli cells and plated on LB+KAN+IPTG+X-gal plates. Those were incubated in 37 deg. C O/N. Moreover, the purified linear MABEL product was run on the DNA electrophoresis gel to assess the quality of the large fragment (>7 kb) purification process when using Qiagen PCR product purification kit (Aleksandra and Jan)

• 23rd of July:

Cloned parts were excised from working vector and inserted into pSB1C3. A 2h restriction with XbaI/ PstI and an O/N ligation was performed to achieve that (Hugo and Dainius)

The transformation resulting from the blunt end ligation was successful. Six colonies were chosen and propagated into 5ml LB medium + KAN. Following 7h incubation in 37 deg. C the cultures were propagated into fresh 5ml LB + KAN + 2% lactose to induce expression of pdc_adhB fusion protein. The non fusion cultures were set up and induced at the same time to have a point of reference (Aleksandra and Jan)

JM109 cells were made chemically competent. E. coli and B. subtilis were patched onto fresh LB medium to be used in other experiments. Some CML plates were prepared (Aleksandra and Jan)

Recipes (or protocols if you prefer so)

• 2xLB medium:

Tryptone, 20g Yeast extract, 10g NaCl, 10g (when making more medium add 20g) Dissolve in 800 ml dH2O, adjust pH to 7.0 with NaOH/HCl, adjust volume to 1 litre and autoclave.

NOTE: Use this medium when diluting the culture with high volumes. If possible try to use same volume of 2xLB and the solution you want to add to it as B. subtilis does not grow really well in highly concentrated LB.

• Preparation of competent E. coli cells:

TSS buffer is required for this process. 24 ml TSS:

-17 ml LB -5 ml 40% w/v PEG 3350 -1 ml 1 M MgCl2 filter sterylise the mix above and add: -1 ml DMSO

Procedure:

Propagate E. coli from plate into 50 ml of LB medium. Grow until OD600 of about 0.2 to 0.5 is obtained. Pellet 1 ml of culture for each eppendorf of competent cells. Remove supernatant and add 100 ul of ice-cold TSS buffer. Incubate with TSS for 30 min on ice and store in -80 deg.C

• Transformation of competent E. coli cells:

1.Use 100ul aliquots of competent E. coli cells from the -80 deg. C freezer.

2.Place cells directly on ice. Try to limit the exposure to heat (i.e. do not touch the bottom of the eppendorf)

3.Add 2 ul of plasmid DNA to the cells and incubate on ice for 30 - 60 minutes.

4.Heat shock the cells in 42 deg. C for 90 seconds (exact timing)

5.After heat shock place the cells on ice for additional 90 seconds.

6.Add 900 ul of LB medium to the cells.

7.Grow in 37 deg. C shaking for 45 - 60 minutes.

8.Plate 100 ul of cells on a plate with appropriate antibiotic.

• Ethanol assay:

Buffer used in the assay: 50 mM tris-HCl pH= 7.5 (0.118g tris base + 0.635g tris.HCl in 100 ml of H2O)

Following solutions were prepared in the buffer:

- yeast ADH: 5 mg/ ml

- NAD+: 20 mM (13.3 mg/ ml)

- PMS: 20 mM (6.1 mg/ ml)

- INTV: 50 mM (25.3 mg/ ml) --> INTV has low solubility; can add few drops of DMSO to dissolve.

- ethanol: 30 mM (1.75 ul/ ml) --> required for the standard absorbance curve

Procedure:

Into 1ml of buffer add:

- 5ul yeast ADH

- 1 ul NAD+

- 1 ul PMS

- 20 ul INTV

mix well

Add 33 ul of the standard ethanol solution (30 mM) and 33 ul of diluted (DF=2) ethanol solution to obtain 1mM and 0.5mM standard responses respectively. The 0 mM EtOH response is obtained by adding 33 ul of H2O. Mix well after addition of the ethanol.

Incubate the assay for 15 min in room temperature. Following that take the OD500 readings which will correspond to the ethanol concentration. You can use H2O as a blank.

To evaluate the levels of EtOH in your bacterial medium spin down the cells from O/N culture and use 33 ul of supernatant as a substrate for the assay. The readings should be taken following exactly the same incubation period as ethanol standard. Make a fresh standard each day you want to analyse bacterial culture.