Team:Nevada/Notebook/Weeks58

Calender Weeks 5-8
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Week 5 - June 27th- July 3rd

E. Coli

Trc Promoter

Lt: Trc promoter was selected for expression of the ADH/PDC and Thioesterase (BTE) genes. Trc promoter was located in the commercial pTRC99A plasmid and transformed into NEB10 β cells. Four colonies were selected from Ampicillin resistant plates and cultured in LB-Amp broth. The cultures were purified using QIAprep Spin Miniprep protocol and the DNA was quantitated using Nanodrop spectrophotometry. Trc promoter was isolated from pTRC99A plasmid using PCR.

Trc promoter was isolated from pTRC99A plasmid using PCR.

Pyruvate Decarboxylase & Alcohol Dehydrogenase

JC: To insert PDC/ADH genes into the σ70 constitutive promoter plasmid, 0.5ug of σ70/pSB1A3 (2190bp) was digested with SpeI and PstI and 0.5ug of PDC/ADH/pSB1C3 (5124bp) was digested with XbaI and PstI. These digestions cut out the red fluorescent protein (rfp) tag on pSB1A3 (rfp=885bp) to aid in colony selection. Digestions were run on a 1% agarose gel, and bands obtained confirmed PDC/ADH (3054bp), pSB1C3 (2070bp), σ70/pSB1A3 (2190), and rfp (885bp). Incomplete digestion of PDC/ADH/pSB1C3 was apparent for sample #8, so the sample was re-digested before ligation.

PDC/ADH-XbaI/PstI and σ70/pSB1A3-SpeI/PstI were ligated and transformed into NEB10 β cells. Single colonies from LB-Ampicillin plates were selected and tested on LB-Amp and LB-Chlor plates. No usable colonies were obtained (all were light pink and grew on both LB-Chl and LB-Amp plates).

Bay Laurel Thioesterase

MT: Four colonies of Part J sigma 70 contiuative promoters was cultured and digested with SpeI and PstI. 3-2 and 3-3 cell lines of Bay Laurel Thioesterase with RBS and terminator (BTE) were digested with XbaI and PstI. All cell lines of sigma 70 and BTE were shown to be fully digested by check with 1% agarose gel. Colony 1 of sigma 70 and 3-2 of BTE were chosen to be ligated together in the J61002 Amp R plasmid that sigma 70 came in. The ligation was transformed in NEB Beta cells and spread on Amp R plates. Twenty-five white colonies were chosen from the transformation and streaked on Amp200 R plates cross-selected on Cm34 R plates. 17/25 of the colonies remained white and none of the colonies grow on the chloramphenicol plates. Ten colonies were chosen for culture, and minipreped.

Cyano
DH5α cells were transformed with the promoters K390015 (petBD+RBS), K390016, and K390017; the integration vector K654056; GLF; and INV. All genes were contained in the plasmid pSB1C3. Transformants were selected for on chloramphenicol plates and cultured in LBccm broth. Plasmid DNA was isolated from the transformants using a QIAgen miniprep kit. Isolated plasmid was digested with EcoRI and PstI to ensure that the correct plasmid transformations took place.

Results/Discussion: The EcoRI and PstI digests did not confirm successful plasmid transformations. This seems to be due to a defect in the restriction enzymes. In order to advance in our research, these isolated plasmids will be submitted for sequencing.

Enzymology
CL:This week we ran the ethanol test assay using ADH. Results were negative as ethanol standards of low concentrations (<20µM) were not being detected. Only when high concentrations of ethanol were added was there any absorbance correlating to ADH activity. We therefore concluded that the ADH enzyme was not sensitive enough to detect ethanol within the concentration ranges we were expecting, and opt to use a more sensitive Alcohol Oxidase enzyme instead. The alternative enzyme was ordered and will be stored until testing. A rough draft protocol for the alcohol oxidase assay was also written up and buffers were prepped.

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Week 6 - July 4th-10th

E. Coli

Trc Promoter

LT:PCR products were cloned into PCR2.1 TOPO vector and transformed into One Shot Top 10 Chemically competent cells using the TOPO TA cloning protocol. Twenty-five colonies were selected from Ampicillin resistant plates streaked on new LB –Amp plates and cultured in LB-Amp broth. QIAprep Spin Miniprep protocol was performed on the cultures and DNA was quantitated using nanodrop spectrophotometry. Results: Nanodrop analysis indicated high levels of RNA contamination. P1 buffer didn’t work properly.

Ten new colonies (#1-10) were streaked and inoculated in LB-Amp broth, purified using the Qiaprep Spin Miniprep protocol, and nanodropped. To confirm that TRC was correctly inserted into the PCR2.1 TOPO vector, an Eco RI and Pst I digest was set up and run on a 1.0% gel. Results: Trc was not successfully inserted into the PCR 2.1 TOPO vector. Bands in the gel correspond to the TOPO vector without insert.

Pyruvate Decarboxylase & Alcohol Dehydrogenase

JC: PDC/ADH was re-digested with XbaI/PstI and run on a 1% agarose gel to confirm digestion. Bands obtained confirmed PDC/ADH (3054bp), and pSB1C3 (2070bp). PDC/ADH-XbaI/PstI and σ70/pSB1A3-SpeI/PstI were re-ligated and transformed into NEB10 β cells.

Bay Laurel Thioesterase

MT: The ten cultures of sigma 70 promoter ligated with BTE into the J61002 Amp R plasmid were digested with EcoRI and PstI. 8/10 of the samples had a band at 2000bp (J61002) and 1200bp (BTE) on a 1% agarose gel. They were compared to BTE/ pSB1C3 digest with EcoRI and PstI, and you can see a slight shift in the size of the BTE suggesting that successful ligation of the sigma 70 with BTE. Six of the samples were sent to the Nevada Genomic Center for sequencing in the forward direction. All six had the entire sigma 70 promoter and the beginning of BTE.

Cyano
Procedure: Submitted isolated pSB1C3 containing K390015, K390016, K390017, K654056, INV, and GLF for sequencing. Prepared 2L of BG11 media for future Synechocystis growth experiments

Results/Discussion: The sequencing data indicated the successful isolation of all genes. Thus, for creating the invertase operon via gibson assembly, K390015 will be used to PCR out the petBD+RBS (light inducible promoter) and INV will be used to PCR out invertase containing the correct overlapping flanking regions. K39005 will also be used to PCR promoter for the GLF operon. K654056 can be used as an integration vector for transforming Synechocystis PCC 6803.

Enzymology
Week 6-7 CL: This week we ordered a Free Fatty Acid Assay Kit from BioSystems as we anticipate that our E. coli modified to produce and secrete free fatty acids part is complete. While I waited for my kit to arrive I helped around the lab and participated in a western blot. The western blot was to detect a Histidine tag on the Bay Laurel thioesterase gene. The blot was attempted and failed three times before we concluded we were using a defective transfer buffer.

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Week 7 - July 11th-17th

E. Coli

Trc Promoter

LT:Fifteen new colonies (#11-25) were recultured, minipreped, digested and run on a 1% gel. (See week 6.) Results: Trc was not successfully inserted into the PCR 2.1 TOPO vector. Bands in the gel correspond to the TOPO vector without insert.

LB- Amp plates were prepared with x-gal . Cultures #1-25 were streaked and incubated overnight for blue/white selection. Results: All colonies were white.

All colonies were white so control cells were spread on the x-gal plates. Results: The control cells appeared very light blue. The x-gal blue/white selection wasn’t helpful for selecting transformed versus non-transformed colonies.

Pyruvate Decarboxylase & Alcohol Dehydrogenase

JC: Single colonies from LB-Amp plates were selected and tested on LB-Amp and LB-Chlor plates. Liquid cultures grown in LB-Amp and minipreps and nanodrop analysis performed.

To verify presence of PDC/ADH genes with the σ70 constitutive promoter, 0.5ug of PDC/ADH/σ70/pSB1A3 was digested with EcoRI and PstI. Digests were run on a 1% agarose gel, and bands confirmed σ70/PDC/ADH (3089bp) and pSB1A3 (2155bp).

Cyano
Procedure: Synechocystis PCC 6803 genomic DNA was isolated using a lysis, denaturation, and ethanol precipitation. This genomic DNA was used to PCR out agp and ThiE for the creation of knockouts of the respective genes using gibson assembly. PCR was performed on CmR, petBD, GLF, and INV from the isolated pSB1C3 plasmids. PCR was also performed on KnR from pUC4K. These PCR reactions were performed using the gibson assembly primers and master mix was prepared with phusion DNA polymerase. DNA was present in 1 ng/ul reaction. All PCR reactions were run on .7% agarose gel at 110 V for 60 minutes.

Results/Discussion: Bands were expected at 4231 bp for agp, 1061 bp for KnR, 219 bp for petBD, 1711 bp for INV, 1548 bp for glf, 894 bp for CmR, and 1031 bp for ThiE. None of these bands appeared on the gel. Thus, PCR failed for all genes and the experiments need to be redone. Since the primers are quite large for gibson assembly parts, the optimum initial annealing temperature for the first three PCR cycles needs to be determined for all genes.

One liter of LB liquid media and stock solutions of ampicillin were made. Ampicillin was added to the LB liquid media and ampicillin plates were poured for future use. Invertase (INV) and glucose facilitator gene (GLF) contained in the pUC57 vector colonies were streaked on ampicillin and chloromphenicol plates to check for growth.

Enzymology
CL:See week 6

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Week 8 - July 18th-24th

E. Coli
Trc Promoter

LT:Half of the PCR products were loaded onto a 1.2% gel to verify that the Trc promoter was successfully isolated. Results: TRC was successfully isolated by PCR.

Remaining PCR products were combined and run on a 1.2% gel. The band correspond to the Trc promoter was cut out and purified using the QIAquick gel extraction of PCR products protocol. Nanodrop analysis was then used to quantitate the amount of DNA present.

Trc promoter was cloned into the TOPO2.1 PCR vector, transformed into One Shot Top 10 Chemically Competent cells, and streaked onto LB-Amp plates with x-gal. Control cells were also plated on LB-Amp plates with x-gal. Results: The transformation seems to have been successful. There were both dark blue and white colonies. The control cells contained only blue colonies!

Fifteen white colonies (#1-15) were selected. Half the colony was single colony streaked onto LB-Amp plates for purification and the other half was inoculated into LB-Amp broth. The cultures were purified using QIAquick miniprep and analyzed using the nanodrop. An Eco RI and Pst I restriction digest was set up and run on a 1.2% gel to confirm that the transformation was successful. Results: The restriction digest did not confirm a successful digest. However, 4 colonies were selected from colonies #1-15 to continue.

Cyano
7/17/11 – PCR temp gradient was created for ThiE solution, used New England Biolabs phusion high-fidelity DNA polymerase protocol. Temp gradient ranges from 72-50 degrees Celsius. Controls of only DNA and only Primer were run with the samples. 10 ul samples were run for each temp gradient
7/18/11 - PCR results were run through a 1% agarose gel. Best results came from ‘F’ which ran at 54.3 Celsius. The DNA from this band was extracted and purified using QIAGEN Gel Extraction Kit
7/19/11 – PCR 50 ul of ThiE at 54.3 Celsius for backup stock. TOPO cloned ThiE that was extracted from gel yesterday. Plated TOPO cells at 100 ul, 75 ul, 50 ul and 25 ul concentrations then placed in incubator overnight
PCR reactions only need one control, of just the primers without DNA.
7/20/11 – 5 colonies of TOPO bacteria grew overnight. Cultured all 5 for purification and confirmation of proper insert (ThiE) Ran gel to confirm that 50 ul ThiE PCR worked, nice clean band at 1 kb marker, saved the rest of the 50 ul stock in -20 C freezer for further use. PCR done on the additional pieces (CmR, PetBD and GLF) used same temp gradient as done with ThiE. Will run a gel of these tomorrow to see what optimal temp is for each sample. If clean bands are seen, we will perform a gel purification and re-PCR those samples. Spoke with Shintani, these additional pieces should just be amplified through PCR until a clean stock is created, then this stock will be used in Gibson.
7/21/11 – Miniprep purified TOPO cultures. Sample “1” did not bloom in culture but grew on stock plate. Purified “2-5” and will save “1” as a backup if no other colonies have the correct insert. Ran temp gradient samples through gels.
GLF had very light bands at 67.6 and 63.5 Celsius temps, the average temp of those two is 65.5 – will try to run more DNA at this temp to see if we can get stronger bands. Maybe increase DNA concentration in solution.
*Shintani gave me his master stock solution of GLF (in puc vector) for next run of PCR. Diluted 1:9 of his solution and stored in freezer in PCR tube (with orange label) will try to PCR this stock at 65.5.
PetBD worked really well at several temps but 63.5 Celsius appears to be the best temp, strong band that was very clean. This worked out so well I might try just running a 50 ul solution at this temp and saving it as backup stock. Confirm the same clean band with a 5 ul run of solution through gel.
CmR did not work at all  I was told K56 was the integration vector sent from Utah State but was unable to confirm that in any of my team’s notebooks. Will double check with David today and see if he has that same number in his note book. If it is correct, maybe need to play with DNA concentration and temps again.
*E. coli group has extra CmR, will ask Megan to bring over some of this stock (pSB1C3 – iGEM vector) for next PCR. Shintani thinks that maybe vials were switched in the beginning (KmR PCR also not working) or something went wrong during purification.
With better stock will run temp gradient PCR on CmR again.
7/22/11: Gel for GLF at 65.5C yielded no bands. Ran PCR of GLF at 63.5C. Faint bands, attempted gel purification, will run confirmation gel on Monday. Ran PCR for PETBD (50ul), which also yielded no bands. Will run another gel for a shorter time period on Monday. Will discuss options/next steps on Monday with the group.

Procedure: PCR was reperformed on KnR, petBD, INV, and agp with a temperature gradient in order to determine the optimum initial annealing temperature for the different parts of the agp knockout-invertase operon. PCR reactions contained phusion DNA polymerase and DNA concentrations of 1 ng/ul reaction. The initial primer annealing temperatures used were 72.0, 70.3, 67.6, 63.5, 58.2, 54.3, 51.6, and 50.0 degrees Celsius. KnR, INV, and agp PCR products were run on .7% agarose gel at 110 V for 1 hour, and petBD PCR product was run on 1.5% agarose gel at 110 V for 1 hour.

Results: No bands were observed at the expected sizes (1360 bp for agp, 1341 bp for KnR, 209 for petBD, and 1768 bp for INV). Thus, the gibson assembly primers are to be reconstructed and reordered for future PCR reactions.

GLF (1605bp) and INV (1728bp) in the pUC57 (2710bp) ampicillin resistant vector were minipreped and 0.5mg of each sample of GLF and INV in the pUC57 ampicillin resistant vector were digested with EcoRI and PstI restriction enzymes and checked on a 1% agarose gel. GLF was properly digested showing bands at about 2000 bp and 1600 bp. Also, the GLF samples grew on chloromphenicol plates. Thus, two GLF samples were sent for sequencing at the Nevada Genomics Center to check if GLF was present in the pSB1C3 vector. The INV digest was not successful, producing a single band for all samples. Samples of GLF and INV in the pUC57 ampicillin resistant vector were obtained from Dr. Shintani and transformed in DH5α E.coli cells on AMP plates. The transformation was successful. As a result, 10 cultures were made for GLF and 10 cultures for INV in 2ml of LB-AMP liquid broth. The sequencing results for GLF from were checked. The sequencing was not complete. Thus, new primers were designed for further sequencing. The GLF and INV in the pUC57 cultures were minipreped and 0.5mg of all 10 GLF and INV minipreps were digested with EcoRI and PstI and checked along with 0.25mg of uncut GLF and INV on a 1% agarose gel. All digested samples for GLF showed two bands at 2700 bp and 1600bp. Samples 3 and 10 showed a third band at about 5000bp. All digested samples for INV showed two bands at 2700 bp and 1700bp. Samples 2 and 3 showed an extra third band at about 5000bp and sample 4 showed four bands, with the fourth band being above the 5000 bp band. Overall, eight GLF and seven INV digested samples appeared correct.

Enzymology
CL: This week we received the FFA assay kit and tested two BTE/PDC transformed cultures (+ 4 negative sigma70 controls); pellets and supernatants both were tested. Results were positive for one of the cultures and results suggested that fatty acids were present in the supernatant as opposed to the cell itself. We decided to do a time course growth on the identified culture.

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