Team:GeorgiaTech/WeekTen

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10/3-10/9

10/3/10

 

For Today:

  1. Run on a gel
  1. aoxa, aoxb next to the troubleshooting pcrs from today, specifically of the PCRS using Ompa-F and Aoxa/b-R since they are similar sizes
  1. Take out plates from incubator. Record observations
  1. Run colony PCRs on at least 20 colonies per construct (yes 20)
  1. Check which primers to use for colony pcr! We can likely use the primers we already have
  2. Run results on gel

 

Results: plated colonies from 10/2/10 (Mitesh & Rob):

Observed that HybB-ompA-Aox1(a/b) constructs were successfully transformed- strong colony growth and red colonies (strange- given that these were supposedly constructs without RFP). The color strongly suggests RFP. Red colony patterns show no consistent trends- some are densely red in the middle of the plate, others mainly around the edges- red intensity varied widely even on the same plate.

 

 

Colony PCR of HybB-ompA-Aox constructs

Picked colonies from plates of HybB-ompA-Aox-RFP and added to 25 ul of water each,10 colonies from Aox1a containing plates, and 10 from Aox1b containing plates:

 

HybB-ompA-Aox1a-RFP: 1.5 mL Tubes 1-10

HybB-ompA-Aox1b-RFP: 1.5 mL Tubes 11-20

 

Used 5 ul for PCR, and added 250 ul of LB media to the rest.

 

Colony PCRs (for each colony): (Rob, Mitesh & Scott)

5 uL of cells

25.5 uL H2O

10 uL GOTAQ 5X Reaction buffer

5 uL HybB-F forward primer

5 uL RFP-R reverse primer

1 uL dNTP 10 mM - (thawed & kept on ice)

0.5 uL polymerase enzyme, TAQ

Total Volume= 50 uL

 

Colony PCRs (for each colony):

5 uL of cells

25.5 uL H2O

10 uL GOTAQ 5X Reaction buffer

5 uL HybB-F forward primer

5 uL Aox1a or b-R reverse primer

1 uL dNTP 10 mM - (thawed & kept on ice)

0.5 uL polymerase enzyme, TAQ

Total Volume= 50 uL

Important: For the PCR tubes, the ones labeled 1,3,5,7,9 are treated with Aox1a reverse primer.

All the even number (2,4,6,...16,18,20) labeled have RFP-R reverse primer in them. And the tubes labeled 11,13,15,17,19 have Aox 1bR reverse primer in them.

PCR start time: 6 PM

 

For Monday:

  1. Check colony pcr on a gel
  1. calculate the predicted sizes and compare to gel results
  1. Continue with colony PCRS if more info is required
  2. Check triple ligations on gel

 

10/4/2010

Protocols

 

1 % Gel to Check colony PCRs from 10/3/2010

Started at 9 am

Order:ladder:1-6|ladder|7-12|ladder|13-14

Important: For the PCR tubes, the ones labeled 1,3,5,7,9 are treated with Aox1a reverse primer.

All the even number (2,4,6,...16,18,20) labeled have RFP-R reverse primer in them. And the tubes labeled 11,13,15,17,19 have Aox 1bR reverse primer in them.

PCR start time: 6 PM

gel start at 10:34 am

 

Predicted Bands:

Hyb-F + RFP-R approx 2100-2200  bp

Hyb-F + Aoxa-R - approx 1500

Hyb-F + Aoxb-R approx 1500

 

Observations- 2200 bp band is seen, but other bands are also observed for the Hyb-F and RFP-R reactions

 

Suggestions:

  1. Troubleshoot by PCR sequencing the basic products (e.g. sequence just HybB in one tube, in the next, just OmpA; in the next, just AOX; in the next, just RFP). This will tell us whether each gene is actually present in the cells PCRed.
  2. Start over again entirely, from the very beginning, digesting each individual gene, ligating, transforming.
  3. Start using controls. When possible, include positive and negative controls.
  1. For example, when doing a double-ligation, for instance, perform experiment alongside designed to fail (e.g. lacking one of the ligation genes) for a negative control.
  2. To see if the plasmid pSB1A3 is causing our problems, transformed this plasmid alone directly into E. coli and plate.
  1. If pSB1A3 turns out to be the problem, can attempt to use a different plasmid backbone. We’ve researched and found plasmid pSB1C3 to have the desired characteristics, including lack of a  promoter, beginning EcoRI and ending SpeI restriction sites.

 

Plan to go forward:

1. Transform “plain” plasmid pSB1A3 into E. coli today 4 OCT 2010. Check for RFP expression.

2. In tandem with step 3, troubleshoot by sequencing the basic gene products in the “bad” HybB-OmpA-AOX contsructs, looking specifically for each gene.

3. In tandem with step 2, re-do the entire construction process from the individual genes up.

4. Transform cells using new biobrick vectors, like psb1c3, and use those instead of psb1a3!

 

NOTE: Need to make more media plates!

 

Protocols

 

Transformation of NB cells using pSB1a3

10 սL Nova Blue cells + 5 սL of pSB1A3 from MiniPrep

 

1. Left cells and plasmid on ice.

2. Added plasmid (5սL) to cells. Mix gently by swirling pipette tip in mixture (DO NOT ASPIRATE).

3. Left cells on ice for 30 min.

4. Applied heat shock of 45 seconds in 42C bath.

5. Put tubes on ice for 2 min.

6. Added 250 սL of LB (room temp.)

7. Incubated 1 hour at 37 C

8. Plated 100սL (x2 plates) and left plates in the 37 degrees incubator  

9. Incubated overnight at 37C.

 

Troubleshooting PCRs

For each test (e.g. HybB, OmpA, AOX1a, etc.)

2 uL of cells

9.4 uL H2O

4 uL GOTAQ 5X Reaction buffer

2 uL forward primer

2 uL reverse primer

0.4 uL dNTP 10 mM - (thawed & kept on ice)

0.2 uL polymerase enzyme, GOTAQ

Total Volume= 20 uL  

 

Combinations

A: HybB-OmpA-AOX1a-pSB1A3 in NovaBlue cells, ligated 2 OCT 2010 (Margo + Scott)

Selected 1 red colony, suspended in 20 uL sterile dH2O

1: HybB forward & reverse primers

2: OmpA forward & reverse primers

3: AOX1a forward & reverse primers

4: RFP forward & reverse primers

 

Selected 1 white colony, suspended in 20 uL sterile dH2O

5: HybB forward & reverse primers

6: OmpA forward & reverse primers

7: AOX1a forward & reverse primers

8: RFP forward & reverse primers

 

B: HybB-OmpA-AOX1b-pSB1A3 in NovaBlue cells, ligated 2 OCT 2010 (Margo + Scott)

Selected 1 red colony, suspended in 20 uL sterile dH2O

1: HybB forward & reverse primers

2: OmpA forward & reverse primers

3: AOX1a forward & reverse primers

4: RFP forward & reverse primers

 

Selected 1 white colony, suspended in 20 uL sterile dH2O

5: HybB forward & reverse primers

6: OmpA forward & reverse primers

7: AOX1a forward & reverse primers

8: RFP forward & reverse primers

 

P: “plain” mini-prepped pSB1A3 plasmid

        RFP forward & reverse primers

 

Ran a PCR on the samples using 1KB ladder -- ran A 1-7

Lane         1: ladder

2: A1

3: A2

4: A3

5: A4

6: A5

7: A6

8: A7

 

Note: need to make a big batch of 1% gels tomorrow since we are running so many samples.

Need more agarose from Gaucher Lab. COMPLETED

Need more EtBr. COMPLETED

Need a 100bp Ladder to see some of this stuff (small constructs) -- we might need to get Ryan to order some.

 

10-5-10

Obtain some more agarose and EtBr from Gaucher lab.

Make 1% gels.

See Protocols page for Preparing 1% Agarose Gels

Ran a gel on the remaining PCR samples from 10-4-10

Following 1 KB ladder, lanes should read in order:

A8, P, B1, B2, B3, B4, B5, B6, B7, B8.

No digital picture available, but one was printed and is in the lab, labelled with the date.

 

  1. Starting construct building strategy over again
  1. Reactions:
  1. HyBb F,R (template biobrick)
  2. OmpA F,R (template ompa vector)
  3. Aox1a F,R (template synthesized gene)
  4. Aox1a F,R2 (template synthesized gene)
  5. Aox1b F,R (template synthesized gene)
  6. Aox1b F,R2 (template synthesized gene)
  7. RFP F,R (template RFP plasmid) (from 9.27.2010 miniprep)
  8. RFP F2,R  (template RFP plasmid) (from 9.27.2010 miniprep)

 

PCR Protocol (Scott)

  1. 26.5 uL H2O
  2. 10 uL PHUSION 5X Reaction buffer
  3. 5 uL forward primer
  4. 5 uL reverse primer
  5. 1 uL dNTP 10 mM - (thawed & kept on ice)
  6. 2 uL template DNA
  7. 0.5 uL polymerase enzyme, PHUSION

Total Volume= 50 uL

started 4:33pm

 

10/6/2010

Goals

  1. The gel from 10/5/2010 of the troubleshooting pcrs, specifically the reaction of pSB1A3 with RFP-F and R, suggests that the vector used for ligation has RFP. We will use anothe rvector from biobrick
  2. We want to transform cells with the new biobrick vector today, miniprep the cells tomorrow morning, digest, and ligate to our hyb.ompa+aox that we have or are making now. Finish by friday is the goal.
  3. Sequence hyb-RFP (for bronze medal requirements)
  4. begin hyb-ompa-rfp building when primers come in
  5. I saw Richard’s sequence was for psb1c3, but we are using psb1a3; this may a primer and digests! Investigate!
  6. Sequence white colonies from the plates on 10/3/2010
  7. For today:
  1. Reconstitute new biobrick vector (psb1A7) COMPLETED
  2. Transform NB cells using new biobrick vector COMPLETED
  3. Check PCRs from 10/5/2010 on gel (tubes in yellow pcr box labeled 1-8 and dated 10.5) COMPLETED
  4. Make Amp plates
  5. Autoclave pipette tips
  1. This involves testing which tips are compatible with ours (we have lots of random tips)

 

Notes on Vector-

Here is an experience from another team concerning transcription of a product during an “off state”:

 

Our team (Davidson College) has used this vector in E. coli strain JM109 extensively. Clones are Amp resistant and are recovered in reasonable yields from mini preps. One drawback is that the vector has read-through transcription that comes into the cloned BioBrick part from both directions. This problem is a major one when an "off state" is critical for the control of a device. Parts without a promoter are expressed in this vector, regardless of orientation (see pSB1A7 Part Design for details). Reverse read-through might be from the Amp resistance gene. Forward read-through might be from a cryptic promoter, since no known genes in the backbone are in the plus orientation.

--Kahaynes 15:48, 23 October 2006 (EDT)

 

Alternative vectors:

  1. pSB1A7 (2010 Kit plate 3, 15G well, name BBa_K126000)
  1. Reasons:
  1. There are double terminators on either side of the multiple cloning site that block any read through or unwanted transcription from the plasmid promoters (plasmid promoters are involved in antibiotic production)
  2. Ampicillin resistance
  3. Already in kit

 

 

Protocols

1. Resuspend psb1A7 DNA in 10uL of autoclaved water.

 

 

3. Run gels of PCR’s on 10-5-10.

 

Order:

  1. HyBb F,R (template biobrick)
  2. OmpA F,R (template ompa vector)
  3. Aox1a F,R (template synthesized gene)
  4. Aox1a F,R2 (template synthesized gene)
  5. Aox1b F,R (template synthesized gene)
  6. Aox1b F,R2 (template synthesized gene)
  7. RFP F,R (template RFP plasmid) (from 9.27.2010 miniprep)
  8. RFP F2,R  (template RFP plasmid) (from 9.27.2010 miniprep)

 

Growing colony of pSB1a3 transformed cells (Scott)

I picked 3 colonies from the plate marked “MFC 9.15.2010 C1 “ from 9.15.2010, with the psb1a3 transformed cells that are slighty pink. I did 3 mL + 3 uL of Carb, and put them in the incubator.

 

PCR of pSB1A3 (direct from well aliquot) using RFP-F,R

  1. 27.5 uL H2O
  2. 10 uL GoTaq 5X Reaction buffer
  3. 5 uL forward primer (RFP-F)
  4. 5 uL reverse primer (RFP-R)
  5. 1 uL dNTP 10 mM - (thawed & kept on ice)
  6. 1 uL template DNA
  7. 0.5 uL polymerase enzyme, GoTaq

Total Volume= 50 uL

Left in block B- Thursday people need to retieve it- Need to gel purify- scroll down to see a lit of things to do for Thursday. These steps are also highligted in blue below.

PCR of mRFP miniprep (direct from well aliquot) using RFP-F3,R

  1. 26.5 uL H2O
  2. 10 uL GoTaq 5X Reaction buffer
  3. 5 uL forward primer (RFP-F3)
  4. 5 uL reverse primer (RFP-R)
  5. 1 uL dNTP 10 mM - (thawed & kept on ice)
  6. 2 uL template DNA
  7. 0.5 uL polymerase enzyme, GoTaq

Total Volume= 50 uL

Left in block B- Thursday people need to retieve it  - Scott knows what to do with this. I don’t. -Debika

 

 

Transformation of NB using pSB1A3 direct from Gel aliquot) -completed (Christina, Debika)

10 սL Nova Blue cells + 5 սL of pSB1A3 from MiniPrep

 

1. Left cells and plasmid on ice.(Scott)

2. Added plasmid (5սL) to cells. Mix gently by swirling pipette tip in mixture (DO NOT ASPIRATE).

3. Left cells on ice for 30 min.

4. Applied heat shock of 45 seconds in 42C bath. (Debika)

5. Put tubes on ice for 2 min. (I messed up and put in LB in a minute instead of 2 minutes. Left it in ice again for a minute after adding LB). Don’t know how that will affect our results. Sorry if this transformation doesn’t work).

6. Added 250 սL of LB (room temp.)

7. Incubated 1 hour at 37 C

8. Plated 100սL (x2 plates) and left plates in the 37 degrees incubator. (Christina)  

9. Incubated overnight at 37C.  

 

Transformation of NB using pSB1A7 direct from Gel aliquot) -completed (Christina)

10 սL Nova Blue cells + 5 սL of pSB1A3 from MiniPrep

  1. Add 1uL of resuspended psb1A7 in 10uL of competent cells (Novablue). (thawed on ice)

See Protocols page for Heat Shock Transformation

 

Note: The incubation step was skipped, which likely will lead to little growth

 

Meeting Notes

Priority List

Critical (bronze medal)

  1. hyb.ompa.aox construct (in pSB1A7)
  2. hyb.ompa.RFP construct (in pSB1A7) (Scott)
  3. Sequencing of constructs and conformation with standard
  4. Biobrick

Need (silver)

  1. Calorimetric/Heat  (Rob, Christian)
  2. Periplasmic Expression Picture (Fluorescent Microscope) (Scott)
  3. Cold Shock Quantification (hybB)
  4. Modeling (Gita, Mitesh)
  1. Liquid culture
  2. Solid Media

        Want

  1. Confirm pSB1A3 has RFP in it
  1. Pick colony from plates, liquid culture. (COMPLETED)(SCOTT)  “MFC 9.15.2010 C1 “

Thursday: Mini-prep, off to sequencing. Ask Ryan or Megan

    ii     Aliquot from well, PCR (COMPLETED, DEBIKA, left in right side block overnight)

Thursday: gel purify, off to sequencing. Ask Ryan or Megan

 

Detailed Plan

Today (wed)

Critical Actions

  1. hyb.ompa.rfp construct
  1. Start PCR of RFP using new primer using a plasmid with ryan’s rfp (pcold and rfp, or the gaucher lab rfp plasmid) (Debika, completed)

 

Want Actions

  1. confirm PSB1A3 has RFP
  1. Scott
  1. Pick colony from original psb1a3 plates  “MFC 9.15.2010 C1 “ and put in liq culture (completed)
  1. Debika
  1. Start PCR of psb1a3 directly from well, using primers RFP-F and RFP-R (Debika, completed)
  1. Christina, Debika,
  1. transformation of NB cells using original psb1a3 aliquot (completed)

 

Other Actions

  1. order psb1a7 sequencing primers (the forward psb1a3-F primer is ok, but we need a reverse primer)

 

Thursday

  1. perform a heat shock transformation of psb1a7 -- this could not be done on Wed. because no plates were left to perform this. Had to make plates first.
  1. Add 1uL of resuspended psb1A7 in 10uL of competent cells (Novablue). (thawed on ice)

See Protocols page for Heat Shock Transformation

 

  1. Mini-prep of psB1A3, send sequence w/ RFP F,R
  2. Gel-purify psb1A3 pcr, send off to sequencing w/ RFP F,R

Friday

  1. Start liquid culture of psB1A7
  1.  
  2. Digest - Debika (12-2 pm)
  3. Ligate, transform - Mitesh, Scott (5pm)

Saturday

  1. Colony PCR of constructs (10 each)
  2. Mini-prep of psb1A7- Scott (9am)
  3. Run gel
  1. hybB F, AOX R
  2. hybB F, ompA R
  3. ompA F, AOX R

 

Need controls for everything from now on!

 

Controls: (Can’t read Scott’s handwriting, sorry Scott! This stuff is still on the whiteboard in the lab)

Ligate

  1. leave out a piece of the ligation so we know it won’t work (- control)
  2. continue to use this throughout the transformation

Transformation control

  1. Just digest psB1A7 use it to transform (negative control

 

10/7/2010 (Thursday)

GOALS:

 

  1. perform a heat shock transformation of psb1a7 -- this could not be done on Wed. because no plates were left to perform this. Had to make plates first. (completed Christina, Rob)
  1. Mini-prep of psB1A3 (completed, Christina, Rob)
  2. send sequence w/ RFP F,R
  3. Gel-purify psb1A3 pcr, send off to sequencing w/ RFP F,R
  1. Make gel in Hammer Lab Chamber (the orange one) (gel completed, christina)
  1. Gel tray is max 80 or so ml
  2. perform gel extraction (I can do this in afternoon, scott)

 

Results and Observations from plates made on 10-6-10:

  1. psb1a3 had growth; no pink colonies (may be slight, can ask Ryan as she is expert)
  1. made a starter culture from these plates and see if they turn pink.
  1. psb1a7 had no growth - plates thrown out.

 

Protocols:

 

Moved the plates of the psb1a7, psb1a3 transformations to fridge -- psb1A7 plates thrown out. (Scott)

 

Make starter cultures from psb1A3/NB plates made on 10/6/10.(Christina)

 

perform a heat shock transformation of psb1a7 -- this could not be done on Wed. because no plates were left to perform this. Had to make plates first (Christina)

Add 1uL of resuspended psb1A7 in 10uL of competent cells (Novablue). (thawed on ice)

See Protocols page for Heat Shock Transformation

 

Mini-prep of psB1A3 from starter cultures grown on 9-6-10 (Christina)

 

Autoclaved a variety of pipette tip boxes to stock up(Christina)

 

make a new 1% gel in the orange pcr chamber (the chamber is the casting tray -- GENIUS!) (Christina)

See Protocols page for Preparing 1% Agarose Gels

 

PCR purifcation of psb1a3 pcr wiith RFP-F, RFP-R

See Protocols page for PCR Purifacation

 

Gel extraction of PCR from psb1a3 using primers RFP-F, RFP-R (Scott, Gita)

1. Excised DNA fragment from the agarose gel with a clean, sharp scalpel.

2. Weighed the gel slice in a colorless tube. Add 3 volumes of Buffer QG to 1 volume of gel (100 mg or approximately 100 μL).

3. Incubated at 50ºC for 10 min (or until the gel slice had completely dissolved). To help dissolve gel, mixed by vortexing the tube every 2 – 3 min during the incubation.

4. After the gel slice has completely dissolved, checked that the color of the mixture is yellow (similar to Buffer QG without dissolved agarose).

5. Added 1 gel volume of isopropanol to the sample and mixed.

6. Placed a QIAquick spin column in a provided 2 mL collection tube.

7. To bind DNA, applied the sample to the QIAquick column, and centrifuged for 1 min.

8. Discarded flow-through and placed QIAquick column back in the same collection tube.

9. Recommended: Added 0.5 mL of Buffer GQ to QIAquick column and centrifuged for 1 min.

10. To wash, added 0.75 mL of Buffer PE to QIAquick column and centrifuged for 1 min.

11. Discarded the flow-through and centrifuged the QIAquick column for an additional 1 min at 17,900 x g (13,000 rpm).

12. Placeed QIAQuick column into a clean 1.5 mL microcentrifuge tube.

13. To elute DNA, added 30  μL water (pH 7.0 – 8.5), let the column stand for 1 min, and then centrifuged for 1 min.

 

RE Digest Recipe for RFP-F3R (that Debika did this yesterday)(Christian is doing the digest today)

12.5 uL H20

5uL 10X Promega Buffer B

6 uL RFP-F3R (167.4 ng/uL 10.6.2010)

5 uL BSA (1ug/uL, to a final conc of .1mg/ml)

0.75  uL SpeI

0.75  uL XmaI

Total=50 ul total

Run 3 hours in the heating block in our lab (37c, put water in the heating blocks)

Start 5pm

 

10/8/2010

Goals

  1. Nanospec the gel extract done on 10/7/2010 (of psb1a3 RFP-FR, 700 bp band)
  2. Run 4 uL of the gel extract on the gel and take picture (to prove psb1a3 has rfp!)
  3. Send off for sequencing:
  1. gel extract with RFP FR
  2. the miniprep of psb1a3 with RFP FR (miniprep from thursday)
  1. Repeat transformation of psb1a7!
  2. PCR purification of digest from (10/7/2010) of RFP F3R

See Protocols page for PCR Purification

  1. run on gel to check for 700 bp band
  2. if ok, then
  1. ligate to Hyb.ompa and psb1a3 or psb1a7 (which vector)?

Observations

The transformation of psb1a7 into NB did not work. We should check whether the strain is compatible with the plasmid.  

The colonies from the transformation of psb1a3 directly from well into NB have turned slightly pink.

Liquid cultures of psb1a3 colonies from plates from 10.6.2010 appear brown with no pink. However, when we pelleted them for miniprep, the pellet was pink!

 

minprep of psb1a3 liq culture from palte from10.6.2010

 

Transformation of pSB1A7 in NB cells (with + control)

Megan suggested we use fresh NB cells (from Gaucher cells), use a positive control (known good plasmids)

2 reactions:

10 սL Nova Blue cells + 5 սL of mRFP from Gaucher Lab (labeled mRFP miniprep 3/11/09)

10 սL Nova Blue cells + 2սL of psb1a7 from  well aliquot

1. Left cells and plasmid on ice.(Scott)

2. Added plasmid (5սL) to cells. Mix gently by swirling pipette tip in mixture (DO NOT ASPIRATE).

3. Left cells on ice for 30 min.

4. Applied heat shock of 45 seconds in 42C bath. (Debika)

5. Put tubes on ice for 2 min.

6. Added 250 սL of LB (room temp.)

7. Incubated 1 hour at 37 C. - Scoot will take over from here. I left 4 plates for you on the bench Scott- Debika

8. Plated 100սL (x2 plates) and left plates in the 37 degrees incubator.

9. Incubated overnight at 37C.  (Scott)

 

PCR purification of digest from (10/7/2010) of RFP F3R (Gita)

See Protocols page for PCR Purification

notes: elute in 30 uL!

 

Nanospec

  1. purified digest of RFP-F3R (labeled with 10.8.2010) = 18.1 ng/uL
  2. Gel extract of RFP FR (tube labeled 1, date 10.7.2010) = 84 ng/uL
  3. Gel extract of RFP FR (tube labeled 2, date 10.7.2010) = 91.3 ng/uL
  4. psb1a3 miniprep
  1. tube 1: 64 ng/uL
  2. tube 2 :56 ng/uL

 

Run on 1% gel

  1. Gel extractions from 10.7.2010 of psb1a3+ RFP-FR (2 tubes)
  2. purified, digested RFP-F3R from today, 10.8.2010

 

 

For tomorrow

  1. high priority
  1. pick colonies of psb1a7 (if succesful) and transfer to liquid culture
  2. tranform cells using psb1c3, since it is the vector we have to submit in.
  3. ligate RFP F3R to hyb.ompa and psb1a7 (likely have to be done sunday)
  1. autoclave more water
  2. Find some chloramphenicol since we have to submit parts in psb1c3 and it has chloramphenicol resistance
  3. low priority
  1. run pcr on psb1a3 minipreps today to check for rfp

 

10/9/2010

Goals

  1. Troubleshoot psb1a7, psb1a3
  1. List of wells, inserts, and sequences (http://partsregistry.org/assembly/libraries.cgi?id=31)

Notes

  1. Troubleshoot psb1a7
  1. does it have a cbbd toxic gene in it?
  1. No, it has an insert coding for a antibody chain, part: K126000

(http://partsregistry.org/wiki/index.php?title=Part:BBa_K126000) (http://partsregistry.org/assembly/plates.cgi?id=1259)

 

  1. can we digest (is it digested) and ligate it directly from the well to our parts?
  1. should we pcr it first?
  1. do we have a ccdb tolerant strain?

 

  1. Trobuleshoot psb1a3
  1. psb1a3 has RFP (http://partsregistry.org/partsdb/get_part.cgi?part=pSB1A3)
  2. BBa_J04450 = RFP
  1. tranform cells using psb1c3, since it is the vector we have to submit in.
  1. Have plasmid backbone from kit (Where is it?)
  2. Has RFP insert for in well Plate 1 - A3 (http://partsregistry.org/assembly/plates.cgi?id=1257)

 

Protocols

RE Double Digest Recipe for pSB1A3 (from 10/8/2010)

6.5 uL H20

3uL 10X Promega Buffer E

16 uL pSB1A3 (10.8.2010, 64 ng/uL)(tube 1)

3 uL BSA (1ug/uL, to a final conc of .1mg/ml)

0.75 uL SpeI

0.75 uL EcoRI

Total=30 ul total

Run 3 hours in the heating block in our lab (37c, put water in the heating blocks)

Predict a insert (1000 bp) and plasmid (2000 bp)

RE Digest Recipe for pSB1A3 (from 10/8/2010)

5.0 uL H20

2.5 uL 10X Promega Buffer E

16 uL pSB1A3 (10.8.2010, 50 ng/uL)(tube 2)

3 uL BSA (1ug/uL, to a final conc of .1mg/ml)

0.75 uL SpeI

Total=30 ul total

Run 3 hours in the heating block in our lab (37c, put water in the heating blocks)

Digest start::12pm

For Tomorrow:

  1. PREFORM PCR on WHITE colonies to check for what is in them: triple ligation plates from Oct
  2. Ask Gaucher lab if they have 1) ccdb resistance strains 2) vector lacking promoters and have amp resistance 3) the three tubes of plasmid backbone from the standard iGem kit
  3. Need more Promega Buffer E

 

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