Our initial idea to prove our concept of antitermination was to use flourescent proteins as reporters. This approach gives the opportunity to measure the termination and antitermination efficiency of our designed BioBricks in vivo as well as in vitro, the latter using a translation kit based on E.Coli lysate.
We decided to use the flourescent proteins GFP and RFP, as their spectra do not overlap and we would not measure any FRET. We would use GFP fluorescence as internal control and RFP fluorescence as signal to detect termination/antitermination by our switch we cloned in between the coding sequences of the proteins. Both protein sequences are under the control of one (L-arabinose induced) promoter.

When measuring the termination of our BioBricks and the antitermination by their corresponding signal-RNA, we should be able to observe an increasing RFP emission compared to the GFP emission upon induced signal-RNA production in the cells/in the kit:

Wiith these measurements, it should also be possible to observe differences in efficiency of termination as well as antitermination between our designed switches.

Measurements with the malachite green aptamer as reporter

A second possibility to measure parameters of our switches we came up with, was the idea to investigate our system on the transcriptional level only. Therefore, we decided to use malachite green as reporter. Malachite green in a fluorescent dye, whose emission increasing dramaticly (about 3000 times) upon binding of a specific RNA-aptamer.

#

---concept to be desribed, as well as literature--- <ref>refs</ref>

To study the switches on the transcriptional level gives the advantage, that we would have less interferences and possible artefacts. Also, we are not sure how cellular mechanisms like degradation of RNases or interacting factors as well as molecular crowding influence our systems.

We made constructs comprising of a sigma(70)-binding promoter followed by a short nonsense sequence, the switches and the aptamer sequence.
Also we made constructs, where the transcription of the signal-RNA is under the control of a sigma(70) promoter. These two linear DNA-constructs, together with the e.coli RNA-polymerase and the right buffer conditions should represent an easy-to-handle measurement kit on the transcriptional level.

Results

We ...blablabla Read more

Flourescent proteins

Unfortunatly, we had to change the reporter construct two times during our experiments as several problems occured in our measurements:

First Try: based on the measurement plasmid pSB1A10

At the beginning, we decided to use the reporter plasmid pSB1A10 from the registry. It consists of the fluorescent proteins eGFP and mRFP1. Each sequence includes a ribosome binding site and a stop-codon; the two genes are divided by a cloning side including the BioBrick cleavage sites.
In front of the eGFP sequence, the plasmid includes an arabinose-inducable promoter. The plasmid also contains an ampicilline resistence.

We cloned our switches into the cloning site of the measurement plasmid and used an empty cloning site as control; our signal-RNAs we cloned into the pSB1K3 vector, together with the BioBricks R0011 (Lac promoter) and B0014 (double terminator of transcription). Afterwards, we cut pSB1K3 with Aat2 and Pst1 and pSB1A10 with Nsi1 and Aat2 and ligated those fragments of each plasmid that contained our Bricks to get a Monsterplasmid.
We had to do so, as both plasmids contain the same ori mechanism. In addition, having both the switch and the signal RNA transcribed from the same plasmid gives us a high local concentration of the signal, once its transcription is induced.

We transformed BL21(DE3) cells with the plasmid. We set up cultures, induced the arabinose promoter and measured the GFP and mRFP1 excitation/emission spectra within time.

Unfortunatly, we were ot able to detect any RFP signal, not even in the positive control with no switch in between the GFP/RFP sequences.

From these experiments, we concluded, that the mRNA of the RFP variant used was instable and rapidly degraded by RNases, so the RFP was not synthesized in the cells. This was also the conclusion from XXX...

As solution to this, we decided to design a measurement plasmid ourselves:

---

Second Try: A measurement plasmid of our own design

To design our own plasmid to overcome the problems that occurred in our first try gave us tghe possibility to overcome several other problems:

Third Try: One promoter for each protein

We decided to use the measuremnt plasmid we developed in our second try but to clone another L-arabinose induced promoter into the plasmid, in front of our switch followed by the mCherry sequence.

In this way, we still can use GFP fluorescence as internal control, because both protein transcription is under the control of a promoter of identical design.

Though we are still not able to tell exactly why our previous measurements did not work, but with this construct we measured the first time fluorescence of the mCherry protein in our positive control.

On this page you can find our protocols for standard molecular biology procedure as well as the full notebook containing lab progress.

Protocols

Gels

Agarose Gels

• 1-3 % agarose gels were used
• TAE buffer
  • 0.4 M Tris
  • 0.01 M EDTA
  • 0.01 M acetic acid
  • pH=8.0

Stain

• SybrGold stain
  • Cover Gel with 1x TAE
  • Add SybrGold to a 1:10000 dilution
  • cover with aluminium foil (light sensitive)
  • shake&incubate 20 min (for 2% Agarose Gels at least 45 min!)

• SybrSafe
  • used just like SybrGold

Molecular weight marker

• all molecular weight marker were purchased from NEB
• in use:
  • low molecular weight
  • 1 kb
  • 2-log

Polyacrylamide Gels

• Preparation of denaturing gels

Gel type	1 big gel	2 big gels	1 small gel	2 small gels
Urea	28.8 g	57.6 g	x	x
Acrylamide 40%	22.5 ml	45 ml	x	x
Buffer 10x	6 ml	12 ml	x	x
End volume (reach by adding water)	60 ml	120 ml	x	x
APS	600 µl	1200 µl	x	x
TEMED	60 µl	120 µl	x	x

• Dissolve Urea in Acrylamide-buffer mixture (use Ultrasound bath), this may take more than an hour!
• Tighten the Gel chamber
• add water to desired end volume
• Add APS, then TEMED, mix
• Pipette mixture into gel chamber
• Add desired comb
• let gel polymerize overnight; add buffer in the evening

Running of Gels mix samples 1:1 with formamide loading dye (stored @ -20°C) carefully remove comb blow air into pockets with a 50 µl syringe fill samples into pockets run the gel (usually about 200 V)

PCR

used protocols

a) Taq Polymerase 'Hot Start'

PCR Pippeting plan:

1 µl template

1 µl dNTP 10 µM

1 µl G1004 (Primer) 10 µM

1 µl G1005 (Primer) 10 µM

5 µl 10x Taq-buffer  (500 mM KCl, 100 mM Tris-HCl (pH 8.3), 15 mM MgCl₂) 

0,2 µl Taq-Polymerase (add last) 5,000 U/ml

40.8 µl Water

Final volume 50µl

Processing: ( program saved as IGEMPCR )

• preheating of PCR chamber to 94 °C

   --> insert sample

• 2 min at 94 °C
• loop 35x:

     - 30 sat 94°C (according to IGEM protocols)

     - 30 s at 56 °C

     - 45s at 72°C

• 7 min at 72°C
• stay at 4°C
  

b) colony PCR

• Colony PCR
  • pick colonies and resuspend them in 20 µl LB+Antibiotic (each)
  • PCR of 2 µl of each sample, 2 µl as negative control (Program: ColonyPCR, modified), store remaining 18 µl for overnight cultures
  • afterwards, mix 15 µl of each PCR product with 3 µl GLPn and load to Gel
  • make overnight cultures of positive clones by adding the remaining 18 µl to 5 ml LB+AB

program:colonypcr '

• preheating of PCR chamber to 94 °C

   --> insert sample

• 5 min 30 sec at 94 °C
• loop 35x:
  • 30 sat 94°C (according to IGEM protocols)
  • 30 s at 58 °C
  • 60s at 72°C
• 7 min at 72°C
• stay at 4°C
  

DNA Purification

PCR samples

ZYMO RESEARCH DNA Clean&Concentration Kit

Protocol and Information

1. In a 1.5 ml microcentrifuge tube, add 2-7 volumes of DNA Binding Buffer to each volume of DNA sample (see table below). Mix briefly by vortexing.
   
   

Application	DNA Binding Buffer : Sample	Example
Plasmid, genomic DNA (>2 kb)	2 : 1	200 μl : 100 μl
PCR, cDNA, DNA fragment	5 : 1	500 μl : 100 μl
ssDNA (e.g., M13 phage)	7 : 1	700 μl : 100 μl

1. Transfer mixture to a provided Zymo-Spin™ Column1 in a Collection Tube.
   
2. Centrifuge at ≥10,000 x g for 30 seconds. Discard the flow-through.
   
3. Add 200 μl Wash Buffer to the column. Centrifuge at ≥10,000 x g for 30 seconds. Repeat wash step.
   
4. Add ≥6 μl water2,3 directly to the column matrix. Transfer the column to a 1.5 ml microcentrifuge tube and centrifuge at ≥10,000 x g for 30 seconds to elute the DNA.
   Ultra-pure DNA in water is now ready for use.
   

QIAquick purification Kit

Handbook

Procedure
1. Add 5 volumes of Buffer PB to 1 volume of the PCR sample and mix. It is not necessary to remove mineral oil or kerosene. For example, add 500 μl of Buffer PB to 100 μl PCR sample (not including oil).
2. If pH indicator I has beein added to Buffer PB, check that the color of the mixture is yellow. If the color of the mixture is orange or violet, add 10 μl of 3 M sodium acetate, pH 5.0, and mix. The color of the mixture will turn to yellow.
3. Place a QIAquick spin column in a provided 2 ml collection tube.
4. To bind DNA, apply the sample to the QIAquick column and centrifuge for 30–60 s. We changed it to 3 min @ 6000rpm !
5. Discard flow-through. Place the QIAquick column back into the same tube. Collection tubes are re-used to reduce plastic waste.
6. To wash, add 0.75 ml Buffer PE to the QIAquick column and centrifuge for 30–60 s.
7. Discard flow-through and place the QIAquick column back in the same tube. Centrifuge the column for an additional 1 min.repeat!
IMPORTANT: Residual ethanol from Buffer PE will not be completely removed unless the flow-through is discarded before this additional centrifugation.
8. Place QIAquick column in a clean 1.5 ml microcentrifuge tube.
9. To elute DNA, add 50 μl Buffer EB (10 mM Tris·Cl, pH 8.5) or water (pH 7.0–8.5) to the center of the QIAquick membrane and centrifuge the column for 1 min. Alternatively, for increased DNA concentration, add 30 μl elution buffer to the center of the QIAquick membrane, let the column stand for 1 min, and then centrifuge.
IMPORTANT: Ensure that the elution buffer is dispensed directly onto the QIAquick membrane for complete elution of bound DNA. The average eluate volume is 48 μl from 50 μl elution buffer volume, and 28 μl from 30 μl elution buffer. Elution efficiency is dependent on pH. The maximum elution efficiency is achieved between pH 7.0 and 8.5. When using water, make sure that the pH value is within this range, and store DNA at –20°C as DNA may degrade in the absence of a buffering agent. The purified DNA can also be eluted in TE buffer (10 mM Tris·Cl, 1 mM EDTA, pH 8.0), but the EDTA may inhibit subsequent enzymatic reactions.
10. If the purified DNA is to be analyzed on a gel, add 1 volume of Loading Dye to 5 volumes of purified DNA. Mix the solution by pipetting up and down before loading the gel.

Gel samples

ZYMO RESEARCH Gel DNA Recovery Kit

Product informartion

Protocol

1. Excise the DNA fragment1 from the agarose gel using a razor blade or scalpel and transfer it to a 1.5 ml microcentrifuge tube.
2. Add 3 volumes of ADB to each volume of agarose excised from the gel (e.g. for 100 μl (mg) of agarose gel slice add 300 μl of ADB).
3. Incubate at 37-55 °C for 5-10 minutes until the gel slice is completely dissolved2. For DNA fragments >8 kb, following the incubation step, add one additional volume (equal to that of the gel slice) of water to the mixture for better DNA recovery (e.g. 100 μl agarose, 300 μl ADB and 100 μl water).
4. Transfer the melted agarose solution to a Zymo-SpinTM I Column in a Collection Tube.
5. Centrifuge at ≥10,000 x g for 30-60 seconds. Discard the flow-through.
6. Add 200 μl of Wash Buffer to the column and centrifuge at ≥10,000 x g for 30 seconds. Discard the flow-through. Repeat the wash step.
7. Add ≥6 μl of water3,4 directly to the column matrix. Place column into a 1.5 ml tube and centrifuge ≥10,000 x g for 30-60 seconds to elute DNA.
   Ultra-pure DNA in water is now ready for use.
   

• add other kits here...

Restriction

Enzyme	10 units is sufficient, generally 1µl is used
DNA	1 µg
10X NEBuffer	5 µl (1X)
BSA	Add to a final concentration of 100 µg/ml (1X) if necessary
Total Reaction Volume	50 µl
Incubation Time	1 - 1.5 hour
Incubation Temperature Enzyme dependent	XbaI, SpeI, PstI, SpeI : 37 °C

activity of restriction enzymes in NEB buffers

Biobrick standard

Protocols for IGEM standard digestion

Dephosphorylation

using Antarctic Phosphatase

1. Add 1/10 volume of 10X Antarctic Phosphatase Reaction Buffer to 1-5 µg of DNA cut with any restriction endonuclease in any buffer.
2. Add 1 µl of Antarctic Phosphatase (5 units) and mix.
3. Incubate for 15 minutes at 37°C for 5´ extensions or blunt-ends, 60 minutes for 3´ extensions.
4. Heat inactivate (or as required to inactivate the restriction enzyme) for 5 minutes at 65°C.
5. Proceed with ligation.

from NEB

Ligation

Using T4 Ligase, New England Labs

• 1 µl T4 Ligase (10.000 U)
• 50 ng plasmid
• 3x mol(plasmid) insert
• 2 µl T4 Ligase 10x buffer
• add H₂O to reach final volume of 20 µl
  

• incubation at 22°C for 1 h
• storing at 16 °C for 40 min
  

Biobrick Standard

Standard BioBrick assembly

Transformation

At Woehlke's S1-Lab !!!

1. Thaw competent cells on Ice
2. Add DNA, pipette gently to mix
3. Let sit for 30 minutes on ice
4. Incubate cells for 45 seconds at 42°C
5. Incubate cells on ice for 2 min
6. Add 1 ml LB0
7. Incubate for 1 hour at 37oC on shaker
8. Spread 100-300 μl onto a plate made with appropriate antibiotic.
9. Grow overnight at 37 °C.
10. Save the rest of the transformants in liquid culture at 4 °C

modified from open wetware

Miniprep

Preparation of BioBricks from distribution 2008

Sequencing

• Monsterplasmids contain GATC-Standard-Primer pBR1 (CGAAAAGTGCCACCTGAC ) directly in front of AATII cleavage site.
• Monsterplasmids contain GATC-Standard-Primer pGFP-FP () approx. 100 bp upstream of Biobrick insert site.

 !!! Please always fill in iGEM-Sequencing-YYMMDD (e.g. iGEM-Sequencing-100625 for today´s date) as internal billing number!

Notebook