Team:METU-Ankara

From 2011.igem.org

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<h2>Lab Protocols</h2>
<h2>Lab Protocols</h2>
<h3>Clonning procedures</h3>
<h3>Clonning procedures</h3>
-
 
+
<ol type="1">
 +
      <li><strong>Getting the DNA parts</strong></li>
 +
              <ol type="a">
 +
              <li><strong>For parts in kit plates</strong></li>
 +
  </b>
 +
                    <ol>
 +
                    <li>With a pipette tip, punch a hole through the foil cover into the corresponding well of the Biobrick<sup>TM</sup>-standard part that you want.</li>
 +
                    <li>Pipette 10 uL of dH2O (distilled water) into the well. Pipette up and down a few times and let sit for 5 minutes to make sure the dried DNA is fully re-suspended.</li>
 +
                    <li><a href="http://partsregistry.org/Help:Transformation_Protocol" target="_blank">Transform</a>
 +
1 or 2 uL of the re-suspended DNA into desired competent cells, plate your transformation with the appropriate antibiotic and grow overnight.</li>
 +
                    <li>Pick a single colony and inoculate LB medium (again, with the correct antibiotic) and grow for 16 hours.</li>
 +
                    <li>Use the resulting culture to <a href="http://openwetware.org/wiki/Miniprep/Kit-free_high-throughput_protocol" target="_blank">miniprep</a> the DNA and make your own glycerol stock.</li>
 +
                    </ol>
 +
 +
              <li><strong>For new synthesized DNA parts</strong></li>
 +
                   
 +
                    <ol>
 +
                    <li>The DNA parts are sent in nmol values in each. These data are determined for all of them individually</li>
 +
                    <li>As a stock solution preparation, these DNA parts are pipetted with PCR water or TE buffer which is 100 times of DNA amount. The final solution is prepared as 100uM.</li>
 +
                    <li>For each transformation procedures, the 10uM of stock DNA part in water is transformed. 1uL is taken from stock DNA solution and is added to 9uL PCR water.</li>
 +
                    </ol>
 +
              </ol>
 +
              <li><strong>Preparation  of Competent Cells</strong>
 +
                <ol>
 +
                  <ol>
 +
                    <li>Inoculate a single colony of E. Coli cells into 50 ml  LB medium. Grow overnight at 37 C with moderate shaking (250rpm)</li>
 +
                    <li>Inoculate  4 mL of the culture into 400 mL LB medium in a sterile 2-liter flask. Grow at  37 C shaking at 250 rpm to an OD590 of 0.375.
 +
                      <p><em>This  procedure requires that cells be growing rapidly (early- or mid-log phase).  Accordingly, it is very important that the growing cells have sufficient air.  Overgrowth of culture (beyond OD590 of 0.4) decreases the efficiency of  transformation.</em>                        </p>
 +
                    </li>
 +
                    <li>Aliquot culture into eight 50 mL prechilled, sterile polypropylene tubes and leave the tubes on ice 5 to 10 min.
 +
                      <p><em>Cells should be kept cold for all subsequent steps.<br />
 +
                      Larger tubes or bottles can be used to centrifuge cells if volumes of all subsequent solutions are increased in direct proportion. </em>                        </p>
 +
                    </li>
 +
                    <li>Centrifuge  cells 7 min at 1600 g (3000 rpm in JS -5.2),   4 C.</li>
 +
                    <p>Allow  centrifuge to decelerate without breake.<br />
 +
                      <em>We have not  attempted to determine whether deceleration without braking is critical to this  procedure. However, we do not use the breake for this step or for the  subsequent centrifugation steps. </em>                    </p>
 +
                    <li>Pour off subernant and resuspend each pellet in 10 ml ice-cold CaCl2 solution.Re-suspension should be performed very gently and all cells kept on ice.</li>
 +
                    <li>Cetrifuge cells 5 min at 1100  g, 4 C. Discard supernatant and re-suspend each pellet in 10 mL ice-cold CaCl2 solution. Keep re-suspend cells on ice for 30 min.</li>
 +
                    <li>Centrifuge cells 5 min at 1100 g, 4 C. Discard supernatant and re-suspend each pellet in 2 mL ice-cold CaCl2 solution.
 +
                      <p><em>It is important to re-suspend this final pellet well. The suspension may be left on ice for several days.</em>                        </p>
 +
                    </li>
 +
                    <li>Dispense cells into prechilled, sterile polypropylene tubes (250 ml aliquots are convenient). Freeze immediately at -70 C.</li>
 +
                  </ol>
 +
                </ol>
 +
              </li>
 +
              <li><strong>Transformation</strong>              </li>
 +
 
 +
  <ol>
 +
                <ol>
 +
                  <li>Aliquot  10 ng of DNA in a volume 10 to 25  mL  into a sterile 15 mL round bottom test tube and place on ice.</li>
 +
                  <p><em>Plasmid DNA  can be used directly from ligation reactions. When this is done , more DNA is  usually used. However, if there is &lt;1 mg of DNA in the ligation reaction, or  if the ligation reaction is from low gelling/melting temperature agarose, it is  wise to dilute the ligation mix.</em></p>
 +
                  <li>Rapidly  thaw competent cells by warming between hands and dispense 100 mL immediately  into test tubes containing DNA. Gently swirl tubes to mix, then place on ice  for 10 min.</li>
 +
                  <p><em>Competent  cells should be used immediately after thawing. Remaining cells should be  discarded rather than refrozen</em></p>
 +
                  <li>Heat  shock cells by placing tubes into a 42 C water bath for 2 min</li>
 +
                  <p><em>Alternatively  incubate at 37 C for 5 min.</em></p>
 +
                  <li>Add 1 ml  LB medium to each tube. Place each tube on a roler drum at 250 rpm for 1 hr at  37 C.</li>
 +
                  <li>Plate  aliquots of transformatin culture on LB /ampicillin or other approprate  antibiotic- containing plates.</li><p><em>It is  convenient to plate several different dilutions of each transformation culture.  The remainder of the mixture can be stored at 4 C for subsequent platings.</em></p>
 +
                  <li>When  plates are dry, incubate 12 to 16 hr at 37 C.</li>
 +
                </ol>
 +
  </ol>
 +
  <li><strong>Plasmid isolation</strong></li>
 +
  <p>This procedure is performed with Fermentas GeneJET™ Plasmid Miniprep Kit</p>
 +
  <ol>
 +
    <ol>
 +
      <ol>
 +
      </ol>
 +
                <li>Pick a single  colony</li>
 +
                <li> Inoculate  in 5 mL LB medium for high-copy or 10 mL for low-copy of LB medium supplemented  with the appropriate selection antibiotic.</li>
 +
                <li> Incubate at  225 rpm not longer than 12-14 h at 37 C .</li>
 +
      <li> Centrifuge  at 4000 rpm for 5 min at 4 C .</li>
 +
                <li> Discard the  supernatant and keep pellet.</li>
 +
                <li>  Resuspended  the pellet with 250 ul  Resuspension solution. (Bacteria should be resuspended completely by vortexing  until no cell clumps remain)</li>
 +
                <li>Transfer the  cell suspension to eppendorf.</li>
 +
         
 +
                <li> Add 250 uL Lysis Solution and mix gently by  inverting the tube 4-6 times until the solution becomes slightly clearPlate  aliquots of transformatin culture on LB /ampicillin or other approprate  antibiotic- containing plates.</li>
 +
        <p><em>Do not  vortex!</em><br />
 +
        <em>Do not incubate for more than 5 min. (To avoid denaturation of  supercoiled plasmid DNA!)</em></p>
 +
        <li>Add 350  uL Neutralization solutionand mix immediately and throughly by inverting the  tube 4-6 times.</li>
 +
        <p><em>(The neutralized bacterial lysate is cloudy and viscous)  (&quot;throughly&quot; to avoid localized precipitation of bacterial cell  debris)</em></p>
 +
        <li>Centrifuge  at 13000 rpm for 5 min to precipitate cell debris and chromosomal DNA.</li>
 +
        <li>Transfer  the supernatant to spin column (about 600 uL).</li>
 +
        <p><em>(Avoid disturbing or transferring the white precipitate)</em></p>
 +
        <li>Centrifuge  at 13000 rpm for 1 min.        </li>
 +
        <li>Discard  the flow-through.        </li>
 +
      <li> Place the  column back into same collection tube.</li>
 +
        <li> Add 500 uL  Wash solution to spin column.</li>
 +
        <li> Centrifuge  at 13000 for 1 min</li>
 +
        <li> Discard  the flow-through.</li>
 +
        <li> Repeat  this step with using 500 uL Wash solution.</li>
 +
        <li> Discard  the flow-through</li>
 +
        <li> Centrifuge  at 13000 rpm for an additional 1 min to remove residual<strong> </strong>Wash solution.<br />
 +
          (This step is  essential to avoid residual ethanol in plasmid preps)</li>
 +
        <li> Transfer spin column into a fresh 1.5 mL epp.</li>
 +
        <li> Add 50 uL Elution buffer into center of the  spin column membrane to elute the plasmid DNA</li>
 +
        <p><em>Do not contact the membrane with pipette tip!</em></p>
 +
        <li>Incubate  for 2 min at 25 C.  </li>
 +
        <p><em>To increase  yield incubation is done for 2 min at heat block at 42 C</em></p>
 +
        <li>Centrifuge  at 13000 for 2 min.</li>
 +
        <li>Discard  the column and store the purified plasmid DNA at -20 C.</li>
 +
        <p><em>OPTIONAL= additional elution step with elution buffer or water. This  step increases the yield by 10-20 %.</em><br />
 +
          <em>NOTE:  For elution of plasmids ≥ 20 kb, prewarm  Elution buffer to 70 C before applying.</em></p>
 +
    </ol>
 +
  </ol>
 +
  <li><strong>Restriction  digestion</strong></li>
 +
 
 +
  <p>This procedure  is performed with NEB  BioBrick™ Assembly  Kit</p>
 +
 
 +
<ul>
 +
  <li>Digest  Upstream Part with EcoRI-HF and Spel<br />
 +
    500 ng  Upstream Part Plasmid<br />
 +
    1 uL EcorI-HF<br />
 +
    1 uL Spe I<br />
 +
    5 uL  10*NE  Buffer 2<br />
 +
    0.5 uL 100*  BSA<br />
 +
    To 50 uL add  dH2O<br />
 +
    <br />
 +
  </li>
 +
  <li>Digest  downstream part will  Xbal and PstI<br />
 +
    500 ng  Downstream Part Plasmid<br />
 +
    1 ul XbaI<br />
 +
    5 uL 10*NE  Buffer 2<br />
 +
    0.5 uL 100*  BSA<br />
 +
  To 50 uL add  dH2O<br />
 +
  <br />
 +
  </li>
 +
  <li>Digest  the destination plasmid with EcorI-HF and Pst I:</li>
 +
 
 +
<p>The destination plasmid DNA should either be prepared with PCR or  contain the toxic gene (e.g, ccdB, sacB) in the cloning site to avoid the need  for gene purification.<br />
 +
The Destination Plasmid should also have a different antibiotic  resistance marker from both the plasmid containing the Upstream Part and the  plasmid containing the Downstream Part to avoid the need to purify the Upstream  and Downstream Parts.<br />
 +
500 ng  Destination Plasmid DNA<br />
 +
1 uL EcorI- HF<br />
 +
1 uL PstI<br />
 +
15 uL 10* NE  Buffer 2<br />
 +
0.5 uL 100*BSA<br />
 +
To 50 uL add  dH2O<br />
 +
 <br />
 +
Incubate all 3  restriction digest reactions at 37 C for 10 min and then heat inactivate at 80  C for 20 min.</p>
 +
</ul>
 +
<li><strong>AGE (Confirmation)</strong></li>
 +
<h3>Background</h3>
 +
<ul><li>EtBr stains only dsDNA. You cannot see ssDNA on gel</li>
 +
<li>Minimum amount of DNA load:</li>
 +
<p>200 ng (Aysu)<br />
 +
  •  Each band of 1kb ladder is approx. 125 ng (2.5 ul loaded) and can be seen on gel</p>
 +
</ul>
 +
 
 +
<h3>Preparetion</h3>
 +
<ul><li>50X TAE (Tris-Acetate) Buffer<br />
 +
 
 +
121 g/0.5 L Tris<br />
 +
28.6 g/0.5 L Glacial Acetic Acid
 +
<br />
 +
7.31 g/0.5 L EDTA
 +
<br />
 +
pH 8.0<br />
 +
 
 +
</li>
 +
<li>Sterile 1.5 mL eppendorf tubes</li>
 +
<li>Sterile long pipette tips</li>
 +
<li>DNA standards
 +
  <ul>
 +
    <li>  [Aysu]: Promega 1.0 kb (1.0-10Kbp), 100 bp (0.1-1.0 Kbp)</li>
 +
  </ul>
 +
</li>
 +
<li>TAE Buffer</li>
 +
<li>EtBr sln (10 mg/mL). Purchase as solution ! Store at RT. <strong>Light-sensitive and carcinogenic !</strong></li>
 +
<li>Sample loading buffer. Store at 4 C.</li>
 +
</ul>
 +
<h3>Protocol</h3>
 +
<ul><li>Prepare 360 ml, 1X TAE running buffer</li>
 +
 
 +
 
 +
  <li>Prepare  gel compartment with tape (do not use parafilm)</li> 
 +
  <li>Prepare  60 ml, 1% agarose gel (0.6 g agarose <u>in 60 ml</u> <u>1X TAE buffer)</u>
 +
    <ul>
 +
      <li>1-2 min  in microwave. Check and swirl after each 30 sec. It must be dissolved completely.</li>
 +
      </ul>
 +
  </li>
 +
  <li>Add 1.0  ul EtBr (10 mg/ml) per 10 ml gel solution, swirl to mix</li>
 +
  <li>Add add 4  ul EtBr (10 mg/ml) per 100 ml running buffer.</li>
 +
  <li>Pour gel  into gel compartment. Put comb.</li>
 +
  <li> After gel solidifies (30 min), take  out the comb and load buffer to one well to measure its capacity.</li>
 +
  <li>Position the  gel compartment and fill gel chamber with running buffer.</li>
 +
  <li> Prepare samples and standards (ladder)</li>
 +
  <li> Prepare samples by mixing 4 ul 6X  Loading Buffer + 20 ul sample</li>
 +
  <li> Load the samples (for 24 ul sample, set  pipette 24 ul).</li>
 +
 
 +
  <p><em>Do not push the tip to the bottom of the wells. Make a 45 degree angle and support the pipette tip on the edge of the well. Don’t worry, gel will not brake when you take support. Slowly release the sample. Do not use second pipet push not to risk air injection.</em></p>
 +
  <li>Make the  connections: Black (-) on sample side, Red (+) opposite side</li>
 +
  <li>Run at 60V<br />
 +
      5-10V/cm (distance between anode and cathode) is recommended.<br />
 +
      90V causes high heat generation for our unit. Use 60V maximum.<br />
 +
      For overnight runs: 2V is too low, causes diffusion<br />
 +
    35V / 4hrs / ¾ progress</li>
 +
  <li>Gel can  be stored in 4 C until next day after completion</li>
 +
</ul>
 +
<h3>Gel Photo</h3>
 +
<ul><li>Adjust zoom and position using visible light</li>
 +
 
 +
 
 +
 
 +
 
 +
  <li>Before  turning on UV load your settings file which has the following parameters:
 +
    <ul>
 +
      <li>Preview tab,  all three options checked</li>
 +
      <li> Active  image</li>
 +
      <li> Dynamic  integration, auto exposure, 10 frames</li>
 +
      <li> 50/50  brigthness/contrast</li>
 +
      <li> 0/0 hue/saturation</li>
 +
      </ul>
 +
  </li> 
 +
  <li> Maximize brigthness with camera knob  (counterclockwise)</li>
 +
  <li> Turn on UV light</li>
 +
  <li>  Lower brightness from camera knob if necessary</li>
 +
  <p>&nbsp;</p>
 +
</ul>
 +
 
 +
</ol> 
</div>
</div>
</div>
</div>

Revision as of 00:07, 21 September 2011

Methan<b>E.COLIc</b> : Decreasing the Greenhouse effects and Saving the workers life in one system

MethanE.COLIc : Decreasing the Greenhouse effects and Saving the workers life in one system

Firedamp explosions are frequently seen cases at all mines over the world. In Turkey every year, 50 miners lose their lives because of firedamp explosions. Firedamp is a flammable gas found in coal mines and it mainly contains methane. Beside its explosive property, methane is also the main contributor to global warming. However recent mine mechanisms release obtained methane into air. By offers of Synthetic biology, we aimed to design a device which will work on E.coli that provides solutions for side effects of methane. Device that we are planning to construct involves the genes of bacteria (Methylococcus capsulatus) and insect (Drosophilia melanogaster) Our compact system in E.coli is fabricated as sensation of methane, the conversion of methane to methanol and then entrapment of methanol to handle for biofuel and death of bacteria at 42 C by kill switch mechanism.

When project is analyzed in stepwise, there are successive 4 steps of our modelled system in modified organism. As mentioned in subtitles, methane is sensed, then converted to methanol and methanol is entrapped and to elute methanol the cells are dead.

 t


 t


 t


 t


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Introduction

MethanE.COLIc project is designed to solve one of the problems of Turkey on worker security in mines, by constructing the natural parts of organisms.The main reason for us to choose such a project is that in Turkey- and also in many countries- each year, huge numbers of workers in mines lost their life due to deficiencies and conditions in their working areas (mines). The release of Grizu gas leads to subsidence of mines and so death of workers.This project is also designed to solve one of universal problem; global warming. Methane gas is a potential greenhouse gas.This project focuses on sensing the ambient methane gas and converting to one of the bio-fuel sources, methanol. Methanol is entrapped by product of one of the constructs of project, and then cells are dead by kill switch device of project to elute methanosol.



Steps

Team

Hello everyone!We are Metu Ankara IGEM team.Our team consists of high motivated,social and enjoyable “undergraduate and graduate scientists” from departments of physics, chemistry ,biology and computer education & instructional technology. We are such a team that complete each other so that we all experienced team spirit in IGEM. This makes us happy while doing experiences even in the hot summer.Our slogan is “ all for one, one for all”!!Then, who are we?


Our Advisors

  • Prof. Dr. Mahinur S. Akkaya
  • Burak Yılmaz
  • Sinan Umu

Team leader :Ceren Şeref

Ceren has just finished the junior year in biological sciences department in METU. It’s her second year in iGEM competition. She’s planning to study about neuroscience-especially on Alzheimer’s disease. She believes synthetic biology approaches can be a very good way of drug development in neuroscience field. She enjoys climbing, listening to music and singing.

Sibel Ataol

Sibel is first semester student in Master's program of Biomedical engineering at Middle East Technical University indeed she is graduated from Biology Department at METU. This is the second year of her in IGEM team from METU.she is one of the experienced in team and elder sister:) As a vice team lead, planing the experiments and cloning strategies and motivating team are the responsibilities of her. Studying in bioengineering and regenerative sciences is her desire for future.

Funda Guzey

She is a senior student of Biological Sciences at Middle East Technical University. This is her third year in iGEM competition. She gained a lot of experiences in this summer. One of the her interests is Synthetic Biology. However, her main interest is Biomedical and Tissue Engineering. She feels lucky to have such a wonderful team and is glad to share a wonderful summer with her team.

Gökcan Aydoğan

Gökcan has just finished the third year of the B.Sc. Chemistry degree at METU. This is his first year in IGEM team. He has been a huge fan of Synthetic Biology ever since he understands nothing about the concept. Everyday, he tries hard to get the picture. In his free time, he likes gaming, drawing cartoon and eating, eating, eating...

Filiz Ormancı

She is a fourth year student at the Department of Physics at Middle East Technical University. This is the first year of her in iGEM team. She wants to study on the usage of optical instruments in biophysics. She likes team working and sharing the success. She is always positive and happy... ehm..also a “soothsayer”. She enjoys playing musical instruments mainly violin and learning different languages.

G. Simge YÜZ

She is a recent graduate student of Chemistry and a fourth year student of Biological Sciences. This is the first year of her in iGEM team. She wants to study on neuropharmacology in the field of neuroscience. She is glad to join to METU-Ankara-iGEM team. She enjoys dancing especially Argentine tango and swimming. She is also a member of Flashmob Ankara Society

Yunus ALPAGU

Yunus is a third year student in biology department at Middle East Technical University in Turkey. This is his first year in iGEM team.He is interested in regenerative medicine, stem cells, biomaterials and tissue engineering. His favourite TV series is ‘Fringe’ and he likes playing tennis and volleyball.He is glad to join to METU-Ankara-iGEM team.

Pelin İspir

Pelin is currently studying the biology department of Middle East Technical University in Turkey. She is interested in stem cell, developmental biology,tissue engineering, and conservation biology.This is the first year of her in İGEM.She really enjoys with being this team and dealing with the mystery of synthetic biology.She enjoys listening latin musics and flamenco.

İbrahim Kutay Ozturk

Kutay is a graduate of Molecular Biology and Genetics, and now doing his M.Sc. in Biotechnology department at METU. This is his first year in IGEM team. He is interested in plant-based drugs, plant-pathogen interaction, biofuel production and bioremediation. He enjoys playing basketball, watching movies, and listening to music.

Miktat Aktaş

He graduated from Computer Education & Instructional Technology Department of Middle East Technical University last semester and he contributes this genius team as a coder for website. He wants to be a successful academician in his department at METU. He likes swimming and everything related to computers and automobiles.

Cihan Efe Kılıç

I am a third year student at the Department of Chemistry at Middle East Technical University. This is the first year of mine in iGEM team. I faced synthetic biology on my Biochemistry course. I want to study on the Electrochemistry-Enzyme immobilization. I believe that synthetic biology will give some benefits for my future work. I like team working and sharing the success. I like to cool staff with liquid nitrogen J I enjoys playing musical instruments flute and martial arts.

M. Akif AĞCA

Kutay is a graduate of Molecular Biology and Genetics, and now doing his M.Sc. in Biotechnology department at METU. This is his first year in IGEM team. He is interested in plant-based drugs, plant-pathogen interaction, biofuel production and bioremediation. He enjoys playing basketball, watching movies, and listening to music.

Advisor:Burak Yılmaz

I am a recent graduate of METU Molecular Biology and Genetics department and now studying towards my masters degree on Molecular Bioengineering at METU. My interest in synthetic biology did start during my undergraduate years and after graduation I started up the Sentegen company which is the first biotechnology based company focused on synthetic biology in Turkey. I continue my research and training in synthetic biology while also contributing to the development of the field in my country. We need new scientific revolutions to solve huge problems of life and emerging field of synthetic biology is best candidate for biotechnological revolution. I am interested in synthetic biology applications, along with Lab-on-a-Chip devices for molecular biology techniques, and we are designing gene synthesis chips to produce biobricks - raw materials of garage biology- faster and cheaper. I enjoy snowboarding, cycling and writing poems.

...

...

WET LAB

Whole summer in lab work we aimed to design 7 new E.coli compatible Biobricks and 1 composite part from 2011 kit plate distributions, also we aimed to characterize each part by protein analysis and fluorescence protein measurements.

We achieved design and compatibility of parts in E.coli, however not all parts’ characterization is achieved. Only the genes of designed composite part from kit plate is characterized by GFP measurements.

In this section you can find out more details on all our wet lab works. You can also find our data under results subtitle and information about design of our parts-biobricks with explanations in literature. It also contains materials and protocols, and finally There is safety questions list on our safety considerations both in the lab and on a wider environmental scale.

Overview

MethanE.COLIc project arises from sustainty and conservancy of human health and safety. Therefore while we were constructing the organismal device we also wanted to inform people from all age and we wanted to increase the public awareness on our project; methane gas based (firedamp) explosions and the greenhouse effect of methane gas.

Our aim is to inform people in each age. After brainstorming and searching, we planned the content of information and activities according to following subtitles.

Future Work


Methane explosion is the main problem since the very beginning of the coal mines. All countries tried different systems to solve this methane problem. When we decided to join iGEM 2011 competition firstly, it was very hard to chose a project from our brainstorms. All member of this group come up with a very reasonable idea for our team and we evaluate them all were seemed very beneficial for humanity. However, one day we face the problem of methane explosions on the news and at that time we decided to create new idea for this problem. After a long literature research, we found how seriously dangerous the methane gas and how people deal with this big problem on coal mines

  1. Australia
  2. Belgium
  3. Canada
  4. Chile
  5. China
  6. France
  7. New Zealand
  8. Poland
  9. Russia
  10. Australia
  11. United States

These are the countries which have been faced with too big methane explosions true out their history. After a certain research we found that to deal up this problem, companies spent lots of money for effective solutions.
Regenerative Thermal Oxidizer from MEGTEC capable of handling 60,000 scfm of VAM. At a methane concentration of about 0.7% a unit this size generates 50,000 carbon credits per year. This unit costs about US$ 1,5 million Elizabeth Obediente from CO2IMPACT at a methane upgrading facility at a coal mine in Alabama. The gas is stripped of impurities and upgraded to 96% methane per volume and then compressed and then sold to the natural gas pipeline. Ventilation Air Methane (VAM): VAM units cost about $20-$30 USD per scfm.

At some mines, downtime is considerable, causing expensive losses to the mine. Ventilation cost cuts can be up to half of the original cost of the ventilation system. In one study, a mine with 400 ft3/ton of methane using vertical wells to pre-drain will result in an estimated US$ 11 million over 20 years in reduced ventilation costs, not including carbon and energy revenue[iii] (U.S. Environmental Protection Agency, 1999). Like many solution system for methane problem, the tree examples of solution of methane problem did not satisfied us, so we created our simple and very effective way to deal with the methane.( http://www.co2impact.com/cmm.html )

According to our methane E colic project, we aimed:

  • Save the coal workers’ life
  • Save the nature
  • Process a new energy
  • Cheap system

Save the coal workers’ life

When we produce our project, we stop the search the worlds system and turn back to our country, so we saw that methane (CH3) is a big problem to get rid of our mines too. The way carry out on our county has some missing parts on safety. While we were proceeding our project, we focus on this part mainly and we have shaped it according to this.
We aimed to collect the methane gas from coal mines to the tanks which are filled with water. When the methane passes the legal percent of %1, according to our project, we dissolve the gas on water tanks. After that we put tablets which include our bacteria on the tanks , so the methane and methanol process will begin with this step.



Years Death workers on Turkey
1983 103
1990 330
1995 40
2003 17
2004 3
2005 18
2006 21
2007 7
2008 43

According to Prof. Dr. Mustafa ÖZTÜRK’s research (Vice President of Parliamentary Commission for the environment on turkey), this the death workers amount since 1983 to 2008 on Turkey’s coal mines.
Our way, collecting all methane gas from the mine to tanks, not only make methane free working space for workers, but also could make the space more workable and safer.

Save the nature

During our research for safety systems for methane all over the world, we saw that in most ways, methane release to the atmosphere with or without some elements and chemicals. Just a few systems are used methane to produce new energy or something else.

We noticed that methane gas is twenty four times harmful than the carbon monoxide gas for the atmosphere. According to our project, on the way that converting methane gas to methanol form, we prevent methane to make any damage to the nature on gas form.

Process a new energy

During the research process for our project, we also realized that energy is the most important thing on today and future life. Today, all energy sources are almost over including petroleum. People are searching new energy source. As the last news from china, everyone saw that nuclear energy is not a secure and trustable way to get energy.

On this century, people understand the nature’s value for human life. Now renewable energy systems are built all around the world like wind turbines and sun batteries.

According to our project, we planed that methanol could be used for making bio-fuel instead of ethanol. For the bio-fuel, ethanol is collecting from especially from the corps. However, on this way, we use corps unnecessarily. Studies suggest that vehicles that run on 85 per cent methanol blends, as well as petrol, actually have performance capabilities that equal or surpass vehicles running on petrol alone.

Also, according to Dr. Robert Zubrin, Methanol is cheaper than ethanol. It can also be made from a broader variety of biomass material, as well as from coal and natural gas. And methanol is the safest motor fuel.(American enterprise, February 13th, 2006)

Cheap system

There are lots of system use now for methane gas and the gas explosions on mines. However, when we look closer to them, they are too expensive to build for a mine. If we notice also there are global economic problems nowadays, it seems not possible that companies may not be to get enough precaution for their workers, even their own life especially on the developing countries.

On the other hand, we put all the bacteria that we produce in a capsule tablet. They are totally harmless on this form. When we put them in the water tanks, they will come to life and start their work.

This process does not cost million dollars or does not get a lot of time for building very big facilities. It is very cheap and has very easy process time.

Our project is open for research and development. For the future of it, we planned to put smelling part to our bacteria for making workers area more fresh and comfortable. In addition, we can design a system for our bacteria to send it in the mine and maybe start the process inside the mine. Furthermore, we put also biosensor part the bacteria and the bacteria measure the percent of the gas level with itself.

PartnerShip

Videos

In Africa 1999

In Ukraine, 2001

In UK, 2006

In Siberia, 2007

In Turkey, 2009

In Turkey, 2010

In Chile, 2010

In Russia, 2010

In New Zeland, 2010

In Virginia, 2011

In Ukraine, 2011

In Mexico, 2011

In Pakistan, 2011

Software Tool

BioGuide is a Biological System Design tool. It has been developed in 2010 by the team METU TURKEY SOFTWARE. You can check the page for detailed information about the project :
https://2010.igem.org/Team:METU_Turkey_Software

Here is rough draft of BioGuide Paper you can read for technical details;

BioGuide.pdf

This year;

We have completed biological system design part of BioGuide and enabled wet lab teams to use it.

You can watch the how to video of BioGuide to see what and how you can do with it;



Here is how METU ANKARA wet lab team is using BioGuide;

This year we are using it while building one of our devices, kill switch composite. Kill switch composite consists of 4 main parts which are in 2011 kit plate distributions; T7 promoter, RNA thermometer, GFP and lysis casette. The upstream part of this composite is T7 promoter (BBa_I712074) which is strong promoter from T7 bacteriophage mostly used expression system and so for strong transcription T7 promoter expression system is chosen.

We also tried the inducible promoters (pLac-IPTG inducer) to design and express the lysis casette. We desired to use a promoter that could be induced and enhance the expression to control and manipulate the translation of device. When we typed IPTG on input box of Bioguide we had reached the possible promoters that could be induced by IPTG. This program gave their standard biobrick codes and finally we got these parts by knowing their location in kit plate.

In downstream of promoter there is RNA thermometer(ROSE) coding region which determines the transcription of our lysis composite part. We had reached this part by coding the temperature 42 in input box of BioGuide. RNA thermometer (BBa_K115001) is temperature sensitive at which 42C translation initiates.

In downstream of RNA thermometer, green fluorescence protein(BBa_E0040) is ligated. This ligation is done to measure expression level and to comment on RNA thermometer efficiency. We typed GFP in output box since we wanted to measure fluorescence.

We had designed this composite and it's parts mostly by processing the BioGuide program that made our job easier in intense lab works. We reached the shortest path with our input and output parameters for this device to construct by BioGuide

Methane sensing

i) Introduction

In our methane.colic project, the first critical point is to sense the ambient methane gas. While in literature search, we have focused on the methane and DNA or methane and regulator protein interaction which binds to DNA after binding to methane. In structure, methane consists of one carbon atom and four hydrogen atom which means it is smaller in size and weight. Therefore it is hard to find any study based on methane interaction with DNA or protein to regulate transcription. This made us search for carbon hydrogen bond interaction with any oligo or protein to trigger transcription of any metabolite product. So that we also searched the literature for any organism which utilizes any alkane chain and alkane which regulates the transcription of organismal metabolites by interaction with DNA or protein. Since bacteria are environmental adapting organisms, it is possible to find any alkane to regulate the transcription of degradation metabolism. Then we have found the organism, Pseudomonas oleovorans to analyze the alkane degradation of organism for its carbon source.

ii) Background

Many microorganisms live in the environments where the conditions changing frequently and so the evolution is inevitable for mechanisms to withstand unfavorable situations. Therefore microorganisms can use their specific and sensitive mechanisms for sensing the required nutrients for them or any pollution to affect their sustainity. Otherwise they can expose to mutations which change the gene expression and gain new functionalities. In case they have ability to survive in such conditions.

While we were scanning the literature based on methane and alkane degrading organisms we have found some organisms that sensitive to methane presence and have mechanisms to activate transcription of related gene clusters.

We analyzed the soil bacteria, Pseudomonas oleovorans. This strain can assimilate the alkane for its carbon source and one of the microbial whole cell –biosensor. They have a gene cluster which codes for degradative pathway and includes the activator which interacts especially with linear alkanes. This activator protein, AlkS, in the presence of alkanes, induces the transcription from PalkB promoter which initiates the expression of genes code for assimilation of alkanes. We have analyzed the related articles in which the promoter region is studied and showed that it is expressed in E.coli correctly because of the corresponding RNA polymerase binding regions.

REFERENCE:
  1. Canosa, I. & Yuste, L. (2000). A positive feedback mechanism controls expression of AlkS, the transcriptional regulator of the Pseudomonas oleovorans alkane degradation pathway. Molecular Microbiology, 35 (4), 791-799.

iii) Modelling

Since the parts that we have found belongs to yeast organism, it was hard to us to manipulate it in bacteria E.coli. We designed the tests of this part by characterizing one of the subunits of methane monooxgenase (MMo). For the functional activity of monooxygenase enzyme, there are required 3 subunits as A,B and C. The A subunit of methane monooxygenase is 210 kDa protein that is supposed as the methane binding active site of monoxygenase complex. This protein consists of non-haem iron and contains p-hydroxo bridge structure. We planned the experiments of this step as characterization of protein A by PCR amplification with specific primers of full construct device to obtained the sequence of protein A. The methane gas is applied to cell culture with our modelled device then the cells were centrifuged and the gas concentration is measured from supernatant.

Lab Protocols

Clonning procedures

  1. Getting the DNA parts
    1. For parts in kit plates
      1. With a pipette tip, punch a hole through the foil cover into the corresponding well of the BiobrickTM-standard part that you want.
      2. Pipette 10 uL of dH2O (distilled water) into the well. Pipette up and down a few times and let sit for 5 minutes to make sure the dried DNA is fully re-suspended.
      3. Transform 1 or 2 uL of the re-suspended DNA into desired competent cells, plate your transformation with the appropriate antibiotic and grow overnight.
      4. Pick a single colony and inoculate LB medium (again, with the correct antibiotic) and grow for 16 hours.
      5. Use the resulting culture to miniprep the DNA and make your own glycerol stock.
    2. For new synthesized DNA parts
      1. The DNA parts are sent in nmol values in each. These data are determined for all of them individually
      2. As a stock solution preparation, these DNA parts are pipetted with PCR water or TE buffer which is 100 times of DNA amount. The final solution is prepared as 100uM.
      3. For each transformation procedures, the 10uM of stock DNA part in water is transformed. 1uL is taken from stock DNA solution and is added to 9uL PCR water.
  2. Preparation of Competent Cells
      1. Inoculate a single colony of E. Coli cells into 50 ml LB medium. Grow overnight at 37 C with moderate shaking (250rpm)
      2. Inoculate 4 mL of the culture into 400 mL LB medium in a sterile 2-liter flask. Grow at 37 C shaking at 250 rpm to an OD590 of 0.375.

        This procedure requires that cells be growing rapidly (early- or mid-log phase). Accordingly, it is very important that the growing cells have sufficient air. Overgrowth of culture (beyond OD590 of 0.4) decreases the efficiency of transformation.

      3. Aliquot culture into eight 50 mL prechilled, sterile polypropylene tubes and leave the tubes on ice 5 to 10 min.

        Cells should be kept cold for all subsequent steps.
        Larger tubes or bottles can be used to centrifuge cells if volumes of all subsequent solutions are increased in direct proportion.

      4. Centrifuge cells 7 min at 1600 g (3000 rpm in JS -5.2),  4 C.

        5. Allow centrifuge to decelerate without breake.
        We have not attempted to determine whether deceleration without braking is critical to this procedure. However, we do not use the breake for this step or for the subsequent centrifugation steps.

      5. Pour off subernant and resuspend each pellet in 10 ml ice-cold CaCl2 solution.Re-suspension should be performed very gently and all cells kept on ice.
      6. Cetrifuge cells 5 min at 1100 g, 4 C. Discard supernatant and re-suspend each pellet in 10 mL ice-cold CaCl2 solution. Keep re-suspend cells on ice for 30 min.
      7. Centrifuge cells 5 min at 1100 g, 4 C. Discard supernatant and re-suspend each pellet in 2 mL ice-cold CaCl2 solution.

        It is important to re-suspend this final pellet well. The suspension may be left on ice for several days.

      8. Dispense cells into prechilled, sterile polypropylene tubes (250 ml aliquots are convenient). Freeze immediately at -70 C.
  3. Transformation
      1. Aliquot 10 ng of DNA in a volume 10 to 25  mL into a sterile 15 mL round bottom test tube and place on ice.

        2. Plasmid DNA can be used directly from ligation reactions. When this is done , more DNA is usually used. However, if there is <1 mg of DNA in the ligation reaction, or if the ligation reaction is from low gelling/melting temperature agarose, it is wise to dilute the ligation mix.

      2. Rapidly thaw competent cells by warming between hands and dispense 100 mL immediately into test tubes containing DNA. Gently swirl tubes to mix, then place on ice for 10 min.

        3. Competent cells should be used immediately after thawing. Remaining cells should be discarded rather than refrozen

      3. Heat shock cells by placing tubes into a 42 C water bath for 2 min

        4. Alternatively incubate at 37 C for 5 min.

      4. Add 1 ml LB medium to each tube. Place each tube on a roler drum at 250 rpm for 1 hr at 37 C.
      5. Plate aliquots of transformatin culture on LB /ampicillin or other approprate antibiotic- containing plates.

        6. It is convenient to plate several different dilutions of each transformation culture. The remainder of the mixture can be stored at 4 C for subsequent platings.

      6. When plates are dry, incubate 12 to 16 hr at 37 C.
  4. Plasmid isolation

    5. This procedure is performed with Fermentas GeneJET™ Plasmid Miniprep Kit

      1. Pick a single colony
      2. Inoculate in 5 mL LB medium for high-copy or 10 mL for low-copy of LB medium supplemented with the appropriate selection antibiotic.
      3. Incubate at 225 rpm not longer than 12-14 h at 37 C .
      4. Centrifuge at 4000 rpm for 5 min at 4 C .
      5. Discard the supernatant and keep pellet.
      6. Resuspended  the pellet with 250 ul Resuspension solution. (Bacteria should be resuspended completely by vortexing until no cell clumps remain)
      7. Transfer the cell suspension to eppendorf.
      8. Add 250 uL Lysis Solution and mix gently by inverting the tube 4-6 times until the solution becomes slightly clearPlate aliquots of transformatin culture on LB /ampicillin or other approprate antibiotic- containing plates.

        9. Do not vortex!
        Do not incubate for more than 5 min. (To avoid denaturation of supercoiled plasmid DNA!)

      9. Add 350 uL Neutralization solutionand mix immediately and throughly by inverting the tube 4-6 times.

        10. (The neutralized bacterial lysate is cloudy and viscous) ("throughly" to avoid localized precipitation of bacterial cell debris)

      10. Centrifuge at 13000 rpm for 5 min to precipitate cell debris and chromosomal DNA.
      11. Transfer the supernatant to spin column (about 600 uL).

        12. (Avoid disturbing or transferring the white precipitate)

      12. Centrifuge at 13000 rpm for 1 min.
      13. Discard the flow-through.
      14. Place the column back into same collection tube.
      15. Add 500 uL Wash solution to spin column.
      16. Centrifuge at 13000 for 1 min
      17. Discard the flow-through.
      18. Repeat this step with using 500 uL Wash solution.
      19. Discard the flow-through
      20. Centrifuge at 13000 rpm for an additional 1 min to remove residual Wash solution.
        (This step is essential to avoid residual ethanol in plasmid preps)
      21. Transfer spin column into a fresh 1.5 mL epp.
      22. Add 50 uL Elution buffer into center of the spin column membrane to elute the plasmid DNA

        23. Do not contact the membrane with pipette tip!

      23. Incubate for 2 min at 25 C. 

        24. To increase yield incubation is done for 2 min at heat block at 42 C

      24. Centrifuge at 13000 for 2 min.
      25. Discard the column and store the purified plasmid DNA at -20 C.

        26. OPTIONAL= additional elution step with elution buffer or water. This step increases the yield by 10-20 %.
        NOTE:  For elution of plasmids ≥ 20 kb, prewarm Elution buffer to 70 C before applying.

  5. Restriction digestion

    6. This procedure is performed with NEB  BioBrick™ Assembly Kit

    • Digest Upstream Part with EcoRI-HF and Spel
      500 ng Upstream Part Plasmid
      1 uL EcorI-HF
      1 uL Spe I
      5 uL 10*NE  Buffer 2
      0.5 uL 100* BSA
      To 50 uL add dH2O

    • Digest downstream part will  Xbal and PstI
      500 ng Downstream Part Plasmid
      1 ul XbaI
      5 uL 10*NE Buffer 2
      0.5 uL 100* BSA
      To 50 uL add dH2O

    • Digest the destination plasmid with EcorI-HF and Pst I:

      • The destination plasmid DNA should either be prepared with PCR or contain the toxic gene (e.g, ccdB, sacB) in the cloning site to avoid the need for gene purification.
      The Destination Plasmid should also have a different antibiotic resistance marker from both the plasmid containing the Upstream Part and the plasmid containing the Downstream Part to avoid the need to purify the Upstream and Downstream Parts.
      500 ng Destination Plasmid DNA
      1 uL EcorI- HF
      1 uL PstI
      15 uL 10* NE Buffer 2
      0.5 uL 100*BSA
      To 50 uL add dH2O
       
      Incubate all 3 restriction digest reactions at 37 C for 10 min and then heat inactivate at 80 C for 20 min.

  6. AGE (Confirmation)

    7. Background

    • EtBr stains only dsDNA. You cannot see ssDNA on gel
    • Minimum amount of DNA load:

      • 200 ng (Aysu)
      • Each band of 1kb ladder is approx. 125 ng (2.5 ul loaded) and can be seen on gel

    Preparetion

    • 50X TAE (Tris-Acetate) Buffer
      121 g/0.5 L Tris
      28.6 g/0.5 L Glacial Acetic Acid
      7.31 g/0.5 L EDTA
      pH 8.0
    • Sterile 1.5 mL eppendorf tubes
    • Sterile long pipette tips
    • DNA standards
      • [Aysu]: Promega 1.0 kb (1.0-10Kbp), 100 bp (0.1-1.0 Kbp)
    • TAE Buffer
    • EtBr sln (10 mg/mL). Purchase as solution ! Store at RT. Light-sensitive and carcinogenic !
    • Sample loading buffer. Store at 4 C.

    Protocol

    • Prepare 360 ml, 1X TAE running buffer
    • Prepare gel compartment with tape (do not use parafilm)
    • Prepare 60 ml, 1% agarose gel (0.6 g agarose in 60 ml 1X TAE buffer)
      • 1-2 min in microwave. Check and swirl after each 30 sec. It must be dissolved completely.
    • Add 1.0 ul EtBr (10 mg/ml) per 10 ml gel solution, swirl to mix
    • Add add 4 ul EtBr (10 mg/ml) per 100 ml running buffer.
    • Pour gel into gel compartment. Put comb.
    • After gel solidifies (30 min), take out the comb and load buffer to one well to measure its capacity.
    • Position the gel compartment and fill gel chamber with running buffer.
    • Prepare samples and standards (ladder)
    • Prepare samples by mixing 4 ul 6X Loading Buffer + 20 ul sample
    • Load the samples (for 24 ul sample, set pipette 24 ul).

      • Do not push the tip to the bottom of the wells. Make a 45 degree angle and support the pipette tip on the edge of the well. Don’t worry, gel will not brake when you take support. Slowly release the sample. Do not use second pipet push not to risk air injection.

    • Make the connections: Black (-) on sample side, Red (+) opposite side
    • Run at 60V
      5-10V/cm (distance between anode and cathode) is recommended.
      90V causes high heat generation for our unit. Use 60V maximum.
      For overnight runs: 2V is too low, causes diffusion
      35V / 4hrs / ¾ progress
    • Gel can be stored in 4 C until next day after completion

    Gel Photo

    • Adjust zoom and position using visible light
    • Before turning on UV load your settings file which has the following parameters:
      • Preview tab, all three options checked
      • Active image
      • Dynamic integration, auto exposure, 10 frames
      • 50/50 brigthness/contrast
      • 0/0 hue/saturation
    • Maximize brigthness with camera knob (counterclockwise)
    • Turn on UV light
    • Lower brightness from camera knob if necessary

      •  

Online Lectures

Anybody interested and novice in Synthetic Biology can use the lecture;

Here is our animation; Industrial Revolution 2 After Synthetic Biology, to introduce the basics of the field;

Here is Our Online Lecture, Click the picture to go;

Click picture to reach Online Lectures

Contact

i) Introduction

When examined in order, conversion is the second step of device system. While in literature searches, it is found that methanotrophs which live in either extreme conditions or in deep oceans, the process is the same, methane is converted to methanol which is the oxygenated form of hydrocarbon group. The searches directed us to organism Methylococcus capsulatus which is one of the mostly studied organisms among methanotrophs. We designed the conversion part of this organism and modified coding operon according to E.coli strain to enhance the expression. The monoxygenase coding part with protein A, B and C products are designed for conversion step of this project.

ii) Background

Methanotrophs - methane oxidizing bacteria- are ubiquitous in the environment and play an important role in mitigating global warming because they are a unique group of gram-negative bacteria that grow aerobically on methane as sole source of carbon and energy (Hanson and Hanson 1996). They are also potentially interesting for industrial applications such as production of bulk chemicals or bioremediation. Methanotrophs converts methane to methanol and subsequently to formaldehyde which is assimilated or further oxidized to CO2 for biosynthesis of cellular forms.In this biosynthesis pathway the conversion of methane to methanol is catalysed by methane monooxygenase (MMO) which is a non-specific enzyme complex that also catalyse the oxidation of a wide range of aliphatic, alicyclic and aromatic compounds (Colby et a l . , 1977; Higgins et a l . ,1979). The first step in the oxidation of methane to precursors of organic compounds is the conversion to methanol by methane monooxygenase, the key enzyme, which exists in two forms: the cytoplasmic, soluble methane monooxygenase (sMMO) and the membrane-bound, particulate methane monooxygenase (pMMO). sMMO components have been expressed in heterologous and homologous hosts. Therefore we searched more on soluble form of monooxygenase enzyme. When analyzed in detail, pMMo differs from sMMo by copper ion concentration. Copper ions have been shown to play a key role in regulating the expression of both MMO enzyme complexes. When its concentration increases the differentiation goes through particulate form. Here we analyzed the soluble form of methane monooxygenase to express in heterologous host.

a) Soluble Methane Monooxygenase

In contrast to pMMO, sMMO has extremely broad substrate specificity and can oxidise a wide range of non-growth substrates such as alkanes, alkenes and aromatic compounds thus making it the more attractive enzyme for co-oxidation reactions. sMMO is expressed only under conditions in which the copper-to-biomass ratio is low, i.e. under “low-copper” growth conditions, when copper ions are omitted from the trace elements solution of a standard mineral salts medium or cells are grown in a fermentor to high cell densities.There is also some evidence that copper ions inhibit the activity of sMMO (Jahng and Wood 1996). Like many other multi-component oxygenase systems, sMMO contains a component of approximately 16 kDa, Protein B, which serves an “effector” or regulatory role. The activity of Protein B may be regulated by proteolysis at its amino terminus (Lloyd et al. 1997). At low concentrations, Protein B converts the hydroxylase from an oxidase and stabilizes intermediates necessary for oxygen activation. Saturating amounts of Protein B dramatically increase the rates of formation of intermediates and accelerate catalysis of methane to methanol by sMMO (Lee and Lipscomb 1999). When analyzed, the most extensively characterised sMMO enzymes are those from Methylococcus capsulatus (Bath) and Methylosinus trichosporium OB3b (reviewed in Lipscomb 1994; Deeth and Dalton 1998). Therefore we preferred to study on Methylococcus capsulatus (Bath) for monooxygenase.The sMMO is a non-haem iron-containing enzyme complex consisting of three components. The hydroxylase consists of three subunits of 60, 45 and 20 kDa arranged in an α2 β2 γ2 configuration. sMMO genes are clustered on the chromosome of Methylococcus capsulatus (Bath) and Methylosinus trichosporium OB3b. mmoX, mmoY and mmoZ encode the α-, β- and γ-subunits respectively of the hydroxylase. mmoB and mmoC code for Protein B and the reductase component. Interestingly, mmoB lies between mmoY and mmoZ; an ORF of unknown function, designated orfY, with a coding capacity of 12 kDa, lies between mmoZ and mmoC in all genes clusters analysed to date (McDonald et al. 1997).

REFERENCE:

  1. J. Colin Murrell · Bettina Gilbert · Ian R. McDonald, (2000), Molecular biology and regulation of methane monooxygenase Arch Microbiology(2000) 173 :325–33
  2. Colby, J . & Dalton, H. (1978). Resolution of the methane monooxygenase of Methylococcus capsulatus (Bath) into three components. Biochemical Journal 171,461-468
  3. Hanson Te&Hanson RS(1996) Methanotrophic bacteria.American Society forMicrobiology.Microbiol. Rev., Jun 1996, 439-471, Vol 60, No. 2
  4. Charlotte, A., West, G. & Horward, D. (1992). Functional expression in Escherichia coli of proteins B and C from soluble methane monooxygenase of Methylococcus capsulatus (Bath. Journal of General Microbiology, (138), 1301-1307.

iii) Modelling

For this step of MethanE.COLIc project, the experiments were planned and modelled as protein characterizations. The protein B and C were previously characterized and analyzed proteins in literature. Based on this publications we planned the experiments as purifying protein from cell extract then SDS-PAGE analysis.

Public Awareness

5-10 year old group

For this age group, we prepared and modified one of the national child game. In this game there is a circle of group of child, one is not included in that circle. It runs around the circle and labels one of the participants in circle. When recognizes, it chases that one with singing that special song. In our modified game, the one that out of circle was our restriction enzyme due to our group in video, we assigned the enzymes into two,also they are double digestion enzymes. These ones wore white caps in video. And we have three insert groups which wore red, green and yellow caps. The blue capped ones were our backbone.
During (By this game and at the begining of) this game we told to kids what is DNA, enzyme and insert, and what we have done as Synthetic Biology.


10-17 year old group

This group consists of high school aged children groups.Through out the workshop, we have paired them as two groups. Firstly we have explained Synthetic Biolgy and what Synthetic Biology is able to do. After these training, we told them our project and taught them basic molecular biology procedures and what are required for basic synthetic biology based experiments. We have done the experiments(cloning procedures) together and also they did individually. We also encouraged them to join iGEM High School division.

18-24 year old group

This group consists of METU students. We arranged the Physics lectures in METU by contacting with instructor. To give an effective presentation (Due to physics is an service course in METU), we have reached to students in several departments. We had told our project individually and told them what is Synthetic Biology, we gained many volunteers to join METU-iGEM team for the following years. Also in METU we have an online lecture application as METU open course ware. For this web page, we have prepare the course notes and they were uploaded to reach many students from all around to inform and contact for further relations about Synthetic Biology.
Moreover, we distributed hand outs about our project and synthetic biology at METU campus, when the new students registrations were done. We aimed to inform students about our project and synthetic biology to attract their attention on the issue.

Online lecture link:&nbsp: http://ocw.metu.edu.tr/course/view.php?id=137

Above 24 year old

For this group of people we met with group of engineers in Turkey who work in mining fields in Turkey. We have told our project in details and we have consulted them on background of our project. What are the conditions in mines, what are the general regulations for worker safety and what are the rooted controls for any gas release are the points which we asked and discussed on.

List of Engineers:

Turkish Architects and Engineers Association members:

NO NAME & SURNAME INSTITUTION CITY
1 Başak GÜLEKEN ERKUNT DÖKÜM A.Ş. ANKARA
2 Saliha SİVRİ ETİ MADEN İŞLETMELERİ ANKARA
3 Aynur ODAMAN KOSGEB ANKARA
4 Mehmet Şevki TÜRÜDÜ MADEN TETKİK ARAMA KURUMU ANKARA
5 Galip Şevket YİNSEL MİTAŞ A.Ş ANKARA
6 Cemil Hakan GÜR ORTA DOĞU TEKNİK ÜNİVERSİTESİ ANKARA


Contact

Entrapment

i) Introduction

After conversion of methane to methanol, the successive step is the entrapment of methanol. Methanol is an alcohol form of hydrocarbon methane and includes hydroxyl group. Hydroxyl radical groups are highly reactive and, and so short-lived; however, they form an important part of radical chemistry. Hydroxyl groups are especially important in biological systems and their chemistry because free radicals tend to form hydrogen bonds both as donor and acceptor. This property is also related to their ability to increase hydrophilicity and water solubility. Therefore hydroxyl free radicals cause damage to oxidative cells and cellular membranes. In order to produce the methanol for further industrial manufacturing in cellular organism, the organismal conditions should be adjusted. In the light of this, for our bacterial system we transferred the protein coding sequence(named as LUSH) of Drosophilia melanogaster to attack to free methanols and hydroxyl group. Here is some structural information about protein LUSH.

ii) Background

LUSH is an alcohol-sensitive odorant binding protein expressed in the olfactory organs of Drosophila melanogaster, and it is used as a model system to investigate the biophysical nature of alcohol-protein interactions at alcohol concentrations that produce intoxication in humans. In this study, by using NMR spectroscopy, they have identified the regions of LUSH that show increased conformational stability on binding alcohols. These residues primarily line the alcohol-binding pocket. A direct measure of the degree of stability that alcohol imparts on LUSH has been provided. LUSH was originally identified as responsible for mediating an avoidance response to short-chain n-alcohols.

The general structure of odorant binding proteins consists of six α-helices surrounding a hydrophobic ligand- binding pocket which differs in size and shape between each protein. All these odorant binding proteins have a set of six cysteines that form three conserved disulfide bonds. In the study, by observing the X-ray crystal structures of LUSH-alcohol complexes, it was found that alcohol binds to a single site in the protein formed by a network of concerted hydrogen-binding residues located at one end of hyrophobic pocket. This binding site has some sequence and/or structural similarities to regions of several ligand gated ion channels (LGICs) that have previously been implicated in inferring sensitivity to alcohol. It is hypothesized in the study that the alcohol-binding site in LUSH may represent a more general structural motif for functionally relevant alcohol-binding sites in proteins. The characterization of the effects of n-alcohols on the structure and stability of LUSH is presented. Also, in the absence of ligand, LUSH exists in vitro in a partially unstructured state and binding of alcohols shifts the solution conformation to a more compact folded state which is accompanied by an increase in the overall protein stability. Those regions of the protein that show the largest changes in local dynamics on binding alcohol have been identified and it have been shown that these are predominantly associated with the residues that line the alcohol-binding pocket. The results provide a quantitative measure of the ability of short-chain alcohols to stabilize protein structure at physiological relevant concentrations.

REFERENCE:

  1. Bucci, B. K., Kruse, S. W. & Thode, A. B. (2006). Effect of n-Alcohols on the Structure and Stability of the Drosophila Odorant Binding Protein LUSH. Biochemistry, 45 1693-1701
  2. Thode, A. B., Kruse, S. W. & Nix, J. C. (2008). The role of multiple hydrogen bonding groups in specific alcohol binding sites in proteins: Insights from structural studies of LUSH. J.Mol Biol, 376 (5), 1360-1376

iii) Modelling

In MethanE.COLIc project, LUSH protein is designed to hold methanol; the conversion product of methane. Methanol is bounded to LUSH protein through its hydroxyl group. In device experiments of this part, we planned to isolate and denaturate protein and then refold in presence of methanol and we planned to analyze the alcohol bounded protein in X-ray diffraction crystallogrophy.

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Kill switch

i) Introduction

In this project the last step is the death of our bacteria to elute the protein(LUSH) bounded product methanol which is one of the precursors of biofuel. In our modified bacteria, the death of cells occurs by temperature dependent cell lysis device. The expression of this device takes place at 42 C since there is an RNA thermometer part in upstream of this device. At the downstream of this device there is an lysis casette. When transcription initiated at 42C holin and endolysin is expressed from this device and make cell dead.

ii) Background

This composite part consists of promoter, RNA thermometer, GFP and lysis casette. The upstream part of this composite is T7 promoter (BBa_I712074) which is strong promoter from T7 bacteriophage. For strong transcription T7 promoter expression system is chosen. In downstream of promoter there is RNA thermometer(ROSE) coding region which determines the transcription of our lysis composite part. RNA thermometer (BBa_K115001) is temperature sensitive that at 42C translation initiates. That means, up to 42 C RNA thermometer is in dimer form and at 42C it becomes linear. In downstream of RNA thermometer, green fluorescence protein(BBa_E0040) is ligated. This ligation is done to measure expression level and to comment on RNA thermometer efficiency. The last ligate to this composite is bacteriophage 21 lysis casette (BBa_K124003). This lysis casette induces lysis in E.coli. This gene cassette consists of the S protein (Holin), R protein (Endolysin), and Rz protein. When translation initiates at 42 C then the following coding gene begins to produce the proteins which lyse the cell.

iii) Modelling

In MethanE.COLIc project, this composite is modelled to lyse and kill the bacteria when switched on at 42C. In experimental design, we ligated this composite without lysis casette (with promoter, ROSE and GFP) We planned two control groups. One is T7 promoter and GFP ligate, this is designed to measure expression level of T7 promoter by reading the GFP expression. The second control group is T7 promoter, ROSE and GFP ligate, this is designed to measure the expression level of T7 promoter with ROSE ligate at 37 C. The device experiment is done with T7 promoter ROSE and GFP ligate at 42 C in which the GFP expression is expected.

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Fun & Learn

Flashmob!



In order to reach to huge amounts of people who are in several age groups, we have designed a flashmob related with our project- in molecular level- .(A flash mob (or flashmob) is a group of people who assemble suddenly in a public place, perform an unusual and sometimes seemingly pointless act for a brief time, then disperse, often for the purposes of entertainment, satire, artistic expression or—in rare cases—violence. Flash mobs are organized via telecommunications, social media, or viral emails ).One of our group member who is a member of Flashmob society helped us for arrangements.. We use Flashmob in order to explain what is our project and increase the public awareness about Synthetic biology and particularly our project. Flashmob event took place at one of the biggest shopping malls in Ankara where people often strolled around. Afterwards, we had interviewed with people who watched our sketch and informed people about nearly limitless capabilities of synthetic biology. Indeed we had prepared hand outs that contains interesting statistical data about methane and it’s side effects, also information about iGEM

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