Team:Fatih Turkey/Notebook

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You are provided with this team page template with which to start the iGEM season. You may choose to personalize it to fit your team but keep the same "look." Or you may choose to take your team wiki to a different level and design your own wiki. You can find some examples <a href="https://2008.igem.org/Help:Template/Examples">HERE</a>.
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<div id="header">
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<a href="https://2011.igem.org/" style="position:absolute; right:10px; top:5px;"><img src="https://static.igem.org/mediawiki/2011/9/9c/Igem_basic_logo.png"/></a>
 +
<!-- Logo -->
 +
<div>
 +
<div class="logo">
 +
<a href="https://2011.igem.org/Team:Fatih_Turkey">
 +
<img width="258" src="https://static.igem.org/mediawiki/2011/b/b6/Fatih_turkey_logo.png">
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<!-- Menu -->
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<div class="nav-main">
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<div id="topmenu" class="ddsmoothmenu">
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<li>
 +
<a href="https://2011.igem.org/Team:Fatih_Turkey">Home</a>
 +
</li>
 +
<li>
 +
<a href="https://2011.igem.org/Team:Fatih_Turkey/Project">Project</a>
 +
<ul>
 +
<li><a href="https://2011.igem.org/Team:Fatih_Turkey/Project">Overall Project</a></li>
 +
<li><a href="https://2011.igem.org/Team:Fatih_Turkey/LALF">LALF</a></li>
 +
<li><a href="https://2011.igem.org/Team:Fatih_Turkey/Reflectin">Reflectin</a></li>
 +
<li><a href="https://2011.igem.org/Team:Fatih_Turkey/Biofilm">Biofilm</a></li>
 +
<li><a href="https://2011.igem.org/Team:Fatih_Turkey/Experiments">Experiments</a></li>
 +
<li><a href="https://2011.igem.org/Team:Fatih_Turkey/Parts">Parts</a></li>
 +
<li><a href="https://2011.igem.org/Team:Fatih_Turkey/Future_Plan">Future Plan</a></li>
 +
</ul>
 +
</li>
 +
<li>
 +
<a href="https://2011.igem.org/Team:Fatih_Turkey/Data_Page">Data Page</a>
 +
</li>
 +
<li><a href="https://2011.igem.org/Team:Fatih_Turkey/Team">Team</a>
 +
<ul>
 +
                                                                                <li><a
 +
href="https://2011.igem.org/Team:Fatih_Turkey/Members">Members</a></li>
 +
                                                                                  <li><a
 +
href="https://2011.igem.org/Team:Fatih_Turkey/Gallery">Gallery</a></li>
 +
                                                                                  <li><a
 +
href="https://2011.igem.org/Team:Fatih_Turkey/Europe_Jamboree">Europe Jamboree</a></li>
 +
</ul>
 +
</li>
 +
<li>
 +
<a href="https://2011.igem.org/Team:Fatih_Turkey/Human_Practice">Human Practice</a>
 +
<ul>
 +
<li><a href="https://2011.igem.org/Team:Fatih_Turkey/Sporocide">Sporicide</a></li>
 +
<li><a href="https://2011.igem.org/Team:Fatih_Turkey/iGEM_for_7_to_77">iGEM for 7 to 77</a></li>
 +
<li><a href="https://2011.igem.org/Team:Fatih_Turkey/game">Game</a></li>
 +
<li><a href="https://2011.igem.org/Team:Fatih_Turkey/canvas_times">Canvas Times</a></li>
 +
                                                                                <li><a
 +
href="https://2011.igem.org/Team:Fatih_Turkey/Safety">Safety</a></li>
 +
<li><a href="https://2011.igem.org/Team:Fatih_Turkey/collaboration">Collaboration</a></li>
 +
</ul>
 +
</li>
 +
<li>
 +
<a href="https://2011.igem.org/Team:Fatih_Turkey/Lab_Garage">Lab Garage</a>
 +
<ul>
 +
<li><a href="https://2011.igem.org/Team:Fatih_Turkey/Notebook">Notebook</a></li>
 +
<li><a href="https://2011.igem.org/Team:Fatih_Turkey/Procedures">Procedures</a></li>
 +
</ul>
 +
</li>
 +
                                                            </ul>
 +
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 +
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 +
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 +
</div>
 +
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 +
<!-- End Header -->
 +
<div class="bar-title-whole">
 +
  <div class="bar-title">
 +
      <h2 style="font-family: Verdana, Arial, SunSans-Regular, sans-serif;">Lab Garage</h2>
 +
      <h5 style="font-family: Verdana, Arial, SunSans-Regular, sans-serif;">Notebook</h5>
 +
    </div>
 +
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 +
  <div class="bar-title-sh"></div>
 +
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    <div style="margin-left: 40px;">
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        <span style="float: left;">Week: </span>
 +
        <ul id="haftalar">
 +
            <li class="active"><a href="https://2011.igem.org/Team:Fatih_Turkey/Notebook">1</a></li>
 +
            <li><a href="https://2011.igem.org/Team:Fatih_Turkey/Notebook2">2</a></li>
 +
            <li><a href="https://2011.igem.org/Team:Fatih_Turkey/Notebook3">3</a></li>
 +
            <li><a href="https://2011.igem.org/Team:Fatih_Turkey/Notebook4">4</a></li>
 +
            <li><a href="https://2011.igem.org/Team:Fatih_Turkey/Notebook5">5</a></li>
 +
            <li><a href="https://2011.igem.org/Team:Fatih_Turkey/Notebook6">6</a></li>
 +
            <li><a href="https://2011.igem.org/Team:Fatih_Turkey/Notebook7">7</a></li>
 +
            <li><a href="https://2011.igem.org/Team:Fatih_Turkey/Notebook8">8</a></li>
 +
            <li><a href="https://2011.igem.org/Team:Fatih_Turkey/Notebook9">9</a></li>
 +
            <li><a href="https://2011.igem.org/Team:Fatih_Turkey/Notebook10">10</a></li>
 +
            <li><a href="https://2011.igem.org/Team:Fatih_Turkey/Notebook11">11</a></li>
 +
            <li><a href="https://2011.igem.org/Team:Fatih_Turkey/Notebook12">12</a></li>
 +
            <li><a href="https://2011.igem.org/Team:Fatih_Turkey/Notebook13">13</a></li>
 +
        </ul>
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 +
 
 +
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<div id="warning" style="text-align: center; font-weight: bold; font-size: small; color: #f6f6f6; padding: 5px;">
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You <strong>MUST</strong> have a team description page, a project abstract, a complete project description, a lab notebook, and a safety page. PLEASE keep all of your pages within your teams namespace.
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                <div style="width: 840px; border: solid 3px #666; border-radius: 10px; padding-left: 30px;padding-right: 30px; margin:center ">
 +
<h4>14.07.11</h4>
-
<!-- *** End of the alert box *** -->
+
PROBLEMS AND SOLUTIONS<br><br>
 +
# Prepare to competent materials;<br>
-
{|align="justify"
+
*We prepared the competent materials for tomorrow<br>
-
|You can write a background of your team here.  Give us a background of your team, the members, etc.  Or tell us more about something of your choosing.
+
-
|[[Image:Fatih_Turkey_logo.png|200px|right|frame]]
+
-
|-
+
-
|
+
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''Tell us more about your project.  Give us background.  Use this is the abstract of your project.  Be descriptive but concise (1-2 paragraphs)''
+
-
|[[Image:Fatih_Turkey_team.png|right|frame|Your team picture]]
+
-
|-
+
-
|
+
-
|align="center"|[[Team:Fatih_Turkey | Team Example]]
+
-
|}
+
-
<!--- The Mission, Experiments --->
+
(tomorrow we will prepare the competents of b. subtilis and it will be 5th time:))<br>
-
{| style="color:#1b2c8a;background-color:#0c6;" cellpadding="3" cellspacing="1" border="1" bordercolor="#fff" width="62%" align="center"
+
*we prepared our b subtilis plates for using tomorrow<br>
-
!align="center"|[[Team:Fatih_Turkey|Home]]
+
-
!align="center"|[[Team:Fatih_Turkey/Team|Team]]
+
-
!align="center"|[https://igem.org/Team.cgi?year=2010&team_name=Fatih_Turkey Official Team Profile]
+
-
!align="center"|[[Team:Fatih_Turkey/Project|Project]]
+
-
!align="center"|[[Team:Fatih_Turkey/Parts|Parts Submitted to the Registry]]
+
-
!align="center"|[[Team:Fatih_Turkey/Modeling|Modeling]]
+
-
!align="center"|[[Team:Fatih_Turkey/Notebook|Notebook]]
+
-
!align="center"|[[Team:Fatih_Turkey/Safety|Safety]]
+
-
!align="center"|[[Team:Fatih_Turkey/Attributions|Attributions]]
+
-
|}
+
 +
*we have two plates for competent, one of them is wild type and other stain is ATCC6633<br>
-
==Notebook==
+
*we named them not to confuse, the ATCC663 strain's new name is Ahmet, wild type bacteria's new name is Mahmut :)<br>those names are turkish male names<br><br>
-
You should make use of the calendar feature on the wiki and start a lab notebook. This may be looked at by the judges to see how your work progressed throughout the summer. It is a very useful organizational tool as well.
+
# Transformation;<br>
 +
 
 +
*we couldn't get the expected results at transformation of b. subtilis in this week today we will try to make the most succesful transformation ever :)<br>
 +
 
 +
The Problems and The Solutions:<br>
 +
 
 +
-We decided to some changeings at our procedure of competent<br>
 +
 
 +
*incubation time will be a hour, firstly we will add the DNA to b. subtilis pellet without medium B then we will shake the mix for 30 min. and we  will add medium B on this mix than we will shake new mix again for 30 min.<br>
 +
 
 +
*amount of DNA will be increased<br><br>
 +
 
 +
SITUATION<br>
 +
 
 +
Transformation; we prepared 4 plates for transformation<br>
 +
 
 +
1. plate : b. subtilis pellet + 6 microliter plasmid ---&gt; incubation/shaker30 min.--&gt; adding 100 microliter medium B ---&gt;incubation/shaker30min. ---&gt;spreading 5ug/ml Chm plate<br>
 +
 
 +
2. plate: b subtilis pellet + 10 microliter plasmid ---&gt; incubation/shaker30 min.--&gt; adding 100 microliter medium B ---&gt;incubation/shaker30min.----&gt; spreading 5ug/ml  Chm plate<br>
 +
 
 +
3. plate: b subtilis pellet + adding 100 microliter medium B ---&gt; incubation/sahker 30 min.---&gt;adding 10 microliter plasmid ---&gt; incubation/shaker30min.----&gt; spreading 5ug/ml Chm plate<br>
 +
 
 +
4.plate: b subtilis pellet + adding 100 microliter medium B ---&gt; incubation/sahker 30 min.---&gt;adding 6 microliter plasmid ---&gt; incubation/shaker30min.----&gt; spreading 5ug/ml Chm plate<br>
 +
          <h4>16.07.11</h4><br><br>
 +
 
 +
1.       Plasmidisolationwasdone. (K090402/01)<br>
 +
 
 +
2.       Competentcellpreparationwasaccomplished. (Mahmut)<br>
 +
 
 +
a.       Three Eppendorfswereexposedtotransformationprocess.<br>
 +
 
 +
b.      NineteenEppendorfswerestocked in -80 C byglycerolstockprocedure.<br>
 +
 
 +
3.       Onemediabottle LB (200 ml) wasprepared.<br>
 +
 
 +
4.       Fourteenplateswithoutantibioticswerestocked.<br>
 +
 
 +
5.       Fentonreagentexperimentwastested.<br>
 +
 
 +
a.       Twofalcons(50 ml) thatincludedoneE.colicolonyperfalconwereprepared. Exposedtoincubation at 37 C.OD650 of falconsweremeasured as 0,37 and 0,08. Theonethat has bigger OD650 wasseperated as 1 ml culturetofourEppendorfs.<br>
 +
 
 +
b.      Oneepp. wasindicated as control. OnewasincludedFentonreagent (FR) dissolvedoxygen, onewasincluded FR withdistilledwaterandlastonewasincluded x10 FR withdistilledwater.<br>
 +
 
 +
c.       All of theEppendorfswereexposedto FR solutionsfor 30 minutes.<br>
 +
 
 +
d.      FourplateswerepreaparedbyspreadingperEppendorfsthat had beenprepared in step 5b. <br>Fourplateswerealsopreparedalternativelybystreaking.<br>
 +
 
 +
6.       500 ul FR withdistilledwaterwas put in 1,5 ml Eppendorf; exposedtoheatshock at 50 C hopingthat it wouldreflectblue-greencolorwhichindicatesthesoluitonlosesitskillingactivity. Itdid not happen.<br>
 +
 
 +
<a href="https://static.igem.org/mediawiki/igem.org/d/da/16%2C07%2C2011.pdf">https://static.igem.org/mediawiki/igem.org/d/da/16%2C07%2C2011.pdf</a><br><br>
 +
<h4>20.07.11</h4><br><br>
 +
 
 +
<a href="https://static.igem.org/mediawiki/igem.org/7/7f/20_07_11.png">https://static.igem.org/mediawiki/igem.org/7/7f/20_07_11.png</a><br>
 +
 
 +
<a href="https://static.igem.org/mediawiki/2011/4/41/Dcd.png">https://static.igem.org/mediawiki/2011/4/41/Dcd.png</a><br>
 +
 
 +
<a href="https://static.igem.org/mediawiki/2011/6/64/Vs.png">https://static.igem.org/mediawiki/2011/6/64/Vs.png</a><br>
 +
 
 +
<a href="https://static.igem.org/mediawiki/2011/b/b7/Fg.png">https://static.igem.org/mediawiki/2011/b/b7/Fg.png</a><br><br>
 +
 
 +
 
 +
<strong>DISCUSSION</strong><br><br>
 +
 
 +
As a conclusion we observed Distilled water including Fenton Reagent (DFR) is more effective than Oxygenated water including Fenton Reagent (OFR) in E.coli. When 25 uL OFR and DFR have been added in E.coli cultures,  82% of DFR treated culture is dead and 47% of OFR treated culture ‘s dead. We didn’t see any colony which included 50 uL and more DFR.  However, after 75 uL and more addition of OFR, any colony formation has not been observed.<br>
 +
 
 +
On the other hand we observed OFR is more effective than DFR in Bacillus subtilis.When 10 uL OFR and DFR have been added in Bacillus subtilis cultures,38% of DFR treated culture is dead and 98.3% of OFR treated culture’s dead. Not only the 25 uL OFR treated but also 25 uL DFR treated culture is dead.<br>
 +
 
 +
If we want to compare E.coli and B. subtilis, we can say that Fenton Reagent application is more fatal for Bacillus subtilis. Both 25 uL OFR and DFR treated Bacillus subtilis culture is dead but 25 uL OFR and DFR treated E.coli culture is still alive.<br><br>
 +
 
 +
&nbsp;
 +
 
 +
5 mL lb which include E.coli has been prepared in the morning then when the culture grown up it has been stroke in lb-agar which contain corn starch and no antibiotics.<br>
 +
 
 +
The wiki arrangement has been kept on.<br>
 +
 
 +
The fridge has been tidied up.<br>
 +
 
 +
400 mL lb-agar with ampisilin has been prepared.<br>
 +
 
 +
E.coli which have GFP, RFP and CFP has been stocked in glycerol. At the same time this cultures have been spreaded.<br>
 +
 
 +
Sporocide experiment has been done.<br><br>
 +
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2011 © Fatih Medical School
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Latest revision as of 19:32, 28 October 2011

deneme baslik

Lab Garage

Notebook
Week:

14.07.11

PROBLEMS AND SOLUTIONS

# Prepare to competent materials;
*We prepared the competent materials for tomorrow
(tomorrow we will prepare the competents of b. subtilis and it will be 5th time:))
*we prepared our b subtilis plates for using tomorrow
*we have two plates for competent, one of them is wild type and other stain is ATCC6633
*we named them not to confuse, the ATCC663 strain's new name is Ahmet, wild type bacteria's new name is Mahmut :)
those names are turkish male names

# Transformation;
*we couldn't get the expected results at transformation of b. subtilis in this week today we will try to make the most succesful transformation ever :)
The Problems and The Solutions:
-We decided to some changeings at our procedure of competent
*incubation time will be a hour, firstly we will add the DNA to b. subtilis pellet without medium B then we will shake the mix for 30 min. and we  will add medium B on this mix than we will shake new mix again for 30 min.
*amount of DNA will be increased

SITUATION
Transformation; we prepared 4 plates for transformation
1. plate : b. subtilis pellet + 6 microliter plasmid ---> incubation/shaker30 min.--> adding 100 microliter medium B --->incubation/shaker30min. --->spreading 5ug/ml Chm plate
2. plate: b subtilis pellet + 10 microliter plasmid ---> incubation/shaker30 min.--> adding 100 microliter medium B --->incubation/shaker30min.----> spreading 5ug/ml  Chm plate
3. plate: b subtilis pellet + adding 100 microliter medium B ---> incubation/sahker 30 min.--->adding 10 microliter plasmid ---> incubation/shaker30min.----> spreading 5ug/ml Chm plate
4.plate: b subtilis pellet + adding 100 microliter medium B ---> incubation/sahker 30 min.--->adding 6 microliter plasmid ---> incubation/shaker30min.----> spreading 5ug/ml Chm plate

16.07.11



1.       Plasmidisolationwasdone. (K090402/01)
2.       Competentcellpreparationwasaccomplished. (Mahmut)
a.       Three Eppendorfswereexposedtotransformationprocess.
b.      NineteenEppendorfswerestocked in -80 C byglycerolstockprocedure.
3.       Onemediabottle LB (200 ml) wasprepared.
4.       Fourteenplateswithoutantibioticswerestocked.
5.       Fentonreagentexperimentwastested.
a.       Twofalcons(50 ml) thatincludedoneE.colicolonyperfalconwereprepared. Exposedtoincubation at 37 C.OD650 of falconsweremeasured as 0,37 and 0,08. Theonethat has bigger OD650 wasseperated as 1 ml culturetofourEppendorfs.
b.      Oneepp. wasindicated as control. OnewasincludedFentonreagent (FR) dissolvedoxygen, onewasincluded FR withdistilledwaterandlastonewasincluded x10 FR withdistilledwater.
c.       All of theEppendorfswereexposedto FR solutionsfor 30 minutes.
d.      FourplateswerepreaparedbyspreadingperEppendorfsthat had beenprepared in step 5b.
Fourplateswerealsopreparedalternativelybystreaking.
6.       500 ul FR withdistilledwaterwas put in 1,5 ml Eppendorf; exposedtoheatshock at 50 C hopingthat it wouldreflectblue-greencolorwhichindicatesthesoluitonlosesitskillingactivity. Itdid not happen.
https://static.igem.org/mediawiki/igem.org/d/da/16%2C07%2C2011.pdf

20.07.11



https://static.igem.org/mediawiki/igem.org/7/7f/20_07_11.png
https://static.igem.org/mediawiki/2011/4/41/Dcd.png
https://static.igem.org/mediawiki/2011/6/64/Vs.png
https://static.igem.org/mediawiki/2011/b/b7/Fg.png

DISCUSSION

As a conclusion we observed Distilled water including Fenton Reagent (DFR) is more effective than Oxygenated water including Fenton Reagent (OFR) in E.coli. When 25 uL OFR and DFR have been added in E.coli cultures,  82% of DFR treated culture is dead and 47% of OFR treated culture ‘s dead. We didn’t see any colony which included 50 uL and more DFR.  However, after 75 uL and more addition of OFR, any colony formation has not been observed.
On the other hand we observed OFR is more effective than DFR in Bacillus subtilis.When 10 uL OFR and DFR have been added in Bacillus subtilis cultures,38% of DFR treated culture is dead and 98.3% of OFR treated culture’s dead. Not only the 25 uL OFR treated but also 25 uL DFR treated culture is dead.
If we want to compare E.coli and B. subtilis, we can say that Fenton Reagent application is more fatal for Bacillus subtilis. Both 25 uL OFR and DFR treated Bacillus subtilis culture is dead but 25 uL OFR and DFR treated E.coli culture is still alive.

  5 mL lb which include E.coli has been prepared in the morning then when the culture grown up it has been stroke in lb-agar which contain corn starch and no antibiotics.
The wiki arrangement has been kept on.
The fridge has been tidied up.
400 mL lb-agar with ampisilin has been prepared.
E.coli which have GFP, RFP and CFP has been stocked in glycerol. At the same time this cultures have been spreaded.
Sporocide experiment has been done.

2011 © Fatih Medical School

Retrieved from "http://2011.igem.org/Team:Fatih_Turkey/Notebook"