Team:BYU Provo/Large Phage

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{{TeamBYUProvo}}
{{TeamBYUProvo}}
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==March==
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{| width="100%"
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===3/15/13===
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| colspan="2" | [[File:LargePhagePic-1.JPG|960px|center]]
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===3/18/13===
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<br>
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===3/20/13===
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===3/22/13===
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<font color="#333399" size="3" font face="Calibri">
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===3/25/13===
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: [[Team:BYU_Provo/Small_Phage|Overview]]
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===3/27/13===
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: [[Team:BYU Provo/Notebook/LargePhage/Winterexp|March-April]]
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===3/29/13===
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: [[Team:BYU Provo/Notebook/LargePhage/Springexp|May-June]]
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==April==
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: [[Team:BYU Provo/Notebook/LargePhage/Summerexp|July-August]]
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===4/1/13===
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===4/4/13===
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: [[Team:BYU Provo/Notebook/LargePhage/Fallexp|September-October]]
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===4/5/13===
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</font>
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===4/8/13===
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===4/10/13===
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<font color="#333399" size="5" font face="Calibri"> '''Overview'''</font>
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===4/12/13===
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<br>
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===4/15/13===
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<font color="#333399" size="3" font face="Calibri">
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**still needs work
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:The goal of the Large Phage Project is to make a mutant phage that has a capsid much larger than the normal ~200nm T4 capsid. Our intent is to create a protocol where large phage with stable phenotypes will form making it possible to "pick a size" when using phage as a delivery system. The impact of these large phage could mean the difference in making a drug treatment effective and efficient.
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:Through the use of our mutagen 5'bromodeoxyuridine, a good mutagenesis protocol and the use of a sensitive cesium chloride gradient. We were able to mutagenize and isolate giant mutant t4 phage.
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[[File:EMpic-1.jpg|400px]]
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==May==
 
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===5/1/13===
 
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===5/3/13===
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</font>
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===5/6/13===
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|}
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===5/8/13===
 
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{{TeamBYUProvoFooter}}
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===5/13/13===
 
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===5/15/13===
 
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===5/17/13===
 
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===5/20/13===
 
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Today we need to run a dilution series to test the titer of our mutated phage stock.
 
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We also need to start selecting for small plaques and learning how to pick them and titer them out.
 
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We also should run a UV test on the mutated phage stock compared to the normal stock.
 
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We picked one plaque off of the 180 sec UV plate sample. We suspended it in 1 mL of broth, and then UV-ed 20 uL samples at 45 second intervals. The number of plaques decreased the longer the samples sat under UV light.  The samples were irradiated from 0 sec to 4 min 30 sec.
 
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As a control, we diluted the T4Do stock to 10^-6 and tested 20 uL at 45 sec intervals (up to 6 min) under UV light.
 
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Also, we diluted the T4 mutagenized stock to 10^-6 and tested 20 uL at 45 sec intervals (up to 4 min 30 sec) under UV light.
 
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UV tests were done by placing 20 uL spots on parafilm and placed in a BSL-2 hood with the UV light turned on.
 
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===5/22/13===
 
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Results from 5/20/13 -
 
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We left the plates in the incubator for 48 hours, which caused contamination on many plates to grow.
 
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When checked at 24 hours, the T4 mutagenized stock had a web plate at 10^-3 and less than 5 plaques at 10^-6. This experiment will need to be redone from 10^0 down through 10^-6.  The whole mutagenesis may need to be redone if this only represents a dilution of our titer when we were trying to grow it in liquid culture.
 
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(We infected with ___ mL of phage at ___ titer in ____ vol of resuspended bacteria.)
 
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Under UV light, the T4Do stock (diluted to 10^-6) has 19 plaques after being irradiated for six minutes (down from almost cleared at 0 min).
 
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Under UV light, the 180 sec UV plate spot (diluted in 1 mL) has a few hundred plaques on it, but the amount dropped significantly at 4 min 30 sec from when it was UV-ed for 0 min.
 
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We will re-titer the T4-Mut stock so we can learn whether it was diluted or whether an infection worked.
 
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We will also re-run the UV test comparing the T4-Mut (10^-3) with the T4-Do stock (at 10^-6) for survivability. The mutagenized phage should survive better.
 
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Since the loss of plaques seemed to level off for the T4Do stock at 5:15 (23 plaques) and 6 min (19 plaques), we will test a 7 min and 8 min timepoint to see if it stays level, suggesting these phage have multiple genomes and are severely mutated.
 
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[[File:Apple.jpeg|600px|thumb|center|T4 mutant 0 and 1.5 minutes under UV light.]]
 
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[[File:Blackberry1.jpeg|600px|thumb|center|T4 mutant 3 and 4.5 minutes under UV light.]]
 
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[[File:Cranberry.jpeg|600px|thumb|center|T4 mutant 6 minutes under UV light.]]
 
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[[File:Dingleberry.jpeg|600px|thumb|center|T4 mutant 7.5 minutes under UV light.]]
 
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[[File:Eggplant.jpeg|600px|thumb|center|T4 mutant 9 minutes under UV light.]]
 
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[[File:Eggplant.jpeg|600px|thumb|center|T4 mutant 0 and 1.5 minutes under UV light.]]
 
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===5/24/13===
 
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===5/27/13===
 
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===5/29/13===
 
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===5/31/13===
 
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==June==
 
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===6/3/13===
 
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===6/5/13===
 
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===6/10/13===
 
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===6/19/13===
 
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===6/24/13===
 
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===6/26/13===
 
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===6/28/13===
 
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==July==
 
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===7/1/13===
 
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===7/3/13===
 
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===7/31/13===
 
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==August==
 
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===8/2/13===
 
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===8/5/13===
 
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===8/9/13===
 
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===8/26/13===
 
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===8/28/13===
 
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===8/30/13===
 
==September==
==September==

Latest revision as of 19:26, 6 September 2013

LargePhagePic-1.JPG


Overview
March-April
May-June
July-August
September-October

Overview


    • still needs work
The goal of the Large Phage Project is to make a mutant phage that has a capsid much larger than the normal ~200nm T4 capsid. Our intent is to create a protocol where large phage with stable phenotypes will form making it possible to "pick a size" when using phage as a delivery system. The impact of these large phage could mean the difference in making a drug treatment effective and efficient.
Through the use of our mutagen 5'bromodeoxyuridine, a good mutagenesis protocol and the use of a sensitive cesium chloride gradient. We were able to mutagenize and isolate giant mutant t4 phage.

EMpic-1.jpg




Contents

September

9/2/13

9/4/13

9/6/13

9/9/13

9/11/13

9/13/13

9/16/13

9/18/13

9/20/13

9/23/13

9/25/13

9/27/13

9/30/13