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Team:MSOE Milwaukee/Week3
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| - | + | <br><FONT color = 'green' size="+20">Week 3</FONT><BR><BR> | |
<H1 align = left>Monday</H1> | <H1 align = left>Monday</H1> | ||
| - | <p>As a team, we finally decided on inputs and outputs for our project. After a long discussion, we chose Eucalyptol as our output because we wanted a more rare or hard to obtain substance. For our input, we chose to use the spent grains from beer production here in Milwaukee. This provided us with direction to further our research on the pathways and enzymes involved.</p><br> | + | <p style="text-align:justify">As a team, we finally decided on inputs and outputs for our project. After a long discussion, we chose Eucalyptol as our output because we wanted a more rare or hard to obtain substance. For our input, we chose to use the spent grains from beer production here in Milwaukee. This provided us with direction to further our research on the pathways and enzymes involved.</p><br> |
<H1 align = left>Tuesday</H1> | <H1 align = left>Tuesday</H1> | ||
| - | <p>In small groups we researched the different pathways and enzymes involved in the output of Eucalyptol and found the pathways incorporated in its production. The glucose from the spent grains will travel into the citric acid cycle, then through the mevalonate pathway, and then a final enzyme will synthesize the Eucalyptol from Geranyl-PP. We found the different enzymes incorporated in the different pathways that do not already exist in </i>E.coli</i> and found their sequences in online databases.</p><br> | + | <p style="text-align:justify">In small groups we researched the different pathways and enzymes involved in the output of Eucalyptol and found the pathways incorporated in its production. The glucose from the spent grains will travel into the citric acid cycle, then through the mevalonate pathway, and then a final enzyme will synthesize the Eucalyptol from Geranyl-PP. We found the different enzymes incorporated in the different pathways that do not already exist in </i>E.coli</i> and found their sequences in online databases.</p><br> |
<H1 align = left>Wednesday</H1> | <H1 align = left>Wednesday</H1> | ||
| - | <p>To continue our research, we looked at different promoters, terminators, and plasmids in the parts registry that are available for our use. We also looked at past iGEM projects to investigate which ones they used and their reasoning behind that to help us make our decision. We decided on using the T7 promoter to control the expression of our genes and the standard double terminator.</p><br> | + | <p style="text-align:justify">To continue our research, we looked at different promoters, terminators, and plasmids in the parts registry that are available for our use. We also looked at past iGEM projects to investigate which ones they used and their reasoning behind that to help us make our decision. We decided on using the T7 promoter to control the expression of our genes and the standard double terminator.</p><br> |
<H1 align = left>Thursday</H1> | <H1 align = left>Thursday</H1> | ||
| - | <p>In groups, we researched the possible locations of where to incorporate terminators and promoters in the biobrick parts, and we decided to use one promoter and one terminator for each biobrick part or gene to promote stable gene expression. We also decided to use | + | <p style="text-align:justify">In groups, we researched the possible locations of where to incorporate terminators and promoters in the biobrick parts, and we decided to use one promoter and one terminator for each biobrick part or gene to promote stable gene expression. We also decided to use three genes or two biobrick parts per plasmid to optimize expression and ensure that the plasmids do not reach capacity. Our plan is to group our output genes as follows: |
<br><br> | <br><br> | ||
| - | *Plasmid 1: HMG-CoA synthase | + | *Plasmid 1: HMG-CoA synthase, HMG-CoA reductase, and Mevalonate kinase<br> |
| - | *Plasmid 2: | + | *Plasmid 2: Phosphomevalonate kinase, Mevalonate-5-pyrophosphate decarboxylase, and 1,8-cineole synthase<br> |
| - | + | ||
<H1 align = left>Friday</H1> | <H1 align = left>Friday</H1> | ||
| - | <p></p> | + | <p style="text-align:justify">Individually, we further researched plasmids, promoters, and the strains of </i>E.coli</i>. We determined that using the DE3 or the BL21 strain of </i>E.coli</i> would be most beneficial to us because it is an expression strain and is compatible with the the T7 promoter we would like to use. We also determined that we would like to continue our research on plasmids, but that the pSTV28 plasmid vector was of itnerest because it is a low copy plasmid and more suited to our use than the standard plasmids available in the iGEM kit. </p> |
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{{Team:MSOE:Notebook}} | {{Team:MSOE:Notebook}} | ||
Latest revision as of 13:40, 22 August 2013
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Week 3
Monday
As a team, we finally decided on inputs and outputs for our project. After a long discussion, we chose Eucalyptol as our output because we wanted a more rare or hard to obtain substance. For our input, we chose to use the spent grains from beer production here in Milwaukee. This provided us with direction to further our research on the pathways and enzymes involved.
Tuesday
In small groups we researched the different pathways and enzymes involved in the output of Eucalyptol and found the pathways incorporated in its production. The glucose from the spent grains will travel into the citric acid cycle, then through the mevalonate pathway, and then a final enzyme will synthesize the Eucalyptol from Geranyl-PP. We found the different enzymes incorporated in the different pathways that do not already exist in E.coli and found their sequences in online databases.
Wednesday
To continue our research, we looked at different promoters, terminators, and plasmids in the parts registry that are available for our use. We also looked at past iGEM projects to investigate which ones they used and their reasoning behind that to help us make our decision. We decided on using the T7 promoter to control the expression of our genes and the standard double terminator.
Thursday
In groups, we researched the possible locations of where to incorporate terminators and promoters in the biobrick parts, and we decided to use one promoter and one terminator for each biobrick part or gene to promote stable gene expression. We also decided to use three genes or two biobrick parts per plasmid to optimize expression and ensure that the plasmids do not reach capacity. Our plan is to group our output genes as follows:
*Plasmid 1: HMG-CoA synthase, HMG-CoA reductase, and Mevalonate kinase
*Plasmid 2: Phosphomevalonate kinase, Mevalonate-5-pyrophosphate decarboxylase, and 1,8-cineole synthase
Friday
Individually, we further researched plasmids, promoters, and the strains of E.coli. We determined that using the DE3 or the BL21 strain of E.coli would be most beneficial to us because it is an expression strain and is compatible with the the T7 promoter we would like to use. We also determined that we would like to continue our research on plasmids, but that the pSTV28 plasmid vector was of itnerest because it is a low copy plasmid and more suited to our use than the standard plasmids available in the iGEM kit.
