Team:Cambridge/Signalling/Primers

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Signalling Overview Vectors Constructs Primers Experiments Lab Notebook

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Agr Primers

These primers are to extract each part of the Agr operon so that a Bacillus RBS can replace the E. coli RBS currently attached to the genes.

agr senders

Agr_B_F
*5' GTTTCTT C GAATTC GCGGCCGC  T  TCTAG ATGaactattttgacaacaa 3'
 
Agr_B_R 
*5' TT C CTGCAG CGGCCGC  T  ACTAGT A TTATTA  tttcagatcctctttgatg 3'

Agr_D_F
*5' CTT C GAATTC GCGGCCGC  T  TCTAG atgaatactctgttcaatctgtttt 3'

Agr_D_R
*5' TT C CTGCAG CGGCCGC  T  ACTAGT A TTATTA ttcatgcagctgggtcagct 3'

agr receivers

Agr_C_F
*5' GTTTCTT C GAATTC GCGGCCGC  T  TCTAG atgattctgatgttcaccat 3' 

Agr_C_R
*5' TT C CTGCAG CGGCCGC  T  ACTAGT A TTATTA gttattgatgatttcgactt 3' 

Agr_A_F
*5' GTTTCTT C GAATTC GCGGCCGC  T  TCTAG  atggaaatcgcactggcta 3'

Agr_A_R
*5' TT C CTGCAG CGGCCGC  T  ACTAGT A TTATTA  gattttcttgacattgcgta 3'

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-====Promoter Primers====
-Temperatures were calculated using https://www.finnzymes.fi/tm_determination.html.
-The uppercase letters match the plasmid sequence, while the lowercase letters are 'bumper bases' for restriction cuts and the biobrick prefix and suffixes. Bumper bases, biobrick prefixes, and plasmid DNA are separated by spaces.
-{| class="wikitable" border="1"
-|-
-! Primer name
-! Parent vector
-! init. length
-! init. Tm
-! init. GC%
-! final length
-! final Tm
-! final GC
-|-
-|pXyl promoter forward
-|pSG1154 (ECE153)
-| 26
-| 58.7+3
-| 15.3%
-| 50
-| 80.0+3
-| 34.0%
-|-
-|colspan="8" align=center|<pre>at gaattcgcggccgcttctagag TTCATGAAAAACTAAAAAAAATATTG</pre>
-|-
-|pXyl promoter reverse
-|pSG1154 (ECE153)
-| 26 bp
-| 63.0+3
-| 26.6 %
-| 50
-| 79.5+3
-| 44.0%
-|-
-|colspan="8" align=center|<pre>gat ctgcagcggccgctactagta TATGTCATATTGTAAGTAAGTTGCAC</pre>
-|-
-|pSpac promoter forward
-|pMUTIN-YFP (ECE151)
-| 22
-| 58.5+3
-| 36.3%
-| 46
-| 82.6+3
-| 45.6%
-|-
-|colspan="8" align=center|<pre>at gaattcgcggccgcttctagag AGAACAACCTCTGCTAAAATTC</pre>
-|-
-|pSpac promoter reverse
-|pMUTIN-YFP (ECE151)
-| 21
-| 59.3+3
-| 38.0%
-| 45
-| 80.4+3
-| 46.6%
-|-
-|colspan="8" align=center|<pre>tat ctgcagcggccgctactagta AAGCTTAATTGTTATCCGCTC</pre>
-|-
-|pPac promoter forward
-|pMUTIN-YFP (ECE151)
-| 21
-| 61.7+3
-| 38.0%
-| 45
-| 84.5+3
-| 46.6%
-|-
-|colspan="8" align=center|<pre>at gaattcgcggccgcttctagag AAACGAGGTCATCATTTCCTT</pre>
-|-
-|pPac promoter reverse
-|pMUTIN-YFP (ECE151)
-| 26
-| 57.7+3
-| 26.6%
-| 50
-| 82.1+3
-| 46.0%
-|-
-|colspan="8" align=center|<pre>cgc ctgcagcggccgctactagta CAAATGTAGTCTTTGAAAGTATTACA</pre>
-|-
-|pUpp promoter forward
-|pAD45-25 (ECE166)
-| 22
-| 58.8+3
-| 27.2%
-| 46
-| 82.6+3
-| 41.3%
-|-
-|colspan="8" align=center|<pre>at gaattcgcggccgcttctagag GATGAATAAATTTTGGCGATAT</pre>
-|-
-|pUpp promoter reverse
-|pAD45-25 (ECE166)
-| 25
-| 60.9+3
-| 36.0%
-| 49
-| 80.3+3
-| 44.8%
-|-
-|colspan="8" align=center|<pre>tat ctgcagcggccgctactagta GAGGATCAAATACATACAGTTTTCC</pre>
-|-
-|}
-====Bacillus Biobrick pBSINT1 Primers====
-{| class="wikitable" border="1"
-|-
-! Primer name
-! Parent vector
-! init. length
-! init. Tm
-! init. GC%
-! final length
-! final Tm
-! final GC
-|-
-|pBSINT1 bla+rep forward
-|pSB1A3
-|
-|
-|
-| 20
-| 62.9
-| 50.0%
-|-
-|colspan="8" align=center|<pre> GCAGGAAAGAACATGTGAGC</pre>
-|-
-|pBSINT1 bla+rep reverse
-|pSB1A3
-|
-|
-|
-| 20
-| 66.7
-| 50.0%
-|-
-|colspan="8" align=center|<pre>GCACTTTTCGGGGAAATGTG</pre>
-|-
-|pBSINT1 amyE front forward
-|pDG1661 (ECE112)
-| 20
-| 63.6
-| 50.0%
-| 35
-| 83.2+3
-| 51.4%
-|-
-|colspan="8" align=center|<pre> ttccccgaaaagtgc ccagtcttcacatcggtttg</pre>
-|-
-|pBSINT1 amyE front reverse
-|pDG1661 (ECE112)
-| 20
-| 66.7
-| 55.0%
-| 35
-| 83.1+3
-| 57.1%
-|-
-|colspan="8" align=center|<pre>agacgtcaggtggca ctgcccgtatttcgcgtaag</pre>
-|-
-|pBSINT1 amyE back+cat forward
-|pDG1661 (ECE112)
-| 19
-| 63.2
-| 47.3%
-| 34
-| 78.1+3
-| 47.0%
-|-
-|colspan="8" align=center|<pre>ctcaaaggcggtaat tttcgctacgctcaaatcc</pre>
-|-
-|pBSINT1 amyE back+cat reverse
-|pDG1661 (ECE112)
-| 20
-| 66.5
-| 55.0%
-| 35
-| 81.5+3
-| 51.4%
-|-
-|colspan="8" align=center|<pre>catgttctttcctgc cctacaatccatgccaaccc</pre>
-|-
-|VF
-|pSB1A3
-|
-|
-|
-| 20
-| 63.8
-| 50.0%
-|-
-|colspan="8" align=center|<pre>tgccacctgacgtctaagaa</pre>
-|-
-|VR
-|pSB1A3
-|
-|
-|
-| 20
-| 63.4
-| 50.0%
-|-
-|colspan="8" align=center|<pre>tat ctgcagcggccgctactagta GAGGATCAAATACATACAGTTTTCC</pre>
-|-
-|}
-====Bacillus RBS Primers====
-We made primer sets for 2 ribosomal binding sites in Bacillus of differing binding strengths. We expect B._sub_RBSs to bind very strongly because it is the consensus sequence for RBS in B. subtilis. Because of its small size, we also made detection primers for use with VF & VR (or temperature compatible alternates) to detect the RBS within the insert,
-<pre>
-B. subtilis consensus RBS - http://www.ncbi.nlm.nih.gov/pubmed/10446248
-B._sub_RBSs_F
-*5' GAATTCGCGGCCGCTTCTAGAG AAAGGAGG TGTTA 3'
-B._sub_RBSs_R
-*5' CTGCAGCGGCCGCTACTAGTAACA CCTCCTTT CTCT 3'</pre>
-<pre>RBS modified from ECE112 SpoVG RBS - http://www.bgsc.org/Catalogs/Catpart4.pdf
-B._sub_RBSw_F
-*5' GAATTCGCGGCCGCTTCTAGAG AGAGGTGG TGTTA 3'
-B._sub_RBSw_R
-*5' CTGCAGCGGCCGCTACTAGTAACA CCACCTCT CTCT 3'</pre>
-{| class="wikitable" border="1"
-|-
-! Primer name
-! final length
-! final Tm
-! final GC
-|-
-|RBS s Detection forward
-| 20
-| 62.3
-| 55.0%
-|-
-|colspan="8" align=center|<pre>CCGCTTCTAGAG AAAGGAGG</pre>
-|-
-|RBS w Detection forward
-| 20
-| 63.4
-| 60.0%
-|-
-|colspan="8" align=center|<pre>CCGCTTCTAGAG AGAGGTGG</pre>
-|-
-|}
 ====Agr Primers====
 *These primers are to extract each part of the Agr operon so that a Bacillus RBS can replace the E. coli RBS currently attached to the genes.