Difference between revisions of "Part:BBa K606059:Experience"

 
 
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This experience page is provided so that any user may enter their experience using this part.<BR>Please enter
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= Characterization tRNA amber suppressor=
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how you used this part and how it worked out.
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==Protocol==
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In order to characterize the tRNA amber suppressor, as well as the pHyperspank, a special part was made: Pveg-SpoVG-GFP amber-TT.
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A double transformation was done with minipreps of two plasmids of different antibiotic resistances : pSB1C3 holding the tRNA under the control of pHyperspank and pSB1AK3 holding the GFP with the amber codon under the control of a constitutive promotor. Two groups of cultures of each picked colony were made. One group was cultured in rich medium without IPTG whilst the other group was cultured in rich medium with IPTG (4mM in 10mL). A culture of the strain holding GFP amber alone was grown in parallel. The two tubes of each colony were compared along with the negative control (GFP amber alone). Cultures were then diluted for microscopy, glycerols, and future experiments. We used the following strains to characterize this system:
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'''GFP amber'''
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Strain holding GFPmut3B, mutated with a single amber mutation under the control of the constitutive promotor Pveg, in the plasmid pSB1AK3 (AmpR).
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'''tRNA amber suppressor'''
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Strain holding the tRNA amber suppressor, under the control of  IPTG inducible strong promotor pHyperspank, in the plasmid pSB1C3 (CmR).
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'''Double transformant'''
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Double transformant of the two previous constructs in their plasmids respectively.
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Two groups of cultures are grown: with or without IPTG.
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Direct observation under fluorescence lamp and microscopy was used to characterize this system.
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<br>We have also <b><a href="http://2011.igem.org/Team:Paris_Bettencourt/Experiments/pHyperSpank">characterised the pHyperSpank promoter</a></b>, compatible with <i>B.subtilis</i> and which is used in this system.
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==Characterization of the tRNA biobrick (fluorescence lamp)==
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The cultures of strains having transformed both tRNA amber suppressor and GFP amber were strongly fluorescent, while the culture of the GFP amber alone as well as the culture of the colony without IPTG induction showed basal fluorescence.
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[[Image:GFPamberwithtRNA.jpg|350px|thumb|center|On the left, the culture of the strain holding GFP amber alone under the control of Pveg (constitutive promotor). On the right, the culture of the double transformant with IPTG induction (4mM)]]
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==Characterization of the tRNA biobrick (microscopy)==
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{| border="1" class="wikitable" style="text-align: center;"
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|+GFP amber / E-coli at 37°C
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|-
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|[[Image:Trnaminus gfp amber trans 1.jpg|350px|thumb|center|E-Coli  at 37°C  (trans image)]]
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|[[Image:Trnaminus_gfp_amber_fluo_1.jpg|350px|thumb|center|E-Coli  at 37°C  (gfp image)]]
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|-
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|[[Image:Trnaminus gfp amber trans 2.jpg|350px|thumb|center|E-Coli  at 37°C  (trans image)]]
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|[[Image:Trnaminus gfp amber fluo 2.jpg|350px|thumb|center|E-Coli  at 37°C  (gfp image)]]
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|}
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{| border="1" class="wikitable" style="text-align: center;"
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|+GFP amber +tRNA amber -IPTG/ E-coli at 37°C
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|-
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|[[Image:Trna_noiptg_gfp_amber_trans_.jpg|350px|thumb|center|E-Coli  at 37°C  (trans image)]]
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|[[Image:Trna noiptg gfp amber fluo 1.jpg|350px|thumb|center|E-Coli  at 37°C  (gfp image)]]
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|-
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|[[Image:Trna noiptg gfp amber trans 2.jpg|350px|thumb|center|E-Coli  at 37°C  (trans image)]]
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|[[Image:Trna noiptg gfp amber fluo 2.jpg|350px|thumb|center|E-Coli  at 37°C  (gfp image)]]
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|}
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{| border="1" class="wikitable" style="text-align: center;"
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|+GFP amber +tRNA amber +IPTG/ E-coli at 37°C
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|-
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|[[Image:Trna iptg gfp amber trans 3.jpg|350px|thumb|center|E-Coli  induced with IPTG at 37°C  (trans image)]]
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|[[Image:Trna iptg gfp amber fluo 3.jpg|350px|thumb|center|E-Coli induced with IPTG at 37°C  (gfp image)]]
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|-
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|[[Image:Trna iptg gfp amber trans 4.jpg|350px|thumb|center|E-Coli induced with IPTG at 37°C  (trans image)]]
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|[[Image:Trna iptg gfp amber fluo 4.jpg|350px|thumb|center|E-Coli  induced with IPTG at 37°C  (gfp image)]]
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|}
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<html>
 
===Applications of BBa_K606059===
 
===Applications of BBa_K606059===
  

Latest revision as of 19:49, 19 October 2011

Characterization tRNA amber suppressor

Protocol

In order to characterize the tRNA amber suppressor, as well as the pHyperspank, a special part was made: Pveg-SpoVG-GFP amber-TT. A double transformation was done with minipreps of two plasmids of different antibiotic resistances : pSB1C3 holding the tRNA under the control of pHyperspank and pSB1AK3 holding the GFP with the amber codon under the control of a constitutive promotor. Two groups of cultures of each picked colony were made. One group was cultured in rich medium without IPTG whilst the other group was cultured in rich medium with IPTG (4mM in 10mL). A culture of the strain holding GFP amber alone was grown in parallel. The two tubes of each colony were compared along with the negative control (GFP amber alone). Cultures were then diluted for microscopy, glycerols, and future experiments. We used the following strains to characterize this system:

GFP amber Strain holding GFPmut3B, mutated with a single amber mutation under the control of the constitutive promotor Pveg, in the plasmid pSB1AK3 (AmpR).

tRNA amber suppressor Strain holding the tRNA amber suppressor, under the control of IPTG inducible strong promotor pHyperspank, in the plasmid pSB1C3 (CmR).

Double transformant Double transformant of the two previous constructs in their plasmids respectively. Two groups of cultures are grown: with or without IPTG.

Direct observation under fluorescence lamp and microscopy was used to characterize this system.
We have also characterised the pHyperSpank promoter, compatible with B.subtilis and which is used in this system.

Characterization of the tRNA biobrick (fluorescence lamp)

The cultures of strains having transformed both tRNA amber suppressor and GFP amber were strongly fluorescent, while the culture of the GFP amber alone as well as the culture of the colony without IPTG induction showed basal fluorescence.

On the left, the culture of the strain holding GFP amber alone under the control of Pveg (constitutive promotor). On the right, the culture of the double transformant with IPTG induction (4mM)

Characterization of the tRNA biobrick (microscopy)

GFP amber / E-coli at 37°C
E-Coli at 37°C (trans image)
E-Coli at 37°C (gfp image)
E-Coli at 37°C (trans image)
E-Coli at 37°C (gfp image)
GFP amber +tRNA amber -IPTG/ E-coli at 37°C
E-Coli at 37°C (trans image)
E-Coli at 37°C (gfp image)
E-Coli at 37°C (trans image)
E-Coli at 37°C (gfp image)
GFP amber +tRNA amber +IPTG/ E-coli at 37°C
E-Coli induced with IPTG at 37°C (trans image)
E-Coli induced with IPTG at 37°C (gfp image)
E-Coli induced with IPTG at 37°C (trans image)
E-Coli induced with IPTG at 37°C (gfp image)


===Applications of BBa_K606059=== ===User Reviews=== BBa_K606059 StartReviews BBa_K606059 EndReviews