Difference between revisions of "Part:BBa K2656106"

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{|class='wikitable'
 
{|class='wikitable'
|colspan=4|Table 1. Optimized parameters for the BBa_K2656106.
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|colspan=4|Table 1. Optimized parameters for the constitutive model with TU BBa_K2656106.
 
|-
 
|-
 
|'''Parameter'''
 
|'''Parameter'''
 
|'''Value'''
 
|'''Value'''
 
|-
 
|-
|Translation rate p
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|Constitutive transcription rate CR
|p =  
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|CR = 539.5 min-1
 
|-
 
|-
 
|Dilution rate μ
 
|Dilution rate μ
| μ =  
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| μ = 0.0058 min-1
 +
 
 
|-
 
|-
 
| PoI degradation rate  
 
| PoI degradation rate  

Revision as of 07:45, 16 October 2018


GFP transcriptional unit 2

Transcriptional unit assembled with a one-pot [http://2018.igem.org/Team:Valencia_UPV/Design Level 1] Golden Gate reaction using BsaI type IIS endonuclease (Figure 1).

TU.
Figure 1. Transcriptional unit assembled. Golden Gote scars: standardized overhangs for promoter, RBS, CDS and terminator

This transcriptional unit is composed of the following standardized parts from our [http://2018.igem.org/Team:Valencia_UPV/Part_Collection Part Collection]:

This transcriptional unit has been used to characterize the constitutive BBa_K2656005 promoter. Following this [http://2018.igem.org/Team:Valencia_UPV/Modeling#http://2018.igem.org/Team:Valencia_UPV/Experiments#exp_protocol experimental protocol], we have obtained the parameters to valide our [http://2018.igem.org/Team:Valencia_UPV/Modeling#models constitutive model] and so the results of the next graph have been obtained after an [http://2018.igem.org/Team:Valencia_UPV/Modeling#optimization optimization] and decision-making process, in which the optimal parameters have been selected and the constituent model for each objective has been simulated and compared with the experimental data.

[[File:|900px|thumb|none|alt=Promoter experiment.|Figure 1. Promoter expression experiment with composite parts BBa_K2656105, BBa_K2656106 and BBa_K2656107]]

Table 1. Optimized parameters for the constitutive model with TU BBa_K2656106.
Parameter Value
Constitutive transcription rate CR CR = 539.5 min-1
Dilution rate μ μ = 0.0058 min-1
PoI degradation rate Promoter Experiment: dp =



Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 11
    Illegal NheI site found at 34
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]