Difference between revisions of "Part:BBa K3137005"

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[[Image:sapp2.jpg|500px|center|thumb|Figure 2. Effect of different anti-phage parts on the growth of <i>E. coli</i> BL21]]
 
[[Image:sapp2.jpg|500px|center|thumb|Figure 2. Effect of different anti-phage parts on the growth of <i>E. coli</i> BL21]]
  
We used the Entropy Weight Method (EWM) to determine the weight of each growth point to select the most similarly modified strain (the highest correlation), which is the component that has the least impact on bacterial growth. At the same time, after consulting the industry experts, we revised the weights according to the experts' recommendations to evaluate the components again, making them more in line with the real situation of production, that is, the most suitable components for industrial production. Using GRA's two evaluations of the four components at different weights, we selected the component gntR.(Fig 3)
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We used the Entropy Weight Method (EWM) to determine the weight of each growth point to select the most similarly modified strain (the highest correlation), which is the component that has the least impact on bacterial growth. At the same time, after consulting the industry experts, we revised the weights according to the experts' recommendations to evaluate the components again, making them more in line with the real situation of production, that is, the most suitable components for industrial production. Using GRA's two evaluations of the four components at different weights, we selected the component <i>gntR</i>.(Fig 3)
  
 
[[Image:sapp3.png|800px|center|thumb|Figure 3. EWM weight & advice weight and the results of GRA for selecting most suitable strain]]
 
[[Image:sapp3.png|800px|center|thumb|Figure 3. EWM weight & advice weight and the results of GRA for selecting most suitable strain]]

Revision as of 08:29, 21 October 2019


gntR

The Gluconate repressor GntR, is a transcription factor that negatively regulates the operon involved in the catabolism of d-gluconate via the Entner-Doudoroff pathway and represses genes involved in the different systems related to d-gluconate uptake: gluconate Ⅰ and gluconate Ⅱ.

Usage and Biology

To get more efficient phage resistant parts, we used the ARTP(Atmospheric and room temperature plasma) mutagenesis system and Comparative Genomics to obtain 4 mutant bacterial and 4 key mutant sites (nuoE, yhjH, rzpD And gntR).Resistance tests on these key sites were performed respectively(Fig 1).

Figure 1. Resistance test for T4 phage of NuoE, YhjH, RzpD and GntR


Since it is not possible to directly see from the figure which component has the least influence on the growth of the bacteria, we use the Grey Relation Analysis (GRA) method to analyze the growth curve (Fig 2) of the bacteria connecting the various components.

Figure 2. Effect of different anti-phage parts on the growth of E. coli BL21

We used the Entropy Weight Method (EWM) to determine the weight of each growth point to select the most similarly modified strain (the highest correlation), which is the component that has the least impact on bacterial growth. At the same time, after consulting the industry experts, we revised the weights according to the experts' recommendations to evaluate the components again, making them more in line with the real situation of production, that is, the most suitable components for industrial production. Using GRA's two evaluations of the four components at different weights, we selected the component gntR.(Fig 3)

Figure 3. EWM weight & advice weight and the results of GRA for selecting most suitable strain


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 425
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]