Difference between revisions of "Part:BBa K3490020"

 
Line 3: Line 3:
 
<partinfo>BBa_K3490020 short</partinfo>
 
<partinfo>BBa_K3490020 short</partinfo>
  
According to research, HicA is a toxin promoting mRNA degradation, leading to the hibernation of bacteria, while HicB is an antitoxin that can neutralize the effect of HicA. Hence, through regulating the expression of hicA and hicB genes, we can control the growth of bacteria, hibernating the bacteria before the contact lens is used.
+
<br>Overview
Since contact lens are sealed during the process of production, it is impossible to regulate the growth switch through chemical induction; hence, we turned to external stimuli such as light, temperature, etc. At first, we used EL222 to regulate the system (a blue light-sensitive protein), pBlind (a promoter activated by EL222), FLP, and FRT to change the orientation of our promoter, which is activated by blue light. In other words, we have to illuminate the contact lens with blue light for 30 minutes before use.
+
First, the production stage is when we are culturing our bacteria. Without any arabinose addition during culture, the bacteria will be able to grow normally. After the production process, we will put the bacteria and arabinose into the contact lens together, so the pBAD promoter will transcribe hicA, causing the bacteria to hibernate. When we need to resuscitate the bacteria, EL222 will be activated by blue light to induce pBlind promoter, and then FLP will be transcribed. FLP will act on the FRT sites to change the orientation of the constitutive promoter, as a result, the bacteria will start to transcribe hicB to neutralize HicA and thus continue to grow.
+
  
  

Revision as of 15:13, 24 October 2020


Regulating the growth rate of bacteria.


Overview


Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 1512
    Illegal SpeI site found at 1830
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 1512
    Illegal NheI site found at 7
    Illegal NheI site found at 30
    Illegal NheI site found at 2789
    Illegal SpeI site found at 1830
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 1512
    Illegal BamHI site found at 2729
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 1512
    Illegal SpeI site found at 1830
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 1512
    Illegal SpeI site found at 1830
    Illegal NgoMIV site found at 142
    Illegal AgeI site found at 367
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 2225
    Illegal BsaI.rc site found at 2265