Composite
ara_gp5.7

Part:BBa_K3790232

Designed by: Chongwen Cao   Group: iGEM21_Fudan   (2021-10-17)
Revision as of 19:57, 21 October 2021 by Chongwen (Talk | contribs) (Introduction)


T7 gene product 5.7 driven by pBAD/araC


Introduction

2021 Fudan

In order to turn the host bacteria into ‘factories’ that concentrate on manufacturing parts of the virus, some phages have the ability to shut off the endogenous transcription of host bacteria. As for T7 phage, there’re three gene products collaboratively realizing the function, which are gp0.7, gp2 and gp5.7.

Gp0.7 and gp2 are early phage genes, which means they are transcribed by the hosts’ RNA polymerase at the very beginning of the infection process. Gp0.7 is a protein kinase without strong specificity. Some said that since it can phosphorylate RNAP of E.coli., it can somehow help inhibit the transcription, while others mentioned that there might be other mechanism. In general, the function of gp0.7 is complicated and not well studied yet. It can interfere with transcription somehow, but the effect is not notable enough.

Gp2 is a small protein that can bind to both the 1.1 domain of σ70 factor and the β’ subunit of the host’s RNAP, thus inhibiting the transcription initiated by σ70-RNAP complex very effectively.

However, in stressful conditions, such as platform stage, E.coli. will mainly use σS factors to initiate transcription, which makes gp2 less effective to shut off transcription. Therefore, gp5.7 is needed for phage to infect E.coli. in stationary phase of growth. Gp5.7 is coded by a mid-stage phage gene. It can bind to σS factors and RNAPs of E.coli. in order to inhibit the transcription initiated by σS-RNAP complex.


Usage and Biology

Experimental Results

Reference

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1205
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 1144
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 979
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 961


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Categories
Parameters
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