Coding

Part:BBa_K3142014

Designed by: Luo Xiaolin   Group: iGEM19_SZPT-CHINA   (2019-10-13)


PT-αcrp + acmA

PT-αcrp is a Glucose starved promoter,which is response to glucose starvation It can be used to Initiate gene expressing in response to glucose starvation.AcmA is an Endo-βN-acetylmuramidase that dissociates the reducing group of N-acetylmuramic acid from Gram-positive bacteria to autolyze the lactic acid bacteria.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 26
    Illegal XbaI site found at 729
    Illegal PstI site found at 253
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 26
    Illegal PstI site found at 253
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 26
    Illegal BamHI site found at 1
    Illegal BamHI site found at 681
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 26
    Illegal XbaI site found at 729
    Illegal PstI site found at 253
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 26
    Illegal XbaI site found at 729
    Illegal PstI site found at 253
  • 1000
    COMPATIBLE WITH RFC[1000]


SZPT-China

To ensure that the transgenic bacteria are not harmful to the environment, we constructed the autolytic enzyme gene acmA of the lactic acid bacteria downstream of the glucose starvation promoter. The results of the construction of the recombinant plasmid pMG36e-pα-crp-acmA named pMG36e-P-a are shown in Fig. 1. The results of LAB MG1363 and LAB MG1363 with pMG36e-p - a after induction of recombinant bacteria by different glucose concentrations are shown in Fig. 2. The results showed that when the concentration of glucose in the environment was less than 0.05%, the growth of recombinant bacteria was significantly inhibited.

20191021205946.png
P-A1231.png

Reference

  • William Henry Bothfeld, Grace Kapov, and Keith Tyo. A glucose-sensing toggle switch for autonomous, high productivity genetic control. ACS Synth. 2017, 6(7):1296-1304.
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