Difference between revisions of "Part:BBa K4591010"
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<p>BslA: BslA has the ability to form a hydrophobic layer on the surface of Bacillus subtilis.</p> | <p>BslA: BslA has the ability to form a hydrophobic layer on the surface of Bacillus subtilis.</p> | ||
− | <p>tetR:TetR is a secretion protein that binds to the upstream teto of the reporter module, inhibiting the expression of the fluorescent sfGFP gene.</p> | + | <p>tetR:TetR is a secretion protein that binds to the upstream teto of the reporter module, inhibiting the expression of the fluorescent <i>sfGFP</i> gene.</p> |
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Latest revision as of 11:20, 12 October 2023
Pm-MstX-BslA-tetR-Pxyl-cre-T500
Usage and Biology
In order to improve the degradation efficiency of engineered bacteria, we designed the gene circuit of attached module. The expression of genes related to this route can promote the formation of a biofilm on the surface of Bacillus subtilis, greatly improve the adhesion ability of engineered bacteria, reduce the mobility of engineered bacteria, and improve the degradation efficiency of PET. This module includes the Xylsmut-Pm biosensor, the membrane integrin MstX for membrane protein expression in Bacillus subtilis, and the hydrophobic protein BslA.
Basic components of the circuit
Pm-xylsmut: Xylsmut is a biosensor that recognizes TPA, a degradation product of PET, and activates the Pm promoter, which initiates the expression of downstream genes.
MstX: MstX increase the phosphorylation of Spo0A to express proteins and polysaccharides required for biofilm formation and prevent flagellar rotation. Promote the formation of engineered bacteria biofilm.
BslA: BslA has the ability to form a hydrophobic layer on the surface of Bacillus subtilis.
tetR:TetR is a secretion protein that binds to the upstream teto of the reporter module, inhibiting the expression of the fluorescent sfGFP gene.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 2294