Difference between revisions of "Part:BBa K3332097"
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<partinfo>BBa_K3332097 short</partinfo> | <partinfo>BBa_K3332097 short</partinfo> | ||
− | Subunits of phosphonate ABC transporter, permease protein phnE, from S.meliloti 1021. We use K823004 to construct a new part that can transport glyphosate to cytoplasm. | + | Subunits of phosphonate ABC transporter, permease protein phnE, from ''S.meliloti'' 1021. We use<partinfo>BBa_ K823004</partinfo> to construct a new part that can transport glyphosate to cytoplasm. |
===Biology=== | ===Biology=== |
Revision as of 22:09, 27 October 2020
J23100-B0034-phnJ-B0015-J23100-RBS-phnE1-RBS-phnE2
Subunits of phosphonate ABC transporter, permease protein phnE, from S.meliloti 1021. We useNo part name specified with partinfo tag. to construct a new part that can transport glyphosate to cytoplasm.
Biology
Phn system is a gene cluster for organophosphorus transport and degradation in many microorganisms. Enterobacterales use phnHIJK genes to encode C-P lyase.PhnJ protein is an essential subunit that can crack C-P bond.
Usage
We ligased the J23100-B0034-phnJ-B0015 (BBa_K3332024) and the part J23100-B0034-phnE1-B0034-phnE2(BBa_K3332067) on the expression vector pSB1C3 by standard assembly. Then the ligation mixture was transformed into E. coli DH5α & E. coli BL21(DE3), enabled the E. coli to degrade glyphosate at higher efficiency.
Characterization
Agarose Gel Electrophoresis
After receiving the synthesized DNA, digestion was done to certify that the plasmid was correct, and the experimental results were shown in figure 1.
2. Enzyme activity
We use Negative Control, experiment groups phnEE and phnEEJ to verify that phnJ can enhance the degradation of glyphosate by the chassis bacteria by our detection system. The phnJ-phnE1E2 gene cluster enhances the degration of glyphosate by the chassis bacteria compared to the blank control, but it has no difference with the phnE1E2 group, indicating that exogenous phnJ can’t bind to the endogenous PhnHIK well.
The result is shown in Fig.2(Experiment groups in Fig.2
Negative Control: J23100-B0034_pSB1C3
phnE1E2: J23100-B0034-phnE1-B0034-phnE2_pSB1C3,
phnJ-phnE1E2: J23100-B0034-phnJ-B0015-J23100-B0034-phnE1-B0034-phnE2_pSB1C3,
Mut21-phnJ-phnE1E2: J23100-B0034-phnJ_mutR21M-B0015- J23100-B0034-phnE1-B0034-phnE2_pSB1C3
Mut1640-phnJ-phnE1E2: J23100-B0034-phnJ_mutT16S&R40Y-B0015-J23100-B0034-phnE1-B0034-phnE2_pSB1C3
RNAi system-phnJ-phnO-phnE1E2: J23101-OmpA 5'UTR-phnF 0.97-Hfq binding sequence-J23101- OmpA 5'UTR-phnJ 0.69-Hfq binding sequence- BBa_J61048-J23100-B0034-phnJ-B0015-J23100-phnO-B0015-J23100-B0034-phnE1-B0034-phnE2_pSB1C3).
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30
Illegal NheI site found at 1057
Illegal NheI site found at 2583
Illegal NheI site found at 2606
Illegal NotI site found at 2750 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 3234
Illegal NgoMIV site found at 3256
Illegal AgeI site found at 2209 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 3246