Difference between revisions of "Part:BBa K3332022"
Acetyl Zheng (Talk | contribs) (→Usage) |
Acetyl Zheng (Talk | contribs) (→Usage) |
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===Usage=== | ===Usage=== | ||
− | We ligased the coding sequences of phnE1 and phnE2 ( | + | We ligased the coding sequences of phnE1 and phnE2 (RBS-phnE1-RBS-phnE2) and the part J23100-RBS-phnE1-RBS-phnE2-J23100-RBS-phnJ-Terminator(<partinfo>BBa_K3332097</partinfo>) 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 transport glyphosate to cytoplasm at higher efficiency. |
===Characterization=== | ===Characterization=== |
Revision as of 17:41, 27 October 2020
phnC
Subunit of phosphonate ABC transporter, ATP binding protein, from S.meliloti 1021.Use BBa_K823004 to construct a new part that can transport glyphosate to cytoplasm.
Biology
Phn system is a gene cluster for organophosphorus transportation and degradation in many microorganisms. Sinorhizobium meliloti 1021 encodes ABC transporter by phnEE, phnC, phnD gene. This transporter can transport glyphosate to cytoplasm. The phnC gene encodes ATP-binding protein and the phnD encodes phosphonate binding protein of the ABC transporter.
Usage
We ligased the coding sequences of phnE1 and phnE2 (RBS-phnE1-RBS-phnE2) and the part J23100-RBS-phnE1-RBS-phnE2-J23100-RBS-phnJ-Terminator(BBa_K3332097) 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 transport glyphosate to cytoplasm at higher efficiency.
Characterization
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 112
Illegal NgoMIV site found at 181
Illegal NgoMIV site found at 420
Illegal NgoMIV site found at 424
Illegal NgoMIV site found at 805
Illegal NgoMIV site found at 829 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 192
Illegal SapI.rc site found at 358