Part:BBa_K590063
mamHIEJKL_pLacGFP_pGA3K3
This part is made by [http://2011.igem.org/Team:Washington UW iGEM Team 2011] using Gibson cloning method. It includes mamH, I, E, J, K, L all in a pGA3K3 vector. This part is contributed to the [http://2011.igem.org/Team:Washington/Magnetosomes/Magnet_Toolkit Magnetosome toolkit], it also serves as an evidence that the Gibson Assembly method is capable of combining multiple inserts to make large constructs (10 kb in this case).
Usage and Biology
We first extracted mamHI, mamE, mamJ, mamKL from the Magnetospirillum magneticum strain AMB-1, then we used Gibson assembly method to fuse the 4 groups of genes together to make a large HIEJKL insert. We then performed a two-fragment Gibson assembly reaction to combine the insert with a plasmid backbone pGA3k3 with an inducible promoter (R0011).
Below is a gel image of singly-cut mamHIEJKL(~9000bp) on pGA3K3.
After Gibson cloning and transformation into an E. coli BL21 lacIq strain, we induced gene expression with IPTG. Though these cells do not have any superfolder GFP-tagged mam genes (see sfGFP-mamK and sfGFP-mamI for reference), the cells appeared to be forming chains (see image below). We plan to continue characterizing this subsystem of the mamAB operon.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 12370
Illegal PstI site found at 5183
Illegal PstI site found at 8860 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 12370
Illegal NheI site found at 11025
Illegal PstI site found at 5183
Illegal PstI site found at 8860 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 12370
Illegal BglII site found at 8564
Illegal BglII site found at 12385
Illegal BamHI site found at 9642
Illegal XhoI site found at 89
Illegal XhoI site found at 6383
Illegal XhoI site found at 9657
Illegal XhoI site found at 9818
Illegal XhoI site found at 10661 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 12370
Illegal PstI site found at 5183
Illegal PstI site found at 8860 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 12370
Illegal PstI site found at 5183
Illegal PstI site found at 8860
Illegal NgoMIV site found at 238
Illegal NgoMIV site found at 1254
Illegal NgoMIV site found at 2589
Illegal NgoMIV site found at 3920
Illegal NgoMIV site found at 6770
Illegal NgoMIV site found at 8586
Illegal NgoMIV site found at 8953
Illegal AgeI site found at 5857
Illegal AgeI site found at 6272
Illegal AgeI site found at 11111
Illegal AgeI site found at 11434 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 651
Illegal BsaI site found at 1986
Illegal BsaI site found at 3317
Illegal BsaI.rc site found at 6963
Illegal BsaI.rc site found at 12139
Illegal SapI site found at 825
Illegal SapI site found at 2160
Illegal SapI site found at 3491
Illegal SapI.rc site found at 9232
Illegal SapI.rc site found at 9553
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