Difference between revisions of "Part:BBa K606003"
(5 intermediate revisions by one other user not shown) | |||
Line 2: | Line 2: | ||
<partinfo>BBa_K606003 short</partinfo> | <partinfo>BBa_K606003 short</partinfo> | ||
− | This plasmid is | + | This plasmid is a multihost plasmid, replicated both in E. Coli at high copy number (>200) and low copy in B. Subtilis (about 20). |
This plasmid is ideal for importing parts in Subtilis: all the cloning can be done in E. Coli, as well as the amplification. Once the plasmid is extracted, you can incorporate it directly in B. Subtilis using electroporation. | This plasmid is ideal for importing parts in Subtilis: all the cloning can be done in E. Coli, as well as the amplification. Once the plasmid is extracted, you can incorporate it directly in B. Subtilis using electroporation. | ||
Line 12: | Line 12: | ||
Beware, there is a pT7 promoter hided in the original sequence of one of the plasmid. This plasmid may be incompatible if you are working in a system with T7 polymerase. | Beware, there is a pT7 promoter hided in the original sequence of one of the plasmid. This plasmid may be incompatible if you are working in a system with T7 polymerase. | ||
− | + | This plasmid was properly characterized. You can find out all the remarks and comments on our wiki at this page [http://2011.igem.org/Team:Paris_Bettencourt/MultiHost]. | |
+ | |||
===Usage and Biology=== | ===Usage and Biology=== | ||
+ | |||
+ | Move your constructions from E. Coli to B. Subtilis, and express your proteins. We encourage you tu use this plasmid in combination with the pVeg promoter (BBa_K143012) and SpoVg RBS (K143021) | ||
+ | |||
<!-- --> | <!-- --> |
Latest revision as of 12:30, 19 September 2011
Multi-host replicative plasmid, for B. Subtilis and E. Coli
This plasmid is a multihost plasmid, replicated both in E. Coli at high copy number (>200) and low copy in B. Subtilis (about 20).
This plasmid is ideal for importing parts in Subtilis: all the cloning can be done in E. Coli, as well as the amplification. Once the plasmid is extracted, you can incorporate it directly in B. Subtilis using electroporation.
This plasmid is Ampicilyn resistant in E. Coli, and is tetracycline resistant in both B. Subtilis and E. Coli.
The biobrick BBa_J04450 is inserted between the E X and SP site, as a negative cloning control in E. Coli
Beware, there is a pT7 promoter hided in the original sequence of one of the plasmid. This plasmid may be incompatible if you are working in a system with T7 polymerase.
This plasmid was properly characterized. You can find out all the remarks and comments on our wiki at this page [http://2011.igem.org/Team:Paris_Bettencourt/MultiHost].
Usage and Biology
Move your constructions from E. Coli to B. Subtilis, and express your proteins. We encourage you tu use this plasmid in combination with the pVeg promoter (BBa_K143012) and SpoVg RBS (K143021)
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 17
Illegal XbaI site found at 2
Illegal SpeI site found at 5918
Illegal PstI site found at 5904 - 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 17
Illegal SpeI site found at 5918
Illegal PstI site found at 5904
Illegal NotI site found at 9
Illegal NotI site found at 5909 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 17 - 23INCOMPATIBLE WITH RFC[23]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 17
Illegal XbaI site found at 2
Illegal SpeI site found at 5918
Illegal PstI site found at 5904 - 25INCOMPATIBLE WITH RFC[25]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 17
Illegal XbaI site found at 2
Illegal SpeI site found at 5918
Illegal PstI site found at 5904
Illegal NgoMIV site found at 3573 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal BsaI site found at 2560
Illegal BsaI site found at 4550
Illegal SapI.rc site found at 5632