Difference between revisions of "Part:BBa K2633006"
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| − | This organism is a transformable gram-negative bacterium which was isolated from surface-sterilized switchgrass (''Panicum virgatum'') roots. It is capable of reinfecting roots of ''Brachypodium distachyon''. ''Enterobacter ludwigii'' can be transformed using | + | This organism is a transformable gram-negative bacterium which was isolated from surface-sterilized switchgrass (''Panicum virgatum'') roots. It is capable of reinfecting roots of ''Brachypodium distachyon''. ''Enterobacter ludwigii'' can be transformed using [http://2018.igem.org/Team:MichiganState/Experiments electroporation]. It is susceptible to chloramphenicol and streptinomycin. Contact Julian Liber (liberjul@msu.edu) if a sample of this strain is desired. |
MichiganState 2018 transformed this chassis using plasmids with the[https://parts.igem.org/Part:pSB1C3 pSB1C3 backbone], this first documented use of this plasmid in an ''Enterobacter'' species. The part we designed for expression of an ''acdS''-eGFP fusion is [https://parts.igem.org/Part:BBa_K2633000 BBa_K2633000], which allows for fluorescent microscopy of the bacteria ''in situ'' and expression of the plant growth promoting enzyme ACC deaminase. | MichiganState 2018 transformed this chassis using plasmids with the[https://parts.igem.org/Part:pSB1C3 pSB1C3 backbone], this first documented use of this plasmid in an ''Enterobacter'' species. The part we designed for expression of an ''acdS''-eGFP fusion is [https://parts.igem.org/Part:BBa_K2633000 BBa_K2633000], which allows for fluorescent microscopy of the bacteria ''in situ'' and expression of the plant growth promoting enzyme ACC deaminase. | ||
Revision as of 17:37, 17 October 2018
Enterobacter ludwigii FCP2-01
This organism is a transformable gram-negative bacterium which was isolated from surface-sterilized switchgrass (Panicum virgatum) roots. It is capable of reinfecting roots of Brachypodium distachyon. Enterobacter ludwigii can be transformed using [http://2018.igem.org/Team:MichiganState/Experiments electroporation]. It is susceptible to chloramphenicol and streptinomycin. Contact Julian Liber (liberjul@msu.edu) if a sample of this strain is desired.
MichiganState 2018 transformed this chassis using plasmids with thepSB1C3 backbone, this first documented use of this plasmid in an Enterobacter species. The part we designed for expression of an acdS-eGFP fusion is BBa_K2633000, which allows for fluorescent microscopy of the bacteria in situ and expression of the plant growth promoting enzyme ACC deaminase.
The 16S rRNA gene sequence can be found here[1]. The Hsp60 sequence can be found here[2].
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Unknown
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Unknown
- 23INCOMPATIBLE WITH RFC[23]Unknown
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]