Part:BBa_K1010001:Design
RBS (B0034) + NphR (PNP-responsive positive regulator) + Terminator (B0015)
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 862
Illegal XhoI site found at 978 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 270
Illegal NgoMIV site found at 925 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
Position 684 is mutated from A to G to avoid a Pst1 restriction site.
Source
This part comes from a 5-kb EcoRI DNA fragment cloned from Rhodococcus sp. Strain PN1 involved in PNP oxidation.(Masahiro Takeo et al. 2008.).
References
Takeo, Masahiro, Masumi Murakami, Sanae Niihara, Kenta Yamamoto, Munehiro Nishimura, Dai-ichiro Kato, and Seiji Negoro. "Mechanism of 4-nitrophenol oxidation in Rhodococcus sp. Strain PN1: characterization of the two-component 4-nitrophenol hydroxylase and regulation of its expression." Journal of bacteriology 190, no. 22 (2008): 7367-7374.
Yamamoto, Kenta, Munehiro Nishimura, Dai-ichiro Kato, Masahiro Takeo, and Seiji Negoro. "Identification and characterization of another 4-nitrophenol degradation gene cluster, nps, in Rhodococcus sp. strain PN1." Journal of bioscience and bioengineering 111, no. 6 (2011): 687-694.