Difference between revisions of "Part:BBa K1957008"
(Additional information and images) |
m |
||
Line 3: | Line 3: | ||
<partinfo>BBa_K1957008 short</partinfo> | <partinfo>BBa_K1957008 short</partinfo> | ||
− | One of the three subunits that make up NiFe Hydrogenase in Shewanella oneidensis. Specifically this is the HyaB subunit, which is the membrane-bound subunit. This subunit has a strep-II tag on its | + | One of the three subunits that make up NiFe Hydrogenase in Shewanella oneidensis. Specifically this is the HyaB subunit, which is the membrane-bound subunit. This subunit has a strep-II tag on its N-terminal for downstream protein assays. This gene encodes one out of the three subunits that can be used to make the entire NiFe hydrogenase construct. |
[[File:T--NRP-UEA-Norwich--Gel_PCR_Colony_NiFe_.jpg|thumb|none|'''Figure 1: PCR Colony of NiFe Hydrogenase subunits'''. Lanes 8 to 10 have HyaB N-terminus gene insert, which is 1830bp. Ladder is Hyperladder Kb, sizes shown in bp]] | [[File:T--NRP-UEA-Norwich--Gel_PCR_Colony_NiFe_.jpg|thumb|none|'''Figure 1: PCR Colony of NiFe Hydrogenase subunits'''. Lanes 8 to 10 have HyaB N-terminus gene insert, which is 1830bp. Ladder is Hyperladder Kb, sizes shown in bp]] |
Latest revision as of 18:25, 13 October 2016
HyaB N-terminally tagged subunit of NiFe Hydrogenase
One of the three subunits that make up NiFe Hydrogenase in Shewanella oneidensis. Specifically this is the HyaB subunit, which is the membrane-bound subunit. This subunit has a strep-II tag on its N-terminal for downstream protein assays. This gene encodes one out of the three subunits that can be used to make the entire NiFe hydrogenase construct.
Colonies from lanes 9 and 10 were sent off for sequencing. After sequencing data came back and confirmed the correct gene insert, the DNA from the colony of lane 10 was submitted into the registry.
Restriction site incompatibility, [1000], is with regards to MoClo or Golden Gate cloning. This restriction site was used in the described Golden Gate cloning experiments in order to assemble the gene cluster into a single expression vector. The Bsal restriction enzyme sites flank the coding sequence, and digestion with Bsal should not disrupt the protein coding sequence. For more details on our Golden Gate cloning strategy and instructions on how to assemble the HyaCBA gene cluster into a single expression vector please see the NRP-UEA 2016 iGEM teams wiki.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 282
Illegal BamHI site found at 1479 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 1067
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1
Illegal BsaI.rc site found at 1766
Illegal SapI.rc site found at 37