Difference between revisions of "Part:BBa K4806004"
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<h2>Constructs</h2> | <h2>Constructs</h2> | ||
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<div class="unterschrift"><b>Fig.1 Construct design</b><br> | <div class="unterschrift"><b>Fig.1 Construct design</b><br> | ||
We designed 3 level 2 constructs containing CYP9Q3 using the modular cloning system (MoClo). | We designed 3 level 2 constructs containing CYP9Q3 using the modular cloning system (MoClo). |
Revision as of 11:46, 20 September 2023
CYP9Q3 gene for Chlamydomonas reinhardtii (Phytobrick)
This basic part contains the coding sequence of CYP9Q3 (B3-B4). This part is codon-optimized for Chlamydomonas reinhardtii and was built as part of the CYPurify Collection. In combination with a promoter like AβSAP(i) (BBa_K4806013) and a terminator like tRPL23 (BBa_K3002006)*, this level 0 part leads to expression and potential detoxification of specific chemicals (Ohkawa & Inui, 2015). To detect the target protein a tag like HA-tag (BBa_K3002017)* is recommended.
Constructs
We designed 3 level 2 constructs containing CYP9Q3 using the modular cloning system (MoClo).
Here are the links to the built constructs:
- 1. CYP9Q3 gene with HA-tag for Chlamydomonas reinhardtii (Phytobrick) (BBa_K4806222)
- 2. CYP9Q3 gene with mStop for Chlamydomonas reinhardtii (Phytobrick) (BBa_K4806223)
- 3. CYP9Q3 gene with mNeonGreen for Chlamydomonas reinhardtii (Phytobrick) (BBa_K4806224)
These constructs were transformed into Chlamydomonas reinhardtii. Besides the CYP9Q3 coding sequence the constructs contain the AβSAP(i)-promotor (BBa_K4806013), either the HA-tag (BBa_K3002017)* or mNeonGreen (BBa_K4806006) for detection or mStop (BBa_K4806009) and the tRPL23-terminator (BBa_K3002006)*. The resistance cassette for spectinomycin is already built in the level 2 vector pMBS807 we are using. The usage of this vector allows the direct assembly of level 0 parts to level 2 constructs, facilitating the cloning time (Niemeyer & Schroda, 2022).
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 1249
Illegal PstI site found at 1429
Illegal PstI site found at 1935 - 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 1249
Illegal PstI site found at 1429
Illegal PstI site found at 1935 - 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1791
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 1249
Illegal PstI site found at 1429
Illegal PstI site found at 1935 - 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 1249
Illegal PstI site found at 1429
Illegal PstI site found at 1935
Illegal NgoMIV site found at 2206 - 1000COMPATIBLE WITH RFC[1000]