Difference between revisions of "Part:BBa K2739009"
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===Usage and Biology=== | ===Usage and Biology=== | ||
In order to enhance the 3HV fraction in PHBV, paralog bktB was introduced into E. coli BL21 (DE3) with co-expression of phaCAB operon from Ralstonia eutropha. | In order to enhance the 3HV fraction in PHBV, paralog bktB was introduced into E. coli BL21 (DE3) with co-expression of phaCAB operon from Ralstonia eutropha. | ||
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+ | https://static.igem.org/mediawiki/parts/8/85/T--Edinburgh_OG_BBa_K2739009--image_1.jpg | ||
<img src="https://static.igem.org/mediawiki/parts/8/85/T--Edinburgh_OG_BBa_K2739009--image_1.jpg" align="left" width="600px"/> | <img src="https://static.igem.org/mediawiki/parts/8/85/T--Edinburgh_OG_BBa_K2739009--image_1.jpg" align="left" width="600px"/> |
Revision as of 22:27, 10 October 2018
Hybrid promoter-PhaCAB-Bktb
This composite part is designed to investigate the effect of PHBV production using PHA synthetic pathway (PHA operon) with BtkB co-expressed. The BktB was isolated from R. eutropha H16 and being recognised as a phaA paralogous, which allows the formation of 3-ketovaleryl-CoA and leads to PHBV production.
Usage and Biology
In order to enhance the 3HV fraction in PHBV, paralog bktB was introduced into E. coli BL21 (DE3) with co-expression of phaCAB operon from Ralstonia eutropha.
<img src="" align="left" width="600px"/>
the effects on PHBV production of having only phaA, only bktBand both two genes
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 979
Illegal BglII site found at 1804 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 285
Illegal NgoMIV site found at 356
Illegal NgoMIV site found at 956
Illegal NgoMIV site found at 1268
Illegal NgoMIV site found at 1547
Illegal NgoMIV site found at 2199
Illegal NgoMIV site found at 2221 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 4065
Illegal BsaI site found at 5108