Difference between revisions of "Part:BBa K3731004"
Line 17: | Line 17: | ||
<partinfo>BBa_K3731004 parameters</partinfo> | <partinfo>BBa_K3731004 parameters</partinfo> | ||
<!-- --> | <!-- --> | ||
+ | |||
+ | <!--from this--> | ||
+ | ==iGEM2021_Nanjing-China Experiment== | ||
+ | <div> | ||
+ | <b>Group: Nanjing-China 2021</b> | ||
+ | <br> | ||
+ | <b>Author: Hao Yin</b> | ||
+ | <br><br> | ||
+ | <p> | ||
+ | Polyphosphate kinase(PPK) polymerizes the terminal phosphate of ATP to a long chain of polyphosphate(polyP) in a freely reversible reaction.We inserted EPVM into PBBR1MCS-2 vector in order to produce polyP. | ||
+ | |||
+ | </p> | ||
+ | |||
+ | <!--to here--> |
Revision as of 06:58, 30 September 2021
EPVM-PBBR1MCS-2
EPVM-PBBR1MCS-2 is a plasmid which can generate polyP in E.coli BL21. We inserted ppk1, vgb and mazE into the PBBR1MCS-2 vector to construct this part.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal prefix found in sequence at 5166
Illegal suffix found in sequence at 1 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 5166
Illegal SpeI site found at 2
Illegal PstI site found at 16
Illegal NotI site found at 9
Illegal NotI site found at 5172 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 5166
- 23INCOMPATIBLE WITH RFC[23]Illegal prefix found in sequence at 5166
Illegal suffix found in sequence at 2 - 25INCOMPATIBLE WITH RFC[25]Illegal prefix found in sequence at 5166
Illegal XbaI site found at 5181
Illegal SpeI site found at 2
Illegal PstI site found at 16 - 1000COMPATIBLE WITH RFC[1000]
iGEM2021_Nanjing-China Experiment
Group: Nanjing-China 2021
Author: Hao Yin
Polyphosphate kinase(PPK) polymerizes the terminal phosphate of ATP to a long chain of polyphosphate(polyP) in a freely reversible reaction.We inserted EPVM into PBBR1MCS-2 vector in order to produce polyP.