Part:BBa_K4119008
Plac-ΔperR
The upper and lower homology arms (HR-UP, HR-DOWN) were constructed at about 500 bp upstream and downstream of the PerR sequence of the Clostridium tyrobutyricum genome, plus a lactose-inducing promoter and a spacer sequence derived from the PerR , generating the CRISPR array .Then inserted it into the pMTL82151 plasmid, the successful plasmid is transformed into E. coli CA434, and introduced into Clostridium tyrobutyricum, by lactose induction to make the spacer hit the perR sequence on the target genome, thereby utilizing the endogenous CRISPR-Cas system knocks the perR out , eliminates the impediment effect of perR on the growth of Clostridium butyrate, thereby achieving aerobic growth of Clostridium tyrobutyricum.
Result
As can be seen from the sequencing results, the perR fragment has been knocked out.
At different rotational speeds, the growth of the plasmid knockout strain was better than that of the control strain
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 368
Illegal PstI site found at 1597 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 368
Illegal PstI site found at 1597 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 368
Illegal BglII site found at 428 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 368
Illegal PstI site found at 1597 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 368
Illegal PstI site found at 1597 - 1000COMPATIBLE WITH RFC[1000]
None |