TY - JOUR
T1 - Cell-Penetrating Peptide-Mediated Transformation of Large Plasmid DNA into Escherichia coli
AU - Islam, Md Monirul
AU - Odahara, Masaki
AU - Yoshizumi, Takeshi
AU - Oikawa, Kazusato
AU - Kimura, Mitsuhiro
AU - Su'Etsugu, Masayuki
AU - Numata, Keiji
N1 - Funding Information:
This work was supported by a JST ERATO Grant (Grant JPMJER1602) (K.N.) and ImPACT (T.Y.).
Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/5/17
Y1 - 2019/5/17
N2 - The highly efficient genetic transformation of cells is essential for synthetic biology procedures, especially for the transformation of large gene clusters. In this technical note, we present a novel cell-penetrating peptide (CPP)-mediated large-sized plasmid DNA transformation system for Escherichia coli. A large plasmid (pMSR227, 205 kb) was complexed with cationic peptides containing a CPP motif and was successfully transformed into E. coli cells. The transformants containing the plasmid DNA exhibited expression of a reporter gene encoding a red fluorescent protein. The transformation efficiency was significantly higher than that obtained using the heat-shock method and was similar to that of electroporation. This technique can be used as a platform for the simple and highly efficient transformation of large DNA molecules under mild conditions without causing significant damage to DNA, accelerating synthetic biology investigations for the design of genetically engineered microorganisms for industrial purposes.
AB - The highly efficient genetic transformation of cells is essential for synthetic biology procedures, especially for the transformation of large gene clusters. In this technical note, we present a novel cell-penetrating peptide (CPP)-mediated large-sized plasmid DNA transformation system for Escherichia coli. A large plasmid (pMSR227, 205 kb) was complexed with cationic peptides containing a CPP motif and was successfully transformed into E. coli cells. The transformants containing the plasmid DNA exhibited expression of a reporter gene encoding a red fluorescent protein. The transformation efficiency was significantly higher than that obtained using the heat-shock method and was similar to that of electroporation. This technique can be used as a platform for the simple and highly efficient transformation of large DNA molecules under mild conditions without causing significant damage to DNA, accelerating synthetic biology investigations for the design of genetically engineered microorganisms for industrial purposes.
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U2 - 10.1021/acssynbio.9b00055
DO - 10.1021/acssynbio.9b00055
M3 - Article
C2 - 31008591
AN - SCOPUS:85065121009
SN - 2161-5063
VL - 8
SP - 1215
EP - 1218
JO - ACS Synthetic Biology
JF - ACS Synthetic Biology
IS - 5
ER -