Part:BBa_K2918061

Φ29 Right origin of replication (OriR)

Φ29 bacteriophage origin of replication (OriR)

Sequence and Features

Assembly Compatibility:

• 10
  COMPATIBLE WITH RFC[10]
• 12
  COMPATIBLE WITH RFC[12]
• 21
  COMPATIBLE WITH RFC[21]
• 23
  COMPATIBLE WITH RFC[23]
• 25
  COMPATIBLE WITH RFC[25]
• 1000
  COMPATIBLE WITH RFC[1000]

The part has been confirmed by sequencing and there are no mutations.

Usage and Biology

The Φ29 replication mechanism is a unique protein-primed based replication of a linear plasmid. Protein primed replication, unlike the conventional DNA or RNA primed mechanism, greatly simplifies the design of replication systems. The Φ29 replication can be established by using four simple proteins: Φ29 DNA polymerase (DNAP/p2),terminal protein (TP/p3), single stranded binding protein (SSB/p5) and double stranded binding protein (DSB/p6). The replication process begins by binding of the Φ29 DNA polymerase and terminal protein complex at the origins of replication (OriR and OriL), which flank the protein-primed linear plasmid (Nies et al, 2018). The double stranded DNA binding proteins (Nies et al, 2018).

Insert Φ29 replication animation/image!

The Φ29 replication system is promising in many ways:

-The Φ29 DNA Polymerase has the highest processivity of all known single subunit DNA polymerases (Blanco et al, 1988), and can be used for whole genome amplification.
-The Φ29 machinery along with cell free expression systems can be used to establish the three dogmas of biology in-vitro. Setting the basis for artificial cell development.
-The existing DNA-protein covalent bonds offer many possibilities to engineer the terminal proteins with functional peptide sequences.
-We envision that the unique configuration of the double-stranded, protein-capped linear replicon will be a basis for many new engineered protein-DNA complexes.
-Orthogonal replication not only enables replication independent from the host, but the ability to engineer the orthogonal DNA polymerase’s fidelity without introducing mutations in the cell’s genome makes in vivo directed evolution a possibility.

Characterization

to be edited

Strain Construction

The DNA sequence of the part was synthesized by IDT and cloned by restriction-ligation in pICH47732 and the sequence was confirmed by sequencing. The cloning protocol can be found in the MoClo section below.