Part:BBa_K1132010
Tp901 integrase
The site-specific recombination system of temperate lactococcal bacteriophage TP901-1 integrase mediates site-specific recombination system. Originally from temperate lactoccocal bacteriophage TP901-1, this is a serine-type integrase able to invert, integrate or excise a DNA fragment according to the position and orientation of its specific recognition sites, attB and attP. This process is directional and definitive because of the transformation of attB and attP into attL and attR during recombination.
The 180° switch permits to design a lot of regulation tools, such as logical gates that can be found here (https://parts.igem.org/Part:BBa_K1132001, https://parts.igem.org/Part:BBa_K1132002).
Improvement by iGEM Peking 2017
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Contribution by ETH Zurich 2016
Improved by UCAS_China 2024
TP901 is a serine recombinase that mediates a reversible site-specific recombination system first discovered in bacteriophages. This site-specific recombination system is used by bacteriophages to integrate their genes into the host genomic DNA for proliferation and to transfer genes from the host genome to daughter phages by expressing recombination directionality factor (RDF) before the host is lysed and released. Specifically, TP901 can mediate the excision or inversion of genes between a pair of specific recognition sites (attB and attP) and simultaneously convert this pair of sites into another pair of recognition sites (attL and attR). This site-specific recombination is reversible, and when the auxiliary protein RDF is present, the serine recombinase can reduce attL and attR to attB and attP.
It is worth noting that a recombinase can have multiple pairs of mutually orthogonal attB and attP recombination sites. For example, TP901B-TC(BBa_K5276011) and TP901P-TC(BBa_K5276012) are a pair of recombination sites of TP901, while TP901B-AG(BBa_K5276013) and TP901B-AG(BBa_K5276014) are another pair of recombination sites orthogonal to that.
Molecular mechanism
Each recognition site consists of two incompletely symmetrical sequences on the left and right and a 2bp linker sequence between them. We named the left and right sequences of attB (attP) as B (P) type arms.
In the free state, recombinase exists as a dimer (a), and the N-terminal domains (NTD) of the two integrases bind to each other; when attB & attP are present, the C-terminal domain (CTD) of the integrase will bind to the two arms of the binding site respectively (b); after CTD binding, the conformation changes, so that the dimers bound to attB & attP respectively form a tetramer (c); the tetramer conformation activates NTD, causing DNA being cut from the 2bp linker region in the middle of the binding site (e); after cutting, the two integrases on one side will rotate 180° relative to each other (f); and finally form a new attL & attR binding site (g). Therefore, as shown in Figure (g), the newly formed attL and attR are both composed of a B arm and a P arm. Since the two arms connecting the dimer are different, tetramers cannot form without RDF; thus, attL and attR cannot be reconstituted. If RDF is present, similar recombination will occur between the attL and attR sites, transforming back into attB and attP.
The recognition site of the recombinase is directional. If a pair of attB and attP sites are in the same direction, the sequence between them will be removed; if the attB and attP sites are in opposite directions, the sequence between them will be inverted.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 28
Illegal AgeI site found at 1486 - 1000COMPATIBLE WITH RFC[1000]
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