Extremely halophilic archaea polyhydroxy fatty acid ester synthases and encoding gene and application
An archaeal polyhydroxyalkanoate and polyhydroxyalkanoate technology, which is applied to the extreme halophilic archaea polyhydroxyalkanoate synthase and its encoding gene and application fields, and can solve deletion mutants and non-highly expressed strains and other problems, to achieve the effect of increasing the production of PHA and increasing the activity of PHA synthase.
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Embodiment 1
[0033]Example 1, the acquisition of polyhydroxyalkanoate (PHA) synthase and its coding gene (the schematic diagram of the cloning strategy is shown in Figure 1)
[0034] 1. Two subunits of polyhydroxyalkanoate (PHA) synthase (PhaE Hh and PhaC Hh ) and the acquisition of its coding gene
[0035] The extreme halophilic archaea Haloarcula hispanica AS 1.2049 has a very close relationship with the extreme halophilic archaea Haloarcula marismortui ATCC 43049 (GenBank number: AY596297) whose complete genome sequence has been published. There is a PHA synthase subunit gene annotated as phaC in the genome sequence Hm , this laboratory study proved that the ORF of an unannotated gene function adjacent to its upstream encoded another subunit of PHA synthase, and named it phaE Hm . According to phaC in the extreme halophilic archaea Haloarcula marismortui ATCC 43049 Hm and phaE Hm Two pairs of primers, P1 / P2 and P3 / P4, were designed.
[0036] P1: 5′CTA GGATCC ATGTCCAGCAACCCCTTC3′...
Embodiment 2
[0056] Embodiment 2, PHA synthase gene phaEC Hh and phaEC Hh The gene encoding the two subunits of phaE Hh and phaC Hh functional verification of
[0057] 1. Overexpression of the PHA synthase gene phaEC in the extreme halophilic archaea Haloarcula hispanica AS1.2049 Hh , phaE Hh and phaC HhThe construction of recombinant plasmids and the construction of overexpression recombinant engineering bacteria
[0058] The following primers were designed according to the cloned sequence information of the extreme halophilic archaea Haloarcula hispanica AS1.2049:
[0059] PE1:5, ATT GGATCC CAACTCGAAGAAGTGCAG3′( BamHI )
[0060] PE2: 5, GGC GGTACC TTACTCTTTCCAGGTGTTC3′( KpnI )
[0061] PE3:5, CGC CCATGG CAACTCGAAGAAGTGCAG3′( NCOI )
[0062] PE4: 5′ATA GGATCC AATAGTACCTCGGCGGCG3′( BamHI )
[0063] PC1:5, CTA GGATCC ATGTCCAGCAACCCGTTT3′( BamHI )
[0064] PC2: 5′CGT GGTACC TTACAGTTGGTCGAGCCA3′( KpnI )
[0065] 1) Using Haloarcula hispanica AS1.2049 genomic D...
Embodiment 3
[0072] Example 3, PHA synthase gene deletion mutant strain Haloarcula hispanica PHB - 1 construction and its functional verification
[0073] 1. Destruction of phaEC Hh Construction of the homologous recombination integration plasmid pUBPHL
[0074] The construction process of pUBPHL is shown in Figure 2, and the specific implementation is as follows:
[0075] 1) Construction of departure plasmid pUBP
[0076]pUBP2 is a shuttle plasmid for extreme halophilic archaea and Escherichia coli (see the literature Proc. Natl. Acad. Sci. USA 87: 6772-6 for the sequence information and construction method of pUBP2). First, pUBP2 was digested with EcoRI to remove the replicon pHH9 of the halophilic archaea in pUBP2 to obtain a 6.6 kb linear fragment, and then the 6.6 kb linear fragment was self-ligated to form plasmid pUBP, which was used to construct the integration vector pUBPHL.
[0077] 2) Used to destroy phaEC Hh Amplification of the homologous recombination double crossover ar...
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