Pseudoalteromonas sp. and application thereof
A host bacteria, cold-adaptive technology, applied to cold-adaptive host bacteria strains and applications, marine biology field
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Embodiment 1
[0046] Example 1: Preparation method of plasmid deletion strain SM20429
[0047] Pseudoalteromonas BSi20429 strain was eliminated by SDS-high temperature treatment, and the plasmid-deleted strain SM20429 of the strain was obtained. This strain is characterized by the complete loss of the plasmid, which is not integrated into the strain genome and is genetically stable. Compared with the original strain, the strain did not change significantly in character. Specific steps are as follows:
[0048] 1) Pick a single colony of Pseudoalteromonas BSi20429 strain on the plate, inoculate it in 5ml 2216E liquid medium, and culture it at 25°C with shaking at 160rpm until OD 600 is 1.0, the primary bacterial liquid is obtained;
[0049] 2) Transfer 100 μl of bacterial liquid to fresh 5ml 2216E liquid medium, culture at 33°C with shaking at 160rpm until OD 600 about 1.0.
[0050] 3) Take 100 μl of the bacterial liquid and transfer it to 5ml 2216E liquid medium added with 25 μl of 1% S...
Embodiment 2
[0055] Example 2: Construction of autonomously replicating expression vector pWD
[0056] 1. Description
[0057] Size: 7654bp
[0058] E. coli replication elements:
[0059] Origin of replication: origin of replication derived from plasmid pUC19, pUC19 was purchased from Takara Company.
[0060] Selection marker: ampicillin-resistant gene, derived from plasmid pUC19 (purchased from Takara Company).
[0061] Pseudoalteromonas replication elements:
[0062] Origin of replication: origin of replication derived from plasmid pSM429 (GenBank accession number EU627679) extracted from strain Pseudoalteromonas sp.BSi20429.
[0063] Selection marker: chloramphenicol resistance gene, cloned in plasmid pBT (purchased from Stratagene Company)
[0064] Promoter: Lac promoter, derived from plasmid pUC19 (purchased from Takara Company).
[0065] Multiple cloning sites: PstI, XhoI and SalI. See attached figure 2 .
[0066] 2. Construction method
[0067] (i) PCR amplification of a 3...
Embodiment 3
[0076] Embodiment 3: the establishment of transformation system of Pseudoalteromonas cold-adapted
[0077] The present invention adopts the method of electrotransformation, takes SM20429 bacterial strain as host, takes self-replicating plasmid pWD as carrier, establishes the transformation system of Pseudoalteromonas cryotropic, and the steps are as follows:
[0078] 1) Take a cold-adapted host bacterial strain whose strain preservation number is CCTCC M 2010239, inoculate it into 2216E liquid medium, and culture it with shaking at 20°C overnight to obtain a primary bacterial liquid;
[0079] 2) Inoculate the primary bacterial liquid prepared in step 1) into 2216E liquid medium at an inoculum size of 1% by volume, and cultivate to OD at 20°C 600 0.8-1.0, centrifuge at 6000rpm for 5min, collect the bacteria, discard the supernatant, and bathe in ice for 10min to get the bacteria;
[0080] 3) Wash the bacterial cells prepared in step 2) with 20ml of pre-cooled sterile water con...
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