pBACOV vector (Cat. No.: V009316)

pBACOV5396 bp6001200180024003000360042004800oriAmpRAmpR promotertraJoriTkanRrepBaprE promoter from Bacillus subtilisregulatoryaprE signal peptide from Bacillus subtilis for secretory protein expression; aprE-SPmultiple cloning site (MCS)6xHis
Basic Information

Note: pBACOV (Bacillus conjugation vector) is a broad-host-range E. coli–Bacillus shuttle vector (GenBank MG599120.1). Derived from pBE-S, it carries the ColE1 ori and AmpR for E. coli, the pUB110 pUB ori and KanR for Bacillus, an RK2 oriT/traJ module for conjugative "transmating", and an expression cassette with the B. subtilis PaprE promoter, aprE signal peptide, MCS and C-terminal His6 tag. Transmating worked in 9 of 11 species tested; PaprE drove sfGFP in 8.

Name:
pBACOV
Antibiotic Resistance:
Ampicillin, Kanamycin
Length:
5396 bp
Type:
Shuttle vector
Replication origin:
ori
Source/Author:
Heinze S, Kornberger P, Graetz C, Schwarz WH, Zverlov VV, Liebl W.
Copy Number:
High copy number
Growth Strain(s):
Top10
Growth Temperature:
37℃
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Two tubes of lyophilized plasmid will be delivered, each tube is about 5µg.

Plasmid Protocol

1. Centrifuge at 5,000×g for 5 min.

2. Carefully open the tube and add sterile water to dissolve the DNA: add 20 μl for 5 μg plasmid, and 100 μl for 100 μg plasmid.

3. Close the tube and incubate for 10 minutes at room temperature.

4. Briefly vortex the tube and then do a quick spin to concentrate the liquid at the bottom. Speed is less than 5000×g.

5. Store the plasmid at -20 ℃.

6. The concentration of plasmid re-measurement sometimes differs from the nominal value, which may be due to the position of the lyophilized plasmid in the tube, the efficiency of the re-dissolution, the measurement bias, and adsorption on the wall of the tube, therefore, it is recommended to transform and extract the plasmid before using it

General Plasmid Transform Protocol

1. Take one 100μl of the competent cells and thaw it on ice for 10min, add 2μl of plasmid, then ice bath for 30min, then heat-shock it at 42℃ for 60s, do not stir, and then ice bath for 2min.

2. Add 900μl of LB liquid medium without antibiotics, and incubate at 37℃ for 45min (30℃ for 1-1.5 hours) with 180rpm shaking.

3. Centrifuge at 6000rpm for 5min, leave only 100μl of supernatant to resuspend the bacterial precipitate and spread it onto the target plasmid-resistant LB plate.

4. Invert the plate and incubate at 37℃ for 14h, or at 30℃ for 20h.

5. Pick a single colony into LB liquid medium, add the corresponding antibiotics, incubate at 220rpm for 14h, and extract the plasmid according to the experimental needs and the instructions of the plasmid extraction kit.

References

  • Heinze, S., Kornberger, P., Grätz, C. et al. Transmating: conjugative transfer of a new broad host range expression vector to various Bacillus species using a single protocol. BMC Microbiol 18, 56 (2018). https://doi.org/10.1186/s12866-018-1198-4

pBACOV vector (Cat. No.: V009316) Sequence

LOCUS       40924_5654        5396 bp DNA     circular SYN 17-DEC-2018
DEFINITION  Shuttle vector pBACOV, complete sequence.
ACCESSION   .
VERSION     .
KEYWORDS    .
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
REFERENCE   1  (bases 1 to 5396)
  AUTHORS   Heinze S, Kornberger P, Graetz C, Schwarz WH, Zverlov VV, Liebl W.
  TITLE     Conjugative transfer of a new broad host range expression vector to 
            various Bacillus species using a single protocol
  JOURNAL   Unpublished
REFERENCE   2  (bases 1 to 5396)
  AUTHORS   Heinze S, Kornberger P, Graetz C, Schwarz WH, Zverlov VV, Liebl W.
  TITLE     Direct Submission
  JOURNAL   Submitted (01-DEC-2017) Department for Microbiology, Technical 
            University of Munich, Emil-Ramann-Str. 4, Freising, Bavaria 85354, 
            Germany
REFERENCE   3  (bases 1 to 5396)
  TITLE     Direct Submission
REFERENCE   4  (bases 1 to 5396)
  AUTHORS   .
  TITLE     Direct Submission
COMMENT     SGRef: number: 1; type: "Journal Article"; journalName: 
            "Unpublished"
COMMENT     SGRef: number: 2; type: "Journal Article"; journalName: "Submitted 
            (01-DEC-2017) Department for Microbiology, Technical University of 
            Munich, Emil-Ramann-Str. 4, Freising, Bavaria 85354, Germany"
COMMENT     SGRef: number: 3; type: "Journal Article"
COMMENT     ##Assembly-Data-START##
            Sequencing Technology :: Sanger dideoxy sequencing 
            ##Assembly-Data-END##
FEATURES             Location/Qualifiers
     source          1..5396
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     rep_origin      complement(79..667)
                     /direction=LEFT
                     /label=ori
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of 
                     replication"
     CDS             complement(841..1698)
                     /label=AmpR
                     /note="beta-lactamase"
     promoter        complement(1699..1803)
                     /label=AmpR promoter
     CDS             complement(1832..2116)
                     /codon_start=1
                     /gene="traJ"
                     /product="TraJ"
                     /label=traJ
                     /protein_id="AWI97856.1"
                     /translation="MADETKPTRKGSPPIKVYCLPDERRAIEEKAAAAGMSLSAYLLAV
                     GQGYKITGVVDYEHVRELARINGDLGQQKAHYVNHHPNQVFWGRGAVKH"
     gene            complement(1832..2116)
                     /gene="traJ"
                     /label=traJ
                     /note="required for conjugation"
     oriT            complement(2149..2258)
                     /direction=LEFT
                     /label=oriT
                     /note="incP origin of transfer"
     CDS             complement(2515..3276)
                     /codon_start=1
                     /gene="kanR"
                     /product="kanamycin resistance protein"
                     /label=kanR
                     /note="KanR"
                     /protein_id="AWI97857.1"
                     /translation="MNGPIIMTREERMKIVHEIKERILDKYGDDVKAIGVYGSLGRQTD
                     GPYSDIEMMCVMSTEEAEFSHEWTTGEWKVEVNFDSEEILLDYASQVESDWPLTHGQFF
                     SILPIYDSGGYLEKVYQTAKSVEAQTFHDAICALIVEELFEYAGKWRNIRVQGPTTFLP
                     SLTVQVAMAGAMLIGLHHRICYTTSASVLTEAVKQSDLPSGYDHLCQFVMSGQLSDSEK
                     LLESLENFWNGIQEWTERHGYIVDVSKRIPF"
     gene            complement(2515..3276)
                     /gene="kanR"
                     /label=kanR
                     /note="for selection in Bacillus"
     CDS             complement(3448..4449)
                     /label=repB
                     /note="RepB replication protein"
     regulatory      4866..5031
                     /label=aprE promoter from Bacillus subtilis
                     /note="aprE promoter from Bacillus subtilis"
                     /regulatory_class="promoter"
     regulatory      4960..4969
                     /regulatory_class="minus_35_signal"
     regulatory      4987..4992
                     /regulatory_class="minus_10_signal"
     regulatory      5042..5046
                     /regulatory_class="ribosome_binding_site"
     misc_feature    5057..5143
                     /note="aprE signal peptide from Bacillus subtilis for
                     secretory protein expression; aprE-SP"
     misc_feature    5156..5215
                     /label=multiple cloning site (MCS)
                     /note="multiple cloning site (MCS)"
     CDS             5216..5233
                     /label=6xHis
                     /note="6xHis affinity tag"