Basic Vector Information
pUDE151 vector Vector Map
Plasmid Resuspension Protocol:
1. Centrifuge at 5,000×g for 5 min.
2. Carefully open the tube and add 20 μl of sterile water to dissolve the DNA.
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 ℃.
pUDE151 vector Sequence
LOCUS 40924_45428 8101 bp DNA circular SYN 18-DEC-2018
DEFINITION Expression vector pUDE151, complete sequence.
ACCESSION .
VERSION .
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
REFERENCE 1 (bases 1 to 8101)
AUTHORS Kozak BU, van Rossum HM, Benjamin KR, Wu L, Daran JM, Pronk JT, van
Maris AJ.
TITLE Replacement of the Saccharomyces cerevisiae acetyl-CoA synthetases
by alternative pathways for cytosolic acetyl-CoA synthesis
JOURNAL Metab. Eng. (2013) In press
PUBMED 24269999
REFERENCE 2 (bases 1 to 8101)
AUTHORS Kozak BU, van Rossum HM, Benjamin KR, Wu L, Daran J-M.G., Pronk JT,
van Maris AJA.
TITLE Direct Submission
JOURNAL Submitted (31-MAY-2013) Biotechnology, Delft University of
Technology, Julianalaan 67, Delft 2628BC, The Netherlands
REFERENCE 3 (bases 1 to 8101)
TITLE Direct Submission
REFERENCE 4 (bases 1 to 8101)
AUTHORS .
TITLE Direct Submission
COMMENT SGRef: number: 1; type: "Journal Article"; journalName: "Metab. Eng.
(2013) In press"
COMMENT SGRef: number: 2; type: "Journal Article"; journalName: "Submitted
(31-MAY-2013) Biotechnology, Delft University of Technology,
Julianalaan 67, Delft 2628BC, The Netherlands"
COMMENT SGRef: number: 3; type: "Journal Article"
FEATURES Location/Qualifiers
source 1..8101
/mol_type="other DNA"
/organism="synthetic DNA construct"
rep_origin complement(183..771)
/direction=LEFT
/label=ori
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
CDS complement(945..1802)
/label=AmpR
/note="beta-lactamase"
promoter complement(1803..1907)
/label=AmpR promoter
rep_origin complement(1934..3276)
/direction=LEFT
/label=2u ori
/note="yeast 2u plasmid origin of replication"
promoter 3540..3760
/label=URA3 promoter
CDS 3761..4561
/label=URA3
/note="orotidine-5'-phosphate decarboxylase, required for
uracil biosynthesis"
rep_origin complement(4695..5150)
/direction=LEFT
/label=f1 ori
/note="f1 bacteriophage origin of replication; arrow
indicates direction of (+) strand synthesis"
primer_bind 5295..5311
/label=M13 fwd
/note="common sequencing primer, one of multiple similar
variants"
promoter 5321..5339
/label=T7 promoter
/note="promoter for bacteriophage T7 RNA polymerase"
terminator complement(5358..5605)
/label=CYC1 terminator
/note="transcription terminator for CYC1"
primer_bind 5608..5624
/label=KS primer
/note="common sequencing primer, one of multiple similar
variants"
protein_bind 5657..5681
/label=attB2
/note="recombination site for the Gateway(R) BP reaction"
CDS complement(5700..7100)
/gene="eutE"
/label=eutE
/note="Acetaldehyde dehydrogenase (acetylating) EutE from
Escherichia coli (strain K12). Accession#: P77445"
protein_bind complement(7116..7140)
/label=attB1
/note="recombination site for the Gateway(R) BP reaction"
primer_bind complement(7148..7164)
/label=SK primer
/note="common sequencing primer, one of multiple similar
variants"
promoter complement(7170..7814)
/label=GAP promoter
/note="promoter for glyceraldehyde-3-phosphate
dehydrogenase; also known as the TDH3 promoter"
promoter complement(7843..7861)
/label=T3 promoter
/note="promoter for bacteriophage T3 RNA polymerase"
primer_bind complement(7882..7898)
/label=M13 rev
/note="common sequencing primer, one of multiple similar
variants"
protein_bind complement(7906..7922)
/label=lac operator
/note="The lac repressor binds to the lac operator to
inhibit transcription in E. coli. This inhibition can be
relieved by adding lactose or
isopropyl-beta-D-thiogalactopyranoside (IPTG)."
promoter complement(7930..7960)
/label=lac promoter
/note="promoter for the E. coli lac operon"
protein_bind complement(7975..7996)
/label=CAP binding site
/note="CAP binding activates transcription in the presence
of cAMP."
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