Basic Vector Information
- Vector Name:
- p1wtVT-lacI
- Antibiotic Resistance:
- Ampicillin
- Length:
- 5412 bp
- Type:
- Cloning vector
- Replication origin:
- ori
- Source/Author:
- Boehm CR, Grant PK, Haseloff J.
p1wtVT-lacI vector Map
p1wtVT-lacI vector Sequence
LOCUS 40924_2468 5412 bp DNA circular SYN 18-DEC-2018
DEFINITION Cloning vector p1wtVT-lacI, complete sequence.
ACCESSION .
VERSION .
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
REFERENCE 1 (bases 1 to 5412)
AUTHORS Boehm CR, Grant PK, Haseloff J.
TITLE Programmed emergence of a domain of gene expression in a bacterial
population
JOURNAL Unpublished
REFERENCE 2 (bases 1 to 5412)
AUTHORS Boehm CR.
TITLE Direct Submission
JOURNAL Submitted (12-OCT-2016) Plant Sciences, University of Cambridge,
Downing Street, Cambridge, Cambridgeshire CB2 3EA, United Kingdom
REFERENCE 3 (bases 1 to 5412)
TITLE Direct Submission
REFERENCE 4 (bases 1 to 5412)
AUTHORS .
TITLE Direct Submission
COMMENT SGRef: number: 1; type: "Journal Article"; journalName:
"Unpublished"
COMMENT SGRef: number: 2; type: "Journal Article"; journalName: "Submitted
(12-OCT-2016) Plant Sciences, University of Cambridge, Downing
Street, Cambridge, Cambridgeshire CB2 3EA, United Kingdom"
COMMENT SGRef: number: 3; type: "Journal Article"
COMMENT ##Assembly-Data-START##
Sequencing Technology :: Sanger dideoxy sequencing
##Assembly-Data-END##
FEATURES Location/Qualifiers
source 1..5412
/mol_type="other DNA"
/organism="synthetic DNA construct"
rep_origin complement(49..637)
/direction=LEFT
/label=ori
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
promoter 818..836
/label=T7 promoter
/note="promoter for bacteriophage T7 RNA polymerase"
regulatory 872..883
/label=BBa_B0034
/note="BBa_B0034"
/regulatory_class="ribosome_binding_site"
RBS 872..883
/note="strong bacterial ribosome binding site (Elowitz and
Leibler, 2000)"
CDS 890..1606
/label=Venus
/note="yellow fluorescent protein (YFP) with fast and
efficient maturation (Nagai et al., 2002)"
terminator 1629..1700
/label=rrnB T1 terminator
/note="transcription terminator T1 from the E. coli rrnB
gene"
terminator 1716..1743
/label=T7Te terminator
/note="phage T7 early transcription terminator"
regulatory 1750..1784
/label=PJ23101*
/note="PJ23101*"
/regulatory_class="promoter"
RBS 1793..1804
/note="strong bacterial ribosome binding site (Elowitz and
Leibler, 2000)"
CDS 1820..2899
/label=lacI
/note="lac repressor"
CDS 2900..2932
/label=ssrA tag (LVA)
/note="C-terminal peptide that mediates degradation in
bacteria through the ClpXP and ClpAP proteases (McGinness
et al., 2006)"
terminator complement(2983..3026)
/label=rrnB T1 terminator
/note="transcription terminator T1 from the E. coli rrnB
gene"
terminator 3067..3094
/label=T7Te terminator
/note="phage T7 early transcription terminator"
misc_feature 3101..3121
/label=BioBrick suffix
/note="universal suffix for all parts"
CDS complement(3147..4004)
/label=AmpR
/note="beta-lactamase"
promoter complement(4005..4109)
/label=AmpR promoter
terminator complement(4199..4242)
/label=bacterial terminator
/note="putative bacterial transcription terminator"
misc_feature 4245..4266
/label=BioBrick prefix
/note="BioBrick prefix for parts that do not start with
'ATG'"
terminator complement(4273..4300)
/label=T7Te terminator
/note="phage T7 early transcription terminator"
terminator complement(4316..4387)
/label=rrnB T1 terminator
/note="transcription terminator T1 from the E. coli rrnB
gene"
CDS complement(4410..5126)
/label=mTurquoise2
/note="enhanced monomeric variant of CFP (Goedhart et al.,
2012)"
regulatory complement(5127..5144)
/label=BBa_B0034
/note="BBa_B0034"
/regulatory_class="ribosome_binding_site"
RBS 5133..5144
/note="strong bacterial ribosome binding site (Elowitz and
Leibler, 2000)"
regulatory complement(5153..5187)
/label=pJ23101
/note="pJ23101"
/regulatory_class="promoter"
misc_feature 5188..5208
/label=BioBrick suffix
/note="universal suffix for all parts"
terminator 5209..5266
/label=his operon terminator
/note="This putative transcriptin terminator from the E.
coli his operon has a 2-bp deletion introduced during
synthesis. Its efficiency has not been determined."
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