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CR, Grant PK, Haseloff J. TITLE Programmed emergence of a domain of gene expression in a bacterial population JOURNAL Unpublished REFERENCE 2 (bases 1 to 5412) AUTHORS Boehm CR.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 TITLE Direct Submission COMMENT SGRef: number: 1; type: "Journal Article"; journalName: "Unpublished" COMMENT SGRef: number: 2; type: "Journal Article"; journalName: "Submitted (12-OCT-2016) Plant Sciences, University of Cambridge, Downing Street, Cambridge,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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