p1eng3VT-lacI vector (V009778)

Basic Vector Information

Vector Name:
p1eng3VT-lacI
Antibiotic Resistance:
Ampicillin
Length:
5431 bp
Type:
Cloning vector
Replication origin:
ori
Source/Author:
Boehm CR, Grant PK, Haseloff J.

p1eng3VT-lacI vector Map

p1eng3VT-lacI5431 bp60012001800240030003600420048005400oriRBSVenusrrnB T1 terminatorT7Te terminatorPJ23101*RBSlacIssrA tag (LVA)rrnB T1 terminatorT7Te terminatorBioBrick suffixAmpRAmpR promoterbacterial terminatorBioBrick prefixT7Te terminatorrrnB T1 terminatormTurquoise2BBa_B0034pJ23101BioBrick suffixhis operon terminator

p1eng3VT-lacI vector Sequence

LOCUS       40924_2453        5431 bp DNA     circular SYN 18-DEC-2018
DEFINITION  Cloning vector p1eng3VT-lacI, complete sequence.
ACCESSION   .
VERSION     .
KEYWORDS    .
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
REFERENCE   1  (bases 1 to 5431)
  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  JOURNAL   Unpublished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 5431)
  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 5431)
  TITLE     Direct Submission
REFERENCE   4  (bases 1 to 5431)
  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            "Unpublished"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..5431
                     /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"
     RBS             875..897
                     /label=RBS
                     /note="efficient ribosome binding site from bacteriophage
                     T7 gene 10 (Olins and Rangwala, 1989)"
     CDS             909..1625
                     /label=Venus
                     /note="yellow fluorescent protein (YFP) with fast and
                     efficient maturation (Nagai et al., 2002)"
     terminator      1648..1719
                     /label=rrnB T1 terminator
                     /note="transcription terminator T1 from the E. coli rrnB
                     gene"
     terminator      1735..1762
                     /label=T7Te terminator
                     /note="phage T7 early transcription terminator"
     regulatory      1769..1803
                     /label=PJ23101*
                     /note="PJ23101*"
                     /regulatory_class="promoter"
     RBS             1812..1823
                     /note="strong bacterial ribosome binding site (Elowitz and 
                     Leibler, 2000)"
     CDS             1839..2918
                     /label=lacI
                     /note="lac repressor"
     CDS             2919..2951
                     /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(3002..3045)
                     /label=rrnB T1 terminator
                     /note="transcription terminator T1 from the E. coli rrnB
                     gene"
     terminator      3086..3113
                     /label=T7Te terminator
                     /note="phage T7 early transcription terminator"
     misc_feature    3120..3140
                     /label=BioBrick suffix
                     /note="universal suffix for all parts"
     CDS             complement(3166..4023)
                     /label=AmpR
                     /note="beta-lactamase"
     promoter        complement(4024..4128)
                     /label=AmpR promoter
     terminator      complement(4218..4261)
                     /label=bacterial terminator
                     /note="putative bacterial transcription terminator"
     misc_feature    4264..4285
                     /label=BioBrick prefix
                     /note="BioBrick prefix for parts that do not start with
                     'ATG'"
     terminator      complement(4292..4319)
                     /label=T7Te terminator
                     /note="phage T7 early transcription terminator"
     terminator      complement(4335..4406)
                     /label=rrnB T1 terminator
                     /note="transcription terminator T1 from the E. coli rrnB
                     gene"
     CDS             complement(4429..5145)
                     /label=mTurquoise2
                     /note="enhanced monomeric variant of CFP (Goedhart et al., 
                     2012)"
     regulatory      complement(5146..5163)
                     /label=BBa_B0034
                     /note="BBa_B0034"
                     /regulatory_class="ribosome_binding_site"
     RBS             5152..5163
                     /note="strong bacterial ribosome binding site (Elowitz and 
                     Leibler, 2000)"
     regulatory      complement(5172..5206)
                     /label=pJ23101
                     /note="pJ23101"
                     /regulatory_class="promoter"
     misc_feature    5207..5227
                     /label=BioBrick suffix
                     /note="universal suffix for all parts"
     terminator      5228..5285
                     /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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