Basic Vector Information
- Vector Name:
- pNOR10-20
- Antibiotic Resistance:
- Chloramphenicol
- Length:
- 5027 bp
- Type:
- Cloning vector
- Replication origin:
- ori
- Source/Author:
- Anderson JC, Voigt CA, Arkin AP.
- Promoter:
- araBAD
pNOR10-20 vector Map
pNOR10-20 vector Sequence
LOCUS 40924_33417 5027 bp DNA circular SYN 18-DEC-2018
DEFINITION Cloning vector pNOR10-20, complete sequence.
ACCESSION .
VERSION .
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
REFERENCE 1 (bases 1 to 5027)
AUTHORS Anderson JC, Voigt CA, Arkin AP.
TITLE Environmental signal integration by a modular AND gate
JOURNAL Mol. Syst. Biol. 3, 133 (2007)
PUBMED 17700541
REFERENCE 2 (bases 1 to 5027)
AUTHORS Salis HM, Mirsky EA, Voigt CA.
TITLE Automated design of synthetic ribosome binding sites to control
protein expression
JOURNAL Nat. Biotechnol. 27 (10), 946-950 (2009)
PUBMED 19801975
REFERENCE 3 (bases 1 to 5027)
AUTHORS Tamsir A, Tabor JJ, Voigt CA.
TITLE Robust multicellular computing using genetically encoded NOR gates
and chemical 'wires'
JOURNAL Nature 469 (7329), 212-215 (2011)
PUBMED 21150903
REFERENCE 4 (bases 1 to 5027)
AUTHORS Moser F, Voigt CA.
TITLE Genetic Circuit Performance under Conditions Relevant for Industrial
Bioreactors
JOURNAL Unpublished
REFERENCE 5 (bases 1 to 5027)
AUTHORS Anderson JC, Moser F, Tamsir A, Salis H.
TITLE Direct Submission
JOURNAL Submitted (06-JAN-2012) Biological Engineering, MIT, 500 Tech
Square, Rm 209D, Cambridge, MA 02139, USA
REFERENCE 6 (bases 1 to 5027)
TITLE Direct Submission
REFERENCE 7 (bases 1 to 5027)
AUTHORS .
TITLE Direct Submission
COMMENT SGRef: number: 1; type: "Journal Article"; journalName: "Mol. Syst.
Biol. 3, 133 (2007)"
COMMENT SGRef: number: 2; type: "Journal Article"; journalName: "Nat.
Biotechnol."; date: "2009"; volume: "27"; issue: "10"; pages:
"946-950"
COMMENT SGRef: number: 3; type: "Journal Article"; journalName: "Nature";
date: "2011"; volume: "469"; issue: "7329"; pages: "212-215"
COMMENT SGRef: number: 4; type: "Journal Article"; journalName:
"Unpublished"
COMMENT SGRef: number: 5; type: "Journal Article"; journalName: "Submitted
(06-JAN-2012) Biological Engineering, MIT, 500 Tech Square, Rm 209D,
Cambridge, MA 02139, USA"
COMMENT SGRef: number: 6; type: "Journal Article"
FEATURES Location/Qualifiers
source 1..5027
/mol_type="other DNA"
/organism="synthetic DNA construct"
terminator complement(78..121)
/label=bacterial terminator
/note="putative bacterial transcription terminator"
misc_feature 124..145
/label=BioBrick prefix
/note="BioBrick prefix for parts that do not start with
'ATG'"
promoter 145..429
/label=araBAD promoter
/note="promoter of the L-arabinose operon of E. coli; the
araC regulatory gene is transcribed in the opposite
direction (Guzman et al., 1995)"
protein_bind 458..476
/label=tet operator
/note="bacterial operator O2 for the tetR and tetA genes"
regulatory 506..511
/label=Ptet BBa_R0040
/note="Ptet BBa_R0040"
/regulatory_class="promoter"
regulatory 520..530
/label=BBa_B0033
/note="BBa_B0033"
/regulatory_class="ribosome_binding_site"
CDS 537..1247
/label=lambda repressor
/note="phage lambda repressor"
CDS 1248..1280
/label=ssrA tag (LVA)
/note="C-terminal peptide that mediates degradation in
bacteria through the ClpXP and ClpAP proteases (McGinness
et al., 2006)"
terminator 1328..1399
/label=rrnB T1 terminator
/note="transcription terminator T1 from the E. coli rrnB
gene"
terminator 1415..1442
/label=T7Te terminator
/note="phage T7 early transcription terminator"
regulatory 1455..1489
/label=BBa_J23117
/note="BBa_J23117"
/regulatory_class="promoter"
regulatory 1498..1509
/label=BBa_B0034
/note="BBa_B0034"
/regulatory_class="ribosome_binding_site"
RBS 1498..1509
/note="strong bacterial ribosome binding site (Elowitz and
Leibler, 2000)"
CDS 1516..2391
/label=araC
/note="L-arabinose regulatory protein"
CDS 2421..3041
/label=TetR
/note="tetracycline repressor TetR"
misc_feature 3048..3068
/label=BioBrick suffix
/note="universal suffix for all parts"
terminator 3069..3128
/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."
rep_origin complement(3375..3963)
/direction=LEFT
/label=ori
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
terminator complement(4051..4145)
/label=lambda t0 terminator
/note="transcription terminator from phage lambda"
CDS complement(4169..4825)
/label=CmR
/note="chloramphenicol acetyltransferase"
promoter complement(4826..4928)
/label=cat promoter
/note="promoter of the E. coli cat gene encoding
chloramphenicol acetyltransferase"
This page is informational only.