Basic Vector Information
- Vector Name:
- pT18mob2
- Length:
- 3549 bp
- Type:
- Cloning vector
- Replication origin:
- ori
- Source/Author:
- Tauch A, Kirchner O, Loffler B, Gotker S, Puhler A, Kalinowski J.
pT18mob2 vector Map
pT18mob2 vector Sequence
LOCUS 40924_42114 3549 bp DNA circular SYN 18-DEC-2018 DEFINITION Cloning vector pT18mob2, complete sequence. ACCESSION . VERSION . KEYWORDS . SOURCE synthetic DNA construct ORGANISM synthetic DNA construct REFERENCE 1 (bases 1 to 3549) AUTHORS Tauch A, Kirchner O, Loffler B, Gotker S, Puhler A, Kalinowski J. TITLE Efficient electrotransformation of corynebacterium diphtheriae with a mini-replicon derived from the Corynebacterium glutamicum plasmid pGA1 JOURNAL Curr. Microbiol. 45 (5), 362-367 (2002) PUBMED 12232668 REFERENCE 2 (bases 1 to 3549) AUTHORS Kirchner O, Tauch A. TITLE Tools for genetic engineering in the amino acid-producing bacterium Corynebacterium glutamicum JOURNAL J. Biotechnol. 104 (1-3), 287-299 (2003) PUBMED 12948646 REFERENCE 3 (bases 1 to 3549) AUTHORS Kirchner O, Tauch A. TITLE Direct Submission JOURNAL Submitted (22-JAN-2003) Department of Genetics, University of Bielefeld, Universitaetsstrasse 25, Bielefeld D-33615, Germany REFERENCE 4 (bases 1 to 3549) TITLE Direct Submission REFERENCE 5 (bases 1 to 3549) AUTHORS . TITLE Direct Submission COMMENT SGRef: number: 1; type: "Journal Article"; journalName: "Curr. Microbiol."; date: "2002"; volume: "45"; issue: "5"; pages: "362-367" COMMENT SGRef: number: 2; type: "Journal Article"; journalName: "J. Biotechnol. 104 (1-3), 287-299 (2003)" COMMENT SGRef: number: 3; type: "Journal Article"; journalName: "Submitted (22-JAN-2003) Department of Genetics, University of Bielefeld, Universitaetsstrasse 25, Bielefeld D-33615, Germany" COMMENT SGRef: number: 4; type: "Journal Article" FEATURES Location/Qualifiers source 1..3549 /mol_type="other DNA" /organism="synthetic DNA construct" misc_feature 1..57 /label=MCS /note="pUC18/19 multiple cloning site" primer_bind complement(61..77) /label=M13 fwd /note="common sequencing primer, one of multiple similar variants" CDS complement(1017..1028) /codon_start=1 /label=Factor Xa site /note="Factor Xa recognition and cleavage site" /translation="IEGR" oriT complement(2232..2339) /direction=LEFT /label=oriT /note="incP origin of transfer" rep_origin 2551..3139 /label=ori /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of replication" protein_bind 3427..3448 /label=CAP binding site /note="CAP binding activates transcription in the presence of cAMP." promoter 3463..3493 /label=lac promoter /note="promoter for the E. coli lac operon" protein_bind 3501..3517 /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)." primer_bind 3525..3541 /label=M13 rev /note="common sequencing primer, one of multiple similar variants"
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