LOCUS Exported 3035 bp ds-DNA circular SYN 18-DEC-2018
DEFINITION Cloning vector pK18mob2, complete sequence.
ACCESSION AY222814
VERSION .
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
REFERENCE 1 (bases 1 to 3035)
AUTHORS Tauch A, Zheng Z, Puhler A, Kalinowski J.
TITLE Corynebacterium striatum chloramphenicol resistance transposon
Tn5564: genetic organization and transposition in Corynebacterium
glutamicum
JOURNAL Plasmid 40 (2), 126-139 (1998)
PUBMED 9735314
REFERENCE 2 (bases 1 to 3035)
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 3035)
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 3035)
AUTHORS .
TITLE Direct Submission
FEATURES Location/Qualifiers
source 1..3035
/organism="Cloning vector pK18mob2"
/lab_host="Escherichia coli"
/mol_type="genomic DNA"
/db_xref="taxon:224984"
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 584..1378
/codon_start=1
/gene="aph(3)-IIa"
/product="Aph(3)-IIa"
/label=aph(3)-IIa
/note="aminoglycoside phosphotransferase"
/protein_id="AAO66594.1"
/translation="MIEQDGLHAGSPAAWVERLFGYDWAQQTIGCSDAAVFRLSAQGRP
VLFVKTDLSGALNELQDEAARLSWLATTGVPCAAVLDVVTEAGRDWLLLGEVPGQDLLS
SHLAPAEKVSIMADAMRRLHTLDPATCPFDHQAKHRIERARTRMEAGLVDQDDLDEEHQ
GLAPAELFARLKARMPDGEDLVVTHGDACLPNIMVENGRFSGFIDCGRLGVADRYQDIA
LATRDIAEELGGEWADRFLVLYGIAAPDSQRIAFYRLLDEFF"
gene 584..1378
/gene="aph(3)-IIa"
/label=aph(3)-IIa
oriT 1716..1825
/note="incP origin of transfer"
misc_feature 1763..1861
/label=RP4-mob region
/note="RP4-mob region"
rep_origin 2037..2625
/direction=RIGHT
/label=ori
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
rep_origin 2624..2626
/label=oriV
/note="oriV"
protein_bind 2913..2934
/label=CAP binding site
/bound_moiety="E. coli catabolite activator protein"
/note="CAP binding activates transcription in the presence
of cAMP."
promoter 2949..2979
/label=lac promoter
/note="promoter for the E. coli lac operon"
protein_bind 2987..3003
/label=lac operator
/bound_moiety="lac repressor encoded by lacI"
/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 3011..3027
/label=M13 rev
/note="common sequencing primer, one of multiple similar
variants"
LOCUS Exported 3035 bp ds-DNA circular SYN 18-DEC-2018
DEFINITION Cloning vector pK18mob2, complete sequence.
ACCESSION AY222814
VERSION .
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
REFERENCE 1 (bases 1 to 3035)
AUTHORS Tauch A, Zheng Z, Puhler A, Kalinowski J.
TITLE Corynebacterium striatum chloramphenicol resistance transposon
Tn5564: genetic organization and transposition in Corynebacterium
glutamicum
JOURNAL Plasmid 40 (2), 126-139 (1998)
PUBMED 9735314
REFERENCE 2 (bases 1 to 3035)
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 3035)
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 3035)
AUTHORS .
TITLE Direct Submission
FEATURES Location/Qualifiers
source 1..3035
/organism="Cloning vector pK18mob2"
/lab_host="Escherichia coli"
/mol_type="genomic DNA"
/db_xref="taxon:224984"
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 584..1378
/codon_start=1
/gene="aph(3)-IIa"
/product="Aph(3)-IIa"
/label=aph(3)-IIa
/note="aminoglycoside phosphotransferase"
/protein_id="AAO66594.1"
/translation="MIEQDGLHAGSPAAWVERLFGYDWAQQTIGCSDAAVFRLSAQGRP
VLFVKTDLSGALNELQDEAARLSWLATTGVPCAAVLDVVTEAGRDWLLLGEVPGQDLLS
SHLAPAEKVSIMADAMRRLHTLDPATCPFDHQAKHRIERARTRMEAGLVDQDDLDEEHQ
GLAPAELFARLKARMPDGEDLVVTHGDACLPNIMVENGRFSGFIDCGRLGVADRYQDIA
LATRDIAEELGGEWADRFLVLYGIAAPDSQRIAFYRLLDEFF"
gene 584..1378
/gene="aph(3)-IIa"
/label=aph(3)-IIa
oriT 1716..1825
/note="incP origin of transfer"
misc_feature 1763..1861
/label=RP4-mob region
/note="RP4-mob region"
rep_origin 2037..2625
/direction=RIGHT
/label=ori
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
rep_origin 2624..2626
/label=oriV
/note="oriV"
protein_bind 2913..2934
/label=CAP binding site
/bound_moiety="E. coli catabolite activator protein"
/note="CAP binding activates transcription in the presence
of cAMP."
promoter 2949..2979
/label=lac promoter
/note="promoter for the E. coli lac operon"
protein_bind 2987..3003
/label=lac operator
/bound_moiety="lac repressor encoded by lacI"
/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 3011..3027
/label=M13 rev
/note="common sequencing primer, one of multiple similar
variants"