LOCUS Exported 3554 bp ds-DNA circular SYN 18-DEC-2018
DEFINITION Cloning vector pT19mob2, complete sequence.
ACCESSION AY222819
VERSION .
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
REFERENCE 1 (bases 1 to 3554)
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 2 (bases 1 to 3554)
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 3 (bases 1 to 3554)
AUTHORS .
TITLE Direct Submission
FEATURES Location/Qualifiers
source 1..3554
/organism="Cloning vector pT19mob2"
/lab_host="Escherichia coli"
/mol_type="genomic DNA"
/db_xref="taxon:224989"
misc_feature 1..57
/label=MCS
/note="pUC18/19 multiple cloning site"
primer_bind complement(58..74)
/label=M13 fwd
/note="common sequencing primer, one of multiple similar
variants"
CDS 1006..2160
/codon_start=1
/gene="tetA(Z)"
/product="TetA(Z)"
/label=tetA(Z)
/note="tetracycline exporter"
/protein_id="AAO66599.1"
/translation="MLITATLDAAGLGLVMPILPTLLDQVGAPDDMIPLHVGLLTALYA
IMQFLCAPILGRLSDRFGRRRVLVASLAGATIDYLVLALTDTLWVFYLARAVAGITGAT
NAVTATVIADITPPDQRAKRYGWLGACYGGGMIAGPAIGGLFGGVSPHLPFLVAAALAG
ITLVLSASLLRETRPPGSNGSHAQQPGTAKRTAVPGMLILLAVFGIVQFIGQAPGSTWV
LFTQQRLDWNPVEVGVSLSIFGMVQVFVQAALTGRIVSRIGETRAILVGIAADAIGLIG
LALIASTWAMLPILAALGLGSITLPALQTLLSRRAPEQQQGRLQGTLASLNSLTSIIGP
VTFTGIFALTRTNADGTLWICAAALYVLCALLMIRETCASRRSR"
gene 1006..2160
/gene="tetA(Z)"
/label=tetA(Z)
CDS complement(1018..1029)
/codon_start=1
/product="Factor Xa recognition and cleavage site"
/label=Factor Xa site
/translation="IEGR"
misc_feature 2278..2376
/label=RP4-mob region
/note="RP4-mob region"
rep_origin 2552..3140
/direction=RIGHT
/label=ori
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
rep_origin 3139..3141
/label=oriV
/note="oriV"
protein_bind 3428..3449
/label=CAP binding site
/bound_moiety="E. coli catabolite activator protein"
/note="CAP binding activates transcription in the presence
of cAMP."
promoter 3464..3494
/label=lac promoter
/note="promoter for the E. coli lac operon"
protein_bind 3502..3518
/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 3526..3542
/label=M13 rev
/note="common sequencing primer, one of multiple similar
variants"
CDS 3538..268
/codon_start=1
/gene="lacZ fragment"
/product="LacZ-alpha fragment of beta-galactosidase"
/label=lacZ-alpha
/translation="MTMITPSLHACRSTLEDPRVPSSNSLAVVLQRRDWENPGVTQLNR
LAAHPPFASWRNSEEARTDRPSQQLRSLNGEWRDKLASRCRKHSGRKGC"
LOCUS Exported 3554 bp ds-DNA circular SYN 18-DEC-2018
DEFINITION Cloning vector pT19mob2, complete sequence.
ACCESSION AY222819
VERSION .
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
REFERENCE 1 (bases 1 to 3554)
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 2 (bases 1 to 3554)
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 3 (bases 1 to 3554)
AUTHORS .
TITLE Direct Submission
FEATURES Location/Qualifiers
source 1..3554
/organism="Cloning vector pT19mob2"
/lab_host="Escherichia coli"
/mol_type="genomic DNA"
/db_xref="taxon:224989"
misc_feature 1..57
/label=MCS
/note="pUC18/19 multiple cloning site"
primer_bind complement(58..74)
/label=M13 fwd
/note="common sequencing primer, one of multiple similar
variants"
CDS 1006..2160
/codon_start=1
/gene="tetA(Z)"
/product="TetA(Z)"
/label=tetA(Z)
/note="tetracycline exporter"
/protein_id="AAO66599.1"
/translation="MLITATLDAAGLGLVMPILPTLLDQVGAPDDMIPLHVGLLTALYA
IMQFLCAPILGRLSDRFGRRRVLVASLAGATIDYLVLALTDTLWVFYLARAVAGITGAT
NAVTATVIADITPPDQRAKRYGWLGACYGGGMIAGPAIGGLFGGVSPHLPFLVAAALAG
ITLVLSASLLRETRPPGSNGSHAQQPGTAKRTAVPGMLILLAVFGIVQFIGQAPGSTWV
LFTQQRLDWNPVEVGVSLSIFGMVQVFVQAALTGRIVSRIGETRAILVGIAADAIGLIG
LALIASTWAMLPILAALGLGSITLPALQTLLSRRAPEQQQGRLQGTLASLNSLTSIIGP
VTFTGIFALTRTNADGTLWICAAALYVLCALLMIRETCASRRSR"
gene 1006..2160
/gene="tetA(Z)"
/label=tetA(Z)
CDS complement(1018..1029)
/codon_start=1
/product="Factor Xa recognition and cleavage site"
/label=Factor Xa site
/translation="IEGR"
misc_feature 2278..2376
/label=RP4-mob region
/note="RP4-mob region"
rep_origin 2552..3140
/direction=RIGHT
/label=ori
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
rep_origin 3139..3141
/label=oriV
/note="oriV"
protein_bind 3428..3449
/label=CAP binding site
/bound_moiety="E. coli catabolite activator protein"
/note="CAP binding activates transcription in the presence
of cAMP."
promoter 3464..3494
/label=lac promoter
/note="promoter for the E. coli lac operon"
protein_bind 3502..3518
/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 3526..3542
/label=M13 rev
/note="common sequencing primer, one of multiple similar
variants"
CDS 3538..268
/codon_start=1
/gene="lacZ fragment"
/product="LacZ-alpha fragment of beta-galactosidase"
/label=lacZ-alpha
/translation="MTMITPSLHACRSTLEDPRVPSSNSLAVVLQRRDWENPGVTQLNR
LAAHPPFASWRNSEEARTDRPSQQLRSLNGEWRDKLASRCRKHSGRKGC"