Basic Vector Information
- Vector Name:
- pBACi
- Antibiotic Resistance:
- Chloramphenicol
- Length:
- 9274 bp
- Type:
- Cloning vector
- Replication origin:
- ori
- Source/Author:
- Sato'o Y, Hisatsune J, Sakuma T, Yamamoto T, Sugai M.
- Promoter:
- lac
pBACi vector Map
pBACi vector Sequence
LOCUS V009319 9274 bp DNA circular SYN 17-DEC-2018
DEFINITION Exported.
ACCESSION V009319
VERSION V009319
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
.
REFERENCE 1 (bases 1 to 9274)
AUTHORS Sato'o Y, Hisatsune J, Sakuma T, Yamamoto T, Sugai M.
TITLE Novel CRISPR interference technology, an elementary method for
inspects of Staphylococcus aureus clinical isolates
JOURNAL Unpublished
REFERENCE 2 (bases 1 to 9274)
AUTHORS Sato'o Y, Hisatsune J, Sugai M.
TITLE Direct Submission
JOURNAL Submitted (22-FEB-2016) Contact:Motoyuki Sugai Hiroshima University,
Bacteriology; Minamiku, Kasumi1-2-3, Hiroshima, Hiroshima 734-8551,
Japan URL :http://home.hiroshima-u.ac.jp/saikin/index.html
REFERENCE 3 (bases 1 to 9274)
TITLE Direct Submission
REFERENCE 4 (bases 1 to 9274)
AUTHORS .
TITLE Direct Submission
COMMENT ##Assembly-Data-START##
Assembly Method :: CLC Genomics Workbench v. 7
Sequencing Technology :: Illumina MiSeq
##Assembly-Data-END##
SGRef: number: 1; type: "Journal Article"; journalName:
"Unpublished"
SGRef: number: 2; type: "Journal Article"; journalName: "Submitted
(22-FEB-2016) Contact:Motoyuki Sugai Hiroshima University,
Bacteriology"; volume: " Minamiku, Kasumi1-2-3, Hiroshima, Hiroshima
734-8551, Japan URL :http"; pages:
"//home.hiroshima-u.ac.jp/saikin/index.htm"
SGRef: number: 3; type: "Journal Article"
FEATURES Location/Qualifiers
source 1..9274
/mol_type="other DNA"
/organism="synthetic DNA construct"
protein_bind 1..22
/label="CAP binding site"
/note="CAP binding activates transcription in the presence
of cAMP."
promoter 37..67
/label="lac promoter"
/note="promoter for the E. coli lac operon"
protein_bind 75..91
/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 99..115
/label="M13 rev"
/note="common sequencing primer, one of multiple similar
variants"
repeat_region 414..449
/rpt_unit_seq="gttttagagctatgctgttttgaatggtcccaaaac"
misc_feature complement(450..455)
/label="BsaI recognition site"
/note="BsaI recognition site"
misc_feature 473..478
/label="BsaI recognition site"
/note="BsaI recognition site"
repeat_region 480..515
/label="DR"
/note="direct repeat for the Streptococcus pyogenes
CRISPR/Cas system"
misc_feature complement(516..647)
/label="crRNA leader"
/note="crRNA leader sequence for the Streptococcus pyogenes
CRISPR/Cas system"
CDS complement(671..4774)
/label="dCas9"
/note="catalytically dead mutant of the Cas9 endonuclease
from the Streptococcus pyogenes Type II CRISPR/Cas system"
misc_RNA 5070..5148
/label="tracrRNA"
/note="trans-activating CRISPR RNA for the Streptococcus
pyogenes CRISPR/Cas9 system"
primer_bind complement(5456..5472)
/label="M13 fwd"
/note="common sequencing primer, one of multiple similar
variants"
rep_origin 5823..6411
/direction=RIGHT
/label="ori"
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
CDS complement(6988..7635)
/gene="cat"
/label="Chloramphenicol acetyltransferase"
/note="Chloramphenicol acetyltransferase from
Staphylococcus aureus. Accession#: P00485"
CDS complement(7917..8918)
/label="repB"
/note="RepB replication protein"
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