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CRISPR interference technology, an elementary method for inspects of Staphylococcus aureus clinical isolates JOURNAL Unpublished REFERENCE 2 (bases 1 to 9274) AUTHORS Sato'o Y, Hisatsune J, Sugai M. TITLE Direct Submission JOURNAL Submitted (22-FEB-2016) Contact:Motoyuki Sugai Hiroshima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Sequencing Technology :: Illumina MiSeq ##Assembly-Data-END## SGRef: number: 1; type: "Journal Article"; journalName: "Unpublished" SGRef: number: 2; type: "Journal Article"; journalName: "Submitted (22-FEB-2016) Contact:Motoyuki Sugai Hiroshima University, Bacteriology"; volume: "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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