pARG1B vector (V009458)

Basic Vector Information

Vector Name:
pARG1B
Antibiotic Resistance:
Ampicillin
Length:
5287 bp
Type:
S. pombe expression vector
Replication origin:
ori
Host:
Yeast
Source/Author:
Matsuyama A, Shirai A, Yoshida M.
Promoter:
TEF1

pARG1B vector Map

pARG1B5287 bp6001200180024003000360042004800ADH1 terminatorderived from Schizosaccharomyces pombeTEF1 promoterEM7 promoterBSDCYC1 terminatorM13 fwdf1 oriAmpR promoterAmpRoriCAP binding sitelac promoterlac operatorM13 rev

pARG1B vector Sequence

LOCUS       40924_4729        5287 bp DNA     circular SYN 18-DEC-2018
DEFINITION  S. pombe expression vector pARG1B DNA, complete sequence.
ACCESSION   .
VERSION     .
KEYWORDS    .
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
REFERENCE   1  (bases 1 to 5287)
  AUTHORS   Matsuyama A, Shirai A, Yoshida M.
  TITLE     A novel series of vectors for chromosomal integration in fission 
            yeast
  JOURNAL   Biochem. Biophys. Res. Commun. 374 (2), 315-319 (2008)
  PUBMED    18634753
REFERENCE   2  (bases 1 to 5287)
  AUTHORS   Matsuyama A, Shirai A, Yoshida M.
  TITLE     Fission yeast integration vector pARG1B
  JOURNAL   Published Only in Database (2007)
REFERENCE   3  (bases 1 to 5287)
  AUTHORS   Matsuyama A, Shirai A, Yoshida M.
  TITLE     Direct Submission
  JOURNAL   Submitted (15-OCT-2007) Contact:Akihisa Matsuyama RIKEN, Chemical 
            Genetics Laboratory; Hirosawa 2-1, Wako, Saitama 351-0198, Japan URL
            :http://cgl.riken.go.jp/
REFERENCE   4  (bases 1 to 5287)
  TITLE     Direct Submission
REFERENCE   5  (bases 1 to 5287)
  AUTHORS   .
  TITLE     Direct Submission
COMMENT     SGRef: number: 1; type: "Journal Article"; journalName: "Biochem. 
            Biophys. Res. Commun."; date: "2008"; volume: "374"; issue: "2"; 
            pages: "315-319"
COMMENT     SGRef: number: 2; type: "Journal Article"; journalName: "Published 
            Only in Database (2007)"
COMMENT     SGRef: number: 3; type: "Journal Article"; journalName: "Submitted 
            (15-OCT-2007) Contact:Akihisa Matsuyama RIKEN, Chemical Genetics 
            Laboratory; Hirosawa 2-1, Wako, Saitama 351-0198, Japan URL 
            :http://cgl.riken.go.jp/"
COMMENT     SGRef: number: 4; type: "Journal Article"
COMMENT     Fission yeast expression vector.
FEATURES             Location/Qualifiers
     source          1..5287
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     terminator      21..208
                     /label=ADH1 terminator
                     /note="transcription terminator for the S. cerevisiae
                     alcohol dehydrogenase 1 (ADH1) gene"
     misc_feature    241..894
                     /pseudo
                     /gene="arg1"
                     /label=derived from Schizosaccharomyces pombe
                     /note="derived from Schizosaccharomyces pombe"
     CDS             241..894
                     /pseudo
                     /codon_start=1
                     /gene="arg1"
                     /label=arg1
                     /note="NotI site is created at the middle of this fragment 
                     (551-558)."
                     /translation="SRSC*R*GLLFV*QGRS*IH*LHLWRSCYIFGSCSS*SC*TCR*S
                     MLQISP**QPFLQRACH*AI*CH**FFGKK*RYCWPHKNFLCQLWY*GQ*DSLEVRS*G
                     GRV*EVWRREESNCLL**LFPRPFFGIS*YHCEPQI*TWFPTITS*CRPSRL**PCIHR
                     AICQ*QNCGCYCRARSR*RWYLSCQA*IFDCFAQGL**GWCFFNL**NSMRTWSQ"
     gene            241..894
                     /pseudo
                     /gene="arg1"
                     /label=arg1
     promoter        902..1309
                     /label=TEF1 promoter
                     /note="promoter for EF-1-alpha"
     promoter        1316..1363
                     /label=EM7 promoter
                     /note="synthetic bacterial promoter"
     CDS             1382..1777
                     /codon_start=1
                     /label=BSD
                     /note="blasticidin S deaminase"
                     /translation="MAKPLSQEESTLIERATATINSIPISEDYSVASAALSSDGRIFTG
                     VNVYHFTGGPCAELVVLGTAAAAAAGNLTCIVAIGNENRGILSPCGRCRQVLLDLHPGI
                     KAIVKDSDGQPTAVGIRELLPSGYVWEG"
     terminator      1874..2121
                     /label=CYC1 terminator
                     /note="transcription terminator for CYC1"
     primer_bind     complement(2147..2163)
                     /label=M13 fwd
                     /note="common sequencing primer, one of multiple similar 
                     variants"
     rep_origin      2376..2831
                     /label=f1 ori
                     /note="f1 bacteriophage origin of replication; arrow
                     indicates direction of (+) strand synthesis"
     promoter        3113..3217
                     /label=AmpR promoter
     CDS             3218..4075
                     /codon_start=1
                     /label=AmpR
                     /note="beta-lactamase"
                     /translation="MSIQHFRVALIPFFAAFCLPVFAHPETLVKVKDAEDQLGARVGYI
                     ELDLNSGKILESFRPEERFPMMSTFKVLLCGAVLSRIDAGQEQLGRRIHYSQNDLVEYS
                     PVTEKHLTDGMTVRELCSAAITMSDNTAANLLLTTIGGPKELTAFLHNMGDHVTRLDRW
                     EPELNEAIPNDERDTTMPVAMATTLRKLLTGELLTLASRQQLIDWMEADKVAGPLLRSA
                     LPAGWFIADKSGAGERGSRGIIAALGPDGKPSRIVVIYTTGSQATMDERNRQIAEIGAS
                     LIKHW"
     rep_origin      4249..4837
                     /label=ori
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of 
                     replication"
     protein_bind    5125..5146
                     /label=CAP binding site
                     /note="CAP binding activates transcription in the presence
                     of cAMP."
     promoter        5161..5191
                     /label=lac promoter
                     /note="promoter for the E. coli lac operon"
     protein_bind    5199..5215
                     /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     5223..5239
                     /label=M13 rev
                     /note="common sequencing primer, one of multiple similar 
                     variants"

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