pPink-HC

Pichia pastoris integrating vector for high-copy expression in the PichiaPink™ system.

Sequence Author: Thermo Fisher (Invitrogen)

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PluTI (7505) SfoI (7503) NarI (7502) KasI (7501) NdeI (7450) AatII (7201) ZraI (7199) AhdI (6279) AflII (4776) PshAI (4737) BmgBI (4458) SpeI (4323) EcoNI (4191) PsiI (3998) BglII (1) Eco53kI (206) SacI (208) PmeI (413) XcmI (706) EcoRI (941) RsrII (948) SphI (958) StuI (964) Bsu36I (966) Acc65I (970) KpnI (974) NgoMIV (977) NaeI (979) FseI (981) SwaI (987) EcoRV (1015) BsrGI (1184) MluI (1191) BamHI (1272) NotI - SacII (1279) PpADE2 HC promoter NheI (1362) BmtI (1366) BbsI (2031) DraIII (2316) BsaAI (3032) BsgI (3139) AscI - BssHII (3192) NruI (3278) BsaBI (3383) pPink-HC 7667 bp
PluTI  (7505)
1 site
G G C G C C C C G C G G

Efficient cleavage requires at least two copies of the PluTI recognition sequence.
SfoI  (7503)
1 site
G G C G C C C C G C G G
NarI  (7502)
1 site
G G C G C C C C G C G G

Efficient cleavage requires at least two copies of the NarI recognition sequence.
KasI  (7501)
1 site
G G C G C C C C G C G G
NdeI  (7450)
1 site
C A T A T G G T A T A C

Prolonged incubation with NdeI may lead to removal of additional nucleotides.
AatII  (7201)
1 site
G A C G T C C T G C A G
ZraI  (7199)
1 site
G A C G T C C T G C A G
AhdI  (6279)
1 site
G A C N N N N N G T C C T G N N N N N C A G

The 1-base overhangs produced by AhdI may be hard to ligate.
Sticky ends from different AhdI sites may not be compatible.
AflII  (4776)
1 site
C T T A A G G A A T T C
PshAI  (4737)
1 site
G A C N N N N G T C C T G N N N N C A G

PshAI quickly loses activity at 37°C, but can be used at 25°C for long incubations.
BmgBI  (4458)
1 site
C A C G T C G T G C A G

This recognition sequence is asymmetric, so ligating blunt ends generated by BmgBI will not always regenerate a BmgBI site.
SpeI  (4323)
1 site
A C T A G T T G A T C A
EcoNI  (4191)
1 site
C C T N N N N N A G G G G A N N N N N T C C

The 1-base overhangs produced by EcoNI may be hard to ligate.
Sticky ends from different EcoNI sites may not be compatible.
PsiI  (3998)
1 site
T T A T A A A A T A T T
BglII  (1)
1 site
A G A T C T T C T A G A
Eco53kI  (206)
1 site
G A G C T C C T C G A G
SacI  (208)
1 site
G A G C T C C T C G A G
PmeI  (413)
1 site
G T T T A A A C C A A A T T T G
XcmI  (706)
1 site
C C A N N N N N N N N N T G G G G T N N N N N N N N N A C C

The 1-base overhangs produced by XcmI may be hard to ligate.
Sticky ends from different XcmI sites may not be compatible.
EcoRI  (941)
1 site
G A A T T C C T T A A G
RsrII  (948)
1 site
C G G W C C G G C C W G G C

Efficient cleavage requires at least two copies of the RsrII recognition sequence.
Sticky ends from different RsrII sites may not be compatible.
For full activity, add fresh DTT.
SphI  (958)
1 site
G C A T G C C G T A C G
StuI  (964)
1 site
A G G C C T T C C G G A
Bsu36I  (966)
1 site
C C T N A G G G G A N T C C

Sticky ends from different Bsu36I sites may not be compatible.
Acc65I  (970)
1 site
G G T A C C C C A T G G
KpnI  (974)
1 site
G G T A C C C C A T G G
NgoMIV  (977)
1 site
G C C G G C C G G C C G

Efficient cleavage requires at least two copies of the NgoMIV recognition sequence.
NaeI  (979)
1 site
G C C G G C C G G C C G

Efficient cleavage requires at least two copies of the NaeI recognition sequence.
FseI  (981)
1 site
G G C C G G C C C C G G C C G G

FseI gradually loses activity when stored at -20°C.
SwaI  (987)
1 site
A T T T A A A T T A A A T T T A

SwaI is typically used at 25°C, but is 50% active at 37°C.
EcoRV  (1015)
1 site
G A T A T C C T A T A G

EcoRV is reportedly more prone than its isoschizomer Eco32I to delete a base after cleavage.
BsrGI  (1184)
1 site
T G T A C A A C A T G T

BsrGI is typically used at 37°C, but is even more active at 60°C.
MluI  (1191)
1 site
A C G C G T T G C G C A
BamHI  (1272)
1 site
G G A T C C C C T A G G

After cleavage, BamHI-HF® (but not the original BamHI) can remain bound to DNA and alter its electrophoretic mobility.
NotI  (1279)
1 site
G C G G C C G C C G C C G G C G
SacII  (1279)
1 site
C C G C G G G G C G C C

Efficient cleavage requires at least two copies of the SacII recognition sequence.
NheI  (1362)
1 site
G C T A G C C G A T C G
BmtI  (1366)
1 site
G C T A G C C G A T C G
BbsI  (2031)
1 site
G A A G A C N N C T T C T G N N ( N ) 4

Sticky ends from different BbsI sites may not be compatible.
BbsI gradually loses activity when stored at -20°C.
DraIII  (2316)
1 site
C A C N N N G T G G T G N N N C A C

Sticky ends from different DraIII sites may not be compatible.
BsaAI  (3032)
1 site
Y A C G T R R T G C A Y
BsgI  (3139)
1 site
G T G C A G ( N ) 14 N N C A C G T C ( N ) 14

Efficient cleavage requires at least two copies of the BsgI recognition sequence.
Sticky ends from different BsgI sites may not be compatible.
For full activity, add fresh S-adenosylmethionine (SAM).
AscI  (3192)
1 site
G G C G C G C C C C G C G C G G
BssHII  (3192)
1 site
G C G C G C C G C G C G

BssHII is typically used at 50°C, but is 75% active at 37°C.
NruI  (3278)
1 site
T C G C G A A G C G C T
BsaBI  (3383)
1 site
G A T N N N N A T C C T A N N N N T A G
PpADE2
1299 .. 2990  =  1692 bp
563 amino acids  =  61.4 kDa
Product: phosphoribosylaminoimidazole carboxylase from Pichia pastoris
essential for the biosynthesis of purine nucleotides, including adenine
PpADE2
1299 .. 2990  =  1692 bp
563 amino acids  =  61.4 kDa
Product: phosphoribosylaminoimidazole carboxylase from Pichia pastoris
essential for the biosynthesis of purine nucleotides, including adenine
PpTRP2
3367 .. 4983  =  1617 bp
538 amino acids  =  60.8 kDa
Product: anthranilate synthase from Pichia pastoris
catalyzes the initial step of tryptophan biosynthesis
PpTRP2
3367 .. 4983  =  1617 bp
538 amino acids  =  60.8 kDa
Product: anthranilate synthase from Pichia pastoris
catalyzes the initial step of tryptophan biosynthesis
AOX1 promoter
2 .. 940  =  939 bp
inducible promoter, regulated by methanol
AOX1 promoter
2 .. 940  =  939 bp
inducible promoter, regulated by methanol
AmpR
6206 .. 7066  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 2:  
   6206 .. 6997  =  792 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
6206 .. 7066  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 1:  signal sequence  
   6998 .. 7066  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
6206 .. 7066  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
ori
5447 .. 6035  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
5447 .. 6035  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
CYC1 terminator
1017 .. 1266  =  250 bp
transcription terminator for CYC1
CYC1 terminator
1017 .. 1266  =  250 bp
transcription terminator for CYC1
PpTRP2 promoter
3217 .. 3366  =  150 bp
promoter for Pichia pastoris TRP2
PpTRP2 promoter
3217 .. 3366  =  150 bp
promoter for Pichia pastoris TRP2
AmpR promoter
7067 .. 7171  =  105 bp
AmpR promoter
7067 .. 7171  =  105 bp
MCS
941 .. 991  =  51 bp
multiple cloning site
MCS
941 .. 991  =  51 bp
multiple cloning site
PpADE2 HC promoter
1286 .. 1298  =  13 bp
weak 13-bp promoter fragment that requires high-copy integration for efficient expression
PpADE2 HC promoter
1286 .. 1298  =  13 bp
weak 13-bp promoter fragment that requires high-copy integration for efficient expression
ORF:  3367 .. 4983  =  1617 bp
ORF:  538 amino acids  =  60.8 kDa
ORF:  486 .. 725  =  240 bp
ORF:  79 amino acids  =  9.2 kDa
ORF:  1299 .. 2990  =  1692 bp
ORF:  563 amino acids  =  61.4 kDa
ORF:  6336 .. 6602  =  267 bp
ORF:  88 amino acids  =  9.2 kDa
ORF:  7452 .. 33  =  249 bp
ORF:  82 amino acids  =  9.8 kDa
ORF:  7412 .. 47  =  303 bp
ORF:  100 amino acids  =  11.8 kDa
ORF:  3558 .. 3803  =  246 bp
ORF:  81 amino acids  =  8.5 kDa
ORF:  6206 .. 7066  =  861 bp
ORF:  286 amino acids  =  31.6 kDa
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