Innovative Tools for Molecular and Cell Biology

Innovative Tools for Molecular and Cell Biology

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pPICHOLI Shuttle Vector System

High-Efficient Protein Expression in Pichia pastoris & E. coli

Vector Maps of pPICHOLI

Vector map of pPICHOLI 1
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Vector map of pPICHOLI 1

Vector map of pPICHOLI 2
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Vector map of pPICHOLI 2

Vector map of pPICHOLI 3
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Vector map of pPICHOLI 3

Vector map of pPICHOLI-HA
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Vector map of pPICHOLI-HA

Features

  • The prokaryotic expression system is simple to handle and allows a cost-effective and high-level production of heterologous proteins
  • P. pastoris/pPICHOLI system is a powerful eukaryotic expression system showing rapid growth at high densities combined with the strong AOX or CUP1 promoter, respectively
  • Ideally suited for expression of soluble proteins with post-translational modifications and those (eukaryotic) proteins causing problems when expressed in E. coli (e.g. proteins toxic to E. coli)
  • Easy cloning and high transformation efficiencies
  • Convenient affinity purification and detection of recombinant proteins

Description

  • The pPICHOLI vectors have been designed for heterologous gene expression in the yeast P. pastoris as well as in the prokaryote E. coli. The vectors contain an inducible (yeast) alcohol oxidase (AOX) promoter and an E. coli T7 promoter as well as sequences allowing autonomous replication both in P. pastoris and E. coli. Thus, vector linearization is no longer required and small amounts of DNA are sufficient to successfully transform P. pastoris. The integrated PARS sequence enables simple recovery of plasmids from yeast. Time-consuming subcloning into a number of expression vectors including testing for a successful gene expression is no longer necessary. A multiple cloning site enables convenient ligation of DNA fragments into the vectors.
Vector map of pPICHOLI-C
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Vector map of pPICHOLI-C
Note: BamHI is not a singular restriction site. pPICHOLI-C has no T7 Promoter.

 Sequence data of the cloning site of pPICHOLI-1

Sequence data of the cloning site of pPICHOLI-1. pPICHOLI-2 is lacking one of the G bases, pPICHOLI-3 is lacking both G bases (dark shaded box) upstream of the SalI restriction site. The ATG start codon and the TAA stop codon are marked in bold and italic. pPICHOLI-HA includes the 6xHis tag upstream of the BamHI restriction site and a HA tag (instead of the biotinylation sequence) downstram of the BamHI restriction site.

The pPICHOLI Vectors

  • The dual expression vectors pPICHOLI and pPICHOLI-HA combine eukaryotic and prokaryotic promoter elements. Phage T7 promoter, including the ribosomal binding site of the major capsid protein, promotes the efficient bacterial expression and is placed downstream of the P. pastoris promoter. The strong alcohol oxidase promoter (AOX) is tightly regulated, since protein expression is completely repressed when grown on glucose and maximally induced when grown on methanol. pPICHOLI is available with a multiple cloning site in three different reading frames to simplify cloning in frame with the tags (pPICHOLI-1, pPICHOLI-2, pPICHOLI-3). pICHOLI-1 (3579 bp) has two G bases directly upstream of the SalI site. pPICHOLI-2 (3578) and pPICHOLI-3 (3577 bp), respectively, are lacking one or both of these G bases.
  • Our pPICHOLI-HA vector includes a HA (hemagglutinin) epitope instead of the biotinylation sequence.
  • pPICHOLI-C carries the CUP1 promoter of Saccharomyces cerevisiae (instead of the AOX promoter) which has been shown to greatly reduce the induction time. pPICHOLI-C has no T7 promoter and is not suited for prokaryotic protein expression.
  • Because of the use of a common selection marker zeocin, the sizes of the shuttle vectors remain small (~3.6 and 3.2 kb, respectively), hence they remain convenient for handling, cloning and transformation. By integration of a Pichia specific autonomous replicating sequence (PARS1) into the pPICHOLI vectors, linearization is no longer required and the transformation efficiency is increased up to 105 transformants/µg DNA. Additionally, plasmids can be easily recovered from P. pastoris. The pPICHOLI dual expression vectors include an RGS(His)6 tag as well as an additional in vivo biotinylation sequence for sensitive detection and rapid purification of expressed proteins. Owing to the strong affinity of biotin to avidin, capture and screening assays are facilitated.

Kit Content

ProductAmount
pPICHOLI-1 vector DNA10 µg
pPICHOLI-2 vector DNA10 µg
pPICHOLI-3 vector DNA10 µg
pPICHOLI-C vector DNA10 µg
pPICHOLI-HA vector DNA10 µg
Sequencing primers500 pmol each

ORDER INFORMATION

  • For shipping and storage information please click on Order#.
Order# Description Amount Price Data Sheet
PPICH pPICHOLI vectors DNA 5 x 10 µg 534,00 PDF
  • All prices are in EURO excl. VAT and shipping. For further pricing and order information please ask your local distributor.

  • Once the DNA has been dissolved in sterile water or buffer we recommend storage at -20°C.

Download

  • pPICHOLI Vectors Handbook (PDF)

Vector maps and Sequences

  • Vector map of pPICHOLI-1 (pic)
  • Vector map of pPICHOLI-2 (pic)
  • Vector map of pPICHOLI-3 (pic)
  • Vector map of pPICHOLI-HA (pic)
  • Vector map of pPICHOLI-C (pic)
  • Sequence of pPICHOLI-1 (txt)
  • Sequence of pPICHOLI-2 (txt)
  • Sequence of pPICHOLI-3 (txt)
  • Sequence of pPICHOLI-HA (txt)
  • Sequence of pPICHOLI-C (txt)