Table 1 List of plasmids used in this work.

From: Improvement in the production of the human recombinant enzyme N-acetylgalactosamine-6-sulfatase (rhGALNS) in Escherichia coli using synthetic biology approaches

Plasmid

Description

Selection Marker

Source of reference

pGEX-5X-GALNSopt

pGEX-5X-3 plasmid encoding the enzyme N-acetylgalactosamine-6-sulfatase codon-optimized for expression in E. coli

AmpR

This study

pGEXosmY

Modification of the pGEX-5X-GALNSopt plasmid where the promoter tac was replaced by the osmY promoter with its corresponding RBS

AmpR

This study

pGEXproUmod

Modification of the pGEX-5X-GALNSopt plasmid where the promoter tac was replaced by the proU mod promoter with its corresponding RBS

AmpR

This study

pACYCDuet™-1

Bicistronic plasmid used as a control and to clone all the chaperones used in this study

CmR

Novagen, Merck Milipore

pDuet::GroS

Plasmids for the overexpression of the genes groS, groL, groS and groL, dnaK, dnaJ, dnaK and dnaJ, ibpA, ibpB, ibpA and ibpB, dsbA, dsbB, dsbA and dsbB, grpE, and clpB (respectively) driven by the lac promoter. Backbone pACYCDuet™-1

CmR

This study

pDuet::GroL

pDuet::GroSL

pDuet::DnaK

pDuet::DnaJ

pDuet::DnaKJ

pDuet::IbpA

pDuet::IbpB

pDuet::IbpAB

pDuet::DsbA

pDuet::DsbB

pDuet::DsbAB

pDuet::GrpE

pDuet::ClpB