Development of a gene synthesis platform for the efficient large scale production of small genes encoding animal toxins. Issue 1 (December 2016)
- Record Type:
- Journal Article
- Title:
- Development of a gene synthesis platform for the efficient large scale production of small genes encoding animal toxins. Issue 1 (December 2016)
- Main Title:
- Development of a gene synthesis platform for the efficient large scale production of small genes encoding animal toxins
- Authors:
- Sequeira, Ana
Brás, Joana
Guerreiro, Catarina
Vincentelli, Renaud
Fontes, Carlos - Abstract:
- Abstract Background Gene synthesis is becoming an important tool in many fields of recombinant DNA technology, including recombinant protein production.De novo gene synthesis is quickly replacing the classical cloning and mutagenesis procedures and allows generating nucleic acids for which no template is available. In addition, when coupled with efficient gene design algorithms that optimize codon usage, it leads to high levels of recombinant protein expression. Results Here, we describe the development of an optimized gene synthesis platform that was applied to the large scale production of small genes encoding venom peptides. This improved gene synthesis method uses a PCR-based protocol to assemble synthetic DNA from pools of overlapping oligonucleotides and was developed to synthesise multiples genes simultaneously. This technology incorporates an accurate, automated and cost effective ligation independent cloning step to directly integrate the synthetic genes into an effectiveEscherichia coli expression vector. The robustness of this technology to generate large libraries of dozens to thousands of synthetic nucleic acids was demonstrated through the parallel and simultaneous synthesis of 96 genes encoding animal toxins. Conclusions An automated platform was developed for the large-scale synthesis of small genes encoding eukaryotic toxins. Large scale recombinant expression of synthetic genes encoding eukaryotic toxins will allow exploring the extraordinary potency andAbstract Background Gene synthesis is becoming an important tool in many fields of recombinant DNA technology, including recombinant protein production.De novo gene synthesis is quickly replacing the classical cloning and mutagenesis procedures and allows generating nucleic acids for which no template is available. In addition, when coupled with efficient gene design algorithms that optimize codon usage, it leads to high levels of recombinant protein expression. Results Here, we describe the development of an optimized gene synthesis platform that was applied to the large scale production of small genes encoding venom peptides. This improved gene synthesis method uses a PCR-based protocol to assemble synthetic DNA from pools of overlapping oligonucleotides and was developed to synthesise multiples genes simultaneously. This technology incorporates an accurate, automated and cost effective ligation independent cloning step to directly integrate the synthetic genes into an effectiveEscherichia coli expression vector. The robustness of this technology to generate large libraries of dozens to thousands of synthetic nucleic acids was demonstrated through the parallel and simultaneous synthesis of 96 genes encoding animal toxins. Conclusions An automated platform was developed for the large-scale synthesis of small genes encoding eukaryotic toxins. Large scale recombinant expression of synthetic genes encoding eukaryotic toxins will allow exploring the extraordinary potency and pharmacological diversity of animal venoms, an increasingly valuable but unexplored source of lead molecules for drug discovery. … (more)
- Is Part Of:
- BMC biotechnology. Volume 16:Issue 1(2016)
- Journal:
- BMC biotechnology
- Issue:
- Volume 16:Issue 1(2016)
- Issue Display:
- Volume 16, Issue 1 (2016)
- Year:
- 2016
- Volume:
- 16
- Issue:
- 1
- Issue Sort Value:
- 2016-0016-0001-0000
- Page Start:
- 1
- Page End:
- 13
- Publication Date:
- 2016-12
- Subjects:
- Gene synthesis -- Assembly PCR -- Gene design -- Venom peptides
Biotechnology -- Periodicals
660.605 - Journal URLs:
- http://www.biomedcentral.com/bmcbiotechnol/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=14 ↗
http://link.springer.com/ ↗ - DOI:
- 10.1186/s12896-016-0316-3 ↗
- Languages:
- English
- ISSNs:
- 1472-6750
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 9962.xml