Enhancing functional expression of heterologous proteins through random substitution of genetic codes in the 5' coding region. Issue 4 (16th January 2015)
- Record Type:
- Journal Article
- Title:
- Enhancing functional expression of heterologous proteins through random substitution of genetic codes in the 5' coding region. Issue 4 (16th January 2015)
- Main Title:
- Enhancing functional expression of heterologous proteins through random substitution of genetic codes in the 5' coding region
- Authors:
- Cheong, Dae‐Eun
Ko, Kyong‐Cheol
Han, Yunjon
Jeon, Ho‐Geun
Sung, Bong Hyun
Kim, Geun‐Joong
Choi, Jong Hyun
Song, Jae Jun - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <sec id="bit25478-sec-0001" sec-type="section"> <p>Recent studies using heterologous protein expression systems suggest that synonymous codons affect not only the expression but also the properties of the expressed protein. However, practical application of this information is challenging, and to date, efforts to employ bioinformatics tools to design synonymous codon mixes have been only marginally successful. Here, we sought to enhance the functional expression of heterologous protein in <italic>Escherichia coli</italic> through completely random substitution of the first ten codons with synonymous codons, using a previously isolated exocellulase CelEdx‐SF301 as the model protein. Synonymous codon variants were generated by PCR using forward primers with mixed nucleotides at the third position in each codon and a conventional reverse primer. The resulting PCR products were inserted upstream of the fluorescent protein mCherry without linkers. After transformation and cultivation, colonies exhibiting red fluorescence were selected, and the activity of SF301‐mCherry fusion proteins was tested. Synonymous codon variant fusion proteins exhibited 35‐ to 530‐fold increases in functional expression compared with wild‐type controls. Unlike results from other reports, we found that the stability of mRNA secondary structure in the 5' untranslated region and codon rarity were not correlated with functional expression<abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <sec id="bit25478-sec-0001" sec-type="section"> <p>Recent studies using heterologous protein expression systems suggest that synonymous codons affect not only the expression but also the properties of the expressed protein. However, practical application of this information is challenging, and to date, efforts to employ bioinformatics tools to design synonymous codon mixes have been only marginally successful. Here, we sought to enhance the functional expression of heterologous protein in <italic>Escherichia coli</italic> through completely random substitution of the first ten codons with synonymous codons, using a previously isolated exocellulase CelEdx‐SF301 as the model protein. Synonymous codon variants were generated by PCR using forward primers with mixed nucleotides at the third position in each codon and a conventional reverse primer. The resulting PCR products were inserted upstream of the fluorescent protein mCherry without linkers. After transformation and cultivation, colonies exhibiting red fluorescence were selected, and the activity of SF301‐mCherry fusion proteins was tested. Synonymous codon variant fusion proteins exhibited 35‐ to 530‐fold increases in functional expression compared with wild‐type controls. Unlike results from other reports, we found that the stability of mRNA secondary structure in the 5' untranslated region and codon rarity were not correlated with functional expression level. Our work demonstrates that a completely random mixed of synonymous codons effectively enhances functional expression levels without the need for amino acid substitutions. Biotechnol. Bioeng. 2015;112: 822–826. © 2014 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Biotechnology and bioengineering. Volume 112:Issue 4(2015:Apr.)
- Journal:
- Biotechnology and bioengineering
- Issue:
- Volume 112:Issue 4(2015:Apr.)
- Issue Display:
- Volume 112, Issue 4 (2015)
- Year:
- 2015
- Volume:
- 112
- Issue:
- 4
- Issue Sort Value:
- 2015-0112-0004-0000
- Page Start:
- 822
- Page End:
- 826
- Publication Date:
- 2015-01-16
- Subjects:
- Biotechnology -- Periodicals
Bioengineering -- Periodicals
660.6 - Journal URLs:
- http://onlinelibrary.wiley.com/doi/10.1002/bip.v101.5/issuetoc ↗
http://www.interscience.wiley.com ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/bit.25478 ↗
- Languages:
- English
- ISSNs:
- 0006-3592
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2089.850000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3050.xml