Please use this identifier to cite or link to this item: https://doi.org/10.1186/1754-1611-3-2
Title: Synthesizing non-natural parts from natural genomic template
Authors: Dhar, P.K
Thwin, C.S
Tun, K
Tsumoto, Y
Maurer-Stroh, S 
Eisenhaber, F
Surana, U 
Keywords: bacterial protein
protein Eka1
protein Eka2
protein Eka3
protein Eka4
protein Eka5
protein Eka6
unclassified drug
amino acid sequence
article
cell growth
controlled study
DNA template
Escherichia coli
growth inhibition
nonhuman
phenotype
priority journal
protein analysis
protein database
protein expression
protein synthesis
protein tertiary structure
sequence analysis
Western blotting
wild type
Issue Date: 2009
Publisher: BMC
Citation: Dhar, P.K, Thwin, C.S, Tun, K, Tsumoto, Y, Maurer-Stroh, S, Eisenhaber, F, Surana, U (2009). Synthesizing non-natural parts from natural genomic template. Journal of Biological Engineering 3 : 2. ScholarBank@NUS Repository. https://doi.org/10.1186/1754-1611-3-2
Rights: Attribution 4.0 International
Abstract: Background: The current knowledge of genes and proteins comes from 'naturally designed' coding and non-coding regions. It would be interesting to move beyond natural boundaries and make user-defined parts. To explore this possibility we made six non-natural proteins in E. coli. We also studied their potential tertiary structure and phenotypic outcomes. Results: The chosen intergenic sequences were amplified and expressed using pBAD 202/D-TOPO vector. All six proteins showed significantly low similarity to the known proteins in the NCBI protein database. The protein expression was confirmed through Western blot. The endogenous expression of one of the proteins resulted in the cell growth inhibition. The growth inhibition was completely rescued by culturing cells in the inducer-free medium. Computational structure prediction suggests globular tertiary structure for two of the six non-natural proteins synthesized. Conclusion: To our best knowledge, this is the first study that demonstrates artificial synthesis of non-natural proteins from existing genomic template, their potential tertiary structure and phenotypic outcome. The work presented in this paper opens up a new avenue of investigating fundamental biology. Our approach can also be used to synthesize large numbers of non-natural RNA and protein parts for useful applications. © 2009 Dhar et al; licensee BioMed Central Ltd.
Source Title: Journal of Biological Engineering
URI: https://scholarbank.nus.edu.sg/handle/10635/178228
ISSN: 1754-1611
DOI: 10.1186/1754-1611-3-2
Rights: Attribution 4.0 International
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