Part:BBa_K844003
Spider Silk 1x Subunit "F" (Fewest tRNA codon optimized)
Spider silk (1x) 2E subunit optimized to use the fewest number of tRNA codons; contains two elasticity domains and one strength domain.
Usage and Biology
The sequence for this subunit was derived from the 2E silk subunit from Brooks et al. (2008), which is based on the native sequence of the MaSp2 silk gene in Argiope aurantia. The 2E silk subunit contains codons for only six amino acids in the following proportions: glycine (44.1%), glutamine (17.6%), proline (14.7%), alanine (11.8%), serine (7.4%), and tyrosine (4.4%). The native Argiope aurantia codon usage profile is significantly different from E. coli ’s and the GC% of the DNA molecule itself (75%) is significantly different from the average GC% of native E. coli genes (51%). These features can make the native form of the gene difficult and slow to produce for the ribosomes in the cell as the necessary tRNA molecules are present in lower concentrations in E. coli and the genetic machinery of E. coli is not adapted to opening DNA of high GC% when making mRNA, and thus lower amounts of spider silk mRNA are produced.
This part is designed for use as an internal subunit in a longer spider silk construct. This part should be preceded by the BBa_K844007 silk subunit, which is identical to this subunit but contains an added Met (ATG) start codon upstream, and should be followed by either more repeats of this subunit or end with a BBa_K844000 part, which contains a 10-Histidine tag and a double stop codon (TAATAA).
The silk subunit contains four main domains: two elasticity domains, a linker domain, and a strength domain. The elasticity domains contains sequences coding for beta-helices and beta-spiral in the protein; these structures increase the elasticity of the spider silk. The linker domain joins the strength and elasticity domains together. The strength domain will form beta-sheets and strengthen the silk fibers by cross-linking silk strands.
Codon Optimization Procedure
This part was designed by entering the 2E DNA sequence into the Gene Designer software from DNA 2.0 and translating it. Codon optimization was performed, not using the Gene Designer software algorithm, but by hand. First, the list of tRNA genes in E. coli K-12 (which is very closely related to the lab strains of DH5α and BL21) was obtained from the [http://gtrnadb.ucsc.edu/Esch_coli_K12/eschColi_K12-tRNAs.fa Genomic tRNA Database], and the list of codons that were recognized by these tRNA anti-codons for each of the six amino acids present in the 2E construct was generated. New codons were selected so that they contained the minimum possible GC% for that amino acid and were included on the list of recognized anti-codons by known E. coli tRNA genes. The “F” construct BBa_K844003 was designed using the fewest possible codons (1 codon per amino acid).
Silk Subunit Amino Acid Composition:
Related parts:
BBa_K844001 – the native spider silk (1x) 1E subunit with one elasticity domains and one strength domain (no sequence manipulation)
BBa_K844002 – the native spider silk (1x) 2E subunit with two elasticity domains and one strength domain (no sequence manipulation)
BBa_K844004 – another codon optimized spider silk subunit, but with either one or two codons used for each amino acid
BBa_K844007 – this spider silk subunit with an added Met (ATG) start codon at the 5’ end
References:
Brooks AE, Stricker SM, Joshi SB, Kamerzell TJ, Middaugh CR, and Lewis RV. 2008. Properties of synthetic spider silk fibers based on Argiope aurantia MaSp2. Biomacromolecules 9:1506–10.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
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