Difference between revisions of "Part:BBa K1554002:Design"

(→‎Design Notes)
(→‎References)
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===References===
 
===References===
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[1] Choi MY, Han KS, Boo KS, Jurenka RA (2002) Pheromone biosynthetic pathways in the moths Helicoverpa zea and Helicoverpa assulta. Insect Biochem Mol Biol. 32, 1353-9.
 +
 +
[2] Wang HL, Zhao CH, Wang CZ (2005) Comparative study of sex pheromone composition and biosynthesis in Helicoverpa armigera, H. assulta and their hybrid. Insect Biochem Mol Biol. 35, 575-83.
 +
 +
[3] Fu X, Fukuzawa M, Tabata J, Tatsuki S, Ishikawa Y (2005) Sex pheromone biosynthesis in Ostrinia zaguliaevi, a congener of the European corn borer moth O. nubilalis. Insect Biochem Mol Biol. 35, 621-6.
 +
 +
[4] Matsumoto S (2010) Molecular mechanisms underlying sex pheromone production in moths. Biosci Biotechnol Biochem. 74, 223-31.
 +
 +
[5] Gu SH, Wu KM, Guo YY, Pickett JA, Field LM, Zhou JJ et al (2013) Identification of genes expressed in the sex pheromone gland of the black cutworm Agrotis ipsilon with putative roles in sex pheromone biosynthesis and transport. BMC Genomics. 14, 636.
 +
 +
[6] Hagström Å, Wang HL, Liénard MA, Lassance JM, Johansson T, Löfstedt C (2013) A moth pheromone brewery: production of (Z)-11-hexadecenol by heterologous co-expression of two biosynthetic genes from a noctuid moth in a yeast cell factory. Microb Cell Fact. 12,
 +
125.
 +
 +
[7] Ding BJ, Hofvander P, Wang HL, Durrett TP, Stymne S, Löfstedt C (2014) A plant factory for moth pheromone production. Nat Commun. 5, 3353.
 +
 +
[8] Hagström AK, Liénard MA, Groot AT, Hedenström E, Löfstedt C Semi-selective fatty acyl reductases from four heliothine moths influence the specific pheromone composition. PLoS One. 7, e37230.

Revision as of 11:49, 28 September 2014


AtrΔ11


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

Codon optimization for Nicotiana benthamiana was performed before ordering sequence by gBlock. A KKYR k-del was also attached as it was shown to have better performance (Ding 2014).

Source

Ordered by gBlock after performing codon optimization for Nicotiana benthamiana from Helicoverpa armigera's gene.

References

[1] Choi MY, Han KS, Boo KS, Jurenka RA (2002) Pheromone biosynthetic pathways in the moths Helicoverpa zea and Helicoverpa assulta. Insect Biochem Mol Biol. 32, 1353-9.

[2] Wang HL, Zhao CH, Wang CZ (2005) Comparative study of sex pheromone composition and biosynthesis in Helicoverpa armigera, H. assulta and their hybrid. Insect Biochem Mol Biol. 35, 575-83.

[3] Fu X, Fukuzawa M, Tabata J, Tatsuki S, Ishikawa Y (2005) Sex pheromone biosynthesis in Ostrinia zaguliaevi, a congener of the European corn borer moth O. nubilalis. Insect Biochem Mol Biol. 35, 621-6.

[4] Matsumoto S (2010) Molecular mechanisms underlying sex pheromone production in moths. Biosci Biotechnol Biochem. 74, 223-31.

[5] Gu SH, Wu KM, Guo YY, Pickett JA, Field LM, Zhou JJ et al (2013) Identification of genes expressed in the sex pheromone gland of the black cutworm Agrotis ipsilon with putative roles in sex pheromone biosynthesis and transport. BMC Genomics. 14, 636.

[6] Hagström Å, Wang HL, Liénard MA, Lassance JM, Johansson T, Löfstedt C (2013) A moth pheromone brewery: production of (Z)-11-hexadecenol by heterologous co-expression of two biosynthetic genes from a noctuid moth in a yeast cell factory. Microb Cell Fact. 12, 125.

[7] Ding BJ, Hofvander P, Wang HL, Durrett TP, Stymne S, Löfstedt C (2014) A plant factory for moth pheromone production. Nat Commun. 5, 3353.

[8] Hagström AK, Liénard MA, Groot AT, Hedenström E, Löfstedt C Semi-selective fatty acyl reductases from four heliothine moths influence the specific pheromone composition. PLoS One. 7, e37230.