Transgenic amorpha-4, 11-diene synthesis

Chemistry: molecular biology and microbiology – Enzyme – proenzyme; compositions thereof; process for... – Lyase

Reexamination Certificate

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C435S252300, C435S320100, C536S023200

Reexamination Certificate

active

07541172

ABSTRACT:
The present invention relates to an isolated DNA sequence encoding a polypeptide having the biological activity of amorpha-4,11-diene synthase. This DNA sequence can be used for the transformation of bacteria, yeasts and plants for the production of amorpha-4,11-diene, a specific precursor in the synthesis of artemisinin, in the respective organisms. The invention also relates to these organisms.

REFERENCES:
patent: 6342380 (2002-01-01), Colby et al.
patent: 6495354 (2002-12-01), Chappell et al.
patent: 7091027 (2006-08-01), Wallaart et al.
Attwood et al. [Comput. Chem. 2001, col. 54(4), pp. 329-39].
Ponting [Brief. Bioinform. Mar. 2001, vol. 2(1), pp. 19-29].
Accession No. AF327526 (Liu et al., 2001).
Guo et al. (PNAS 101(25):9205-9210, 2004).
Attwood et al., “Which craft is best in bioinformatics?,” Computers & Chemistry, 25(4): 329-339 (2001).
Back et al., “Cloning and bacterial expression of a sesquiterpene cyclase fromHyoscyamus muticusand its molecular comparison to related terpene cyclases,” J. Biol. Chem., 270(13):7375-7381 (1995).
Back et al., “Expression of a plant sesquiterpene cyclase gene inEscherichia coli,” Archives of Biochemistry and Biophysics, 315(2): 527-532 (1994).
Back et al., “Identifying functional domains within terpene cyclases using a domain-swapping strategy,” Proc. Natl. Acad. Sci. USA, 93: 6841-6845 (1996).
Bohlmann et al., “Cadina-4,11-diene fromViguiera oblongifolia,” Phytochemistry, 23(5): 1183-1184 (1984).
Brodelius et al., “Metabolic engineering of plant secondary metabolism: a tool to improve the productivity of plant cell cultures?,” Abstract Papers of the American Chemical Society, p. AGFD026, abstract (1997).
Brodelius, “Metabolic engineering of secondary metabolism inVanilla planifoliaandArtemisia annua,” Book of Abstracts, 211thACS National Meeting, abstract (Mar. 24-28, 1996).
Chang et al., “Improvement of heterologous protein prouctivity using recombinantYarrowia lipolyticaand cyclic fed-batch process strategy,” Biotechnology and Bioengineering, 59(3): 379-385 (1998).
Chen et al., “One-step transformation of the dimorphic yeastYarrowia lipolytica,” Appl. Microbiol. Biotechnol., 48: 232-235 (1997).
Facchini et al., “Gene family for an elicitor-induced sesquiterpene cyclase in tobacco,” Proc. Natl. Acad. Sci. USA., 89: 11088-11092 (1992).
Hohn et al., “Expression of a fungal sesquiterpene cyclase gene in transgenic tobacco,” Plant Physiol., 97: 460-462 (1991).
Koepp et al., “Cyclization of geranylgeranyl diphosphate to taxa-4(5),11(12)-diene is the committed step of taxol biosynthesis in pacific yew,” J. Biol. Chem., 270(15): 8686-8690 (1995).
Matsushita et al., “Cloning and analysis of a cDNA encoding farnesyl diphosphate synthase fromArtemisia annua,” Gene, 172(2): 207-209 (1996).
Müller et al., “Comparison of expression systems in the yeastsSaccharomyces cerevisiae, Hansenula polymorpha, Klyveromyces lactis, Schizosaccharomyces pombeandYarrowia lipolytica. Cloning of two novel promoters fromYarrowia lipolytics,” Yeast, 14: 1267-1283 (1998).
Omirulleh et al., “Activity of a chimeric promoter with the doubled CaMV 35S enhancer element in protoplast-derived cells and transgenic plants in maize,” Plant Molecular Biology, 21: 415-428 (1993).
Park et al., “Expression, secretion, and processing of rice α-amylase in the yeastYarrowia lipolytica,” Journal of Biological Chemistry, 272(11): 6876-6881 (1997).
Ponting, “Issues in predicting protein function from sequence,” Briefings in Bioinformatics, 2(1): 19-29 (2001).
Rogers et al., “Gene transfer in plants: production of transformed plants using Ti plasmid vectors,” Methods in Enzymology, 118: 627-640 (1986).
Sequence alignment between Accession No. AF327526 (Liu et al., “Cloning of sesquiterpene cyclase gene fromArtemisia annua,” submitted Dec. 2001 to the EMBL, GenBank, and DDBJ databases) and Applicants' SEQ ID No. 13, 2001.
Shimada et al., “Increased carotenoid production by the food yeastCandida utilisthrough metabolic engineering of the Isoprenoid Pathway,” Applied and Environmental Microbiology, 64(7): 2676-2680 (1998).
Starks et al., “Structural basis for cyclic terpene biosynthesis by tobacco 5-epi-aristolochene synthase,” Science, 277: 1815-1820 (1997).
Tharaud et al., “Secretion of human blood coagulation factor XIIIa by the yeastYarrowia lipolytica,” Gene, 121: 111-119 (1992).
Van Geldre et al., “State of the art of the production of the antimalarial compound artemisinin in plants,” Plant Molecular Biology, 33(2): 199-209 (1997).
Vergauwe et al., “Agrobacterium tumefaciens-mediated transformation ofArtemisia annuaL. and regeneration of transgenic plants,” Plant Cell Reports, 15(12): 929-933 (1996).
Wallaart et al., “Bioconversion of dihydroarteannuinic acid into the new antimalarial drug artemisinin,” Pharmacy World and Science, 16(3): C4, abstract (1994).
Woerdenbag et al., “Progress in the research of artemisinin-related antimalarials: an update,” Pharmacy World and Science, 16(4): 169-180 (1994).
Yanisch-Perron et al., “Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 Vectors,” Gene 33: 103-119 (1985).
Preliminary Amendment filed Feb. 26, 2001, in U.S. Appl. No. 09/763,822, now U.S. Patent 7,091,027.
Sequence Amendment filed Jul. 29, 2002, in U.S. Appl. No. 09/763,822, now U.S. Patent 7,091,027.
Response to Notification of Defective Response and Sequence Amendment filed May 5, 2003, in U.S. Appl. No. 09/763,822, now U.S. Patent 7,091,027.
Restriction Requirement mailed Apr. 22, 2004, in U.S. Appl. No. 09/763,822, now U.S. Patent 7,091,027.
Election with Traverse filed May 25, 2004, in U.S. Appl. No. 09/763,822, now U.S. Patent 7,091,027.
Non-Final Office Action mailed Jun. 18, 2004, in U.S. Appl. No. 09/763,822, now U.S. Patent 7,091,027.
Amendment filed Sep. 20, 2004, in U.S. Appl. No. 09/763,822, now U.S. Patent 7,091,027.
Non-Final Office Action mailed Dec. 1, 2004, in U.S. Appl. No. 09/763,822, now U.S. Patent 7,091,027.
Amendment filed Jun. 1, 2005, in U.S. Appl. No. 09/763,822, now U.S. Patent 7,091,027.
Final Office Action mailed Sep. 30, 2005, in U.S. Appl. No. 09/763,822, now U.S. Patent 7,091,027.
Amendment After Final filed Feb. 24, 2006, in U.S. Appl. No. 09/763,822, now U.S. Patent 7,091,027.
Notice of Allowance and Fee(s) due mailed Mar. 24, 2006, in U.S. Appl. No. 09/763,822, now U.S. Patent 7,091,027.

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