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		+	The goal of the project is to express the four previously mentioned genes, crtI, crtYB, crtE, and CCD1, needed for the beta-ionone synthesis pathway in yeast.
		+	*Each of the four genes is first synthesized.
		+	*Then a restriction site and section homologous to a suitable section of the yeast genome is added to the ends of the genes.
		+	*In parallel, a cassette containing a gene that allows for separation of transformed yeast from untransformed (such as ampicillin resistance) is modified in the same way.
		+	*The gene and cassette are then ligated together using the restriction sites.
		+	*

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Revision as of 02:03, 28 September 2011

Modeling

The pathway for producing beta-carotene as shown in "High-Level Production of Beta-Carotene in Saccharomyces cerevisiae by Successive Transformation with Carotenogenic Genes from Xanthophyllomyces dendrorhous" by Rene Verwaal et. Al. Yeast naturally produce GGPP but no other intermediates in beta-carotene pathway, crtYB and crtI are needed to to complete the pathway for beta-carotene production. Notice crtYB codes for two proteins needed in the pathway. CrtE further improves beta-carotene production as it aides in the production of the starting product, GGPP.

The pathway for producing beta-ionone from beta-carotene as shown in "Functional Characterization of a Carotenoid Cleavage Dioxygenase 1 and Its Relation to the Carotenoid Accumulation and Volatile Emission During the Floral Development of Osmanthus Fragrans Lour" by Susanne Baldermann et. Al. This process only involves the expression of one gene, CCD, which codes for enzymatic oxidative cleavage 1 and 2, which cleaves the ends of beta-carotene to produce two beta-ionone molecules.

The goal of the project is to express the four previously mentioned genes, crtI, crtYB, crtE, and CCD1, needed for the beta-ionone synthesis pathway in yeast.

• Each of the four genes is first synthesized.
• Then a restriction site and section homologous to a suitable section of the yeast genome is added to the ends of the genes.
• In parallel, a cassette containing a gene that allows for separation of transformed yeast from untransformed (such as ampicillin resistance) is modified in the same way.
• The gene and cassette are then ligated together using the restriction sites.