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− | < | + | <h1> Patenting a New Form of Taxol Fermentation </h1> |
− | <p> | + | <h2> Abstract </h2> |
− | + | <p> Taxol, also known as pacilitaxel, is a widely used chemotherapy drug typically | |
− | + | extracted from the Yew tree. Mere extraction, however, does not yield sustainable returns | |
+ | because too-frequent extraction involves destroying the Yew tree source. Demand for Taxol | ||
+ | has outstripped supply, and scientists have turned to developing Taxol in plant cells followed | ||
+ | by industrial fermentation. The Duke University International Genetically Engineered | ||
+ | Machine Project looks to go a step further, by generating Taxol in bacteria cell cultures | ||
+ | instead of plant cell cultures. In order to use this invention to boost the market supply of | ||
+ | Taxol, the IGEM team will eventually need a corporate or non-profit partner, and this partner | ||
+ | will only be incentivized to participate if the IGEM team can offer exclusive licensing. Thus, the | ||
+ | success of IGEM’s new genetically engineered bacteria largely hinges on its patentability with | ||
+ | the United States Patent and Trademark Office. This report walks through the relevant patent | ||
+ | requirements, analyzes the case law, and comes to the conclusion that IGEM’s new genetically | ||
+ | engineered bacteria meets the conditions for successful patentability. </p> | ||
+ | <br> | ||
+ | <h2> Introduction <h2> | ||
+ | <p> Prior research has already shown Taxol to be an effective chemical in combatting | ||
+ | cancer. As explained by a professor at the University of Massachusetts-Amherst, the | ||
+ | compound “binds to micro-tubules, which are important in cell division, and prevents the | ||
+ | cancer cells from dividing properly.” <br> | ||
+ | However, just because a product is useful does not mean supply has kept pace with | ||
+ | rising demand. Taxol is primarily obtained by extracting it from Yew trees, which naturally | ||
+ | synthesize the product. Given the solvents and treatment necessary to do so, however, this | ||
+ | approach also destroys the very same Yew trees in the process. As such, extraction is | ||
+ | unlikely to achieve demand-supply equilibrium in the market. Researchers have since | ||
+ | pivoted to modifying plant cell cultures to produce Taxol and other significant precursors | ||
+ | found along the metabolic pathway. These plant cell cultures are in turn used in industrial | ||
+ | processes designed to produce Taxol on a substantial scale. Even this, however, is not the | ||
+ | most efficient solution to the current shortage—the plant cell’s complex infrastructure and | ||
+ | subsequent energy needs have prevented the cell’s resources from being fully directed | ||
+ | towards Taxol production. Low product yield is typically the result. <br> | ||
+ | The 2016 Duke University International Genetically Engineered Machine team’s goal | ||
+ | is to produce Taxol more efficiently, by using bacteria cell cultures rather than plant cells. | ||
+ | The process of optimizing bacteria to produce a product for later industrial fermentation | ||
+ | has already been demonstrated, but its application to Taxol has not. The IGEM team has | ||
+ | worked on characterizing five enzymes involved in the natural process of Taxol production, | ||
+ | and then merging them into one strain by genetically engineering the DNA of the bacteria | ||
+ | culture. At the end of this process, the bacteria culture produces Taxol, with less energy | ||
+ | expenditure than was required in plant cells and subsequently higher yield. <br> | ||
+ | But a more efficient process is meaningless if the means to boost market supply are | ||
+ | not available, which requires cooperation with a biopharmaceutical company. The Duke | ||
+ | IGEM project does not on its own have the resources to mass produce Taxol through | ||
+ | industrial fermentation, so licensing the new bacteria cell culture to a pharmaceutical | ||
+ | manufacturer is the logical next step. <br> <br> | ||
+ | “A company that owns rights in a patent, know-how, or other IP asset, but cannot or | ||
+ | does not want to be involved in the manufacturing of products, could benefit from | ||
+ | licensing out of such IP assets by relying on the better manufacturing capacity, | ||
+ | wider distribution outlets, greater local knowledge and management expertise of | ||
+ | another company (the licensee)” <br> <br> | ||
+ | Details of such a licensing agreement would need to be worked out in individual contract | ||
+ | negotiations. For example, the manufacturer might require more research by IGEM at the | ||
+ | front-end before agreeing to commercialize the product5. Before any negotiation can take | ||
+ | place, however, the manufacturer needs reassurance the venture will be profitable. These | ||
+ | industries are not in the business of charity. Acquiring a patent on the new genetically | ||
+ | engineered bacteria will provide the necessary financial incentive. <br> | ||
+ | The remainder of this report will outline the fundamentals of patent law and | ||
+ | requirements to getting a patent approved by the United States Patent and Trademark | ||
+ | Office. It will explain out the main roadblocks towards getting approved, but will ultimately | ||
+ | provide a case for a successful patent prosecution. </p> | ||
</html> | </html> |
Revision as of 02:03, 19 October 2016
Patenting a New Form of Taxol Fermentation
Abstract
Taxol, also known as pacilitaxel, is a widely used chemotherapy drug typically extracted from the Yew tree. Mere extraction, however, does not yield sustainable returns because too-frequent extraction involves destroying the Yew tree source. Demand for Taxol has outstripped supply, and scientists have turned to developing Taxol in plant cells followed by industrial fermentation. The Duke University International Genetically Engineered Machine Project looks to go a step further, by generating Taxol in bacteria cell cultures instead of plant cell cultures. In order to use this invention to boost the market supply of Taxol, the IGEM team will eventually need a corporate or non-profit partner, and this partner will only be incentivized to participate if the IGEM team can offer exclusive licensing. Thus, the success of IGEM’s new genetically engineered bacteria largely hinges on its patentability with the United States Patent and Trademark Office. This report walks through the relevant patent requirements, analyzes the case law, and comes to the conclusion that IGEM’s new genetically engineered bacteria meets the conditions for successful patentability.
Introduction
Prior research has already shown Taxol to be an effective chemical in combatting
cancer. As explained by a professor at the University of Massachusetts-Amherst, the
compound “binds to micro-tubules, which are important in cell division, and prevents the
cancer cells from dividing properly.”
However, just because a product is useful does not mean supply has kept pace with
rising demand. Taxol is primarily obtained by extracting it from Yew trees, which naturally
synthesize the product. Given the solvents and treatment necessary to do so, however, this
approach also destroys the very same Yew trees in the process. As such, extraction is
unlikely to achieve demand-supply equilibrium in the market. Researchers have since
pivoted to modifying plant cell cultures to produce Taxol and other significant precursors
found along the metabolic pathway. These plant cell cultures are in turn used in industrial
processes designed to produce Taxol on a substantial scale. Even this, however, is not the
most efficient solution to the current shortage—the plant cell’s complex infrastructure and
subsequent energy needs have prevented the cell’s resources from being fully directed
towards Taxol production. Low product yield is typically the result.
The 2016 Duke University International Genetically Engineered Machine team’s goal
is to produce Taxol more efficiently, by using bacteria cell cultures rather than plant cells.
The process of optimizing bacteria to produce a product for later industrial fermentation
has already been demonstrated, but its application to Taxol has not. The IGEM team has
worked on characterizing five enzymes involved in the natural process of Taxol production,
and then merging them into one strain by genetically engineering the DNA of the bacteria
culture. At the end of this process, the bacteria culture produces Taxol, with less energy
expenditure than was required in plant cells and subsequently higher yield.
But a more efficient process is meaningless if the means to boost market supply are
not available, which requires cooperation with a biopharmaceutical company. The Duke
IGEM project does not on its own have the resources to mass produce Taxol through
industrial fermentation, so licensing the new bacteria cell culture to a pharmaceutical
manufacturer is the logical next step.
“A company that owns rights in a patent, know-how, or other IP asset, but cannot or
does not want to be involved in the manufacturing of products, could benefit from
licensing out of such IP assets by relying on the better manufacturing capacity,
wider distribution outlets, greater local knowledge and management expertise of
another company (the licensee)”
Details of such a licensing agreement would need to be worked out in individual contract
negotiations. For example, the manufacturer might require more research by IGEM at the
front-end before agreeing to commercialize the product5. Before any negotiation can take
place, however, the manufacturer needs reassurance the venture will be profitable. These
industries are not in the business of charity. Acquiring a patent on the new genetically
engineered bacteria will provide the necessary financial incentive.
The remainder of this report will outline the fundamentals of patent law and
requirements to getting a patent approved by the United States Patent and Trademark
Office. It will explain out the main roadblocks towards getting approved, but will ultimately
provide a case for a successful patent prosecution.