Appeal 2007-1069 Application 10/334,990 In our opinion, Lilly is not the proper standard to apply to the claims in this appeal. In Lilly, at issue was the written description of a novel DNA genus. Lilly, 119 F.3d at 1563, 1567, 43 USPQ2d at 1401, 1405. In this case, DNA sequences for the claimed enzymes were known in the prior art. It is unnecessary for a patent application to provide a description of nucleotide sequences which are already known in the prior art. Falko- Gunter Falkner v. Inglis, 448 F.3d 1357, 1367, 79 USPQ2d 1001, 1008 (Fed. Cir. 2006). As explained in Capon v. Eshhar, 418 F.3d 1349, 1358, 76 USPQ2d 1078, 1084-5 (Fed. Cir. 2005): The “written description” requirement must be applied in the context of the particular invention and the state of the knowledge. The Board’s rule that the nucleotide sequences of the chimeric genes must be fully presented, although the nucleotide sequences of the component DNA are known, is an inappropriate generalization. When the prior art includes the nucleotide information, precedent does not set a per se rule that the information must be determined afresh. Both parties state that a person experienced in the field of this invention would know that these known DNA segments would retain their DNA sequences when linked by known methods. Both parties explain that their invention is not in discovering which DNA segments are related to the immune response, for that is in the prior art, but in the novel combination of the DNA segments to achieve a novel result. Here, the claimed enzymes – hydantoinase, hydantoin racemase, and D- or L-carbamoylase – were well-known and characterized in the prior art. As explained by Appellants, enzyme activities for each of the three enzyme classes were known in the art prior to the filing date of the application (Br. 13). Conserved amino acid motifs had been established for each enzyme class (Br. 16, 18, 20 (Tables 1-3)). Nucleotide information for these 7Page: Previous 1 2 3 4 5 6 7 8 9 10 11 12 13 Next
Last modified: September 9, 2013