Ex Parte BORNSCHEUER et al - Page 23




              Appeal No. 2005-1745                                                                                     
              Application No. 09/161,680                                                                               
              of the filing date sought” that they were in possession of the invention as now claimed.                 
              Lockwood v. American Airlines, 107 F.3d at 1572, 41 USPQ2d at 1966; Vas-Cath v.                          
              Mahurkar, 935 F.2d at 1563-64, 19 USPQ2d at 1117.                                                        


              VI.  Another issue                                                                                       
                     In the event of further prosecution, the examiner may wish to consider whether                    
              the claims are patentable under 35 U.S.C. § 103 in view of Greener alone or in                           
              combination with another reference.  Greener discloses a method of generating a new                      
              catalytic activity of two enzymes, $-lactamase and alkaline phosphatase by introducing a                 
              DNA sequence encoding said enzymes into the E. coli strain XL1-Red and incubating                        
              the transformed E. coli to generate mutations in the DNA sequence.  Greener further                      
              discloses transferring the mutated DNA sequence into a strain which lacked the enzyme                    
              activity, incubating this strain in the presence of a selection medium, and selecting                    
              microorganisms which showed a new activity.  Greener still further discloses the XL1-                    
              Red mutator strain can be used “for introducing random mutations in a clones gene                        
              when a genetic selection or screen for variants is available.”  Greener, p. 384, last para.              
              Greener also describes “[t]he advantage in using XL1-Red for random mutagenesis                          
              (over e.g., chemical mutagenesis or a PCR-based protocol) is that the mutation rate can                  






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