Ex parte BERG - Page 3




          Appeal No. 93-3114                                                          
          Application 07/825,465                                                      
          Examiner’s Answer, p.3).  Representative Claim 1 reads:                     
                    1.   A method for treating cattle and sheep                       
               to prevent foot rot or liver necrosis comprising                       
               administering a Fusobacterium necrophorum bacterin,                    
               which is a B-propiolactone inactivated Fusobacterium                   
                    necrophorum isolate, to the animal being treated.                 
          1.   Rejections based on Maas                                               
               Claim 1 stands rejected under 35 U.S.C. § 102(b) because               
          Maas purportedly describes the claimed process, and under                   
          35 U.S.C. § 102(f) because applicant signed a statement that                
          he actually examined the Maas dissertation prior to the June                
          7, 1990, the filing date of applicant’s parent application.                 
               A.   Maas’ disclosure                                                  
               In Chapter III, “The Immune Responses of Mice and Cattle               
          to Fusobacterium Necrophorum,” at pages 101-102, bridging                   
          paragraph, Maas describes the preparation of vaccines                       
          (emphasis added):                                                           
                   Three whole-cell monovalent F. necrophorum                        
               vaccines (FN 2101, FN 2382, and FN 3080) were                          
               prepared.  The bacteria were removed from the                          
               surface of plate cultures (BHIBA) with a sterile                       
               loop and suspended in sterile 0.1 M PBS at pH 7.1                      
               to a turbidity comparable to a No. 5 tube of a                         
               McFarland nephelometer set.  Beta-propiolactone                        
               (BPL) . . . was added (0.1% v/v).  The resulting                       
               mixtures were incubated for 4 days at 4 C to kill                      
               the bacteria. . . . [T]he vaccines were then warmed                    
               at 37 C for 4 hours to eliminate the concentration                     
               of (BPL)(Staples, 1981).  A low viscosity aluminum                     
               hydroxide gel (10% v/v) . . . was added as an                          
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