Ex parte TREICHLER et al. - Page 5




              Appeal No. 1995-2518                                                                                        
              Application 07/895,581                                                                                      


              Bussey taken with Achstetter, Hinnen, and Meyhack in further view of Strathern.                             
                     Claim 57 stands rejected under 35 U.S.C. § 103 as being unpatentable over                            
              Bussey taken with Achstetter, Hinnen, and Meyhack in further view of Kingsman.                              
                     We have chosen to group the grounds of rejection before us under                                     
              35 U.S.C. § 103, since all three rejections depend on the examiner's consideration of                       
              Bussey, Achstetter, Hinnen and Meyhack.  Appellants have argued the separate rejections                     
              of claim 56 and 57 only to the extent that it is urged that the rejection of these claims should            
              fail for the same reasons advanced relative to the first rejection. (Principal Brief, page 8).              
                     In describing Bussey, the examiner states (Answer, page 4):                                          

                     Bussey et al. disclose strains of S. cerevisiae with a null mutation of the KEX1 gene                
                     (col 3) obtained by gene disruption (col 6, lines 6-11) so that it allows for the                    
                     production of desired protein precursors retaining the C-terminal residues (col 6,                   
                     lines 20-27).  While Bussey et al. do not explicitly disclose the additional yscA,                   
                     yscB, yscY and yscS proteolytic activities, Bussey et al. nevertheless set forth the                 
                     teaching of producing proteins where the C-terminal is intact and the post                           
                     translational processing can be tailored as Bussey et al. disclose that the                          
                     processing can be carried out in vitro to process the selected secreted proteins                     
                     which means that the heterologous protein is obtained from the transformed yeast                     
                     with the C-terminal intact and unmodified and a yeast without an active ysc" gene                    
                     would not have been expected to have an active ysc" gene     product . . . .                         
                                                                                                                         

              The examiner relies on Achstetter as disclosing (Answer, page 4):                                           
                     [t]he isolation of yeast strains in which the genes coding for yscA, B, Y, and S                     
                     contain mutations (pages 141-142 and 145) and which also teaches that                                
                     proteinase yscB deficiency results in a decrease in protein degradation of                           
                     40-60%. . .                                                                                          


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