Barton et al or Fischhoff et al v. Adang et al. - Page 107




          Interference 103,781                                                        

          modified sequence which contains a greater number of codons                 
          preferred by the intended plant host than did said coding                   
          sequence” (Claim 1 of Adang’s involved U.S. Patent 5,380,831).              
          Dr. Adang testified as follows (AR 0111, l. 21, - AR 0112,                  
          l. 16):                                                                     
                    A.  There’s a series of experiments based on                      
               constructing a series of gene deletions of the natural Bt              
               genes.  There’s a series of experiments directed towards               
               transgenic expression systems.  The most extensively worked            
               with was electroporation.  We also contemplated, designed              
               some experiments with heli cell extracts.  We then                     
               eventually had a series of experiments with using heat                 
               shock promoters and constructs.                                        
                                      . . . . .                                       
                    At some point also we then began to do experiments                
               . . . testing Shaw Kamen sequences in transgenic expression            
               systems.  So each of those experiments were for the purpose            
               of identifying the gene part, region that needed or would              
               benefit from fixing most, would reduce our work load of                
               synthesis.  Then we could go and rebuild the gene upon codon           
               preference and codon frequency.                                        
          By the series of experiments identified, Dr. Adang had “hoped”              
          (AR 0112, l. 23, - AR 0113, l. 8)(emphasis added):                          
               . . . we would . . . use that information on what region               
               would be sort of the focus.  And then . . . we could come              
               back and make these - make codon changes in those regions.             
               . . . [Y]ou would have solved the problem of - solved any              
               sort of codon problems and at the same time solved any                 
               instability problems.  And you get higher expression.  But             
               basically it’s a way of not having to build a . . . whole              
               gene, upon - and save time and cost.                                   
               Dr. Adang was then asked if there came a time when the                 
          effort to find a suitable destabilizing region was abandoned                

                                        -107-                                         





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