Cloning and expression of Escherichia coli O157∶H7 Stx2B subunit
	    		
		   		
	    	
    	
    	
   		
        
        	
        		- VernacularTitle:肠出血性大肠杆菌O157∶H7志贺样毒素2B亚基的表达
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Yiqiang DING
			        		
			        		;
		        		
		        		
		        		
			        		Changjun WANG
			        		
			        		;
		        		
		        		
		        		
			        		Shouyi YU
			        		
			        		
		        		
		        		
		        		
		        		
		        		
			        		
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		EHEC O157∶H7;
			        		
			        		
			        		
				        		Shiga-like toxin 2B subunit;
			        		
			        		
			        		
				        		Cloning and expression
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Journal of Medical Postgraduates
	            		
	            		 2003;0(06):-
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	Objective: To clone,identify and express the Shigalike toxin 2B(Stx2B) subunit gene of EHEC O157∶H7.Methods: A pair of primers were designed based on the Stx2B subunit gene sequence of EHEC O157∶H7.The Stx2B gene was amplified from the EHEC O157∶H7 chromosome by PCR and cloned into the pMD18-T vector.Thereafter,the gene was cut from the pMD18-T vector and cloned into the prokaryotic expression plasmid pET-28a vector.Then the recombinant plasmids were transformed into E. coli BL21(DE3) and the transformed host strain induced by IPTG.The expression protein was detected by SDS-PAGE and Western-blot analyses.Results: The Stx2B gene was successfully cloned into pMD18-T and pET-28a vectors,and the expressed protein identified by SDS-PAGE and Western blot.The molecular mass(Mr) of the expressed product was about 7 500,and the expression rate about 40%. Conclusion: The Stx2B gene was successfully cloned and effectively expressed in the prokaryotic expression system.