Insights into the biosynthesis of septacidin l-heptosamine moiety unveils a VOC family sugar epimerase.
	    		
		   		
		   			
		   		
	    	
    	 
    	10.1016/j.apsb.2022.05.031
   		
        
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Meng CHEN
			        		
			        		
			        		
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			        		Zhengyan GUO
			        		
			        		
			        		
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			        		Jinyuan SUN
			        		
			        		
			        		
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			        		Wei TANG
			        		
			        		
			        		
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			        		Min WANG
			        		
			        		
			        		
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			        		Yue TANG
			        		
			        		
			        		
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			        		Pengwei LI
			        		
			        		
			        		
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			        		Bian WU
			        		
			        		
			        		
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			        		Yihua CHEN
			        		
			        		
			        		
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			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. State Key Laboratory of Microbial Resources & CAS Key Laboratory of Microbial Physiological and Metabolic Engineering, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		Biosynthesis;
			        		
			        		
			        		
				        		Catalytic mechanism;
			        		
			        		
			        		
				        		Deprotonation/reprotonation;
			        		
			        		
			        		
				        		Hemiketal;
			        		
			        		
			        		
				        		Natural product;
			        		
			        		
			        		
				        		Septacidin;
			        		
			        		
			        		
				        		VOC epimerase;
			        		
			        		
			        		
				        		l-heptose
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Acta Pharmaceutica Sinica B
	            		
	            		 2023;13(2):765-774
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:English
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	l-Heptopyranoses are important components of bacterial polysaccharides and biological active secondary metabolites like septacidin (SEP), which represents a group of nucleoside antibiotics with antitumor, antifungal, and pain-relief activities. However, little is known about the formation mechanisms of those l-heptose moieties. In this study, we deciphered the biosynthetic pathway of the l,l-gluco-heptosamine moiety in SEPs by functional characterizing four genes and proposed that SepI initiates the process by oxidizing the 4'-hydroxyl of l-glycero-α-d-manno-heptose moiety of SEP-328 ( 2) to a keto group. Subsequently, SepJ (C5 epimerase) and SepA (C3 epimerase) shape the 4'-keto-l-heptopyranose moiety by sequential epimerization reactions. At the last step, an aminotransferase SepG installs the 4'-amino group of the l,l-gluco-heptosamine moiety to generate SEP-327 ( 3). An interesting phenomenon is that the SEP intermediates with 4'-keto-l-heptopyranose moieties exist as special bicyclic sugars with hemiacetal-hemiketal structures. Notably, l-pyranose is usually converted from d-pyranose by bifunctional C3/C5 epimerase. SepA is an unprecedented monofunctional l-pyranose C3 epimerase. Further in silico and experimental studies revealed that it represents an overlooked metal dependent-sugar epimerase family bearing vicinal oxygen chelate (VOC) architecture.