Enhanced production and identification of antioxidants in in vitro cultures of the cacti Mammillaria candida and Turbinicarpus laui
                 
        Academic Article in Scopus 
                     
         
            
    
    
     
        
    
          
      
    
      
            Overview 
              
            Identity 
              
            Additional document info 
              
    View All 
      
 
        
        
            
                 
         
            Overview 
        
            
                    abstract    
                
    
    	© 2019, Springer-Verlag GmbH Germany, part of Springer Nature. Cacti are an important source of metabolites but present limitations for their commercial exploitation, like slow growth and a decrease of wild populations. An alternative to obtain their biocompounds without affecting the natural environment are the in vitro culture techniques. We established in vitro cultures from Mammillaria candida Scheidweiler and Turbinicarpus laui Glass and Foster and used different stresses to increase metabolites and antioxidant activity. The cultures were exposed to 1.25% polyethylene glycol to induce a moderate drought stress, 50 g L ¿1 sucrose to generate an osmotic stress, chitosan (1.25 to 5 mg mL ¿1 ) to simulate a biotic attack, or to UV light. Chitosan was the best elicitor improving 1.5 times the concentration of phenolics, 9 to 10 times the content of flavonoids and betalains, and 16% the antioxidant activity in M. candida suspensions. In T. laui suspensions, this elicitor duplicates the flavonoids content and antioxidant activity. The antioxidant levels in elicited suspensions increased 5 to 10 times in relation to plant tubercles. Eleven compounds were identified in M. candida suspensions being digalloyl rhamnoside and epicatequin gallate the most abundant; in the T. laui suspensions, 16 compounds were detected and the most abundant were 17-decarboxi neobetanin and derivatives of luteolin. Thus, cacti in vitro culture is an efficient system to obtain high level of metabolites of biological interest. 
     
                 
              
            
                    
                
              
            
                    status    
                
              
            
                    publication date    
                
              
            
                    published in    
                
              
         
          
        
        
            
                 
         
            Identity 
        
            
                    Digital Object Identifier (DOI)    
                
              
            
                    PubMed ID    
                
              
         
          
        
        
            
                 
         
            Additional document info 
        
            
                    has global citation frequency    
                
              
            
                    start page    
                
              
            
                    end page    
                
              
            
                    volume