Abstract
Two potent anti-MRSA tanshinone glycosides (1 and 2) were discovered by targeted microbial biotransformation, along with rapid identification via MS/MS networking. Serial reactions including dehydrogenation, demethylations, reduction, glycosylation and methylation have been observed after incubation of tanshinone IIA and fungus Mucor rouxianus AS 3.3447. In addition, tanshinosides B (2) showed potent activities against serial clinical isolates of oxacillin-resistant Staphylococcus aureus with MIC values of 0.78 μg/mL. This is the first study that shows a significant increase in the level and activities of tanshinone glycosides relative to the substrate tanshinone IIA.
Research Department	
              
          Research Journal	
              Synthetic and Systems Biotechnology
          Research Publisher	
              Sciencedirect
          Research Rank	
              1
          Research Vol	
              1
          Research Website	
              http://www.sciencedirect.com/science/article/pii/S2405805X15300223
          Research Year	
              2016
          Research Member	
          
      Research Abstract	
               
 
 
          