Towards the biotechnological isomerization of branched sugars: D-tagatose-3-epimerase equilibrates both enantiomers of 4-C-methyl-ribulose with both enantiomers of 4-C-methyl-xylulose

Slični predmeti

• Green syntheses of new 2-C-methyl aldohexoses and 5-C-methyl ketohexoses: D-tagatose-3-epimerase (DTE)-a promiscuous enzyme
  od: Jones, N, i dr.
  Izdano: (2008)
• A concise approach to the synthesis of all twelve 5-deoxyhexoses: D-tagatose-3-epimerase-a reagent that is both specific and general
  od: Rao, D, i dr.
  Izdano: (2009)
• Carbon-branched carbohydrate chirons: practical access to both enantiomers of 2-C-methyl-ribono-1,4-lactone and 2-C-methyl-arabinonolactone
  od: Booth, K, i dr.
  Izdano: (2008)
• Conversion of L-rhamnose into ten of the sixteen 1-and 6-deoxyketohexoses in water with three reagents: D-tagatose-3-epimerase equilibrates C3 epimers of deoxyketoses
  od: Gullapalli, P, i dr.
  Izdano: (2010)
• Doubly carbon-branched pentoses: synthesis of both enantiomers of 2.4-di-C-methyl arabinose and 2-deoxy-2,4-di-C-methyl arabinose using only acetonide protection
  od: Booth, K, i dr.
  Izdano: (2009)