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mixture and the extraction with organic solvents. As a result, it would be desirable to employ ω‐TAs for the transamination exclusively in organic solvents. Mutti et al. employed nine different lyophilized crude cell‐free extracts of (R)‐selective and (S)‐selective ω‐TAs for the asymmetric amination of ketones in organic solvents with 2‐propylamine as amine donor. The best enzyme activity for the transamination was found for methyl tert‐butyl ether (MTBE) at a water activity of 0.6 that allowed excellent stereoselectivity of optically pure amines (e.e. > 99%) and a conversion rate > 99% [9].

Chemical reaction depicting the oxidation/transamination cascade reactions for the biosynthesis of 6-aminohexanoic acid from cyclohexanol.

      Source: Based on Sattler et al. [8].

      The use of organic solvent MTBE has also been applied for the production of optically pure 1,2‐amino‐alcohols such as valinol from corresponding prochiral hydroxyl ketone using ω‐TAs [9]. Chiral 1,2‐amino‐alcohols are common building blocks embedded in many synthetic and naturally occurring molecules having biological activity, and valinol is a typical example of the versatile vicinal amino alcohols. Thus, the reductive amination of isopropyl methyl alcohol ketone can be performed in MTBE using 2‐propyl amine as amino donor to yield either (R)‐valinol or (S)‐valinol by the choice of (R)‐ and (S)‐selective ω‐TAs. The use of (R)‐selective ω‐TA purified from Bacillus megaterium afforded the (R)‐valinol with an ideal optical purity (>99% e.e.), although a low conversion rate of 15%. The (S)‐selective ω‐TA originating from Arthrobacter sp. can produce the (S)‐valinol with a much better conversion rate (95%) and a perfect stereoselectivity (>99% e.e.) [10].

Chemical reaction depicting synthesis of sitagliptin from prositagliptin ketone using immobilized transaminase in organic solvent.

      Source: Truppo et al. [12].

      The ubiquitous glycosyltransferases (GTs) are responsible for the synthesis of the diverse and complex array of oligosaccharides and glycoconjugates found in nature. The chemical diversity and complexity of glycoconjugates, reflecting the various chemical moieties, epimer at each chiral center, anomeric configuration, linkage position, and branching, require that the enzymes that catalyze their synthesis, degradation, and modification need to be highly specific [16]. The synthesis of most cell–surface glycoforms in mammalian systems is performed by Leloir‐type glycosyltransferases. They usually show environmental conditions sensitive and often demand special buffers or detergents for solubilization [15, 17, 18]. A large number of eukaryotic Leloir glycosyltransferases have been cloned to date [14, 19, 20] to give highly regio‐ and stereospecific with respect to glycosidic linkage formation and provide products in high yield. In addition, these enzymes exhibit substrate specificity that transfers a given carbohydrate from the sugar nucleotide donor substrate to a specific hydroxyl group of the acceptor sugar.

Chemical reaction depicting galactosyltransferase catalyzed glycosylation with UDP-2-d-Gal as donor.

      Source: Based on Wohlgemuth [14]; Křen and Thiem [15]; Koeller and Wong [18].

Chemical reaction depicting method for avoiding product inhibition in GalT-catalyzed glycosylation by in situ regenerating and recycling of sugar nucleotides.