Reductive reactions carbonyl reductases

Studies on metabolic stability using hepatocyte suspensions are not feasible for automation/HTS, but these studies do provide rather complete profiles of hepatic biotransformation without the supplements of cofactors and cosubstrates. The use of S9 in metabolic stability studies can be evaluated in a manner similar to that used for the microsomal assays, but with the possible addition of a broader panel of cofactors or cosubstrates. These include NADPH for CYP/FMO-mediated reactions, NADH for xanthine oxidoreductase and quinone oxidoreductase 2, NADPH-dependent reductions by carbonyl reductases, and NADPH/NADH-dependent reductions catalyzed by aldo-keto reductases, uridine 5 -diphosphate... 

The enantioselective reduction of alkyl 3-oxobutanoates by carbonyl reductase (SI) from C. magnoliae was also performed in organic-aqueous two-phase reaction system (Figure 8.15) [llc,d]. 

The Reduction Reactions. The object of the next three reactions (steps 4 to 6 in fig. 18.12a) is to reduce the 3-carbonyl group to a methylene group. The carbonyl is first reduced to a hydroxyl by 3-ketoacyl-ACP reductase. Next, the hydroxyl is removed by a dehydration reaction catalyzed by 3-hydroxyacyl-ACP dehydrase with the formation of a trans double bond. This double bond is reduced by NADPH catalyzed by 2,3-trans-enoyl-ACP reductase. Chemically, these reactions are nearly the same as the reverse of three steps in the j6-oxidation pathway except that the hydroxyl group is in the D-configuration for fatty acid synthesis and in the L-configuration for /3 oxidation (compare figs. 18.4a and 18.12a). Also remember that different cofactors, enzymes and cellular compartments are used in the reactions of fatty acid biosynthesis and degradation. 

Reduction of ethyl 2 -ketopantothenate to ethyl 2 -d-pantothenate ((g) in Fig. 8). The rate of condensation of ketopantolactone or D-pantolactone with ethyl (3-alanine, yielding ethyl 2 -ketopantothenate (0 in Fig. 8) or ethyl D-panto-thenate, respectively, is quite fast compared to the condensation of ketopantolactone or D-pantolactone with (3-alanine, and the reaction with ethyl (3-alanine proceeds more stoichiometrically [117]. Since the enzymatic hydrolysis of ethyl D-pantothenate has been established [118], if the stereoselective reduction of ethyl 2 -ketopantothenate to ethyl D-pantothenate is possible, both the troublesome resolution and the incomplete condensation might be avoided at the same time. Carbonyl reductase of C. macedoniensis is used for this purpose. Washed cells of the yeast converted ethyl 2 -ketopantothenate (80 g/1) almost specifically to ethyl D-pantothenate (> 98% e.e.), with a molar yield of 97.2% [103]. In a similar manner, 2 -ketopantothenonitrile (50 g/1) was converted to D-pan-tothenonitrile (93.6% e.e.), with a molar yield of 95.6%, on incubation with Sporidiobolus salmonicolor cells as a catalyst [104],... 

A number of functional groups, such as nitro, diazo, carbonyls, disulfides, sulfoxides, and alkenes, are susceptible to reduction. In many cases it is difficult to determine whether these reactions proceed nonenzymatically by the action of biological reducing agents such as NADPFI, NADH, and FAD or through the mediation of functional enzyme systems. As noted above, the molybdenum hydroxylases can carry out, in vitro, a number of reduction reactions, including nitro, azo, A-oxidc, and sulfoxide reduction. Although the in vivo consequences of this are not yet clear, much of the distribution of reductases described below may be, in whole or in part, the distribution of molybdenum hydroxylases. 

Oxidoreductases these enzymes catalyze redox reactions. Examples are oxidases that catalyze oxidation of a substrate by reducing molecular oxygen (02), and peroxidases that reduce H202. Laccases (EC 1.10.3.2) are oxidases that catalyze the oxidation of (poly)phenolic substrates. Reductases and dehydrogenases (EC 1.1.1) catalyze the reduction of carbonyls, using NADH/NADPH cofactors. Catalases (EC 1.11.1.6) catalyze the decomposition of H202 to 02 and H20. 

Besides the involvement in the de novo biosynthesis of BH4, SR may also participate in the pterin salvage pathway by catalyzing the conversion of sepiapterin (Figure 14, 47) into 7,8-dihydrobiopterin (46) that is then transformed to BH4 by dihydrofolate reductase (DHFR EC 1.5.1.3). Both reactions consume NADPH. Although SR is sufficient to complete the BH4 biosynthesis, a family of alternative NADPH-dependent aldo—keto reductases, including carbonyl reductases (CR), aldose reductases (AR), and the 3a-hydroxysteroid dehydrogenase type 2 (AKR1C3) may participate in the diketo reduction of the carbonyl side chain in Moreover, based on the discover) of the autosomal recessive deficiency for SR, which presents... 

The reductive biotransformation of drugs has been one of the least studied reactions, and many of the enzymes that are involved have not been well characterized. Some of the enzymes that catalyze reductive reactions of drugs are the cytochrome P450s, molybdenum reductases, alcohol dehydrogenases, carbonyl reductases, NADPH cytochrome P450 reductase, NAD(P)H— quinone oxidoreductases, and enzymes of the intestinal microflora (Matsunaga et al., 2006 Rosemond and Walsh, 2004). 

The most sustainable strategy is to avoid the use of solvents completely. Only one reported example for discussing bioreduction in neat substrates is the asymmetric reduction of ketone with lyophilized E. coli cells overexpressing carbonyl reductase from Candida parapsUosis, which produced enantiomerically pure alcohols in large amounts (Figure 9.4). The reaction setup only requires a substrate, a cosubstrate... 

NAD(P)H-dependent catalytic reduction reactions such as carbonyl or enoate reductases and hydroxy acid or amino acid dehydrogenases [14],... 

Reduction Carbonyl groups. The carbonyl group (-(C=0)-) is reduced through a reaction that is catalyzed by an aldo-keto reductase requiring NADH as a cofactor. A large number of aromatic and aliphatic ketones are reduced to the corresponding alcohols these reductions are frequently stereospecific. a,P-Unsaturated ketones are typically metabolized to saturated alcohols. 

Step (2) Reduction of the Carbonyl Group The acetoacetyl-ACP formed in the condensation step now undergoes reduction of the carbonyl group at C-3 to form d-j8-hydroxybutyryl-ACP. This reaction is catalyzed by /3-ketoacyl-ACP reductase (KR) and the electron donor is NADPH. Notice that the D-j3-hydroxybutyryl group does not have the same stereoisomeric form as the l-j8-hydroxyacyl intermediate in fatty acid oxidation (see Fig. 17-8). 

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