Regioselective Biocatalytic Transformations Employing Transaminases and Tyrosine Phenol Lyases
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Regioselective reactions allow the differentiation between two or more chemically identical reactive centers within the same molecule. They are highly desirable transformations in organic synthesis, as they avoid additional chemical operations and sophisticated protection/deprotection strategies. In this context, enzymes, which present exquisite selectivity and reactivity, have been widely employed as catalysts in numerous regioselective transformations. This review focuses on two recently developed biocatalytic processes that present outstanding regioselectity: the transaminase-catalyzed asymmetric amination of di- and triketo compounds, and the stereoselective C–C coupling between phenol derivatives, ammonia and pyruvate for the synthesis of tyrosine analogues, catalyzed by tyrosine phenol lyases. Additionally, elegant and straightforward cascades that have combined the aforementioned biotransformations with other enzymatic and/or chemocatalytic processes are compiled in this contribution. Overall, this review aims to provide a general view of the synthetic possibilities that two relatively recently described regio- and stereoselective biotransformations can provide.
KeywordsBiocatalysis Regioselectivity Identical functional group differentiation Transaminase Tyrosine phenol lyase Protecting-group-free
Over the last 15 years, biocatalysis has emerged as a valuable tool in organic chemistry that provides straightforward and efficient alternatives to the traditional chemical and chemocatalytic approaches used in synthesis. Among the various advantages of the use of enzymes for synthetic purposes, the most important is probably their inherent selectivity . When enzymes catalyze the transformation of a substrate, they can distinguish between different stereoisomers or different orientations of prochiral/meso compounds (stereoselectivity), between different functional groups (chemoselectivity), or between functional groups that are chemically identical but situated in different positions within the same molecule (regioselectivity) .
Regioselective transformations are highly desirable in organic synthesis as they avoid additional reaction steps and sophisticated protection/deprotection strategies [3, 4], thus resulting in simpler, higher-yielding and more cost-effective synthesis routes. Consequently, protecting-group-free strategies are considered superior to traditional protection-based routes and have received well-deserved recognition [5, 6]. In the field of biocatalysis, regioselective reactions have been described for numerous enzyme classes, whereby hydrolytic enzymes have been studied in most detail [7, 8]. For instance, in carbohydrate chemistry, lipases can catalyze the selective acylation of a single primary  or secondary alcohol  in the presence of several other primary or secondary hydroxyl groups, respectively. Among other selective transformations, lipases also catalyze the monoamidation of glutamic acid diesters , the monodeacetylation of di- or triacetoxyacetophenones by transesterification , and the monoacetylation of dihydroxybenzene derivatives with vinyl acetate . Likewise, dinitriles have been hydrolyzed to the corresponding monocarboxylic acids by nitrilases  or to monoamides by nitrile hydratases  with moderate to excellent regioselectivity. Epoxide hydrolases showing opposite regioselectivity on the (S)- and (R)-enantiomer of the same substrate have been used for the enantioconvergent hydrolysis of racemic mixtures of oxiranes [16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28] into vicinal diols. Methyl transferases perform highly regioselective methylations in vivo and have also been successfully employed in biocatalysis for regioselective alkyl transfer, in some cases using non-natural derivatives of the S-adenosyl methionine (SAM) cofactor as alkyl donors [29, 30, 31, 32, 33]. Oxidoreductases are also capable of differentiating between identical functional groups: Alcohol dehydrogenases have been found to reduce one carbonyl group of diketo compounds with very high regio- and enantioselectivity [34, 35], and both native and evolved P450 monooxygenases have successfully been applied in the regio- and stereoselective hydroxylation of arenes, linear alkanes, terpenes, and steroids [36, 37, 38, 39, 40, 41, 42, 43, 44, 45]. Also worth mentioning is the oxidative monocleavage of dialkenes at the expense of molecular oxygen that has been achieved using an enzyme preparation from the fungus Trametes hirsuta .
Among the different regioselective enzymatic reactions existing in literature, in this contribution we will focus on two biotransformations that have gained particular relevance in the last few years. These are the monoamination of multiketo compounds catalyzed by transaminases, and the para-selective C–C bond formation reaction mediated by tyrosine phenol lyases on para-unsubstituted phenols. In addition, examples of cascades that have employed either of these biotransformations in combination with further biocatalytic processes for the regio- and stereoselective synthesis of nitrogen heterocycles and tyrosine derivatives will be discussed in this review.
2 Regioselective Transformations Catalyzed by Transaminases
Optically pure amines are valuable building blocks in the synthesis of pharmaceuticals and agrochemicals. In addition, versatile applications as resolving agents, chiral auxiliaries and organocatalytic reagents have been reported for this compound class . Therefore, synthetic organic chemists have historically devoted great effort to the development of efficient and versatile strategies for the stereoselective synthesis of chiral amines. These efforts have also led to the development of several biocatalytic methods for chiral amine synthesis, which rely on enzymes such as lipases, amine oxidases, imine reductases, and transaminases, among others [48, 49, 50, 51]. Transaminases (TAs, EC 2.6.1.X) are pyridoxal 5′-phosphate (PLP)-dependent enzymes that mediate the stereoselective transfer of an amino group from an amine donor to a carbonyl acceptor. Depending on the stereopreference of the selected enzyme, (S)- or (R)-amines can be accessed in high optical purity starting from the prochiral ketones [52, 53, 54, 55, 56]. Taking advantage of their potential, these biocatalysts have been implemented in pharmaceutical synthesis during the last decade. An outstanding example is the TA-catalyzed stereoselective amination that has replaced a rhodium(I)-mediated asymmetric enamine hydrogenation as the key step in the manufacture of the antidiabetic drug Sitagliptin .
Focusing on the scope of this contribution, TAs have been successfully applied to regioselective transformations. In particular, the asymmetric monoamination of di- and triketones has been achieved. Most wild-type TAs present a high selectivity for the sterically less demanding ketone moiety, in particular methyl ketones, while carbonyl groups with more bulky substituents remain untouched. This selectivity was exploited for the regio- and stereoselective monoamination of diketones without the use of protecting groups . 1,5-Diketo compounds were exclusively converted into one out of the two possible regioisomeric aminoketone intermediates. These species spontaneously cyclized, yielding the corresponding Δ1-piperideines in optically pure form (Scheme 1). By choosing TAs with suitable stereopreference, both enantiomers of the piperideines could be accessed in up to > 99% conversion and ee.
Diastereoselective reduction of the cyclic imines thus formed gave access to the corresponding 2,6-disubstituted piperidines. For instance, the two enantiomers of the alkaloids dihydropinidine  and isosolenopsin  were synthesized in three steps from the commercially available 6-methyl-3,4-dihydropyran-2-one with overall yields of 61–72% over three steps (Scheme 2a). Grignard reactions gave access to the corresponding 1,5-diketone compounds, which were regio- and stereoselectively transformed into the Δ1-piperideines through transaminase-catalyzed reactions. The cyclic imines were readily reduced by hydrogenation with palladium on charcoal (Pd/C) as catalyst, affording the cis-disubstituted piperidines with excellent diastereoselectivity (> 98% de). In a similar fashion, both enantiomers of the alkaloid epi-dihydropinidine (Scheme 2b) were accessed in high yield (up to 91% over two steps) and moderate diastereoselectivity when the enantiopure imine intermediate was treated with LiAlH4 in the presence of Et3Al . This reduction reaction, in contrast to the Pd/C-catalyzed hydrogenation, affords predominantly the anti-diastereoisomers.
An extension of this concept was recently used in the chemo-enzymatic asymmetric synthesis of both enantiomers of the ant venom alkaloid xenovenine . A key step in this process is the biocatalytic amination of a triketone intermediate, which was prepared in two steps starting from commercially available 2-(n-heptyl)furan (Scheme 3). Two enantiocomplementary TAs from Arthrobacter sp. mediated the regio- and stereoselective amination of the least sterically demanding carbonyl group, followed by the spontaneous cyclization of the resulting intermediate. The five-membered cyclic amine obtained was aromatized to the corresponding pyrrolizidine by subjecting the crude product of the biotransformation to a 0.1% v/v solution of acetic acid in methanol. Finally, the hydrogenation of this compound catalyzed by Pd/C in the presence of camphorsulphonic acid (CSA) led to the desired (5Z, 8E)-diastereoisomer, independently of the substrate enantiomer. Thus, the naturally occurring (+)-enantiomer was obtained in 30% isolated yield over the three steps by treating the triketone with the (R)-TA from Arthrobacter sp., whereas the (S)-TA from Arthrobacter sp. led to the formation of (–)-xenovenine in 48% yield. Both antipodes were isolated in enantio- and diastereomerically pure form.
Taking further advantage of this methodology, an elegant multienzymatic approach combining TAs and mononoamine oxidases (MAOs) has been described for the asymmetric synthesis of 2,5-disubstituted pyrrolidines [62, 63]. The authors employed two commercially available transaminases with opposite stereopreference, ATA-113 and ATA-117, for the regio- and stereoselective synthesis of (S)- and (R)-Δ1-pyrrolines, respectively. In this case, hydrogenation of the cyclic imines over Pd/C proceeded with poor diastereoselectivity and was hence not a suitable method for obtaining the corresponding disubstituted pyrrolidines as pure stereoisomers. Instead, the authors implemented a ‘cyclic deracemisation’ system using monoamine oxidase and ammonia–borane to obtain the desired chiral pyrrolidines in excellent optical purity (Scheme 4). The non-selective reducing agent NH3·BH3 reduces the cyclic imine to a mixture of diasteroisomers of the desired amine. Engineered variants of monoamine oxidase from Aspergillus niger (MAO-N) catalyze the selective oxidation of the (5S)-diastereomer back to the imine. Successive rounds of reduction and oxidation, which take place concurrently in the same reaction vessel, lead to accumulation of the (5R)-configured pyrrolidine in > 99% de. Due to the complementary regioselectivity displayed by the TAs and the MAO-N variants, the stereochemistry of C2 (established by the TA) was not affected by MAO-N. Consequently, the cascade proceeded with excellent enantio- and diasteroselectivity (up to > 99% ee and > 99% de) for almost all cases studied.
Due to the fact that this contribution focuses only on regioselective processes, TA-catalyzed conversion of ketones in the presence of ester groups within the same molecule [64, 65, 66], or the differentiation between aldehyde and ketone groups are out of the scope of this review [67, 68].
3 Regioselective Transformations Catalyzed by Tyrosine Phenol Lyases
The formation of carbon–carbon (C–C) bonds is the key reaction in organic synthesis that builds the carbon framework of every organic molecule by connecting smaller and simpler substructures. The development and identification of new biocatalysts able to mediate C–C couplings with high control of chemo-, regio- and stereoselectivity has undoubtedly expanded the chemist’s toolbox for the synthesis of multifunctional products . For instance, the chemical synthesis of tyrosine derivatives, which are valuable building blocks in the synthesis of several anti-cancer therapeutics [70, 71], comprises several laborious and time-consuming steps. In contrast, PLP-dependent tyrosine phenol lyases (TPLs, EC 184.108.40.206) can catalyze the regio- and stereoselective reversible formation of tyrosine from pyruvate, phenols and ammonia in a single and “green” reaction [72, 73, 74]. TPLs are not limited to phenol as substrate, however: For instance, the TPL from Erwinia herbicola has been used to convert catechol into l-dihydroxyphenylalanine (l-DOPA) [75, 76], and this reaction has very recently been applied to a bacterial system with an expanded genetic code that can biosynthesize DOPA and employ it for protein synthesis . An engineered variant of TPL from Citrobacter freundii (M379V) has been shown to accept a range of 2-substituted phenols as substrates, hence giving access to non-natural, monosubstituted l-tyrosine derivatives in moderate to excellent conversions (52–99%) and excellent optical purity (ee > 99%; Scheme 5). In all cases the C–C coupling occurred with excellent regioselectivity; therefore, only the product bearing the substituent in position 3′ of tyrosine was detected .
Moreover, different enzyme engineering approaches have taken advantage of the activity shown by TPLs to successfully incorporate unnatural amino acids (UAAs) into recombinant proteins. While traditional mutagenesis is limited to the ‘chemical space’ of the 20 proteinogenic amino acids, the introduction of non-natural residues gives access to novel side-chain functionalities that can lead to more robust enzymes with enhanced catalytic properties . For instance, a double variant of the TPL from Citrobacter freundii (M288S/F448C) has been used to catalyze the formation of the metal-chelating UAA 2-amino-3-(8-hydroxyquinolin-5-yl)propanoic acid (HqAla, Scheme 6) from 8-hydroxyquinoline, ammonium chloride and pyruvate in high yield. After purification, HqAla was site-specifically incorporated into green fluorescent proteins, enabling them to sense Cu2+ ions, which opens the door for biosensing applications . In addition, examples of improved enzymatic activity and modified selectivity resulting from the incorporation of UAAs were also reported by the same authors. In one study, a single variant of the Symbiobacterium sp. TPL (M379V) was used to access 3-methoxytyrosine (OMeY, Scheme 6) from 2-methoxyphenol. The tyrosine analog was selectively incorporated at a defined site in myoglobin, increasing the oxygen reduction activity of the protein and changing the predominant reaction product from H2O2 to water . Likewise, the genetic incorporation of 3-methylthiotyrosine (SMeY, Scheme 6), also synthesized by a TPL-catalyzed coupling, into myoglobin provided a protein fourfold more active than the original enzyme towards the reduction of hydroxylamine to ammonia . Both modifications mimic the active-site environment of other heme enzymes, namely cytochrome c oxidase (OMeY) and cyctochrome c nitrite reductase (SMeY). The preparation of various fluorotyrosines by TPL-catalysed C–C coupling as well as the incorporation of these UAAs into peptides and proteins has also been reported [83, 84].
The excellent performance shown by TPLs for the regio- and stereoselective preparation of l-tyrosine derivatives has enabled the coupling of this reaction to other biocatalytic processes, resulting in several elegant multi-enzymatic cascades. For instance, the combined use of a P450 monoxygenase with the TPL variant M379V from Citrobacter freundii gave access to tyrosine analogs from substituted benzenes, pyruvate and ammonia in a one-pot two-step cascade (Scheme 7a) . In the first step, monosubstituted arenes were regioselectively hydroxylated in the ortho-position by the monooxygenase P450 BM3 at the expense of oxygen and NADPH, yielding the corresponding phenols. These compounds were excellent substrates for the subsequent TPL-catalyzed process, and the desired amino acids were obtained in moderate to good conversion (up to 72%) and chemoselectivity (up to 80%). In some cases, a lower selectivity was observed as a result of an undesired P450-mediated overoxidation of the monosubstituted phenol intermediates.
More recently, the regioselective transformation catalyzed by TPL was successfully combined with a tyrosine ammonia lyase (TAL) from Rhodobacter sphaeroides, which mediated the ammonia elimination that gave access to p-coumaric acid derivatives from phenols. This biocatalytic process constituted the first direct para-selective alkenylation of these derivatives without the presence of an auxiliary group in para-position. Only pyruvate was used as stoichiometric reagent, as the ammonia that is consumed in the TPL-catalyzed coupling was internally regenerated in the elimination step mediated by the TAL, thus making water the sole coproduct . Seven phenols (including halogenated derivatives) were thus transformed into the α,β-unsaturated carboxylic acids with high to excellent conversions and perfect selectivity towards the E-isomer (Scheme 7b). The addition of a ferulic acid decarboxylase (FAD) to the bienzymatic process just described resulted in the formation of para-vinylphenols via decarboxylation of the corresponding p-coumaric acid derivatives (Scheme 7c). The FAD-catalyzed decarboxylation is an irreversible transformation that drives the equilibrium towards product formation, and consequently 2-, 3-, and 2,3-substituted phenols were transformed into the para-vinylated products in excellent conversion (> 99%) for all the cases studied . To highlight the importance of this contribution, it must be mentioned that, while vinyl arenes are important building blocks in organic chemistry, their synthesis from unprotected phenols is not straightforward. The chemical reaction with SnCl4·Bu3N leads to ortho functionalization , whereas the synthesis of para-vinylphenols involves transition-metal-catalyzed couplings in which the presence of auxiliary groups at the para-position is strictly necessary [89, 90].
In another bienzymatic approach, l-tyrosine formed by a TPL reaction was used as substrate for immobilized cells containing a heterologously expressed tyrosine decarboxylase (TDC). The latter mediated the decarboxylation of l-tyrosine, yielding tyramine [2-(p-hydroxyphenyl)ethylamine], a bioactive metabolite and valuable intermediate in the synthesis of pharmaceutical drugs . The authors were able to scale up the two-step enzymatic process converting 15 L of pyruvate fermentation broth into the l-tyrosine intermediate in 94% isolated yield. The decarboxylation reaction provided the desired tyramine in 91% yield, thus reaching 86% overall yield after the two biocatalytic reactions (Scheme 7d).
Likewise, the TPL-catalyzed regio- and enantioselective tyrosine formation allowed the preparation of enantiopure (R)- and (S)-p-hydroxyphenyl lactic acids when it was combined with two additional biocatalytic reactions that employed an l-amino acid deaminase (l-ADD) and an enantioselective hydroxyacid dehydrogenase, respectively . This elegant three-step cascade was performed in one pot and subdivided into two different modules that were run sequentially. The first module comprised the l-tyrosine formation catalyzed by the TPL from Citrobacter freundii M379V, whereas the second module consisted of two biocatalytic transformations: the oxidative deamination mediated by the l-ADD from Proteus myxofaciens and the reduction of the resulting 2-keto acid derivatives using as catalysts the two stereocomplementary 2-hydroxyisocaproate dehydrogenases from Lactobacillus paracasei (L-HicDH) and Lactobacillus confusus (d-HicDH) (Scheme 7e). The TPL–L-ADD–HicDH cascade led to the transformation of p-unsubstituted phenols to both enantiomers of the corresponding p-hydroxyphenyl lactic acids in excellent conversion (92% to > 99%), high isolated yield (58–85%) and excellent optical purity (96% to > 97%) for all the cases studied.
4 Conclusion and Outlook
Enzyme catalysis has become a well-established discipline that provides valuable and efficient tools for the synthesis of pharmaceuticals and other bioactive compounds with excellent chemo-, regio- and stereoselectivity. This contribution focuses on two regioselective processes that, by definition, allow the differentiation between two or more chemically identical functional groups at different positions of a substrate molecule. Thus, several examples of asymmetric monoamination of di- and triketones catalyzed by transaminases have been discussed in detail. Likewise, a compilation of strategies that have taken advantage of the ability presented by tyrosine phenol lyases to distinguish between different sites of phenols, leading to the synthesis of l-tyrosine analogues, have also been described in this review. Both these regioselective processes have attained well-deserved recognition in recent years as a consequence of having shortened sophisticated and time-consuming synthesis routes for the preparation of drugs and important building blocks, thus resulting in protecting-group-free strategies with considerably higher yield and overall efficiency than traditional approaches.
Overall, transaminases and tyrosine phenol lyases catalyze highly selective and versatile transformations with a large potential for synthetic application, especially when combined with other enzymatic or chemocatalytic reactions. They thus represent a valuable extension of the organic chemist’s toolbox for the preparation of chiral target molecules.
Open access funding provided by University of Graz. The authors gratefully acknowledge BIOMIN Holding GmbH (Tulln, Austria) for financial support to Dr. Lía Martínez-Montero.
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