Enzymatic synthesis of chiral organophosphothioates from prochiral precursors

Article abstract of DOI:10.1021/ja017840d

The phosphotriesterase from Pseudomonas diminuta has been shown to selectively cleave the pro-R p-nitrophenolate substituent from bis-p-nitrophenyl alkyl phosphothioate esters. When the alkyl substituent is methyl, ethyl, or isopropyl the enantiomeric exc

Full text of DOI:10.1021/ja017840d

Published on Web 03/14/2002
Enzymatic Synthesis of Chiral Organophosphothioates from Prochiral
Precursors
Wen-Shan Li, Yingchun Li, Craig M. Hill, Karin T. Lum, and Frank M. Raushel*
Department of Chemistry, Texas A&M UniVersity, P.O. Box 30012, College Station, Texas 77842-3012
Received December 20, 2001
Significant progress has been made in the development of
enzyme-based methods for the preparative syntheses of chiral
building blocks.1 As an example, the native bacterial phosphotri-
esterase (PTE) from Pseudomonas diminuta has been shown to be
a highly effective catalyst for the kinetic resolution of racemic
mixtures of organophosphate triesters.2 Differential rates of hy-
drolysis for pairs of chiral enantiomers with the wild-type enzyme
have enabled the isolation of pure stereoisomers in very high yield.1
Moreover, rational reconstruction of the substrate binding site cavity
within PTE through site-directed mutagenesis has altered the
catalytic properties where the inherent stereoselectivity of the native
PTE has been enhanced, relaxed, or reVersed.3 Tsai and co-workers
have also shown that the stereoselective properties of adenylate
kinase can be manipulated through mutagenesis.4 The reversal of
Figure 1. Time course for the hydrolysis of 1 (0.022 mM) by KOH and
stereoselectivity for PTE has allowed the isolation of either
stereoisomer in a racemic mixture through the judicious choice of
a specific mutant from an enzyme library constructed with modified
catalytic properties.2,3
the mutant G60A at pH 9.0 and 25 °C. The reaction was monitored at 400
nm.
and chemical nerve agents that are known to inactivate acetyl
cholinesterase.5 The enzymatic reaction is initiated by the direct
nucleophilic attack of the hydrolytic water molecule on the
phosphorus center.6 The three-dimensional structure of Zn/Zn-
PTE with a bound substrate analogue, diethyl 4-methylbenzylphos-
phonate, has led to the identification of three distinct binding pockets
that are responsible for the orientation and selectivity of substrates
within the active site of the enzyme.7 These binding sub-sites have
been designated as the small, large, and leaVing group pockets.
Prior stereochemical investigations with the native enzyme predict
that the wild-type PTE will selectively cleave the pro-R substituent
from compounds 1-4.3
Scheme 1
The prochiral substrates 1-4 were synthesized by standard
methods.8 A graphical illustration of the reaction time course,
monitored at 400 nm, catalyzed by the mutant G60A and KOH for
the hydrolysis of substrate 1 is presented in Figure 1. These data
demonstrate that a single p-nitrophenolate group is cleaved from
the prochiral starting material and that the reaction proceeds to the
same extent enzymatically or with the addition of KOH.
The relative stereoselectivity for the enzymatic hydrolysis of
compounds 1-4 was established by 31P NMR spectroscopy, using
strychnine as a chiral shift reagent. Illustrated in Figure 2a is the
31P NMR spectrum of the KOH-derived hydrolysis products from
1 in the presence of (-)-strychnine. Resonances for each of the
two chiral acids (5a and 5b) are observed at ∼80.3 ppm with a
chemical shift difference of 0.05 ppm. Shown in Figure 2b,c are
NMR spectra of authentic (SP)- and (RP)-stereoisomers of 5,
respectively. The relative downfield resonance for the (SP)-isomer
was confirmed by the addition of a small amount of racemic 5
(Figure 2d). When 1 was hydrolyzed by wild-type PTE there was
a preponderance of a single stereoisomeric product (Figure 2e) that
was confirmed to be the (RP)-isomer of 5 after the addition of a
small amount of racemic material (Figure 2f). The measured
In this communication, we describe a novel enzymatic approach
toward the efficient generation of chiral enantiomers of alkyl
phosphothioates and related alkyl phosphonothioates through the
stereoselective hydrolysis of prochiral starting materials. The
preferential hydrolysis of a single prochiral p-nitrophenolate from
bis-p-nitrophenyl methyl phosphonothioate (1) and bis-p-nitrophenyl
alkyl phosphothioates (2-4) will generate the chiral products 5-8.
The wild-type PTE is known to catalyze the hydrolysis of
phosphorus centers with complete inVersion of configuration.5,6
Therefore, cleavage of the pro-R substituent from substrates 1-4
will generate products 5a-8a, whereas hydrolysis of the pro-S
substituent will form products 5b-8b. The expected reaction
products and stereochemical configurations are summarized in
Scheme 1.
The phosphotriesterase from Pseudomonas diminuta is a zinc-
containing enzyme that catalyzes the hydrolysis of a variety of
organophosphorus compounds, including an array of insecticides
* Address correspondence to this author. E-mail: raushel@tamu.edu.
9
3498
J. AM. CHEM. SOC. 2002, 124, 3498-3499
10.1021/ja017840d CCC: $22.00 © 2002 American Chemical Society

C O M M U N I C A T I O N S
Table 1. Kinetic Constants and Enantiomeric Excess (ee) for the Enzymatic Hydrolysis of Prochiral Substrates 1-4a,b
enantiomeric excess (%)
enzyme
5
6
7
8
1kcat (min-1
)
2kcat (min-1
)
3kcat (min-1
)
4kcat (min-1
24
0.1
)
wild-type
G60A
86 (RP)
96 (RP)
32 (RP)
14 (SP)
9 (RP)
49 (SP)
85 (SP)
23 (SP)
58 (SP)
99 (SP)
99 (SP)
99 (SP)
63 (SP)
46 (SP)
36 (SP)
35 (SP)
10 (SP)
24 (RP)
99 (SP)
99 (SP)
99 (SP)
87 (SP)
75 (SP)
99 (SP)
99 (SP)
9 (RP)
99 (SP)
87 (SP)
99 (SP)
96 (SP)
47 (SP)
86 (SP)
81 (SP)
88 (RP)
42 (SP)
96
110
3
310
290
5
4
6
9
0.4
5
2
420
190
5
1
6
3
2
2
2
H254G/H257W/L303T
I106A/H257Y/S308A
I106G/F132G/H257Y
1.0
0.4
0.4
0.2
0.4
0.4
0.4
3
55
26
4
69
96
I106A/F132A/H257Y
I106A/F132A/H257W
I106G/F132G/H257Y/S308G
I106A/F132A/H254G/H257W
87 (SP)
a Products 5a/5b, 6a/6b, 7a/7b, and 8a/8a/8b were solved by addition of (-)-strychnine in CDCl3. They displayed two distinguishable 31P NMR resonances
at 80.34/80.29, 56.05/56.07, 55.07/55.11, and 53.39/53.43 ppm, respectively. The enantiomeric excess was determined from the integral ratios. b Reaction
conditions: 10% dioxane/CHES (0.5 M, pH ) 9.0) with 0.113 mM 1-4.
Figure 3. X-ray structures for the strychnine salts of (RP)-5 (left) and (SP)-5
(right) (-)-strychnine salts.
The chiral thiophosphates generated by these enzymatic methods
can be further utilized as chiral synthons for more complex synthetic
elaborations. The chiral p-nitrophenyl methylphosphonothionic acid
(RP)-5a, generated by G60A, was successfully converted into (RP)-
S-methyl-p-nitrophenyl methylphosphonothiolate by reacting 5a
with excess CH3I in anhydrous benzene.9 Products of this type can
be utilized as precursors for synthesizing diverse examples of chiral
Figure 2. 31P NMR spectra of (-)-strychnine salts of 5a/5b: (a) hydrolysis
of 1 by KOH; (b) authentic (SP)-5; (c) authentic (RP)-5; (d) authentic (SP)-5
plus racemic 5; (e) product from hydrolysis of 5 by wild-type PTE; (f)
addition of racemic 5 to spectrum 2e.
organophosphorus compounds.
In summary, we have demonstrated that formation of chiral
organophosphothioic acids can be prepared through the stereose-
lective hydrolysis of prochiral substrates using engineered mutants
of phosphotriesterase. Moreover, the prochiral stereoselectivity
inherent to the wild-type PTE can be manipulated by specific
modifications to the substrate binding domain within the active site
of this protein.
enantiomeric excess (ee) was 86%. The product ratios for com-
pounds 2-4 were determined in an identical manner and the
corresponding ee values are presented in Table 1 along with the
kinetic constants for the wild-type PTE and selected mutants.
The absolute stereochemistry of the phosphorus centers for the
(RP)- and (SP)-enantiomers of 5 was confirmed by X-ray diffraction
analysis of the isolated (-)-strychnine salts (Figure 3). The racemic
methylphosphonothionic acid (5) was prepared by hydrolysis of 1
with KOH and converted into the corresponding (-)-strychnine
salt. The individual isomers were isolated by successive recrystal-
lizations from MeOH/H2O (10:1) followed by isopropyl alcohol/
H2O (10:1).
Acknowledgment. We thank Dr. Joseph Ribenspies for the
X-ray structural analysis. This work was supported in part by the
NIH (GM 33894), ONR (N00014-99-0235), and Texas Advanced
Technology Program (366-0076-2001).
References
(1) Koeller, K. M; Wong, C. H. Nature. 2001, 409, 232.
(2) Wu, F.; Li, W.-S.; Chen-Goodspeed, M.; Sogorb, M. A.; Raushel, F. M.
J. Am. Chem. Soc. 2000, 122, 10206.
The wild-type PTE cleaves the pro-R substituent from com-
pounds 1-4 with a stereoselectivity that is greater than previously
observed for a related series of racemic organophosphate triesters.3
The enhancement in the observed stereoselectivity for the wild-
type PTE with this series of thiophosphate esters is likely due to a
more rate limiting dependence on the specific step for P-O bond
cleavage during overall substrate turnover. The utilization of certain
variants of the wild-type PTE, where the size and shape of the
substrate binding cavity has been specifically modified through site-
directed mutagenesis, has altered the stereoselectivity to the point
where the pro-S substituent is preferentially cleaved from some of
the prochiral substrates. A nearly complete reversal in stereoselec-
tivity was observed for substrate 5 with the mutant I106A/F132A/
H257W whereas a relaxation in the stereoselectivity was obtained
for compounds 6, 7, and 8.
(3) (a) Chen-Goodspeed, M.; Sogorb, M. A.; Wu, F.; Hong, S. B.; Raushel,
F. M. Biochemistry 2001, 122, 10206. (b) Chen-Goodspeed, M.; Sogorb,
M. A.; Wu, F.; Hong, S.-B.; Raushel, F. M. Biochemistry 2001, 122,
10206.
(4) (a) Jiang, R. T.; Dahnke, T.; Tsai, M. D. J. Am. Chem. Soc. 1991, 113,
5485. (b) Dahnke, T.; Jiang, R. T.; Tsai, M. D. J. Am. Chem. Soc. 1991.
113. 9388.
(5) Raushel, F. M.; Holden, H. M. AdV. Enzymol. Relat. Areas Mol. Biol.
2000, 74, 51.
(6) Lewis, V. E.; Donarski, W. J.; Wild, J. R.; Raushel, F. M. Biochemistry
1988, 27, 1591.
(7) Vanhooke, J. L.; Benning, M. M.; Raushel, F. M.; Holden, H. M.
Biochemistry 1996, 35, 6020.
(8) A new approach was developed to synthesize 2-4 through the intermedi-
ate, tris(4-nitrophenyl)thiophosphate, which was reacted with the corre-
sponding alcohol in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene
at 0-25 °C. The prochiral substrates 2-4 were isolated by chromatography
or recrystallization (MeOH) in high overall yield (84-96%).
(9) 1H NMR (300 MHz, CDCl3) δ 2.04 (d, J ) 15.6 Hz, 3H), 2.32 (d, J )
13.6 Hz, 3H), 7.44 (dd, J ) 8.8, 1.4 Hz, 2H), 8.25 (d, J ) 8.8 Hz, 2H).
JA017840D
9
J. AM. CHEM. SOC. VOL. 124, NO. 14, 2002 3499