Patent US4659671A successfully refreshed from Google Patents.
← Back to Patent Explorer
US4659671A Expired / Lapsed US ⏱️ 0.0 years remaining

Enzymatic separation of racemic mixtures of hydroxy compounds

Assignee: Massachusetts Institute of Technology
•
Filing: 1983-07-01
•
Granted: 1987-04-21
•
Expires: 2003-07-01
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract The invention constitutes an enzymatic method for resolution of a racemic mixture of hydroxy compounds. A D,L mixture of the hydroxy compound is phosphorylated to form the D,L monoorthophosphate esters of the hydroxy compound. Thereafter, the D,L mixture of phosphorylated compounds is treated with a stereospecific phosphatase, such as wheat germ acid phosphatase, which causes the hydrolysis of substantially only one optical isomer of the monoorthophosphate ester. The resulting hydrolyzed isomer of the hydroxy compound is then separated from the remaining monoorthophosphate ester.

Inventors

  • 👤 Alexander M. Klibanov

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 18:25
CPC Classifications
C; C12; C12P; C12P7/00; C12P7/02; C12P7/04; C12P13/00; C12P13/04; C12P13/08; C12P41/00; C12P41/003; C12P41/004

Claims Analysis

Total Claims: 12
Claim 1
Independent Claim 62 words
A method for resolution of a racemic threonine, comprising the following steps: a. reacting the racemic threonine and phosphorus oxychloride to form a monoorthophosphate ester of threonine; b. contacting the monoorthophosphate ester with wheat germ acid phosphatase under conditions whereby said phosphatase preferentially hydrolyzes the L-monoorthophosphate ester of threonine to yield L-threonine; and c. separating L-threonine; and the monoorthophosphate ester of D-threonine.
Claim 2
Independent Claim 62 words
A method for resolution of a racemic threonine, comprising the following steps: a. reacting the racemic threonine and phosphorus oxychloride to form a monoorthophosphate ester of threonine; b. contacting the monoorthophosphate ester with wheat germ acid phosphatase under conditions whereby said phosphatase preferentially hydrolyzes the L-monoorthophosphate ester of threonine to yield L-threonine; and c. separating L-threonine; and the monoorthophosphate ester of D-threonine.
Claim 3
Independent Claim 64 words
A method of resolution of a racemic threonine, comprising the steps of: a. phosphorylating the racemic threonine to form a monoorthophosphate ester of threonine; b. contacting the monoorthophosphate ester with wheat germ acid phosphatase or potato acid phosphatase under conditions such that the phosphatase preferentially hydrolyzes the L-monoorthophosphate ester of threonine to yield L-threonine; and c. separating L-threonine and the monoorthophosphate ester of D-threonine.
Claim 4
Independent Claim 64 words
A method of resolution of a racemic threonine, comprising the steps of: a. phosphorylating the racemic threonine to form a monoorthophosphate ester of threonine; b. contacting the monoorthophosphate ester with wheat germ acid phosphatase or potato acid phosphatase under conditions such that the phosphatase preferentially hydrolyzes the L-monoorthophosphate ester of threonine to yield L-threonine; and c. separating L-threonine and the monoorthophosphate ester of D-threonine.
Claim 5
Dependent Claim 18 words
A method of claim 2, wherein the racemic threonine is phorphorylated by reacting the threonine with phosphorus oxychloride.
Claim 6
Dependent Claim 14 words
A method of claim 2, wherein the phosphatase is immobilized in a solid phase.
Claim 7
Dependent Claim 42 words
A method of claim 2, further comprising the steps of: d. inducing racemization of the monoorthophosphate ester of D-threonine; and e. subjecting the resulting mixture to steps b and e until a desired amount of the racemic threonine is converted to L-threonine.
Claim 8
Independent Claim 77 words
A method for resolving a racemic mixture of 1,2-dichloro-3-hydroxy propane, comprising the steps of: a. phosphorylating the racemic 1-chloro-2-hydroxypropane to form a phosphate ester of 1-chloro-2-hydroxypropane; b. contacting the phosphate ester of 1-chlorohydroxypropane with wheat germ acid phosphatase or potato acid phosphatase under conditions such that the phosphatase preferentially catalyzes the hydrolysis of one optical isomer the phosphate ester; and c. separating the hydrolyzed optical isomer of 1-chloro-2-hydroxypropane and the phosphate ester of the other optical isomer.
Claim 9
Independent Claim 77 words
A method for resolving a racemic mixture of 1,2-dichloro-3-hydroxy propane, comprising the steps of: a. phosphorylating the racemic 1-chloro-2-hydroxypropane to form a phosphate ester of 1-chloro-2-hydroxypropane; b. contacting the phosphate ester of 1-chlorohydroxypropane with wheat germ acid phosphatase or potato acid phosphatase under conditions such that the phosphatase preferentially catalyzes the hydrolysis of one optical isomer the phosphate ester; and c. separating the hydrolyzed optical isomer of 1-chloro-2-hydroxypropane and the phosphate ester of the other optical isomer.
Claim 10
Dependent Claim 18 words
A method of claim 6, wherein the racemic threonine is phorphorylated by reacting the threonine with phosphorus oxychloride.
Claim 11
Dependent Claim 14 words
A method of claim 2, wherein the phosphatase is immobilized in a solid phase.
Claim 12
Dependent Claim 44 words
A method of claim 2, further comprising the steps of: d. inducing racemization of the monoorthophosphate ester of 1-chloro-2-hydroxypropane; and e. subjecting the resulting mixture to steps b and e until a desired amount of the racemic 1-chloro-2-hydroxypropane is converted to the optical isomer.

References Cited (Backward Citations)

US3347752A Cited
US3386888A Cited
US3607651A Cited
US3635795A Cited
US3666399A Cited
US3813317A Cited
US3878043A Cited
US3997543A Cited
US4022664A Cited
US4202943A Cited
US4226941A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1990-04-20 1990-10-20 1991-04-21 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1994-04-20 1994-10-20 1995-04-21 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1998-04-20 1998-10-20 1999-04-21 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag