Chemistry: molecular biology and microbiology – Micro-organism – tissue cell culture or enzyme using process... – Preparing oxygen-containing organic compound
Reexamination Certificate
2001-08-02
2003-05-13
Lilling, Herbert J. (Department: 1651)
Chemistry: molecular biology and microbiology
Micro-organism, tissue cell culture or enzyme using process...
Preparing oxygen-containing organic compound
C435S170000, C435S227000, C435S232000
Reexamination Certificate
active
06562603
ABSTRACT:
This application claims benefit to Provisional Ser. No. 60/223,044 filed Aug. 4, 2000.
FIELD OF THE INVENTION
This invention relates to a process for the preparation of a 3-hydroxycarboxylic acid from a 3-hydroxynitrile. More particularly, 3-hydroxyvaleronitrile is converted to 3-hydroxyvaleric acid in high yield at 100% conversion, using as catalyst the nitrile hydratase and amidase activities, or the nitrilase activity, of a microbial cell. 3-Hydroxyvaleric acid is used as a substitute for &egr;-caprolactone in the preparation of highly branched polyesters.
BACKGROUND OF THE INVENTION
Precise macromolecular engineering is becoming a major trend in polymer technology to satisfy the demand for new properties, improved cost effectiveness, ecology, and quality. Functional polymers with branched, compact structures and terminally located reactive groups are expected to exhibit superior performance/cost characteristics, by virtue of their lower inherent viscosity and higher reactivity versus conventional linear statistical copolymers. Preparation of these polymers can be accomplished by copolymerizing hyperbranching hydroxycarboxylic acid comonomers (hyperbranching AB
n
type, where A and B are moieties with hydroxyl- or carboxyl-derived reactive groups, n is 2 or more) (Hult et al., pp. 656-658 and Voit et al., pp. 658-659 in Concise Polymeric Materials Encyclopedia, ed. J. C. Salomone, CRC Press, New York, 1999) and a variety of linear hydroxycarboxylic acid comonomers (linear AB type), including 3-hydroxyvaleric acid.
3-Hydroxyvaleric acid is also useful as a (co)monomer for making linear polyesters. Polyesters are useful as thermoplastic, thermoset, semicrystalline, amphorous, rigid, and elastomeric materials. They are the basis of fibers, films, moldings, and coatings (Goodman, pp. 793-799 in Concise Encyclopedia of Polymer Science and Engineering, ed. J. I. Kroschwitz, John Wiley & Sons, New York, 1990).
3-Hydroxyvaleric acid has been prepared by the &bgr;-hydroxylation of valeric acid in fermentation using
Candida rugosa
(Hasegawa et al.,
J. Ferment. Technol.
59:257 -262 (1981); JP 59053838 B4), and a single enantiomer of 3-hydroxyvaleric acid was similarly prepared by fermentative &bgr;-hydroxylation of valeric acid with
Pseudomonas putida, Pseudomonas fluorescens, Arthrobacter oxydans
and
Arthrobacter crystallopietes
(U.S. Pat. No. 3,553,081). These methods for fermentative oxidation of valeric acid typically produce 3-hydroxyvaleric acid at low product concentrations, and require an elaborate and expensive separation of 3-hydroxyvaleric acid from the fermentation broth. (R)-(−)-3-Hydroxyvaleric acid has been prepared by the chemical degradation (Seebach et al.,
Helv. Chim. Acta
77:2007-2034 (1994)) or by fermentative autodegradation (WO 9929889) of poly(3-hydroxybutyrate/3-hydroxyvalerate), but degradation of hydroxybutyric acid/hydroxyvaleric acid copolymers also requires a difficult separation of 3-hydroxybutyric acid from the co-product 3-hydroxyvaleric acid. (R)-(−)-3-Hydroxyvaleric acid has also been prepared by the enzymatic reduction of 3-oxovaleric acid (Bayer et al.,
Appl. Microbiol. Biotechnol.
42:543-547 (1994)) or by the asymmetric hydrogenation of methyl 3-oxovalerate followed by saponification (Burk et al.,
Organometallics
9:2653-2655 (1990)).
Nitriles are readily converted to the corresponding carboxylic acids by a variety of chemical processes. These processes typically require strongly acidic or basic reaction conditions and high reaction temperatures, and usually produce unwanted byproducts and/or large amounts of inorganic salts as unwanted waste. Reaction conditions for the chemical hydrolysis of nitriles which additionally have a hydroxyl group, such as for the conversion of 3-hydroxyvaleronitrile to 3-hydroxyvaleric acid, will usually also result in the undesirable elimination of primary, secondary, or tertiary hydroxyl groups to produce carbon—carbon double bonds.
The enzyme-catalyzed hydrolysis of nitriles substrates to the corresponding carboxylic acids is often preferred to chemical methods, since the reactions are often run at ambient temperature, do not require the use of strongly acidic or basic reaction conditions, and produce the desired product with high selectivity at high conversion.
A combination of two enzymes, nitrile hydratase and amidase, can be used to convert aliphatic nitrites to the corresponding carboxylic acid in aqueous solution. The aliphatic nitrile is initially converted to an amide by the nitrile hydratase, then the amide is subsequently converted by the amidase to the corresponding carboxylic acid. A wide variety of bacterial genera are known to possess a diverse spectrum of nitrile hydratase and amidase activities (Sugai et al.,
Biosci. Biotech. Biochem.
61:1419-1427 (1997)), including Rhodococcus, Pseudomonas, Alcaligenes, Arthrobacter, Bacillus, Bacteridium, Brevibacterium, Corynebacterium and Micrococcus. The fungus
Fusarium merismoides
TG-1 has also been used as catalyst for the hydrolysis of aliphatic nitrites and dinitriles (Asano et al.,
Agric. Biol. Chem.
44:2497-2498 (1980)). Immobilized nitrile hydratase and amidase from Rhodococcus sp. (SP409 from Novo Industri) was used to hydrolyze 3-hydroxypropionitrile, 3-hydroxyheptanenitrile, 3-hydroxyoctanenitrile, and 3-hydroxynonanenitrile to the corresponding 3-hydroxycarboxylic acids in 63%, 62% and 83% yields, respectively (de Raadt et al.,
J. Chem. Soc
. Perkin Trans. 1, 137-140 (1992)). The formation of the corresponding amide was also observed by TLC. In contrast, the purified nitrile hydratase of
Bacillus pallidus
Dac521 hydrolyzed a variety of aliphatic nitrites, but did not hydrolyze 3-hydroxypropionitrile (Cramp et al.,
Biochim. Biophys. Acta
1431:249-260 (1999)).
A single enzyme, nitrilase, also converts a nitrile to the corresponding carboxylic acid and ammonia in aqueous solution, but without the intermediate formation of an amide. Kobayashi et al. (
Tetrahedron
46:5587-5590 (1990);
J. Bacteriology
172:4807-4815 (1990)) have described an aliphatic nitrilase isolated from
Rhodococcus rhodochrous
K22 which catalyzed the hydrolysis of a variety of aliphatic nitrites to the corresponding carboxylic acids. A nitrilase from
Comamonas testosteroni
has been isolated that can convert a range of aliphatic &agr;,&ohgr;-dinitriles to either the corresponding &ohgr;-cyanocarboxylic acids or dicarboxylic acids (CA 2,103,616; Lévy-Schil et al.,
Gene
161:15-20 (1995)). Aliphatic nitrilases are also produced by
Rhodococcus rhodochrous
NIMBI 11216 (Bengis-Garber et al.,
Appl. Microbiol. Biotechnol.
32:11-16 (1989); Gradley et al.,
Biotechnology Lett.
16:41-46 (1994)),
Rhodococcus rhodochrous
PA-34 (Bhalla et al.,
Appl. Microbiol. Biotechnol.
37:184-190 (1992)),
Fusarium oxysporum
f. sp.
melonis
(Goldlust et al.,
Biotechnol. Appl. Biochem.
11:581-601 (1989)), Acinetobacter sp. AK 226 (Yamamoto et al.,
Agric. Biol. Chem.
55:1459-1473 (1991)),
Alcaligenes faecalis
ATCC 8750 (Yamamoto et al.,
J. Ferment. Bioeng.
73:425-430 (1992)), and
Acidovorax facilis
72W (Gavagan et al.,
J. Org. Chem.
63:4792-4801 (1998)).
The problem to be solved, therefore, is to provide new catalysts useful for converting nitrites to their corresponding carboxylic acids at high yield. More specifically, the ability to convert a nitrile functional group in a compound to the corresponding carboxylic acid in the presence of a hydroxyl group that can undergo elimination would be extremely useful.
SUMMARY OF THE INVENTION
A process is disclosed for hydrolyzing 3-hydroxynitrile to 3-hydroxycarboxylic acid. The process includes the steps of (a) contacting a 3-hydroxynitrile in an aqueous reaction mixture with an enzyme catalyst characterized by 1) nitrile hydratase and amidase activity or 2) nitrilase activity; and (b) optionally, recovering the 3-hydroxycarboxylic acid produced in step (a). More particularly, 3-hydroxyvaleronitrile is converted in the invention to 3-hydroxyvaleric acid in high yield at up to 100% conversion, using as an
Bramucci Michael G.
Dicosimo Robert
Fallon Robert
Gavagan John E.
Herkes Frank
E. I. du Pont de Nemours and Company
Lilling Herbert J.
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