CA2191713C - Process for recovering polyhydroxyalkanoates using centrifugal fractionation - Google Patents
Process for recovering polyhydroxyalkanoates using centrifugal fractionation Download PDFInfo
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- CA2191713C CA2191713C CA002191713A CA2191713A CA2191713C CA 2191713 C CA2191713 C CA 2191713C CA 002191713 A CA002191713 A CA 002191713A CA 2191713 A CA2191713 A CA 2191713A CA 2191713 C CA2191713 C CA 2191713C
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- polyhydroxyalkanoate
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/88—Post-polymerisation treatment
- C08G63/89—Recovery of the polymer
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/62—Carboxylic acid esters
- C12P7/625—Polyesters of hydroxy carboxylic acids
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/06—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from hydroxycarboxylic acids
Abstract
The present invention relates to a process for recovering polyhydroxyalkanoate from a biological source material containing the polyhydroxyalkanoate, the process comprising: a) comminuting the biological source material; b) suspending the comminuted biological source material in a fluid; c) partitioning the polyhydroxyalkanoate from the other components of the biological source material by centrifugal fractionation to form a solid-solid separation; and d) recovering the polyhydroxyalkanoate.
Description
WO 95/33065 21 ~ 171 ~ PCT/US95/06651 PROCESS FOR RECOVERING POLYHYDROXYALKANOATES USING
CENTRIFUGAL FRACTIONATION
TECHNICAL FIELD
The present invention relates to processes for isolating specific resin components from other biomass components. More specifically, the present invention relates to a process for the recovery of a polyhydroxyalkanoate from a biological system, such as a plant or bacteria, by using centrifugal fractionation.
BACKGROUND
Commodity polymers are typically produced from petrochemical sources by well-known synthetic means. However, recent advances in technology have resulted in the promise of new sources of commodity polymers. Particularly promising is the production of plastic resins using living organisms ("bioplastic"), including genetically manipulated bacteria and crop plants, which are designed to produce polymers such as polyhydroxyalkanoate (PHA); a number of bacteria which naturally produce PHA are also promising sources of PHA. (see for example, NovEL
BIODEGRADABLE MICROBIAL POLYMERS, E.A. DBWeS, ed., NATO ASI SerleS, Series E: Applied Sciences - Vol. 186, Kluwer Academic Publishers (1990);
Poirier, Y., D.E. Dennis, K. Klomparens and C. Somerville, "Polyhydroxybutyrate, a biodegradable thermoplastic, produced in transgenic plants", SCIENCE, Vol. 256, pp. 520-523 (1992)). In a large scale production, for example agricultural production, the harvesting and purifying of such bioplastic from the biomass debris is a critical step for determining the practical feasibility of such technology.
The separation of polymeric lipids such as PHA from a large-scale biological source, such as an agricultural crop, is not a trivial task. The conventional separation methods used extensively in the extraction of low molecular weight lipids are not practical to employ in a resin isolation process. For example, a simple mechanical press is impractical because, unlike separating vegetable oils from oil-seeds, solid plastics cannot be squeezed out of crops by mechanical pressing.
Solvent extraction is also impractical for a number of reasons. A
solution of polymer develops an extremely high viscosity, even at relatively WO 95/33065 ~ ~ ~ ~ ~ ~ ~ PCT/US95/06651
CENTRIFUGAL FRACTIONATION
TECHNICAL FIELD
The present invention relates to processes for isolating specific resin components from other biomass components. More specifically, the present invention relates to a process for the recovery of a polyhydroxyalkanoate from a biological system, such as a plant or bacteria, by using centrifugal fractionation.
BACKGROUND
Commodity polymers are typically produced from petrochemical sources by well-known synthetic means. However, recent advances in technology have resulted in the promise of new sources of commodity polymers. Particularly promising is the production of plastic resins using living organisms ("bioplastic"), including genetically manipulated bacteria and crop plants, which are designed to produce polymers such as polyhydroxyalkanoate (PHA); a number of bacteria which naturally produce PHA are also promising sources of PHA. (see for example, NovEL
BIODEGRADABLE MICROBIAL POLYMERS, E.A. DBWeS, ed., NATO ASI SerleS, Series E: Applied Sciences - Vol. 186, Kluwer Academic Publishers (1990);
Poirier, Y., D.E. Dennis, K. Klomparens and C. Somerville, "Polyhydroxybutyrate, a biodegradable thermoplastic, produced in transgenic plants", SCIENCE, Vol. 256, pp. 520-523 (1992)). In a large scale production, for example agricultural production, the harvesting and purifying of such bioplastic from the biomass debris is a critical step for determining the practical feasibility of such technology.
The separation of polymeric lipids such as PHA from a large-scale biological source, such as an agricultural crop, is not a trivial task. The conventional separation methods used extensively in the extraction of low molecular weight lipids are not practical to employ in a resin isolation process. For example, a simple mechanical press is impractical because, unlike separating vegetable oils from oil-seeds, solid plastics cannot be squeezed out of crops by mechanical pressing.
Solvent extraction is also impractical for a number of reasons. A
solution of polymer develops an extremely high viscosity, even at relatively WO 95/33065 ~ ~ ~ ~ ~ ~ ~ PCT/US95/06651
2 low concentration, thereby making the solution extremely difficult to work with. Furthermore, the stripping of solvent from polymer is a slow and difficult process. A commonly used solvent for the extraction of PHA from bacteria is chloroform. However, the use of a large amount of such a solvent, potentially harmful to health and environment if accidentally released, near the harvesting site would be undesirable.
Separation of PHA by sedimentational methods should be, in principle, possible. However, simple gravitational (1-G force) settling in a liquid suspending medium is, in fact, quite impractical. The rate of settling is extremely slow. In addition, such slow settling is easily disrupted by the Brownian motion of the fine PHA particles induced by the thermal fluctuation of the suspending fluid molecules surrounding the particles. Furthermore, the extended period of time required to settle very fine PHA particles introduces the problem of bacterial contamination and subsequent biodegradation of the particle suspension.
Based on the foregoing, there is a need for a simple and economical process for recovering bioplastics from a large-scale biological source.
Such a process would preferably be easily adaptable as an integral part of the agricultural production of bioplastics.
It is therefore an object of the present invention to provide a process for recovering bioplastics from a biological source material.
SUMMARY
The present invention relates to a process for recovering polyhydroxyalkanoate from a biological source material containing the polyhydroxyalkanoate, the process comprising: a) comminuting the biological source material; b) suspending the comminuted biological source material in a fluid; c) partitioning the polyhydroxyalkanoate from the other components of the biological source material by centrifugal fractionation to form a solid-solid separation; and d) recovering the polyhdroxyalkanoate.
DETAILED DESCRIPTION
The present invention answers the need for a process for recovering bioplastics from a biological source material.
The following is a list of definitions for terms used herein.
"g/sec" means grams per second.
"g/min" means grams per minute.
"p" means micron(s).
"psi" means pounds per square inch.
"MPa" means mega Pascal, which is equivalent to about 145 psi.
Separation of PHA by sedimentational methods should be, in principle, possible. However, simple gravitational (1-G force) settling in a liquid suspending medium is, in fact, quite impractical. The rate of settling is extremely slow. In addition, such slow settling is easily disrupted by the Brownian motion of the fine PHA particles induced by the thermal fluctuation of the suspending fluid molecules surrounding the particles. Furthermore, the extended period of time required to settle very fine PHA particles introduces the problem of bacterial contamination and subsequent biodegradation of the particle suspension.
Based on the foregoing, there is a need for a simple and economical process for recovering bioplastics from a large-scale biological source.
Such a process would preferably be easily adaptable as an integral part of the agricultural production of bioplastics.
It is therefore an object of the present invention to provide a process for recovering bioplastics from a biological source material.
SUMMARY
The present invention relates to a process for recovering polyhydroxyalkanoate from a biological source material containing the polyhydroxyalkanoate, the process comprising: a) comminuting the biological source material; b) suspending the comminuted biological source material in a fluid; c) partitioning the polyhydroxyalkanoate from the other components of the biological source material by centrifugal fractionation to form a solid-solid separation; and d) recovering the polyhdroxyalkanoate.
DETAILED DESCRIPTION
The present invention answers the need for a process for recovering bioplastics from a biological source material.
The following is a list of definitions for terms used herein.
"g/sec" means grams per second.
"g/min" means grams per minute.
"p" means micron(s).
"psi" means pounds per square inch.
"MPa" means mega Pascal, which is equivalent to about 145 psi.
3 "Fractionation" means the separation and/or isolation of components of a mixuture. The invention described herein preferably achieves such fractionation due to differences in the density and/or particle size of the various components.
"Solid-solid separation" and "solid-solid fractionation" mean the separation or partitioning of components in a sample wherein each fraction comprises a component in a solid state. For example, a separation resulting in a fraction comprising PHA granules suspended in a fluid medium and a fraction comprising other insoluble biomass is considered a solid-solid separation.
"Liquid-solid separation" and "liquid-solid fractionation" mean the separation or partitioning of components in a sample wherein at least one fraction contains an otherwise solid component in liquid state, and at least one fraction comprises a component in a solid state. For example, a separation resulting in a fraction comprising PHA dissolved in a solvent and a fraction comprising other insoluble biomass is considered a liquid-solid separation.
"Polyhydroxyalkanoate" and "PHA" mean a polymer having the following general structure:
R O
I II
O~CH~~CH2~nC
n wherein R is preferably an alkyl or alkenyl, m is 1 or 2, and n is an integer.
The structure enclosed in brackets is commonly referred to as a repeating unit. The terms polyhydroxyalkanoate and PHA include polymers containing one or more different repeating units. Examples of preferred PHAs recoverable by the present process included those disclosed in Canadian Patent Application S.N. 2,181,791; Canadian Patent Application S.N.
2,181,796; Canadian Patent Application S.N. 2,181,795; and European Patent Application Ser. No. 533 144, Shiotani and Kobayashi, published March 24, 1993.
"Recovering polyhydroxyalkanoate from a biological source material", in addition to referring to the recovery of the partilcular PHA produced by a biological source material which produces a single PHA, also refers to the recovery of one or more types of PHA when the biological source material produces more than one type of PHA.
W x~., J
2i9~> »
"Alkyl" means a carbon-containing chain which may be straight, branched or cyclic, preferably straight; substituted (mono- or poly-) or unsubstituted; and saturated.
"Alkenyl" means a carbon-containing chain which may be straight, branched or cyclic, preferably straight; substituted (mono- or poly-) or unsubstituted; and monounsaturated (i.e., one double or triple bond in the chain), or polyunsaturated (i.e., two or more double bonds in the chain, two or more triple bonds in the chain, or one or more double and one or more triple bonds in the chain).
"Comprising" means that other steps and other ingredients which do not affect the end result can be added. This term encompasses the terms "consisting of and "consisting essentially of'.
All percentages are by weight of total composition unless specifically stated otherwise.
The present invention relates to a process for recovering (i.e., isolating) polyhydroxyalkanoate from a biological source material containing the polyhydroxyalkanoate, the process comprising centrifugal fractionation of the biological source material such that the polyhydroxyalkanoate is partitioned from the other components of the biological source material by solid-solid separation.
PHA components found in biological systems (e.g., conventional, or genetically engineered bacteria or genetically engineered plants) tend to settle at rates different from other cellular components such as proteins and carbohydrates when they are suspended in a common fluid medium. The difference in the sedimentation rate results in the spatial segregation of mixed particulates into multiple layers (fractionation) each containing predominantly a single component.
According to the Stokes' law of sedimentation, there are two major factors affecting the sedimentation rates of particles: differences in the density and size of suspended particles. These factors independently control the separation efficiency of the fractionation process.
Density is an intrinsic property of the material to be separated.
Generally, there is no easy way of manipulating the density of an individual component to be fractionated. The density difference between particles in a composition is not always large enough to achieve substantial fractionation of one component from the rest. When the densities of the components are sufficiently different, a high degree of separation can be achieved, particularly when a suspending medium having an intermediate density is used. The density of PHA is sufficiently different from other biomass components, such as proteins and carbohydrates, to achieve some degree of fractionation.
Differences in particle size also contribute greatly to the effectiveness of the fractionation process. PHA is generally stored in biological systems in the form of very fine granules having a diameter of about or below 1 ~.. The particle size of PHA granules are therefore much smaller as compared to other cellular components from the disrupted cell. In addition, particle size can be further manipulated by a post-harvest processing which includes grinding or colloid-milling. Specific types of biological source material and the process are discussed in more detail below.
Biological Source Material Sources from which PHA is recovered via the process of the present invention include single-cell organisms such as bacteria or fungi and higher organisms such as plants (herein collectively referred to as "biological source material" or "BSM"). While such BSM could be wild-type organisms, they are preferably genetically manipulated species specifically designed for the production of a specific PHA of interest to the grower. Such genetically manipulated organisms are produced by incorporating the genetic information necessary to produce PHA. Typically, such genetic information is derived from bacteria which naturally produce PHA.
Plants useful in the present invention include any genetically engineered plant designed to produce PHA. Preferred plants include agricultural crops such cereal grains, oil seeds and tuber plants; more preferably, avocado, barley, beets, broad bean, buckwheat, carrot, coconut, copra, corn (maize), cottonseed, gourd, lentils, lima bean, millet, mung bean, oat, oilpalm, peas, peanut, potato, pumpkin, rapeseed (e.g., canola), rice, sorghum, soybean, sugarbeet, sugar cane, sunflower, sweetpotato, tobacco, wheat, and yam. Such genetically altered fruit-bearing plants useful in the process of the present invention include, but are not limited to apple, apricot, banana, cantaloupe, cherries, grapes, kumquat, lemon, lime, orange, papaya, peaches, pear, pineapple, tangerines, tomato, and watermelon. Preferably the plants are genetically engineered to produced PHA pursuant to the methods disclosed in Poirier, Y., D.E. Dennis, K.
Klomparens and C. Somerville, "Polyhydroxybutyrate, a biodegradable thermoplastic, produced in transgenic plants", SCIENCE, Vol. 256, pp. 520-523 (1992); WO Patent No. 95/05472 and WO Patent No. 93/02187.
Particularly preferred plants are soybean, potato, corn and coconut plants genetically engineered to produce PHA.
Bacteria useful in the present invention include any genetically engineered bacteria designed to produce PHA, as well as bacteria which naturally produce PHA. Examples of such bacteria include those disclosed In NOVEL BIODEGRADABLE MICROBIAL POLYMERS, E.A. DaweS, ed., NATO ASI
Series, Series E: Applied Sciences - Vol. 186, Kluwer Academic Publishers (1990); US Patent 5,250,430, Peoples and Sinskey, issued October 5, 1993;
US Patent 5,245,023, Peoples and Sinskey, issued September 14, 1993;
US Patent 5,229,279, Peoples and Sinskey, issued JUIy 20, 1993; and US
Patent 5,149,644, Lubitz, issued September 22, 1992.
It is preferable that the BSM contain a sufficient quantity of PHA to make the process economically desirable. Preferably, the initial content of PHA in the source material should be at least about 5% of the total dry weight; more preferably at least about 25%; more preferably at least about 50%; more preferably still, at least about 75%.
Isolation Process The process of the present invention preferably involves the following unit-operation steps: pretreatment, size reduction, suspension, and centrifugal separation. The optimal range of unit operation conditions or individual devices will vary considerably according to the type of raw BSMs used.
The pretreatment of source materials comprising PHA is preferred in order to remove low molecular weight contaminants readily soluble in appropriate solvents, such as sugars, oils and sometimes moisture. A
variety of standard pretreatment methods used for the processing of food crops are known to those skilled in the art and may be readily employed for the pretreatment step of the present invention. Examples of such pretreatment steps include oil extraction (for example, see BAILEY'S
INDUSTRIAL OIL AND FAT PRODUCTS, THIRD ED., Johne Wiley and Sons: New York (1964), pp. 663-713), water washing (for example, see US Patent 2,881,076, Sair, issued April 7, 1959), and alcohol washing (for example, see Eldridge, A.C., W.J. Wolf, A.M. Nash and A.K. Smith, "Alcohol Washing Of Soybean Protein", AGRICULTURAL AND FOOD CHEMISTRY, July-August, 1963, pp. 323-328).
-~A
The pretreated material comprising PHA granules is then pulverized (e.g., dry milling) to small fragments, by first using a common vibratory or hammer mill. The pulverization of source material by dry milling, particularly for agricultural crop plants comprising PHA granules, preferably produces grain flour of a particle size finer than about 500 ~ in diameter, more preferably finer than about 300 ~, more preferably still, finer than about 100 The comminuted material is then dispersed in a suspending fluid such as water, chlorinated carbon solvents (e.g., chloroform, carbon tetrachloride, or dichlorethane), various organic solvents (e.g., ethanol, methanol, acetone, methyl ethyl ketone, ethyl acetate, hexane, heptane, pentane, or mixtures thereof), or supercritical fluids (e.g., carbon dioxide or nitrous oxide); preferably water. If the suspending fluid is water, the water is preferably heated to promote hydration of certain non-PHA components prior to the wet milling to a temperature preferably not exceeding 90°C. If a suspending medium having an intermediate density between the PHA and other biomass is desired, then the suspending medium is preferably an aqueous solution of an organic or inorganic salt, or an aqueous solution of a water-soluble sugar. Useful organic salts include, but are not limited to, potassium glycolate, potassium citrate, potassium lactate, potassium malate, and dipotassium tartrate. Useful inorganic salts include, but are not limited to, sodium chloride, potassium chloride, calcium chloride, magnesium chloride, and calcium sulfate. Useful water-soluble sugars include, but are not limited to, sucrose, glucose, and raffinose.
The material is further treated by wet milling using a device such as a colloid mill, sonicator, or homoginizer, to obtain the desired particle size distribution for the dispersed solids. For wet milling, the comminuted material is suspended in a fluid. Preferred fluids include, but are not limited to water; ethanol; and aqueous solutions of organic salts, inorganic salts or sugars. The wet milling should preferably produce suspensions having an average particle size of smaller than about 50 ~.
The suspension mixture of PHA and other biomass components is then processed with a centrifugal device to fractionate PHA-rich particles from the other biomass. Preferred centrifugal devices include, but are not limited to, centrifuge, ultracentrifuge, or hydrocyclone separator. An industrial scale centrifugal separation device may be used in the process of the present invention for fractionation of the PHA, so long as the device provides sufficient "G" force (i.e., sedimentational force field created, for WO 95/33065 2191 ~ ~ ~ PCT/US95106651 example, by centrifugal effect expressed in terms of the equivalent to gravitational force) to achieve the sedimentation of solid particles above the rate necessary to overcome the Brownian motion of particles to be settled.
The centrifugal force field employed in the process of the present invention is preferably at least about 10 G (i.e., ten times faster than simple gravimetric settling) to achieve rapid and efficient fractionation of PHA from other biomass components. More preferably, the centrifugal force field is at least about 100 G, more preferably at least about 1,000 G, more preferably at least about 10,000 G, more preferably still at least about 100,000 G.
In one embodiment of the present invention, a hydrocyclone is employed as the centrifugal device. A hydrocyclone consists of a conical cavity with an eccentric inlet port and two exit ports above and below the conical cavity. The vortex flow created by the off-centered high-speed injection of fluid creates a centrifugal force resulting in the sedimentation of heavy particles toward the inner wall of the conical cavity. The heavier portion will exit predominantly from the smaller tip of the cone, while the lighter portion will exit from the wider part of the cone. The centrifugal force field increases in a hydrocyclone with the inlet feed rate and decreases with the diameter of the conical cavity. For example, in a typical 1 cm diameter hydrocyclone, it is possible to achieve well above 100 G of centrifugal force by maintaining the feed rate of suspension above several tens of gallons per minute. (See, for example, Day, R.W., "Hydrocyclones in Process and Pollution Control", CHEMICAL ENGINEERING PROGRESS, Vol. 69, pp. 67-72 (1973); and US Patent 2,754,968, Vegter and Hage, issued July 17, 1956;
and KIRK-OTHMER ENCYCLOPEDIA OF CHEMICAL TECHNOLOGY, THIRD ED., Vol.
12, pp. 1-29, John Wiley and Sons, (1990)). Hydrocyclones useful in the present invention are available from a variety of manufactureres including Dorr-Oliver, Inc. (Milford, CT), Yardney Water Management Systems, Inc.
(Riverside, CA), and Quality Solids Separation Co. (Houston, TX).
In another embodiment of the present invention, a continuous centrifuge may be employed as the centrifugal device. A continuous centrifuge comprises a rapidly rotating cylinder having a feed suspension flowing inside the cylinder. As a result of the rotation, centrifugal force is created thereby promoting sedimentation of heavier components toward the inner wall of the rotating cylinder. The sedimentate is continuously collected by a scraping mechanism while the supernatant is removed as effluent. A typical industrial scale centrifuge operating at several thousand rpm can easily produce a centrifugal force well above 100 G. (See, for .. 2191713 example, Ambler, C.M., "The Evaluation of Centrifuge Performance", CHEMICAL ENGINEERING PROGRESS, VOI. 48, pp. 150-158, (1952); and KIRK-OTHMER ENCYCLOPEDIA OF CHEMICAL TECHNOLOGY, THIRD ED., VOI. 12, pp. 1-29, John Wiley and Sons, (1990)). Centrifuges useful in the present invention are available from a variety of manufacturers, including Humboldt Decanter, Inc. (Atlanta, GA), Western States Machine Co. (Hamilton, OH), and Bird Machine Co. (South Walpole, MA).
Preferably, the process of the present invention yields at least about 70% of the PHA in the source material, more preferably at least about 80%, more preferably still at least about 90%.
Preferably, at least about 85% of the dry mass of the PHA-rich fraction isolated by the process of the present invention is PHA, more preferably at least about 95%, more preferably still at least about 99%.
The PHAs recovered by the process of this invention are useful for forming a variety of plastic articles, including those disclosed in Canadian Patent Application S.N. 2,181,791; Canadian Patent Application S.N.
2,181,796 and Canadian Patent Application S.N. 2,181,795. Such plastic articles include, but are not limited to, films, sheets, foams, fibers, nonwovens, elastomers, adhesive and molded articles. Such plastic articles can be further incorporated into a variey of useful products including, but not limited to, personal cleansing wipes; disposable health care products such as bandages, wound dressings, wound cleansing pads, surgical gowns, surgical covers, surgical pads; other institutional and health care disposables such as gowns, wipes, pads, bedding items such as sheets and pillowcases, foam mattress pads.
The following non-limiting examples illustrate the methods of the present invention.
Isolation of POly~3-hKdroxybutyrate-co-3-hydroxyoctanoate) from Soybeans Soybeans, from a genetically altered soybean plant, comprising poly(3-hydroxybutyrate-co-hydroxyoctanoate) are roll milled to form thin flakes. The low molecular weight lipids and oils contained in the flakes are initially removed by pressing the flakes. The remaining low molecular lipids and oils are subsequently extracted from the flakes by using hexane as a solvent. The resulting defatted soybean flakes are dried and pulverized using a vibratory energy mill (Sweco*, Florence, KY) to produce a flour having an average particle size of less than 80 p. The flour is then hydrated * Trademark A
in water at 65°C for 30 minutes to produce a suspension containing 7%
solids by weight. The suspension is then passed through a colloid mill (Littleford Day, Florence, KY) once to assure complete mixing. The suspension is then passed through a homogenizer (Model 3M, APV Gaulin, Willimington, MA) operated at 8,000 psi, two times, to produce a suspension mixture consisting of fine granules of polymer having an average particle size of less than 1 ~ and other soybean biomass debris comprising proteins and carbohydrates. The homogenized suspension of soybeans is fed to a hydrocyclone (DOXIE *TYPE-A, Dorr-Oliver, Milford, CT) with a heavy duty pump (Model 4678-10S, Northern Pump, Minneapolis, MN) at a feed rate of 150 g/sec under a nominal pressure of 3 MPa.
The effluent stream coming out the top section of the hydrocyclone contains most of the polymer granules. This portion of the suspension is spray dried and washed with 40% water / 60% ethanol mixture to remove soluble residual components such as sugars, to produce a cake of poly(3-hydroxybutyrate-co-hydroxyoctanoate) granules with a purity of greater than 95%, and a yield of about 85% with respect to the starting material.
Isolation of Poly(3-hydroxybutyrate-co-hydroxyhexanoate) from Maize Grains of maize (corn), from a genetically altered maize plant, comprising poly(3-hydroxybutyrate-co-3-hydroxyhexanoate are hammer milled to form meals.
The low molecular weight lipids and oils contained in the meals are removed first by pressing the flakes and are then further extracted by using hexane as the solvent and washed with 40% water / 60% ethanol mixture to remove other soluble components such as sugars. The resulting defatted and desugared maize meals are dried and comminuted using a vibratory energy mill (Sweco, Florence, KY) to produce a flour having an average particle size of less than 80 ~,. The flour is then hydrated in water at 65°C for 30 min to produce a suspension containing 7% solids by weight. The suspension is then passed through a colloid mill (Littleford Day, Florence, KY) once to assure complete mixing. The suspension is then passed twice through a homogenizer (Model 3M, Gaulin, Willmington, MA) operated at 8,000 psi to produce a suspension mixture consisting of fine granules of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate having an average particle size of less than 1 ~ and other maize biomass debris comprising proteins and carbohydrates.
The homogenized suspension of soybeans is fed to a continuous centrifuge (6"
Solid Bowl Centrifuge, Bird Machine Co., South Walpole, MA) at a feed rate of 1,500 g/min. The * Trademark _..,~.,.
,-~._.
supernatant effluent stream coming out the continuous centrifuge is spray dried to produce a cake of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate granules with a purity higher than 98%, and a yield of about 85% with respect to the starting material.
Isolation of Polv(3-hvdroxvbutvrate-3-hvdroxvvalerate) from Tobacco Tobacco leaves, from a genetically altered tobacco plant, comprising poly(3-hydroxybutyrate-co-3-hydroxyvalerate) are hammer milled to form a flour. The low molecular weight soluble components contained in the flakes are removed by washing first with hexane and then with a 40% water / 60%
ethanol mixture to produce a dry flour having an average particle size of less than 80 ~. The flour is then hydrated in water at 65 °C for 30 min to produce a suspension containing 7% solids by weight. The suspension is then passed through a colloid mill (Littleford Day, Florence, KY) once to assure complete mixing. The suspension is then passed twice through a homogenizer (Model 3M, Gaulin, Wilmington, MA) operated at 8,000 psi to produce a suspension mixture consisting of fine granules of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) having an average particle size of less than 1 a and other tobacco biomass debris. The homogenized suspension of tobacco is fed to a continuous centrifuge (6" Solid Bowl Centrifuge, Bird Machine Co., South Walpole, MA) at a feed rate of 1,500 g/min. The supernatant effluent stream coming out the continuous centrifuge is spray dried to produce a cake of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) granules with a purity higher than 95%, and a yield of about 85% with respect to the starting material.
Isolation of Polv(3-hvdroxvbutvrate-co-3-hvdroxvdecanoate) from Coconuts Coconuts, from a genetically altered coconut tree, comprising poly(3-hydroxybutyrate-co-3-hydroxydecanoate) are shredded to form thin flakes.
The low molecular weight lipids and oils contained in the flakes are extracted by using hexane as a solvent. Soluble sugars are also removed by using a 40% water / 60% ethanol mixture. The resulting defatted and desugared coconut flakes are dried and pulverized using a vibratory energy mill (Sweco, Florence, KY) to produce a flour having an average particle size of less than 80 ~. The flour is then hydrated in water at 65°C for min to produce a suspension containing 7°~ solids by weight. The suspension is then passed through a colloid mill (Littleford Day, Florence, KY) once to assure complete mixing. The suspension is then passed twice WO 95/33065 2191713 pCT/LTS95106651 through a homogenizer (Model 3M, Gaulin, Wilmington, MA) operated at 8,000 psi to produce a suspension mixture consisting of fine granules of poly(3-hydroxybutyrate-co-3-hydroxydecanoate) having an average particle size of less than 1 ~ and other coconut biomass debris. The homogenized suspension of coconuts is fed to a hydrocyclone (Doxie Type-A, Dorr-Oliver, Milford, CT) with a heavy duty pump (Model 4678-10S, Northern Pump, Minneapolis, MN) at a feed rate of 200 g/sec under a nominal pressure of 4 MPa. The effluent stream coming out the top section of the hydrocyclone will contain most of the poly(3-hydroxybutyrate-co-3-hydroxydecanoate) granules. This portion of the suspension is spray dried to produce a cake of poly(3-hydroxybutyrate-co-3-hydroxydecanoate) granules with a purity higher than 95%, and a yield of about 85% with respect to the starting material.
Isolation of Polv(3-hvdroxvbutvrate-co-3-hydroxyheptanoate) from Potatoes Potato flakes, from potatoes obtained from a genetically altered potato plant, comprising poly(3-hydroxybutyrate-co-3-hydroxyheptanoate) are washed with water and then hydrated at 65°C for 30 min to produce a suspension containing 7% solids by weight. The suspension is then passed through a colloid mill (Littleford, Day, Florence, KY]) once to assure complete mixing. The suspension is then passed twice through a homogenizer (Model 3M, Gaulin, Wilmington, MA) operated at 8,000 psi to produce a suspension mixture consisting of fine granules of poly(3-hydroxybutyrate-co-3-hydroxyheptanoate) having an average particle size of less than 1 p and other potato biomass debris. The homogenized suspension of potato is fed to a continuous centrifuge (6" Solid Bowl Centrifuge, Bird Machine Co., South Walpole, MA) at a feed rate of 1,500 g/min. The supernatant effluent stream coming out of the continuous centrifuge is spray dried to produce a cake of poly(3-hydroxybutyrate-co-3-hydroxyheptanoate) granules with a purity higher than 95%, and a yield of about 85% with respect to the starting material.
Isolation of Poly(3-hvdroxybutyrate) from A. eutrophus A culture of A. eutrophus which naturally produces poly(3-hydroxybutyrate) is treated with an ultrasonic sonicator (Branson Ultrasonics Corp., Danbury, CT) to produce a suspension mixture consisting of fine granules of poly(3-hydroxybutyrate) having an average particle size of less than 1 ~ and other bacterial biomass debris containing about 20%
solids by weight. The homogenized suspension of bacterial components is fed to a hydrocyclone (Doxie type-A, Dorr-Oliver, Milford, CT) with a heavy duty pump pressure of 4 MPa. The effluent stream coming out the top section of the hydrocyclone contains most of the poly(3-hydroxybutyrate) granules. This portion of the suspension is spray dried to produce a cake of poly(3-hydroxybutyrate) granules with a purity higher than 95%, and a yield of about 90% with respect to the starting material.
Isolation of Poly(3-hydroxybutyrate) from E. coli A culture of E. coli which has been genetically manipulated to produce poly(3-hydroxybutyrate) is treated with an ultrasonic sonicator (Branson Ultrasonics Corp., Danbury, CT) to produce a suspension mixture consisting of fine granules of poly(3-hydroxybutyrate) having an average particle size of less than 1 ~, an other bacterial biomass debris containing about 5% solids by weight. The homogenized suspension of bacterial components is fed to a hydrocyclone (Doxie type-A, Dorr-Oliver, Milford, CT) with a heavy duty pump pressure of 4 MPa. The effluent stream coming out the top section of the hydrocyclone contains most of the poly(3-hydroxybutyrate) granules. This portion of the suspension is spray dried to produce a cake of poly(3-hydroxybutyrate) granules with a purity higher than 95%, and a yield of about 90% with respect to the starting material.
It is understood that the examples and embodiments described herein are for illustrative purposes only and that various modifications or changes in light thereof will be suggested to one skilled in the art and are to be included in the spirit and purview of this application and scope of the appended claims.
"Solid-solid separation" and "solid-solid fractionation" mean the separation or partitioning of components in a sample wherein each fraction comprises a component in a solid state. For example, a separation resulting in a fraction comprising PHA granules suspended in a fluid medium and a fraction comprising other insoluble biomass is considered a solid-solid separation.
"Liquid-solid separation" and "liquid-solid fractionation" mean the separation or partitioning of components in a sample wherein at least one fraction contains an otherwise solid component in liquid state, and at least one fraction comprises a component in a solid state. For example, a separation resulting in a fraction comprising PHA dissolved in a solvent and a fraction comprising other insoluble biomass is considered a liquid-solid separation.
"Polyhydroxyalkanoate" and "PHA" mean a polymer having the following general structure:
R O
I II
O~CH~~CH2~nC
n wherein R is preferably an alkyl or alkenyl, m is 1 or 2, and n is an integer.
The structure enclosed in brackets is commonly referred to as a repeating unit. The terms polyhydroxyalkanoate and PHA include polymers containing one or more different repeating units. Examples of preferred PHAs recoverable by the present process included those disclosed in Canadian Patent Application S.N. 2,181,791; Canadian Patent Application S.N.
2,181,796; Canadian Patent Application S.N. 2,181,795; and European Patent Application Ser. No. 533 144, Shiotani and Kobayashi, published March 24, 1993.
"Recovering polyhydroxyalkanoate from a biological source material", in addition to referring to the recovery of the partilcular PHA produced by a biological source material which produces a single PHA, also refers to the recovery of one or more types of PHA when the biological source material produces more than one type of PHA.
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"Alkyl" means a carbon-containing chain which may be straight, branched or cyclic, preferably straight; substituted (mono- or poly-) or unsubstituted; and saturated.
"Alkenyl" means a carbon-containing chain which may be straight, branched or cyclic, preferably straight; substituted (mono- or poly-) or unsubstituted; and monounsaturated (i.e., one double or triple bond in the chain), or polyunsaturated (i.e., two or more double bonds in the chain, two or more triple bonds in the chain, or one or more double and one or more triple bonds in the chain).
"Comprising" means that other steps and other ingredients which do not affect the end result can be added. This term encompasses the terms "consisting of and "consisting essentially of'.
All percentages are by weight of total composition unless specifically stated otherwise.
The present invention relates to a process for recovering (i.e., isolating) polyhydroxyalkanoate from a biological source material containing the polyhydroxyalkanoate, the process comprising centrifugal fractionation of the biological source material such that the polyhydroxyalkanoate is partitioned from the other components of the biological source material by solid-solid separation.
PHA components found in biological systems (e.g., conventional, or genetically engineered bacteria or genetically engineered plants) tend to settle at rates different from other cellular components such as proteins and carbohydrates when they are suspended in a common fluid medium. The difference in the sedimentation rate results in the spatial segregation of mixed particulates into multiple layers (fractionation) each containing predominantly a single component.
According to the Stokes' law of sedimentation, there are two major factors affecting the sedimentation rates of particles: differences in the density and size of suspended particles. These factors independently control the separation efficiency of the fractionation process.
Density is an intrinsic property of the material to be separated.
Generally, there is no easy way of manipulating the density of an individual component to be fractionated. The density difference between particles in a composition is not always large enough to achieve substantial fractionation of one component from the rest. When the densities of the components are sufficiently different, a high degree of separation can be achieved, particularly when a suspending medium having an intermediate density is used. The density of PHA is sufficiently different from other biomass components, such as proteins and carbohydrates, to achieve some degree of fractionation.
Differences in particle size also contribute greatly to the effectiveness of the fractionation process. PHA is generally stored in biological systems in the form of very fine granules having a diameter of about or below 1 ~.. The particle size of PHA granules are therefore much smaller as compared to other cellular components from the disrupted cell. In addition, particle size can be further manipulated by a post-harvest processing which includes grinding or colloid-milling. Specific types of biological source material and the process are discussed in more detail below.
Biological Source Material Sources from which PHA is recovered via the process of the present invention include single-cell organisms such as bacteria or fungi and higher organisms such as plants (herein collectively referred to as "biological source material" or "BSM"). While such BSM could be wild-type organisms, they are preferably genetically manipulated species specifically designed for the production of a specific PHA of interest to the grower. Such genetically manipulated organisms are produced by incorporating the genetic information necessary to produce PHA. Typically, such genetic information is derived from bacteria which naturally produce PHA.
Plants useful in the present invention include any genetically engineered plant designed to produce PHA. Preferred plants include agricultural crops such cereal grains, oil seeds and tuber plants; more preferably, avocado, barley, beets, broad bean, buckwheat, carrot, coconut, copra, corn (maize), cottonseed, gourd, lentils, lima bean, millet, mung bean, oat, oilpalm, peas, peanut, potato, pumpkin, rapeseed (e.g., canola), rice, sorghum, soybean, sugarbeet, sugar cane, sunflower, sweetpotato, tobacco, wheat, and yam. Such genetically altered fruit-bearing plants useful in the process of the present invention include, but are not limited to apple, apricot, banana, cantaloupe, cherries, grapes, kumquat, lemon, lime, orange, papaya, peaches, pear, pineapple, tangerines, tomato, and watermelon. Preferably the plants are genetically engineered to produced PHA pursuant to the methods disclosed in Poirier, Y., D.E. Dennis, K.
Klomparens and C. Somerville, "Polyhydroxybutyrate, a biodegradable thermoplastic, produced in transgenic plants", SCIENCE, Vol. 256, pp. 520-523 (1992); WO Patent No. 95/05472 and WO Patent No. 93/02187.
Particularly preferred plants are soybean, potato, corn and coconut plants genetically engineered to produce PHA.
Bacteria useful in the present invention include any genetically engineered bacteria designed to produce PHA, as well as bacteria which naturally produce PHA. Examples of such bacteria include those disclosed In NOVEL BIODEGRADABLE MICROBIAL POLYMERS, E.A. DaweS, ed., NATO ASI
Series, Series E: Applied Sciences - Vol. 186, Kluwer Academic Publishers (1990); US Patent 5,250,430, Peoples and Sinskey, issued October 5, 1993;
US Patent 5,245,023, Peoples and Sinskey, issued September 14, 1993;
US Patent 5,229,279, Peoples and Sinskey, issued JUIy 20, 1993; and US
Patent 5,149,644, Lubitz, issued September 22, 1992.
It is preferable that the BSM contain a sufficient quantity of PHA to make the process economically desirable. Preferably, the initial content of PHA in the source material should be at least about 5% of the total dry weight; more preferably at least about 25%; more preferably at least about 50%; more preferably still, at least about 75%.
Isolation Process The process of the present invention preferably involves the following unit-operation steps: pretreatment, size reduction, suspension, and centrifugal separation. The optimal range of unit operation conditions or individual devices will vary considerably according to the type of raw BSMs used.
The pretreatment of source materials comprising PHA is preferred in order to remove low molecular weight contaminants readily soluble in appropriate solvents, such as sugars, oils and sometimes moisture. A
variety of standard pretreatment methods used for the processing of food crops are known to those skilled in the art and may be readily employed for the pretreatment step of the present invention. Examples of such pretreatment steps include oil extraction (for example, see BAILEY'S
INDUSTRIAL OIL AND FAT PRODUCTS, THIRD ED., Johne Wiley and Sons: New York (1964), pp. 663-713), water washing (for example, see US Patent 2,881,076, Sair, issued April 7, 1959), and alcohol washing (for example, see Eldridge, A.C., W.J. Wolf, A.M. Nash and A.K. Smith, "Alcohol Washing Of Soybean Protein", AGRICULTURAL AND FOOD CHEMISTRY, July-August, 1963, pp. 323-328).
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The pretreated material comprising PHA granules is then pulverized (e.g., dry milling) to small fragments, by first using a common vibratory or hammer mill. The pulverization of source material by dry milling, particularly for agricultural crop plants comprising PHA granules, preferably produces grain flour of a particle size finer than about 500 ~ in diameter, more preferably finer than about 300 ~, more preferably still, finer than about 100 The comminuted material is then dispersed in a suspending fluid such as water, chlorinated carbon solvents (e.g., chloroform, carbon tetrachloride, or dichlorethane), various organic solvents (e.g., ethanol, methanol, acetone, methyl ethyl ketone, ethyl acetate, hexane, heptane, pentane, or mixtures thereof), or supercritical fluids (e.g., carbon dioxide or nitrous oxide); preferably water. If the suspending fluid is water, the water is preferably heated to promote hydration of certain non-PHA components prior to the wet milling to a temperature preferably not exceeding 90°C. If a suspending medium having an intermediate density between the PHA and other biomass is desired, then the suspending medium is preferably an aqueous solution of an organic or inorganic salt, or an aqueous solution of a water-soluble sugar. Useful organic salts include, but are not limited to, potassium glycolate, potassium citrate, potassium lactate, potassium malate, and dipotassium tartrate. Useful inorganic salts include, but are not limited to, sodium chloride, potassium chloride, calcium chloride, magnesium chloride, and calcium sulfate. Useful water-soluble sugars include, but are not limited to, sucrose, glucose, and raffinose.
The material is further treated by wet milling using a device such as a colloid mill, sonicator, or homoginizer, to obtain the desired particle size distribution for the dispersed solids. For wet milling, the comminuted material is suspended in a fluid. Preferred fluids include, but are not limited to water; ethanol; and aqueous solutions of organic salts, inorganic salts or sugars. The wet milling should preferably produce suspensions having an average particle size of smaller than about 50 ~.
The suspension mixture of PHA and other biomass components is then processed with a centrifugal device to fractionate PHA-rich particles from the other biomass. Preferred centrifugal devices include, but are not limited to, centrifuge, ultracentrifuge, or hydrocyclone separator. An industrial scale centrifugal separation device may be used in the process of the present invention for fractionation of the PHA, so long as the device provides sufficient "G" force (i.e., sedimentational force field created, for WO 95/33065 2191 ~ ~ ~ PCT/US95106651 example, by centrifugal effect expressed in terms of the equivalent to gravitational force) to achieve the sedimentation of solid particles above the rate necessary to overcome the Brownian motion of particles to be settled.
The centrifugal force field employed in the process of the present invention is preferably at least about 10 G (i.e., ten times faster than simple gravimetric settling) to achieve rapid and efficient fractionation of PHA from other biomass components. More preferably, the centrifugal force field is at least about 100 G, more preferably at least about 1,000 G, more preferably at least about 10,000 G, more preferably still at least about 100,000 G.
In one embodiment of the present invention, a hydrocyclone is employed as the centrifugal device. A hydrocyclone consists of a conical cavity with an eccentric inlet port and two exit ports above and below the conical cavity. The vortex flow created by the off-centered high-speed injection of fluid creates a centrifugal force resulting in the sedimentation of heavy particles toward the inner wall of the conical cavity. The heavier portion will exit predominantly from the smaller tip of the cone, while the lighter portion will exit from the wider part of the cone. The centrifugal force field increases in a hydrocyclone with the inlet feed rate and decreases with the diameter of the conical cavity. For example, in a typical 1 cm diameter hydrocyclone, it is possible to achieve well above 100 G of centrifugal force by maintaining the feed rate of suspension above several tens of gallons per minute. (See, for example, Day, R.W., "Hydrocyclones in Process and Pollution Control", CHEMICAL ENGINEERING PROGRESS, Vol. 69, pp. 67-72 (1973); and US Patent 2,754,968, Vegter and Hage, issued July 17, 1956;
and KIRK-OTHMER ENCYCLOPEDIA OF CHEMICAL TECHNOLOGY, THIRD ED., Vol.
12, pp. 1-29, John Wiley and Sons, (1990)). Hydrocyclones useful in the present invention are available from a variety of manufactureres including Dorr-Oliver, Inc. (Milford, CT), Yardney Water Management Systems, Inc.
(Riverside, CA), and Quality Solids Separation Co. (Houston, TX).
In another embodiment of the present invention, a continuous centrifuge may be employed as the centrifugal device. A continuous centrifuge comprises a rapidly rotating cylinder having a feed suspension flowing inside the cylinder. As a result of the rotation, centrifugal force is created thereby promoting sedimentation of heavier components toward the inner wall of the rotating cylinder. The sedimentate is continuously collected by a scraping mechanism while the supernatant is removed as effluent. A typical industrial scale centrifuge operating at several thousand rpm can easily produce a centrifugal force well above 100 G. (See, for .. 2191713 example, Ambler, C.M., "The Evaluation of Centrifuge Performance", CHEMICAL ENGINEERING PROGRESS, VOI. 48, pp. 150-158, (1952); and KIRK-OTHMER ENCYCLOPEDIA OF CHEMICAL TECHNOLOGY, THIRD ED., VOI. 12, pp. 1-29, John Wiley and Sons, (1990)). Centrifuges useful in the present invention are available from a variety of manufacturers, including Humboldt Decanter, Inc. (Atlanta, GA), Western States Machine Co. (Hamilton, OH), and Bird Machine Co. (South Walpole, MA).
Preferably, the process of the present invention yields at least about 70% of the PHA in the source material, more preferably at least about 80%, more preferably still at least about 90%.
Preferably, at least about 85% of the dry mass of the PHA-rich fraction isolated by the process of the present invention is PHA, more preferably at least about 95%, more preferably still at least about 99%.
The PHAs recovered by the process of this invention are useful for forming a variety of plastic articles, including those disclosed in Canadian Patent Application S.N. 2,181,791; Canadian Patent Application S.N.
2,181,796 and Canadian Patent Application S.N. 2,181,795. Such plastic articles include, but are not limited to, films, sheets, foams, fibers, nonwovens, elastomers, adhesive and molded articles. Such plastic articles can be further incorporated into a variey of useful products including, but not limited to, personal cleansing wipes; disposable health care products such as bandages, wound dressings, wound cleansing pads, surgical gowns, surgical covers, surgical pads; other institutional and health care disposables such as gowns, wipes, pads, bedding items such as sheets and pillowcases, foam mattress pads.
The following non-limiting examples illustrate the methods of the present invention.
Isolation of POly~3-hKdroxybutyrate-co-3-hydroxyoctanoate) from Soybeans Soybeans, from a genetically altered soybean plant, comprising poly(3-hydroxybutyrate-co-hydroxyoctanoate) are roll milled to form thin flakes. The low molecular weight lipids and oils contained in the flakes are initially removed by pressing the flakes. The remaining low molecular lipids and oils are subsequently extracted from the flakes by using hexane as a solvent. The resulting defatted soybean flakes are dried and pulverized using a vibratory energy mill (Sweco*, Florence, KY) to produce a flour having an average particle size of less than 80 p. The flour is then hydrated * Trademark A
in water at 65°C for 30 minutes to produce a suspension containing 7%
solids by weight. The suspension is then passed through a colloid mill (Littleford Day, Florence, KY) once to assure complete mixing. The suspension is then passed through a homogenizer (Model 3M, APV Gaulin, Willimington, MA) operated at 8,000 psi, two times, to produce a suspension mixture consisting of fine granules of polymer having an average particle size of less than 1 ~ and other soybean biomass debris comprising proteins and carbohydrates. The homogenized suspension of soybeans is fed to a hydrocyclone (DOXIE *TYPE-A, Dorr-Oliver, Milford, CT) with a heavy duty pump (Model 4678-10S, Northern Pump, Minneapolis, MN) at a feed rate of 150 g/sec under a nominal pressure of 3 MPa.
The effluent stream coming out the top section of the hydrocyclone contains most of the polymer granules. This portion of the suspension is spray dried and washed with 40% water / 60% ethanol mixture to remove soluble residual components such as sugars, to produce a cake of poly(3-hydroxybutyrate-co-hydroxyoctanoate) granules with a purity of greater than 95%, and a yield of about 85% with respect to the starting material.
Isolation of Poly(3-hydroxybutyrate-co-hydroxyhexanoate) from Maize Grains of maize (corn), from a genetically altered maize plant, comprising poly(3-hydroxybutyrate-co-3-hydroxyhexanoate are hammer milled to form meals.
The low molecular weight lipids and oils contained in the meals are removed first by pressing the flakes and are then further extracted by using hexane as the solvent and washed with 40% water / 60% ethanol mixture to remove other soluble components such as sugars. The resulting defatted and desugared maize meals are dried and comminuted using a vibratory energy mill (Sweco, Florence, KY) to produce a flour having an average particle size of less than 80 ~,. The flour is then hydrated in water at 65°C for 30 min to produce a suspension containing 7% solids by weight. The suspension is then passed through a colloid mill (Littleford Day, Florence, KY) once to assure complete mixing. The suspension is then passed twice through a homogenizer (Model 3M, Gaulin, Willmington, MA) operated at 8,000 psi to produce a suspension mixture consisting of fine granules of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate having an average particle size of less than 1 ~ and other maize biomass debris comprising proteins and carbohydrates.
The homogenized suspension of soybeans is fed to a continuous centrifuge (6"
Solid Bowl Centrifuge, Bird Machine Co., South Walpole, MA) at a feed rate of 1,500 g/min. The * Trademark _..,~.,.
,-~._.
supernatant effluent stream coming out the continuous centrifuge is spray dried to produce a cake of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate granules with a purity higher than 98%, and a yield of about 85% with respect to the starting material.
Isolation of Polv(3-hvdroxvbutvrate-3-hvdroxvvalerate) from Tobacco Tobacco leaves, from a genetically altered tobacco plant, comprising poly(3-hydroxybutyrate-co-3-hydroxyvalerate) are hammer milled to form a flour. The low molecular weight soluble components contained in the flakes are removed by washing first with hexane and then with a 40% water / 60%
ethanol mixture to produce a dry flour having an average particle size of less than 80 ~. The flour is then hydrated in water at 65 °C for 30 min to produce a suspension containing 7% solids by weight. The suspension is then passed through a colloid mill (Littleford Day, Florence, KY) once to assure complete mixing. The suspension is then passed twice through a homogenizer (Model 3M, Gaulin, Wilmington, MA) operated at 8,000 psi to produce a suspension mixture consisting of fine granules of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) having an average particle size of less than 1 a and other tobacco biomass debris. The homogenized suspension of tobacco is fed to a continuous centrifuge (6" Solid Bowl Centrifuge, Bird Machine Co., South Walpole, MA) at a feed rate of 1,500 g/min. The supernatant effluent stream coming out the continuous centrifuge is spray dried to produce a cake of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) granules with a purity higher than 95%, and a yield of about 85% with respect to the starting material.
Isolation of Polv(3-hvdroxvbutvrate-co-3-hvdroxvdecanoate) from Coconuts Coconuts, from a genetically altered coconut tree, comprising poly(3-hydroxybutyrate-co-3-hydroxydecanoate) are shredded to form thin flakes.
The low molecular weight lipids and oils contained in the flakes are extracted by using hexane as a solvent. Soluble sugars are also removed by using a 40% water / 60% ethanol mixture. The resulting defatted and desugared coconut flakes are dried and pulverized using a vibratory energy mill (Sweco, Florence, KY) to produce a flour having an average particle size of less than 80 ~. The flour is then hydrated in water at 65°C for min to produce a suspension containing 7°~ solids by weight. The suspension is then passed through a colloid mill (Littleford Day, Florence, KY) once to assure complete mixing. The suspension is then passed twice WO 95/33065 2191713 pCT/LTS95106651 through a homogenizer (Model 3M, Gaulin, Wilmington, MA) operated at 8,000 psi to produce a suspension mixture consisting of fine granules of poly(3-hydroxybutyrate-co-3-hydroxydecanoate) having an average particle size of less than 1 ~ and other coconut biomass debris. The homogenized suspension of coconuts is fed to a hydrocyclone (Doxie Type-A, Dorr-Oliver, Milford, CT) with a heavy duty pump (Model 4678-10S, Northern Pump, Minneapolis, MN) at a feed rate of 200 g/sec under a nominal pressure of 4 MPa. The effluent stream coming out the top section of the hydrocyclone will contain most of the poly(3-hydroxybutyrate-co-3-hydroxydecanoate) granules. This portion of the suspension is spray dried to produce a cake of poly(3-hydroxybutyrate-co-3-hydroxydecanoate) granules with a purity higher than 95%, and a yield of about 85% with respect to the starting material.
Isolation of Polv(3-hvdroxvbutvrate-co-3-hydroxyheptanoate) from Potatoes Potato flakes, from potatoes obtained from a genetically altered potato plant, comprising poly(3-hydroxybutyrate-co-3-hydroxyheptanoate) are washed with water and then hydrated at 65°C for 30 min to produce a suspension containing 7% solids by weight. The suspension is then passed through a colloid mill (Littleford, Day, Florence, KY]) once to assure complete mixing. The suspension is then passed twice through a homogenizer (Model 3M, Gaulin, Wilmington, MA) operated at 8,000 psi to produce a suspension mixture consisting of fine granules of poly(3-hydroxybutyrate-co-3-hydroxyheptanoate) having an average particle size of less than 1 p and other potato biomass debris. The homogenized suspension of potato is fed to a continuous centrifuge (6" Solid Bowl Centrifuge, Bird Machine Co., South Walpole, MA) at a feed rate of 1,500 g/min. The supernatant effluent stream coming out of the continuous centrifuge is spray dried to produce a cake of poly(3-hydroxybutyrate-co-3-hydroxyheptanoate) granules with a purity higher than 95%, and a yield of about 85% with respect to the starting material.
Isolation of Poly(3-hvdroxybutyrate) from A. eutrophus A culture of A. eutrophus which naturally produces poly(3-hydroxybutyrate) is treated with an ultrasonic sonicator (Branson Ultrasonics Corp., Danbury, CT) to produce a suspension mixture consisting of fine granules of poly(3-hydroxybutyrate) having an average particle size of less than 1 ~ and other bacterial biomass debris containing about 20%
solids by weight. The homogenized suspension of bacterial components is fed to a hydrocyclone (Doxie type-A, Dorr-Oliver, Milford, CT) with a heavy duty pump pressure of 4 MPa. The effluent stream coming out the top section of the hydrocyclone contains most of the poly(3-hydroxybutyrate) granules. This portion of the suspension is spray dried to produce a cake of poly(3-hydroxybutyrate) granules with a purity higher than 95%, and a yield of about 90% with respect to the starting material.
Isolation of Poly(3-hydroxybutyrate) from E. coli A culture of E. coli which has been genetically manipulated to produce poly(3-hydroxybutyrate) is treated with an ultrasonic sonicator (Branson Ultrasonics Corp., Danbury, CT) to produce a suspension mixture consisting of fine granules of poly(3-hydroxybutyrate) having an average particle size of less than 1 ~, an other bacterial biomass debris containing about 5% solids by weight. The homogenized suspension of bacterial components is fed to a hydrocyclone (Doxie type-A, Dorr-Oliver, Milford, CT) with a heavy duty pump pressure of 4 MPa. The effluent stream coming out the top section of the hydrocyclone contains most of the poly(3-hydroxybutyrate) granules. This portion of the suspension is spray dried to produce a cake of poly(3-hydroxybutyrate) granules with a purity higher than 95%, and a yield of about 90% with respect to the starting material.
It is understood that the examples and embodiments described herein are for illustrative purposes only and that various modifications or changes in light thereof will be suggested to one skilled in the art and are to be included in the spirit and purview of this application and scope of the appended claims.
Claims (21)
1. A process for recovering polyhydroxyalkanoate from a biological source material containing the polyhydroxyalkanoate, the process comprising:
(a) comminuting the biological source material;
(b) suspending the comminuted biological source material in a fluid; and (c) partitioning the polyhydroxyalkanoate from the other components of the biological source material by centrifugal fractionation to form a solid-solid separation; and (d) recovering the polyhdroxyalkanoate.
(a) comminuting the biological source material;
(b) suspending the comminuted biological source material in a fluid; and (c) partitioning the polyhydroxyalkanoate from the other components of the biological source material by centrifugal fractionation to form a solid-solid separation; and (d) recovering the polyhdroxyalkanoate.
2. The process of Claim 1, wherein the biological source material is plant material.
3. The process of Claim 2, wherein the biological source material is avocado, barley, beets, broad bean, buckwheat, carrot, coconut, copra, corn, cottonseed, gourd, lentils, lima bean, millet, mung bean, oat, oilpalm, peas, peanut, potato, pumpkin, rapeseed, rice, sorghum, soybean, sugarbeet, sugar cane, sunflower, sweetpotato, tobacco, wheat, yam, apple, apricot, banana, cantaloupe, cherries, grapes, kumquat, lemon, lime, orange, papaya, peaches, pear, pineapple, tangerines, tomato, or watermelon.
4. The process of Claim 3, wherein the biological source material is soybean.
5. The process of Claim 3, wherein the biological source material is corn.
6. The process of Claim 3, wherein the biological source material is potato.
7. The process of Claim 2, wherein the centrifugal fractionation is carried out by a hydrocyclone.
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8. The process of Claim 2, wherein the centrifugal fractionation is carried out by centrifugation.
9. A polyhydroxyalkanoate of high yield and purity suitable for large scale production of plastic articles, as recovered by the process of Claim 2.
10. A polyhydroxyalkanoate of high yield and purity suitable for large scale production of plastic articles, as recovered by the process of Claim 3.
11. A polyhydroxyalkanoate of high yield and purity suitable for large scale production of plastic articles, as recovered by the process of Claim 4.
12. The polyhydroxyalkanoate of high yield and purity suitable for large scale production of plastic articles, as recovered by the process of Claim 5.
13. A polyhydroxyalkanoate of high yield and purity suitable for large scale production of plastic articles, as recovered by the process of Claim 6.
14. A polyhydroxyalkanoate of high yield and purity suitable for large scale production of plastic articles, as recovered by the process of Claim 7.
15. A polyhydroxyalkanoate of high yield and purity suitable for large scale production of plastic articles, as recovered by the process of Claim 8.
16. The process of Claim 1, wherein the biological source material is bacteria.
17. The process of Claim 16, wherein the centrifugal fractionation is carried out by a hydrocyclone.
18. The process of Claim 16, wherein the centrifugal fractionation is carried out by centrifugation.
19. A polyhydroxyalkanoate of high yield and purity suitable for large scale production of plastic articles, as recovered by the process of Claim 16.
20. A polyhydroxyalkanoate of high yield and purity suitable for large scale production of plastic articles, as recovered by the process of Claim 17.
21. A polyhydroxyalkanoate of high yield and purity suitable for large scale production of plastic articles, as recovered by the process of Claim 18.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25182894A | 1994-06-01 | 1994-06-01 | |
| US08/251,828 | 1994-06-01 | ||
| PCT/US1995/006651 WO1995033065A1 (en) | 1994-06-01 | 1995-05-25 | Process for recovering polyhydroxyalkanoates using centrifugal fractionation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2191713A1 CA2191713A1 (en) | 1995-12-07 |
| CA2191713C true CA2191713C (en) | 2000-08-29 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002191713A Expired - Fee Related CA2191713C (en) | 1994-06-01 | 1995-05-25 | Process for recovering polyhydroxyalkanoates using centrifugal fractionation |
Country Status (18)
| Country | Link |
|---|---|
| US (2) | US5918747A (en) |
| EP (1) | EP0763126B1 (en) |
| JP (1) | JPH10501134A (en) |
| CN (1) | CN1071379C (en) |
| AT (1) | ATE182363T1 (en) |
| AU (1) | AU701964B2 (en) |
| BR (1) | BR9507830A (en) |
| CA (1) | CA2191713C (en) |
| DE (1) | DE69510937T2 (en) |
| DK (1) | DK0763126T3 (en) |
| ES (1) | ES2133780T3 (en) |
| FI (1) | FI114217B (en) |
| GR (1) | GR3030840T3 (en) |
| HK (1) | HK1013112A1 (en) |
| HU (1) | HU9603303D0 (en) |
| MX (1) | MX9605952A (en) |
| TW (1) | TW273521B (en) |
| WO (1) | WO1995033065A1 (en) |
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| DE19633475C2 (en) * | 1996-08-20 | 2002-03-14 | Buna Sow Leuna Olefinverb Gmbh | Process for the production of polyhydroxyalkanoates and their use |
| US6087471A (en) * | 1997-04-15 | 2000-07-11 | Monsanto Company | High temperature PHA extraction using PHA-poor solvents |
| US6043063A (en) * | 1997-04-15 | 2000-03-28 | Monsanto Company | Methods of PHA extraction and recovery using non-halogenated solvents |
| EP1044278A1 (en) * | 1998-01-05 | 2000-10-18 | Monsanto Company | Biosynthesis of medium chain length polyhydroxyalkanoates |
| CN1070534C (en) * | 1998-01-23 | 2001-09-05 | 清华大学 | Method for separating and refining polyhydroxy fatty acid ester in bacteria cell from bacteria |
| US6485775B1 (en) * | 1998-10-16 | 2002-11-26 | Basic American, Inc. | Starchy food-based fine particle fat substitute |
| ATE337743T1 (en) | 2000-06-09 | 2006-09-15 | Procter & Gamble | GLOVE CONTAINING POLYHYDROXYALKANOATES |
| US7335390B2 (en) * | 2003-03-06 | 2008-02-26 | Microsoy Corporation | Composition containing soybean flakes and potato flakes, method for making a food product therefrom, and said food product |
| AU2004293501B2 (en) * | 2003-11-28 | 2009-10-29 | Phb Industrial S.A. | Process for recovering polyhydroxialkanoates ("PHAs") from cellular biomass |
| US7582456B2 (en) | 2003-12-19 | 2009-09-01 | Tianan Biologic Material Co., Ltd. Ningbo | Method for separating, extracting and purifying poly-β-hydroxyalkanoates (PHAs) directly from bacterial fermentation broth |
| US7301000B2 (en) | 2004-09-15 | 2007-11-27 | The Procter & Gamble Company | Nucleating agents for polyhydroxyalkanoates |
| CN101300354A (en) * | 2005-09-08 | 2008-11-05 | 梅雷迪安公司 | Deregulated bacteria with improved polyhydroxyalkanoate production |
| US8076504B2 (en) * | 2007-12-31 | 2011-12-13 | The University Of North Dakota | Method for production of short chain carboxylic acids and esters from biomass and product of same |
| CN102115994B (en) * | 2010-01-06 | 2012-08-29 | 安琪酵母股份有限公司 | Method for treating lignocellulose raw material |
| SG11201903508XA (en) | 2016-10-18 | 2019-05-30 | Meredian Bioplastics Inc | Crystal nucleating agents for polyhydroxyalkanoates |
| US11584110B2 (en) | 2020-07-30 | 2023-02-21 | Pepsico, Inc. | Multi-layered packaging films |
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| US3036959A (en) * | 1960-09-26 | 1962-05-29 | Grace W R & Co | Process for preparing poly-beta-hydroxy-butyric acid |
| US3275610A (en) * | 1964-03-24 | 1966-09-27 | Mobil Oil Corp | Microbial synthesis of polymers |
| US3895003A (en) * | 1971-06-25 | 1975-07-15 | Procter & Gamble | Process for producing protein concentrate using air classification |
| US3828017A (en) * | 1973-03-16 | 1974-08-06 | Us Agriculture | Process for isolating proteins using liquid fluorocarbons and low density hydrocarbon solvents |
| US3869438A (en) * | 1973-03-16 | 1975-03-04 | Us Agriculture | Process for isolating oil-seed proteins using liquid fluorocarbons |
| GB1561856A (en) * | 1977-01-24 | 1980-03-05 | Pfeifer & Langen | Method of preparing refined starch hydrolysates mainlyconsisting of monosaccharides disaccharides and higher saccharides from starch-containing cereals |
| US4146534A (en) * | 1977-04-14 | 1979-03-27 | Ralston Purina Company | Liquid cyclone process |
| US4175075A (en) * | 1978-07-07 | 1979-11-20 | The Procter & Gamble Company | Isolation of protein from vegetable seeds |
| US4174315A (en) * | 1978-07-07 | 1979-11-13 | The Procter & Gamble Company | Isolation of protein from vegetable seed material |
| US4174314A (en) * | 1978-07-07 | 1979-11-13 | The Procter & Gamble Company | Density fractionation process to recover vegetable seed proteins |
| US4215040A (en) * | 1978-12-22 | 1980-07-29 | The Procter & Gamble Company | Density separation process |
| EP0015123B1 (en) * | 1979-02-21 | 1982-12-22 | Imperial Chemical Industries Plc | A process for the extraction of poly-3-hydroxy-butyric acid from microbial cells |
| EP0046335A3 (en) * | 1980-08-18 | 1982-03-10 | Imperial Chemical Industries Plc | Extraction of poly(beta-hydroxybutyric acid) |
| CN1016177B (en) * | 1988-11-05 | 1992-04-08 | 化学工业部晨光化工研究院一分院 | Method for preparation of heat-resistant highly polymerized hydroxy-benzoic acid polyester |
| CA1334430C (en) * | 1989-04-06 | 1995-02-14 | Claude Chavarie | Separation of poly-.beta.-hydroxyalkanoic acids from microbial biomass |
| US5334520A (en) * | 1990-05-25 | 1994-08-02 | Center For Innovative Technology | Production of poly-beta-hydroxybutyrate in transformed escherichia coli |
| CA2062816C (en) * | 1989-07-10 | 2006-09-12 | Oliver P. Peoples | Method for producing novel polyester biopolymers |
| WO1991013207A1 (en) * | 1990-02-21 | 1991-09-05 | Pulp And Paper Research Institute Of Canada | POLY-β-HYDROXYALKANOATES FOR USE IN FIBRE CONSTRUCTS AND FILMS |
| US5451456A (en) * | 1990-02-21 | 1995-09-19 | Pulp And Paper Research Institute Of Canada | Latex of poly-β-hydroxyalkanoates for treating fiber constructs and coating paper |
| GB9108756D0 (en) * | 1991-04-24 | 1991-06-12 | Ici Plc | Production of polyalkanoate in plants |
| JP2777757B2 (en) * | 1991-09-17 | 1998-07-23 | 鐘淵化学工業株式会社 | Copolymer and method for producing the same |
| US5281691A (en) * | 1992-06-19 | 1994-01-25 | Eastman Kodak Company | Poly(3-hydroxyalkanoates) |
| ES2062955B1 (en) * | 1993-04-29 | 1995-06-16 | Repsol Quimica Sa | PROCEDURE FOR THE EXTRACTION OF POLYHYDROXYALKANOATES FROM HALOPHILIC BACTERIA THAT CONTAIN IT. |
-
1995
- 1995-05-25 HU HU9603303A patent/HU9603303D0/en unknown
- 1995-05-25 DE DE69510937T patent/DE69510937T2/en not_active Expired - Fee Related
- 1995-05-25 CA CA002191713A patent/CA2191713C/en not_active Expired - Fee Related
- 1995-05-25 WO PCT/US1995/006651 patent/WO1995033065A1/en active IP Right Grant
- 1995-05-25 JP JP8501043A patent/JPH10501134A/en active Pending
- 1995-05-25 ES ES95921415T patent/ES2133780T3/en not_active Expired - Lifetime
- 1995-05-25 AU AU26500/95A patent/AU701964B2/en not_active Ceased
- 1995-05-25 EP EP95921415A patent/EP0763126B1/en not_active Expired - Lifetime
- 1995-05-25 MX MX9605952A patent/MX9605952A/en unknown
- 1995-05-25 BR BR9507830A patent/BR9507830A/en not_active IP Right Cessation
- 1995-05-25 CN CN95193867A patent/CN1071379C/en not_active Expired - Fee Related
- 1995-05-25 AT AT95921415T patent/ATE182363T1/en not_active IP Right Cessation
- 1995-05-25 DK DK95921415T patent/DK0763126T3/en active
- 1995-06-09 TW TW084105894A patent/TW273521B/zh active
-
1996
- 1996-11-29 FI FI964785A patent/FI114217B/en not_active IP Right Cessation
-
1997
- 1997-07-13 US US08/910,869 patent/US5918747A/en not_active Expired - Fee Related
- 1997-08-19 US US08/915,307 patent/US5899339A/en not_active Expired - Fee Related
-
1998
- 1998-12-21 HK HK98114433A patent/HK1013112A1/en not_active IP Right Cessation
-
1999
- 1999-07-22 GR GR990401694T patent/GR3030840T3/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FI964785A0 (en) | 1996-11-29 |
| EP0763126A1 (en) | 1997-03-19 |
| AU2650095A (en) | 1995-12-21 |
| GR3030840T3 (en) | 1999-11-30 |
| US5899339A (en) | 1999-05-04 |
| ATE182363T1 (en) | 1999-08-15 |
| HK1013112A1 (en) | 1999-08-13 |
| ES2133780T3 (en) | 1999-09-16 |
| CN1152943A (en) | 1997-06-25 |
| FI114217B (en) | 2004-09-15 |
| DK0763126T3 (en) | 1999-11-29 |
| JPH10501134A (en) | 1998-02-03 |
| BR9507830A (en) | 1997-09-16 |
| TW273521B (en) | 1996-04-01 |
| MX9605952A (en) | 1997-12-31 |
| FI964785A (en) | 1997-01-29 |
| CN1071379C (en) | 2001-09-19 |
| US5918747A (en) | 1999-07-06 |
| HU9603303D0 (en) | 1997-01-28 |
| CA2191713A1 (en) | 1995-12-07 |
| AU701964B2 (en) | 1999-02-11 |
| DE69510937T2 (en) | 2000-02-17 |
| DE69510937D1 (en) | 1999-08-26 |
| WO1995033065A1 (en) | 1995-12-07 |
| EP0763126B1 (en) | 1999-07-21 |
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