Methods and compositions for degradation of nitroaromatic and nitramine pollutants
The invention relates to novel Methylobacterium species that are capable of degrading nitroaromatic and nitramine compounds. Compositions, kits and methods of using the Methylobacterium species for the degradation of nitroaromatic and nitramine pollutants are provided. More specifically, compositions and methods for the degradation or bioremediation of nitroaromatic and nitramine explosives and explosive residues are provided.
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This application is a divisional patent application of U.S. patent application Ser. No. 10/873,659, filed Jun. 22, 2004, which claims the priority of U.S. provisional patent application No. 60/483,736, filed Jun. 30, 2003, the entirety of which is incorporated herein by reference.
BACKGROUND OF THE INVENTION Nitroaromatic and nitramine compounds comprise a class of pollutants known to have both toxic and carcinogenic properties. Nitroaromatic and nitramine pollutants are frequently generated in the production of explosives, such as TNT (2,4,6-trinotrotoluene), RDX (Royal demolition explosive; hexahydro-1,3,5-trinitro-1,3,5-triazine) and HMX (High melting point explosive; octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine) (see
First synthesized in 1863, TNT was used in the dye industry before becoming in the 20th century the main conventional explosive used worldwide. However, because of a higher stability and detonation power, nitramines HMX and RDX are at the present time the most widespread conventional explosives. Manufacture of nitro-substituted explosives, testing and firing ranges, and destruction of ammunition stocks have generated toxic wastes leading to large-scale contamination of soils and groundwater (44). Seven nitro-substituted explosives, including TNT and RDX, have been listed as priority pollutants by the U.S. Environmental Protection Agency (EPA) (25). RDX, formerly used as a rat poison, is in addition considered as possible carcinogen by the EPA (2, 28). HMX has been listed as an EPA contaminant of concern (48). A lifetime health advisory of 2 μg L−1 of TNT in drinking water and a water-quality limit of 105 μg L−1 of RDX have been recommended (7, 37). Physicochemical properties, biodegradation, and toxicity of nitro-substituted explosives have been extensively reviewed in the literature (12, 18, 38, 43, 45, 53).
The toxicity of TNT has been reported since the First World War among English ammunition workers. From laboratory studies TNT, RDX, and HMX have been found to be toxic for most classes of organisms, including bacteria (46, 57), algae (46, 57), plants (35), earthworms (36), aquatic invertebrates (46, 48), animals (22, 42), mammals (28, 48), and humans (3, 22).
Traditional treatments of toxic ammunition wastes (i.e. open burning/open detonation (OB/OD), adsorption onto activated carbon, photooxidation (UV/O3), etc.) are costly, damaging for the environment, and in most cases practically infeasible.
Biotransformation of energetic pollutants TNT, RDX, and HMX have been reported for different classes of organisms, including bacteria, fungi, and plants (12, 18, 29, 33, 38, 41, 53). Metabolism of TNT typically involves a sequential reduction of the nitro groups to form toxic aromatic amino derivatives, which are poorly further transformed (29, 33). Except with white-rot fungi, that secrete powerful ligninolytic peroxidases (8, 54), no significant mineralization has been detected in biological systems (29). In contrast to TNT, whose limiting degradation step is the aromatic ring fission, as soon as nitramines RDX and HMX undergo a change of the molecular structure, the ring collapses to generate small aliphatic metabolites (17, 53). While other decomposition mechanisms have been reported (i.e. concerted decomposition, bimolecular elimination, or hydrolysis (17)), biotransformation of RDX and HMX frequently involves an initial reduction of the nitro groups to form nitroso and hydroxylamino derivatives (31). The latter decompose to unstable aliphatic nitramines, eventually converted into N2O and CO2 (17,18). Due to different conformations, HMX (crown-type) is chemically more stable and therefore less amenable to biodegradation than RDX (chair-type) (17).
Bacteria of the genus Methylobacterium are strictly aerobic, facultative methylotrophic, Gram-negative, rod-shaped bacteria that are able to grow on one-carbon compounds, i.e. methanol or methylamine (13, 30, 51). Members of the genus Methylobacterium, which belongs to the α-2 subclass of Proteobacteria, are distributed in a wide diversity of natural and human-made habitats, including soils, air, dust, fresh water, aquatic sediments, marine environments, water supplies, bathrooms, and masonry (19, 51). Some species have been described as opportunistic human pathogens (51). In addition, methylotrophic bacteria colonize the roots and the leaves of terrestrial and aquatic plant species (21, 34, 51). These bacteria are often red to pink due to the presence of carotenoids and referred as pink-pigmented facultative methylotrophs (PPFMs). Methylobacterium bacteria are highly resistant to dehydration, freezing, chlorination, UV light, ionizing radiations, and elevated temperatures (51).
SUMMARY OF THE INVENTIONThe invention provides novel strains of Methylobacterium species and methods for using them and other species of the genus Methylobacterium. These bacteria are shown herein to have the capacity to degrade nitroaromatic and nitramine compounds, including, for example the explosives TNT, HMX and RDX and their derivatives. The capacity of the newly identified bacteria to degrade such nitroaromatic and nitramine compounds provides new methods for the decontamination of environmental materials containing such compounds. Degradation of nitroaromatic and nitramine compounds is generally accomplished by contacting the bacteria with the compounds. The contacting can be performed in the environment, or in isolation using materials, e.g., soil, sediment or wastewater removed from the environment.
The invention also provides compositions, preparations and kits comprising the new Methylobacterium species and methods of making them.
In one aspect, the invention encompasses a method for degrading a nitroaromatic or nitramine compound (or compounds), the method comprising contacting the compound with an isolated bacterium having all identifying characteristics of the Methylobacterium species, strain BJ001 having ATCC Accession No. PTA-5125 and NCIMB Accession No. 13946, whereby the concentration of the compound is reduced and one or more degradation products is produced.
In one embodiment, the compound is an explosive or high energy compound.
In another embodiment, the compound is selected from the group consisting of TNT, RDX and HMX.
In another embodiment, the degradation products of the degrading have reduced toxicity relative to the toxicity of the nitroaromatic or nitramine compound or compounds degraded.
In another embodiment, the compound is substantially mineralized to CO2 and H2O by the method.
In another embodiment, the contacting comprises distributing a composition comprising said bacterium over an area in which one seeks to degrade such a compound or a mixture of such compounds.
In another embodiment, the composition comprising the bacterium is distributed over an area of soil, fresh water or sediment contaminated by such a compound or a mixture of such compounds.
In another embodiment, the contacting comprises combining a composition comprising such a bacterium with soil, water or sediment obtained from a site contaminated with such a compound or a mixture of such compounds.
In another embodiment, the contacting comprises combining a preparation comprising an isolated bacterium having all identifying characteristics of the Methylobacterium sp. BJ001 having ATCC Accession No. PTA-5125 and NCIMB Accession No. 13946 with a sample comprising a nitroaromatic or nitramine compound or a mixture of such compounds. In another embodiment, the preparation further comprises one or more additional microorganisms. In another embodiment, the preparation comprises one or more additional species of Methylobacterium. In another embodiment, the sample is a soil sample.
In another embodiment, the preparation further comprises one or more nutrients for the Methylobacterium.
In another embodiment, the method comprises the addition of one or more soil amendments to a soil sample. The one or more soil amendments can comprise a material, such as manure, wood chips or sawdust, potato scraps, apple pomace, and corncobs, among others, or any carbon source suitable to support the growth of Methylobacterium bacteria. Soil amendment materials can be used in varying proportions, depending upon the composition of the soil to be decontaminated and the type of amendment used, from for example a soil to amendment ratio of 1000:1 (w/w), 500:1, 200:1, 100:1, 50:1, 10:1, 5:1, or even 1:1, 1:2, 1:5 or 1:10.
In another aspect, the invention encompasses a method of identifying a Methylobacterium that degrades a nitroaromatic or nitramine compound, the method comprising: contacting tissue from a tree with a sterile preparation of growth medium that supports the growth of Methylobacterium species; incubating the preparation of growth medium under conditions that permit the growth of Methylobacterium species; isolating a pure culture of a Methylobacterium species from the growth medium; and contacting the isolated Methylobacterium species with a nitramine or nitroaromatic compound; and determining whether the nitroaromatic or nitramine compound is degraded, wherein degradation of the nitramine or nitroaromatic compound identifies the Methylobacterium as a species that degrades a nitroaromatic or nitramine compound.
In one embodiment, the tissue is from a Poplar tree.
In another embodiment, the tissue from a tree is a surface-sterilized tissue explant, tissue grown in tissue culture, or a regenerated plantlet.
In another embodiment, the growth medium comprises LB, NA or modified Jayasuriya's medium.
In another aspect, the invention provides an isolated Methylobacterium having the identifying characteristics of the Methylobacterium sp. BJ001 having ATCC Accession No. PTA-5125 and NCIMB Accession No. 13946.
In another aspect, the invention provides an isolated Methylobacterium which is the Methylobacterium sp. BJ001 having ATCC Accession No. PTA-5125 and NCIMB Accession No. 13946.
In another aspect, the invention provides a method of preparing Methylobacterium sp. BJ001 comprising: inoculating a sterile preparation of growth medium that supports the growth of Methylobacterium species with a cell of Methylobacterium sp. BJ001 having the identifying characteristics of ATCC Accession No. PTA-5125 and NCIMB Accession No. 13946; and incubating the preparation of growth medium to produce a preparation of the Methylobacterium sp. BJ001.
In one embodiment, the growth medium comprises Luria Bertani (LB) medium, Nutrient Agar (NA) or modified Jayasuriya's medium.
In another aspect, the invention encompasses a composition comprising an isolated Methylobacterium having all identifying characteristics of the Methylobacterium sp. BJ001 having ATCC Accession No. PTA-5125 and NCIMB Accession No. 13946, and a high energy compound, including, for example, a nitramine or nitroaromatic explosive.
In one embodiment, the nitramine or nitroaromatic explosive is one or more of TNT, RDX and HMX.
In another embodiment, the composition further comprises one or more additional microorganisms. In another embodiment, one or more of such additional microorganisms belong to the genus Methylobacterium.
In another embodiment, the composition further comprises one or more nutrients for the Methylobacterium.
In another aspect, a preparation of Methylobacterium sp. BJ001, having ATCC Accession No. PTA-5125 and NCIMB Accession No. 13946 is provided, the preparation having a concentration of at least 1% (v/v) of the Methylobacterium inoculum. In one embodiment, the preparation has a cell concentration of 1% to about 95% by volume.
In another aspect, there is provided a composition comprising an aqueous slurry of solid material comprising a nitroaromatic or nitramine compound, and a Methylobacterium species having the identifying characteristics of Methylobacterium sp. BJ001 having ATCC Accession No. PTA-5125 and NCIMB Accession No. 13946, the aqueous slurry being 30% solid material (w/w).
In one embodiment, the Methylobacterium species is present at a density of 109 cells/ml or greater.
In another embodiment, the composition has a pH in the range of pH 3.0 to pH 11.0. In another embodiment, the pH is in the range of pH 6.0 to pH 8.0. In another embodiment, the composition is at a temperature of 4° C. to 41° C. In another embodiment, the composition of is at a temperature of 15° C. to 37° C.
In another embodiment, the composition is at an oxygen saturation of 5% to 100%. In another embodiment, the composition is at an oxygen saturation of 20% to 100%.
In another aspect, a preparation is provided comprising viable, dried Methylobacterium sp. BJ001 having ATCC Accession No. PTA-5125 and NCIMB Accession No. 13946.
In one embodiment, the preparation further comprises an additional microbial species. In one embodiment, the additional microbial species comprises a bacterial species belonging to the genus Methylobacterium.
In another embodiment, the preparation further comprises one or more nutrients for the Methylobacterium. Such nutrient(s) aid the bacterium in growth upon recovery from the dried state. Such nutrients include, as non-limiting examples, methanol, ethanol, formate, succinate and fructose.
In another aspect, there is provided a Methylobacterium isolated by the steps of: contacting a Poplar tissue with a sterile preparation of growth medium that supports the growth of Methylobacterium species; and isolating a single red or pink-colored bacterial colony from said preparation.
In one embodiment, the growth medium that supports the growth of Methylobacterium species is LB medium.
In another embodiment, the Methylobacterium degrades a nitroaromatic or nitramine compound.
In another embodiment, the Methylobacterium degrades a high energy compound.
In another embodiment, the Methylobacterium degrades TNT, RDX or HMX.
In another embodiment, the Poplar tissue comprises a tissue explant from a Poplar tree.
In another embodiment, the Poplar tree is Populus deltoides x nigra DN34.
In another embodiment, the Poplar tissue is from tissue culture.
In another embodiment, the Poplar tissue is tissue from a regenerated plantlet.
In another aspect, there is provided a kit for the degradation of a nitramine or nitroaromatic compound, the kit comprising a Methylobacterium having the identifying characteristics of the species having ATCC Accession No. PTA-5125 and NCIMB Accession No. 13946.
Definitions:
As used herein, the term “degrading” refers to the conversion of a nitroaromatic or nitramine compound to a form that has reduced toxicity compared to the starting compound. “Degrading” requires the cleavage of one or more chemical bonds in a nitroaromatic or nitramine target compound. A “degradation product” is a composition resulting from degrading a nitramine or nitroaromatic compound. The term “degradation product” encompasses products ranging from a compound differing from a starting nitramine or nitroaromatic compound by one or more chemical bonds, to a fully mineralized degradation product of such nitramine or nitroaromatic compound. The degradation of nitroaromatic and nitramine compounds can be measured by HPLC and radioactive tracer assays as described herein. Nutrients include, for example, carbon sources (e.g., carbohydrates, methanol, succinate, etc.) minerals, vitamins, nitrogen sources, and phosphorus sources.
As used herein, the term “reduced toxicity” means that the product or products of a degradation process are less toxic to a test organism under conditions in which the compound degraded is toxic to that organism. Toxicity is commonly expressed in terms of the LD50, the dose of a toxin at which 50% of a test organism is killed. Generally, toxicity of a compound is “reduced” relative to a parent compound if the LD50 of the compound is at least 10% higher than the LD50 of the parent compound.
As used herein, the term “reduced concentration” when used in reference to a nitroaromatic or nitramine compound means that the concentration of the compound is reduced by at least 1%, and preferably more, e.g., at least 5%, 10%, 20% or more, up to and including 100% (no compound remaining), relative to the concentration prior to the combination of a sample with a Methylobacterium species as described herein.
As used herein, the term “explosive” refers to a nitroaromatic or nitramine compound that explodes upon application of heat or shock. The term “high energy compound” also refers to a nitroaromatic or nitramine compound that explodes upon application of heat or shock.
As used herein, the term “nitroaromatic” refers to an aromatic hydrocarbon compound containing one or more nitro groups in place of a hydrogen atom or atoms.
As used herein, the term “nitramine” refers to a compound comprising the chemical structure R1R2N—NO2 where R1 and R2 can be any substituent. Preferred nitramines are heterocyclic nitramines, such as RDX and HMX.
As used herein, the term “isolated,” when used in reference to a Methylobacterium strain, means that the bacterium is not physically associated with a tissue of a tree of the genus Populus. An “isolated” bacterium is preferably, but not necessarily a pure culture of the bacterium.
As used herein, the term “identifying characteristics,” when used in reference to Methylobacterium sp. BJ001, means the bacterium is a strictly aerobic, facultative methylotrophic, Gram negative rod, and can grow on one-carbon compounds including methanol, methane, formaldehyde, and methylamine. Additional “identifying characteristics” include growth on fructose, acetate, betaine, tartrate, formate, propionate, oxalate, lactate, salicylate, pyruvate, succinate, fumarate, glycerol and ethanol, but lack of growth on saccharaose, arabinose, galactose, glucose, lactose, mannose, xylose, fucose, iso-propanol, n-butanol, inositol, mannitol, sorbitol, aspartate, glutamate, citrate, sebacate, dimethylamine, trimethylamine, chloromethane, dichloromethane, methyl tert-butyl ether, TNT, RDX and HMX. Additional “identifying characteristics” include the presence of the following enzymatic activities: oxidase, catalase, alkaline phosphatase, C4 and C8 esterases, valine arylamidase, α-chymotrypsin, acid phosphatase and naphthol-AS-BI-phosphohydrolase. (Using biochemical assays, strain BJ001 is tested positive for the following enzymatic reactions: Akaline phosphatase (2-naphthyl phosphate), esterase C4 (2-naphtyl butyrate), esterase C8 (2-naphthyl carylate), valine arylamidase (L-valyl-2-naphtyhlamide), α-chymotrypsine (N-glutaryl-phenylalanine-2-naphtylamide), acid phosphatase (2-naphtyl phosphate), and naphtol-AS-BI-phosphohydrolase (naphtol-AS-BI-phosphate or 6-Bromo-2-phosphohydroxy-3-naphthoic acid α-anisidide)). Methylobacterium species according to the invention have greater than or equal to 95% 16S ribosomal DNA and 16S-23S IGS DNA sequence similarity to the 16S rDNA and 16S-23S IGS sequence provided in
As used herein, the term “mineralized” means that a compound has been completely transformed to CO2, H2O, and a mineral form of nitrogen, i.e., N2, NOx or NH4. The term “substantially mineralized” means that at least 10%, and preferably more (e.g., 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or more, up to and including 100%) of a given amount of a nitroaromatic or nitramine compound (e.g., a nitroaromatic or nitramine explosive) is mineralized.
As used herein, the term “distributing” means applying a composition comprising a bacterium to an area of contaminated soil or water. The composition is preferably applied in a substantially uniform manner, although uniformity is not absolutely required. Distribution can include, for example, spraying or sowing a composition in liquid, solid or semi-solid form. Distribution can also be accomplished by mixing an inoculum of bacterium-containing composition into a soil sample removed from a contaminated site.
As used herein, the term “environment” refers to an area contaminated with a nitramine or nitroaromatic compound, the area being a body of water (e.g., stream, lake or pond, man-made or natural) and/or the ground or sediment under the water, or a piece of land (e.g., a field, landfill, industrial manufacturing or storage site).
As used herein, the phrase “growth medium that supports the growth of Methylobacterium species” refers to a sterile preparation which supports the growth of Methylobacterium sp. BJ001. Non-limiting examples include LB medium, NA medium, modified Jayasuriya's medium, and DSMZ (Deutsche Sammlung von Mikroorganismen und Zellkulturen, Braunschweig, Germany) Methylobacterium Medium 125. One of skill in the art can readily determine whether a given medium preparation supports the growth of Methylobacterium sp. BJ001 or other Methylobacterium species, e.g., by inoculating the medium with strain BJ001 or other Methylobacterium species and incubating it at 28° C., thereafter monitoring bacterial growth by, e.g., OD600 or other suitable means.
As used herein, the term “modified Jayasuriya's medium” refers to an aqueous medium in which 1 liter contains 1.74 g of K2HPO4, 1.38 g NaH2PO4.H2O, 0.54 g Na2SO4, 0.2 g MgSO4.7H2O, 25 mg CaCl2.2H2O, 3.5 mg FeCl2.4H2O, and 2 ml of mineral solution (Wolfe's Trace Mineral Solution, ATCC Catalog No. MD-TMS). The medium has a pH of 7.0. For the growth of Methylobacterium sp. BJ001, the modified Jayasuriya's medium is supplemented with 0.5% w/v fructose, 0.2% w/v succinate or 0.5% v/v methanol and 1.2 g/L NH4NO3.
As used herein, the phrase “conditions that support the growth of Methylobacterium species” refers to culture conditions including a growth medium that supports the growth of Methylobacterium species as the term is defined herein, pH 3.0 to pH 11.0 (preferably about pH 6.0 to about pH 8.0), temperature of 4° C. to 41° C. (preferably about 15° C. to about 37° C.), and oxygen concentration of 5% to 100% saturation (preferably about 20% to about 100% saturation).
As used herein, the term “tissue explant” refers to living tissue removed from a plant. Tissue explants can come from any living tissue of the plant, e.g., the roots, stem, leaves, etc.
As used herein, the phrase “surface sterilized” means a plant tissue has been treated to kill all bacteria on the outside of the plant tissue. Surface sterilization can be achieved, for example, by successive immersion in 10% v/v bleaching solution (initially 5.25% sodium hypochloride (NaClO)) for 20 min, in 1.0% v/v Iodophor Sanitizer (National Chemicals, Inc., Winona, Minn.) for 5 min, in 70% v/v ethanol for 2 min, followed by rinsing with sterile DI water.
As used herein, the term “regenerated plantlet” refers to a plant grown from a plant cell tissue culture or plant explant by a vegetative way.
As used herein, the term “viable” means that the bacterium is capable of growth and division. Viability is tested by inoculation into medium and incubation under conditions permissive for growth of the bacterium.
As used herein, the term “dried” when referring to a bacterial preparation means a preparation of cells retaining less than 10% residual moisture, preferably, under 5%, even more preferably, less than 3.5-4% residual moisture, most preferably about 2-3% residual moisture. The amount of residual moisture can be evaluated by any method known to those skilled in the art, which include, but are not limited to, i) Karl Fischer Thermal method, ii) Thermogravimetry/Mass Spectometry (TG/MS), iii) Moisture evolution method and Vapor pressure moisture method, iv) gas chromatography, v) Near infrared reflectance (NIR) spectroscopy, vi) Gravimetric (loss-on-drying) method, vii) Differential scanning calorimetry (DSC), and viii) Thermally stimulated polarization current (TSPC).
As used herein, the term “nutrient” means an organic or inorganic chemical moiety that is taken up by and promotes the growth or metabolism of Methylobacterium sp. BJ001. “Nutrients” as used herein include, for example, carbon sources (e.g., carbohydrates, organic acids, methanol, etc.), minerals, vitamins, nitrogen sources, and phosphorus sources.
As used herein, the term “soil amendment” refers to a composition used to modify nitramine- or nitroaromatic-contaminated soil in a manner that increases the ability of the soil to support the nitroaromatic- or nitramine-degrading activity of a Methylobacterium species as described herein (i.e., the amendment increases the nitramine or nitroaromatic degradation activity of a Methylobacterium species by at least 5% relative to the same soil without that amendment). Without wishing to be bound by any one mechanism of action, a soil amendment can, for example, effectively dilute the concentration of agents toxic to the bacterium, provide vitamins or nutrients (e.g., carbon source, nitrogen, etc.) to the Methylobacterium species, adjust the pH, modify the soil's water-retention ability or increase the ease of or degree of aeration of the soil. Exemplary soil amendments include, for example, sand, manure, wood chips, paper shreddings, sawdust, vegetable scrap products of industrial scale food processing (e.g., apple pomace, potato scraps, corncobs, or other vegetable scraps from industrial food processing operations), vermiculite, straw, rice hulls, peat, alfalfa, and grass.
BRIEF DESCRIPTION OF THE DRAWINGS
Methylobacteria as described herein are capable of degrading nitramine and nitroaromatic compounds, which tend to be toxic, to less toxic forms and/or to fully degraded (i.e., mineralized) forms. While not limited to explosive compounds or their partial degradation products or derivatives, nitramine (e.g., heterocyclic nitramine) and nitroaromatic compounds are common contaminants resulting from the production or use of a number of widely used explosive compounds, as described herein above. Such compounds tend to contaminate soil, groundwater and sediments located near sites of production and use of the explosives. By introduction of the novel Methylobacterium strain described herein, alone or together with additional microorganisms, including other Methylobacterium species, to contaminated soil, groundwater or sediment either still in the environment or in isolation, the species described herein can be used in programs of environmental decontamination.
Methylobacterium Species According to the Invention
Methylobacterium sp. strain BJ001 as disclosed herein was isolated from tissues of the hybrid poplar Populus deltoides x nigra DN34. The strain BJ001 was isolated as described herein below.
A. Bacterial Isolation, Growth, and Maintenance.
A pink-pigmented bacterium was isolated from poplar tissue cultures and plantlets (Populus deltoides x nigra DN34) cultivated under axenic conditions. Tissue cultures in liquid medium and intact plantlets (regenerated from in vitro tissues) did not show microbial contamination. However, plant tissues plated on modified MS semi-solid medium frequently turned red, while excised plantlets showed the development of bright-red colonies spreading from the plant material (
For plant tissue cultures and explants, Imperial Carolina hybrid poplar cuttings (Populus deltoides x nigra DN34) were obtained from Hramoor Nursery (Manistee, Mich.). Explants from small trees routinely maintained in hydroponic cultures (i.e. 10-mm pieces of young stems and leaves) were surface-sterilized by successive immersion in 10% v/v bleaching solution (initially 5.25% sodium hypochloride (NaClO)) for 20 min, in 1.0% v/v Iodophor Sanitizer (National Chemicals, Inc., Winona, Minn.) for 5 min, in 70% v/v ethanol for 2 min, and then rinsed with sterile DI water (55). Sterilized explants grew on semi-solid medium consisting of Murashige and Skoog (MS) medium (pH 5.8) containing 20 g L−1 sucrose, 1.0 g L−1 phytagel, 3.0 g L−1 phytagar, and 5.0 mg L−1 2,4-dichlorophenoxyacetic acid (2,4-D) and 1.0 mg L−1 6-furfurylaminopurine (kinetin) as growth regulators. The medium was sterilized by autoclaving 25 min at 121° C., 1 atm. After one month of incubation in the dark, actively developing callus material was transferred in sterile liquid MS medium and incubated under agitation (125 rpm) under a 16-h/8-h light/dark photoperiod. After about one month, tissue cultures developed in the form of spherical green cell aggregates (10-20 mm diameter). Tissue cultures were used directly for in vitro experiments as a laboratory plant model and for the regeneration of small plantlets: Green tissues were incubated on root induction medium (semi-solid MS medium supplemented with 203 μg L−1 indole-3-butyric acid (IBA) as growth regulator) for 2-4 weeks and then transferred to shoot induction medium (semi-solid MS medium supplemented with 113 μg L−1 6-benzylaminopurine (BA), 110 μg L−1 6-(4-hydroxy-3-methylbut-2-enylamino)purine (zeatin), and 5 μg L−1 IBA as growth regulators). Plantlets were cultivated under axenic conditions in Magenta boxes with vented lid (Osmotek Lifeline, Rehovot, Israel) under a 16-h/8-h photoperiod.
The isolated Methylobacterium sp. BJ001 (also referred to herein as BJ001T, for the “type” strain for this new species) described herein has been deposited under the terms of the Budapest Treaty with both the American Type Culture Collection (Manassas Va.; Accession No. PTA-5125; date of deposit, Apr. 9, 2003) and the National Collections of Industrial and Marine Bacteria (NCIMB; Aberdeen, Scotland, UK; Accession No. 13946; date of deposit, Mar. 13, 2003). The deposits were made for a term of at least thirty (30) years and at least five (5) years after the most recent request for the furnishing of a sample of the deposit is received by the depository, or for the effective term of the patent, whichever is longer, and will be replaced if it becomes non-viable during that period.
Large volumes of Methylobacterium culture can be prepared in LB or other suitable medium. Preparations for application in bioremediation, e.g., dried preparations or microbial mats can be made using methods known in the art. Methylobacterium species are generally quite resistant to desiccation, so standard methods of preparing dried bacteria can be used as known to those skilled in the art or, for example, as disclosed in U.S. Pat. Nos. 6,322,994, 5,733,774 and 5,695,541, each of which is incorporated herein by reference. Dried forms of the bacteria have the advantage of increased storage and transport stability relative to liquid suspensions. U.S. Pat. No. 6,033,559, incorporated herein by reference, describes the preparation of microbial mats for use in bioremediation.
In order to maintain a selective pressure for methylotroph isolation, bacteria were alternatively cultivated in liquid minimal medium supplemented with methanol 0.5% v/v as a carbon source, and ammonium nitrate (NH4NO3) 1.2 g L−1 (i.e. 3.0 mM N) as a nitrogen source. Minimal medium, consisting of modified Jayasuriya's medium, contained in 1 L DI water K2HPO4, 1.74 g; NaH2PO4.H2O, 1.38 g; Na2SO4, 0.54 g; MgSO4.7H2O, 0.2 g; CaCl2.2H2O, 25 mg; FeCl2.4H2O, 3.5 mg; and mineral solution, 2 ml, at pH 7.0 (16).
C. Morphological, Biochemical, and Physiological Analysis.
Gram staining was carried out according to standard protocols (9). Scanning electron microscopy (SEM) observations were performed on fixed material prepared for routine examination using the following procedure: A concentrated bacterial suspension was immersion-fixed in a solution of 2.5% glutaraldehyde in 0.1 M cacodylate buffer (pH 7.2). Fixation was allowed to proceed overnight at 4° C. Fixed material was collected by centrifugation and rinsed with cacodylate buffer three times for one hour. Samples were then post-fixed with an osmium tetroxide solution (1.0% OsO4 and 1.5% ferrocyanide in cacodylate buffer) for one hour and dehydrated by successive immersion in a graded ethanol series (25, 50, 75, 95, and 100% v/v EtOH) for 20-30 min each. Dehydrated samples were critical point dried, mounted on stubs, and sputter coated with a gold/palladium mixture. The cells were visualized using a Hitachi S-4000 scanning electron microscope (Tokyo, Japan) equipped with a field emission electron source. Digitized images were collected with an iXRF digital image capturing system (IXRF Systems, Houston, Texas). Morphology is shown in
A dehydrated carbon source utilization test was based on a set of 49 organic compounds and was performed using the API50CH system (Biomerieux, Montalieu-Vercieu, France). In addition, the isolated bacterium was cultivated in 50-ml conical flasks on minimal liquid medium supplemented with 1.2 g L−1 of NH4NO3 (3.0 mM N) and various carbon sources added to a final concentration of 0.5% v/v (liquid substrates) or 5 g L−1 (solid substrates), except formaldehyde, 0.05% v/v; TNT, 1.0 g L−1; RDX, 1.0 g L−1; and HMX, 1.0 g L−1. Flasks were inoculated and incubated for one week at room temperature with agitation. Carbon source utilization was determined by the biomass dry weight after two weeks of incubation. A biochemical test based on a set of 19 enzymatic assays was performed using API ZYM system (Biomerieux).
The bacterium was shown to grow on different C1-carbon sources, including methanol, methylamine, and formaldehyde, which is a particular attribute of the genus Methylobacterium. Other carbon substrates sustaining growth of Methylobacterium sp. BJ001 included fructose, glycerol, ethanol, and a wide range of organic acids. On the other hand, no growth was observed on saccharose, arabinose, galactose, iso-propanol, n-butanol, chloromethane, dichloromethane, TNT, RDX, or HMX. Using further biochemical assays, strain BJ001 tested positive for the following enzymatic reactions: Akline phosphatase, esterases (C4 and C8), valine arylamidase, α-chymotrypsine, acid phosphatase, and naphtol-AS-BI-phosphohydrolase.
D. Characterization of the Isolated Bacterium by 16S and 16S-23S IGS rDNA Analysis.
General techniques for DNA manipulations were carried out according to standard protocols (1,39). Bacterial genomic DNA was extracted by centrifugation from 4-day pre-grown cell suspensions using a DNeasy Tissue Kit (Qiagen, Inc., Valencia, Calif.). Extracted DNA was further purified by phenol-chloroform extraction and ethanol precipitation (1). For 16S rDNA PCR amplification, the following universal primers were synthesized: Forward bacterial primer 27f (positions 11-27 of bacterial 16S rDNA, according to Escherichia coli numbering) and reverse bacterial primer 1513r (positions 1492-1513 of bacterial 16S rDNA, E. coli numbering). For 16S-23S IGS rDNA amplification, a forward primer 926f (positions 901-926 of bacterial 16S rDNA, E. coli numbering) and a reverse primer 115r/23S (positions 97-115 of bacterial 23S rDNA, E. coli numbering) were used (49). PCR amplifications were carried out on a Matercycler Gradient (Eppendorf AG, Hamburg, Germany) by the following steps: Initial denaturation at 94° C. for 3 min; 30 cycles of denaturation at 94° C. for 1 min, elongation at 54-56° C. for 1 min, and extension at 72° C. for 90 sec; and final extension at 72° C. for 10 min (49). PCR products were first analyzed by agarose gel electrophoresis (AGE) according to standard protocols (39). PCR products were then purified using a Qiagen PCR Purification Kit. Retrieved sequences were submitted for sequencing at the University of Iowa DNA Core Facility (Iowa City, Iowa). Sequencing was carried out by Sanger-based fluorescent identification of bases on an ABI 3700 electrophoresis detector (The Institute for Bioanalytics, Branford, Conn.) and using separately both the forward and the reverse primers used for amplification. The determined rDNA sequences, as well as reference sequences retrieved from NCBI GenBank (U.S. National Library of Medicine, Bethesda, Md.), were aligned by ClustalW Multiple Alignment, BioEdit (version 5.0.9.) software (Raleigh, N.C.). The tree topology was inferred by the “neighbor-joining” method using Mega2 (version 2.1.) software (27).
16S and 16S-23 S IGS rDNA sequences from Methylobacterium sp. BJ001 (ATCC PTA-5125; NCIMB 13946) have been deposited to NCBI GenBank database under the accession numbers AY214142 and AY214143 respectively (both sequences are provided in
Using 16S ribosomal DNA (rDNA) and 16S-23S intergenic spacer (IGS) rDNA analysis as described above, the isolated strain was identified as a Methylobacterium sp. A phylogenetic tree based on the 16S rDNA sequence and showing the location of Methylobacterium sp. BJ001 is displayed in
Identified Methylobacterium sp. BJ001 isolated from poplar tissues (Populus deltoides x nigra DN34) belongs to the α-2 subclass of Proteobacteria and, as noted above, has been shown to be related to M. extorquens. M. extorquens is a widely distributed methylotrophic bacterium, frequently associated with plant leaves and roots (51). Members of the genus Methylobacterium are known to be common inhabitants of the rhizosphere and the phyllosphere of plants and have been described as chronic contaminants of plant tissue cultures (20, 21, 30, 51). However, this is the first identified close association between a Methylobacterium species and a poplar tree (Populus sp.).
A transient red coloration of plant tissues, as well as red colonies spreading only from wounded plant materials, suggests that Methylobacterium sp. BJ001 is an endophyte. Surface sterilization of original explants and manipulations under sterile conditions should ensure microbe-free plant tissues, except in the case of endophytic bacteria. A recently identified fourth branch of rhizobia (a heterogenous lade gathering bacteria fixing nitrogen in symbiosis with leguminous plants) includes members of the genus Methylobacterium (47). The ability shown by Methylobacterium sp. BJ001 to grow on nitrogen-free medium suggests that the bacteria can fix atmospheric nitrogen. The ability of Methylobacterium sp. BJ001 to metabolize fructose faster than any other carbon sources-fructose is the first hexose produced by photosynthesis-also supports an endophytic ecology.
E. Compositions Comprising Methylobacterium Species, Including the Novel Strain BJ001
Compositions comprising the Methylobacterium species disclosed herein are provided according to one aspect of the invention. Such compositions include, for example, a composition comprising an isolated Methylobacterium having all identifying characteristics of the Methylobacterium sp. BJ001 deposited with ATCC at Accession No. PTA-5125, and at NCIMB at Accession No. 13946, or other Methylobacterium species, and such a composition further comprising a nitramine or nitroaromatic compound or compounds. The nitramine or nitroaromatic compound or compounds can be, for example, an explosive or a derivative (e.g., a partial breakdown product) thereof. The explosive can be, for example, TNT, RDX or HMX or derivatives thereof described herein below or known in the art.
Uses of Methylobacterium Species
The nitramine- and nitroaromatic-compound degrading capacities of the Methylobacterium species disclosed herein can be exploited for the decontamination of sites and materials contaminated with such compounds. Exemplary nitramine and nitroaromatic compounds and approaches to their degradation and decontamination of such sites and materials are described herein below.
A. Nitramine and Nitroaromatic Compounds
A number of nitramine and nitroaromatic compounds can be substrates for degradation by the novel Methylobacterium species described herein. These include, but are not limited to 2,4,6-trinitrotoluene (TNT) and degradation products or derivatives thereof (e.g., 2,4-dinitrotoluene, 4-amino-2,6-dinitrotoluene), octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) and degradation products or derivatives thereof (e.g., octahydro-1,3,5-trinitro-7-nitroso-1,3,5,7-tetrazocine, octahydro-1,3-dinitro-5,7-dinitroso-1,3,5,7-tetrazocine, octahydro-1,5-dinitro-3,7-dinitroso-1,3,5,7-tetrazocine, octahydro-1-nitro-3,5,7-trinitroso-1,3,5,7-tetrazocine, octahydro-1,3,5,7-tetranitroso-1,3,5,7-tetrazocine), 1,3,5-trinitro-1,3,5-triazine (RDX) and degradation products and derivatives thereof (e.g., hexahydro-1-nitroso-3,5-dinitro-1,3,5-triazine (MNX), hexahydro-1,3-dinitroso-5-nitro-1,3,5-triazine (DNX), and hexahydro-1,3,5-trinitroso-1,3,5-triazine (TNX). Methylobacterium sp. BJ001 is shown herein to degrade TNT, HMX and RDX. Because TNT (a representative nitroaromatic compound), and RDX and HMX (representative nitramines) present chemical structures and moieties that are characteristic of their respective groups of compounds, the metabolic chemistry applied by the Methylobacterium species described herein to degrading any of various nitroaromatics and nitramines would be substantially the same as applied to TNT, HMX and RDX. For example, degrading a nitroaromatic would require removal of the nitro groups and cleavage of the aromatic ring(s). The fact that the isolated strain can rapidly degrade TNT indicates that the strain would be capable of degrading any of various other nitroaromatics. Similarly, degrading a nitramine would require removal of nitro groups and cleavage of the alkylamino backbone of the molecule. The fact that the isolated strain can efficiently degrade RDX and HMX indicates that the strains would be capable of degrading any of various other nitramines. Other nitroaromatic compounds may include, for example, nitrobenzene, all isomers of dinitrobenzene (e.g., 1,3-dinitrobenzene), trinitrobenzene (e.g., 1,3,5-trinitrobenzene), nitrotoluene (e.g., 2-nitrotoluene), dinitrotoluene (e.g., 2,4-dinitrotoluene), trinitrotoluene (e.g., 2,4,5-trinitrotoluene), nitrophenol (e.g., 2-nitrophenol), dinitrophenol (e.g., 1,3-dinitrophenol), trinitrophenol (e.g., picric acid), and degradation products or derivatives thereof (e.g., aminobenzene, 1-amino-3-nitrobenzene, 1-amino-3,5-dinitrobenzene, 2-aminotoluene, 2-amino-4-nitrotoluene, 2-amino-4,5-dinitrotoluene, aminophenol, 2-amino-4-nitrophenol, 2-amino-4,6-dinitrophenol). Other energetic compounds may include nitrocellulose, nitroglycerine, pentaerytriol tetranitrate, tetryl, etc. The fact that the isolated strain can efficiently degrade TNT, RDX, and HMX individually indicates that the strain would be capable of degrading mixtures of them, and mixtures of any of the energetic compounds and their degradation products and derivatives thereof listed above. Mixtures of energetic compounds and degradation products and derivatives may originate from blending in the environment as a result of utilization and release of different parent compounds, and/or from the partial in situ biodegradation of parents compounds. Mixture of energetic compounds and degradation products and derivatives may originate from blending before utilization and release in the environment (e.g.,) and/or from the partial in situ biodegradation of original mixtures.
B. Degradation of Nitroaromatic and Nitramine Compounds
In one embodiment, a method is provided for the degradation of nitroaromatic and nitramine compounds in the environment or elsewhere. In general, this involves contacting the compounds with one or more Methylobacterium species, including strain BJ001. The Methylobacterium sp. BJ001 has an advantage in being a naturally-occurring species found as an endosymbiont of Poplar tissues. The natural occurrence of the bacterium indicates that it is safe to use in the open environment.
In one aspect, contaminated soil, sediment, sludge, or wastewater is contacted with the Methylobacterium species. The contaminated material can be contacted with a preparation of the bacteria while the material is still in the environment. For example, the Methylobacterium preparation can be applied to open fields, lagoons, ponds, or other areas contaminated with nitroaromatic or nitramine compounds. Methods of application can include, for example, spraying, broadcasting, sowing or otherwise distributing a preparation of the bacteria onto or into the area to be treated. If necessary or desired, the preparation can be mixed into the soil, sediment, sludge or wastewater, for example, by tilling, plowing or stirring. Such mixing can be performed once, upon application, or repeatedly (e.g., 2, 3, 4 or more times) over the course of decontamination, or even continuously during the process. Whereas the Methylobacterium species are strictly aerobic, breakdown of contaminants can be aided by increasing the aeration of the material being decontaminated. Thus, in one embodiment, continuous or frequent mixing or turning of the material during the process is preferred. Soil, sediment or water samples from the area being treated can be monitored (e.g., by HPLC as described herein, or by other suitable means, e.g., gas chromatography/mass spectrometry (GC/MS)) for nitroaromatic and nitramine contaminant levels at various time intervals (daily, weekly, etc.) to determine the progress of the decontamination.
Where relatively dry soil is to be decontaminated in the open environment, it can be beneficial to increase the hydration of the soil in order to encourage growth of the bacteria. This can be accomplished through standard irrigation means well known to those skilled in the art. Care should be taken in the process, however, to avoid increasing runoff or spreading of contaminants in the irrigation water. Generally, water should not exceed about 50% of the moisture-holding capacity of the soil.
In another aspect, contaminated soil, sediment, sludge, wastewater or other contaminated material is removed from the open environment and contacted with the Methylobacterium species in isolation, for example, in a container or trough. Preferably such container is lined. This approach is referred to herein as “composting,” and can be particularly useful, as a non-limiting example, in situations in which the level of contamination is particularly high, such that the contaminant(s) present a toxic threat to the bacteria themselves. In this situation, it can be helpful to compost the material by first mixing it with an amount of non-contaminated material, e.g., soil, manure, wood chips, potato scraps, apple pomace, or other material that effectively dilutes the concentration of contaminant(s) to a level wherein the bacteria are not killed, thereby permitting them to degrade the contaminant(s). These or other additional materials can also be added to provide nutrients to maintain the health of the bacteria. The composting can be performed under controlled conditions of pH (ranging from about pH 3.0 to about pH 11.0, preferably about pH 6.0 to about pH 8.0), temperature (about 4° C. to about 41° C., preferably about 15° C. to about 37° C.), oxygen (about 5% to about 100% saturation, preferably about 20% to about 100% saturation) and hydration (to about 40% wt/wt). After inoculation, the contents of the container can be turned or agitated so as to maintain aeration and ensure contact of the bacteria with contaminants to be degraded. Samples of the composting material can be monitored by, for example, HPLC or other suitable method, to follow the progress of decontamination. It is contemplated that the process could be scaled up from a “batch” process to a continuous feed process, wherein the material is slowly moved through zones in the container as new material is added behind it, emerging from the end after full decontamination. Composting as a general means of degrading nitroaromatic and nitramine compounds such as TNT, RDX and HMX is also described by, for example, Williams et al., 1992, J. Ind. Microbiol. 9: 137-144, Griest et al., 1993, Environ. Toxicol. Chem. 12: 1105-1116, Jarvis et al., 1998, Ecotoxicol. Environ. Safety 39: 131-135 and Bruns-Nagel et al., 2000, Composting (Humification) of Nitroaromatic Compounds. In: Spain et al., (eds) Biodegradation of Nitroaromatic Compounds and Explosives. CRC Press, Boca Raton, pp 357-394.
In yet another aspect, the material to be decontaminated can be mixed with water to create a slurry of the material, for example, about a 30% w/w slurry. Bacteria are added and the slurry is fermented or cultured under conditions conducive to the decontamination of the slurry by the bacteria. Conditions such as pH (ranging from about pH 3.0 to about pH 11.0, preferably about pH 6.0 to about pH 8.0), temperature (about 4° C. to about 41° C., preferably about 15° C. to about 37° C.), and oxygen (about 5% to about 100% saturation, preferably about 20% to about 100% saturation) can be controlled in the slurry. The slurry should be agitated or stirred to maximize both contact of contaminants with the bacteria and aeration. As above, additional nutrients can be added if necessary or desired. Samples can be monitored at various intervals by, for example, HPLC in order to follow the decontamination process.
Where necessary or desired, removal of contaminated material from an environmental site to a site for bioremediation as described herein can be accomplished, for example, by excavation and transport using equipment well known in the field. Where the contaminated material is, for example, wastewater or runoff, the liquids can be pumped from the site and transported by standard methods of transporting liquids. Alternatively, contaminated liquid materials can be absorbed with, for example, paper or other absorbent materials, and those materials now containing the contaminated water can be transported to a facility for decontamination.
In each of the aspects described herein, it is contemplated that other bacteria (including other members of the genus Methylobacterium) can also be added for their combined effect on the decontamination process. Additional microbes can be naturally present in, for example, livestock manure. Where manure is used in any aspect of the methods or compositions described herein, it is preferable to avoid manure from animals, e.g., cattle, that are routinely treated with antibiotics, as the antibiotics may have adverse effects on the Methylobacterium. One source that does not tend to be tainted with antibiotics is horse manure.
Other microbes that can be included in preparations of the Methylobacterium species include, as non-limiting examples, aerobic microbes such as Pseudomonas species (e.g., P. fluorescens (e.g., ATCC 12842), P. aeruginosa (e.g., ATCC 10145), P. pseudoalcaligenes JS52 (Fiorella & Spain, 1997, Appl. Environ. Microbiol. 63: 2007-2015), P. savastanoi (e.g., ATCC 13492), P. putida (e.g., ATCC 17391), Pseudomonas strain C1S1 (Duque et al., 1993, J. Bacteriol. 175: 2278-2283), Rhodococcus species (e.g., R. erythropolis HLPM-1; Lenke & Knackmuss, 1992, Appl. Environ. Microbiol. 58: 2933-2937), Enterobacter sp (e.g., E. cloacae, French et al., 1998, Appl. Environ. Microbiol. 64: 2864-2868), and Mycobacterium sp. (E.g., Mycobacterium vaccae (Vanderberg et al., 1995, Appl. Microbiol Biotechnol. 43: 937-945), among others. Preparations of anaerobic bacteria can also be combined with preparations of the Methylobacterium species described herein, including, as non-limiting examples, Clostridium species (e.g., C. bifermentans (e.g., ATCC 17836), C. acetobutylicum (e.g., ATCC 39236) and others. Sulfate-reducing bacteria can also be included in compositions with the Methylobacterium species described herein, including, as a non-limiting example, Desulfovibrio species. Fungi, including for example, white rot fungi species such as Phanerochaete chrysosporium (e.g., ATCC 34541) and Phlebia radiata (e.g., ATCC 52891), can also be included. Further microbial isolates that can be included with the Methylobacterium species described herein include, for example, those Arthrobacter species described in U.S. Pat. No. 5,478,743, incorporated herein by reference (ATCC Accession Nos. include, for example, 55546, 55547, 55548 and 55549), microbial species described in U.S. Pat. No. 5,455,173, incorporated herein by reference (e.g., ATCC Accession Nos. 55559, 55560, and 55561), and members of the consortium of species disclosed in U.S. Pat. No. 5,543,324 (e.g., the consortia at ATCC Accession No. 55381 and 55382, which include, for example, Arthrobacter uratoxydans, Aurobacterium saperdae, Bacillus cereus, Flavobacterium esteroaromaticum, Micrococcus luteus, Micrococcus varians, Pseudomonas putida and Ochrobacterium anthropi), among others.
Where microbes in addition to the Methylobacterium species described herein are employed, the proportion of Methylobacterium species to other microbe(s) can range from, for example, about 1000:1 to about 1:1000, e.g., about 500:1, about 200:1, about 100:1, about 10:1, about 1:1, about 1:10, about 1:100, or about 1:200. These proportions can be an organism to organism ratio or, for example, a weight to weight ratio.
The Methylobacterium species preparation can be provided in the form of a liquid suspension or slurry that is sprayed onto or into a material to be decontaminated. Dried preparations of the bacteria can also be used for inoculation, and are discussed herein above.
C. Determination of Nitroaromatic and Nitramine Compound Degradation
For degradation in experimental cultures, the analysis of nitro-substituted compounds (e.g., TNT, RDX, HMX, and their metabolites) can be performed by reverse phase HPLC (HP Series 1100; Hewlett-Packard, Palo Alto, Calif.) on a C18 Supelcosil® LC-18 column (25 cm×4.6 mm, 5 μm; Supelco, Bellefonte, Pa.). The system is equipped with a UV-visible photodiode array detector (HP Series 1100), a mass spectrometry detector (Agilent 1100 Series LC/MSD, Palo Alto, Calif.), and a Radiomatic Flo-One β radio-chromatograph (Packard Bioscience, Meriden, Calif.) for the detection of 14C-radioactive compounds. The mobile phase consists of AcCN:0.1% w/v ammonium acetate (NH4CH3COO) running at a flow rate of 1 ml min−1. For mass analyses, a Zorbax 80 Å Extended-C18 column (2.1×100 mm, 3.5 μm; Agilent) running at flow rate of 0.2 ml min−1 is used. The mass spectrometer is equipped with an electrospray ionization source (ESI) used in negative mode. Operating parameters are as follows: Capillary voltage, 3.0 kV; drying gas flow, 12.01 min−1; nebulizer pressure, 35 psig; drying gas temperature, 350° C. TNT and its metabolites are detected by their M−H ion masses, while RDX, HMX, and their metabolites were detected by their M+60−H (acetate) ion masses.
14C-Radioactivity in solution, in extracts, and in CO2 traps is analyzed with a Beckman liquid scintillation counter (LSC) LS 60001C (Beckman Coulter, Fullerton, Calif.) using Ultima Gold XR® (Packard Bioscience) as scintillation cocktail.
Radioactivity remaining in cells is analyzed by bio-oxidation using a biological oxidizer Harvey OX600 (R. J. Harvey Instrument, Hillsdale, N.J.). 14CO2 contained in outgoing gases was trapped into 10 ml of 14Carbon® scintillation cocktail (R. J. Harvey Instrument) and the radioactivity is determined by LSC.
Bacterial growth is recorded by the OD at 600 nm and the biomass dry weight. Cell dry weight is determined by harvesting cells by filtration on glass fiber and drying overnight at 105° C. Cell concentration is determined by direct counting using a hemocytometer (Hausser Scientific, Horsham, Pa.). Photometric data are converted to biomass dry weight and to cell concentration using standard curves.
For the determination of degradation of nitroaromatic and nitramine compounds, such as TNT, RDX and HMX in, for example, environmental samples being decontaminated as described herein, HPLC can be used as for experimental analyses described above, as can other suitable methods of analysis. With an HPLC instrument, detection of the subject compound and its transformation and degradation products can be performed using a diode-array detector, measuring UV absorption at selected absorption maxima and/or continuous scanning over a suitable wavelength range. The U.S. Environmental Protection Agency (EPA) has a standard set of conditions used to measure nitroaromatics and nitramines in soil. This method, referred to as Method 8330, titled “Determination of Concentration of Nitroaromatics and Nitramines by High-Performance Liquid Chromatography (HPLC)” is incorporated herein by reference and summarized below:
EPA Method 8330 provides three optional procedures for low concentration (parts per billion (ppb) or nanograms per liter (ng L−1) of certain explosives residues in surface or ground water. These options are salting-out extraction, cartridge solid-phase extraction, and membrane solid-phase extraction. Direct injection of diluted and filtered water samples can be used for water samples of higher concentration, and a similar method is used for soils and sediments.
EPA Method 8330 Low-Level Method No. 1: Salting-out with no evaporation:
Aqueous samples of low concentration are extracted using a salting-out extraction procedure with acetonitrile and sodium chloride. The small volume of acetonitrile that remains undissolved above the salt water is drawn off and transferred to a smaller volumetric flask. It is back-extracted by vigorous stirring with a specific volume of salt water. After equilibration, the phases are allowed to separate, and the small volume of acetonitrile residing in the narrow neck of the volumetric flask is removed using a Pasteur pipette. The concentrated extract is diluted 1/1 with reagent-grade water. An aliquot is separated on a C-18 reverse-phase column, determined at 254 nm, and confirmed on a CN reverse-phase column.
EPA Method 8330 Low-Level Method No. 2: Cartridge solid-phase extraction:
Extraction cartridges are fitted with frits at one end, then packed tightly with Porapak RDX. A second frit is placed over the open ends of the cartridges to retain the material inside. Using a Visiprep Solid-Phase Extraction Manifold (Supelco), the aqueous samples are extracted through the cartridges; the cartridges are then eluted using acetonitrile. The resulting eluate is diluted 1/1 with reagent-grade water prior to analysis.
EPA Method 8330 Low-Level Method No. 3: Membrane solid-phase extraction:
Empore styrene-divinyl benzene (SDB) RPS disks are placed in a vacuum filter apparatus and soaked with acetonitrile. The acetonitrile is pulled through the disk, followed by reagent-grade water. Just before all the water has been pulled through, the vacuum is turned off and an aqueous water sample aliquot is placed in the reservoir. Turning the vacuum back on, the aliquot and any remaining water is pulled through the membrane. Air is then pulled through the disks for a short time to remove any excess water. Once they are dry, acetonitrile is added to the reservoir and allowed to soak into the membrane. Next, the acetonitrile is pulled through the disks into a test tube that has been fitted into the vacuum flask. The resulting extract is removed using a Pasteur pipette and placed into a graduated cylinder where it is diluted 1/1 with reagent-grade water prior to analysis.
EPA Method 8330 High-level direct injection method:
Aqueous samples of higher concentration can be diluted 1/1 (v/v) with methanol or acetonitrile, filtered, separated on a C-18 reverse-phase column, determined at 254 nm, and confirmed on a CN reverse-phase column. If HMX is an important target analyte, methanol is preferred.
EPA Method 8330 Method for soil and sediment samples:
Soil and sediment samples are extracted using acetonitrile in an ultrasonic bath, filtered, and chromatographed, as in the high level direct injection method.
Another method for determining the amount of degradation of a nitrogen-containing compound such as a nitroaromatic or nitramine compound is to analyze the amount of nitrite released during the degradation process. Methods for determining the amount of nitrite released from nitrogen-containing compounds are common and well known in the art. For example, Misko et al. (Anal. Biochem., 214, 11, (1993)) teach a fluorometric assay for the measurement of nitrite in biological samples which is designed to detect nitrite/nitrate. The method is based upon the reaction of nitrite with 2,3-diaminonaphthalene to form the fluorescent product, 1-(H)-naphthotriazole. Carson et al. (U.S. Government Report, DC/WRRC-42, W83-02296, OWRT-A-019-DC(1); Order No. PB83-180331, 31 pp. From: Gov. Rep. Announce. Index (U.S.) 1983, 83 (14), 3113) discuss the determination of nitrite and nitrate in water by reduction to ammonia followed by enzymatic cycling involving the reduction of NO2− and/or NO3− to NH3 with Devarda's metal while simultaneously trapping the released NH3 gas with diluted aqueous HCl. Another nitrite release assay is the method described by Smibert et al. (Method I in Manual of Methods for General Bacteriology, Gerhardt, Murray, Costilow, Nester, Wood, Kreig & Phillips, Editors, p. 419 (1981)). This method involves the colorometric detection of nitrite by mixing a sample suspected of containing nitrite with N-1-naphthyl ethylenediamine HCL and sulfanilic acid, with detection at 540 nm.
Measurement of the levels of total organic carbon (TOC) in culture media is another indication of the level of degradation of microbial carbon sources. Methods for the determination of TOC are common and well known in the art and any suitable method can be used. Sakamoto et al. (Ultrapure Water, 4(9), 24, 26-8, 30-1 (1987)) discuss a method for measuring TOC by wet oxidation and Heanes (Commun. Soil Sci. Plant Anal., 15(10), 1191-213 (1984)) teaches the determination of total organic carbon in soils using chromic acid digestion followed by a spectrophotometric procedure. A review of several methods is provided by Haverty (Ultrapure Water, 1(2), 29-31 (1984)).
Nitroaromatic and nitramine compounds are considered “degraded” when one or more chemical bonds in a nitroaromatic or nitramine target compound are broken. Degradation preferably continues to completion, that is until mineralization of the compound to H2O and CO2 and where none of the starting material is present. However, degradation to a form having reduced toxicity relative to the starting compound(s) is beneficial.
EXAMPLES Example 1 Degradation of Nitroaromatic and Nitramine ExplosivesCell suspensions of Methylobacterium sp. strain BJ001 in pure culture were exposed separately to nitro-substituted explosives TNT, RDX, and HMX. Bioreactors consisted of 250-ml conical flasks equipped with lateral tubing for sample collection and closed by a rubber stopper. Flasks were equipped with a CO2 trap consisting of a 5-ml glass vial containing 1 ml of 1.0 N NaOH. Each bioreactor contained 100 ml of liquid LB medium supplemented with 14C[-U-ring]-TNT (25 mg L−1), 14C[-U-ring]-RDX (20 mg L−1), or 14C[-U-ring]-HMX (2.5 mg L−1). Each flask was inoculated with a concentrated cell suspension (1.0% v/v). The inoculum was prepared from a 48-h old log-phase cell suspension growing in LB medium supplemented with methanol (0.5% v/v) or fructose (0.5% w/v) and incubated under stirring at 28° C. Cells were harvested by centrifugation (30 min, 5,000 rpm) and re-suspended in sterile DI water. The procedure was repeated two times in order to wash the bacterial cells and the final inoculum exhibited an OD600 of 1.0 (i.e. approximately 109 cells ml−1). Bioreactors were incubated at room temperature under agitation (125 rpm). One-ml samples of the solution and the CO2 traps were collected periodically for analysis. Control experiments were carried out with non-inoculated flasks or flasks inoculated with the bacteria, but without toxic compound. Experiments were conducted in triplicate.
Bacteria were shown to fully transform the nitro-substituted explosives over the 55 days of experiment (
While TNT disappeared completely in less than 10 days, no significant mineralization (i.e. release of 14CO2) or decrease of the radioactivity in solution was observed (Table 1). In contrast, RDX and HMX concentrations decreased more slowly (reaching non-detectable levels after 40 days), but with a significant release of 14CO2, corresponding to 58.0±3.0 and 62.0±3.9% of the initial radioactivity respectively (
Radiochromatograms of the solution initially containing 14C-TNT showed a single peak eluted after 18.9 min, which corresponded to TNT (
Radiochromatograms of the solution containing RDX at the beginning of the experiment showed a single peak eluted after 8.7 min (
Analyses of nitro-substituted compounds (i.e. TNT, RDX, HMX, and their metabolites) were performed by reverse phase HPLC (HP Series 1100; Hewlett-Packard, Palo Alto, Calif.) on a C18 Supelcosil® LC-18 column (25 cm×4.6 mm, 5 μm; Supelco, Bellefonte, Pa.). The system was equipped with a UV-visible photodiode array detector (HP Series 1100), a mass spectrometry detector (Agilent 1100 Series LC/MSD, Palo Alto, Calif.), and a Radiomatic Flo-One β radio-chromatograph (Packard Bioscience, Meriden, Calif.) for the detection of 14C-radioactive compounds. The mobile phase consisted of AcCN:0.1% w/v ammonium acetate (NH4CH3COO) running at a flow rate of 1 ml min−1. For mass analyses, a Zorbax 80 Å Extended-C18 column (2.1×100 mm, 3.5 μm; Agilent) running at flow rate of 0.2 ml min−1 was used. The mass spectrometer was equipped with an electrospray ionization source (ESI) used in negative mode. Operating parameters were as follows: Capillary voltage, 3.0 kV; drying gas flow, 12.01 min−1; nebulizer pressure, 35 psig; drying gas temperature, 350° C. TNT and its metabolites were detected by their M−H ion masses, while RDX, HMX, and their metabolites were detected by their M+60−H (acetate) ion masses. 14C-Radioactivity in solution, in extracts, and in CO2 traps was analyzed with a Beckman liquid scintillation counter (LSC) LS 60001C (Beckman Coulter, Fullerton, Calif.) using Ultima Gold XR® (Packard Bioscience) as scintillation cocktail.
Radioactivity remaining in cells was analyzed by bio-oxidation using a biological oxidizer Harvey OX600 (R. J. Harvey Instrument, Hillsdale, N.J.). 14CO2 contained into outgoing gases was trapped into 10 ml of 14Carbon® scintillation cocktail (R. J. Harvey Instrument) and the radioactivity was determined by LSC.
Bacterial growth was recorded by the OD at 600 nm and the biomass dry weight. Cell dry weight was determined by harvesting cells by filtration on glass fiber and drying overnight at 105° C. Cell concentration was determined by direct counting using a hemocytometer (Hausser Scientific, Horsham, Pa.). Photometric data were converted to biomass dry weight and to cell concentration using standard curves.
To determine whether the transformation/mineralization of nitro-substituted explosives was metabolic or co-metabolic (i.e., associated or not with a carbon or nitrogen utilization), additional degradation experiments using growing cells were carried out in minimal liquid medium supplemented with the following carbon and/or nitrogen sources (See Table 2): Fructose (5 g L−1) and NH4NO3 (1.2 g L−1 or 3 mM N), fructose only, NH4NO3 only, and no fructose and no NH4NO3. Bioreactors consisted of 30-ml serum vials equipped with a CO2 trap composed of a 4-ml glass tube containing 500 μl of 1.0 N NaOH. Each bioreactor contained 10 ml of liquid medium supplemented separately with 14C-[U-ring]-TNT (25 mg L−1), 14C-[U-ring]-RDX (20 mg L−1), or 14C-[U-ring]-HMX (2.5 mg L−1) and were inoculated with a concentrated cell suspension (1.0% v/v). Control experiments consisted in the same set of media but without addition of TNT, RDX, or HMX. For each set of experiments, LB medium and non-inoculated minimal medium were used as positive and negative control media respectively. Bioreactors were incubated as previously described.
Similar degradation experiments were carried out with other members of the genus Methylobacterium, M. extorquens (ATCC 14718), M. organophilum (ATCC 27886), M. rhodesianum (ATCC 21611) growing on LB medium supplemented with succinate (2.0 g L−1).
In all sets of experiments (with and without 14C-TNT, 14C-RDX, or 14C-HMX; see Table 2), only minimal media supplemented with fructose (5.0 g L−1) supported bacterial growth (reaching 0.7-1.1 g dry biomass L−1after the 20 days), regardless the presence of a nitrogen source. Significant mineralization of nitramines (accounting for 7.0-7.7% of the initial 14C-RDX and 5.0-6.8% of the initial 14C-HMX) were observed under the same conditions, i.e. in the presence of fructose. No significant mineralization of 14C-TNT was recorded. Mineralization rates of nitramines 14C-RDX and 14C-HMX were shown to be higher when the bacteria were grown on LB medium (i.e. 18.1 and 15.5% of the initial radioactivity respectively). Interestingly, nitrogen-free control medium (i.e. without TNT, RDX, or HMX) was able to sustain bacterial, growth (reaching 1.1 g dry biomass L−1), as long as a carbon source (i.e. fructose) was provided. For all sets of experiments, neither significant biomass growth nor release of 14CO2 was recorded in the absence of a carbon source or from non-inoculated control flasks.
The ability to mineralize nitramines RDX and HMX was investigated among other representative members of the genus Methylobacterium. Methylobacterium strains tested were able to significantly degrade nitramine explosives. Strain BJ001 exhibited higher mineralization rates (Table 3).
The data show that Methylobacterium species strain BJ001 transforms TNT and mineralizes RDX and HMX into CO2. The transient generation of reduction derivatives early in the degradation process (i.e. ADNTs and DANTs from TNT, MNX from RDX) indicates that the metabolism of explosives by Methylobacterium sp. BJ001 began with a reduction reaction. Bacterial transformation of heterocyclic nitramines frequently involves an initial reduction step (31) and nitroso metabolites have been previously detected, both under aerobic and anaerobic conditions (15, 18). Initial nitroreductase-catalyzed reduction of the nitro groups is known to occur either via a two-electron transfer (type I), generating nitroso derivatives, or via a one-electron transfer (type II), producing nitramine anion radicals (17, 18). The detection of MNX (and possibly methylenedinitramine) indicates that the metabolism of RDX by Methylobacterium sp. BJ001 followed a two-electron reduction pathway.
On the other hand, being a highly oxidized molecule, TNT can be reduced by many different organisms (57). The stepwise reduction of the nitro groups, with the subsequent generation of reduction derivatives (i.e. hydroxylaminodinitrotoluenes (OHADNTs), ADNTs, and DANTs), is known to be the major transformation pathway of TNT, even though NADPH-dependent reductive hydrogenation of the aromatic ring (with the formation of (di)hydride-Meisenheimer complex) has been reported (29).
However, following these early reduction steps, the fates of the nitro aromatic explosive TNT and of heterocyclic nitramines RDX and HMX diverge considerably. Indeed, while the metabolism of 14C-RDX and 14C-HMX by Methylobacterium sp. BJ001 resulted in an extensive release of 14CO2, no significant mineralization of 14C-TNT was observed. Mineralization of RDX and HMX by aerobic bacteria is well documented (17, 53). However, several bacterial strains were reported to convert RDX and HMX into nitroso derivatives, which accumulate in the medium, suggesting that they are neither mineralized nor serving as carbon or nitrogen sources (24). It is a common feature that a slight change in the chemical structure of hetero cyclic nitramines—such as the reduction of a nitro group—destabilizes the entire molecule (inner C—N bonds are less than 2 kcal mol−1), resulting in a ring cleavage generating various aliphatic hydroxylamines and nitramines (17, 18, 53). The latter may decompose and/or rearrange, eventually producing methanol (CH3OH), formaldehyde (CHO), CO2, and N2O (17, 31). However, besides the formation of 14CO2, no clear conclusion can be stated about the ability of Methylobacterium sp. BJ001 to use heterocyclic nitramines as carbon and/or nitrogen sources. The inability of the bacterium to grow on RDX or HMX when added in high concentration (as applied for carbon source-utilization tests) might be the result of a toxic effect, while concentrations of RDX and HMX as low as 20 and 2.5 mg L−1 (as applied for degradation experiments) would hardly sustain a significant bacterial growth on minimal medium. On the other hand, the apparent capacity of Methylobacterium sp. BJ001 to fix atmospheric nitrogen prevents any conclusion about the potential use of RDX and HMX as sole nitrogen sources. It is emphasized, however, that whether or not Methylobacterium sp. BJ001 can utilize RDX or HMX as a sole carbon and/or nitrogen source has no real bearing on its ability to degrade these compounds to less toxic forms, or its use in bioremediation of materials contaminated with such compounds.
In contrast to RDX and HMX, which are easily broken down upon the initial reduction, nitroaromatic TNT is not well mineralized. Indeed, even though TNT was very quickly transformed (i.e. reduced) by Methylobacterium sp. BJ001, no significant release of CO2 was recorded. For several decades, bacterial metabolism of nitroaromatic compounds has been known to lead to the formation of “dead-end” reduced derivatives not further transformed. Even though the reduction of nitro groups (electron withdrawing) into amino groups (electron donor) increases the reactivity of the aromatic ring, only very limited mineralization of TNT (less than 5.0%) has been observed in bacterial systems (29, 33). On the other hand, several reports have described a denitration of TNT with a release of nitrite (NO2), which can be used by bacteria as a nitrogen source (6, 29, 56). However, the potential of Methylobacterium sp. BJ001 for fixing nitrogen prevents any conclusion about a possible utilization of TNT as a nitrogen source. Although bacterial transformation of TNT did not lead to a complete detoxification (i.e. mineralization), recalcitrant reduction metabolites are significantly less toxic than parent TNT (28) and may be bound to soil particles and humic acids, or conjugated to organic molecules, resulting in a reduction of bioavailability and toxicity (3).
Example 2 Taxonomic Analysis of BJ001T The bacterium isolated from poplar tissues, BJ001T, was identified by phylogenetic analysis as a Methylobacterium sp. (
BJ001T differed from its closest relatives (i.e., M. thiocyanate, M. extorquens, M. zatmanii, and M. rhodesianum) by carbon-source utilization features summarized in Table 4: M. thiocyanate grows on glucose, arabinose, glutamate, citrate, and cyanate and thiocyanate, M. zatmanii grows on trimethylamine, and M. rhodesianum grows on dimethylamine, which did not support the growth of BJ001T; on the other hand, M. extorquens does not use fructose, M. zatmanii does not use betaine, and M. rhodesianum does not use tartrate, which were all substrates for BJ001T (79, 83, 68, 58). Fructose, the first hexose synthesized by plant photosynthesis, is an optimal carbon substrate for BJ001T. Carbon and nitrogen source utilization and enzymatic reactions of BJ001T are shown in Tables 7-9.
On the basis of 16S and 16S-23S IGS rDNA sequence similarities, DNA-DNA hybridization values, its carbon-source utilization pattern, including the use of methane, and its endophytic association with poplar trees, BJ001T is a novel Methylobacterium species, named herein Methylobacterium populum sp. nov.
Example 3 Description of Methylobacterium populum sp. nov.Methylobacterium populum (po.pu.lum N. L. neut. adj. Populum of Populus, the Latin name of poplar).
The cells are aerobic, Gram-negative, asporogenous rods (0.8-1.0×1.0-10.0 μm) occurring singly, in pairs, or in rosettes. Cells are motile by one single polar or lateral flagella. Colonies are pink to red, slow growing, 0.1-0.2 mm in diameter after 4 days at 28° C. on LB or nutrient agar (NA) plates. The pink pigment is water-insoluble and has absorption maxima at 390, 473, 505, and 534 nm in a mixture of chloroform:methanol 1:1. The cells tested positive for the following enzymatic reactions: Catalase, oxidase, alkaline phosphatase, esterases (C4 and C8), valine arylamidase, α-chymotrypsine, acid phosphatase, and napthol-AS-BI-phosphohydrolase.
The cells utilized the following carbon-sources: D-fructose, glycerol, methanol, ethanol, formate, acetate, succinate, lactate, tartrate, pyruvate, fumarate, salicylate, formaldehyde, methylamine, methane, and betaine. Cells grow on LB and NA plates at 28° C. The cells do not use D- or L-arabinose, D-fucose, D-galactose, D-glucose, D-lactose, D-mannose, D-xylose, sucrose, iso-propanol, n-butanol, inositol, mannitol, sorbitol, L-aspartate, L-glutamate, glycine, citrate, sebacate, dimethylamine, trimethylamine, chloromethane, dichloromethane, cyanate or thiocyanate.
The utilized nitrogen-sources are ammonium, nitrate, L-alanine, L-aspartate, L-glutamate, L-glutamine, glycine, L-tryptophane, and methylamine.
The cellular fatty acids are hexadecanoate (palmitic acid, C16:0), 6.4±0.4% (n=3); cis-9-octadecenoate (oleic acid, C18:19), 81.6±2.1% (n=3); and octadecanoate (stearic acid, C18:0), 11.9±0.3% (n=3).
Optimal pH is 7.0. Cells do not grow at pH 4.0 or 9.0.
Optimal temperature is 20-30° C. Cells do not grow at 15 or 40° C.
Cells do not grow in the presence of 2.0% NaCl.
The G+C content is 70.4±0.3% (n=3). The GenBank accession number for the 16S and 16S-23S IGS rDNA sequence is AY251818.
The type strain, BJ001T, was isolated from internal poplar tissues (Populus deltoides x nigra DN34) obtained from Hramoor Nursery (Manistee, Mich.) and has been deposited in the American Type Culture Collection as ATCC BAA-705T and at the National Collection of Industrial, Food, and Marine Bacteria as NCIMB 13946T.
All chemicals used in the experiments described herein were of analytical grade and were purchased from Fluka (Ronkonkoma, N.Y.) or Sigma (St Louis, Mo.). Plant growth regulators and Phytagar were from Sigma. Phytagel was purchased from Gibco BRL (Rockville, Md.). 14C-[U-ring]-RDX and 14C-[U-ring]-HMX was purchased from DuPont NEN (Boston, Mass.) and exhibited an initial specific activity of 8.3 and 6.8 mCi mmol−1 respectively. Both 14C-RDX and 14C-HMX were mixed with corresponding non-labeled compounds to obtain final specific activities of 4.5-9.1 and 3.0-1.6 nCi mmol−1 for 14C-RDX and 14C-HMX respectively. 14C-[U-ring]-TNT was purchased from PerkinElmer Life Science (Boston, Mass.) and exhibited an initial activity of 40.0 mCi mmol−1. 14C-TNT was mixed with non-labeled TNT to give a final specific activity of 2.1-3.3 nCi mmol−1.
All patents, patent applications, and published references cited herein are hereby incorporated by reference in their entirety. While this invention has been particularly shown and described with references to preferred embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the scope of the invention encompassed by the appended claims.
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+, Growth; −, no growth; v, variable; w, weak growth; ND, not determined
+, Growth; 0, no growth
a1.25 mM
bAtmosphere methane:oxygen 95:5, 90:10, and 80:10%
cSolid medium
+, Growth; 0, no growth
+, Growth; 0, no growth
+, Growth/positive reaction; 0, no growth/negative reaction
aCarried out according to Gerhardt et al. (9)
Claims
1. (canceled)
2. An isolated Methylobacterium comprising a nucleotide sequence having at least 95% identity to the 16S ribosomal DNA and 16S-23S IGS DNA sequence of nucleotides 1-2110 of SEQ ID NO: 1, and wherein said isolated Methylobacterium degrades nitramine and nitroaromatic compounds.
3. A composition comprising:
- a Methylobacterium comprising a nucleotide sequence having at least 95% identity to the 16S ribosomal DNA and 16S-23S IGS DNA sequence of nucleotides 1-2110 of SEQ ID NO: 1, and wherein said isolated Methylobacterium degrades nitramine and nitroaromatic compounds; and
- a nitroaromatic or a nitramine compound.
4. A composition comprising:
- an aqueous slurry of solid material comprising a nitroaromatic or a nitramine compound, wherein said aqueous slurry is 30% solid material (w/w); and
- a Methylobacterium comprising a nucleotide sequence having at least 95% identity to the 16S ribosomal DNA and 16S-23S IGS DNA sequence of nucleotides 1-2110 of SEQ ID NO: 1, and wherein said isolated Methylobacterium degrades nitramine and nitroaromatic compounds.
5. The composition of claim 3, wherein said Methylobacterium species is present at a density of 109 cells/ml or greater.
6. The composition of claim 3, having a pH in the range of pH 3.0 to pH 11.0.
7. The composition of claim 6, wherein the pH is in the range of pH 6.0 to pH 8.0.
8. The composition of claim 3 which is at an oxygen saturation of 5% to 100%
9. The composition of claim 8 which is at an oxygen saturation of 20% to 100%.
10. The composition of claim 3, further comprising an additional microbial species.
11. The composition of claim 10, wherein said additional microbial species is another member of the genus Methylobacterium.
12. A preparation comprising a viable, dried Methylobacterium comprising a nucleotide sequence having at least 95% identity to the 16S ribosomal DNA and 16S-23S IGS DNA sequence of nucleotides 1-2110 of SEQ ID NO: 1, and wherein said viable, dried Methylobacterium degrades nitramine and nitroaromatic compounds
13. The preparation of claim 12, further comprising an additional microbial species.
14. The preparation of claim 13, wherein said additional microbial species is another member of the genus Methylobacterium.
15. The preparation of claim 12, further comprising one or more nutrients for said Methylobacterium.
16. A kit for the degradation of a nitramine or nitroaromatic compound, the kit comprising a Methylobacterium comprising a nucleotide sequence having at least 95% identity to the 16S ribosomal DNA and 16S-23S IGS DNA sequence of nucleotides 1-2110 of SEQ ID NO: 1, and wherein said isolated Methylobacterium degrades nitramine and nitroaromatic compounds.
Type: Application
Filed: May 8, 2007
Publication Date: Feb 7, 2008
Applicant:
Inventors: Jerald Schnoor (Iowa City, IA), Beniot Van Aken (Iowa City, IA)
Application Number: 11/800,919
International Classification: C12N 1/20 (20060101);
