WO1999027953A1 - Chemoprotective bacterial strains - Google Patents
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- WO1999027953A1 WO1999027953A1 PCT/US1998/025315 US9825315W WO9927953A1 WO 1999027953 A1 WO1999027953 A1 WO 1999027953A1 US 9825315 W US9825315 W US 9825315W WO 9927953 A1 WO9927953 A1 WO 9927953A1
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING THEREOF
- A23C9/00—Milk preparations; Milk powder or milk powder preparations
- A23C9/12—Fermented milk preparations; Treatment using microorganisms or enzymes
- A23C9/123—Fermented milk preparations; Treatment using microorganisms or enzymes using only microorganisms of the genus lactobacteriaceae; Yoghurt
- A23C9/1234—Fermented milk preparations; Treatment using microorganisms or enzymes using only microorganisms of the genus lactobacteriaceae; Yoghurt characterised by using a Lactobacillus sp. other than Lactobacillus Bulgaricus, including Bificlobacterium sp.
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/66—Microorganisms or materials therefrom
- A61K35/74—Bacteria
- A61K35/741—Probiotics
- A61K35/744—Lactic acid bacteria, e.g. enterococci, pediococci, lactococci, streptococci or leuconostocs
- A61K35/747—Lactobacilli, e.g. L. acidophilus or L. brevis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/43—Enzymes; Proenzymes; Derivatives thereof
- A61K38/44—Oxidoreductases (1)
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/43—Enzymes; Proenzymes; Derivatives thereof
- A61K38/45—Transferases (2)
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
- A61P39/02—Antidotes
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y106/00—Oxidoreductases acting on NADH or NADPH (1.6)
- C12Y106/02—Oxidoreductases acting on NADH or NADPH (1.6) with a heme protein as acceptor (1.6.2)
- C12Y106/02004—NADPH-hemoprotein reductase (1.6.2.4), i.e. NADP-cytochrome P450-reductase
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y205/00—Transferases transferring alkyl or aryl groups, other than methyl groups (2.5)
- C12Y205/01—Transferases transferring alkyl or aryl groups, other than methyl groups (2.5) transferring alkyl or aryl groups, other than methyl groups (2.5.1)
- C12Y205/01018—Glutathione transferase (2.5.1.18)
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Definitions
- the present invention relates to the field of genetically engineered bacteria for therapeutic and prophylactic use.
- the invention provides recombinant probiotic bacteria expressing enzymes that facilitate detoxification of carcinogens, and methods for their use in prevention and treatment of certain forms of cancer.
- procarcinogens promutagens
- GI procarcinogens Dietary intake of such procarcinogens not only contributes to colorectal and other types of gastrointestinal (GI) cancers, but also can increase the risk of all kinds of cancer, once the procarcinogen is absorbed into the body's circulation from the GI tract.
- a significant additional source of GI procarcinogen consumption is from tobacco byproducts. These can include procarcinogens generated during roasting of tobacco leaves and then solubilized in saliva and swallowed during the normal use of chewing or smokeless tobacco. These can also include the procarcinogens present in tobacco smoke that are solubilized in saliva and swallowed during smoking of tobacco products .
- procarcinogens are also of concern in livestock, where acute forms of toxicity, including death, can result from oral consumption and GI absorption of naturally-occurring plant toxins.
- Another area in which consumption of specific procarcinogens is of concern is populated environments that are heavily contaminated with specific environmental contaminants whose identities are known.
- Detoxification systems in cells of the GI tract are the first line of defense against procarcinogens and other ingested xenobiotic compounds.
- the enzymes of detoxification convert reactive compounds to less reactive species, and/or to species that can be more easily excreted from the cell. Enzymes of this system are often polymorphic: one isozy e may have a higher specificity toward a particular xenobiotic chemical than another.
- the enzymes of detoxification have been classified into two groups: Phase I and Phase II. Phase I enzymes function to render the xenobiotic compound reactive, whereafter it can be acted on by the Phase II enzymes .
- Cyt P450 contains a heme group which acts as the cofactor in the catalysis of oxygenation of the procarcinogens, thereby providing a reactive chemical group for the Phase II family to conjugate to a second molecule, which increases the hydrophilicity of the resulting compound.
- a prominent member of the Phase II family is glutathione S-transferase (GST) . It catalyzes the conjugation of glutathione, the tripeptide ⁇ -glutamyl- cysteinylglycine, to a variety of toxic electrophilic compounds.
- This invention provides compositions and methods for supplementing the detoxification systems of GI cells to protect the body from ingested procarcinogens and other toxic substances.
- compositions of the invention comprise probiotic microorganisms which have been genetically modified to express mammalian enzymes involved in Phase I and Phase II detoxification.
- the probiotic microorganisms are GI tract- colonizing or -associated bacteria, such as various strains of Lactobacillus .
- the invention is practiced by feeding the engineered probiotic organisms to an animal or human.
- the organisms colonize or otherwise become associated with the GI tract of the individual, whereupon they grow and multiply, continuing to produce the detoxifying enzymes.
- these bacteria scavenge and detoxify food procarcinogens, releasing the biologically innocuous metabolites into the bowel contents for excretion.
- the overall bioavailability of carcinogens is thereby reduced, which reduces the risk and incidence of all types of cancers, and GI cancers in particular.
- the probiotic microorganism is selected from the group consisting of Lactobacillus , Lactococcus , Bifidobacteria , Eubacteria and non-pathogenic strains of Escherichia coli .
- the enzymes are selected from the group consisting of cytochrome P450, NADPH-cytochrome P450 reductase, glutathione-S-transferase , gamma-glutamylcysteine synthetase, N-acetyltransferase, aldehyde dehydrogenase, and aldehyde reductase.
- the procarcinogenic or toxic substances are selected from the group consisting of polycyclic aromatic hydrocarbons, mycotoxins, arylamines, heterocyclic amines, nitrosamines and benzene.
- genes encoding three classes of recombinant drug- metabolizing enzymes are used to transform probiotic bacteria. These genes encode (1) one or more of the commonly available forms of Cyt P450 for Phase I metabolism, (2) a common form of the enzyme NADPH-P450 reductase that associates with, and contributes electrons to, Cyt P450 to enable efficient Phase I metabolism; and (3) either common or unique forms of glutathione S- transferase (GST) for Phase II metabolism to produce nonreactive conjugates.
- GST glutathione S- transferase
- a plurality of different probiotic microorganisms are used, which express a plurality of different enzymes.
- the above- described metabolically fortified bacteria are used in products like yogurt to populate the human GI tract, and by so-doing, put in place a system that steadfastly acts to capture and detoxify procarcinogen molecules as they are presented to the GI mucosal surface where the bacteria reside.
- FIG. 1 Schematic diagram showing the specific detoxification and elimination of the procarcinogen, benzo(a) pyrene by recombinant probiotic bacteria expressing cytochrome P450, NADPH P450 reductase and glutathione S-transferase. Other major procarcinogen contaminants of human food and their detoxification steps are also depicted.
- Figure 2. Schematic diagram showing two examples, Construct 1 and Construct 2, which contain functional expression cassettes for each of three recombinant drug-metabolizing enzymes in a preferred embodiment of the invention.
- Construct 1 is 9742 nucleotides, with components as follows: Cyt P450 1A1 cDNA at bases 1-1625; NADPH Cyt P450 reductase at bases 1637-4099; M13 origin of replication at bases 4267-4665; ⁇ -lactamase CDS at bases 4082-5732; ColEl origin at bases 5792-6491; Human GST pi cassette at bases 6786-7678; Laq I q at bases 8136-9402; Taq promoter at bases 9577-9629; Taq promoter at bases 9652-9736.
- Construct 2 is 9641 nucleotides, with components as follows: Cyt P450 1A2 cDNA at bases 1-1523; NADPH Cyt P450 reductase at bases 1535-3997; M13 origin of replication at bases 4165-4563; ⁇ -lactamase CDS at bases 4700-5630; ColEl origin at bases 5690-6389; Human GST pi cassette at bases 6684-7576; Laq I q at bases 8034-9300; Taq promoter at bases 9455-9527; Taq promoter at bases 9550-9634. Additional variants of these are also used, in which additional cytochrome P450 and/or GST cDNAs are exchanged at the indicated sites.
- FIG. 3 Western immunoblot showing rec cytochrome P450 1A1 production in E . coli DH5 cells transformed with the Construct 1 plasmid. Cultures were induced overnight with IPTG. Bacterial membranes were prepared according to Parikh et al. (1997) . Proteins (75 ⁇ g of bacterial membrane protein per lane) were separated on 12.5% SDS-PAGE and transferred to a nitrocellulose membrane. Immunoblotting was performed using an ECL kit according to the manufacturer's protocol (Pierce
- CYP450 1A1 (57 kDa) was detected using a polyclonal goat anti-rabbit secondary antibody conjugated to horseradish peroxidase
- Lane 1 is Control (pIC20r) ; Lane 2 is pCW lAl/reductase; Lane 3 is pCW lAl/reductase/GST pi (construct 1) ; Lane 4 is a blank lane; Lane 5 is molecular weight markers (kDa) .
- FIG. 4 Western immunoblot showing rec cytochrome P450 1A2 production in E . coll DH5 ⁇ cells transformed with the Construct 2 plasmid. Cultures were induced overnight with IPTG. Bacterial membranes were prepared according to Pa ikh et al. (1997). Proteins (100 ⁇ g of bacterial membrane protein per lane) were separated on 12.5% SDS-PAGE and transferred to a nitrocellulose membrane.
- CYP450 1A2 was visualized using a goat anti-human CYP 1A2 polyclonal antibody (1:2000 dilution; RDI Research Diagnostics, Inc.) and a swine anti-goat secondary antibody conjugated to horseradish peroxidase (1:5000, Boehringer Mannheim) with chemiluminescent substrate (Pierce Biochemicals,
- Lane 1 is molecular weight markers (kDa) ; Lane 2 is purified CYP 450 1A2 (0.2 ⁇ g, Panvera Biochemicals); Lane 3 is purified CYP 450 1A2 (0.4 ⁇ g, Panvera Biochemicals) ; Lane 4 is control (pIC20r) ; Lanes 5 and 6 are blank; Lane 7 is pCW 1A2/reductase; Lane 8 is pCW lA2/reductase/GST pi clone #3 (construct 2) .
- FIG. 1 Western immunoblot showing rec NADPH-P450 reductase production in E . coli DH5 cells transformed with Construct 1 or Construct 2 plasmids. Cultures were induced overnight with IPTG. Bacterial membranes were prepared according to Parikh et al. (1997) . Proteins (100 ⁇ g of bacterial membrane protein per lane) were separated on 12.5% SDS-PAGE and transferred to a nitrocellulose membrane. Immunoblotting was performed using an ECL kit according to the manufacturer's protocol (Pierce Biochemicals, Rockford). A polyclonal rabbit anti-human CYP450 1A1 antibody (RDI Research Diagnostics) was used as the primary antibody (1:1000 dilution).
- P450 reductase (77 kDa) was detected using a polyclonal goat anti-rabbit secondary antibody conjugated to horseradish peroxidase (1:5000 dilution) and chemiluminescent substrate. The gel was overloaded, leading to smearing of the 77 kDa P450 reductase band.
- Lane 1 is rat liver extract showing NADPH-P450 reductase; Lane 2 is blank; Lane 3 is the control (pIC20r) ; Lane 4 is pCW lAl/reductase; Lane 5 is pCW 1A1 reductase/GST pi (Construct 1) ; Lane 6 is pCW lA2/reductase/GST pi (Construct 2) ; Lane 7 is blank; Lane 8 is molecular weight markers (kDa) .
- FIG. 1 Western immunoblot showing rec GST pi production in E . coli DH5 cells transformed with Construct 1 or Construct 2 plasmid ⁇ . Cultures were induced overnight with IPTG. Bacterial membranes were prepared according to Parikh et al. (1997). Proteins (50 ⁇ g of crude bacterial supernate per lane) were separated on 12.5% SDS-PAGE and transferred to a nitrocellulose membrane. Immunoblotting was performed using an ECL kit according to the manufacturer's protocol (Pierce Biochemicals, Rockford) . A polyclonal rabbit anti-GST pi antibody (RDI Research Diagnostics) was used as the primary antibody (1:1000 dilution).
- GST pi was detected using a polyclonal goat anti-rabbit secondary antibody conjugated to horseradish peroxidase (1:5000 dilution) and chemiluminescent substrate.
- Lane 1 is molecular weight markers (kDa) ;
- Lane 2 is purified human GST pi (0.1 ⁇ g) ;
- Lane 3 is the control (pIC20r) ;
- Lane 4 is pCW 1A1/OR;
- Lane 5 is pCW 1A1/0R-GST;
- Lane 6 is pCW 1A2/0R;
- Lane 7 is pCW 1A2/OR-GST pi.
- FIG. 7 Reduced carbon monoxide difference spectrum of rec cytochrome P450 1A2 in membranes of bacterial cells transformed with Construct 2 plasmid.
- Intact difference spectrum illustrates that the cytochrome P450 1A2 apoprotein synthesized in the bacterial cells is properly binding the heme prosthetic group produced by the bacterial cells to yield functional holoenzyme.
- the rec cytochrome P450 content of the bacterial membranes was determined by measuring the absorbance difference at 450 nm between the reduced hemoprotein (Fe+2) versus the reduced hemoprotein bound to carbon monoxide (Fe+2-C0) .
- Figure 8 Results of Ames mutagenesis assay showing linear, dose-dependent induction of mutations in TA98 tester strain using benzo (a) pyrene as the procarcinogen.
- a TA98 Salmonella tester strain containing a mutation in the histidine operon was preincubated with benzo (a) pyrene (B(a)P) and a 10% S9 mixture for 30 minutes at 37°C prior to the Ames assay. Following the preincubation, a histidine/biotin top agar was added to the contents listed above and plated on minimal glucose plates. Spontaneous reversion of TA98 to histidine independence by B(a)P was measured by counting the number of colonies on the minimal glucose plates after a 48 hour incubation at 37°C.
- compositions of the invention comprise recombinant probiotic bacteria engineered to express one or more isofor s of two critical mammalian detoxification enzymes, cytochrome P450 (Cyt P450) and glutathione-S- transferase (GST) , as well as the important contributor to the Phase I metabolism step, NADPH-P450 reductase.
- Cyt P450 cytochrome P450
- GST glutathione-S- transferase
- the Cyt P450 enzyme catalyzes the first step in the detoxification, converting a non-reactive procarcinogen to a reactive species that can be further processed.
- the GST enzyme then conjugates the intermediate product of the Cyt P450-catalyzed reaction to glutathione, which is normally present in bacterial cells at millimolar concentrations to yield a biologically-inert, water-soluble metabolite.
- One possible step in further engineering the probiotic bacteria would be to integrate and stably express two cDNAs encoding the heavy and light subunits of the enzyme gamma-glutamylcysteine synthetase ( ⁇ -GCS) .
- ⁇ -GCS gamma-glutamylcysteine synthetase
- recombinant enzymes can also be expressed in probiotic bacteria to direct the detoxification of procarcinogens; examples include one or more isoforms of N-acetyltransferase, aldehyde dehydrogenase, and aldehyde reductase to metabolize aflatoxin. This would broaden the scope of environmental toxins that could be safely detoxified by probiotic bacteria of the invention.
- These recombinant gene products are stably expressed in strains of probiotic bacteria, such as Lactobacillus acidophilus , which are generally accepted as being "friendly floral" strains, i.e., strains that grow well within the human or other mammalian GI ecosystem without producing or secreting detrimental bacterial toxins.
- the substrates for the two-step drug metabolism catalyzed by the fortified recombinant bacteria of the invention are molecules that are generally referred to herein as "procarcinogens.” These are environmental contaminants that humans come in contact with, most commonly, through smoking or gastrointestinal absorption. Some examples of procarcinogens that commonly appear in the daily human diet are illustrated in Figure 1. These and additional procarcinogens that commonly occur in the production and packaging of human foods were recently studied and listed in a prioritized manner in a book recently published by a study group of the U. S. National Academy of Sciences (Carcinogens and Anticarcinoqens in the Human Diet, National Academy Press, Washington, D.C., 1996) .
- the procarcinogens consumed in a daily diet usually are not highly water soluble. Therefore, they are readily absorbed from the lumenal contents of the stomach, as well as the small and large intestine. Once absorbed, the procarcinogens distribute throughout the body, where they are stored or metabolized by cellular Cyt P450s to yield highly reactive, electrophilic "proximate" carcinogens which can now, because of their highly reactive nature, attack DNA and induce mutation (see Figure 1) .
- the accrued result of this chronic DNA modification can be either cell death (a cytotoxic result) or transformation to a cancer cell (a neoplastic transformational result) .
- the fortified bacteria of the present invention that stably express the mammalian detoxification enzymes can aid in averting systemic distribution of procarcinogens by detoxifying them in the GI lumen, before they can be absorbed into the system.
- the fortified bacteria residing in the GI lumen can routinely mix with ingested, partially digested, hydrated food. After absorbing the procarcinogens and converting them to safe, biologically inert metabolites, the bacteria will secrete the innocuous metabolites back into the GI lumenal contents to be excreted.
- the fortified bacteria of the invention will serve not only to lower the risk of GI associated cancers, but also will contribute to lower risks of all types of cancer.
- the following basic steps should be followed in order to practice the present invention: (1) select the detoxifying enzymes desired for expression in probiotic bacteria; (2) clone the enzyme-encoding genes in a form suitable for expression in the selected probiotic " bacteria; (3) transform the bacteria with the cloned genes, such that the bacteria express functional enzymes; and (4) feed the recombinant bacteria to animal or human subjects for which protection from procarcinogens is desired. Each of these steps is described in greater detail below.
- the recombinant bacteria of the present invention are engineered to express enzymes involved in the two-step detoxification mechanism described above.
- enzymes include, but are not limited to: (1) selected substrate-specific isoforms of Cyt P450; (2) one or more isoforms or recombinant variants of GST; (3) a form of NADPH-P450 oxidoreductase, an enzyme that produces reducing equivalents consumed by Cyt P450 during its oxidation of the procarcinogen molecule; (4) one or more isoforms of N-acetyltransferase, (5) aldehyde dehydrogenase, (6) aldehyde reductase, and (7) heavy and light subunits of the enzyme ⁇ -GCS.
- cytochrome P450 isozymes are capable of metabolizing the large majority of environmental procarcinogens encountered by humans (Guengerich, 1996) .
- Candidate cytochrome P450 isozymes include CYP IBl, CYP 1A1, 1A2 and 2E1.
- CYP IBl a form that was first described several years ago (Gehly, Fahl, et al., J. Biol. Chem. 254 : 5041-5048, 1979) because of its unique specificity for metabolizing polycyclic aromatic hydrocarbon (PAH) substrates, has now been cloned and can be efficiently expressed in bacterial cells (Savas et al., Arch. Bioch. Biophys.
- CYP 1A2 is a logical candidate because of its capacity to oxidize the carcinogenic arylamines and heterocyclic amines found in broiled meats.
- CYP 2E1 is a logical candidate because of its ability to metabolize nitrosamines and benzene.
- Certain P450s like CYP 2D6 will need to be approached cautiously in clinical trials because its substrate specificity includes several drugs, such as antidepressants, which adult humans fairly commonly consume .
- Cytosolic members of mammalian GSTs are dimeric proteins that have four classes (Alpha, Mu, Pi, and Theta) .
- Alpha-class GSTs to detoxify alkylating compounds is well documented.
- GSTs catalyze the nucleophilic attack of the thiolate anion of the tripeptide glutathione (GSH) on the electrophilic functional group of a hydrophobic substrate.
- GSH tripeptide glutathione
- the hydrophobic electrophilic compounds that serve as substrates for GSTs undergo catalytic conjugation to GSH to become more polar, less toxic, and more readily excretable from the cells as glutathionyl conjugates.
- GST isoforms Because of their evolutionary heritage of conjugating large numbers of structurally diverse electrophilic metabolites that mammals encounter, the spectrum of GST isoforms required to accommodate the Phase I metabolites generated by the above CYP450s is smaller (Hayes & Pulford, Crit. Rev. Bioch. Mol. Biol. 30: 445-600, 1995) . Generally, all GST isoforms are capable of catalyzing the conjugation of most electrophiles, but there can be sizable differences in the rates at which the isofor -catalyzed reactions proceed.
- the GST pi isoform is capable of conjugating very diverse groups of organic electrophiles including P.AH epoxides and diol-epoxides .
- the GST alpha class isoform, Yc is very efficient at conjugating aflatoxin- epoxide, while other alpha class isoforms are efficient at detoxifying alkylating drugs like melphalan and cytoxan.
- Other broad rules of specificity are described in the GST review by Hayes (Hayes & Pulford, 1995, supra) .
- a gene encoding a wild-type GST is used.
- recombinant GSTs having increased enzymatic activity are used.
- Such recombinant GSTs are known in the art (Gulick & Fahl, Proc. Natl. Acad. Sci. USA 92 : 8140-8144, 1995; and are described in commonly-owned U.S. Patent Application Serial No. 08/297,431, incorporated by reference herein.
- a panel of, e.g., six to eight recombinant plasmids are generated, which express, e.g. , three or four different cDNAs encoding Cyt P450s with different substrate specificity and, e.g., two or three different cDNAs encoding GSTs with different substrate specificity.
- These different cDNAs also may be expressed in different probiotic bacteria having complementary biological features. Mixing clones of different bacteria expressing different forms of detoxifying enzymes will enable metabolism of broad mixtures of procarcinogens, or very specific procarcinogens, depending on the desired application.
- Probiotic bacteria suitable for the present invention include any non pathogenic, preferably physiologically beneficial, bacteria that colonize or are otherwise associated with or resident in the gastrointestinal tract of the selected subject animal or human.
- these bacteria are species of the genus Lactobacillus .
- other genera may be utilized, including, but not limited to: Lactococcus , Bifidobacteria , Eubacteria and non-pathogenic strains of Escherichia coli (see Gibson and Roberfroid, J. Nutrition 125: 1401-1412, 1995).
- Lactobacilli are a large and diverse group of Gram-positive bacilli that are common components of the normal indigenous flora of humans and other animals. Lactobacilli are considered "health promoting," but in any event are rarely pathogenic, making them good candidates for use in the present invention. Indeed, Lactobacilli have been exploited recently as vaccine delivery vehicles, i.e. expressing antigens in the GI tract of immune-functional individuals for purposes of eliciting an immune response (see, e.g., Rush et al., Chapter 6 in Gram-Positive Bacteria as Vaccine Vehicles for Mucosal Immunization, (G. Pozzi & J.M. Wells, eds.), Austin Bioscience, 1997) .
- Different strains and species of Lactobacillus are differentially capable of colonizing or becoming otherwise associated with the GI tract of a particular animal.
- Two approaches can be used in selecting appropriate strains for delivery of detoxifying enzymes to a particular animal species (including humans): (1) selection of strains known to be capable of colonizing mucosal surfaces of the animal (e.g., Lactobacillus GG is known to colonize the human GI tract); and/or (2) selection of strains naturally found in foods, which may have limited interactions with the host GI tract, but nevertheless may inhabit the GI tract for significant periods of time.
- the fate of viable Lactobacillus cells within the GI system of mammals depends on a number of variables.
- the bacterial cells simply mix with the undigested fiber of ingested food and move along the GI system. In this situation there is little colonization by the Lactobacillus cells.
- cells will find host sites within the mucosal matrix, stay there and replicate (i.e., "colonize"). The factors that determine the ability of cells to colonize or merely populate sites within the GI system are not fully understood.
- Some parameters that affect the ability of probiotic bacteria to colonize include: the pH of the particular GI site, acidophilus means "acid lover” meaning these strains can accommodate the low pH of the stomach and duodenum; the oxygen content of the site; the strain of bacteria; and the ability to compete for nutrients with other types of bacteria that are encountered on the mucosal surface of GI epithelium.
- acidophilus means "acid lover” meaning these strains can accommodate the low pH of the stomach and duodenum
- the oxygen content of the site the strain of bacteria
- the ability to compete for nutrients with other types of bacteria that are encountered on the mucosal surface of GI epithelium selection of appropriate strains can be made on the basis of how long such production is desired in the individual undergoing the treatment.
- combinations of different strains, some transient and others colonizing can be used to provide short and long- term protection.
- Lactobacillus species have been demonstrated amenable to transformation and expression/secretion of recombinant proteins.
- Lactobacilli can be genetically modified by way of two mechanisms: (1) via introduction of an ectopic plasmid carrying a foreign gene; or (2) via stable integration of a foreign gene into the genome.
- One advantage to this latter approach is that it avoids potential loss of the foreign gene, which can result from plasmid shedding during expansion of the bacterial cultures.
- the potential lower expression associated with stable integration of the foreign gene could be offset by the more stable retention of that gene and resulting ability of the bacteria to express the detoxifying enzymes for an extended period of time.
- Lactobacillus species Moreover, the art describes the successful introduction and expression of foreign genetic material in a variety of Lactobacillus species, including L . casei , L . pi ant arum , L . paracasei , L . acidophilus , L . fermentum and L . zeae , among others (Rush et al., 1997, supra ; Rush et al., Microbiol. Biotechnol. 4J : 537-542, 1997; Hols et al., Microbiology 143: 2733-2741, 1997).
- Example 2 below describes vector design and a protocol for transformation of an L . gasseri strain that colonizes the murine upper GI tract.
- This protocol follows standard protocols for transformation of Lactobacillus by electroporation (see, e.g., Aukrust et al., Chapter 20 in Methods in Molecular Biology, Vol. 47, (J.A. Nickoloff, ed.), Humana Press Inc., Totowa, N.J.).
- the vectors presently available in the art for transforming Lactobacillus were not designed for consumption by humans or animals.
- most of the vectors utilize antibiotic resistance as a selection means. Since it is undesirable to introduce antibiotic resistance into an animal or human, the currently available vectors should be modified to comprise a different selection means, such as a color indicator. Selection means that do not rely on antibiotic resistance are known in the art and are available.
- Example 1 describes the transformation of E . coli with a recombinant plasmid encoding a Cyt-P450, NADPH-P450 reductase and a GST.
- the recombinant probiotic bacteria are produced, they are used to protect against ingested procarcinogens and other toxic agents.
- the mode of administration is by oral or nasal injection, or by feeding (alone or incorporated into the subject's feed or food) .
- the Lactobacillus acidophilus that is presently widely available commercially is sold as gel capsules containing a lyophilized mixture of bacterial cells and a solid support such as mannitol. When the gel capsule is ingested with liquid, the lyophilized cells are re- hydrated and become viable, clonogenic bacteria.
- the recombinant Lactobacillus cells are added to food by sprinkling in the powdered, lyophilized preparation.
- the re-hydrated, viable - Lactobacillus cells will then populate and/or colonize at sites throughout the upper and lower gastrointestinal system.
- the recombinant bacteria are used to produce fermented milk products, such as yogurt and kefir, in the same manner that non-recombinant lactobacilli would be used.
- the fortified probacteria are mixed into a product such as chewing tobacco.
- the bacteria are mobilized to begin scavenging the procarcinogens to preemptively detoxify them before they are absorbed by oral, esophageal, gastric and intestinal epithelial cells.
- Another application of this invention in humans is directed to populated environments that are heavily contaminated with environmental contaminants whose identities are known, whose consumption by inhabitants is known, and the toxic impact upon the inhabitants consuming contaminated groundwater and produce is also known.
- environmental contaminants whose identities are known, whose consumption by inhabitants is known, and the toxic impact upon the inhabitants consuming contaminated groundwater and produce is also known.
- Gladowice, Poland, and other industrialized Eastern bloc sites the level of environmental contamination has been estimated to be greater than that which could be environmentally remediated within the next 100 years.
- the fortified bacteria are mixed into feed for agriculturally important animals, such as cows, pigs and chickens.
- livestock crops e.g., aflatoxin from Aspergillus flavus in peanut butter
- Decreasing the procarcinogen "load" to the animals should be easier and more cost-effective than attempting to remove them from the milk or meat consumer products.
- the toxic element in Leucaena the amino acid analogue mimosine
- recCytochrome P450 1A1 or 1A2 recNADPH-P450 Reductase and recGST pi in Escherichia coli : Detoxification of Benzo (a) pyrene ⁇ a Common Food Procarcinogen
- Benzo (a) pyrene has long been known to be tumorigenic when fed or applied topically to experimental animals, and has served as a prototype for chemical carcinogens. It is metabolized by the cytochrome P450 enzymes to form the 7,8-epoxide, which is then metabolized by epoxide hydrolase to form the BP-7,8-diol. The compound is further oxidized by cytochrome P450s to BPDE. BPDE was demonstrated to be a substrate of GST for glutathione conjugation. The ability of GST expression in cells to confer BPDE resistance is known. However, co-expression of Cyt P450 and GST in recombinant bacteria heretofore has not been reported.
- Construct 1 and Construct 2 Expression Plasmids The design and structure of two examples of expression plasmids, Construct 1 and Construct 2, are presented in Figure 2.
- Construct 1 we started with the pCWIAlOR vector constructed by Parikh, Guengerich et al. (Nature Biotech. 15: 784-788, 1997). This bicistronic expression vector containing a full length cDNAs for both CYP 1A1 and human NADPH P450-reductase was kindly provided by Dr. Fred Guengerich, Vanderbilt University. Dr.
- Guengerich has likewise provided the same vector in which the P450 site contains cDNAs encoding human CYP 1A2 , 2E1, 2C9, 2D6, or 3A4.
- a cDNA encoding human CYP IBl, modified for efficient expression in bacteria, has been provided by Dr. Colin Jefcoate, University of Wisconsin. With these cDNAs, the sequences of which are publicly available, a variety of P450 expression vectors can be constructed using standard methods.
- An expression cassette containing a lac i promoter sequence joined to a cDNA encoding the human GST pi isozyme was prepared by PCR amplifying this roughly 700 bp sequence from the pGFLEX vector created in our laboratory (Manoharan et al., Gene 193: 229-237, 1997) and ligating it into a unique restriction site on the pCWIAlOR vector.
- the resulting plasmid, Construct 1 (or Construct 2 where the lac i-GST cassette is ligated into pCWlA20R) was transformed into DH5 cells, and the transformed cells were streaked on a LB-a p plate.
- plasmids were prepared using the PERFECTprep Plasmid DNA Preparation kit.
- the plasmids were checked for correct incorporation by diagnostic restriction digests, and the successful constructs were sequenced to further confirm correct incorporation, using AmpliTaq DNA polymerase.
- Construct 2 plasmid DNA was grown overnight at 37 " C in LB-amp. A 5-ml aliquot was then diluted 1:100 in modified TB [12g bactotryptone, 24g yeast extract, 2g bactopeptone, and 4ml glycerol (liter -1 ) ] containing lOOmg ampicillin liter "* , 1. OmM thiamine, and 0.25ml of trace elements solution (liter " J . Composition of the trace elements solution: [27g FeCl ?
- Membrane fraction preparation The procedure of Gillam et al. (1993, supra) was used. Cells were chilled on ice and harvested by centrifugation at 5,000g for 10 minutes. The cell pellet was weighed and resuspended in lOOmM Tris-acetate buffer (pH 7.6) containing 500mM sucrose and 0.5mM EDTA (15ml buffer per g of wet weight cells) . Following the addition of lysozyme (0.2mg ml ""1 ), the suspension was diluted twofold with chilled H0, and then incubated on ice for 30 minutes. The resulting spheroplasts were pelleted at
- Spheroplasts were lysed in an ice-salt bath using a Branson Cell Disruptor 185 (Branson Sonic Power Co., Danbury, CT) , and centrifuged at 10,000g for 20 minutes at 4°C. Supernatant was removed and centrifuged at 180,000g for 65 minutes at 4°C. The membrane fraction was resuspended in 50mM Tris-acetate buffer (pH 7.6) containing 250mM sucrose and 0.25mM EDTA using gentle homogenization.
- recNADPH-P450 reductase and recGST pi are provided in the description of Figure 7 and in the tables.
- Ethoxyresorufin O-deethylation was measured by fluorescence spectroscopy as described by Parikh et al. (1997) .
- Replicate clones of washed bacterial cells containing either pCW lAl/reductase/GST pi (Construct 1) or pCW lA2/reductase/GST pi (Construct 2) were mixed with
- the level of recNADPH P450 reductase in bacterial membranes was measured by its ability to catalyze the reduction of cytochrome c.
- Bacterial membranes isolated from replicate clones of bacterial cells containing either Construct 1 or Construct 2 were preincubated with 0.5 mM horse heart cytochrome c in 0.3 M potassium phosphate buffer, pH 7.7 for 2 min at 30°C before the addition of 10 mM NADPH. The formation of reduced cytochrome c was monitored at 550 nm.
- Table 3 GSH Conjugation of Chloro-dinitro-benzene
- CDNB recGlutathione-S-Transferase
- mice were anesthetized with nembutal and then surgically opened with a ventral, midline incision. Ligatures (untied) were placed around the esophagus near the stomach entry and around the small bowel just distal to the duodenum. The small bowel was cut, the feeding needle was inserted orally into the mouse and threaded down to the esophageal opening to the stomach.
- the incubation material was filtered through a 0.2 ⁇ sterile filter, and the filtrate was then used to reconstitute cofactor/TA98 Ames assay incubations.
- the carcinogen/mutagen component of the Ames incubations was contributed by the benzo (a) pyrene that had been carried through the preceding bacterial incubations in the mouse stomach. No metabolism of the benzo (a) pyrene (originally, 24 nmol) by the bacterial cells in the mouse stomach incubation (i.e., the pIC20r control cells) would mean a largely intact carryover of the benzo (a) pyrene to the Ames assay and a resulting high TA98 colony count.
- Lactobacillus species are amenable to transformation by electroporation.
- MRS broth 10.0 g peptone, 8.0 g meat extract, 4.0 g yeast extract, 20.0 g glucose, 1 mL onooleate (Tween 80), 2.0 g K 2 HP0 4 , 5.0 g sodium acetate'3H20 , 2.0 g (NH 3 ) .- citrate, 0.2 g MgSO 7H0, 0.05 g MnSOj'4H : 0, distilled water to l L.
- MRSSM MRS with 0.5 M Sucrose, 0.1 M MgCl .
- Electroporation solutions 1) SM: 326 g sucrose (952 mM) , 0.71 g MgCl ' 6H.0 (3.5 mM) , distilled water to 1 L.
- DNA Dissolve plasmid pGK12 in TE (lOmM Tris-HCl, 1 mM EDTA, pH 7.5) to 0.10-1.0 ⁇ g/ ⁇ L. Ligation mixtures should be ethanol precipitated and washed, then dissolved in TE before electroporation.
- SM or 100 mL of 1 mM MgC12 according to an alternate procedure
- Pellets were again resuspended in 100 mL of SM or, in an alternate procedure, 30% PEG, then washed and re-pelleted as above. Cells were resuspended in 1 mL of SM (or 30% PEG according to an alternate procedure) . Aliquots containing 10 9 -10 10 cells/mL were transferred to mi-cro tubes for electroporation. The DNA in a volume ⁇ 1/20 of the cell suspension volume was added immediately before electroporation. The mixture was transferred to an ice cold electroporation cuvette with a 2-mm electrode gap. Different electric pulses were delivered as shown in Table 6.
- Table 7 shows the results of electroporation experiments demonstrating efficient delivery and expression of a plasmid-encoded drug resistance gene in a probiotic bacterial strain, Lactobacillus brevis , that is reported in the literature to successfully colonize human intestinal sites.
- Expression of the erythromycin resistance gene from the pKTH2121 plasmid expression cassette is of special significance because this vector and its expression cassette configuration provide the likely model of how the drug metabolizing enzyme cDNA sequences of the invention are expressed.
- Table 7 Electroporation of Gram-Positive Shuttle Vectors into Lactobacillus brevis cells. Plasmid # Erythromycin'" colonies pGK12 1000 pKTH2121 30 pGKnucMCS 50 a. 2.0 ⁇ g//mL erythromycin was used for selection of plas id-containing transformants . b. 2-mm electrode gap cuvettes were used in the electroporations . c. The electroporation settings were 2.5 kV, 200 ⁇ , and 25 ⁇ F. d.
- Positive control + pKTH2121 + Lactobacillus brevis cells were electroporated as described above and by Raya et al.(1992). Following selection of colonies for 48 hours on Lactobacilli MRS plates containing 2 ⁇ g/mL erythromycin, portions of the colonies were picked and smeared onto small discs impregnated with the ⁇ -lactamase substrate, nitrocefin
Abstract
Description
Claims
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IL13626698A IL136266A0 (en) | 1997-11-28 | 1998-11-27 | Chemoprotective bacterial strains |
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JP2000522938A JP2001524530A (en) | 1997-11-28 | 1998-11-27 | Chemoprotective bacterial strain |
CA002311613A CA2311613A1 (en) | 1997-11-28 | 1998-11-27 | Chemoprotective bacterial strains |
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FR2810337A1 (en) * | 2000-06-20 | 2001-12-21 | Univ Clermont Auvergne | New microorganisms expressing heterologous gene, useful e.g. for detoxification, have high survival rates in stomach and colon |
KR100386144B1 (en) * | 1999-06-24 | 2003-06-02 | 와카모토 세이야꾸 가부시끼가이샤 | Food or drink product with a disinfection property of helicobacter pylori |
WO2004076657A2 (en) | 2003-02-28 | 2004-09-10 | Mcgill University | Cell and enzyme compositions for modulating bile acids, cholesterol and triglycerides |
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JP2012197313A (en) * | 2012-06-25 | 2012-10-18 | Snow Brand Milk Products Co Ltd | Agent for promoting bone formation and inhibiting bone resorption |
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- 1998-11-27 EP EP98960523A patent/EP1032413A1/en not_active Withdrawn
- 1998-11-27 AU AU16105/99A patent/AU754020B2/en not_active Ceased
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- 1998-11-27 JP JP2000522938A patent/JP2001524530A/en active Pending
- 1998-11-27 WO PCT/US1998/025315 patent/WO1999027953A1/en active IP Right Grant
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Cited By (8)
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KR100386144B1 (en) * | 1999-06-24 | 2003-06-02 | 와카모토 세이야꾸 가부시끼가이샤 | Food or drink product with a disinfection property of helicobacter pylori |
FR2810337A1 (en) * | 2000-06-20 | 2001-12-21 | Univ Clermont Auvergne | New microorganisms expressing heterologous gene, useful e.g. for detoxification, have high survival rates in stomach and colon |
WO2001098461A1 (en) * | 2000-06-20 | 2001-12-27 | Universite D'auvergne | Micro-organisms active in the digestive environment |
WO2004076657A2 (en) | 2003-02-28 | 2004-09-10 | Mcgill University | Cell and enzyme compositions for modulating bile acids, cholesterol and triglycerides |
WO2004076657A3 (en) * | 2003-02-28 | 2004-12-29 | Univ Mcgill | Cell and enzyme compositions for modulating bile acids, cholesterol and triglycerides |
US7939061B2 (en) | 2003-02-28 | 2011-05-10 | Micropharma Limited | Cell and enzyme compositions for modulating bile acids, cholesterol and triglycerides |
US8932578B2 (en) | 2003-02-28 | 2015-01-13 | Uas Laboratories Llc | Cell and enzyme compositions for modulating ale acids, cholesterol and triglycerides |
US9637729B2 (en) | 2003-02-28 | 2017-05-02 | Uas Laboratories Llc | Cell and enzyme compositions for modulating bile acids, cholesterol and triglycerides |
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JP2001524530A (en) | 2001-12-04 |
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