초록 ▼

The present invention relates to the use of compositions for isolating and/or stabilizing nucleic acids in or from microorganisms?such as prokaryotes, fungi, protozoa or algae. The composition contains, as an essential ingredient, a cationic compound of general formulaY+R1R2R3R4X?whereinY may denote

The present invention relates to the use of compositions for isolating and/or stabilizing nucleic acids in or from microorganisms?such as prokaryotes, fungi, protozoa or algae. The composition contains, as an essential ingredient, a cationic compound of general formulaY+R1R2R3R4X?whereinY may denote nitrogen or phosphorus,R1, R2, R3 and R4 independently of one another may denote an unbranched or branched C1-C20-alkyl and/or a C6-C20-aryl group as well as a C6-C26-aralkyl group, andX? may denote an anion of an inorganic or organic, mono- or polybasic acid.

대표청구항 ▼

1. A method for stabilizing nucleic acids in or from microorganisms comprising administering to the microorganism a composition containing a cationic compound of general formula 1:Y+R1R2R3R4X???(1) whereinY represents nitrogen or phosphorus; R1, R2, R3 and R4, independently, represent an unbranched

1. A method for stabilizing nucleic acids in or from microorganisms comprising administering to the microorganism a composition containing a cationic compound of general formula 1:Y+R1R2R3R4X???(1) whereinY represents nitrogen or phosphorus; R1, R2, R3 and R4, independently, represent an unbranched or branched C1-C20-alkyl group and/or a C7-C20-aryl group as well as a C6-C26-arallcyl group; X? represents an anion of an inorganic or organic, mono- or polybasic acid; and at least one proton donor. 2. The method according to claim 1, wherein Y denotes nitrogen.3. The method according to claim 1, wherein R1 denotes a higher alkyl group with 12, 14 or 16 carbon atoms and R2, R3 and R4 each represent a methyl group.4. The method according to claim 1 or 3, wherein the anion X? is an anion of hydrohalic acids or anions of mono- or dibasic organic acids.5. The method according to claim 4, wherein the anion is selected from the group consisting of bromide, chloride, phosphate, sulphate, formate, acetate, propionate, oxalate, malonate, succinate and citrate.6. The method according claim 1, wherein the proton donor is selected from the group consisting of saturated aliphatic monocarboxylic acids, the unsaturated alkenyl-carboxylic acids, the saturated and/or unsaturated aliphatic C2-C6-dicarboxylic acids and/or tricarboxylic acids, the aliphatic ketodicarboxylic acids, the amino acids or the inorganic acids or the salts thereof, and combinations thereof.7. The method according to claim 6, wherein the aliphatic monocarboxylic acid comprises a C1-C6-alkyl-carboxylic acid selected from the group consisting of acetic acid, propionic acid, n-butyric acid, n-valeric acid, isovaleric acid, ethyl-methyl-acetic acid (2-methyl-butyric acid), 2,2-dimethylpropionic acid (pivalic acid), n-hexanoic acid, n-octanoic acid, n-decanoic acid or n-dodecanoic acid (lauric acid) or mixtures thereof.8. The method according to claim 6, wherein the aliphatic alkenyl-carboxylic acid is selected from the group consisting of acrylic acid (propenoic acid), methacrylic acid, crotonic acid, isocrotonic acid or vinylacetic acid or mixtures thereof.9. The method according to claim 6, wherein the saturated aliphatic C2-C6-dicarboxylic acid is selected from the group consisting of oxalic acid, malonic acid, succinic acid, glutaric acid or adipic acid or mixtures thereof.10. The method according to claim 9, wherein the aliphatic dicarboxylic acid is oxalic acid or succinic acid or mixtures thereof.11. The method according to claim 6, wherein the aliphatic hydroxy-di- and -tricarboxylic acids are selected from the group consisting of tartronic acid, D-(+), L-(?)- or DL-malic acid, (2R,3R)-(+)-tartaric acid, (2S,3S)-(?)-tartaric acid, meso-tartaric acid, citric acid, and mixtures thereof.12. The method according to claim 6, wherein the unsaturated dicarboxylic acid is maleic and/or fumaric acid or mixtures thereof.13. The method according to claim 6, wherein the unsaturated tricarboxylic acid is aconitic acid.14. The method according to claim 6, wherein the aliphatic ketodicarboxylic acids are mesoxalic acid or oxaloacetic acid, or mixtures thereof.15. The method according to claim 6, wherein the amino acids are selected from the group consisting of aminoacetic acid (glycine), α-aminopropionic acid (alanine), α-amino-iso-valeric acid (valine), α-amino-iso-caproic acid (leucine) and α-amino-β-methylvaleric acid (isoleucine), and mixtures thereof.16. The method according to claim 1, wherein the composition is in the form of an aqueous solution.17. The method according to claim 16, wherein the cationic compound is present in the composition in a concentration in a range from 0.01% (W/V) to 10% (W/V).18. The method according to claim 1, wherein the nucleic acids originate from prokaryotes, the Archaebacteria or the Eubacteria.19. The method according to claim 18, wherein the nucleic acids originate from Gram-positive bacteria.20. The method according to claim 19, wherein the nucleic acids originate from Bacillus, Staphylococcus, Streptomyces, Flavobacterium, Mycobacterium, Streptococcus, Clostridiae, Listeria, Peptococcus, Peptostreptococcus, Enterococcus, Corynebacterium, Propionibacterium or Lactobacillus. 21. The method according to claim 18, wherein the nucleic acids originate from Gram-negative bacteria.22. The method according to claim 21, wherein the nucleic acids originate from Escherichia, Pseudomonas, Klebsiella, Salmonella, Sinorhizobium, Campylobacter, Neisseria, Vibrio, Shigella, Serratia, Enterobacter, Acinetobacter, Proteus, Yersinia, Brucella, Haemophilus, Bacteroides, Helicobacter, Bordetella, Legionella or Pasteurella. 23. The method according to claim 18, wherein the nucleic acids originate from Chlamydia. 24. The method according to claim 18, wherein the nucleic acids originate from phototropic bacteria.25. The method according to claim 18, wherein the nucleic acids originate from Mycoplasma. 26. The method according to claim 18, wherein the nucleic acids originate from Rickettsia. 27. The method according to claim 18, wherein the nucleic acids originate from Spirochetes. 28. The method according to claim 18, wherein the nucleic acids originate from Spirilla. 29. The method according to claim 1, wherein the nucleic acids originate from eukaryotic microorganisms.30. The method according to claim 29, wherein the nucleic acids originate from fungi of the Dermatophyte group, the yeasts, the moulds and the biphasic fungi.31. The method according to claim 30, wherein the nucleic acids originate from the yeasts Saccharomyces, Candida or Cryptococcus. 32. The method according to claim 30, wherein the nucleic acids originate from moulds of the group Aspergillus. 33. The method according to claim 30, wherein the nucleic acids originate from moulds of the group Penicillium. 34. The method according to claim 30, wherein the nucleic acids originate from moulds of the group Mucor. 35. The method according to claim 29, wherein the nucleic acids originate from algae.36. The method according to claim 29, wherein the nucleic acids originate from protozoa.37. The method according to claim 1, wherein said microorganism is lysed by enzymatic, mechanical, thermal or chemical methods, or combination thereof.38. The method according to claim 1, wherein said composition has a pH in the range from 2 to 12.39. A kit for stabilization of nucleic acids in or from microorganisms comprising a composition according to claim 1 and instructions for combining said composition with a solution containing nucleic acids, in or from microorganisms, to be stabilized.40. A mixture comprising a biological sample comprising prokaryotes, fungi, protozoa or algae and a composition according to claim 1, optionally together with other excipients.