PL429362A1 - Nowa, niespecyficzna termolabilna nukleaza aktywna w niskich temperaturach i wysokich stężeniach soli - Google Patents
Nowa, niespecyficzna termolabilna nukleaza aktywna w niskich temperaturach i wysokich stężeniach soliInfo
- Publication number
- PL429362A1 PL429362A1 PL429362A PL42936219A PL429362A1 PL 429362 A1 PL429362 A1 PL 429362A1 PL 429362 A PL429362 A PL 429362A PL 42936219 A PL42936219 A PL 42936219A PL 429362 A1 PL429362 A1 PL 429362A1
- Authority
- PL
- Poland
- Prior art keywords
- mvi
- nuclease
- thermolabile
- active fragment
- enzymatically active
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/14—Hydrolases (3)
- C12N9/16—Hydrolases (3) acting on ester bonds (3.1)
- C12N9/22—Ribonucleases [RNase]; Deoxyribonucleases [DNase]
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/20—Bacteria; Culture media therefor
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/52—Genes encoding for enzymes or proenzymes
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/70—Vectors or expression systems specially adapted for E. coli
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/26—Preparation of nitrogen-containing carbohydrates
- C12P19/28—N-glycosides
- C12P19/30—Nucleotides
- C12P19/34—Polynucleotides, e.g. nucleic acids, oligoribonucleotides
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P21/00—Preparation of peptides or proteins
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6844—Nucleic acid amplification reactions
- C12Q1/6848—Nucleic acid amplification reactions characterised by the means for preventing contamination or increasing the specificity or sensitivity of an amplification reaction
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y301/00—Hydrolases acting on ester bonds (3.1)
- C12Y301/21—Endodeoxyribonucleases producing 5'-phosphomonoesters (3.1.21)
- C12Y301/21001—Deoxyribonuclease I (3.1.21.1)
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Genetics & Genomics (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Microbiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biophysics (AREA)
- Physics & Mathematics (AREA)
- Plant Pathology (AREA)
- Medicinal Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- General Chemical & Material Sciences (AREA)
- Tropical Medicine & Parasitology (AREA)
- Virology (AREA)
- Analytical Chemistry (AREA)
- Immunology (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Przedmiotem wynalazku jest nowa termolabilna nukleaza Mvi lub jej enzymatycznie aktywny fragment, gdzie nukleaza ma sekwencję SEQ.Nr 2 lub sekwencję, która jest co najmniej w 40% z nią identyczna. Przedmiotem wynalazku jest gen kodujący nukleazę Mvi lub jej enzymatycznie aktywny fragment posiadający; cząsteczka kwasu nukleinowego kodująca nukleazę Mvi lub jej enzymatycznie aktywny fragment; plazmid ekspresyjny zawierający sekwencję genu kodującego Mvi; Rekombinantowy szczep Escherichia coli BL21 (DE3)-RlL pD454-Mvi; sposób wytwarzania białka nukleazy Mvi; zastosowanie nukleazy Mvi w procesach oczyszczania białek rekombinantowych o znacząco obniżonej zawartości DNA oraz do dekontaminacji reakcji PCR i RT PCR dla uzyskana zwiększonej czułości i specyficzności odpowiednich analiz genetycznych; Zastosowanie nukleazy Mvi w procesach oczyszczania białek rekombinantowych, w szczególności enzymów, przeciwciał, antygenów szczepionkowych, przygotowania preparatów używanych w terapiach komórkowych, i innych białkach terapeutycznych.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL429362A PL429362A1 (pl) | 2019-03-22 | 2019-03-22 | Nowa, niespecyficzna termolabilna nukleaza aktywna w niskich temperaturach i wysokich stężeniach soli |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL429362A PL429362A1 (pl) | 2019-03-22 | 2019-03-22 | Nowa, niespecyficzna termolabilna nukleaza aktywna w niskich temperaturach i wysokich stężeniach soli |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL429362A1 true PL429362A1 (pl) | 2020-10-05 |
Family
ID=72669246
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL429362A PL429362A1 (pl) | 2019-03-22 | 2019-03-22 | Nowa, niespecyficzna termolabilna nukleaza aktywna w niskich temperaturach i wysokich stężeniach soli |
Country Status (1)
| Country | Link |
|---|---|
| PL (1) | PL429362A1 (pl) |
-
2019
- 2019-03-22 PL PL429362A patent/PL429362A1/pl unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Yadavalli et al. | Bacterial small membrane proteins: the swiss army knife of regulators at the lipid bilayer | |
| Van Melderen et al. | ATP-dependent degradation of CcdA by Lon protease: effects of secondary structure and heterologous subunit interactions | |
| Iwanczyk et al. | Role of the PDZ domains in Escherichia coli DegP protein | |
| Puri et al. | HspQ functions as a unique specificity-enhancing factor for the AAA+ Lon protease | |
| CN108473969B9 (zh) | 用于增强生产的rna相关酶的修饰 | |
| Becker et al. | Existence of two distinct aspartyl-tRNA synthetases in Thermus thermophilus. Structural and biochemical properties of the two enzymes | |
| KR100361049B1 (ko) | 천연적으로 폴딩 및 분비되는 단백질의 제조방법 | |
| Anisenko et al. | Human Ku70 protein binds hairpin RNA and double stranded DNA through two different sites | |
| Nadeau et al. | 83‐kilodalton heat shock proteins of trypanosomes are potent peptide‐stimulated ATPases | |
| Budzik et al. | Sortase D forms the covalent bond that links BcpB to the tip of Bacillus cereus pili | |
| PL431144A1 (pl) | Nowa, niespecyficzna termolabilna nukleaza aktywna w niskiej temperaturze, szerokim zakresie pH oraz wysokich stężeniach soli | |
| Mangel et al. | [27] Omptin: An Escherichia coli outer membrane proteinase that activates plasminogen | |
| Nemoto et al. | Characterization of the glutamyl endopeptidase from Staphylococcus aureus expressed in Escherichia coli | |
| Mohajeri et al. | Cloning and expression of recombinant human endostatin in periplasm of escherichia coli expression system | |
| US20150329606A1 (en) | Method for preparing c1q recombinant protein | |
| PL429362A1 (pl) | Nowa, niespecyficzna termolabilna nukleaza aktywna w niskich temperaturach i wysokich stężeniach soli | |
| Wang et al. | Purification and characterization of glutathione binding protein GsiB from Escherichia coli | |
| Shafaati et al. | Expression and characterization of hemagglutinin–neuraminidase protein from Newcastle disease virus in Bacillus subtilis WB800 | |
| Lin et al. | Two enzymes, TilS and HprT, can form a complex to function as a transcriptional activator for the cell division protease gene ftsH in Bacillus subtilis | |
| CN104610443A (zh) | 一种高稳定性重组降钙素原、制备方法及用途 | |
| KR100801810B1 (ko) | 슈퍼-항원 융합 단백질들 및 그 용도 | |
| Stone et al. | Design and characterization of a protein superagonist of IL‐15 fused with IL‐15Rα and a high‐affinity T cell receptor | |
| JP2012147772A (ja) | 組換えプラスミドベクターおよびそれを用いたタンパク質の製造方法 | |
| Hung et al. | Recombinant production of the amino terminal cytoplasmic region of dengue virus non-structural protein 4A for structural studies | |
| Andrianova et al. | Role of α-helical domains in functioning of ATP-dependent Lon protease of Escherichia coli |