AU2001259829A1 - Chemoenzymatic synthesis of neotame - Google Patents
Chemoenzymatic synthesis of neotameInfo
- Publication number
- AU2001259829A1 AU2001259829A1 AU2001259829A AU5982901A AU2001259829A1 AU 2001259829 A1 AU2001259829 A1 AU 2001259829A1 AU 2001259829 A AU2001259829 A AU 2001259829A AU 5982901 A AU5982901 A AU 5982901A AU 2001259829 A1 AU2001259829 A1 AU 2001259829A1
- Authority
- AU
- Australia
- Prior art keywords
- neotame
- chemoenzymatic synthesis
- chemoenzymatic
- synthesis
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06104—Dipeptides with the first amino acid being acidic
- C07K5/06113—Asp- or Asn-amino acid
-
- 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
- C12P21/02—Preparation of peptides or proteins having a known sequence of two or more amino acids, e.g. glutathione
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Zoology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Wood Science & Technology (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biotechnology (AREA)
- Biophysics (AREA)
- Medicinal Chemistry (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/570,408 | 2000-05-12 | ||
US09/570,408 US6627431B1 (en) | 2000-05-12 | 2000-05-12 | Chemoenzymatic synthesis of neotame |
PCT/US2001/040676 WO2001085977A2 (en) | 2000-05-12 | 2001-05-07 | Chemoenzymatic synthesis of neotame |
Publications (1)
Publication Number | Publication Date |
---|---|
AU2001259829A1 true AU2001259829A1 (en) | 2001-11-20 |
Family
ID=24279530
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2001259829A Abandoned AU2001259829A1 (en) | 2000-05-12 | 2001-05-07 | Chemoenzymatic synthesis of neotame |
Country Status (3)
Country | Link |
---|---|
US (1) | US6627431B1 (en) |
AU (1) | AU2001259829A1 (en) |
WO (1) | WO2001085977A2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110563797A (en) * | 2019-10-12 | 2019-12-13 | 山东奔月生物科技股份有限公司 | Method for removing viscous components in neotame |
CN110818774A (en) * | 2019-11-21 | 2020-02-21 | 暨南大学 | Synthetic method of 40000 times dipeptide high-power sweetener |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3933781A (en) | 1973-11-05 | 1976-01-20 | Monsanto Company | Process for the preparation of α-L-aspartyl-L-phenylalanine alkyl esters |
US4293648A (en) | 1979-12-12 | 1981-10-06 | G. D. Searle & Co. | Process for esterification of α-L-aspartyl-L-phenylalanine |
JPS6274297A (en) | 1985-09-30 | 1987-04-06 | Asahi Chem Ind Co Ltd | Production of alpha-l-aspartyl-l-phenylalanine methyl ester |
FR2697844B1 (en) | 1992-11-12 | 1995-01-27 | Claude Nofre | New compounds derived from dipeptides or dipeptide analogues useful as sweetening agents, process for their preparation. |
FR2719590B1 (en) | 1994-05-09 | 1996-07-26 | Claude Nofre | Improved process for the preparation of a compound derived from aspartame useful as a sweetening agent. |
US5773261A (en) * | 1996-08-26 | 1998-06-30 | The Nutrasweet Company | Regioselective α-hydrolysis of amino acid diesters using pig liver esterase |
US5728862A (en) | 1997-01-29 | 1998-03-17 | The Nutrasweet Company | Method for preparing and purifying an N-alkylated aspartame derivative |
AU1832500A (en) | 1998-11-25 | 2000-06-19 | Nutrasweet Company, The | Purification of N-(N-(3,3-dimethylbutyl)-l-alpha-aspartyl)-l-phenylalanine 1-methyl ester via crystallization |
US6077962A (en) | 1998-12-24 | 2000-06-20 | The Nutrasweet Company | N-3, 3-dimethylbutyl-L-aspartic acid and esters thereof, the process of preparing the same, and the process for preparing N-(N-(3,3-dimethylbutyl) -α L-aspartyl)-L- phenylalanine 1-methyl ester therefrom |
-
2000
- 2000-05-12 US US09/570,408 patent/US6627431B1/en not_active Expired - Fee Related
-
2001
- 2001-05-07 WO PCT/US2001/040676 patent/WO2001085977A2/en active Application Filing
- 2001-05-07 AU AU2001259829A patent/AU2001259829A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
WO2001085977A3 (en) | 2002-08-15 |
US6627431B1 (en) | 2003-09-30 |
WO2001085977A2 (en) | 2001-11-15 |
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