Engineering of Cascade Reactions and Alditol Oxidase for High‐Yielding Synthesis of (R)‐Phenylethanolamine from Styrene, l‐Phenylalanine, Glycerol or Glucose. Issue 17 (5th August 2022)
- Record Type:
- Journal Article
- Title:
- Engineering of Cascade Reactions and Alditol Oxidase for High‐Yielding Synthesis of (R)‐Phenylethanolamine from Styrene, l‐Phenylalanine, Glycerol or Glucose. Issue 17 (5th August 2022)
- Main Title:
- Engineering of Cascade Reactions and Alditol Oxidase for High‐Yielding Synthesis of (R)‐Phenylethanolamine from Styrene, l‐Phenylalanine, Glycerol or Glucose
- Authors:
- Wang, Zilong
Li, Xirui
Li, Zhi - Abstract:
- Abstract: ( R )‐phenylethanolamine (PEA) is a useful and valuable chiral chemical and requires enantioselective and efficient synthesis method. A novel SMO‐StEH‐AldO‐CvTA‐catalyzed cascade reaction was established to convert styrene to ( R )‐PEA via epoxidation‐hydrolysis‐oxidation‐amination. The key transformation of ( R )‐1‐phenyl‐1, 2‐ethanediol to ( R )‐PEA in the cascade was achieved in 94 % conversion via AldO‐CvTA. The limiting enzyme AldO was engineered through directed evolution, yielding a mutant AldO(MVIK) with 3‐fold enhanced catalytic efficiency. The use of AldO(MVIK) in the 4‐enzyme cascade significantly increased the productivity than the use of AldO, yielding 34.6 mM ( R )‐PEA with >99 % ee . By incorporating deamination and decarboxylation enzymes, a 6‐enzyme cascade was engineered to produce 23.7 mM ( R )‐PEA from l ‐phenylalanine. Coupling of l ‐phenylalanine biosynthesis pathway with 6‐enzyme cascade enabled synthesis of ( R )‐PEA from glycerol or glucose, producing 6.8 mM and 6.5 mM ( R )‐PEA, respectively. The developed cascade biotransformations provide direct synthesis of ( R )‐PEA from either simple chemicals or renewable feedstocks. Abstract : Biotransformations : Novel 4‐ and 6‐enzyme cascades were developed for one‐pot synthesis of ( R )‐PEA with high ee and high yield from styrene and l ‐phenylalanine, respectively. The limiting enzyme in the cascade, AldO, was successfully engineered to enhance activity. Coupling of l ‐Phe biosynthesis pathwayAbstract: ( R )‐phenylethanolamine (PEA) is a useful and valuable chiral chemical and requires enantioselective and efficient synthesis method. A novel SMO‐StEH‐AldO‐CvTA‐catalyzed cascade reaction was established to convert styrene to ( R )‐PEA via epoxidation‐hydrolysis‐oxidation‐amination. The key transformation of ( R )‐1‐phenyl‐1, 2‐ethanediol to ( R )‐PEA in the cascade was achieved in 94 % conversion via AldO‐CvTA. The limiting enzyme AldO was engineered through directed evolution, yielding a mutant AldO(MVIK) with 3‐fold enhanced catalytic efficiency. The use of AldO(MVIK) in the 4‐enzyme cascade significantly increased the productivity than the use of AldO, yielding 34.6 mM ( R )‐PEA with >99 % ee . By incorporating deamination and decarboxylation enzymes, a 6‐enzyme cascade was engineered to produce 23.7 mM ( R )‐PEA from l ‐phenylalanine. Coupling of l ‐phenylalanine biosynthesis pathway with 6‐enzyme cascade enabled synthesis of ( R )‐PEA from glycerol or glucose, producing 6.8 mM and 6.5 mM ( R )‐PEA, respectively. The developed cascade biotransformations provide direct synthesis of ( R )‐PEA from either simple chemicals or renewable feedstocks. Abstract : Biotransformations : Novel 4‐ and 6‐enzyme cascades were developed for one‐pot synthesis of ( R )‐PEA with high ee and high yield from styrene and l ‐phenylalanine, respectively. The limiting enzyme in the cascade, AldO, was successfully engineered to enhance activity. Coupling of l ‐Phe biosynthesis pathway with 6‐enzyme cascade achieved synthesis of ( R )‐PEA from glycerol or glucose, respectively. … (more)
- Is Part Of:
- ChemCatChem. Volume 14:Issue 17(2022)
- Journal:
- ChemCatChem
- Issue:
- Volume 14:Issue 17(2022)
- Issue Display:
- Volume 14, Issue 17 (2022)
- Year:
- 2022
- Volume:
- 14
- Issue:
- 17
- Issue Sort Value:
- 2022-0014-0017-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-08-05
- Subjects:
- alditol oxidase -- cascade biotransformations -- protein engineering -- renewable resources -- styrene
Catalysis -- Periodicals
541.39505 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1867-3899 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cctc.202200418 ↗
- Languages:
- English
- ISSNs:
- 1867-3880
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 23305.xml