Literature DB >> 33067683

Recent advances in biocatalytic derivatization of L-tyrosine.

Xu Tan1,2, Wei Song1,2, Xiulai Chen2,3, Liming Liu2,3, Jing Wu4.   

Abstract

L-Tyrosine is an aromatic, polar, non-essential amino acid that contains a highly reactive α-amino, α-carboxyl, and phenolic hydroxyl group. Derivatization of these functional groups can produce chemicals, such as L-3,4-dihydroxyphenylalanine, tyramine, 4-hydroxyphenylpyruvic acid, and benzylisoquinoline alkaloids, which are widely employed in the pharmaceutical, food, and cosmetics industries. In this review, we summarize typical L-tyrosine derivatizations catalyzed by enzymatic biocatalysts, as well as the strategies and challenges associated with their production processes. Finally, we discuss future perspectives pertaining to the enzymatic production of L-tyrosine derivatives.Key points• Summary of recent advances in enzyme-catalyzed L-tyrosine derivatization.• Highlights of relevant strategies involved in L-tyrosine derivatives biosynthesis.• Future perspectives on industrial applications of L-tyrosine derivatization.

Entities:  

Keywords:  Derivatization; Enzyme catalysis; Group modification; L-Tyrosine

Mesh:

Substances:

Year:  2020        PMID: 33067683     DOI: 10.1007/s00253-020-10949-6

Source DB:  PubMed          Journal:  Appl Microbiol Biotechnol        ISSN: 0175-7598            Impact factor:   4.813


  49 in total

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3.  Biochemical and Mechanistic Characterization of the Fungal Reverse N-1-Dimethylallyltryptophan Synthase DMATS1Ff.

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Journal:  ACS Chem Biol       Date:  2019-12-05       Impact factor: 5.100

4.  Biocontrolled formal inversion or retention of L-α-amino acids to enantiopure (R)- or (S)-hydroxyacids.

Authors:  Eduardo Busto; Nina Richter; Barbara Grischek; Wolfgang Kroutil
Journal:  Chemistry       Date:  2014-07-22       Impact factor: 5.236

5.  Synthesis of Microcin SF608 through nucleophilic opening of an oxabicyclo[2.2.1]heptane.

Authors:  Stefan Diethelm; Corinna S Schindler; Erick M Carreira
Journal:  Org Lett       Date:  2010-09-03       Impact factor: 6.005

Review 6.  Carboxylic acid reductases (CARs): An industrial perspective.

Authors:  Sasha R Derrington; Nicholas J Turner; Scott P France
Journal:  J Biotechnol       Date:  2019-08-17       Impact factor: 3.307

7.  Understanding Which Residues of the Active Site and Loop Structure of a Tyrosine Aminomutase Define Its Mutase and Lyase Activities.

Authors:  Gayanthi Attanayake; Tyler Walter; Kevin D Walker
Journal:  Biochemistry       Date:  2018-05-30       Impact factor: 3.162

Review 8.  Engineering enzymes for noncanonical amino acid synthesis.

Authors:  Patrick J Almhjell; Christina E Boville; Frances H Arnold
Journal:  Chem Soc Rev       Date:  2018-10-03       Impact factor: 54.564

9.  Determination of Alkyl-Donor Promiscuity of Tyrosine-O-Prenyltransferase SirD from Leptosphaeria maculans.

Authors:  Chandrasekhar Bandari; Erin M Scull; Johanna M Masterson; Rachel H Q Tran; Steven B Foster; Kenneth M Nicholas; Shanteri Singh
Journal:  Chembiochem       Date:  2017-10-27       Impact factor: 3.164

10.  Promiscuous enzymatic activity-aided multiple-pathway network design for metabolic flux rearrangement in hydroxytyrosol biosynthesis.

Authors:  Wei Chen; Jun Yao; Jie Meng; Wenjing Han; Yong Tao; Yihua Chen; Yixin Guo; Guizhi Shi; Yang He; Jian-Ming Jin; Shuang-Yan Tang
Journal:  Nat Commun       Date:  2019-02-27       Impact factor: 14.919

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  1 in total

1.  Cost-Effective Production of L-DOPA by Tyrosinase-Immobilized Polyhydroxyalkanoate Nanogranules in Engineered Halomonas bluephagenesis TD01.

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Journal:  Molecules       Date:  2021-06-22       Impact factor: 4.411

  1 in total

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