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Bioproduction of Enantiopure ( R )‐ and ( S )‐2‐Phenylglycinols from Styrenes and Renewable Feedstocks
Author(s) -
Sekar Balaji Sundara,
Mao Jiwei,
Lukito Benedict Ryan,
Wang Zilong,
Li Zhi
Publication year - 2021
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.202001322
Subject(s) - enantiopure drug , transamination , chemistry , enantioselective synthesis , biocatalysis , organic chemistry , hydrolysis , decarboxylation , phenylalanine , chemical synthesis , stereochemistry , enzyme , amino acid , catalysis , reaction mechanism , biochemistry , in vitro
Enantiopure ( R )‐ and ( S )‐2‐phenylglycinols are important chiral building blocks for pharmaceutical manufacturing. Several chemical and enzymatic methods for their synthesis were reported, either involving multi‐step synthesis or starting from a relatively complex chemical. Here, we developed one‐pot simple syntheses of enantiopure ( R )‐ and ( S )‐2‐phenylglycinols from cheap starting materials and renewable feedstocks. Enzyme cascades consisting of epoxidation‐hydrolysis‐oxidation‐transamination were developed to convert styrene 2 a to ( R )‐ and ( S )‐2‐phenylglycinol 1 a , with butanediol dehydrogenase for alcohol oxidation as well as BmTA and NfTA for ( R )‐ and ( S )‐enantioselective transamination, respectively. The engineered E. coli strains expressing the cascades produced 1015 mg/L ( R )‐ 1 a in >99% ee and 315 mg/L ( S )‐ 1 a in 91% ee , respectively, from styrene 2 a . The same cascade also converted substituted styrenes 2 b – k and indene 2 l into substituted ( R )‐phenylglycinols 1 b – k and (1 R , 2 R )‐1‐amino‐2‐indanol 1 l in 95–>99% ee . To transform bio‐based L ‐phenylalanine 6 to ( R )‐ 1 a and ( S )‐ 1 a , ( R )‐ and ( S )‐enantioselective enzyme cascades for deamination‐decarboxylation‐epoxidation‐hydrolysis‐oxidation‐transamination were developed. The engineered E. coli strains produced ( R )‐ 1 a and ( S )‐ 1 a in high ee at 576 mg/L and 356 mg/L, respectively, from L ‐phenylalanine 6 , as the first synthesis of these compounds from a bio‐based chemical. Finally, L ‐phenylalanine biosynthesis pathway was combined with ( R )‐ or ( S )‐enantioselective cascade in one strain or coupled strains, to achieve the first synthesis of ( R )‐ 1 a and ( S )‐ 1 a from a renewable feedstock. The coupled strain approach enhanced the production, affording 274 and 384 mg/L ( R )‐ 1 a and 274 and 301 mg/L ( S )‐ 1 a , from glucose and glycerol, respectively. The developed methods could be potentially useful to produce these high‐value chemicals from cheap starting materials and renewable feedstocks in a green and sustainable manner.