Green Routes for the Production of Enantiopure Benzylisoquinoline Alkaloids

Int J Mol Sci. 2017 Nov 20;18(11):2464. doi: 10.3390/ijms18112464.

Abstract

Benzylisoquinoline alkaloids (BIAs) are among the most important plant secondary metabolites, in that they include a number of biologically active substances widely employed as pharmaceuticals. Isolation of BIAs from their natural sources is an expensive and time-consuming procedure as they accumulate in very low levels in plant. Moreover, total synthesis is challenging due to the presence of stereogenic centers. In view of these considerations, green and scalable methods for BIA synthesis using fully enzymatic approaches are getting more and more attention. The aim of this paper is to review fully enzymatic strategies for producing the benzylisoquinoline central precursor, (S)-norcoclaurine and its derivatives. Specifically, we will detail the current status of synthesis of BIAs in microbial hosts as well as using isolated and recombinant enzymes.

Keywords: alkaloids; benzylisoquinoline alkaloids; green synthesis; microbial factories; recombinant enzymes.

Publication types

  • Review

MeSH terms

  • Alkaloids / chemical synthesis*
  • Alkaloids / chemistry
  • Alkaloids / metabolism
  • Bacteria / chemistry
  • Bacteria / enzymology
  • Bacteria / genetics
  • Benzylisoquinolines / chemical synthesis*
  • Benzylisoquinolines / chemistry
  • Benzylisoquinolines / metabolism
  • Bioreactors*
  • Escherichia coli / enzymology
  • Escherichia coli / genetics
  • Plants / chemistry
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Saccharomyces cerevisiae / enzymology
  • Saccharomyces cerevisiae / genetics
  • Tetrahydroisoquinolines / chemical synthesis*
  • Tetrahydroisoquinolines / chemistry
  • Tetrahydroisoquinolines / metabolism

Substances

  • Alkaloids
  • Benzylisoquinolines
  • Recombinant Proteins
  • Tetrahydroisoquinolines
  • higenamine