Anchoring a plant cytochrome P450 via PsaM to the thylakoids in Synechococcus sp. PCC 7002: evidence for light-driven biosynthesis.

PLoS One

Center for Synthetic Biology "bioSYNergy", the VILLUM Research Center "Plant Plasticity", Copenhagen Plant Science Center, Department of Plant and Environmental Sciences, University of Copenhagen, Frederiksberg C, Copenhagen, Denmark.

Published: March 2015

AI Article Synopsis

  • Plants create a diverse range of specialized metabolites that have valuable bioactive properties, often used in pharmaceuticals, but their low production levels and complex structures make chemical synthesis challenging.
  • By harnessing the electrons generated during photosynthesis, researchers developed a method to produce these plant compounds in photosynthetic microorganisms by linking a biosynthetic enzyme to photosystem I.
  • The study successfully fused the cytochrome P450 enzyme from Sorghum bicolor with a photosystem I subunit in the cyanobacterium Synechococcus sp. PCC 7002, demonstrating that this engineered enzyme can drive light-powered biosynthesis of valuable metabolites both inside and outside the organism.

Article Abstract

Plants produce an immense variety of specialized metabolites, many of which are of high value as their bioactive properties make them useful as for instance pharmaceuticals. The compounds are often produced at low levels in the plant, and due to their complex structures, chemical synthesis may not be feasible. Here, we take advantage of the reducing equivalents generated in photosynthesis in developing an approach for producing plant bioactive natural compounds in a photosynthetic microorganism by functionally coupling a biosynthetic enzyme to photosystem I. This enables driving of the enzymatic reactions with electrons extracted from the photosynthetic electron transport chain. As a proof of concept, we have genetically fused the soluble catalytic domain of the cytochrome P450 CYP79A1, originating from the endoplasmic reticulum membranes of Sorghum bicolor, to a photosystem I subunit in the cyanobacterium Synechococcus sp. PCC 7002, thereby targeting it to the thylakoids. The engineered enzyme showed light-driven activity both in vivo and in vitro, demonstrating the possibility to achieve light-driven biosynthesis of high-value plant specialized metabolites in cyanobacteria.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4099078PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0102184PLOS

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