Abstract

Sustainable and economically viable support for an ever-increasing global population requires a paradigm shift in agricultural productivity, including the application of biotechnology to generate future crop plants. Current genetic engineering approaches aimed at enhancing the photosynthetic efficiency or composition of the harvested tissues involve relatively simple manipulations of endogenous metabolism. However, radical rewiring of central metabolism using new-to-nature pathways, so-called “synthetic metabolism”, may be needed to really bring about significant step changes. In many cases, this will require re-programming the metabolism of the chloroplast, or other plastids in non-green tissues, through a combination of chloroplast and nuclear engineering. However, current technologies for sophisticated chloroplast engineering (“transplastomics”) of plants are limited to just a handful of species. Moreover, the testing of metabolic rewiring in the chloroplast of plant models is often impractical given their obligate phototrophy, the extended time needed to create stable non-chimeric transplastomic lines, and the technical challenges associated with regeneration of whole plants. In contrast, the unicellular green alga, Chlamydomonas reinhardtii is a facultative heterotroph that allows for extensive modification of chloroplast function, including non-photosynthetic designs. Moreover, chloroplast engineering in C. reinhardtii is facile, with the ability to generate novel lines in a matter of weeks, and a well-defined molecular toolbox allows for rapid iterations of the “Design-Build-Test-Learn” (DBTL) cycle of modern synthetic biology approaches. The recent development of combinatorial DNA assembly pipelines for designing and building transgene clusters, simple methods for marker-free delivery of these clusters into the chloroplast genome, and the pre-existing wealth of knowledge regarding chloroplast gene expression and regulation in C. reinhardtii further adds to the versatility of transplastomics using this organism. Herein, we review the inherent advantages of the algal chloroplast as a simple and tractable testbed for metabolic engineering designs, which could then be implemented in higher plants.

Highlights

  • The latter half of the 20th century witnessed what is widely referred to as the “Green Revolution”

  • We summarise examples of projects for which there is great potential for the algal chloroplast as a synthetic biology (SynBio) testbed for the kind of advanced, step-change modifications needed to power the Green Revolution 2.0

  • There have been reports of over 100 different foreign proteins produced in the Chlamydomonas chloroplast (Larrea-Alvarez and Purton, 2020) Whilst these studies have typically involved the introduction of a single transgene and selection marker into the plastome, reports of multigenic genetic engineering approaches involving up to six transgenes are appearing (Gimpel et al, 2016; Macedo-Osorio et al, 2018; Larrea-Alvarez and Purton, 2020)

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Summary

INTRODUCTION

The latter half of the 20th century witnessed what is widely referred to as the “Green Revolution”. Further radical engineering might include the introduction of nitrogen fixation into the plant tissue (Liu et al, 2018) or new anabolic pathways for key nutrients currently lacking in plants, such as vitamin B12 (Smith et al, 2007) and long-chain polyunsaturated fatty acids (VenegasCalerón et al, 2010) Realising such goals will require approaches beyond conventional breeding and selection, namely sophisticated genetic engineering tools combined with synthetic biology and systems biology technologies for the major crop species, together with a simple model chassis that can serve as a tractable and malleable testbed for exploring these radical ideas. We summarise examples of projects for which there is great potential for the algal chloroplast as a SynBio testbed for the kind of advanced, step-change modifications needed to power the Green Revolution 2.0

CHLOROPLAST GENETIC SYSTEM
ENGINEERING THE CHLAMYDOMONAS
Gene Regulation Tools
Multigenic Expression
The Arrival of Standardised Modular
Whole Plastome Engineering
PRIORITY PROJECTS FOR THE TESTBED
Improving Photosynthesis
Carbon Fixation
Nitrogen Fixation
Engineering Crop Plants for the Production of Novel Metabolites
CONCLUDING REMARKS
AUTHOR CONTRIBUTIONS
Full Text
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