| Literature DB >> 26214707 |
Javier A Gimpel1, Hussam H Nour-Eldin1, Melissa A Scranton1, Daphne Li1, Stephen P Mayfield1.
Abstract
Oxygenic photosynthesis provides the energy to produce all food and most of the fuel on this planet. Photosystem II (PSII) is an essential and rate-limiting component of this process. Understanding and modifying PSII function could provide an opportunity for optimizing photosynthetic biomass production, particularly under specific environmental conditions. PSII is a complex multisubunit enzyme with strong interdependence among its components. In this work, we have deleted the six core genes of PSII in the eukaryotic alga Chlamydomonas reinhardtii and refactored them in a single DNA construct. Complementation of the knockout strain with the core PSII synthetic module from three different green algae resulted in reconstitution of photosynthetic activity to 85, 55, and 53% of that of the wild-type, demonstrating that the PSII core can be exchanged between algae species and retain function. The strains, synthetic cassettes, and refactoring strategy developed for this study demonstrate the potential of synthetic biology approaches for tailoring oxygenic photosynthesis and provide a powerful tool for unraveling PSII structure-function relationships.Entities:
Keywords: Chlamydomonas reinhardtii; chloroplast synthetic biology; microalgae genetic engineering; photosynthesis engineering; photosystem II; refactoring
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Year: 2015 PMID: 26214707 DOI: 10.1021/acssynbio.5b00076
Source DB: PubMed Journal: ACS Synth Biol ISSN: 2161-5063 Impact factor: 5.110