| Literature DB >> 30165733 |
Pierre Crozet1, Francisco J Navarro2, Felix Willmund3, Payam Mehrshahi2, Kamil Bakowski4, Kyle J Lauersen5, Maria-Esther Pérez-Pérez6, Pascaline Auroy7, Aleix Gorchs Rovira2, Susana Sauret-Gueto2, Justus Niemeyer3, Benjamin Spaniol3, Jasmine Theis3, Raphael Trösch3, Lisa-Desiree Westrich3, Konstantinos Vavitsas4, Thomas Baier5, Wolfgang Hübner8, Felix de Carpentier1, Mathieu Cassarini1, Antoine Danon1, Julien Henri1, Christophe H Marchand1, Marcello de Mia1, Kevin Sarkissian1, David C Baulcombe2, Gilles Peltier7, José-Luis Crespo6, Olaf Kruse5, Poul-Erik Jensen4, Michael Schroda3, Alison G Smith2, Stéphane D Lemaire1.
Abstract
Microalgae are regarded as promising organisms to develop innovative concepts based on their photosynthetic capacity that offers more sustainable production than heterotrophic hosts. However, to realize their potential as green cell factories, a major challenge is to make microalgae easier to engineer. A promising approach for rapid and predictable genetic manipulation is to use standardized synthetic biology tools and workflows. To this end we have developed a Modular Cloning toolkit for the green microalga Chlamydomonas reinhardtii. It is based on Golden Gate cloning with standard syntax, and comprises 119 openly distributed genetic parts, most of which have been functionally validated in several strains. It contains promoters, UTRs, terminators, tags, reporters, antibiotic resistance genes, and introns cloned in various positions to allow maximum modularity. The toolkit enables rapid building of engineered cells for both fundamental research and algal biotechnology. This work will make Chlamydomonas the next chassis for sustainable synthetic biology.Entities:
Keywords: Chlamydomonas reinhardtii; algal biotechnology; modular cloning; synthetic biology
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Year: 2018 PMID: 30165733 DOI: 10.1021/acssynbio.8b00251
Source DB: PubMed Journal: ACS Synth Biol ISSN: 2161-5063 Impact factor: 5.110