Unrestrained markerless trait stacking in <i>Nannochloropsis gaditana</i> through combined genome editing and marker recycling technologies

John Verruto(Synthetic Genomics (United States)), Kristie Francis(Synthetic Genomics (United States)), Yingjun Wang(Synthetic Genomics (United States)), Melisa C. Low(Synthetic Genomics (United States)), Jessica Greiner(Synthetic Genomics (United States)), Sarah Tacke(Synthetic Genomics (United States)), Fedor I. Kuzminov(Synthetic Genomics (United States)), W. Marcus Lambert(Synthetic Genomics (United States)), Jay McCarren(Synthetic Genomics (United States)), Imad Ajjawi(Synthetic Genomics (United States)), Nicholas Bauman(Synthetic Genomics (United States)), Ryan Kalb(Synthetic Genomics (United States)), Gregory Hannum(Synthetic Genomics (United States)), Eric R. Moellering(Synthetic Genomics (United States))
Proceedings of the National Academy of Sciences
July 9, 2018
Cited by 95Open Access
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Abstract

Significance Stacking traits in microalgae is limited by a lack of robust genome modification tools and selectable marker availability. This presents a key hurdle in developing strains for renewable products including biofuels. Here, we overcome these limitations by combining inducible Cre recombinase with constitutive Cas9 nuclease expression in the industrial strain, Nannochloropsis gaditana . With this system, we demonstrate marker- and reporter-free recapitulation of an important lipid productivity trait. In addition, we generate a strain harboring seven-gene knockouts within the photosystem antennae encoding genes. The combined use of relatively mature (Cre) and emerging (CAS9) genome modification technologies can thus accelerate the pace of industrial strain development and facilitate basic research into functionally redundant gene families.


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