| Literature DB >> 28943084 |
Yinghong Lu1, Sandra Stegemann1, Shreya Agrawal1, Daniel Karcher1, Stephanie Ruf1, Ralph Bock2.
Abstract
Transgene expression from the plastid (chloroplast) genome provides unique advantages, including high levels of foreign protein accumulation, convenient transgene stacking in operons, and increased biosafety due to exclusion of plastids from pollen transmission [1, 2]. However, applications in biotechnology and synthetic biology are severely restricted by the very small number of plant species whose plastid genomes currently can be transformed [3, 4]. Here we report a simple method for the introduction of useful plastid transgenes into non-transformable species. The transgenes tested comprised a synthetic operon encoding three components of a biosynthetic pathway for producing the high-value ketocarotenoid astaxanthin in the plastids of the cigarette tobacco, Nicotiana tabacum. Transplastomic N. tabacum plants accumulated astaxanthin to up to 1% of the plants' dry weight. We then used grafting, a procedure recently shown to facilitate horizontal genome transfer between plants [5-7], to let the transgenic chloroplast genome move across the graft junction from N. tabacum plants into plants of the nicotine-free tree species Nicotiana glauca. Transplastomic N. glauca trees expressing the synthetic pathway were recovered at high frequency, thus providing a straightforward method for extension of the transplastomic technology to new species.Entities:
Keywords: Nicotiana glauca; Nicotiana tabacum; astaxanthin; carotenoid biosynthesis; horizontal gene transfer; horizontal genome transfer; isoprenoid biosynthesis; ketocarotenoid; plastid transformation; synthetic biology
Mesh:
Substances:
Year: 2017 PMID: 28943084 DOI: 10.1016/j.cub.2017.08.044
Source DB: PubMed Journal: Curr Biol ISSN: 0960-9822 Impact factor: 10.834