AI Article Synopsis

  • - The development of the 'mini-synplastome' provides a new method for introducing synthetic circuits in plant plastids without disturbing the native plastome.
  • - This innovative genome structure is based on the unique organization of dinoflagellate plastomes, featuring multiple minicircles instead of a single genome.
  • - Mini-synplastomes aim to enhance chloroplast biotechnology by allowing easy cloning and predictable transgene expression, while remaining independent from the plant's existing genetic material.

Article Abstract

In the age of synthetic biology, plastid engineering requires a nimble platform to introduce novel synthetic circuits in plants. While effective for integrating relatively small constructs into the plastome, plastid engineering via homologous recombination of transgenes is over 30 years old. Here we show the design-build-test of a novel synthetic genome structure that does not disturb the native plastome: the 'mini-synplastome'. The mini-synplastome was inspired by dinoflagellate plastome organization, which is comprised of numerous minicircles residing in the plastid instead of a single organellar genome molecule. The first mini-synplastome in plants was developed in vitro to meet the following criteria: (i) episomal replication in plastids; (ii) facile cloning; (iii) predictable transgene expression in plastids; (iv) non-integration of vector sequences into the endogenous plastome; and (v) autonomous persistence in the plant over generations in the absence of exogenous selection pressure. Mini-synplastomes are anticipated to revolutionize chloroplast biotechnology, enable facile marker-free plastid engineering, and provide an unparalleled platform for one-step metabolic engineering in plants.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8753362PMC
http://dx.doi.org/10.1111/pbi.13717DOI Listing

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