Gangwon Cheong’s research while affiliated with Gyeongsang National University and other places

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Publications (1)


Stable or transient expression of foreign genes from the nuclear genome and post-translational import of foreign proteins into chloroplasts. Two methods are used for transgene expression following nuclear transformation. In the first method, T-DNA harboring the transgene is stably integrated into the nuclear genome, thereby giving rise to transgenic plants, and in the second method, the non-integrated transgene is expressed from the nucleus and subsequently proteins are synthesized on cytosolic ribosomes and post-translationally imported into chloroplasts
Production of recombinant proteins through sequestration in chloroplasts: a strategy based on nuclear transformation and post-translational protein import
  • Literature Review
  • Publisher preview available

May 2019

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231 Reads

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21 Citations

Plant Cell Reports

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Gangwon Cheong

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Inhwan Hwang

Recently, plants have emerged as a lucrative alternative system for the production of recombinant proteins, as recombinant proteins produced in plants are safer and cheaper than those produced in bacteria and animal cell-based production systems. To obtain high yields in plants, recombinant proteins are produced in chloroplasts using different strategies. The first strategy is based on chloroplast transformation, followed by gene expression and translation in chloroplasts. This has proven to be a powerful approach for the production of proteins at high levels. The second approach is based on nuclear transformation, followed by post-translational import of proteins from the cytosol into chloroplasts. In the nuclear transformation approach, foreign genes are stably integrated into the nuclear genome or transiently expressed in the nucleus by non-integrating T-DNA. Although this approach also has great potential for protein production at high levels, it has not been thoroughly investigated. In this review, we focus on nuclear transformation-based protein expression and its subsequent sequestration in chloroplasts, and summarize the different strategies used for high-level production of recombinant proteins. We also discuss future directions for further improvements in protein production in chloroplasts through nuclear transformation-based gene expression.

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Citations (1)


... Most recombinant proteins are produced through nuclear transformation with land plants as the hosts, and foreign genes are randomly and heterogeneously integrated into different sites of the nuclear genome, which have the advantages of glycosylation and proper protein targeting (León-Bañares et al. 2004). However, nuclear transformation is influenced by the randomness of gene integration, leading to some limitations in the process, such as low gene copy number, gene silencing, and low expression level (Muthamilselvan et al. 2019). Furthermore, chloroplast transformation involves inserting homologous fragments into the chloroplast genome before and after multiple cloning sites in the expression vector. ...

Reference:

Development and research progress of microalgae as a production platform for antimicrobial peptides
Production of recombinant proteins through sequestration in chloroplasts: a strategy based on nuclear transformation and post-translational protein import

Plant Cell Reports