Co-expression of a cyclizing asparaginyl endopeptidase enables efficient production of cyclic peptides in planta. (22nd December 2017)

• Record Type: Journal Article
• Authors: Poon, Simon; Harris, Karen S; Jackson, Mark A; McCorkelle, Owen C; Gilding, Edward K; Durek, Thomas; van der Weerden, Nicole L; Craik, David J; Anderson, Marilyn A
• Is Part Of: Journal of experimental botany. Volume 69:Number 3(2018)
• Page Start: 633
• Page End: 641
• Publication Date: 2017-12-22
• Subjects: Asparaginyl endopeptidase -- cyclic peptide -- cyclotide -- kalata B1 -- Nicotiana benthamiana -- plant-made pharmaceutical -- transient expression -- SFTI; Botany -- Periodicals; Botany, Experimental -- Periodicals; Plant physiology -- Periodicals; 580
• DOI: 10.1093/jxb/erx422
• Languages: English
• ISSNs: 0022-0957

Abstract

Abstract : Backbone-cyclized peptides, which have applications in the pharmaceutical and agricultural industries, can be made efficiently in plants by co-expressing them with a cyclizing enzyme. Abstract: Cyclotides are ultra-stable, backbone-cyclized plant defence peptides that have attracted considerable interest in the pharmaceutical industry. This is due to their range of native bioactivities as well as their ability to stabilize other bioactive peptides within their framework. However, a hindrance to their widespread application is the lack of scalable, cost-effective production strategies. Plant-based production is an attractive, benign option since all biosynthetic steps are performed in planta . Nonetheless, cyclization in non-cyclotide-producing plants is poor. Here, we show that cyclic peptides can be produced efficiently in Nicotiana benthamiana, one of the leading plant-based protein production platforms, by co-expressing cyclotide precursors with asparaginyl endopeptidases that catalyse peptide backbone cyclization. This approach was successful in a range of other plants (tobacco, bush bean, lettuce, and canola), either transiently or stably expressed, and was applicable to both native and engineered cyclic peptides. We also describe the use of the transgenic system to rapidly identify new asparaginyl endopeptidase cyclases and interrogate their substrate sequence requirements. Our results pave the way for exploiting cyclotides for pest protection in transgenic crops as well as large-scale production of cyclic peptide pharmaceuticals in plants.