Expression strategies for the efficient synthesis of antimicrobial peptides in plastids

被引:33
|
作者
Hoelscher, Matthijs P. [1 ,2 ]
Forner, Joachim [1 ]
Calderone, Silvia [1 ,3 ]
Kraemer, Carolin [1 ]
Taylor, Zachary [1 ]
Loiacono, F. Vanessa [1 ]
Agrawal, Shreya [1 ,4 ]
Karcher, Daniel [1 ]
Moratti, Fabio [1 ]
Kroop, Xenia [1 ]
Bock, Ralph [1 ]
机构
[1] Max Planck Inst Mol Pflanzenphysiol, Muhlenberg 1, D-14476 Potsdam, Germany
[2] Univ Utrecht, Pharmaceut, Pharmaceut Sci, Univ Weg 99, NL-3584 CG Utrecht, Netherlands
[3] CSIC IRTA UAB UB, Ctr Res Agr Genom Crag, Campus UAB, Barcelona 08193, Spain
[4] Neoplants, 630 Rue Noetzlin Batiment, F-91190 Gif Sur Yvette, France
基金
欧洲研究理事会;
关键词
HIGH-LEVEL EXPRESSION; RECOMBINANT PRODUCTION; TRANSGENIC TOBACCO; TOMATO PLASTIDS; BASIC RESEARCH; PROTEIN; GENOME; TRANSFORMATION; ANTIBACTERIAL; GRIFFITHSIN;
D O I
10.1038/s41467-022-33516-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Antimicrobial peptides (AMPs) kill microbes or inhibit their growth and are promising next-generation antibiotics. Harnessing their full potential as antimicrobial agents will require methods for cost-effective large-scale production and purification. Here, we explore the possibility to exploit the high protein synthesis capacity of the chloroplast to produce AMPs in plants. Generating a large series of 29 sets of transplastomic tobacco plants expressing nine different AMPs as fusion proteins, we show that high-level constitutive AMP expression results in deleterious plant phenotypes. However, by utilizing inducible expression and fusions to the cleavable carrier protein SUMO, the cytotoxic effects of AMPs and fused AMPs are alleviated and plants with wildtype-like phenotypes are obtained. Importantly, purified AMP fusion proteins display antimicrobial activity independently of proteolytic removal of the carrier. Our work provides expression strategies for the synthesis of toxic polypeptides in chloroplasts, and establishes transplastomic plants as efficient production platform for antimicrobial peptides.
引用
收藏
页数:17
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