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EDITORIAL article

Front. Plant Sci., 28 October 2021
Sec. Plant Metabolism and Chemodiversity
This article is part of the Research Topic Exploring and Engineering Plant Specialized Metabolism: Latest Advances and New Horizons View all 10 articles

Editorial: Exploring and Engineering Plant Specialized Metabolism: Latest Advances and New Horizons

  • 1Institute of Botany, Leibniz University Hannover, Hanover, Germany
  • 2Centre of Biomolecular Drug Research, Leibniz University Hannover, Hanover, Germany
  • 3Key Laboratory of Bio-resource and Eco-environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, China
  • 4Department of Chemistry, Irving K. Barber Faculty of Science, The University of British Columbia, Kelowna, BC, Canada

Plants use specialized metabolic pathways to produce over 200,000 small molecules which often have potent biological activities. Many of these compounds have medicinal, nutritional or other applications. However, the natural supply from the producing plants is often strongly limited, for example because plants produce insufficient quantities or do not produce biomass fast enough. There is therefore an urgent need to improve our understanding of plant specialized metabolism, and to come up with strategies to engineer the underlying pathways. This is especially true in the light of climate change and the mandate to transition to a biobased economy. For that reason, this Research Topic aims to collate recent developments in the area of plant specialized metabolism, with a special focus on cutting-edge methods to explore as well as engineer biosynthetic pathways.

Probably the most important technical progress of the last decade has been achieved in the field of sequencing platforms. Nowadays, obtaining transcriptome and even genome data of non-model plant species is a realistic option even for smaller labs. For example, high-quality genome assemblies up to the chromosome level have been reported recently for medicinal plants such as Senna tora (Kang et al., 2020), Camptotheca acuminata (Zhao et al., 2017; Kang et al., 2021), Ophiorrhiza pumila (Rai et al., 2021), Papaver somniferum (opium poppy; Guo et al., 2018; Li et al., 2020), and Taxus chinensis var. mairei (Xiong et al., 2021) as well as for culinary herbs from the mint family (Lamiaceae; Bornowski et al., 2020; Lichman et al., 2020). This advance opens up numerous avenues to gain a better understanding of plant specialized metabolism on a transcriptome- or genome-wide level.

The importance of sequencing data for investigating the biochemistry of understudied plant species is underlined very well by the publications in this Research Topic: For example, Yamada et al. performed a genome-wide profiling of WRKY transcription factor genes in California poppy (Eschscholzia californica) to study their effect on benzylisoquinoline alkaloid biosynthesis. A similar approach was used by Cao et al. with a focus on MYB transcription factor genes in Chinese Bayberry (Morella rubra) to investigate flavonoid metabolism. Li et al. used genome data from red sage (Salvia miltiorrhiza) to identify TIFY transcription factors involved in regulation of specialized metabolism. Lastly, Zhang et al. combined multiple omics techniques to gain a better understanding of how lipid and fatty acid synthesis is regulated in sesame seeds (Sesamum indicum).

While all of these studies demonstrate well how current omics techniques can be applied to understand regulatory circuits of already known plant metabolic pathways, there remains a much larger number of pathways that have yet to be elucidated. The key challenge here is to identify the genes and enzymes involved in these pathways, which is often a slow and tedious process and requires an efficient bioinformatic and biochemical pipeline. However, several break-through publications in the last years demonstrate that plant pathway elucidation is now becoming increasingly feasible (Caputi et al., 2018; Dang et al., 2018; Christ et al., 2019; Hodgson et al., 2019; Pluskal et al., 2019; Nett et al., 2020). In the course of these and numerous other projects, many unusual and powerful enzymes have been discovered, which are also attractive from a biocatalysis perspective. A particularly important class of enzymes are cytochromes P450, whose broad repertoire of catalytical function was reviewed by Nguyen and Dang. Again, analyzing genome and transcriptome data via state-of-the-art bioinformatics approaches has been key to discovering novel biosynthetic genes and enzymes from plants. Plant biosynthetic gene clusters are now reported more and more frequently, as plant genomic data can be obtained more readily. An overview over currently known plant biosynthetic gene clusters is provided by Bharadwaj et al..

Understanding how plant metabolic pathways work and are regulated is key to engineer them successfully. A strategy that is commonly used is to transfer these pathways into baker's yeast (Saccharomyces cerevisiae) as a versatile and easy-to-handle eukaryotic host system. As reviewed by Utomo et al., this success is particularly based on CRISPR/Cas9-based techniques for multiplex genome editing. However, not only microorganisms are attractive hosts for pathway engineering. Thanks to advancements in the fields of genome editing and plant biochemistry, original producer plants are now often engineered rationally as well. Examples from engineering terpenoid metabolism in glandular trichomes of Lamiaceae plants are reviewed by Mahmoud et al. How a better understanding of plant metabolism can translate into a relevant application is also demonstrated by the article of Koudounas et al.; in their work, they successfully silenced a gene involved in secoiridoid biosynthesis in olives (Olea europaea), which might be valuable to improve the effects of olive oil on human health.

As demonstrated by this Research Topic, the impact of modern sequencing techniques, bioinformatics analysis platforms, state-of-the-art biochemical approaches and new genetic engineering techniques to the field of plant specialized metabolism has been tremendous. This has enabled various biochemical discoveries and engineering applications, which would not have been possible only a few years ago. We are looking forward to seeing further progress in understanding plant specialized metabolism and additional real-world applications of pathway engineering in the years to come.

Author Contributions

All authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication.

Funding

YZ was supported by the Institutional Research Fund of Sichuan University (2020SCUNL106) and the Fundamental Research Funds for the Central Universities (SCU2021D006).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

Bornowski, N., Hamilton, J. P., Liao, P., Wood, J. C., Dudareva, N., and Buell, C. R. (2020). Genome sequencing of four culinary herbs reveals terpenoid genes underlying chemodiversity in the Nepetoideae. DNA Res. 27:dsaa016. doi: 10.1093/dnares/dsaa016

PubMed Abstract | CrossRef Full Text | Google Scholar

Caputi, L., Franke, J., Farrow, S. C., Chung, K., Payne, R. M. E., Nguyen, T.-D., et al. (2018). Missing enzymes in the biosynthesis of the anticancer drug vinblastine in Madagascar periwinkle. Science 360, 1235–1239. doi: 10.1126/science.aat4100

PubMed Abstract | CrossRef Full Text | Google Scholar

Christ, B., Xu, C., Xu, M., Li, F.-S., Wada, N., Mitchell, A. J., et al. (2019). Repeated evolution of cytochrome P450-mediated spiroketal steroid biosynthesis in plants. Nat. Commun. 10:3206. doi: 10.1038/s41467-019-11286-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Dang, T.-T. T., Franke, J., Carqueijeiro, I. S. T., Langley, C., Courdavault, V., and O'Connor, S. E. (2018). Sarpagan bridge enzyme has substrate-controlled cyclization and aromatization modes. Nat. Chem. Biol. 14, 760–763. doi: 10.1038/s41589-018-0078-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Guo, L., Winzer, T., Yang, X., Li, Y., Ning, Z., He, Z., et al. (2018). The opium poppy genome and morphinan production. Science 2018:eaat4096. doi: 10.1126/science.aat4096

PubMed Abstract | CrossRef Full Text | Google Scholar

Hodgson, H., Peña, R. D. L., Stephenson, M. J., Thimmappa, R., Vincent, J. L., Sattely, E. S., et al. (2019). Identification of key enzymes responsible for protolimonoid biosynthesis in plants: opening the door to azadirachtin production. Proc. Natl. Acad. Sci. U. S. A. 2019:201906083. doi: 10.1073/pnas.1906083116

PubMed Abstract | CrossRef Full Text | Google Scholar

Kang, M., Fu, R., Zhang, P., Lou, S., Yang, X., Chen, Y., et al. (2021). A chromosome-level Camptotheca acuminata genome assembly provides insights into the evolutionary origin of camptothecin biosynthesis. Nat. Commun. 12:3531. doi: 10.1038/s41467-021-23872-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Kang, S.-H., Pandey, R. P., Lee, C.-M., Sim, J.-S., Jeong, J.-T., Choi, B.-S., et al. (2020). Genome-enabled discovery of anthraquinone biosynthesis in Senna tora. Nat. Commun. 11:5875. doi: 10.1038/s41467-020-19681-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, Q., Ramasamy, S., Singh, P., Hagel, J. M., Dunemann, S. M., Chen, X., et al. (2020). Gene clustering and copy number variation in alkaloid metabolic pathways of opium poppy. Nat. Commun. 11, 1–13. doi: 10.1038/s41467-020-15040-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Lichman, B. R., Godden, G. T., and Buell, C. R. (2020). Gene and genome duplications in the evolution of chemodiversity: perspectives from studies of Lamiaceae. Curr. Opin. Plant Biol. 55, 74–83. doi: 10.1016/j.pbi.2020.03.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Nett, R. S., Lau, W., and Sattely, E. S. (2020). Discovery and engineering of colchicine alkaloid biosynthesis. Nature 8, 1–6. doi: 10.1038/s41586-020-2546-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Pluskal, T., Torrens-Spence, M. P., Fallon, T. R., Abreu, A. D., Shi, C. H., and Weng, J.-K. (2019). The biosynthetic origin of psychoactive kavalactones in kava. Nat. Plants 5, 867–878. doi: 10.1038/s41477-019-0474-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Rai, A., Hirakawa, H., Nakabayashi, R., Kikuchi, S., Hayashi, K., Rai, M., et al. (2021). Chromosome-level genome assembly of Ophiorrhiza pumila reveals the evolution of camptothecin biosynthesis. Nat. Commun. 12:405. doi: 10.1038/s41467-020-20508-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Xiong, X., Gou, J., Liao, Q., Li, Y., Zhou, Q., Bi, G., et al. (2021). The Taxus genome provides insights into paclitaxel biosynthesis. Nat. Plants 2021, 1–11. doi: 10.1101/2021.04.29.441981

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhao, D., Hamilton, J. P., Pham, G. M., Crisovan, E., Wiegert-Rininger, K., Vaillancourt, B., et al. (2017). De novo genome assembly of Camptotheca acuminata, a natural source of the anti-cancer compound camptothecin. GigaScience 6, 1–7. doi: 10.1093/gigascience/gix065

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: genomics, transcriptomics, plant biochemistry, transcription factors, metabolic engineering

Citation: Franke J, Zhang Y and Dang T-TT (2021) Editorial: Exploring and Engineering Plant Specialized Metabolism: Latest Advances and New Horizons. Front. Plant Sci. 12:783465. doi: 10.3389/fpls.2021.783465

Received: 26 September 2021; Accepted: 11 October 2021;
Published: 28 October 2021.

Edited by:

Reuben J. Peters, Iowa State University, United States

Reviewed by:

Bjoern Hamberger, Michigan State University, United States

Copyright © 2021 Franke, Zhang and Dang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Jakob Franke, jakob.franke@botanik.uni-hannover.de; Yang Zhang, yang.zhang@scu.edu.cn; Thu-Thuy T. Dang, thuy.dang@ubc.ca

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.