The ultimate goal of the Metabolic Diversity group at the IPK is to understand the interplay between plant genes, the environment, and the molecular outcomes of these interactions in order to optimise crop traits that are beneficial to modern agriculture. We define metabolic diversity therefore as the capability of plants to adjust their biosynthetic products when exposed to different abiotic and biotic factors present in their environment. This ability to change rapidly to environmental cues is extremely important for new generations of cultivated plants and the people who depend upon them. We now understand that this metabolic diversity has a strong genetic component to it.
The expected outcomes of the Metabolic Diversity group will range from quantified, targeted metabolites for specific comparisons of primary essential biomolecules to non-targeted metabolic screens. We intend to identify differences among populations of crop plants in order to select agriculturally important traits. The Metabolic Diversity group relies heavily on a combinatorial experimental approach, which integrates biochemistry, molecular biology, and analytical chemistry to analyse primary and secondary metabolic status in combination with phenotypic performance parameters (growth rates, vitality, seed viability and yield).
Besides cereal crops, the Metabolic Diversity group has interest in medicinal crop species and is interested in using novel synthetic biology techniques to produce plant-derived medicinal compounds in a host of alternative organisms. Lastly, the Metabolic Diversity lab aims to contribute to solving a growing problem in modern plant science. Specifically, we intend on making a significant contribution to the assignment of gene functions in the form of annotation of enzyme classes and activities of the high proportion of genes identified as ‘putative’ or more importantly, ‘unknown function’ that are pervasive in complex cultivated crop genomes.
Hypericum perforatum, also known as Saint John’s Wort (SJW), is part of a genus including over 400 species distributed all around the world and characterized by great diversity (Crockett and Robson 2012). Saint John’s Wort is a popular medicinal plant that produces bio active compounds and is recognized for its mild antidepressant properties (Schallau et al 2010; Galla et al 2011; Rizzo 2016). Hypericin is one of the many bioactive compounds produced by SJW that got the attention of the scientific community thanks to its potential use in the treatment of the Alzheimer disease (Sgarbossa et al 2008; Bramanti et al 2010) and to its applications in cancer photodynamic therapy (Garg et al 2010, 2012; Dudek-Peric 2015). Despite the long effort in the study of hypericin production, this biosynthetic pathway remains mostly uncharacterized.
Dr. Paride Rizzo, a postdoc of the D’Auria lab, is interested in the developmental biology of SJW. His research lead to the identification of contrasting phenotypes of glanded and glandless tissues (G-/G+ PT) in the flowers of H. perforatum (Rizzo et al 2019).
We compare these phenotypes to identify the main metabolic and transcriptomic differences between glanded and glandless tissues. Using this combination of genetic and metabolic subtraction, we identify candidate genes for the biosynthesis of hypericin and for the differentiation of dark glands.
Currently the MD group is implementing a pipeline for the test of such genes using expression assays in microorganisms as well as in plants.
Considering the high metabolic cost of synthesizing hypericin and producing glands to keep it compartmentalized, we are curious about the ecological and evolutionary advantages of its biosynthesis. With this in mind, we explore the metabolic and genomic diversity of H. perforatum and combine the phylogenesis of this species with its hypericin production patterns in order to understand if the trait of dark glands formation has a geographical structure and if it is going to be lost in evolution.
While we characterize several genotypes of the species perforatum, we are also addressing the interspecific diversity of the genus Hypericum thanks to a germplasm collection that we are currently growing in our lab.
Our research is embedded in a network of partners including: IPB Halle, Halle University, University of Braunschweig, University of Saskatchewan and University of Heidelberg.
With our research on Hypericum we want to generate new scientific results that will be useful for the implementation of future applications in the pharmaceutical industry and in medical research.
Tropane alkaloids represent a major class of plant-derived secondary metabolites known to occur in the Solanaceae family but are also present in the families Convolvulaceae, Proteaceae, Rhizophoraceae and Erythroxylaceae. The core defining structure of tropane alkaloids is an 8-azabicyclo[3.2.1] octane nucleus. The diversity of tropane alkaloids is achieved by elaboration of this core through different types of modifications. The genus Erythroxylum (family Erythroxylaceae) contains approximately 230 species with ranges spread throughout the tropics including South America and Madagascar.
Erythroxylum coca and Erythroxylum novogranatense are the most widely used species for the production of cocaine. Very little is known as to the biological and ecological roles that cocaine and other tropane alkaloids play in plants. Their anti-cholinergic properties argue strongly in favor of deterrent activity against herbivores. We have begun molecular and biochemical studies in order to elucidate the biochemical steps which lead to the production of tropane alkaloids in E. coca plants.
The terminal step in the production of cocaine or other tropane related esters is thought to be the formation of the acyl ester via the action of an acyltransferase enzyme. In the case of cocaine, this acyltransferase utilizes the substrates methylecgonine and benzoyl CoenzymeA to produce cocaine and free CoA. Our lab has been working for several years on a plant specific family of acyltransferases commonly referred to as the BAHD acyltransferases. Thus far, more than 8 BAHD acyltransferases have been isolated from Erythroxylum coca (E. coca). Recent results show one of these BAHD members exhibits cocaine synthase activity. Members of my group have successfully developed an LC-MS based ‘realtime' enzyme assay for cocaine synthase in order to obtain very accurate kinetic data for characterization studies. We are also using antibodies made against the whole purified protein in order to perform immunoprecipitation and immunohistochemical studies.
In addition to the study of the role of acyltransferases in E. coca, members of the D’Auria lab are also actively pursuing the enzymes that are involved in forming the first and second rings of the tropane core. Most theories to date suggest that the precursor compound is most likely the mono-methylated polyamine putrescine. Benjamin Chavez, a PhD. student in the D’Auria lab, is characterizing the properties of several polyamine synthases that are similar to putrescine methyltransferase and spermine/spermidine synthases. We are also interested in the origins of the benzoic acid portion of cocaine and are combining the tools that we have thus far developed for E. coca to develop this system as a model for benzoic acid biosynthesis.
Using a combination of a LECO HT time-of-flight mass spectrometer, an AGILENT 7890A gas chromatograph equipped with a GERSTEL MPS2XL autosampler, we are able to quantify a large array of polar plant metabolites. Typically, these comprise a number of 60-100 known metabolites like amino acids, organic acids, polyamins, sugars, sugar phosphates etc. and twice the number of metabolites with unknown chemical structure. Routinely we apply in-line derivatization (derivatization of each individual sample prior injection) to improve the quality of our measurements. This enables us to quantify metabolites from large sample numbers in a highly reproducible manner.
A high resolution Bruker Maxis 2 quadrupole time-of-flight mass spectrometer (R = 85000, accuracy = 0.6 ppm) hyphenated with an AGILENT 1290 liquid chromatograph (max 1200 bar) and equipped with a GERSTEL autosampler is used for high throughput metabolite profiling of semi-polar compounds like secondary metabolites, phytosterols, vitamins, hormones... and hydrophobic analytes like lipids, tocoperols, pigments... Typically, several Hundreds to Thousands non-redundant chromatographic features (mz) are quantitatively recorded which can be partially annotated by database queries (KNApSAcK, KEGG) using accurate mass, isotopic pattern and MSMS fragment spectra of the analytes. The liquid chromatograph can be coupled to a mikroplate fraction collector (ADVION Nanomate) to comprehensively isolate separated metabolites for in-depth characterization. The analysis time ranges from 5 min (secondary metabolite profiling, lipid profiles of oil storing organs) to 30 min (comprehensive profiling of semi-polar metabolites, lipid profiling of samples with complex lipidomic composition) and allows reproducible measurements of a large number of samples.
|Chavez||Benjaminfirstname.lastname@example.org||+49 39482 5-587|
|D Auria||Dr. John Charlesemail@example.com||+49 39482 5-176|
|Madappattuparambil Ravindran||Dr. Beenafirstname.lastname@example.org||+49 39482 5-468|
|Pathi||Dr. Krishnaemail@example.com||+49 39482 5-241|
|Rizzo||Dr. Paridefirstname.lastname@example.org||+49 39482 5-787|
|Apelt||Andreaemail@example.com||+49 39482 5-780|
|Hammer||Simonafirstname.lastname@example.org||+49 39482 5-508|
|Helmold||Christineemail@example.com||+49 39482 5-203|
Alseekh S, Aharoni A, Brotman Y, Contrepois K, DAuria J, Ewald J, J C E, Fraser P D, Giavalisco P, Hall R D, Heinemann M, Link H, Luo J, Neumann S, Nielsen J, Perez de Souza L, Saito K, Sauer U, Schroeder F C, Schuster S, Siuzdak G, Skirycz A, Sumner L W, Snyder M P, Tang H, Tohge T, Wang Y, Wen W, Wu S, Xu G, Zamboni N, Fernie A R:
Mass spectrometry-based metabolomics: a guide for annotation, quantification and best reporting practices. Nat. Methods 18 (2021) 747-756. https://dx.doi.org/10.1038/s41592-021-01197-1
Irfan M, Chavez B, Rizzo P, D’Auria J C, Moghe G D:
Evolution-aided engineering of plant specialized metabolism. aBIOTECH 2 (2021) 240-263. https://dx.doi.org/10.1007/s42994-021-00052-3
Kim N, Chavez B, Stewart C, D’Auria J C:
Structure and function of enzymes involved in the biosynthesis of tropane alkaloids. In: Srivastava V, Mehrotra S, Mishra S (Eds.): Tropane alkaloids – pathways, potential and biotechnological applications. Singapore: Springer Nature (2021) 21-50. dx.doi.org/10.1007/978-981-33-4535-5_2 ISBN 978-981-334-534-8
D’Auria J C (Ed.):
Special Issue: Advances in Plant Alkaloid Research; printed edition. (Series: Molecules, Vol. 25) (2020) 278 pp. doi.org/10.3390/books978-3-03943-173-1 ISBN 978-3-03943-172-4 (Hbk); ISBN 978-3-03943-173-1 (PDF)
Isayenkov S, Hilo A, Rizzo P, Tandron Moya Y A, Rolletschek H, Borisjuk L, Radchuk V:
Adaptation strategies of halophytic barley Hordeum marinum spp marinum to high salinity and osmotic stress. Int. J. Mol. Sci. 21 (2020) 9019. https://dx.doi.org/10.3390/ijms21239019
Rizzo P, Altschmied L, Ravindran B M, Rutten T, DAuria J C:
The biochemical and genetic basis for the biosynthesis of bioactive compounds in Hypericum perforatum L., one of the largest medicinal crops in Europe. Genes 11 (2020) E1210. https://dx.doi.org/10.3390/genes11101210
Stark P, Zab C, Porzel A, Franke K, Rizzo P, Wessjohann L A:
PSYCHE-a valuable experiment in plant NMR-metabolomics. Molecules 25 (2020) 5125. https://dx.doi.org/10.3390/molecules25215125
Restrepo D A, Saenz E, Jara-Muñoz O A, Calixto-Botia I F, Rodríguez-Suárez S, Zuleta P, Chavez B G, Sanchez J A, DAuria J C:
Erythroxylum in focus: an interdisciplinary review of an overlooked genus. Molecules 24 (2019) 3788. https://dx.doi.org/10.3390/molecules24203788