Until 2022

Since the development of microbes and higher eukaryotes coevolution has resulted in specific interaction mechanisms. It is well known that symbiotic bacteria and fungi influence the life cycle, and are essential for the homeostasis of many eukaryotes. However, in most cases, the factors driving and influencing the cross-kingdom interactions are unknown.

We focus on the structural identification of microbial chemical mediators that are important to maintain the symbiotic life style of the producing organisms.

To study the chemical signals we apply state-of-the-art analytical tools:

  • Analytical Chemistry (UHPLC, UHPLC-MS, NMR, MALDI etc.)
  • Genome Mining and Molecular Biology
  • Organic Synthesis (total synthesis and natural product derivatization)

Natural Products of Microbial Symbionts of Termites

Fungus-growing termites rear a symbiotic fungus as a food source in specialized combs. Termites have developed several strategies to combat invading fungi species, which can be life-threatening to the insect colony. Especially defensive symbionts support the homeostasis of the colony by secretion of selective antimicrobial and antifungal products.

Natural Products of Microbial Symbionts of Hydractinia

Natural products present in bacterial biofilm induce morphogenesis of larvae of the marine hydroid polyp Hydractinia echinata.

Head

Christine Beemelmanns
Head

Termites and their symbionts

Studying the microbiome of social insects, such as termites, helps to identify new aspects of small-molecule mediated symbiotic relations. At the same time it serves platform to identify new antibacterial and antifungal agents.

Fungus-growing termites

The fungus-growing termite system is a prime example of multilateral symbiosis. The ancient farming symbiosis involves a termite host (Macrotermitinae), a specialized fungal mutualist (Termitomyces) maintained in an optimized fungal garden system (fungus comb), the presence of complex and highly adapted bacterial communities within the insect gut and fungus comb, and the co-evolved garden weed (Pseudoxylaria).

Natural products from protective symbionts

Within this project, we aim to isolate, characterize and understand the role of natural products produced by microorganisms associated with fungus-growing termites. We used various different culturing techniques to isolate termite-associated microbes and pursued the whole genome sequence of several key isolates. Subsequent chemical analysis of our isolates in axenic and co-cultures revealed several new natural product classes showing a diverse set of biological activities.

Biosynthetic pathway analysis

We have sequenced the genomes of selected new microbial species to analyze their biosynthetic potential and potentially detect new natural products. The comparative analysis of the acquired genomic information likely reveals new biosynthetic enzymes and new biochemical transformations.

Documentation

Termine Fungiculture – A Hidden Treasure Trove

Wie ein Antibiotikacocktail Insekten schützt

Funding

  • ChemBioSys (DFG) seit 2016
  • BiBiMac (DFG-ANR) ab 2018

Our collaborations

Microbial Symbionts of Hydractinia

Microbes associated with marine invertebrates are well-known to harbor an enormous biosynthetic potential. We combine new bioassays, genome sequencing and mining strategies to identify the encoded secondary metabolites with unique chemical scaffolds and potential pharmaceutical application.

Microorganisms protect and shape the colonial hydroid polyp Hydraktinia

Morphogenic Signaling Molecules

More and more examples show that bacterially produced small molecules contribute to the host’s fitness and development by acting as biological information carrier to maintain and modulate the multilateral interaction network. But fully characterized examples are still rare, and the mode-of-actions of those molecules are often not well understood.

We are investigating the model system Hydractinia echinata, a marine hydroid polyp, to identify key metabolites that induce biofouling.

The life cycle of the marine hydroid polyp H. echinata has a motile (larvae) and sessil reproductive phase (polyp). The irreversible morphogenesis from the motile larvae to the sessile primary polyp is induced by specific molecules from Pseudoalteromonas spp. But the structure determination and and mode of action of the signaling molecules has been so far elusive. We use a broad range of molecular biology methods to identify the bacterial cues and the receptor in the marine hydroid polyp to understand the interaction mechanisms in more detail.

 

Natural product synthesis and derivatisation

Many natural products are only produced in minor amounts and a full structural characterization is nearly impossible. In addition, many pharmaceutically interesting compounds are too toxic and need derivatisation to improve their pharmacological properties.

Therefore, we are establishing synthetic strategies towards sphingoid-type natural products and functionalized lipids, which represent important signaling molecules in our ecological mdoel systems. 

Synthesis of new NRPS-derived natural products

Based on a comparative genome analysis, we were able to isolate a new natural product - barnesin A. Further bioactivity studies showed that barnesin A is a cysteine ​​protease inhibitor with nanomolar activity. The total synthesis enabled further structural activity studies.

For more details, see Maja's article in ACS ChemBio!

Publications

Schmidt S, Kildgaard S, Guo H, Beemelmanns C, Poulsen M (2021) The chemical ecology of the fungus-farming termite symbiosis. Nat Prod Rep 39(2), 231-248. (Review)
Schorn MA, Verhoeven S, Ridder L, Huber F, Acharya DD, Aksenov AA, Aleti G, Moghaddam JA, Aron AT, Aziz S, Bauermeister A, Bauman KD, Baunach M, Beemelmanns C, Beman JM, Berlanga-Clavero MV, Blacutt AA, Bode HB, Boullie A, Brejnrod A, Bugni TS, Calteau A, Cao L, Carrión VJ, Castelo-Branco R, Chanana S, Chase AB, Chevrette MG, Costa-Lotufo LV, Crawford JM, Currie CR, Cuypers B, Dang T, de Rond T, Demko AM, Dittmann E, Du C, Drozd C, Dujardin JC, Dutton RJ, Edlund A, Fewer DP, Garg N, Gauglitz JM, Gentry EC, Gerwick L, Glukhov E, Gross H, Gugger M, Guillén Matus DG, Helfrich EJN, Hempel BF, Hur JS, Iorio M, Jensen PR, Kang KB, Kaysser L, Kelleher NL, Kim CS, Kim KH, Koester I, König GM, Leao T, Lee SR, Lee YY, Li X, Little JC, Maloney KN, Männle D, Martin HC, McAvoy AC, Metcalf WW, Mohimani H, Molina-Santiago C, Moore BS, Mullowney MW, Muskat M, Nothias LF, O'Neill EC, Parkinson EI, Petras D, Piel J, Pierce EC, Pires K, Reher R, Romero D, Roper MC, Rust M, Saad H, Saenz C, Sanchez LM, Sørensen SJ, Sosio M, Süssmuth RD, Sweeney D, Tahlan K, Thomson RJ, Tobias NJ, Trindade-Silva AE, van Wezel GP, Wang M, Weldon KC, Zhang F, Ziemert N, Duncan KR, Crüsemann M, Rogers S, Dorrestein PC, Medema MH, van der Hooft JJJ (2021) A community resource for paired genomic and metabolomic data mining. Nat Chem Biol 17(4), 363-368.
Seyedi J, Kalbassi MR, Esmaeilbeigi M, Tayemeh MB, Amiri Moghadam J (2021) Toxicity and deleterious impacts of selenium nanoparticles at supranutritional and imbalance levels on male goldfish (Carassius auratus) sperm. J Trace Elem Med Biol 66, 126758.
Sinotte VM, Conlon BH, Seibel E, Schwitalla JW, de Beer ZW, Poulsen M, Bos N (2021) Female-biased sex allocation and lack of inbreeding avoidance in Cubitermes termites. Ecol Evol 11(10), 5598-5605.
Um S, Guo H, Thiengmag S, Benndorf R, Murphy R, Rischer M, Braga D, Poulsen M, de Beer ZW, Lackner G, Beemelmanns C (2021) Comparative genomic and metabolic analysis of Streptomyces sp. RB110 morphotypes illuminates genomic rearrangements and formation of a new 46-membered antimicrobial macrolide. ACS Chem Biol 16(8), 1482-1492.
Um S, Seibel E, Schalk F, Balluf S, Beemelmanns C (2021) Targeted isolation of saalfelduracin B-D from Amycolatopsis saalfeldensis using LC-MS/MS-based molecular networking. J Nat Prod 84(4), 1002-1011.
Vidkjær NH, Schmidt S, Hu H, Bodawatta KH, Beemelmanns C, Poulsen M (2021) Species- and caste-specific gut metabolomes in fungus-farming termites. Metabolites 11(2), 839.
Benndorf R, Martin K, Küfner M, de Beer ZW, Vollmers J, Kaster AK, Beemelmanns C (2020) Actinomadura rubteroloni sp. nov. and Actinomadura macrotermitis sp. nov., isolated from the gut of the fungus growing-termite Macrotermes natalensis. Int J Syst Evol Microbiol 70(10), 5255-5262.
Benndorf R, Schwitalla JW, Martin K, de Beer ZW, Vollmers J, Kaster AK, Poulsen M, Beemelmanns C (2020) Nocardia macrotermitis sp. nov. and Nocardia aurantia sp. nov., isolated from the gut of the fungus-growing termite Macrotermes natalensis. Int J Syst Evol Microbiol 70(10), 5226-5234.
Ghodsi Z, Kalbassi MR, Farzaneh P, Mobarez AM, Beemelmanns C, Amiri Moghaddam J (2020) Immunomodulatory function of antimicrobial peptide Ec-Hepcidin1 modulates the induction of inflammatory gene expression in primary cells of caspian trout (Salmo trutta caspius Kessler, 1877). Fish Shellfish Immunol 104, 55-61.