Biology subjects

Dittmann, E.

Publications and source records attributed to Dittmann, E..

5 recordsLinked to original sources

bioRxiv2026

An Oligomeric Lanthipeptide from Nostoc punctiforme Promotes Host Association During Early Symbiosis with Blasia pusilla

Nitrogen-fixing Nostoc species form symbiotic relationships with diverse plants, yet the role of specialized metabolites in these interactions remains poorly understood. Here, we identify a previously cryptic gene cluster coding for the biosynthesis of the lanthipeptide nostolanthin (nlt), which is rapidly induced upon physical contact between Nostoc punctiforme and the liverwort Blasia pusilla. Despite its robust transcriptional activation, nostolanthin remained undetectable in its native producer by conventional metabolomic analyses. Heterologous reconstitution of the biosynthesis showed that the lanthipeptide synthetase NltM produces a bicyclic class II lanthipeptide containing a non-cyclized dehydroamino acid together with a free cysteine residue. We show that this lanthipeptide undergoes covalent oligomerization into high-molecular-weight assemblies, a process favored under native cyanobacterial expression conditions. An antibody raised against the oligomeric peptide enabled the detection of secreted nostolanthin in cyanobacteria and revealed that it accumulates predominantly in an oligomeric form. Comparative genomics showed that nostolanthin belongs to a larger family of Nif11-type-lanthipeptide biosynthetic gene clusters, consistently associated with homologous two-component regulatory systems. Importantly, oligomeric, but not monomeric nostolanthin, accelerated the establishment of physical contact between Nostoc and B. pusilla. Together, these findings reveal oligomerization by covalent bond formation as a previously unrecognized mode of lanthipeptide maturation and identify nostolanthin as a host-responsive peptide that regulates the transition from a free-living to a symbiotic lifestyle.

microbiology↗

bioRxiv2026

Microcystin-Driven Control of the Carbon-Concentrating Mechanism Shapes CO2 Fixation Dynamics in Microcystis aeruginosa PCC 7806

Bloom-forming cyanobacteria thrive in highly dynamic light environments, yet the mechanisms enabling rapid acclimation to fluctuating irradiance remain poorly understood. Here, we compared light acclimation in the bloom-forming cyanobacterium Microcystis aeruginosa PCC 7806 and the non-bloom-forming model cyanobacterium Synechocystis sp. PCC 6803 and investigated the role of the cyanobacterial toxin microcystin (MC) and its in vivo binding partner RubisCO in this process. Whereas Synechocystis grew faster under sustained high light, Microcystis performed better under low light and responded to transient high-light exposure with a remarkably rapid increase in photosynthetic activity and glycogen accumulation. These responses were markedly attenuated in an MC-deficient mutant. Although RubisCO from Microcystis exhibited pronounced light-dependent changes in activity, MC had only minor effects on RubisCO catalysis, arguing against a direct role in regulating enzyme function. Instead, extracellular MC elicited a transient transcriptional program characterized by induction of inorganic carbon acquisition systems, including the high-affinity bicarbonate transporter BCT1, consistent with activation of the carbon-concentrating mechanism (CCM) and enhanced carbon fixation in vivo. MC further stimulated the expression of photosynthesis-related genes, and altered carboxysome organization, and promoted extracarboxysomal localization of RubisCO. Together, our findings identify MC as a light-responsive signaling molecule that coordinates CCM activity, carbon acquisition, and photosynthetic acclimation, thereby enhancing adaptation of Microcystis to fluctuating irradiance and potentially contributing to its ecological success in cyanobacterial blooms.

microbiology↗

bioRxiv2024

Microcystin shapes the Microcystis phycosphere through community filtering and by influencing cross-feeding interactions

The cyanobacterium Microcystis causes harmful algal blooms (cyanoHABs) that pose a major threat to human health and ecosystem services, particularly due to the prevalence of the potent hepatotoxin microcystin. With their pronounced EPS layer, Microcystis colonies also serve as a hub for heterotrophic phycosphere bacteria. Here, we tested the hypothesis that the genotypic plasticity in its ability to produce microcystin influences the composition and assembly of the Microcystis phycosphere microbiome. In an analysis of individual colonies of a natural Microcystis bloom, we observed a significantly reduced richness of the community in the presence of microcystin biosynthesis genes. A subsequent synthetic community experiment with 21 heterotrophic strains in co-cultivation with either the wild-type strain M. aeruginosa PCC 7806 or the microcystin-free mutant {Delta}mcyB revealed not only a tug-of-war between phototrophic and heterotrophic bacteria, but also a reciprocal dominance of two isolates of the genus Sphingomonas and Flavobacterium. In contrast, an Agrobacterium isolate thrived equally well in both consortia. In substrate utilization tests, Sphingomonas showed the strongest dependence on Microcystis exudates with a clear preference for the wild-type strain. Genome sequencing revealed a high potential for complementary cross-feeding, particularly for the Agrobacterium and Sphingomonas isolates but no potential for microcystin degradation. We postulate that strain-specific functional traits, such as the ability to perform photorespiration and to produce vitamin B12, play a crucial role in the cross-feeding interactions, and that microcystin is one of the determining factors in the Microcystis phycosphere due to its interference with inorganic carbon metabolism.

microbiology↗

bioRxiv2024

Competition and interdependence define multifaceted interactions of symbiotic Nostoc sp. and Agrobacterium sp. under inorganic carbon limitation

Cyanobacteria of the Nostoc genus are capable of forming symbiotic relationships with plants, thus transitioning to a heterotrophic lifestyle in return for providing bioavailable nitrogen to the host. The diazotrophic photoautotrophs also serve as a hub for specialized heterotrophic bacterial communities whose physiological contributions are poorly understood. By comparing the axenic strain Nostoc punctiforme PCC 73102 and the related strains Nostoc sp. KVJ2 and KVJ3, which still maintain their heterotrophic microbiome, we were able to demonstrate an almost obligate dependence of the cyanobacteria on the heterotrophic partners under carbon-limiting conditions. Detailed analysis of the intimate bilateral relationship between N. punctiforme and the isolate Agrobacterium tumefaciens Het4 using shotgun proteomics and microscopy uncovered a complex partnership characterized, among other traits, by competition for iron and facilitation for carbon. Although competitive interactions with A. tumefaciens Het4 compromise nitrogen fixation and stimulate the degradation of cyanophycin, mutualistic dependency prevails under inorganic carbon limitation. Both the absence of the high affinity bicarbonate uptake transporter SbtA and the prevalent extracarboxysomal localization of the carbon-fixing enzyme RubisCO, as detected by immunofluorescence microscopy, suggest that a weak carbon concentrating mechanism in N. punctiforme enforces a dependence on heterotrophic bacteria. Further, immunofluorescence, electron microscopic and proteomic analyses reveal a pronounced extracellular recycling of proteins under N- and C-limiting conditions. Our study shows that the pivotal influence of heterotrophic bacteria on symbiotic Nostoc strains should be considered when analyzing these cyanobacteria, especially in the free-living state. This work also sheds new light on how Nostoc benefits from the organic carbon provided by plant hosts.

microbiology↗

bioRxiv2019

Non-canonical localization of RubisCO under high light conditions in the toxic cyanobacterium Microcystis aeruginosa PCC7806

The frequent production of the hepatotoxin microcystin and its impact on the life-style of bloom-forming cyanobacteria are poorly understood. Here we report that microcystin interferes with the assembly and the subcellular localization of RubisCO, in Microcystis aeruginosa PCC7806. Immunofluorescence, electron microscopic and cellular fractionation studies revealed a pronounced heterogeneity in the subcellular localization of RubisCO. At high cell density, RubisCO particles are largely separate from carboxysomes in M. aeruginosa and relocate to the cytoplasmic membrane under high-light conditions. We hypothesize that the binding of microcystin to RubisCO promotes its membrane association and enables an extreme versatility of the enzyme. Steady-state levels of the RubisCO CO2 fixation product 3-phosphoglycerate are significantly higher in the microcystin-producing wild type. We also detected noticeable amounts of the RubisCO oxygenase reaction product secreted into the medium that may support the mutual interaction of M. aeruginosa with its heterotrophic microbial community.

microbiology↗