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Brueckner, A.

Publications and source records attributed to Brueckner, A..

6 recordsLinked to original sources

Nepeta cataria L. (catnip) can serve as a chassis for the engineering of secondary metabolic pathways.

ObjectiveEvaluation of Nepeta cataria as a host with specific endogenous metabolite background for transient expression and metabolic engineering of secondary biosynthetic sequences. ResultsThe reporter gene GFP::licBM3 as well as three biosynthetic genes leading to the formation of the cannabinoid precursor olivetolic acid were adopted to the modular cloning standard GoldenBraid, transiently expressed in two chemotypes of N. cataria and compared to Nicotiana benthamiana. To estimate the expression efficiency in both hosts, quantification of the reporter activity was carried out with a sensitive and specific lichenase assay. While N. benthamiana exhibited lichenase activity of 676 {+/-} 94 mol g-1 s-1 (Gerasimenko et al. 2019), N. cataria cultivar 1000, and the cultivar Citriodora showed an activity of 37 {+/-} 8 mol g-1 s-1 and 18 {+/-} 4 mol g-1 s-1, respectively. Further, combinatorial expression of genes involved in cannabinoid biosynthetic pathway acylactivating enzyme 1 (aae1), olivetol synthase (ols) and olivetolic acid cyclase (oac) in N. cataria cv. resulted presumably in the in vivo production of olivetolic acid glycosides. ConclusionNepeta cataria is amenable to Agrobacterium-mediated transient expression and could serve as a novel chassis for the engineering of secondary metabolic pathways and transient evaluation of heterologous genes.

plant biology↗

Deficiency in hyaluronan synthase 3 attenuates ruptures in a murine model of abdominal aortic aneurysms by reduced aortic monocyte infiltration

Abdominal aortic aneurysms (AAA) are a common vascular disorder with a high mortality due to the prevalence of aortic ruptures. The underlying pathomechanisms are complex and involve immune cell infiltration and degradation of the vascular extracellular matrix (ECM). Hyaluronan (HA), synthesized at the plasma membrane by three HA synthase isoenzymes (HAS1-3), is not only a major constituent of the ECM but also known to directly affect the phenotype of vascular smooth muscle cells as well as immunological responses. Specifically, the HAS3 isoenzyme has been reported to play a major role in various inflammatory conditions. Therefore, the aim of the present study was to elucidate the role of HAS3-derived HA in the pathogenesis of abdominal aortic aneurysm. To this end, we used a murine model of Angiotensin II (AngII)-induced abdominal aortic aneurysms and dissections (AAAs/AADs) and could demonstrate that genetic depletion of Has3 improves survival in Apoe/Has3 double deficient (Apoe/Has3-DKO) mice via the reduced occurrence of aortic ruptures. Mechanistically, fewer elastica breaks were observed in Apoe/Has3-DKO mice compared to Apoe-KO littermates. This was associated with a decreased infiltration of myeloid immune cells into the vessel wall of Has3-deficient mice while in parallel elevated numbers of circulating leukocytes were detected. RNA seq analysis from aortic tissue pointed towards a disturbed endothelial-myeloid cell communication as a cause for the diminished recruitment of immune cells to the aortic wall. While endothelial cells were unaffected, upregulation of adhesion receptors as well as the HA receptor CD44, known to mediate leukocyte adhesion to the endothelium, was blunted in monocytes from Apoe/Has3-DKO mice in response to AngII treatment. These findings underline the pivotal detrimental role of monocytes HAS3-dependent pericellular HA matrix for an exaggerated immune cell recruitment to inflammatory foci giving here rise for an increased incidence of ruptured aortic aneurysms.

immunology↗

Inhibition of myeloperoxidase prevents thoracic aortic aneurysm formation in Marfan mice

Marfan syndrome (MFS) is the most prevalent inherited connective tissue disorder, still remains uncurable, and is characterized by high mortality at early age driven by dissection and rupture of thoracic aortic aneurysms. MFS is caused by mutations in the fibrillin-1 gene and aberrant TGF{beta} signaling. Here we addressed whether myeloperoxidase (MPO), a leukocyte derived enzyme with potent matrix modulating properties also influences the aortic phenotype in MFS. MFS patients displayed increased circulating MPO levels compared to controls as well as marked aortic MPO deposition. In an MFS mouse model, MPO induced inflammatory endothelial activation and endothelial to mesenchymal transition which triggered aortic leukocyte recruitment. Moreover, MPO directly contributed to adverse extracellular matrix remodeling by promoting oxidative stress and nitration of proteins within the vascular wall. Genetic MPO deficiency and pharmacological MPO inhibition attenuated MFS-related aneurysm formation. We herein identify MPO as a critical mediator of MFS-related thoracic aortic aneurysm formation and - in the absence of any pharmacological treatment so far in this disease - a first anti-inflammatory target to modulate disease progression.

immunology↗

Benzoquinones in the defensive secretion of a bug (Pamillia behrensii): a common chemical trait retrieved in the Heteroptera

Benzoquinones are a phylogenetically widespread compound class within arthropods, appearing in harvestman, millipedes and insects. Whereas the function of benzoquinones as defensive compounds against potential predators and microbes has been well established, the full extent of benzoquinone usage across arthropods, and especially within Insecta, has yet to be established. Adding to the growing list of unique evolutionary origins of benzoquinone employment, we describe in this paper the metathoracic scent gland secretion of the mirid bug Pamillia behrensii, which is composed of heptan-2-one, 2-heptyl acetate, 2,3-dimethyl-1-4-benzoquinone, 2,3-dimethyl-1-4-hydroquinone as well as one unknown compound. Similarly, to many other arthropods that use benzoquinones, Pamillia releases the contents of its gland as a defensive mechanism in response to harassment by other arthropod predators. Morphological investigation of the gland showed that the benzoquinone-producing gland complex of P. behrensii follows a similar blueprint to metathoracic scent glands described in other Heteropterans. Overall, our data further underpins the widespread convergent evolution and use of benzoquinones for defense across the Arthropoda, now including the order Hemiptera.

evolutionary biology↗

Molecular evolutionary trends and biosynthesis pathways in the Oribatida revealed by the genome of Archegozetes longisetosus

Oribatid mites are a specious order of microarthropods within the subphylum Chelicerata, compromising about 11,000 described species. They are ubiquitously distributed across different microhabitats in all terrestrial ecosystems around the world and were among the first animals colonizing terrestrial habitats as decomposers and scavengers. Despite their species richness and ecological importance genomic resources are lacking for oribatids. Here, we present a 190-Mb genome assembly of the clonal, all-female oribatid mite species Archegozetes longisetosus Aoki, a model species used by numerous laboratories for the past 30 years. Comparative genomic and transcriptional analyses revealed patterns of reduced body segmentation and loss of segmental identity gene abd-A within Acariformes, and unexpected expression of key eye development genes in these eyeless mites across developmental stages. Consistent with their soil dwelling lifestyle, investigation of the sensory genes revealed a species-specific expansion of gustatory receptors, the largest chemoreceptor family in the genome used in olfaction, and evidence of horizontally transferred enzymes used in cell wall degradation of plant and fungal matter, both components of the A. longisetosus diet. Oribatid mites are also noted for their biosynthesis capacities and biochemical diversity. Using biochemical and genomic data, we were able to delineate the backbone biosynthesis of monoterpenes, an important class of compounds found in the major exocrine gland system of Oribatida - the oil glands. Given the mites strength as an experimental model, the new high-quality resources provided here will serve as the foundation for molecular research in Oribatida and will enable a broader understanding of chelicerate evolution.

zoology↗

Using weapons instead of perfume - chemical association strategies of the myrmecophilous bug Scolopostethus pacificus (Rhyparochromidae)

A vast diversity of parasites associate with ants. Living in and around ant nests these organisms must overcome ant colony defenses. As ant defensive behavior is mainly mediated by species-specific cuticular hydrocarbons (CHCs) or alarm pheromones, ant-associated parasites can either crack their hosts chemical communication code by modifying their own CHC-profiles or use pro-active strategies like chemical weaponry for distraction and repellency. While the chemical nature of ant-parasite interactions has been intensively studied for highly host specific parasites, the chemical-deceptive strategies of the rather rare ant-resembling Heteropterans are unknown. To gain insight into this system, I studied the bug Scolopostethus pacificus (Barber 1918) which can be found near the nests of the ecologically dominant and aggressive velvety tree ant (Liometopum occidentale, Emery 1895). Using behavioral, chemical and molecular approaches I disentangled the relationship of S. pasificus and its host ant. Chemical profiling of the bug and the ant revealed that the bug does not make use of CHC insignificance or mimicry, but instead uses a cocktail of volatile compounds released from its metathoracic glands that likely moderates encounters with its aggressive host. Feeding trials with armed and artificially disarmed bugs revealed a defensive function of the gland exudates. Targeted molecular gut barcoding showed that S. pasificus does not feed on L. occidentale. These results suggest that chemical weaponry, rather than a chemical code-cracking CHC matching or chemical insignificance, enables S. pasificus to get along with and live in close proximity to its host ant.

zoology↗