Kaiserslautern - Fachbereich Biologie
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Water availability shapes edaphic and lithic cyanobacterial communities in the Atacama Desert
(2019)
In the Atacama Desert, cyanobacteria grow on various substrates such as soils (edaphic) and quartz or granitoid stones (lithic). Both edaphic and lithic cyanobacterial communities have been described but no comparison between both communities of the same locality has yet been undertaken. In the present study, we compared both cyanobacterial communities along a precipitation gradient ranging from the arid National Park Pan de Azúcar (PA), which resembles a large fog oasis in the Atacama Desert extending to the semiarid Santa Gracia Natural Reserve (SG) further south, as well as along a precipitation gradient within PA. Various microscopic techniques, as well as culturing and partial 16S rRNA sequencing, were applied to identify 21 cyanobacterial species; the diversity was found to decline as precipitation levels decreased. Additionally, under increasing xeric stress, lithic community species composition showed higher divergence from the surrounding edaphic community, resulting in indigenous hypolithic and chasmoendolithic cyanobacterial communities. We conclude that rain and fog water, respectively, cause contrasting trends regarding cyanobacterial species richness in the edaphic and lithic microhabitats.
VIPP proteins aid thylakoid biogenesis and membrane maintenance in cyanobacteria, algae, and plants. Some members of the Chlorophyceae contain two VIPP paralogs termed VIPP1 and VIPP2, which originate from an early gene duplication event during the evolution of green algae. VIPP2 is barely expressed under nonstress conditions but accumulates in cells exposed to high light intensities or H2O2, during recovery from heat stress, and in mutants with defective integration (alb3.1) or translocation (secA) of thylakoid membrane proteins. Recombinant VIPP2 forms rod-like structures in vitro and shows a strong affinity for phosphatidylinositol phosphate. Under stress conditions, >70% of VIPP2 is present in membrane fractions and localizes to chloroplast membranes. A vipp2 knock-out mutant displays no growth phenotypes and no defects in the biogenesis or repair of photosystem II. However, after exposure to high light intensities, the vipp2 mutant accumulates less HSP22E/F and more LHCSR3 protein and transcript. This suggests that VIPP2 modulates a retrograde signal for the expression of nuclear genes HSP22E/F and LHCSR3. Immunoprecipitation of VIPP2 from solubilized cells and membrane-enriched fractions revealed major interactions with VIPP1 and minor interactions with HSP22E/F. Our data support a distinct role of VIPP2 in sensing and coping with chloroplast membrane stress.
In cyanobacteria and plants, VIPP1 plays crucial roles in the biogenesis and repair of thylakoid membrane protein complexes and in coping with chloroplast membrane stress. In chloroplasts, VIPP1 localizes in distinct patterns at or close to envelope and thylakoid membranes. In vitro, VIPP1 forms higher-order oligomers of >1 MDa that organize into rings and rods. However, it remains unknown how VIPP1 oligomerization is related to function. Using time-resolved fluorescence anisotropy and sucrose density gradient centrifugation, we show here that Chlamydomonas reinhardtii VIPP1 binds strongly to liposomal membranes containing phosphatidylinositol-4-phosphate (PI4P). Cryo-electron tomography reveals that VIPP1 oligomerizes into rods that can engulf liposomal membranes containing PI4P. These findings place VIPP1 into a group of membrane-shaping proteins including epsin and BAR domain proteins. Moreover, they point to a potential role of phosphatidylinositols in directing the shaping of chloroplast membranes.
Arctic, Antarctic and alpine biological soil crusts (BSCs) are formed by adhesion of soil particles to exopolysaccharides (EPSs) excreted by cyanobacterial and green algal communities, the pioneers and main primary producers in these habitats. These BSCs provide and influence many ecosystem services such as soil erodibility, soil formation and nitrogen (N) and carbon (C) cycles. In cold environments degradation rates are low and BSCs continuously increase soil organic C; therefore, these soils are considered to be CO2 sinks. This work provides a novel, nondestructive and highly comparable method to investigate intact BSCs with a focus on cyanobacteria and green algae and their contribution to soil organic C. A new terminology arose,basedonconfocallaserscanningmicroscopy(CLSM) 2-D biomaps, dividing BSCs into a photosynthetic active layer (PAL) made of active photoautotrophic organisms and a photosynthetic inactive layer (PIL) harbouring remnants of cyanobacteria and green algae glued together by their remaining EPSs. By the application of CLSM image analysis (CLSM–IA) to 3-D biomaps, C coming from photosynthetic activeorganismscouldbevisualizedasdepthprofileswithC peaks at 0.5 to 2mm depth. Additionally, the CO2 sink character of these cold soil habitats dominated by BSCs could be highlighted, demonstrating that the first cubic centimetre of soil consists of between 7 and 17% total organic carbon, identified by loss on ignition.
Membrane proteins are generally soluble only in the presence of detergent micelles or other membrane-mimetic systems, which renders the determination of the protein’s molar mass or oligomeric state difficult. Moreover, the amount of bound detergent varies drastically among different proteins and detergents. However, the type of detergent and its concentration have a great influence on the protein’s structure, stability, and functionality and the success of structural and functional investigations and crystallographic trials. Size-exclusion chromatography, which is commonly used to determine the molar mass of water-soluble proteins, is not suitable for detergent-solubilised proteins because
the protein–detergent complex has a different conformation and, thus, commonly exhibits
a different migration behaviour than globular standard proteins. Thus, calibration curves obtained with standard proteins are not useful for membrane-protein analysis. However,
the combination of size-exclusion chromatography with ultraviolet absorbance, static light scattering, and refractive index detection provides a tool to determine the molar mass of protein–detergent complexes in an absolute manner and allows for distinguishing the contributions of detergent and protein to the complex.
The goal of this thesis was to refine the standard triple-detection size-exclusion chromatography measurement and data analysis procedure for challenging membrane-protein samples, non-standard detergents, and difficult solvents such as concentrated denaturant solutions that were thought to elude routine approaches. To this end, the influence of urea on the performance of the method beyond direct influences on detergents and proteins was investigated with the help of the water-soluble bovine serum albumin. On the basis of
the obtained results, measurement and data analysis procedures were refined for different detergents and protein–detergent complexes comprising the membrane proteins OmpLA and Mistic from Escherichia coli and Bacillus subtilis, respectively.
The investigations on mass and shape of different detergent micelles and the compositions of protein–detergent complexes in aqueous buffer and concentrated urea solutions
showed that triple-detection size-exclusion chromatography provides valuable information
about micelle masses and shapes under various conditions. Moreover, it is perfectly suited for the straightforward analysis of detergent-suspended proteins in terms of composition and oligomeric state not only under native but, more importantly, also under denaturing conditions.
Like many other bacteria, the opportunistic pathogen P. aeruginosa encodes a broad network of enzymes that regulate the intracellular concentration of the second messenger c-di-GMP. One of these enzymes is the phosphodiesterase NbdA that consists of three domains: a membrane anchored, putative sensory MHYT domain, a non-functional diguanylate cyclase domain with degenerated GGDEF motif and an active PDE domain with EAL motif. Analysis of the nbdA open reading frame by 5’-RACE PCR revealed an erroneous annotation of nbdA in the Pseudomonas database with the ORF 170 bp shorter than previously predicted. The newly defined promoter region of nbdA contains recognition sites for the alternative sigma-factor RpoS as well as the transcription factor AmrZ. Promoter analysis within PAO1 wt as well as rpoS and amrZ mutant strains utilizing transcriptional fusions of the nbdA promoter to the reporter gene lacZ revealed transcriptional activation of nbdA by RpoS in stationary growth phase and transcriptional repression by AmrZ. Additionally, no influence of nitrite and neither exogenous nor endogenous NO on nbdA transcription could be shown in this study. However, deletion of the nitrite reductase gene nirS led to a strong increase of nbdA promoter activity which needs to be characterized further. Predicted secondary structures of the 5’-UTR of the nbdA mRNA indicated either an RNA thermometer function of the mRNA or post-transcriptional regulation of nbdA by the RNA binding proteins RsmA and RsmF. Nevertheless, translational studies using fusions of the 5’ UTR of nbdA to the reporter gene bgaB did not verify either of these hypotheses. In general, nbdA translational levels were very low and neither the production of the reporter BgaB nor genomically encoded NbdA could be detected on a western blot. Overproduction of NbdA variants induced many phenotypic changes in motility and biofilm formation. But strains overproducing variants containing the MHYT domain revealed greatly elongated cells and were impaired in surface growth, indicating a misbalance in the membrane protein homeostasis. Therefore, these phenotypes have to be interpreted very critically. Microscopic studies with fluorescently tagged NbdA revealed either a diffuse fluorescent signal of NbdA or the formation of fluorescent foci which were located mainly at the cell poles. Co-localization studies with the polar flagellum and the chemotaxis protein CheA showed that NbdA is not generally localizing to the flagellated cell pole. NbdA localization indicates the control of a specific local c-di-GMP pool in the cell which is most likely involved in MapZ mediated chemotactic flagellar motor switching.
Towards standardized operating procedures for eDNA-based monitoring of marine coastal ecosystems
(2022)
Marine coastal ecosystems are exposed to a variety of anthropogenic impacts, which
often manifest themselves in the pollution of the surrounding ecosystem. Especially on
densely populated coasts or in regions heavily used for aquaculture, changes in the natural
marine habitat can be observed. In order to protect nature and thus its ecosystem services
for humans, more and more environmental protection laws are coming into force.
Exemplary, operators of facilities known to contribute to pollution are obliged to regularly
monitor the condition of the surrounding environment. The purpose of such so-called
compliance monitoring is to determine whether the prescribed regulations are being
followed. The traditional routine involves sampling by ship, during which sediment
samples are taken from the seabed below the aquaculture cages and all macrofauna
organisms found, such as mussels or worms, are taxonomically determined and quantified
by experts. Based on the community of organisms the ecological status of the sample can
then be inferred. Since this method is very labor- and time-consuming, a reorientation of
the scientific community towards alternative monitoring methods is currently taking place.
A bacteria-based eDNA (environmental DNA) metabarcoding system in particular has
proven to be a suitable monitoring tool. With this molecular method, the composition of
the benthic bacterial community is determined using high-throughput sequencing. The
great advantage of this method is that bacteria, due to their short generation times, react
rapidly to various environmental influences. The composition of this community can then
be used to infer the ecological status of the sample under investigation via sequencing
without the need for laborious enumeration and identification of organisms. Additionally,
sequencing costs are more and more decreasing, proposing eDNA metabarcoding-based
monitoring as a faster and cheaper alternative to traditional monitoring. In order to
implement the method in legislation in the long term, standard protocols need to be
developed. Once these are sufficiently validated, the novel methodology can be
incorporated into regulations to support or even replace traditional monitoring. However,
some steps of the eDNA metabarcoding method, from sampling to ecosystem assessment,
are not yet sufficiently standardized, which is why the development of this work was
necessary. Since there is no consensus in the scientific community on (i) the preservation of
environmental samples during transport, (ii) the reproducibility of ecosystem assessment
among different laboratories, (iii) the most appropriate bioinformatic method for ecosystem
assessment, and (iv) the minimum sequencing depth required to determine ecosystem
status, these sub-steps were investigated. It was found that the most common methods
currently used to preserve samples during transport had no discernible effect on the final
ecosystem assessment. Furthermore, sample processing in independent laboratories
allowed the same ecological interpretations based on the bacterial community, which
resulted in concordant ecosystem assessments among laboratories. This indicates the
overall reproducibility of the eDNA metabarcoding-based method, thus enabling its
implementation in standard protocols. Furthermore, it was shown that corresponding
ecosystem assessments can be obtained with the currently used methods for determining
ecological status based on eDNA data. Critical to predictive accuracy is not the method
itself, but a sufficient number of samples that accounts for the natural spatial and temporal
variability of bacterial communities. It was demonstrated that a very shallow sequencing
depth per sample can be sufficient to use machine learning to prediction the ecological
status of the environmental sample. The quality of this classifications did not depend on
the sequencing depth as assumed but was determined by the separability of individual
categories. The results and recommendations of this work contribute directly to the
standardization of ecological assessment of nearshore marine ecosystems. By establishing
these standard protocols, it will be possible to integrate the eDNA metabarcoding-based
method for monitoring compliance of coastal marine ecosystems into legislative
regulations in the future.
Cell division and cell elongation are fundamental processes for growth. In contrast to animal cells, plant cells are surrounded by rigid walls and therefore loosening of the wall is required during elongation. On the other hand, vacuole size has been shown to correlate with cell size and inhibition of vacuolar expansion limits cell growth. However, the specific role of the vacuole during cell elongation is still not fully resolved. Especially the question whether the vacuole is the leading unit during cellular growth or just passively expands upon water uptake remains to be answered. Here, we review recent findings about the contribution of the vacuole to cell elongation. In addition, we also discuss the connection between cell wall status and vacuolar morphology. In particular, we focus on the question whether vacuolar size is dictated by cell size or vice versa and share our personnel view about the sequential steps during cell elongation.
Climate change will have severe consequences on Eastern Boundary Upwelling Systems (EBUS). They host the largest fisheries in the world supporting the life of millions of people due to their tremendous primary production. Therefore, it is of utmost importance to better understand predicted impacts like alternating upwelling intensities and light impediment on the structure and the trophic role of protistan plankton communities as they form the basis of the food web. Numerical models estimate the intensification of the frequency in eddy formation. These ocean features are of particular importance due to their influence on the distribution and diversity of plankton communities and the access to resources, which are still not well understood even to the present day. My PhD thesis entails two subjects conducted during large-scaled cooperation projects REEBUS (Role of Eddies in Eastern Boundary Upwelling Systems) and CUSCO (Coastal Upwelling System in a Changing Ocean).
Subject I of my study was conducted within the multidisciplinary framework REEBUS to investigate the influence of eddies on the biological carbon pump in the Canary Current System (CanCS). More specifically, the aim was to find out how mesoscale cyclonic eddies affect the regional diversity, structure, and trophic role of protistan plankton communities in a subtropical oligotrophic oceanic offshore region.
Samples were taken during the M156 and M160 cruises in the Atlantic Ocean around Cape Verde during July and December 2019, respectively. Three eddies with varying ages of emergence and three water layers (deep chlorophyll maximum DCM, right beneath the DCM and oxygen minimum zone OMZ) were sampled. Additional stations without eddy perturbation were analyzed as references. The effect of oceanic mesoscale cyclonic eddies on protistan plankton communities was analyzed by implementing three approaches. (i) V9 18S rRNA gene amplicons were examined to analyze the diversity and structure of the plankton communities and to infer their role in the biological carbon pump. (ii) By assigning functional traits to taxonomically assigned eDNA sequences, functional richness and ecological strategies (ES) were determined. (iii) Grazing experiments were conducted to assess abundance and carbon transfer from prokaryotes to phagotrophic protists.
All three eddies examined in this study differed in their ASV abundance, diversity, and taxonomic composition with the most pronounced differences in the DCM. Dinoflagellates were the most abundant taxa in all three depth layers. Other dominating taxa were radiolarians, Discoba and haptophytes. The trait-approach could only assign ~15% of all ASVs and revealed in general a relatively high functional richness. But no unique ES was determined within a specific eddy. This indicates pronounced functional redundancy, which is recognized to be correlated with ecosystem resilience and robustness by providing a degree of buffering capacity in the face of biodiversity loss. Elevated microbial abundances as well as bacterivory were clearly associated to mesoscale eddy features, albeit with remarkable seasonal fluctuations. Since eddy activity is expected to increase on a global scale in future climate change scenarios, cyclonic eddies could counteract climate change by enhancing carbon sequestration to abyssal depths. The findings demonstrate that cyclonic eddies are unique, heterogeneous, and abundant ecosystems with trapped water masses in which characteristic protistan plankton develop as the eddies age and migrate westward into subtropical oligotrophic offshore waters. Therefore, eddies influence regional protistan plankton diversity qualitatively and quantitatively.
Subject II of my PhD project contributed to the CUSCO field campaign to identify the influence of varying upwelling intensities in combination with distinct light treatments on the whole food web structure and carbon pump in the Humboldt Current System (HCS) off Peru. To accomplish such a task, eight offshore-mesocosms were deployed and two light scenarios (low light, LL; high light, HL) were created by darkening half of the mesocosms. Upwelling was simulated by injecting distinct proportions (0%, 15%, 30% and 45%) of collected deep-water (DW) into each of the moored mesocosms. My aim was to examine the changes in diversity, structure, and trophic role of protistan plankton communities for the induced manipulations by analyzing the V9 18S rRNA gene amplicons and performing short-term grazing experiments.
The upwelling simulations induced a significant increase in alpha diversity under both light conditions. In austral summer, reflected by HL conditions, a generally higher alpha diversity was recorded compared to the austral winter simulation, instigated by LL treatment. Significant alterations of the protistan plankton community structure could likewise be observed. Diatoms were associated to increased levels of DW addition in the mimicked austral winter situation. Under nutrient depletion, chlorophytes exhibited high relative abundances in the simulated austral winter scenario. Dinoflagellates dominated the austral summer condition in all upwelling simulations. Tendencies of reduced unicellular eukaryotes and increased prokaryotic abundances were determined under light impediment. Protistan-mediated mortality of prokaryotes also decreased by ~30% in the mimicked austral winter scenario.
The findings indicate that the microbial loop is a more relevant factor in the structure of the food web in austral summer and is more focused on the utilization of diatoms in austral winter in the HCS off Peru. It was evident that distinct light intensities coupled with multiple upwelling scenarios could lead to alterations in biochemical cycles, trophic interactions, and ecosystem services. Considering the threat of climate change, the predicted relocation of EBUS could limit primary production and lengthen the food web structure with severe socio-economic consequences.
Compared to our current knowledge of neuronal excitation, little is known about the development and maturation of inhibitory circuits. Recent studies show that inhibitory circuits develop and mature in a similar way like excitatory circuit. One such similarity is the development through excitation, irrespective of its inhibitory nature. Here in this current study, I used the inhibitory projection between the medial nucleus of the trapezoid body (MNTB) and the lateral superior olive (LSO) as a model system to unravel some aspects of the development of inhibitory synapses. In LSO neurons of the rat auditory brainstem, glycine receptor-mediated responses change from depolarizing to hyperpolarizing during the first two postnatal weeks (Kandler and Friauf 1995, J. Neurosci. 15:6890-6904). The depolarizing effect of glycine is due to a high intracellular chloride concentration ([Cl-]i), which induces a reversal potential of glycine (EGly) more positive than the resting membrane potential (Vrest). In older LSO neurons, the hyperpolarizing effect is due to a low [Cl-]i (Ehrlich et al., 1999, J. Physiol. 520:121-137). Aim of the present study was to elucidate the molecular mechanism behind Clhomeostasis in LSO neurons which determines polarity of glycine response. To do so, the role and developmental expression of Cl-cotransporters, such as NKCC1 and KCC2 were investigated. Molecular biological and gramicidin perforated patchclamp experiments revealed, the role of KCC2 as an outward Cl-cotransporter in mature LSO neurons (Balakrishnan et al., 2003, J Neurosci. 23:4134-4145). But, NKCC1 does not appear to be involved in accumulating chloride in immature LSO neurons. Further experiments, indicated the role of GABA and glycine transporters (GAT1 and GLYT2) in accumulating Cl- in immature LSO neurons. Finally, the experiments with hypothyroid animals suggest the possible role of thyroid hormone in the maturation of inhibitory synapse. Altogether, this thesis addressed the molecular mechanism underlying the Cl- regulation in LSO neurons and deciphered it to some extent.