Publications by authors named "Klaus Koren"

Chemical gradients are essential in biological systems, affecting processes like microbial activity in soils and nutrient cycling. Traditional tools, such as microsensors, offer high-resolution data but are limited to one-dimensional measurements. Planar optodes allow for two-dimensional (2D) and three-dimensional (3D) chemical imaging but are often sensitive to temperature changes.

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Optode-based chemical imaging is a rapidly evolving field that has substantially enhanced our understanding of the role of microenvironments and chemical gradients in biogeochemistry, microbial ecology, and biomedical sciences. Progress in sensor chemistry has resulted in a broadened spectrum of analytes, alongside enhancements in sensor performance (e.g.

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In disciplines like toxicology and pharmacology, oxygen (O) respiration is a universal metric for evaluating the effects of chemicals across various model systems, including mammalian and microalgal cells. However, for these cells the common practice is to segregate populations into control and exposure groups, which assumes direct equivalence in their responses and does not take into account heterogeneity among individual cells. This lack of resolution impedes our ability to precisely investigate differences among experimental groups with small or limited sample sizes.

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While the pH cross-sensitivity of chromoionophore-based ion-selective optodes (ISOs) has often been regarded as a significant limitation, this paper demonstrates how this apparent drawback can be transformed into a beneficial feature. The response range of chromoionophore-based ISOs shifts proportionally with changes in the sample pH. Thus, integrating them with a stable pH gradient across the optode surface, such as those provided by immobilized pH gradient (IPG) gels, allows for significant enhancement of the effective measuring range of chromoionophore-based ISOs while preserving their maximum sensitivity.

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Accurate descriptions of the variability in single-cell oxygen consumption and its size-dependency are key to establishing more robust tissue models. By combining microfabricated devices with multiparameter identification algorithms, we demonstrate that single human hepatocytes exhibit an oxygen level-dependent consumption rate and that their maximal oxygen consumption rate is significantly lower than that of typical hepatic cell cultures. Moreover, we found that clusters of two or more cells competing for a limited oxygen supply reduced their maximal consumption rate, highlighting their ability to adapt to local resource availability and the presence of nearby cells.

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Measuring the distribution and dynamics of H2 in microbial electrochemical reactors is valuable to gain insights into the processes behind novel bioelectrochemical technologies, such as microbial electrosynthesis. Here, a microsensor method to measure and profile dissolved H2 concentrations in standard H-cell reactors is described. Graphite cathodes were oriented horizontally to enable the use of a motorized microprofiling system and a stereomicroscope was used to place the H2 microsensor precisely on the cathode surface.

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Cable bacteria are multicellular, filamentous bacteria that use internal conductive fibers to transfer electrons over centimeter distances from donors within anoxic sediment layers to oxygen at the surface. We extracted the fibers and used them as free-standing bio-based electrodes to investigate their electrocatalytic behavior. The fibers catalyzed the reversible interconversion of oxygen and water, and an electric current was running through the fibers even when the potential difference was generated solely by a gradient of oxygen concentration.

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Chemical gradients and uneven distribution of analytes are common in natural and artificial systems. As a result, the ability to visualize chemical distributions in two or more dimensions has gained significant importance in recent years. This has led to the integration of chemical imaging techniques into all domains of analytical chemistry.

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Accurate measurement of pH-dependent analytes is crucial for a wide range of applications, including environmental monitoring, industrial processes, and healthcare diagnostics. In multi-sensor systems, combining data from multiple sensors offers the potential for more comprehensive analysis, yet it is important to be aware of the limitations of this approach. In this paper, we investigate the often-overlooked issue of response time mismatch among sensors, which can introduce significant errors in calculated sum parameters.

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Recycling of phosphorus (P) from waste streams in agriculture is essential to reduce the negative environmental effects of surplus P and the unsustainable mining of geological P resources. Sewage sludge (SS) is an important P source; however, several issues are associated with the handling and application of SS in agriculture. Thus, post-treatments such as pyrolysis of SS into biochar (BC) could address some of these issues.

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Although there is a growing demand for new sensors for environmental monitoring, biofouling continues to plague current sensors and sensing networks. As soon as a sensor is placed in water, the formation of a biofilm begins. Once a biofilm is established, reliable measurements are often no longer possible.

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Dissolved inorganic carbon (DIC) is a key component of the global carbon cycle and plays a critical role in ocean acidification and proliferation of phototrophs. Its quantification at a high spatial resolution is essential for understanding various biogeochemical processes. We present an analytical method for 2D chemical imaging of DIC by combining a conventional CO optode with localized electrochemical acidification from a polyaniline (PANI)-coated stainless-steel mesh electrode.

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Biofouling is a major challenge in environmental sensing. Current mitigation strategies are often expensive, energy consuming or require toxic chemicals. In this contribution electrochemical biofouling control is evaluated as an alternative approach to reduce biofouling on an optical O sensor (optode).

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Simultaneous sensing of metabolic analytes such as pH and O is critical in complex and heterogeneous biological environments where analytes often are interrelated. However, measuring all target analytes at the same time and position is often challenging. A major challenge preventing further progress occurs when sensor signals cannot be directly correlated to analyte concentrations due to additional effects, overshadowing and complicating the actual correlations.

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Total Dissolved Sulfide (TDS) concentrations can either be derived from simultaneous measurement of pH and one of the sulfide species or determined indirectly in samples following an acidification step. Here we report a microsensor that allows for direct measurement of TDS in aquatic media without the need for pH monitoring. An acidic chamber placed in front of a commercial, amperometric HS microsensor allows for the in-situ conversion of dissolved ionic sulfide species to HS, which in turn is oxidized at the transducer anode.

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Soil spatial responses to fire are unclear. Using optical chemical sensing with planar 'optodes', pH and dissolved O concentration were tracked spatially with a resolution of 360 μm per pixel for 72 h after burning soil in the laboratory with a butane torch (∼1300 °C) and then sprinkling water to simulate a postfire moisture event. Imaging data from planar optodes correlated with microbial activity (quantified via RNA transcripts).

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In this letter, we demonstrate 2D acidification of samples at environmental and physiological pH with an electrochemically activated polyaniline (PANI) mesh. A novel sensor-actuator concept is conceived for such a purpose. The sample is sandwiched between the PANI (actuator) and a planar pH optode (sensor) placed at a very close distance (∼0.

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Most tropical corals live in symbiosis with Symbiodiniaceae algae whose photosynthetic production of oxygen (O) may lead to excess O in the diffusive boundary layer (DBL) above the coral surface. When flow is low, cilia-induced mixing of the coral DBL is vital to remove excess O and prevent oxidative stress that may lead to coral bleaching and mortality. Here, we combined particle image velocimetry using O-sensitive nanoparticles (sensPIV) with chlorophyll (Chla)-sensitive hyperspectral imaging to visualize the microscale distribution and dynamics of ciliary flows and O in the coral DBL in relation to the distribution of Symbiodiniaceae Chla in the tissue of the reef building coral, Porites lutea.

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From individual cells to whole organisms, O transport unfolds across micrometer- to millimeter-length scales and can change within milliseconds in response to fluid flows and organismal behavior. The spatiotemporal complexity of these processes makes the accurate assessment of O dynamics via currently available methods difficult or unreliable. Here, we present "sensPIV," a method to simultaneously measure O concentrations and flow fields.

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Optical chemical imaging has established itself as a valuable technique for visualizing analyte distributions in 2D, notably in medical, biological, and environmental applications. In particular for image acquisitions on small scales between few millimeter to the micrometer range, as well as in heterogeneous samples with steep analyte gradients, image resolution is essential. When individual pixels are inspected, however, image noise becomes a metric as relevant as image accuracy and precision, and denoising filters are applied to preserve relevant information.

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The toolbox available for microbiologists to study interspecies interactions is rapidly growing, and with continuously more advanced instruments, we are able to expand our knowledge on establishment and function of microbial communities. However, unravelling molecular interspecies interactions in complex biological systems remains a challenge, and interactions are therefore often studied in simplified communities. Here we perform an in-depth characterization of an observed interspecies interaction between two co-isolated bacteria, and .

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We present a dipping probe total dissolved inorganic carbon (DIC) microsensor based on a localized acidic microenvironment in front of an amperometric CO microsensor. The acidic milieu facilitates conversion of bicarbonate and carbonate to CO, which in turn is reduced at a silver cathode. Interfering oxygen is removed by an acidic CrCl oxygen trap.

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Seeing is believing, as the saying goes, and optical sensors (so-called optodes) are tools that can make chemistry visible. Optodes react reversibly and quickly (seconds to minutes) to changing analyte concentrations, enabling the spatial and temporal visualization of an analyte in complex environments. By being available as planar sensor foils or in the form of nano- or microparticles, optodes are flexible tools suitable for a wide array of applications.

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State-of-the-art electrochemical and optical sensors present distinct advantages and disadvantages when used individually. Combining both methodologies offers interesting synergies and makes it possible to exploit strengths and circumvent possible problems of the individual methods. We report a dynamic sensing concept for buffer capacity by applying water electrolysis to modulate the pH microenvironment in front of an optical pH sensor placed in a flow cell.

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The electric wires of cable bacteria possibly support a unique respiration mode with a few oxygen-reducing cells flaring off electrons, while oxidation of the electron donor and the associated energy conservation and growth is allocated to other cells not exposed to oxygen. Cable bacteria are centimeter-long, multicellular, filamentous Desulfobulbaceae that transport electrons across oxic-anoxic interfaces in aquatic sediments. From observed distortions of the oxic-anoxic interface, we derived oxygen consumption rates of individual cable bacteria and found biomass-specific rates of unheard magnitude in biology.

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