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van Loosdrecht, M. C. M.

Publications and source records attributed to van Loosdrecht, M. C. M..

23 records · Page 2Linked to original sources

Escherichia coli metabolism under short-term repetitive substrate dynamics: Adaptation and trade-offs

BackgroundMicrobial metabolism is highly dependent on the environmental conditions. Especially, the substrate concentration, as well as oxygen availability, determine the metabolic rates. In large-scale bioreactors, microorganisms encounter dynamic conditions in substrate and oxygen availability (mixing limitations), which influence their metabolism and subsequently their physiology. Earlier, single substrate pulse experiments were not able to explain the observed physiological changes generated under large-scale industrial fermentation conditions. ResultsIn this study we applied a repetitive feast-famine regime in an aerobic Escherichia coli culture in a time-scale of seconds. The regime was applied for several generations, allowing cells to adapt to the (repetitive) dynamic environment. The observed response was highly reproducible over the cycles, indicating that cells were indeed fully adapted to the regime. We observed an increase of the specific substrate and oxygen consumption (average) rates during the feast-famine regime, compared to a steady-state (chemostat) reference environment. The increased rates at same (average) growth rate led to a reduced biomass yield (30% lower). Interestingly, this drop was not followed by increased by-product formation, pointing to the existence of energy-spilling reactions and/or less effective ATP synthesis. During the feast-famine cycle, the cells rapidly increased their uptake rate. Within 10 seconds after the beginning of the feeding, the substrate uptake rate was higher (4.68 mol/gCDW/s) than reported during batch growth (3.3 mol/gCDW/s). The high uptake led to an accumulation of several intracellular metabolites, during the feast phase, accounting for up to 34 % of the carbon supplied. Although the metabolite concentrations changed rapidly, the cellular energy charge remained unaffected, suggesting well-controlled balance between ATP producing and ATP consuming reactions. The role of inorganic polyphosphate as an energy buffer is discussed. ConclusionsThe adaptation of the physiology and metabolism of Escherichia coli under substrate dynamics, representative for large-scale fermenters, revealed the existence of several cellular mechanisms coping with stress. Changes in the substrate uptake system, storage potential and energy-spilling processes resulted to be of great importance. These metabolic strategies consist a meaningful step to further tackle reduced microbial performance, observed under large-scale cultivations.

microbiology↗

On anammox activity at low temperature: effect of ladderane composition, process conditions and dominant anammox population

The application of partial nitritation-anammox (PN/A) under mainstream conditions can enable substantial cost savings at wastewater treatment plants (WWTPs), but how process conditions and cell physiology affect anammox performance at psychrophilic temperatures below 15 {degrees}C remains poorly understood. We tested 14 anammox communities, including 8 from globally-installed PN/A processes, for (i) specific activity at 10-30 {degrees}C (batch assays), (ii) composition of membrane lipids (U-HPLC-HRMS/MS), and (iii) microbial community structure (16S rRNA gene amplicon sequencing). Crucially, the key parameters impacting anammox activity were the membrane lipid composition and cultivation temperature. The size of ladderane lipids and the content of bacteriohopanoids were key physiological drivers of anammox performance at low temperatures. Higher contents of (i) short C18 [3]-ladderane alkyl and (ii) large phosphatidylcholine headgroup were determined in anammox more active at 15-30 {degrees}C and 10-15 {degrees}C, respectively. At below 15 {degrees}C, the activation energies of most mesophilic cultures severely increased while those of the psychrophilic cultures remained stable; this indicates that the adaptation of mesophilic cultures to psychrophilic regime necessitates months, but in some cases can take up to 5 years. Interestingly, biomass enriched in the marine genus "Candidatus Scalindua" displayed exceptionally highest activity at 10-20 {degrees}C (0.50 kg-N.kg-VSS-1.d-1 at 10 {degrees}C, Ea10-30 {degrees}C = 51{+/-}16 kJ.mol-1), indicating outstanding potential for nitrogen removal from cold streams. Collectively, our comprehensive study provides essential knowledge of cold adaptation mechanism, will enable more accurate modelling and suggests highly promising target anammox genera for inoculation and set-up of anammox reactors, in particular for mainstream WWTPs. HighlightsO_LILadderane size and cold exposure affected anammox activation energy (Ea). C_LIO_LIEa improved with more C18 [3]-ladderanes over C20 and larger polar headgroup. C_LIO_LILong-term cold exposure reduced Ea at 10-15 {degrees}C, not activity per se. C_LIO_LIMarine "Ca. Scalindua" was exceptionally suitable for cold streams. C_LIO_LIAnammox Ea at 15-30 {degrees}C was 79{+/-}18 kJ.mol-1. C_LI Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=121 SRC="FIGDIR/small/873869v1_ufig1.gif" ALT="Figure 1"> View larger version (25K): org.highwire.dtl.DTLVardef@1c5c3aborg.highwire.dtl.DTLVardef@b11ed2org.highwire.dtl.DTLVardef@5e7ec9org.highwire.dtl.DTLVardef@1d5cba5_HPS_FORMAT_FIGEXP M_FIG C_FIG

microbiology↗

Anticipating xenogenic pollution at the source: Impact of sterilizations on DNA release from microbial cultures

The dissemination of DNA and xenogenic elements across waterways is under scientific and public spotlight due to new gene-editing tools, such as do-it-yourself (DIY) CRISPR-Cas kits. Over decades, prevention of spread of genetically modified organisms (GMOs), antimicrobial resistances (AMR), and pathogens from transgenic systems has focused on microbial inactivation. However, sterilization methods have not been assessed for DNA release and integrity. Here, we investigated the fate of intracellular DNA from cultures of model prokaryotic (Escherichia coli) and eukaryotic (Saccharomyces cerevisiae) cells, commonly used as microbial hosts for genetic modifications, such as in white biotechnology. DNA release was tracked during exposure of these cultures to conventional sterilization methods. Autoclaving, disinfection with glutaraldehyde, and microwaving are used to inactivate broths, healthcare equipment, and GMOs produced at kitchen table. The results show that current sterilization methods are effective on microorganism inactivation but do not safeguard an aqueous residue exempt of biologically reusable xenogenic material, being regular autoclaving the most severe DNA-affecting method. Reappraisal of sterilization methods is required along with risk assessment on the emission of DNA fragments in urban systems and nature.\n\nGraphical abstract O_FIG_DISPLAY_L [Figure 1] M_FIG_DISPLAY C_FIG_DISPLAY

microbiology↗

The environment selects: Modeling energy allocation in microbial communities under dynamic environments

What will be the best metabolic strategy in a competitive environment where oxygen is periodically unavailable? A few decades ago, an accidental, man-made cyclic anaerobic/aerobic environment selected for Polyphosphate Accumulating Organisms (PAOs) and this strategy is now widely used to allow for Enhanced Biological Phosphorus Removal (EBPR) of wastewater. But could it have been predicted? Here, a dynamic resource allocation modeling formalism was used to analyze the impact of selection pressures on metabolic function. With the same meta-network but modified selective pressures, different successful strategies can be predicted: Polyphosphate-AOs, Glycogen-AOs, Polyhydroxyalkanoate-AOs, and regular aerobic heterotrophs. The results demonstrate how storage metabolism allows for different trade-offs between growth yield, robustness, and competitiveness, and highlight how each metabolic function is an important determining factor for a selective advantage in a given environment. This can be seen as an example of when \"Unity in biochemistry\" by A.Kluyver meets \"Everything is everywhere, but the environment selects\" by B.Becking and how microbial ecosystems may be described by the energy allocation phenotype instead of a detailed description of each organism.

systems biology↗

Revealing metabolic flexibility of Candidatus Accumulibacter phosphatis through redox cofactor analysis and metabolic network modeling

Candidatus Accumulibacter phosphatis, a polyphosphate accumulating organism (PAO) growing under alternating anaerobic/aerobic conditions in enhanced biological phosphorus removal (EBPR) systems, displays an intricate metabolic strategy. The organism relies on combining features from either anaerobic- or aerobic-only metabolisms and connecting phases using different reserve polymers. Analysis of the metabolic functions is not trivial, specially without isolates of this microorganism available and without employing advanced metabolic modelling techniques. So far, there is no consensus regarding the type of glycolysis nor the operating mode of the tricarboxylic acid cycle anaerobically. Here, we simulated different conditions using flux balance analyses and a reduced central carbon metabolic network based on previously published meta-omics data and validated with enzyme activity assays. Interestingly, we observed that the polyhydroxyalkanoates (PHA) production was NADH preferring instead of the commonly reported NADPH dependency. This feature allows for higher metabolic flexibility while maintaining a near-optimal carbon conservation and without extra energetic costs, which explains PAOs competitiveness under anaerobic/aerobic shifting environments.

microbiology↗