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Kilpeläinen, P.

Publications and source records attributed to Kilpeläinen, P..

2 recordsLinked to original sources

Unsaturated intercellular vapor pressure is relevant for leaf water heavy isotope enrichment

Leaf intercellular vapor pressure (ei) can be unsaturated, but its effect on leaf water heavy isotope enrichment (LWE) has not yet been quantified. We evaluated the ecological relevance of unsaturated ei for LWE, i.e., for leaf water oxygen-18 and deuterium enrichment, using data from a boreal forest stand and a large-scale dataset. Unsaturated ei can firstly affect LWE by directly decreasing ei in the Craig Gordon model (Mechanism 1), which leads to an increased influence of atmospheric vapor isotopic enrichment above source water ({Delta}v), and a decreased influence of kinetic fractionation by diffusion through the stomata and boundary layer ({varepsilon}k). Unsaturated ei can secondly affect LWE by changing {varepsilon}k (Mechanism 2). To evaluate the effect of Mechanism 1 to LWE, we employed sensitivity tests on LWE model performance using varying measured intercellular relative humidity (RHcellular), or RHcellular fitted to observed LWE. To explore the effects of Mechanism 2 to LWE, we modified the calculation of {varepsilon}k and observed consequences to LWE predictions. Unsaturated ei is relevant to LWE by Mechanism 1, since a lowered RHcellular noticeably changed LWE predictions. It clearly improved deuterium predictions and conditionally improved oxygen-18 predictions. Isotope fractionation by Mechanism 2 is unlikely relevant to oxygen-18 and deuterium enrichment. Unsaturated ei must now be recognized as a variable that introduces error to heavy isotope enrichment models and reconstructions from organic material, via Mechanism 1. We suggest a correction for unsaturated ei for both oxygen-18 and deuterium enrichment using a variable RHcellular calculated from atmospheric relative humidity.

plant biology↗

FMN-dependent oligomerization of putative lactate oxidase from Pediococcus acidilactici

Lactate oxidases belong to a group of FMN-dependent enzymes and they catalyze a conversion of lactate to pyruvate with a release of hydrogen peroxide. Hydrogen peroxide is also utilized as a read out in biosensors to quantitate lactate levels in biological samples. Aerococcus viridans lactate oxidase is the best characterized lactate oxidase and our knowledge of lactate oxidases relies largely to studies conducted with that particular enzyme. Pediococcus acidilactici lactate oxidase is also commercially available for e.g. lactate measurements, but this enzyme has not been characterized before in detail. Here we report structural characterization of the recombinant enzyme and its co-factor dependent oligomerization. The crystal structures revealed two distinct conformations in the loop closing the active site, consistent with previous biochemical studies implicating the role of loop in catalysis. Despite the structural conservation of active site residues when compared to Aerococcus viridans lactate oxidase we were not able to detect either oxidase or monooxygenase activity when L-lactate or other potential alpha hydroxyl acids were used as a substrate. Pediococcus acidilactici lactate oxidase is therefore an example of a misannotation of an FMN-dependent enzyme, which catalyzes likely a so far unknown oxidation reaction.

biochemistry↗