Jochen Schmid

ORCID: 0000-0003-2557-5532
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About
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Research Areas
  • Polysaccharides and Plant Cell Walls
  • Polysaccharides Composition and Applications
  • Enzyme Production and Characterization
  • Microbial Metabolic Engineering and Bioproduction
  • Microbial Metabolites in Food Biotechnology
  • Bacterial Genetics and Biotechnology
  • Analytical Methods in Pharmaceuticals
  • Enzyme Catalysis and Immobilization
  • CRISPR and Genetic Engineering
  • Analytical Chemistry and Chromatography
  • Glycosylation and Glycoproteins Research
  • Stability and Controllability of Differential Equations
  • Biofuel production and bioconversion
  • Genomics and Phylogenetic Studies
  • Advanced Mathematical Modeling in Engineering
  • Mass Spectrometry Techniques and Applications
  • Pharmacogenetics and Drug Metabolism
  • RNA and protein synthesis mechanisms
  • Carbohydrate Chemistry and Synthesis
  • Antibiotics Pharmacokinetics and Efficacy
  • Pharmacological Effects and Assays
  • Seaweed-derived Bioactive Compounds
  • Receptor Mechanisms and Signaling
  • Plant pathogens and resistance mechanisms
  • Manufacturing Process and Optimization

University of Münster
2020-2024

University of Basel
2024

German Center for Infection Research
2024

Technical University of Munich
2012-2023

Fraunhofer Institute for Industrial Mathematics
2023

Universitätsklinikum Erlangen
2022

Norwegian University of Science and Technology
2019-2022

Stadtwerke Straubing (Germany)
2016-2019

Biogen (Germany)
2011-2017

Bucharest University of Economic Studies
2015-2017

The enzyme subclass of glycosyltransferases (GTs; EC 2.4) currently comprises 97 families as specified by CAZy classification. One their important roles is in the biosynthesis disaccharides, oligosaccharides, and polysaccharides catalyzing transfer sugar moieties from activated donor molecules to other molecules. In addition GTs also catalyze onto aglycons, which great relevance for synthesis many high value natural products. Bacterial show a higher sequence similarity comparison mammalian...

10.3389/fmicb.2016.00182 article EN cc-by Frontiers in Microbiology 2016-02-18

The study was conducted in healthy male volunteers to evaluate the absorption, metabolic pattern, and mode of elimination telmisartan, a nonpeptide angiotensin II receptor antagonist. [ 14 C]telmisartan administered orally solution as single 40 mg dose 5 subjects. A further subjects received short‐term intravenous infusion mg. Measurement total C radioactivity plasma showed that about 50% absorbed following oral administration, with maximum concentration observed after 0.5 1 hour. Absolute...

10.1177/009127000004001202 article EN The Journal of Clinical Pharmacology 2000-12-01

Abstract Antamanide is the name we have given to a constituent of fungus Amanita phalloides. This substance counteracts lethal action toxins phalloidine and α‐amanatine if administered white mouse before, or simultaneously with, poisons. Its concentration in is, however, so low that toxic latter predominates. cyclic decapeptide formed from L ‐amino acids alanine, phenylalanine, proline, valine molar ratio 1:4:4:1. The amino‐acid sequence was determined by combination gas chromatography mass...

10.1002/anie.196802041 article EN Angewandte Chemie International Edition 1968-03-01

Abstract Als Antamanid bezeichnen wir einen Inhaltsstoff des grünen Knollenblätterpilzes, Amanita phalloides, der an weißen Maus die tödliche Wirkung Amanitatoxine Phalloidin und α‐Amanitin bei spätestens gleichzeitiger Verabreichung aufhebt. Die Konzentration im Pilz ist allerdings so gering, daß dessen Giftwirkung überwiegt. ein cyclisches Dekapeptid aus den L‐Aminosäuren Alanin, Phenylalanin, Prolin Valin, zueinander Molverhältnis von 1:4:4:1 stehen. Sequenz wurde durch...

10.1002/ange.19680800602 article DE Angewandte Chemie 1968-03-21

1. The metabolism of Meloxicam (ME) and the cytochrome(s) P450 (CYPs) involved were analysed by using primary human hepatocytes, liver microsomes from recombinant B-lymphoblastoid cell lines. 2. While hepatocytes capable converting ME to a 5-hydroxymethyl metabolite (M7) then 5-carboxyderivative (M5), formed mostly only 5-hydroxymethylderivative. kinetics formation M7 biphasic with Km = 13.6 +/- 9.5 381 55.2 microM respectively. corresponding Vmax 33.7 24.2 143 83.9 pmol/min/mg protein 3....

10.1080/004982598239704 article EN Xenobiotica 1998-01-01

Application of state-of-the-art genome editing tools like CRISPR-Cas9 drastically increase the number undomesticated micro-organisms amenable to highly efficient and rapid genetic engineering. Adaptation these new bacterial families can open up entirely possibilities for organisms accelerate as biotechnologically relevant microbial factories, also making products economically competitive. Here, we report implementation a based vector system in Paenibacillus polymyxa, enabling fast reliable...

10.1093/synbio/ysx007 article EN cc-by-nc Synthetic Biology 2017-01-01

Microbial exopolysaccharides (EPS) are multifunctional biogenic polymers, which exist in highly diverse chemical structures. To facilitate a fast determination of the carbohydrate composition novel isolated strains or modified EPS variants screening and analytical method is required. The platform as realized described this article based on analysis via liquid chromatography coupled with ultra violet electrospray ionization ion trap detection 96-well format to detect different sugars, sugar...

10.1016/j.carbpol.2014.12.021 article EN cc-by Carbohydrate Polymers 2015-01-14

Paenibacillus polymyxa is a Gram-positive, non-pathogenic soil bacterium that has been extensively investigated for the production of R-,R-2,3-butanediol in exceptionally high enantiomeric purity. Rational metabolic engineering efforts to increase productivity and product titers were restricted due limited genetic accessibility organism up now. By use CRISPR-Cas9 mediated genome editing, six mutant variants generated compared batch fermentations first time. Downstream processing was...

10.1016/j.ymben.2020.07.009 article EN cc-by Metabolic Engineering 2020-08-06
Katharina S. Appel Carolin Nürnberger Thomas Bahmer Christian Förster Maria Cristina Polidori and 95 more Mirjam Kohls T. Kraus Nora Hettich-Damm Julia Petersen Sabine Blaschke Isabel Bröhl Jana Butzmann Hiwa Dashti Jürgen Deckert Michael Dreher K Fiedler Carsten Finke Ramsia Geisler Frank Hanses Sina M. Hopff Björn‐Erik Ole Jensen Margarethe Konik Kristin Lehnert Susana M. Nunes de Miranda Lazar Mitrov Olga Miljukov Jens‐Peter Reese Gernot Rohde Margarete Scherer Kristin Tausche Johannes Tebbe Jörg Janne Vehreschild Florian Voit Patricia Wagner Martin Weigl Christina Lemhöfer Khaled O. Alsaad Eckard Hamelmann Holger Heidenreich Claudia Hornberg N. S. A. Kulamadayil-Heidenreich P. Maasjosthusmann A. Muna M. Ruwe Christoph Stellbrink N. Buechner Y. Dashti Carl F. Tessmer Barbara Laumerich Ingmar Silberbaur Stephen O. Bader Michael Engelmann André Fuchs A. Langer Bruno Maerkl H Messmann Anna Muzalyova Christoph Roemmele Heidi Altmann Reinhard Berner Svenja Dreßen Tobias Koch Dirk Lindemann Kristin Seele Peter M. Spieth Nicole Toepfner Simone von Bonin Torsten Feldt Verena Keitel Alexander Killer Lisa Knopp Tom Luedde M. Lutterbeck Martha Paluschinski John Pereira Jörg Timm Detlef Kraska Andreas E. Kremer Moritz Leppkes Jonathan M. Mang M. F. Neurath Hans U. Prokosch Jochen Schmid Marcel Vetter Carsten Willam Kathrin Wolf Christophe Arendt Carla Bellinghausen Sabine Cremer Adrian Groh A. Gruenewaldt Yascha Khodamoradi Svenja Klinsing Maria J. G. T. Vehreschild Thomas J. Vogl Marylyn M. Addo Maher Almahfoud Alexander Engels Dominik Jarczak Melanie Kerinn

Abstract Purpose The objective examination of the Post-COVID syndrome (PCS) remains difficult due to heterogeneous definitions and clinical phenotypes. aim study was verify functionality correlates a recently developed PCS score. Methods score applied prospective, multi-center cross-sectoral cohort (in- outpatients with SARS-CoV-2 infection) "National Pandemic Cohort Network (NAPKON, Germany)". Symptom assessment patient-reported outcome measure questionnaires were analyzed at 3 12 months...

10.1007/s15010-024-02226-9 article EN cc-by Infection 2024-04-08

Meloxicam [4-hydroxy-2-methyl-N-(5-methyl-2-thiazolyl)-2H- 1,2-benzothiazine-3-carboxamide-1,1-dioxide] is a new nonsteroidal antiinflammatory drug belonging to the enolic acid group. In crossover study, 30 mg 14C-labeled meloxicam was administered four male healthy volunteers as short-term infusion and an oral solution. The objectives of study were determine mode elimination, excretion balance, in vivo binding characteristics serum proteins, investigate metabolic pattern plasma, urine,...

10.1016/s0090-9556(25)06817-5 article EN Drug Metabolism and Disposition 1995-11-01

In analyzing the reductive power of Escherichia coli K-12 for metabolic engineering approaches, we identified YahK and YjgB, two medium-chain dehydrogenases/reductases subgrouped to cinnamyl alcohol dehydrogenase family, as being important. Identification was achieved using a stepwise purification protocol starting with crude extract. For exact characterization, genes were cloned into pET28a vector expressed N-terminal His tag. Substrate specificity studies revealed that large variety...

10.1007/s00253-012-4474-5 article EN cc-by Applied Microbiology and Biotechnology 2012-10-23
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