On track of new gut bacteria

The Microbial Biology and Metagenomics group at the University of Queensland’s Diamantina Institute uses the BMG LABTECH FLUOstar Omega microplate reader to develop new methods to study the human gut microbiome. The researchers’ aim is to assess how the products that these microbes produce or consume influence digestive health.

Dr Martin Mangold Dr Martin Mangold
Application Specialist, BMG LABTECH HQs
Dr Martin Mangold

Dr Martin Mangold

BMG LABTECH HQs

Application Scientist

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About Dr Martin Mangold

Dr. Martin Mangold works as an Applications Specialist at BMG LABTECH headquarters in Ortenberg, Germany. He studied biology with a focus on biochemistry and cell biology at the University of Bonn before specializing in pharmaceutical sciences and drug interactions in his doctoral studies. During his time in the pharmaceutical department, Dr. Mangold gained expertise in protein sciences, binding and interaction studies, and enzyme kinetics as part of an interdisciplinary team of chemists, pharmacists and biologists. Since 2021, Dr. Mangold has been part of the BMG LABTECH team where he authors application notes, performs training courses and supports scientific customers.

Areas of Expertise

  • Protein science and interaction studies
  • Protein expression and purification
  • Cell biology and cell-based assays
  • Compound screening
  • Enzyme kinetics
  • Biochemistry

Academic Degrees

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PhD in Pharmaceutical Sciences Friedrich-Wilhelm-Universität Bonn
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MSc Degree in Drug Research Friedrich-Wilhelm-Universität Bonn
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BSc Degree in Biology Friedrich-Wilhelm-Universität Bonn

Therefore, automated growth assays of gut bacteria in 96-well microplates are conducted in the FLUOstar Omega microplate reader which allows accurate temperature control, processing of large numbers of samples, documenting growth characteristics and effects from various forms of bioactives. The instrument also includes a robust optimized heavy duty plate transport mechanism that makes long term shaking kinetic experiments possible.

Whilst the FLUOstar Omega’s O2 and CO2 atmospheric control can reduce to as little as 0.1%, growth assays of obligate anaerobic gut bacteria require an absolute anaerobic environment which is made possible by placing the FLUOstar Omega microplate reader in an anaerobic chamber from COY. Using this anaerobic setup, the Diamantina Institute’s Microbial Biology and Metagenomics group are isolating and screening new gut bacteria which may provide further insights into the functional role of the human gut microbiota in influencing human health.

Frequently asked questions

  • What is the significance of tracking new gut bacteria?  

    Tracking new gut bacteria helps in understanding their role in health and disease, potentially leading to targeted therapies and improved microbiome management.
  • Why are microplate readers important for studying bacteria in the gut?

    Microplate readers provide rapid, automated, and reproducible measurements, significantly increasing efficiency and data reliability for different types of studies of the gut microbiome.
  • Why is it important to identify new strains of gut bacteria?  

    Identifying new strains can reveal beneficial or harmful effects on human health, aiding in the development of probiotics or treatments for various conditions.
  • Can tracking gut bacteria help in personalized medicine?  

    Yes, analyzing individual microbiomes allows for tailored dietary recommendations and therapies based on specific bacterial profiles.
  • What practical applications arise from tracking new gut bacteria?  

    Applications include developing targeted probiotics, improving digestive health, and advancing disease prevention strategies.
  • How can microplate readers help track gut bacteria?

    Microplate readers (fluorescence, luminescence, and absorbance) enable high-throughput screening, viability assays, and metabolite measurements, accelerating discovery and tracking of gut microbes.
  • What assays are best for discovering new gut bacteria?

    Viability assays, colony-forming unit proxies, qPCR readouts, reporter assays (fluorescent/luminescent), and metabolite detection (SCFAs, bile acids) are common starting points.
  • Can microplate readers detect live/dead bacteria?

    Yes. Microplate reader assays can be used for viability and metabolic activity measurements (e.g., respirometry, ATP/Luminescence) to differentiate live from non-viable cells in plates.
  • How do you monitor gut bacteria metabolism with a plate reader?

    By measuring metabolic byproducts (e.g., fluorescence or luminescence from enzymatic reporters) and substrate consumption in microplates over time.
  • What data analysis tips help track new gut bacteria effectively?

    Normalize to controls, use kinetic/area-under-curve analyses for growth, apply robust statistics, and integrate multi-omics data for comprehensive profiling.

 

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