# Multidimensional strategy enables scalable metabolome diversity in microbial fermentations

**Authors:** Anton Lindig, Makram Fataeri, Georg Hubmann, Stephan Lütz

PMC · DOI: 10.1038/s41598-026-37748-9 · 2026-01-29

## TL;DR

This study shows how adjusting multiple factors can improve the consistency of natural product production in different microbial cultivation systems.

## Contribution

The paper introduces a multidimensional strategy to enhance metabolome reproducibility across diverse microbial cultivation systems.

## Key findings

- Adjusting ethanol concentration and oxygen availability increased metabolic footprint overlap by 18%.
- Morphology and total mass features are key factors influencing metabolic reproducibility.
- 48 flower plates and stirred tank bioreactors share the highest number of molecular clusters.

## Abstract

Natural products (NPs) are critical sources of new drug leads, but their biosynthesis is highly sensitive to bioprocess parameters and environmental conditions, making NP discovery especially susceptible to challenges in achieving robust scalability and reproducibility of the metabolome across various cultivation systems. Here, we identified key factors that improved the metabolic footprint overlap of Streptomyces griseochromogenes across three cultivation systems, i.e. baffled shake flasks (BSF), 48 flower plates (48 FP), and a stirred tank bioreactor (STR), by 50 %. Using the classical scale-up criterion of constant oxygen availability, the metabolic footprints were found to differ considerably, with only an 18 % overlap in mass feature (MF) number. Efforts to improve overlap by varying ethanol concentration in culture medium and oxygen availability resulted in an 18 % increase. Factor analysis of 80 cultivations including variations in bioprocess conditions, growth, and MF detection identified morphology and total MF number, mainly influenced by the cultivation systems, as key factors in metabolic footprint reproducibility. Molecular network analysis revealed that 48 FP and STR share the highest number of molecular clusters. Our findings reveal that only multidimensional optimization unlocks robust metabolome scalability and reproducibility across cultivation systems, paving the way for the discovery of novel NPs.

The online version contains supplementary material available at 10.1038/s41598-026-37748-9.

## Linked entities

- **Chemicals:** ethanol (PubChem CID 702)
- **Species:** Streptomyces griseochromogenes (taxon 68214)

## Full-text entities

- **Diseases:** MFs (MESH:C536030), SM (MESH:D000068376), FP (MESH:C000719190)
- **Chemicals:** ether (MESH:D004986), amino acid (MESH:D000596), Glucose (MESH:D005947), desferrioxamine (MESH:D003676), platensimycin (MESH:C510909), L-asparagyl-L-asparagyl-L-prolyl-L-serine (-), undecylprodigiosin (MESH:C047347), natamycin (MESH:D010866), purine (MESH:C030985), actinorhodin (MESH:C013390), peptides (MESH:D010455), polystyrene (MESH:D011137), EtOH (MESH:D000431), SMs (MESH:D012493), carbon (MESH:D002244), pristinamycin (MESH:D025762), reactive oxygen species (MESH:D017382), oxygen (MESH:D010100), carbohydrates (MESH:D002241), polyamide (MESH:D009757), glycerol (MESH:D005990), IC202B (MESH:C405822), oxytetracycline (MESH:D010118), platencin (MESH:C520340), water (MESH:D014867), maltose (MESH:D008320), futalosine (MESH:C122040), Des B. (MESH:C007366), alanine (MESH:D000409), proline (MESH:D011392)
- **Species:** Azospirillum brasilense (species) [taxon 192], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Gluconobacter oxydans (species) [taxon 442], Streptomyces (genus) [taxon 1883], Escherichia coli (E. coli, species) [taxon 562], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Streptomyces griseochromogenes (species) [taxon 68214], Homo sapiens (human, species) [taxon 9606], Corynebacterium glutamicum (species) [taxon 1718]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12855292/full.md

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Source: https://tomesphere.com/paper/PMC12855292