# A high-throughput biocatalytic platform for screening isomeric kainoid natural products

**Authors:** Robert A. Shepherd, Manasa Ramachandra, Austin R. Hopiavuori, Melanie C. Jones, Conrad A. Fihn, Alex J. Tabag, Ananya Manjunath, Limar Y. Gad, Chloe R. Whipple, Shaun M.K. McKinnie, Laura M. Sanchez

PMC · DOI: 10.1016/j.xcrp.2025.103092 · Cell reports. Physical science · 2026-03-18

## TL;DR

The paper introduces a fast method using MALDI-TIMS-MS to screen isomeric products from engineered enzymes, enabling high-throughput discovery of improved kainoid synthases.

## Contribution

A MALDI-TIMS-MS platform is developed for high-throughput screening of isomeric kainoid products from enzyme variants.

## Key findings

- Screening of 1,054 KabC variants identified seven with improved KAL formation.
- The workflow retains favorable expression and in vitro stability of enzyme variants.
- MALDI-TIMS-MS is established as a promising tool for isomeric product screening.

## Abstract

The growing field of biocatalysis relies on the generation of large, genetically diverse libraries for downstream colorimetric, fluorogenic, or chromatographic screening. However, challenges remain when assessing enzyme variants in a high-throughput manner whose transformations yield isomeric low-molecular-weight products. The kainoid synthase subfamily of Fe/αKG-dependent dioxygenases produces the isomeric neurochemicals kainic acid (KA) and KA lactone (KAL) in a range of yields and ratios. To enable an improved throughput screening of engineered kainoid synthases, we developed a matrix-assisted laser desorption/ionization-trapped ion mobility spectrometry-mass spectrometry (MALDI-TIMS-MS) platform to directly detect regioisomeric products with near-baseline resolution from bacterial colonies. Screening of 1,054 genetically diversified KabC variants identified seven with improved KAL formation, while retaining favorable expression profiles and improved in vitro stabilities. This workflow establishes MALDI-TIMS-MS as a promising platform for high-throughput isomeric product screening and provides unique enzyme constructs to probe structure-function relationships and for further biocatalytic development.

Shepherd and Ramachandra et al. present a fast, chromatography-free method for resolving isomeric products from engineered enzymes. This platform enables large-scale screening and identifies improved kainoid synthase variants, advancing both biocatalyst discovery and high-throughput analytical workflows.

## Linked entities

- **Chemicals:** kainic acid (PubChem CID 3816), KAL (PubChem CID 146014955)

## Full-text entities

- **Diseases:** epilepsy (MESH:D004827)
- **Chemicals:** His (MESH:D006639), L-ascorbate (MESH:D001205), kanamycin (MESH:D007612), heme (MESH:D006418), coproporphyrin (MESH:D003306), Phosphorus red (MESH:D010758), H2O (MESH:D014867), alpha-ketoglutarate (MESH:D007656), 1,5-DAN (MESH:C510889), KA (MESH:D007608), pyrrolidine (MESH:C032519), Fe (MESH:D007501), 2,5-dihydroxybenzoic acid (MESH:C010925), agar (MESH:D000362), ACN (MESH:C084683), lipids (MESH:D008055), glycerol (MESH:D005990), C10H15NO4 (-), nickel (MESH:D009532), carboxylic acid (MESH:D002264), acid (MESH:D000143), molecular oxygen (MESH:D010100), fatty acid (MESH:D005227), Ni-NTA (MESH:C088321)
- **Species:** Escherichia coli (E. coli, species) [taxon 562], Grateloupia filicina (species) [taxon 31455], Palmaria palmata (dulse, species) [taxon 2822], Palmaria hecatensis (species) [taxon 700710], Rhodophysema elegans (species) [taxon 39578], Mus musculus (house mouse, species) [taxon 10090], Digenea simplex (species) [taxon 945030]
- **Mutations:** Y347F, E128K, S107C, G122N
- **Cell lines:** pET-28a — Oryctolagus cuniculus (Rabbit), Transformed cell line (CVCL_6E94), E. coli BL21(DE3) — Mus musculus (Mouse), Hybridoma (CVCL_B7HM)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12995366/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12995366/full.md

## References

70 references — full list in the complete paper: https://tomesphere.com/paper/PMC12995366/full.md

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Source: https://tomesphere.com/paper/PMC12995366