Author

Tomoya Maeda

Hokkaido UniversityORCID 0000-0002-2024-7794Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:bacteria (other)· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Organism:E. coli· 1 Approach:experimental assay· 1 Approach:genetic perturbation / CRISPR· 1 Research Focus:genome assembly· 1 Research Focus:perturbation response prediction· 1

Frequent Co-Authors

Maude GuillieriD· 1 shared Maxence LejarsiD· 1 shared Saki Mitsumasu· 1 shared Taichi E. TakasukaiD· 1 shared Takahiro NaganoiD· 1 shared Vijay KumariD· 1 shared Yoshinori HasegawaiD· 1 shared Yu Kasuga· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 16 mutual co-author links

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1 shared paperMicrobiology

Maude GuillierORCID

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2 papers

Recent·Most cited

MicrobiologybioRxivPreprintMay 19, 2026

A genomic and proteomic characterization of mannan-degradable Bacillus sp. TTS1, isolated from Tomakomai Forest in Hokkaido

Saki Mitsumasu, Yu Kasuga, Takahiro Nagano…·Taichi E. Takasuka

This study characterizes the genomic and proteomic features of a novel Bacillus sp. TTS1 capable of degrading plant biomass, identifying key enzymes involved in mannan and xylan degradation.

DOI 10.64898/2026.05.18.725066

bacteria (other)proteomics

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MicrobiologyNucleic Acids ResearchPeer-reviewedAug 22, 2025

EASY-CRISPR: a toolbox for high-throughput single-step custom genetic editing in bacteria

Maxence Lejars, Tomoya Maeda, Maude Guillier

EASY-CRISPR enables high-throughput, single-step genetic editing in E. coli using optimized guide RNAs and repair templates to construct genetic tools and mutant libraries.

2 citations

E. coligenetic perturbation / CRISPR

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