Evidence map›Paper›PMID 41273350›Full record

ArticleFEMS yeast research2025

The genetically encoded biosensor HyPer7 enables in-line monitoring of H2O2 accumulation dynamics in the methylotrophic yeast Komagataella phaffii.

Victor Mendes Honorato, Jennifer Staudacher, Mikael Molin, Brigitte Gasser

Abstract read
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Article in FEMS yeast research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Victor Mendes HonoratoDepartment of Biotechnology and Food Science, Institute of Microbiology and Microbial Biotechnology, BOKU University, 1190 Vienna, Austria.
Jennifer StaudacherDepartment of Biotechnology and Food Science, Institute of Microbiology and Microbial Biotechnology, BOKU University, 1190 Vienna, Austria.
Mikael MolinDivision of Systems and Synthetic Biology, Department of Biology and Biological Engineering, Chalmers University of Technology, 405 30 Gothenburg, Sweden.
Brigitte GasserDepartment of Biotechnology and Food Science, Institute of Microbiology and Microbial Biotechnology, BOKU University, 1190 Vienna, Austria.ORCID 0000-0003-2881-6370

Funding

Austrian Science Fund 10.55776/W1224
6 · The paper itself

Abstract

In methylotrophic yeasts such as Komagataella phaffii (syn Pichia pastoris), the initial step of methanol metabolism by alcohol oxidase (Aox) generates hydrogen peroxide (H2O2) as a potentially toxic byproduct. Introduction of the ratiometric, genetically encoded fluorescent H2O2 biosensor HyPer7 in combination with cultivation in a microbioreactor allowed for the first time to in vivo determine H2O2 dynamics upon methanol utilization (MUT). In line monitoring of H2O2 during growth on glucose or methanol revealed a general increase in biosensor oxidation on methanol, with significant oxidation peaks shortly after methanol addition. HyPer7 also detected low endogenous H2O2 levels occurring during respiratory growth in K. phaffii and its signal responded to both external oxidants and reductants. In strains with different MUT phenotypes (K. phaffii deleted for aox1 and/or aox2), HyPer7 demonstrated that H2O2 production is mainly due to Aox1 activity, and explained why strains possessing only Aox2 (MutS) have superior growth and production capacities compared to the wild-type. In conclusion, we present the first application of an H2O2 biosensor in K. phaffii, offering new insights into methanol metabolism and oxidative stress. The findings hold promise for optimizing yeast cell factories and developing more sustainable production processes with reduced oxidative stress in the future.

Indexed as

Biosensing TechniquesHydrogen PeroxideSaccharomycetalesAlcohol OxidoreductasesGlucoseLuminescent ProteinsMethanolOxidation-Reductionalcohol oxidaseAlcohol OxidoreductasesGlucoseHydrogen PeroxideLuminescent ProteinsMethanolalcohol oxidaseH2O2 biosensorHyPer7methanol metabolismmethylotrophic yeastoxidative stress

Identifiers

PMID41273350
PMCPMC12684170

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.