Deep Learning-Based Prediction of Enzyme Optimal pH and Design of Point Mutations to Improve Acid Resistance

An accurate deep learning predictor of enzyme optimal pH is essential to quantitatively describe how pH influences the enzyme catalytic activity. CatOpt, developed in this study, outperformed existing predictors of enzyme optimal pH (RMSE = 0.833 and <i>R</i><sup>2</sup> = 0.479), and could provide good interpretability with informative residue attention weights. The classification of acidophilic and alkaliphilic enzymes and prediction of enzyme optimal pH shifts caused by point mutations showcased the capability of CatOpt as an effective computational tool for identifying enzyme pH preferences. Furthermore, a single point mutation designed with the guidance of CatOpt successfully enhanced the activity of <i>Pyrococcus horikoshii</i> diacetylchitobiose deacetylase at low pH (pH = 4.5/5.5) by approximately 7%, suggesting that CatOpt is a promising <i>in silico</i> enzyme design tool for pH-dependent enzyme activities.

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Publication Details

Journal
ACS Synthetic Biology
Published
2025-11-21
DOI
https://doi.org/10.1021/acssynbio.5c00679
Citations
2
Primary Topic
Enzyme Catalysis and Immobilization
Type
article
Field-Weighted Citation Impact
1.61
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Deep Learning-Based Prediction of Enzyme Optimal pH and Design of Point Mutations to Improve Acid Resistance

Sizhe Qiu, Nan‐Kai Wang, Jin‐Song Shi, Aidong Yang et al.
2 citations
ACS Synthetic Biology
Enzyme Catalysis and Immobilization
1.61
article

Deep Learning-Based Prediction of Enzyme Optimal pH and Design of Point Mutations to Improve Acid Resistance

Sizhe Qiu, Nan‐Kai Wang, Jin‐Song Shi, Aidong Yang, Yishun Lu, Jin-Song Gong
article en
2 citations

Abstract

An accurate deep learning predictor of enzyme optimal pH is essential to quantitatively describe how pH influences the enzyme catalytic activity. CatOpt, developed in this study, outperformed existing predictors of enzyme optimal pH (RMSE = 0.833 and <i>R</i><sup>2</sup> = 0.479), and could provide good interpretability with informative residue attention weights. The classification of acidophilic and alkaliphilic enzymes and prediction of enzyme optimal pH shifts caused by point mutations showcased the capability of CatOpt as an effective computational tool for identifying enzyme pH preferences. Furthermore, a single point mutation designed with the guidance of CatOpt successfully enhanced the activity of <i>Pyrococcus horikoshii</i> diacetylchitobiose deacetylase at low pH (pH = 4.5/5.5) by approximately 7%, suggesting that CatOpt is a promising <i>in silico</i> enzyme design tool for pH-dependent enzyme activities.

ACS Synthetic BiologyVol. 14(12)
Jiangnan University (CN), Jiangsu University (CN), University of Oxford (GB), Yixing People's Hospital (CN), Science Oxford (GB)
Openalex Percentile: Top 14%
Enzyme Catalysis and Immobilization
1.61
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