Evidence map›Paper›PMID 41266391›Full record

ArticleScientific reports2025

Machine learning-guided discovery of thermophilic carbonic anhydrases from environmental metagenomes.

Sornpornpun Pairoh, Wuttichai Mhuantong, Katewadee Boonyapakron, Jirundon Yuvaniyama, Pattanop Kanokratana, Benjarat Bunterngsook, Hataikarn Lekakarn, Nattapol Arunrattanamook, Thanaporn Laothanachareon, Verawat Champreda

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Sornpornpun Pairoh *Enzyme Technology Research Team, Biorefinery Technology and Bioproduct Research Group, National Center for Genetic Engineering and Biotechnology, Khlong Luang, 12120, Pathum Thani, Thailand.
Wuttichai Mhuantong *Enzyme Technology Research Team, Biorefinery Technology and Bioproduct Research Group, National Center for Genetic Engineering and Biotechnology, Khlong Luang, 12120, Pathum Thani, Thailand.
Katewadee BoonyapakronEnzyme Technology Research Team, Biorefinery Technology and Bioproduct Research Group, National Center for Genetic Engineering and Biotechnology, Khlong Luang, 12120, Pathum Thani, Thailand.
Jirundon YuvaniyamaDepartment of Biochemistry and Center for Excellence in Protein and Enzyme Technology, Faculty of Science, Mahidol University, Ratchathewi, Bangkok, 10400, Thailand.
Pattanop KanokratanaEnzyme Technology Research Team, Biorefinery Technology and Bioproduct Research Group, National Center for Genetic Engineering and Biotechnology, Khlong Luang, 12120, Pathum Thani, Thailand.
Benjarat BunterngsookEnzyme Technology Research Team, Biorefinery Technology and Bioproduct Research Group, National Center for Genetic Engineering and Biotechnology, Khlong Luang, 12120, Pathum Thani, Thailand.
Hataikarn LekakarnDepartment of Biotechnology, Faculty of Science and Technology, Thammasat University, Rangsit Campus, Phahonyothin Road, Khlong Luang, 12120, Pathum Thani, Thailand.
Nattapol ArunrattanamookEnzyme Technology Research Team, Biorefinery Technology and Bioproduct Research Group, National Center for Genetic Engineering and Biotechnology, Khlong Luang, 12120, Pathum Thani, Thailand.
Thanaporn LaothanachareonEnzyme Technology Research Team, Biorefinery Technology and Bioproduct Research Group, National Center for Genetic Engineering and Biotechnology, Khlong Luang, 12120, Pathum Thani, Thailand.
Verawat ChampredaBiorefinery Technology and Bioproduct Research Group, National Center for Genetic Engineering and Biotechnology, Khlong Luang, 12120, Pathum Thani, Thailand. verawat@biotec.or.th.

Funding

Program Management Unit for Human Resources & Institutional Development, Research and Innovation (PMU-B) B13F670055
6 · The paper itself

Abstract

Thermophilic carbonic anhydrases (CAs) are promising biocatalysts for carbon capture utilization and storage (CCUS) due to their stability and efficiency at elevated temperatures. This study presents a machine learning (ML)-guided approach to discover thermostable γ-class CA (γ-CA) from metagenomic datasets derived from Fang Hot Spring, Northern Thailand. To develop classification models, two sets of protein descriptors-dipeptide composition (DPC) and physicochemical/biochemical properties (AAindex)-were used to train classification models. Fourteen ML algorithms were systematically evaluated for each feature set. AdaBoost achieved the best performance for the DPC-based model, while LightGBM performed best with AAindex-based features. External validation with known CA sequences confirmed the ability of the models to discriminate thermophilic from non-thermophilic proteins. Applying the optimized models, we screened 1,534 predicted CAs and identified three high-confidence candidates (TtCA, CrCA, and ToCA). These were heterologously expressed in E. coli, purified, and biochemically validated. All candidates exhibited carbonic anhydrase activity, trimeric oligomeric structures, and high melting temperatures (T

Indexed as

Carbonic AnhydrasesHot SpringsMachine LearningMetagenomeAlgorithmsAmino Acid SequenceCarbonic Anhydrases

Identifiers

PMID41266391
PMCPMC12635333

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.