Evidence map›Paper›PMID 40877025›Full record

ArticleJournal of microbiology and biotechnology2025

Establishment of High-Throughput Screening Protocol Based on Isomerase Using

Na Kyeong Koo, Sol Min Han, Seong-Bo Kim, Seung-Ho Baek, Hyun June Park

Abstract read
In one paragraph

Article in Journal of microbiology and biotechnology, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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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

5 authors.

Na Kyeong KooDepartment of Bio-Health Convergence, Duksung Women's University, Seoul 01369, Republic of Korea.
Sol Min HanDepartment of Bio-Health Convergence, Duksung Women's University, Seoul 01369, Republic of Korea.
Seong-Bo KimBio-Living Engineering Major, Yonsei University, Seoul 03722, Republic of Korea.
Seung-Ho BaekCenter for Bio-based Chemistry, Korea Research Institute of Chemical Technology (KRICT), Ulsan 44429, Republic of Korea.
Hyun June ParkDepartment of Bio-Health Convergence, Duksung Women's University, Seoul 01369, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Directed evolution is a powerful tool in protein engineering that generates diverse variant libraries to enhance enzyme functionalities. However, the identification of desirable variants from large mutant libraries requires an efficient high-throughput screening (HTS) technique. In this study, we established a robust HTS protocol for selecting high-activity isomerase variants, specifically using L-rhamnose isomerase (L-RI) consistently; avoid switching between L-RI and L-RhI. L-RI catalyzes the isomerization of D-allulose to D-allose, which allows for activity detection via the reduction of the ketose D-allulose in a colorimetric assay based on Seliwanoff's reaction. Initial optimization was conducted in a single-tube format, where reaction conditions were refined and interfering factors were minimized. This optimized single-tube protocol demonstrated excellent accuracy when validated against high-performance liquid chromatography measurements, confirming its ability to precisely quantify D-allulose depletion. Subsequently, the protocol was successfully adapted to a 96-well plate format, incorporating further optimizations for protein expression and the removal of denatured enzymes. This involved methods such as cell harvest, supernatant removal, and filtration to reduce assay interference. The analytical quality of the established HTS protocol was evaluated using statistical metrics. The results yielded a Z'-factor of 0.449, a signal window (SW) of 5.288, and an assay variability ratio (AVR) of 0.551. All these values meet the acceptance criteria for high-quality of HTS assay. This HTS protocol is highly reliable and applicable for efficient screening of isomerase activity in various industrial and research areas.

Indexed as

Aldose-Ketose IsomerasesGeobacillusHigh-Throughput Screening AssaysBacterial ProteinsChromatography, High Pressure LiquidColorimetryGlucoseAldose-Ketose IsomerasesalloseBacterial ProteinsGlucoseL-rhamnose isomeraseHigh-throughput screeningIsomerizationL-Rhamnose isomeraseSeliwanoff's reaction

Identifiers

PMID40877025
PMCPMC12409428

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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.