A Comparative Biochemical Study of Oleate Hydratases

In the search for more efficient chemical processes to valorize renewable feedstocks, oleate hydratases (Ohys) represent promising biocatalysts. These enzymes can convert cis ‐Δ 9 fatty acids like oleic acid into their hydroxy fatty acid counterparts using only water as co‐reagent and with unparallelled selectivity. A multitude of Ohys has been described, however, direct comparison is hard due to the use of different assays. For this work, we characterized and compared four Ohys across different homologous families (HFams): those from Elizabethkingia meningoseptica ( Em Ohy, HFam11), Stenotrophomonas nitritireducens ( Sn Ohy, HFam11), Rhodococcus erythropolis ( Re Ohy, HFam3), and Rhodococcus pyridinivorans ( Rp Ohy, HFam2). All enzymes, especially Sn Ohy, expressed well in Escherichia coli (28–99 mg/L culture ). FAD occupancy after purification was 51% or lower for all Ohys. Re Ohy had lost the flavin altogether, making supplementation a necessity for its activity. Reduction of the cofactor to FADH 2 clearly showed a favorable effect on the activity of all Ohys, with product yields increasing from modest to 12‐fold. Although Sn Ohy showed the highest initial reaction rates, Em Ohy reached the highest 10‐hydroxystearic acid (10‐HSA) yields at higher oleic acid loading (10 mM) and prolonged reaction times. Thermostability was analyzed by thermal shift assays, with Em Ohy appearing as most thermostable ( T m app = 54 °C).

Authors

Institutions

Publication Details

Journal
ChemBioChem
Published
2026-07-30
DOI
https://doi.org/10.1002/cbic.70487
Primary Topic
Enzyme Catalysis and Immobilization
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A Comparative Biochemical Study of Oleate Hydratases

Peter‐Leon Hagedoorn, Ulf Hanefeld, Alejandro Gran‐Scheuch, Maxim van Delft
ChemBioChem
Enzyme Catalysis and Immobilization
article

A Comparative Biochemical Study of Oleate Hydratases

Peter‐Leon Hagedoorn, Ulf Hanefeld, Alejandro Gran‐Scheuch, Maxim van Delft
article en

Abstract

In the search for more efficient chemical processes to valorize renewable feedstocks, oleate hydratases (Ohys) represent promising biocatalysts. These enzymes can convert cis ‐Δ 9 fatty acids like oleic acid into their hydroxy fatty acid counterparts using only water as co‐reagent and with unparallelled selectivity. A multitude of Ohys has been described, however, direct comparison is hard due to the use of different assays. For this work, we characterized and compared four Ohys across different homologous families (HFams): those from Elizabethkingia meningoseptica ( Em Ohy, HFam11), Stenotrophomonas nitritireducens ( Sn Ohy, HFam11), Rhodococcus erythropolis ( Re Ohy, HFam3), and Rhodococcus pyridinivorans ( Rp Ohy, HFam2). All enzymes, especially Sn Ohy, expressed well in Escherichia coli (28–99 mg/L culture ). FAD occupancy after purification was 51% or lower for all Ohys. Re Ohy had lost the flavin altogether, making supplementation a necessity for its activity. Reduction of the cofactor to FADH 2 clearly showed a favorable effect on the activity of all Ohys, with product yields increasing from modest to 12‐fold. Although Sn Ohy showed the highest initial reaction rates, Em Ohy reached the highest 10‐hydroxystearic acid (10‐HSA) yields at higher oleic acid loading (10 mM) and prolonged reaction times. Thermostability was analyzed by thermal shift assays, with Em Ohy appearing as most thermostable ( T m app = 54 °C).

ChemBioChemVol. 27(15)
Delft University of Technology (NL)
Clean water and sanitation
Openalex Percentile: Top 15%
Enzyme Catalysis and Immobilization
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.