ArticleExtremophiles : life under extreme conditions2019
Recombinant production and characterization of a novel esterase from a hypersaline lake, Acıgöl, by metagenomic approach.
Article in Extremophiles : life under extreme conditions, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 16 citations in OpenAlex.
- Discovery and characterization of an enantioselective family VIII esterase from effluent treatment plant sludge metagenome.Scientific reports · 2025Article
- Pharmaceutical applications of halophilic enzymes.Heliyon · 2025Review
- Identification of Cutinolytic Esterase from Microplastic-Associated Microbiota Using Functional Metagenomics and Its Plastic Degrading Potential.Molecular biotechnology · 2024Article
- Enzymatic Characterization of a Novel HSL Family IV Esterase EstD04 fromMolecules (Basel, Switzerland) · 2023Article
- Molecular Cloning and Characterization of a New Family VI Esterase from an Activated Sludge Metagenome.Microorganisms · 2022Article
- Biotechnological potentials of halophilic microorganisms and their impact on mankind.Beni-Suef University journal of basic and applied sciences · 2022Review
- Characterization of a Novel Esterase Est33 From an Antarctic Bacterium: A Representative of a New Esterase Family.Frontiers in microbiology · 2022Article
- Review
- Identification and Biochemical Characterization of a Novel Hormone-Sensitive Lipase Family Esterase Est19 from the Antarctic BacteriumBiomolecules · 2021Article
- A novel esterase from a soil metagenomic library displaying a broad substrate range.AMB Express · 2021Article
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The aim of this study was to isolate a novel esterase from a hypersaline lake by sequence-based metagenomics. The metagenomic DNA was isolated from the enriched hypersaline lake sediment. Degenerate primers targeting the conserved regions of lipolytic enzymes of halophilic microorganisms were used for polymerase chain reaction (PCR) and a whole gene was identified by genome walking. The gene was composed of 783 bp, which corresponds to 260 amino acids with a molecular weight of 28.2 kDa. The deduced amino acid sequence best matched with the esterase from Halomonas gudaonensis with an identity of 91%. Recombinantly expressed enzyme exhibited maximum activity towards pNP-hexanoate with a k
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