Publication:
Haloadaptation: Insights From Comparative Modeling Studies Between Halotolerant and Non-Halotolerant Dehalogenases

dc.authorscopusid57188622711
dc.authorscopusid13205355000
dc.authorscopusid55279669000
dc.authorscopusid57219859702
dc.authorscopusid10240240100
dc.contributor.authorEdbeib, M.F.
dc.contributor.authorAksoy, H.M.
dc.contributor.authorKaya, Y.
dc.contributor.authorAbdul Wahab, R.A.
dc.contributor.authorHuyop, F.
dc.date.accessioned2020-06-21T12:26:09Z
dc.date.available2020-06-21T12:26:09Z
dc.date.issued2020
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Edbeib] Mohamed Faraj Abdulgader, Department of Animal Production, Bani Waleed University, Bani Walid, Libya, Department of Plant Protection, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Aksoy] Hasan Murat, Department of Plant Protection, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Kaya] Yilmaz, Department of Agricultural Biotechnology, Ondokuz Mayis Üniversitesi, Samsun, Turkey, Department of Biology, Kyrgyz-Turkish Manas University, Bishkek, Bishkek, Kyrgyzstan; [Abdul Wahab] Roswanira Abdul B., Department of Chemistry, Universiti Teknologi Malaysia, Johor Bahru, Johor, Malaysia; [Huyop] Fahrul Zaman, Department of Agricultural Biotechnology, Ondokuz Mayis Üniversitesi, Samsun, Turkey, Department of Biosciences, Universiti Teknologi Malaysia, Johor Bahru, Johor, Malaysiaen_US
dc.description.abstractHalophiles are extremophilic microorganisms that grow optimally at high salt concentrations by producing a myriad of equally halotolerant enzymes. Structural haloadaptation of these enzymes adept to thriving under high-salt environments, though are not fully understood. Herein, the study attempts an in silico investigation to identify and comprehend the evolutionary structural adaptation of a halotolerant dehalogenase, DehHX (GenBank accession number: KR297065) of the halotolerant Pseudomonas halophila, over its non-halotolerant counterpart, DehMX1 (GenBank accession number KY129692) produced by Pseudomonas aeruginosa. GC content of the halotolerant DehHX DNA sequence was distinctively higher (58.9%) than the non-halotolerant dehalogenases (55% average GC). Its acidic residues, Asp and Glu were 8.27% and 12.06%, respectively, compared to an average 5.5% Asp and 7% Glu, in the latter; but lower contents of basic and hydrophobic residues in the DehHX. The secondary structure of DehHX interestingly revealed a lower incidence of α-helix forming regions (29%) and a higher percentage of coils (57%), compared to 49% and 29% in the non-halotolerant homologues, respectively. Simulation models showed the DehHX is stable under a highly saline environment (25% w/v) by adopting a highly negative-charged surface with a concomitant weakly interacting hydrophobic core. The study thus, established that a halotolerant dehalogenase undergoes notable evolutionary structural changes related to GC content over its non-halotolerant counterpart, in order to adapt and thrive under highly saline environments. Communicated by Ramaswamy H. Sarma. © 2019 Informa UK Limited, trading as Taylor & Francis Group.en_US
dc.identifier.doi10.1080/07391102.2019.1657498
dc.identifier.endpage3461en_US
dc.identifier.issn0739-1102
dc.identifier.issn1538-0254
dc.identifier.issue12en_US
dc.identifier.pmid31422756
dc.identifier.scopus2-s2.0-85072023098
dc.identifier.scopusqualityQ1
dc.identifier.startpage3452en_US
dc.identifier.urihttps://doi.org/10.1080/07391102.2019.1657498
dc.identifier.volume38en_US
dc.identifier.wosWOS:000485423000001
dc.identifier.wosqualityQ3
dc.language.isoenen_US
dc.publisherTaylor and Francis Ltd. michael.wagreich@univie.ac.aten_US
dc.relation.ispartofJournal of Biomolecular Structure & Dynamicsen_US
dc.relation.journalJournal of Biomolecular Structure & Dynamicsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectComparative Analysisen_US
dc.subjectDehalogenaseen_US
dc.subjectHaloadaptationen_US
dc.subjectMolecular Dynamicsen_US
dc.subjectStructure Predictionen_US
dc.titleHaloadaptation: Insights From Comparative Modeling Studies Between Halotolerant and Non-Halotolerant Dehalogenasesen_US
dc.typeArticleen_US
dspace.entity.typePublication

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