Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/14138
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSürmeli, Yusuf-
dc.contributor.authorTekedar, Hasan Cihad-
dc.contributor.authorSanli-Mohamed, Gulsah-
dc.date.accessioned2024-01-06T07:21:30Z-
dc.date.available2024-01-06T07:21:30Z-
dc.date.issued2023-
dc.identifier.issn0885-4513-
dc.identifier.issn1470-8744-
dc.identifier.urihttps://doi.org/10.1002/bab.2529-
dc.identifier.urihttps://hdl.handle.net/11147/14138-
dc.description.abstractMicrobial lipases are utilized in various biotechnological areas, including pharmaceuticals, food, biodiesel, and detergents. In this study, we cloned and sequenced Lip21 and Lip33 genes from Geobacillus sp. GS21 and Geobacillus sp. GS33, then we in silico and experimentally analyzed the encoded lipases. For this purpose, Lip21 and Lip33 were cloned, sequenced, and their amino acid sequences were investigated for determination of biophysicochemical characteristics, evolutionary relationships, and sequence similarities. 3D models were built and computationally affirmed by various bioinformatics tools, and enzyme-ligand interactions were investigated by docking analysis using six ligands. Biophysicochemical property of Lip21 and Lip33 was also determined experimentally and the results demonstrated that they had similar isoelectric point (pI) (6.21) and T-m (75.5(degrees)C) values as T-m was revealed by denatured protein analysis of the circular dichroism spectrum and pI was obtained by isoelectric focusing. Phylogeny analysis indicated that Lip21 and Lip33 were the closest to lipases from Geobacillus sp. SBS-4S and Geobacillus thermoleovorans, respectively. Alignment analysis demonstrated that S144-D348-H389 was catalytic triad residues in Lip21 and Lip33, and enzymes possessed a conserved Gly-X-Ser-X-Gly motif containing catalytic serine. 3D structure analysis indicated that Lip21 and Lip33 highly resembled each other and they were alpha/beta hydrolase-fold enzymes with large lid domains. BAN Delta IT analysis results showed that Lip21 and Lip33 had higher thermal stability, compared to other thermostable Geobacillus lipases. Docking results revealed that Lip21- and Lip33-docked complexes possessed common residues (H112, K115, Q162, E163, and S141) that interacted with the substrates, except paranitrophenyl (pNP)-C10 and pNP-C12, indicating that these residues might have a significant action on medium and short-chain fatty acid esters. Thus, Lip21 and Lip33 can be potential candidates for different industrial applications.en_US
dc.language.isoenen_US
dc.publisherWILEYen_US
dc.relation.ispartofBiotechnology and Applied Biochemistryen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectGeobacillusen_US
dc.subjecthomology modelingen_US
dc.subjectmolecular dockingen_US
dc.subjectrecombinant lipaseen_US
dc.subjectthermostable lipaseen_US
dc.subjectBacillus-Thermocatenulatusen_US
dc.subjectBiochemical-Characterizationen_US
dc.subjectStearothermophilusen_US
dc.subjectPurificationen_US
dc.subjectCloningen_US
dc.subjectClassificationen_US
dc.subjectOptimizationen_US
dc.subjectEsterasesen_US
dc.subjectDockingen_US
dc.subjectWeben_US
dc.titleSequence identification and in silico characterization of novel thermophilic lipases from Geobacillus speciesen_US
dc.typeArticleen_US
dc.typeArticle; Early Accessen_US
dc.institutionauthor-
dc.departmentİzmir Institute of Technologyen_US
dc.identifier.wosWOS:001096113400001en_US
dc.identifier.scopus2-s2.0-85175574485en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1002/bab.2529-
dc.identifier.pmid37908087en_US
dc.authorscopusid55758999000-
dc.authorscopusid36680834900-
dc.authorscopusid36680469600-
dc.identifier.wosqualityQ3-
dc.identifier.scopusqualityQ3-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.openairetypeArticle; Early Access-
crisitem.author.dept04.01. Department of Chemistry-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
Show simple item record



CORE Recommender

SCOPUSTM   
Citations

2
checked on Nov 15, 2024

WEB OF SCIENCETM
Citations

2
checked on Nov 9, 2024

Page view(s)

114
checked on Nov 18, 2024

Google ScholarTM

Check




Altmetric


Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.