Sequence Identification and in Silico Characterization of Novel Thermophilic Lipases From Geobacillus Species

dc.contributor.author Sürmeli, Yusuf
dc.contributor.author Tekedar, Hasan Cihad
dc.contributor.author Sanli-Mohamed, Gulsah
dc.date.accessioned 2024-01-06T07:21:30Z
dc.date.available 2024-01-06T07:21:30Z
dc.date.issued 2023
dc.description.abstract Microbial 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.identifier.doi 10.1002/bab.2529
dc.identifier.issn 0885-4513
dc.identifier.issn 1470-8744
dc.identifier.scopus 2-s2.0-85175574485
dc.identifier.uri https://doi.org/10.1002/bab.2529
dc.identifier.uri https://hdl.handle.net/11147/14138
dc.language.iso en en_US
dc.publisher WILEY en_US
dc.relation.ispartof Biotechnology and Applied Biochemistry en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Geobacillus en_US
dc.subject homology modeling en_US
dc.subject molecular docking en_US
dc.subject recombinant lipase en_US
dc.subject thermostable lipase en_US
dc.subject Bacillus-Thermocatenulatus en_US
dc.subject Biochemical-Characterization en_US
dc.subject Stearothermophilus en_US
dc.subject Purification en_US
dc.subject Cloning en_US
dc.subject Classification en_US
dc.subject Optimization en_US
dc.subject Esterases en_US
dc.subject Docking en_US
dc.subject Web en_US
dc.title Sequence Identification and in Silico Characterization of Novel Thermophilic Lipases From Geobacillus Species en_US
dc.type Article en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.institutional
gdc.author.scopusid 55758999000
gdc.author.scopusid 36680834900
gdc.author.scopusid 36680469600
gdc.bip.impulseclass C5
gdc.bip.influenceclass C5
gdc.bip.popularityclass C4
gdc.coar.type text::journal::journal article
gdc.collaboration.industrial false
gdc.description.department İzmir Institute of Technology en_US
gdc.description.departmenttemp [Surmeli, Yusuf] Tekirdag Namik Kemal Univ, Dept Agr Biotechnol, Tekirdag, Turkiye; [Surmeli, Yusuf; Tekedar, Hasan Cihad; Sanli-Mohamed, Gulsah] Izmir Inst Technol, Dept Biotechnol & Bioengn, Izmir, Turkiye; [Tekedar, Hasan Cihad] Mississippi State Univ, Coll Vet Med, Mississippi State, MS USA; [Sanli-Mohamed, Gulsah] Izmir Inst Technol, Dept Chem, Izmir, Turkiye; [Sanli-Mohamed, Gulsah] Izmir Inst Technol, Sci Fac, Dept Chem, Izmir, Turkiye; [Surmeli, Yusuf] Tekirdag Namik Kemal Univ, Fac Agr, Dept Agr Biotechnol, Tekirdag, Turkiye en_US
gdc.description.endpage 175
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q2
gdc.description.startpage 162
gdc.description.volume 71
gdc.description.wosquality Q3
gdc.identifier.openalex W4388134120
gdc.identifier.pmid 37908087
gdc.identifier.wos WOS:001096113400001
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed
gdc.oaire.diamondjournal false
gdc.oaire.impulse 4.0
gdc.oaire.influence 2.6808469E-9
gdc.oaire.isgreen false
gdc.oaire.keywords Bacterial Proteins
gdc.oaire.keywords Enzyme Stability
gdc.oaire.keywords Geobacillus
gdc.oaire.keywords Amino Acid Sequence
gdc.oaire.popularity 5.3361973E-9
gdc.oaire.publicfunded false
gdc.openalex.collaboration International
gdc.openalex.fwci 0.74268163
gdc.openalex.normalizedpercentile 0.72
gdc.opencitations.count 4
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