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

dc.contributor.author Sürmeli,Y.
dc.contributor.author Tekedar,H.C.
dc.contributor.author Şanlı-Mohamed,G.
dc.date.accessioned 2024-03-03T16:41:36Z
dc.date.available 2024-03-03T16:41:36Z
dc.date.issued 2024
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 Tm (75.5°C) values as Tm 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 α/β hydrolase-fold enzymes with large lid domains. BANΔIT 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. © 2023 International Union of Biochemistry and Molecular Biology, Inc. en_US
dc.identifier.doi 10.1002/bab.2529
dc.identifier.issn 8854-513
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/11147/14335
dc.language.iso en en_US
dc.publisher John Wiley and Sons Inc 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.title Sequence Identification and in Silico Characterization of Novel Thermophilic Lipases From Geobacillus Species en_US
dc.type Article en_US
dspace.entity.type Publication
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gdc.bip.impulseclass C5
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gdc.bip.popularityclass C4
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
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gdc.description.department Izmir Institute of Technology en_US
gdc.description.departmenttemp Sürmeli Y., Department of Agricultural Biotechnology, Tekirdağ Namık Kemal University, Tekirdağ, Turkey, Department of Biotechnology and Bioengineering, İzmir Institute of Technology, İzmir, Turkey; Tekedar H.C., Department of Biotechnology and Bioengineering, İzmir Institute of Technology, İzmir, Turkey, College of Veterinary Medicine, Mississippi State University, Mississippi State, MS, United States; Şanlı-Mohamed G., Department of Biotechnology and Bioengineering, İzmir Institute of Technology, İzmir, Turkey, Department of Chemistry, İzmir Institute of Technology, İzmir, Turkey en_US
gdc.description.endpage 175 en_US
gdc.description.issue 1 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q2
gdc.description.startpage 162 en_US
gdc.description.volume 71 en_US
gdc.description.wosquality Q3
gdc.identifier.openalex W4388134120
gdc.identifier.pmid 37908087
gdc.index.type Scopus
gdc.index.type PubMed
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gdc.oaire.influence 2.6808469E-9
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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
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gdc.opencitations.count 4
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