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dc.contributor.authorYetiman, Ahmet Evren
dc.contributor.authorOrtakci, Fatih
dc.date.accessioned2024-04-22T12:37:07Z
dc.date.available2024-04-22T12:37:07Z
dc.date.issued2023en_US
dc.identifier.issn1389-1723
dc.identifier.urihttps://doi.org/10.1016/j.jbiosc.2022.10.008
dc.identifier.urihttps://hdl.handle.net/20.500.12573/2114
dc.description.abstractThis study aimed to perform genomic, probiotic, and metabolic characterization of a novel Liquorilactobacillus nagelii AGA58 isolated from a lactic acid-fermented shalgam beverage to understand its metabolic potentials and probiotic features. AGA58 is gram-positive, motile, catalase-negative and appears as short rods under the light-microscope. The AGA58 chromosome comprises a single linear chromosome of 2,294,635 bp that is predicted to carry 2135 coding sequences, including 45 tRNA genes, 3 mRNA, and 3 rRNA operons. The genome has a G+C content of 36.9%, including 55 pseudogenes and a single intact prophage. AGA58 is micro-anaerobic due to achieving a shorter doubling time and faster growth rate than micro-aerophilic conditions. It carries flagellar biosynthesis protein-encoding genes predicting motile behavior, which was confirmed with the in vitro motility test. AGA58 is an obligatory homofermentative lactobacillus that can ferment hexose sugars such as galactose, glucose, fructose, sucrose, mannose, N-acetyl glucosamine, maltose, and trehalose to lactate through glycolysis. No acid production from pentoses implies that five-carbon sugars are being utilized for purine and pyrimidine synthesis. Putative pyruvate metabolism revealed formate, malate, oxaloacetate, acetate, acetaldehyde, acetoin, and lactate forms from pyruvate. AGA58 is predicted to encode the LuxS gene and biosynthesis of class IIa and Blp family class-II bacteriocins suggesting this bacterium's antimicrobial potential, linked to antagonism tests that AGA58 can inhibit Escherichia coli ATCC 43895, Salmonella enterica serovar Typhimurium ATCC 14028, and Klebsiella pneumonia ATCC 13883. Moreover, AGA58 is tolerant to acid and bile concentrations simulating the human gastrointestinal conditions depicting the probiotic potential of the organism as the first report in literature within the same species.en_US
dc.description.sponsorshipThis work has been supported by Erciyes University Scientific Research Projects Unit with grant number FKB-2020-10551. We thank Mr. Ismail Gumustop for his excellent support in drawing metabolic pathways. We would also like to thank KotilLab for its support during the experiments. The datasets generated and/or analyzed during the current study are available from the corresponding author upon reasonable request. The authors declare no competing interests.en_US
dc.language.isoengen_US
dc.publisherELSEVIERen_US
dc.relation.isversionof10.1016/j.jbiosc.2022.10.008en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectLiquorilactobacillus nageliien_US
dc.subjectComparative genomicsen_US
dc.subjectBacteriocinen_US
dc.subjectMotilityen_US
dc.subjectProbioticen_US
dc.subjectMetabolismen_US
dc.titleGenomic, probiotic, and metabolic potentials of Liquorilactobacillus nagelii AGA58, a novel bacteriocinogenic motile strain isolated from lactic acid-fermented shalgamen_US
dc.typearticleen_US
dc.contributor.departmentAGÜ, Yaşam ve Doğa Bilimleri Fakültesi, Biyomühendislik Bölümüen_US
dc.contributor.authorID0000-0003-1319-0854en_US
dc.contributor.institutionauthorOrtakci, Fatih
dc.identifier.volume135en_US
dc.identifier.issue1en_US
dc.identifier.startpage34en_US
dc.identifier.endpage43en_US
dc.relation.journalJournal of Bioscience and Bioengineeringen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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