Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/4976
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dc.contributor.authorEsposito, Alfonsoen_US
dc.contributor.authorDragićević, Milanen_US
dc.contributor.authorDimkić, Ivicaen_US
dc.contributor.authorDegrassi, Giulianoen_US
dc.contributor.authorPiazza, Silvanoen_US
dc.date.accessioned2022-11-08T10:10:15Z-
dc.date.available2022-11-08T10:10:15Z-
dc.date.issued2022-06-
dc.identifier.citationEsposito, A., Dragićević, M., Dimkić, I., Degrassi, G., Piazza, S., 2022. An in-depth characterization of the carbohydrate active enzymes from Bacillus altitudinis PS213. FEMS Conference on Microbiology in association with Serbian Society of Microbiology, Belgrade, Serbia, Electronic Abstract Book, pp. 907 (569).en_US
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/4976-
dc.descriptionElectronic Abstract Book, pp. 907 (569).en_US
dc.description.abstractBACKGROUND The need for clean energy, renewable resources, and circular economy has fostered the research in plant biomass degradation (PBD) catalyzed by microorganisms. The bovine rumen is among the best studied environments where PBD takes place. In this organ, the plant cell wall components (a combination of cellulose, hemicellulose and pectin) is enzymatically digested by carbohydrate-active enzymes (CAZymes) secreted by the microorganisms living in it. OBJECTIVES In this study, we report the complete circular genome sequence of a Bacillus altitudinis strain PS213, with annotation of the secreted CAZymes encoded in its genome and describe in depth their 3D structure. METHODS The genome was assembled using Unicycler from a combination of long and short reads (Illumina MiSeq and ONT). The predicted proteins were submitted to dbCAN to identify the putative CAZy. The 3D structure of secreted plant cell wall degrading enzymes was estimated using AlphaFold, and compared to experimentally determined structures to infer substrate binding specificity and catalytic mechanism. RESULTS The genome assembly resulted in a single contig of length 3.896.825 with GC%=41.2. It encoded 3955 proteins (avg protein length 287.6 aa), resulting in a coding ratio of 87.6%. We found 97 CAZy proteins, including 24 proteins presenting a secretory signal peptide and 21 proteins annotated as hypothetical proteins. The identification and in-depth description of known and novel CAZymes from B. altitudinis PS213 pave the way toward the improvement of plant biomass degradation processes with multiple possible biotechnological applications in the treatments of different wastes, feed stocks and composting materialsen_US
dc.language.isoenen_US
dc.subjectMicrobial Genomics, ,en_US
dc.subjectCarbohydrate-active enzymes (CAZy)en_US
dc.subjectPlant biomass degradationen_US
dc.titleAn in-depth characterization of the carbohydrate active enzymes from Bacillus altitudinis PS213en_US
dc.typeConference Paperen_US
dc.relation.conferenceFEMS Conference on Microbiology in association with Serbian Society of Microbiology, Belgrade, Serbiaen_US
dc.date.updated2023-10-14-
dc.description.rankM34en_US
dc.description.startpage907en_US
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeConference Paper-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.orcid0000-0002-0425-5938-
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