Please use this identifier to cite or link to this item: https://doi.org/10.1038/srep10521
DC FieldValue
dc.titleCharacterization of a xylanase-producing Cellvibrio mixtus strain J3-8 and its genome analysis
dc.contributor.authorWu, Y.-R
dc.contributor.authorHe, J
dc.date.accessioned2020-09-14T07:40:01Z
dc.date.available2020-09-14T07:40:01Z
dc.date.issued2015
dc.identifier.citationWu, Y.-R, He, J (2015). Characterization of a xylanase-producing Cellvibrio mixtus strain J3-8 and its genome analysis. Scientific Reports 5 : 10521. ScholarBank@NUS Repository. https://doi.org/10.1038/srep10521
dc.identifier.issn2045-2322
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/175996
dc.description.abstractCellvibrio mixtus strain J<inf>3</inf>-8 is a gram-negative, xylanase-producing aerobic soil bacterium isolated from giant snails in Singapore. It is able to produce up to 10.1 U ml-1 of xylanase, which is comparable to xylanase production from known bacterial and fungal strains. Genome sequence analysis of strain J3-8 reveals that the assembled draft genome contains 5,171,890 bp with a G + C content of 46.66%, while open reading frame (ORF) annotations indicate a high density of genes encoding glycoside hydrolase (GH) families involved in (hemi)cellulose hydrolysis. On the basis of 15 identified putative xylanolytic genes, one metabolic pathway in strain J<inf>3</inf>-8 is constructed for utilization of xylan. In addition, a 1,083 bp xylanase gene from strain J<inf>3</inf>-8 represents a new member of GH<inf>11</inf> family. This gene is verified to be novel via phylogenetic analysis. To utilize this novel gene for hydrolysis of xylan to xylose, it is expressed in recombinant E. coli and characterized for its hydrolytic activity. This study shows that strain J<inf>3</inf>-8 is a potential candidate for hydrolysis of lignocellulosic materials.
dc.sourceUnpaywall 20200831
dc.subjectbacterial protein
dc.subjectrecombinant protein
dc.subjectRNA 16S
dc.subjectxylan 1,4 beta xylosidase
dc.subjectamino acid sequence
dc.subjectanimal
dc.subjectbacterial genome
dc.subjectbiosynthesis
dc.subjectCellvibrio
dc.subjectchemistry
dc.subjectclassification
dc.subjectenzymology
dc.subjectEscherichia coli
dc.subjectgenetics
dc.subjectisolation and purification
dc.subjectmetabolism
dc.subjectmicrobiology
dc.subjectmolecular cloning
dc.subjectmolecular genetics
dc.subjectphylogeny
dc.subjectsequence alignment
dc.subjectsequence homology
dc.subjectsnail
dc.subjectAmino Acid Sequence
dc.subjectAnimals
dc.subjectBacterial Proteins
dc.subjectCellvibrio
dc.subjectCloning, Molecular
dc.subjectEscherichia coli
dc.subjectGenome, Bacterial
dc.subjectMolecular Sequence Data
dc.subjectPhylogeny
dc.subjectRecombinant Proteins
dc.subjectRNA, Ribosomal, 16S
dc.subjectSequence Alignment
dc.subjectSequence Homology, Amino Acid
dc.subjectSnails
dc.subjectXylosidases
dc.typeArticle
dc.contributor.departmentCIVIL AND ENVIRONMENTAL ENGINEERING
dc.description.doi10.1038/srep10521
dc.description.sourcetitleScientific Reports
dc.description.volume5
dc.description.page10521
dc.published.statePublished
Appears in Collections:Elements
Staff Publications

Show simple item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_1038_srep10521.pdf3.2 MBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


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