Please use this identifier to cite or link to this item:
https://doi.org/10.1038/srep10521
DC Field | Value | |
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dc.title | Characterization of a xylanase-producing Cellvibrio mixtus strain J3-8 and its genome analysis | |
dc.contributor.author | Wu, Y.-R | |
dc.contributor.author | He, J | |
dc.date.accessioned | 2020-09-14T07:40:01Z | |
dc.date.available | 2020-09-14T07:40:01Z | |
dc.date.issued | 2015 | |
dc.identifier.citation | Wu, 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.issn | 2045-2322 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/175996 | |
dc.description.abstract | Cellvibrio 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.source | Unpaywall 20200831 | |
dc.subject | bacterial protein | |
dc.subject | recombinant protein | |
dc.subject | RNA 16S | |
dc.subject | xylan 1,4 beta xylosidase | |
dc.subject | amino acid sequence | |
dc.subject | animal | |
dc.subject | bacterial genome | |
dc.subject | biosynthesis | |
dc.subject | Cellvibrio | |
dc.subject | chemistry | |
dc.subject | classification | |
dc.subject | enzymology | |
dc.subject | Escherichia coli | |
dc.subject | genetics | |
dc.subject | isolation and purification | |
dc.subject | metabolism | |
dc.subject | microbiology | |
dc.subject | molecular cloning | |
dc.subject | molecular genetics | |
dc.subject | phylogeny | |
dc.subject | sequence alignment | |
dc.subject | sequence homology | |
dc.subject | snail | |
dc.subject | Amino Acid Sequence | |
dc.subject | Animals | |
dc.subject | Bacterial Proteins | |
dc.subject | Cellvibrio | |
dc.subject | Cloning, Molecular | |
dc.subject | Escherichia coli | |
dc.subject | Genome, Bacterial | |
dc.subject | Molecular Sequence Data | |
dc.subject | Phylogeny | |
dc.subject | Recombinant Proteins | |
dc.subject | RNA, Ribosomal, 16S | |
dc.subject | Sequence Alignment | |
dc.subject | Sequence Homology, Amino Acid | |
dc.subject | Snails | |
dc.subject | Xylosidases | |
dc.type | Article | |
dc.contributor.department | CIVIL AND ENVIRONMENTAL ENGINEERING | |
dc.description.doi | 10.1038/srep10521 | |
dc.description.sourcetitle | Scientific Reports | |
dc.description.volume | 5 | |
dc.description.page | 10521 | |
dc.published.state | Published | |
Appears in Collections: | Elements Staff Publications |
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10_1038_srep10521.pdf | 3.2 MB | Adobe PDF | OPEN | None | View/Download |
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