Literature DB >> 23618715

Draft Genome Sequence of Biocontrol Bacterium Brevibacillus brevis Strain FJAT-0809-GLX.

Jianmei Che1, Bo Liu, Yingzhi Lin, Weiqi Tang, Jianyang Tang.   

Abstract

Brevibacillus brevis strain FJAT-0809-GLX had significant inhibition on many plant and animal pathogens. The draft genome sequence of B. brevis FJAT-0809-GLX is 6 Mb in size and consists of 5,677 genes (protein-coding sequences [CDS]), with an average length of 933 bp and a G+C content of 47.30%. Compared with the published B. brevis strain NBRC 100599, 618 specific genes were identified in the strain FJAT-0809-GLX.

Entities:  

Year:  2013        PMID: 23618715      PMCID: PMC3636543          DOI: 10.1128/genomeA.00160-13

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Brevibacillus brevis (formerly Bacillus brevis Nagano [1]) is a Gram-positive and spore-forming bacterium (2). It can secrete large amounts of secondary metabolites, which are important for controlling pathogens. Among them, tyrocidine (3), gramicidin (4–6), gratisin (7), and edeine (8) have been successively isolated and identified. B. brevis could be a promising candidate for use as an antimicrobial agent to improve crop yield and quality, owing to its antagonistic activities against pathogenic bacteria and fungi (2). The first genome of B. brevis, strain NBRC 100599, is available at GenBank. Here, we report the second genome for B. brevis, strain FJAT-0809-GLX. B. brevis FJAT-0809-GLX was isolated from the soil of watermelon rhizosphere in Fujian province, China. It was identified by 16S rRNA gene sequencing and physiological and biochemical analyses (9). Studies showed that it had significant inhibition on many plant and animal pathogens (10–13), such as Ralstonia solanacearum (10), Fusarium oxysporum (10,11), and Escherichia coli K88 (13). It also had an inhibitory effect on the activity of peroxidase (POD) from longan pericarp for keeping fruit fresh (13). Here, we analyzed the genome sequence of this strain to explore the genomic features responsible for its effectiveness as a biocontrol agent. The genome of B. brevis FJAT-0809-GLX was sequenced by Illumina GA IIx with a 400-bp paired-end library. Using SOAPdenovo v1.04 (14), a total of 739 Mb high-quality bases were de novo assembled into 72 contigs, with a total genome size of 6.02 Mb, of which the N50 is 181 kb. The G+C content of the FJAT-0809-GLX genome is approximately 47.3%. In all, 5,677 coding sequences (CDSs) were predicted by Prodigal v2.5 (15), with a mean gene length of 933 bp. The CDSs represent 87.8% of the genome. Functional annotation of the predicted genes was performed by homologous comparison to NR and UniRef (BLASTp, e value ≤ 1E - 5); however, 362 genes did not match any known protein in a current public database. Of the total proteins, 3,830 can be assigned to COG families and 2,048 can be assigned to KEGG. Additionally, 1 rRNA and 80 tRNAs were identified by RNAmmer (16) and tRNAscan-SE 1.21 (17), respectively. Compared with the sequenced genome of B. brevis strain NBRC 100599, 618 strain-specific genes were identified within the genome of strain FJAT-GLX-0809, accounting for 10.89% of the total number of predicted genes, most of which encoded hypothetical and putative uncharacterized proteins. The average amino acid identity (AAI) of orthologous genes is 97.1% between the two strains. The B. brevis FJAT-0809-GLX genome might not only enrich the genome database of B. brevis, but it might also lay the foundation at the genomic level for the research of antimicrobial mechanisms and the development of related products.

Nucleotide sequence accession numbers.

The whole-genome shotgun project for B. brevis FJAT-0809-GLX has been deposited at DDBJ/EMBL/GenBank under the accession no. AHKL00000000. The version described in this paper is the first version, accession no. AHKL01000000.
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1.  De novo assembly of human genomes with massively parallel short read sequencing.

Authors:  Ruiqiang Li; Hongmei Zhu; Jue Ruan; Wubin Qian; Xiaodong Fang; Zhongbin Shi; Yingrui Li; Shengting Li; Gao Shan; Karsten Kristiansen; Songgang Li; Huanming Yang; Jian Wang; Jun Wang
Journal:  Genome Res       Date:  2009-12-17       Impact factor: 9.043

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Journal:  J Bacteriol       Date:  1997-11       Impact factor: 3.490

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Authors:  M Tamaki; M Takimoto; S Sofuku; I Muramatsu
Journal:  J Antibiot (Tokyo)       Date:  1983-06       Impact factor: 2.649

4.  Proposal for two new genera, Brevibacillus gen. nov. and Aneurinibacillus gen. nov.

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Journal:  Int J Syst Bacteriol       Date:  1996-10

5.  Structure activity relationship studies on the antimicrobial activity of novel edeine A and D analogues.

Authors:  Zbigniew Czajgucki; Ryszard Andruszkiewicz; Wojciech Kamysz
Journal:  J Pept Sci       Date:  2006-10       Impact factor: 1.905

6.  Prodigal: prokaryotic gene recognition and translation initiation site identification.

Authors:  Doug Hyatt; Gwo-Liang Chen; Philip F Locascio; Miriam L Land; Frank W Larimer; Loren J Hauser
Journal:  BMC Bioinformatics       Date:  2010-03-08       Impact factor: 3.169

7.  The tRNAscan-SE, snoscan and snoGPS web servers for the detection of tRNAs and snoRNAs.

Authors:  Peter Schattner; Angela N Brooks; Todd M Lowe
Journal:  Nucleic Acids Res       Date:  2005-07-01       Impact factor: 16.971

8.  RNAmmer: consistent and rapid annotation of ribosomal RNA genes.

Authors:  Karin Lagesen; Peter Hallin; Einar Andreas Rødland; Hans-Henrik Staerfeldt; Torbjørn Rognes; David W Ussery
Journal:  Nucleic Acids Res       Date:  2007-04-22       Impact factor: 16.971

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