Complete genome sequence analysis and Pks genes identification of Brevibacillus brevis FJAT-0809-GLX with a broad inhibitory spectrum against phytopathogens.

IF 4 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jianmei Che, Chengchun Lai, Gongti Lai, Bingxing Chen, Liyuan He, Bo Liu
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引用次数: 0

Abstract

Brevibacillus brevis FJAT-0809-GLX has a broad spectrum of antimicrobial activity. Understanding the molecular basis of biocontrol ability of B. brevis will allow us to develop effective microbial agents for sustainable agriculture. In this study, we present the complete and annotated genome sequence of FJAT-0809-GLX. The complete genome size of B. brevis FJAT-0809-GLX was 6,137,019 bp, with 5688 predicted coding sequences (CDS). The average GC content of 47.38%, and there were 44 copies of the rRNAs operon (16S, 23S and 5S RNA), and 127 tRNA genes. A total of 11,162 genes were functionally annotated with the COG, GO, and KEGG databases, and 123 genes belonged to CAZymes. Genomic secondary metabolite analysis indicated 13 clusters encoding potential new antimicrobials. FJAT-0809-GLX was designated as B. brevis according to average nucleotide polymorphism (ANI) and phylogenetic analysis. The pangenome consisted of 7141 homologous genes, and 4469 homologous genes shared by B. brevis FJAT-0809-GLX, B. brevis NBRC100599, B. brevis DSM30, and B. brevis NCTC2611. The number of unique homologous genes of B. brevis FJAT-0809-GLX (419 genes) and B. brevis NBRC100599 (480 genes) were much more than those in B. brevis DSM30 (13 genes), and B. brevis NCTC2611 (6 genes). Nine gene clusters encoding for secondary metabolite biosynthesis were compared in the genome of B. brevis FJAT-0809-GLX with those of B. brevis NBRC100599, B. brevis DSM30 and B. brevis NCTC2611, and the gene clusters encoding for lantipeptide and transatpks-otherks only existed in genome of B. brevis FJAT-0809-GLX. The 11 BbPks genes were included in the B. brevis FJAT-0809-GLX genome, which contained the conserved PS-DH domain. The relative expression of BbPksL, BbPksM2, BbPksM3, BbPksN3, BbPksN4 and BbPksN5 reached a maximum at 120 h and then decreased at 144 h. Our results provided detailed genomic and Pks genes information for the FJAT-0809-GLX strain, and lid a foundation for studying its biocontrol mechanisms.

对具有广泛植物病原体抑制谱的 Brevibacillus brevis FJAT-0809-GLX 进行全基因组序列分析和 Pks 基因鉴定。
Brevibacillus brevis FJAT-0809-GLX 具有广谱的抗菌活性。了解布雷维氏菌生物防治能力的分子基础将有助于我们开发有效的微生物制剂,促进农业可持续发展。在本研究中,我们展示了 FJAT-0809-GLX 的完整基因组序列和注释。B. brevis FJAT-0809-GLX 的完整基因组大小为 6,137,019 bp,有 5688 个预测编码序列(CDS)。平均 GC 含量为 47.38%,rRNAs 操作子(16S、23S 和 5S RNA)有 44 个拷贝,tRNA 基因有 127 个。COG、GO和KEGG数据库共对11162个基因进行了功能注释,其中123个基因属于CAZymes。基因组次生代谢物分析表明有 13 个基因簇编码潜在的新抗菌素。根据平均核苷酸多态性(ANI)和系统进化分析,FJAT-0809-GLX 被命名为 B. brevis。泛基因组包括 7141 个同源基因,其中 4469 个同源基因为 B. brevis FJAT-0809-GLX、B. brevis NBRC100599、B. brevis DSM30 和 B. brevis NCTC2611 所共有。B. brevis FJAT-0809-GLX(419 个基因)和 B. brevis NBRC100599(480 个基因)的独特同源基因数量远远多于 B. brevis DSM30(13 个基因)和 B. brevis NCTC2611(6 个基因)。与 B. brevis NBRC100599、B. brevis DSM30 和 B. brevis NCTC2611 的基因组相比,FJAT-0809-GLX 的基因组中有 9 个编码次生代谢物生物合成的基因簇,而编码兰肽和 transatpks-otherks 的基因簇只存在于 B. brevis FJAT-0809-GLX 的基因组中。在 B. brevis FJAT-0809-GLX 基因组中包含了 11 个 BbPks 基因,其中含有保守的 PS-DH 结构域。我们的研究结果为 FJAT-0809-GLX 菌株提供了详细的基因组和 Pks 基因信息,为研究其生物防治机制奠定了基础。
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来源期刊
World journal of microbiology & biotechnology
World journal of microbiology & biotechnology 工程技术-生物工程与应用微生物
CiteScore
6.30
自引率
2.40%
发文量
257
审稿时长
2.5 months
期刊介绍: World Journal of Microbiology and Biotechnology publishes research papers and review articles on all aspects of Microbiology and Microbial Biotechnology. Since its foundation, the Journal has provided a forum for research work directed toward finding microbiological and biotechnological solutions to global problems. As many of these problems, including crop productivity, public health and waste management, have major impacts in the developing world, the Journal especially reports on advances for and from developing regions. Some topics are not within the scope of the Journal. Please do not submit your manuscript if it falls into one of the following categories: · Virology · Simple isolation of microbes from local sources · Simple descriptions of an environment or reports on a procedure · Veterinary, agricultural and clinical topics in which the main focus is not on a microorganism · Data reporting on host response to microbes · Optimization of a procedure · Description of the biological effects of not fully identified compounds or undefined extracts of natural origin · Data on not fully purified enzymes or procedures in which they are applied All articles published in the Journal are independently refereed.
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