首页 | 本学科首页   官方微博 | 高级检索  
     检索      

胡椒瘟病生防菌 Bacillus subtilis VD18R19 全基因组测序及 比较基因组学分析
引用本文:高圣风,刘爱勤,桑利伟,孙世伟,苟亚峰,王 政,孟倩倩.胡椒瘟病生防菌 Bacillus subtilis VD18R19 全基因组测序及 比较基因组学分析[J].热带作物学报,2018,39(10):2021-2027.
作者姓名:高圣风  刘爱勤  桑利伟  孙世伟  苟亚峰  王 政  孟倩倩
作者单位:1. 中国热带农业科学院香料饮料研究所,海南万宁 571533; 2. 海南省热带香辛饮料作物遗传改良与品质调控重点实验室, 海南万宁 571533
摘    要:Bacillus subtilis VD18R19 具有促进胡椒生长和防治胡椒瘟病的效果,全基因组测序是其分子机理研究和开发 利用的重要基础。本研究采用第二代 Illumina 平台与第三代 PacBio 平台相结合的测序技术,对生防菌 VD18R19 进行 全基因组测序,并进行比较基因组学分析。结果发现,VD18R19 全基因组大小为 4 123 380 bp,GC 含量为 43.80%, 编码基因 4 245 个;含有 tRNA 85 个、rRNA 30 个、sRNA 33 个;含有串联重复序列 60 个,其中小卫星 DNA 43 个、 微卫星 DNA 1 个;共线性分析、core-pan 基因分析及基因家族分析结果均显示 VD18R19 与模式菌株 B. subtilis 168 具 有高度的同源性;antiSMASH 软件预测及同源序列比对结果显示,VD18R19 菌株中含有 6 个抑菌次生代谢产物合成基 因簇,编码 surfactin、plipastatin、bacillibactin、bacilysin、bacillaene、subtilosin A 等抑菌物质,其合成途径涵盖了核 糖体途径、非核糖体途径和聚酮合酶途径。本研究为深入研究生防菌 VD18R19 的分子机理奠定生物信息学基础,有利 于生防菌株及其抑菌次生代谢产物的开发和利用。

关 键 词:枯草芽孢杆菌  全基因组测序  比较基因组学  抑菌物质  基因簇  

Whole Genome Sequencing and Comparative Genomics Analysis of Bacillus subtilis VD18R19 with Biocontrol Activity Against Pepper Phytophtora Rot Disease
GAO Shengfeng LIU Aiqin,SANG Liwei SUN Shiwei GOU Yafeng WANG Zheng MENG Qianqian.Whole Genome Sequencing and Comparative Genomics Analysis of Bacillus subtilis VD18R19 with Biocontrol Activity Against Pepper Phytophtora Rot Disease[J].Chinese Journal of Tropical Crops,2018,39(10):2021-2027.
Authors:GAO Shengfeng LIU Aiqin  SANG Liwei SUN Shiwei GOU Yafeng WANG Zheng MENG Qianqian
Institution:1. Spice and Beverage Research Institute, Chinese Academy of Tropical Agricultural Sciences, Wanning, Hainan 571533, China;  2. Hainan Provincial Key Laboratory of Genetic Improvement and Quality Regulation for Tropical Spice and Beverage Crops, Wanning, Hainan 571533, China
Abstract:Bacillus subtilis VD18R19 has beneficial effects on pepper growth-promoting and bio-control against pepper Phytophtora rot disease. The whole genome sequencing is an important basis for further molecular research and application. The genome was sequenced using a PacBio RS II platform and Illumina HiSeq 4000 platform, and the gene function annotation and comparative genomics analysis were performed using blast alignment tools. The genome is 4 123 380 bp with GC content of 43.80%, 4 245 identified genes, 85 tRNA, 30 rRNA, 33 sRNA, 60 tandem repeat regions including 43 minisatellite DNA and 1 microsatellite DNA. The genome showed highly homologous with the model strain B. subtilis 168 by the analysis of genome synteny, core-pan gene and gene family. It harbors six antibiotic gene clusters, directing synthesis of surfactin, plipastatin, bacillibactin, bacilysin, bacillaene and subtilosin A, through ribosomal synthetases (RS) pathway or non-ribosomal peptide synthetases (NRPS) pathway or polyketide synthases(PKS) pathway. This study would provide a database for further research of diverse molecular biology mechanisms and is helpfull in utilizing the beneficial strain and the functional antibiotics. 
Keywords:Bacillus subtilis  whole genome sequencing  comparative genomics  antibiotic  gene cluster  
本文献已被 CNKI 等数据库收录!
点击此处可从《热带作物学报》浏览原始摘要信息
点击此处可从《热带作物学报》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号