首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Identification and Partial Characterization of the Nonribosomal Peptide Synthetase Gene Responsible for Cereulide Production in Emetic Bacillus cereus
【2h】

Identification and Partial Characterization of the Nonribosomal Peptide Synthetase Gene Responsible for Cereulide Production in Emetic Bacillus cereus

机译:鉴定和部分表征负责蜡样芽孢杆菌蜡样内酯生产的非核糖体肽合成酶基因

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Cereulide, a depsipeptide structurally related to valinomycin, is responsible for the emetic type of gastrointestinal disease caused by Bacillus cereus. Due to its chemical structure, (d-O-Leu-d-Ala-l-O-Val-l-Val)3, cereulide might be synthesized nonribosomally. Therefore, degenerate PCR primers targeted to conserved sequence motifs of known nonribosomal peptide synthetase (NRPS) genes were used to amplify gene fragments from a cereulide-producing B. cereus strain. Sequence analysis of one of the amplicons revealed a DNA fragment whose putative gene product showed significant homology to valine activation NRPS modules. The sequences of the flanking regions of this DNA fragment revealed a complete module that is predicted to activate valine, as well as a putative carboxyl-terminal thioesterase domain of the NRPS gene. Disruption of the peptide synthetase gene by insertion of a kanamycin cassette through homologous recombination produced cereulide-deficient mutants. The valine-activating module was highly conserved when sequences from nine emetic B. cereus strains isolated from diverse geographical locations were compared. Primers were designed based on the NRPS sequence, and the resulting PCR assay, targeting the ces gene, was tested by using a panel of 143 B. cereus group strains and 40 strains of other bacterial species showing PCR bands specific for only the cereulide-producing B. cereus strains.
机译:Cereulide(一种与缬氨霉素结构相关的二肽)是引起蜡状芽孢杆菌引起的肠胃疾病的催吐型疾病。由于其化学结构,(d-O-Leu-d-Ala-1-O-Val-I-Val)3,蜡菊内酯可能是非核糖体合成的。因此,靶向已知的非核糖体肽合成酶(NRPS)基因的保守序列基序的简并PCR引物可用于扩增产蜡状芽孢杆菌的蜡状芽孢杆菌菌株的基因片段。扩增子之一的序列分析揭示了一个DNA片段,其推定的基因产物与缬氨酸激活NRPS模块具有显着的同源性。该DNA片段侧翼区的序列揭示了一个完整的模块,该模块预计将激活缬氨酸以及NRPS基因的一个推定的羧基末端硫酯酶结构域。通过同源重组插入卡那霉素盒而破坏肽合成酶基因,产生了蜡样内酯缺陷型突变体。当比较从不同地理位置分离的九种催产蜡状芽孢杆菌菌株的序列时,缬氨酸激活模块高度保守。根据NRPS序列设计引物,并使用一组143蜡状芽孢杆菌组菌株和40个其他细菌种菌株(仅显示产生蜡状芽孢杆菌的PCR谱带)对针对ces基因的PCR检测进行了测试。蜡状芽孢杆菌菌株。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号