生物
质粒
操纵子
蜡样芽孢杆菌
基因
非核糖体肽
遗传学
突变体
生物合成
细菌
作者
Genia Lücking,Elrike Frenzel,Andrea Rütschle,Sandra Marxen,Timo D. Stark,Thomas Hofmann,Siegfried Scherer,Monika Ehling‐Schulz
标识
DOI:10.3389/fmicb.2015.01101
摘要
The emetic toxin cereulide produced by Bacillus cereus is synthesized by the modular enzyme complex Ces that is encoded on a pXO1-like mega-plasmid. To decipher the role of the genes adjacent to the structural genes cesA/cesB, coding for the nonribosomal peptide synthetase (NRPS), gene inactivation- and overexpression mutants of the emetic strain F4810/72 were constructed and their impact on cereulide biosynthesis was assessed. The hydrolase CesH turned out to be a part of the complex regulatory network controlling cereulide synthesis on a transcriptional Level, while the ABC transporter CesCD was found to be essential for post-translational control of cereulide synthesis. Using a gene inactivation approach, we show that the NRPS activating function of the phosphopantetheinyl transferase (PPtase) embedded in the ces locus was complemented by a chromosomally encoded Sfp-like PPtase, representing an interesting example for the functional interaction between a plasmid encoded NRPS and a chromosomally encoded activation enzyme. In summary, our results highlight the complexity of cereulide biosynthesis and reveal multiple levels of toxin formation control. ces operon internal genes were shown to play a pivotal role by acting at different levels of toxin production, thus complementing the action of the chromosomal key transcriptional regulators AbrB and CodY.
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