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来自荧光假单胞菌的四个编码硝吡咯菌素生物合成的基因。

Four genes from Pseudomonas fluorescens that encode the biosynthesis of pyrrolnitrin.

作者信息

Hammer P E, Hill D S, Lam S T, Van Pée K H, Ligon J M

机构信息

Novartis Crop Protection, Inc., Research Triangle Park, North Carolina 27709, USA.

出版信息

Appl Environ Microbiol. 1997 Jun;63(6):2147-54. doi: 10.1128/aem.63.6.2147-2154.1997.

Abstract

Pyrrolnitrin is a secondary metabolite of Pseudomonas and Burkholderia sp. strains with strong antifungal activity. Production of pyrrolnitrin has been correlated with the ability of some bacteria to control plant diseases caused by fungal pathogens, including the damping-off pathogen Rhizoctonia solani. Pseudomonas fluorescens BL915 has been reported to produce pyrrolnitrin and to be an effective biocontrol agent for this pathogen. We have isolated a 32-kb genomic DNA fragment from this strain that contains genes involved in the biosynthesis of pyrrolnitrin. Marker-exchange mutagenesis of this DNA with Tn5 revealed the presence of a 6.2-kb region that contains genes required for the synthesis of pyrrolnitrin. The nucleotide sequence of the 6.2-kb region was determined and found to contain a cluster of four genes that are required for the production of pyrrolnitrin. Deletion mutations in any of the four genes resulted in a pyrrolnitrin-nonproducing phenotype. The putative coding sequences of the four individual genes were cloned by PCR and fused to the tac promoter from Escherichia coli. In each case, the appropriate tac promoter-pyrrolnitrin gene fusion was shown to complement the pyrrolnitrin-negative phenotype of the corresponding deletion mutant. Transfer of the four gene cluster to E. coli resulted in the production of pyrrolnitrin by this organism, thereby demonstrating that the four genes are sufficient for the production of this metabolite and represent all of the genes required to encode the pathway for pyrrolnitrin biosynthesis.

摘要

硝吡咯菌素是假单胞菌属和伯克霍尔德菌属菌株的次生代谢产物,具有很强的抗真菌活性。硝吡咯菌素的产生与一些细菌控制由真菌病原体引起的植物病害的能力有关,包括猝倒病病原体立枯丝核菌。据报道,荧光假单胞菌BL915能产生硝吡咯菌素,并且是这种病原体的有效生物防治剂。我们从该菌株中分离出一个32 kb的基因组DNA片段,其中包含参与硝吡咯菌素生物合成的基因。用Tn5对该DNA进行标记交换诱变,发现存在一个6.2 kb的区域,其中包含合成硝吡咯菌素所需的基因。测定了该6.2 kb区域的核苷酸序列,发现其中包含一组四个基因,这些基因是产生硝吡咯菌素所必需的。四个基因中的任何一个发生缺失突变都会导致不产生硝吡咯菌素的表型。通过PCR克隆了四个单独基因的推定编码序列,并将其与大肠杆菌的tac启动子融合。在每种情况下,适当的tac启动子-硝吡咯菌素基因融合都显示出能互补相应缺失突变体的硝吡咯菌素阴性表型。将这四个基因簇转移到大肠杆菌中,导致该生物体产生硝吡咯菌素,从而证明这四个基因足以产生这种代谢产物,并且代表了编码硝吡咯菌素生物合成途径所需的所有基因。

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